Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 116461 |
| ensemblid | ENSG00000198860.14 |
| hgncid | 16791 |
| symbol | TSEN15 |
| name | tRNA splicing endonuclease subunit 15 |
| refseq_nuc | NM_052965.4 |
| refseq_prot | NP_443197.1 |
| ensembl_nuc | ENST00000645668.2 |
| ensembl_prot | ENSP00000493902.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 184051730 |
| end | 184074212 |
| strand | + |
| ver | v1.2 |
| region | chr1:184051730-184074212 |
| region5000 | chr1:184046730-184079212 |
| regionname0 | TSEN15_chr1_184051730_184074212 |
| regionname5000 | TSEN15_chr1_184046730_184079212 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 171 | 290 | 83 | 55 | 113 | 13 | 24 | 92 | TSEN15_chr1_184046730_184079212 | TSEN15 | MEERG others(166): Show |
chr1 | 184046730 | 184079212 |
| a0002 | 0/0 | 171 | 130 | 12 | 17 | 80 | 5 | 16 | 63 | TSEN15_chr1_184046730_184079212 | TSEN15 | MEERG others(166): Show |
chr1 | 184046730 | 184079212 |
| a0003 | 0/0 | 171 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | MEERG others(166): Show |
chr1 | 184046730 | 184079212 |
| a0004 | 0/0 | 171 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | MEERG others(166): Show |
chr1 | 184046730 | 184079212 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 513 | 290 | 83 | 55 | 113 | 13 | 24 | TSEN15_chr1_184046730_184079212 | TSEN15 | ATGGA others(508): Show |
chr1 | 184046730 | 184079212 | ||
| a0002c0002 | 0/0 | 513 | 130 | 12 | 17 | 80 | 5 | 16 | TSEN15_chr1_184046730_184079212 | TSEN15 | ATGGA others(508): Show |
chr1 | 184046730 | 184079212 | ||
| a0003c0003 | 0/0 | 513 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | ATGGA others(508): Show |
chr1 | 184046730 | 184079212 | ||
| a0004c0004 | 0/0 | 513 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | ATGGA others(508): Show |
chr1 | 184046730 | 184079212 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1907 | 257 | 59 | 52 | 107 | 13 | 24 | TSEN15_chr1_184046730_184079212 | TSEN15 | ACCAC others(1902): Show |
chr1 | 184046730 | 184079212 |
| a0001c0001t0002 | 0/0 | 1907 | 10 | 9 | 1 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | ACCAC others(1902): Show |
chr1 | 184046730 | 184079212 |
| a0001c0001t0004 | 0/0 | 1907 | 6 | 6 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | ACCAC others(1902): Show |
chr1 | 184046730 | 184079212 |
| a0001c0001t0005 | 0/0 | 1907 | 3 | 1 | 2 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | ACCAC others(1902): Show |
chr1 | 184046730 | 184079212 |
| a0001c0001t0006 | 0/0 | 1907 | 3 | 3 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | ACCAC others(1902): Show |
chr1 | 184046730 | 184079212 |
| a0001c0001t0007 | 0/0 | 1907 | 3 | 0 | 0 | 3 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | ACCAC others(1902): Show |
chr1 | 184046730 | 184079212 |
| a0001c0001t0008 | 0/0 | 1907 | 2 | 0 | 0 | 2 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | ACCAC others(1902): Show |
chr1 | 184046730 | 184079212 |
| a0001c0001t0010 | 0/0 | 1907 | 2 | 2 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | ACCAC others(1902): Show |
chr1 | 184046730 | 184079212 |
| a0001c0001t0011 | 0/0 | 1907 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | ACCAC others(1902): Show |
chr1 | 184046730 | 184079212 |
| a0001c0001t0012 | 0/0 | 1907 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | ACCAC others(1902): Show |
chr1 | 184046730 | 184079212 |
| a0001c0001t0013 | 0/0 | 1907 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | ACCAC others(1902): Show |
chr1 | 184046730 | 184079212 |
| a0001c0001t0014 | 0/0 | 1907 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | ACCAC others(1902): Show |
chr1 | 184046730 | 184079212 |
| a0002c0002t0001 | 0/0 | 1907 | 121 | 10 | 14 | 78 | 4 | 15 | TSEN15_chr1_184046730_184079212 | TSEN15 | ACCAC others(1902): Show |
chr1 | 184046730 | 184079212 |
| a0002c0002t0003 | 0/0 | 1907 | 7 | 2 | 3 | 0 | 1 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | ACCAC others(1902): Show |
chr1 | 184046730 | 184079212 |
| a0002c0002t0009 | 0/0 | 1907 | 2 | 0 | 0 | 2 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | ACCAC others(1902): Show |
chr1 | 184046730 | 184079212 |
| a0003c0003t0001 | 0/0 | 1907 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | ACCAC others(1902): Show |
chr1 | 184046730 | 184079212 |
| a0004c0004t0001 | 0/0 | 1907 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | ACCAC others(1902): Show |
chr1 | 184046730 | 184079212 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 60 | 1 | 5 | 50 | 0 | 4 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0004 | 0/0 | 16 | 1 | 4 | 10 | 0 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0006 | 0/0 | 10 | 1 | 0 | 8 | 1 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0008 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0010 | 0/0 | 7 | 0 | 5 | 0 | 0 | 2 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0011 | 0/0 | 7 | 0 | 5 | 0 | 2 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0012 | 0/0 | 6 | 1 | 2 | 0 | 1 | 2 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0013 | 0/0 | 6 | 2 | 2 | 2 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0014 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0016 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0017 | 1/0 | 4 | 0 | 3 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0022 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0023 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0033 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0002g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0002g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0002g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0004g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0005g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0007g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0007g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0008g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0008g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0010g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0010g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0011g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0012g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0013g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0001c0001t0014g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0002 | 0/0 | 37 | 0 | 1 | 31 | 1 | 4 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0003 | 0/0 | 21 | 4 | 5 | 9 | 0 | 3 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0005 | 0/0 | 15 | 0 | 0 | 12 | 1 | 2 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0026 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0027 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0003g0002 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0002c0002t0009g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0003c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| a0004c0004t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | GBR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00099 | hp2 | a0002 | c0002 | t0003 | g0002 | EUR | GBR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0026 | EUR | GBR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | GBR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | FIN | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0078 | EUR | FIN | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | FIN | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | CHS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00558 | hp2 | a0001 | c0001 | t0007 | g0036 | EAS | CHS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | CHS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | CHS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0026 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0079 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0026 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01070 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01071 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0092 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0034 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0041 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0034 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0041 | AMR | CLM | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | IBS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0056 | AFR | ACB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0133 | AMR | PEL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01978 | hp2 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PEL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | KHV | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | KHV | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | KHV | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02129 | hp2 | a0001 | c0001 | t0012 | g0028 | EAS | KHV | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | KHV | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | CDX | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CDX | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CDX | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | ACB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0081 | AFR | ACB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02615 | hp1 | a0001 | c0001 | t0011 | g0138 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02647 | hp1 | a0001 | c0001 | t0014 | g0102 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0087 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0088 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0083 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02922 | hp2 | a0003 | c0003 | t0001 | g0085 | AFR | ESN | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02965 | hp1 | a0002 | c0002 | t0003 | g0002 | AFR | ESN | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02976 | hp1 | a0001 | c0001 | t0013 | g0080 | AFR | ESN | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0027 | AFR | ESN | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | MSL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | MSL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | MSL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0104 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0137 | SAS | PJL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | BEB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0043 | SAS | BEB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0130 | SAS | STU | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | STU | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | STU | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0073 | SAS | STU | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | STU | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | YRI | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | YRI | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | YRI | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18949 | hp2 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18971 | hp2 | a0002 | c0002 | t0009 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18974 | hp1 | a0001 | c0001 | t0007 | g0044 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19007 | hp1 | a0002 | c0002 | t0009 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19010 | hp1 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | LWK | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | LWK | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | LWK | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19065 | hp1 | a0001 | c0001 | t0008 | g0119 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19072 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19081 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ASW | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0005 | EUR | TSI | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | TSI | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | TSI | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA20905 | hp1 | a0002 | c0002 | t0003 | g0072 | SAS | GIH | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02486 | hp2 | a0001 | c0001 | t0010 | g0135 | AFR | ACB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG06807 | hp1 | a0002 | c0002 | t0003 | g0049 | AFR | USA | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | USA | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | USA | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA21309 | hp1 | a0001 | c0001 | t0010 | g0136 | AFR | LWK | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0082 | AFR | LWK | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0063 | REF | REF | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0017 | REF | REF | TSEN15_chr1_184046730_184079212 | TSEN15 | chr1 | 184046730 | 184079212 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:184051801 | C | A | 1 | a0003 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.46C>A | p.Leu16Met | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/5 | 72/1907 | 46/516 | 16/171 | chr1 | 184051801 | |||
| chr1:184051811 | G | A | 2 | a0002 a0003 |
131 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(128): Show |
missense_variant | MODERATE | c.56G>A | p.Gly19Asp | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/5 | 82/1907 | 56/516 | 19/171 | chr1 | 184051811 | |||
| chr1:184051856 | C | T | 1 | a0004 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.101C>T | p.Ala34Val | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/5 | 127/1907 | 101/516 | 34/171 | chr1 | 184051856 | |||
| chr1:184054395 | A | C | 2 | a0002 a0003 |
131 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(128): Show |
missense_variant | MODERATE | c.177A>C | p.Gln59His | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 2/5 | 203/1907 | 177/516 | 59/171 | chr1 | 184054395 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:184072924 | T | C | 1 | a0002c0002t0003 | 7 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*77T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 77 | chr1 | 184072924 | ||||||
| chr1:184072929 | A | G | 1 | a0001c0001t0010 | 2 | HG02486.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*82A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 82 | chr1 | 184072929 | ||||||
| chr1:184072944 | C | G | 1 | a0001c0001t0010 | 2 | HG02486.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*97C>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 97 | chr1 | 184072944 | ||||||
| chr1:184073193 | C | T | 1 | a0001c0001t0014 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*346C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 346 | chr1 | 184073193 | ||||||
| chr1:184073264 | G | A | 1 | a0001c0001t0010 | 2 | HG02486.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*417G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 417 | chr1 | 184073264 | ||||||
| chr1:184073378 | T | C | 1 | a0001c0001t0011 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*531T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 531 | chr1 | 184073378 | ||||||
| chr1:184073447 | T | G | 1 | a0001c0001t0008 | 2 | NA19010.hp1 NA19065.hp1 |
3_prime_UTR_variant | MODIFIER | c.*600T>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 600 | chr1 | 184073447 | ||||||
| chr1:184073497 | T | C | 1 | a0001c0001t0010 | 2 | HG02486.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*650T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 650 | chr1 | 184073497 | ||||||
| chr1:184073557 | C | G | 1 | a0001c0001t0010 | 2 | HG02486.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*710C>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 710 | chr1 | 184073557 | ||||||
| chr1:184073602 | T | G | 1 | a0001c0001t0004 | 6 | HG02896.hp2 HG02897.hp1 HG03041.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*755T>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 755 | chr1 | 184073602 | ||||||
| chr1:184073643 | A | G | 1 | a0001c0001t0002 | 10 | HG02004.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*796A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 796 | chr1 | 184073643 | ||||||
| chr1:184073681 | C | T | 1 | a0001c0001t0007 | 3 | HG00558.hp2 NA18974.hp1 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*834C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 834 | chr1 | 184073681 | ||||||
| chr1:184073744 | A | G | 1 | a0001c0001t0013 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*897A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 897 | chr1 | 184073744 | ||||||
| chr1:184073806 | T | C | 1 | a0001c0001t0005 | 3 | HG01099.hp1 HG01109.hp1 HG01884.hp2 |
3_prime_UTR_variant | MODIFIER | c.*959T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 959 | chr1 | 184073806 | ||||||
| chr1:184073848 | G | A | 1 | a0001c0001t0005 | 3 | HG01099.hp1 HG01109.hp1 HG01884.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1001G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 1001 | chr1 | 184073848 | ||||||
| chr1:184073895 | T | C | 1 | a0001c0001t0006 | 3 | HG02451.hp1 HG02818.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1048T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 1048 | chr1 | 184073895 | ||||||
| chr1:184073904 | A | G | 1 | a0002c0002t0009 | 2 | NA18971.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1057A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 1057 | chr1 | 184073904 | ||||||
| chr1:184074000 | A | T | 1 | a0001c0001t0010 | 2 | HG02486.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1153A>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 1153 | chr1 | 184074000 | ||||||
| chr1:184074009 | C | A | 2 | a0001c0001t0005 a0001c0001t0010 |
5 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1162C>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 1162 | chr1 | 184074009 | ||||||
| chr1:184074168 | A | G | 1 | a0001c0001t0010 | 2 | HG02486.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1321A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 1321 | chr1 | 184074168 | ||||||
| chr1:184074185 | T | G | 1 | a0001c0001t0012 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1338T>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 5/5 | 1338 | chr1 | 184074185 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:184051975 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.135+85T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184051975 | |||||||
| chr1:184051999 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0139 a0001c0001t0001g0140 |
6 | HG02280.hp2 HG02559.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+109C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184051999 | |||||||
| chr1:184052042 | A | G | 1 | a0001c0001t0001g0054 | 2 | HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.135+152A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184052042 | |||||||
| chr1:184052101 | C | T | 1 | a0001c0001t0011g0138 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.135+211C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184052101 | |||||||
| chr1:184052133 | C | T | 1 | a0002c0002t0001g0137 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.135+243C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184052133 | |||||||
| chr1:184052170 | A | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.135+280A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184052170 | |||||||
| chr1:184052186 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.135+296A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184052186 | |||||||
| chr1:184052187 | G | A | 2 | a0001c0001t0005g0034 a0001c0001t0005g0056 |
3 | HG01099.hp1 HG01109.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.135+297G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184052187 | |||||||
| chr1:184052187 | G | T | 1 | a0002c0002t0001g0133 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.135+297G>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184052187 | |||||||
| chr1:184052485 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.135+595C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184052485 | |||||||
| chr1:184052506 | A | G | 2 | a0001c0001t0005g0034 a0001c0001t0005g0056 |
3 | HG01099.hp1 HG01109.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.135+616A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184052506 | |||||||
| chr1:184052557 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.135+667G>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184052557 | |||||||
| chr1:184052739 | TC | T | 2 | a0002c0002t0001g0024 a0002c0002t0001g0058 |
4 | NA18972.hp1 NA18975.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+852delC | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 184052739 | ||||||
| chr1:184052841 | A | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0053 a0001c0001t0001g0131 |
7 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+951A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184052841 | |||||||
| chr1:184052925 | C | T | 2 | a0001c0001t0005g0034 a0001c0001t0005g0056 |
3 | HG01099.hp1 HG01109.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.135+1035C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184052925 | |||||||
| chr1:184053056 | C | T | 119 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(116): Show |
303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.135+1166C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184053056 | |||||||
| chr1:184053081 | G | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.135+1191G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184053081 | |||||||
| chr1:184053465 | T | C | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.136-889T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184053465 | |||||||
| chr1:184053501 | C | T | 1 | a0002c0002t0001g0130 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.136-853C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184053501 | |||||||
| chr1:184053659 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.136-695G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184053659 | |||||||
| chr1:184053665 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.136-689G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184053665 | |||||||
| chr1:184053697 | A | G | 5 | a0001c0001t0001g0033 a0001c0001t0001g0126 a0001c0001t0001g0127 others(2): Show |
7 | HG02258.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-657A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184053697 | |||||||
| chr1:184053864 | C | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0125 |
4 | HG02723.hp1 HG02809.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-490C>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184053864 | |||||||
| chr1:184053873 | G | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.136-481G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184053873 | |||||||
| chr1:184053887 | G | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0123 a0001c0001t0001g0124 |
8 | HG00735.hp1 HG01255.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-467G>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184053887 | |||||||
| chr1:184053925 | C | T | 22 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(19): Show |
62 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.136-429C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184053925 | |||||||
| chr1:184053943 | A | C | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.136-411A>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184053943 | |||||||
| chr1:184054016 | G | A | 1 | a0002c0002t0003g0072 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.136-338G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184054016 | |||||||
| chr1:184054021 | A | G | 1 | a0001c0001t0011g0138 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.136-333A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184054021 | |||||||
| chr1:184054205 | A | G | 1 | a0001c0001t0011g0138 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.136-149A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184054205 | |||||||
| chr1:184054243 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.136-111A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 1/4 | chr1 | 184054243 | |||||||
| chr1:184054455 | T | G | 1 | a0001c0001t0001g0115 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.217+20T>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 2/4 | chr1 | 184054455 | |||||||
| chr1:184054481 | G | A | 1 | a0002c0002t0001g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.217+46G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 2/4 | chr1 | 184054481 | |||||||
| chr1:184054583 | C | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.218-145C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 2/4 | chr1 | 184054583 | |||||||
| chr1:184054630 | C | T | 3 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0002c0002t0001g0130 |
3 | HG02486.hp2 HG04115.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.218-98C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 2/4 | chr1 | 184054630 | |||||||
| chr1:184054658 | G | C | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.218-70G>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 2/4 | chr1 | 184054658 | |||||||
| chr1:184054712 | A | G | 3 | a0002c0002t0001g0021 a0002c0002t0001g0112 a0002c0002t0001g0113 |
6 | HG00544.hp2 HG00621.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.218-16A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 2/4 | chr1 | 184054712 | |||||||
| chr1:184054914 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.353+51A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184054914 | |||||||
| chr1:184054938 | C | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+75C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184054938 | |||||||
| chr1:184054962 | G | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+99G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184054962 | |||||||
| chr1:184054985 | A | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0110 a0001c0001t0001g0111 |
6 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.353+122A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184054985 | |||||||
| chr1:184055069 | TA | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(143): Show |
409 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(406): Show |
intron_variant | MODIFIER | c.353+216delA | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 184055069 | ||||||
| chr1:184055144 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.353+281G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184055144 | |||||||
| chr1:184055190 | G | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+327G>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184055190 | |||||||
| chr1:184055238 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.353+375A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184055238 | |||||||
| chr1:184055373 | T | C | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | HG01192.hp2 HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.353+510T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184055373 | |||||||
| chr1:184055416 | T | C | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+553T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184055416 | |||||||
| chr1:184055424 | A | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+561A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184055424 | |||||||
| chr1:184055599 | G | A | 5 | a0002c0002t0001g0026 a0002c0002t0001g0041 a0002c0002t0001g0078 others(2): Show |
8 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.353+736G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184055599 | |||||||
| chr1:184055803 | ATAATG | A | 1 | a0001c0001t0001g0015 | 5 | HG01891.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.353+945_353+949del others(5): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 184055803 | ||||||
| chr1:184055896 | G | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+1033G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184055896 | |||||||
| chr1:184055981 | A | AAAAATCT others(301): Show |
1 | a0001c0001t0010g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.353+1133_353+1134i others(310): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 184055981 | ||||||
| chr1:184056293 | T | C | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+1430T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184056293 | |||||||
| chr1:184056422 | T | G | 2 | a0001c0001t0005g0034 a0001c0001t0005g0056 |
3 | HG01099.hp1 HG01109.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.353+1559T>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184056422 | |||||||
| chr1:184056672 | A | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+1809A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184056672 | |||||||
| chr1:184056710 | C | G | 5 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0050 others(2): Show |
10 | HG02004.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.353+1847C>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184056710 | |||||||
| chr1:184056754 | A | C | 1 | a0001c0001t0010g0135 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.353+1891A>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184056754 | |||||||
| chr1:184057013 | T | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+2150T>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184057013 | |||||||
| chr1:184057145 | A | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+2282A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184057145 | |||||||
| chr1:184057153 | C | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+2290C>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184057153 | |||||||
| chr1:184057163 | C | T | 1 | a0002c0002t0001g0107 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.353+2300C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184057163 | |||||||
| chr1:184057169 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.353+2306C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184057169 | |||||||
| chr1:184057205 | A | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+2342A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184057205 | |||||||
| chr1:184057268 | G | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+2405G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184057268 | |||||||
| chr1:184057271 | G | C | 5 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0050 others(2): Show |
10 | HG02004.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.353+2408G>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184057271 | |||||||
| chr1:184057367 | A | G | 1 | a0002c0002t0001g0113 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.353+2504A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184057367 | |||||||
| chr1:184057438 | C | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+2575C>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184057438 | |||||||
| chr1:184057575 | G | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+2712G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184057575 | |||||||
| chr1:184057676 | G | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+2813G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184057676 | |||||||
| chr1:184057801 | G | A | 1 | a0002c0002t0001g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.353+2938G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184057801 | |||||||
| chr1:184058146 | T | G | 1 | a0001c0001t0013g0080 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.353+3283T>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184058146 | |||||||
| chr1:184058209 | C | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+3346C>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184058209 | |||||||
| chr1:184058324 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.353+3461A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184058324 | |||||||
| chr1:184058354 | G | A | 4 | a0001c0001t0005g0034 a0001c0001t0005g0056 a0001c0001t0010g0135 others(1): Show |
5 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.353+3491G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184058354 | |||||||
| chr1:184058542 | T | C | 34 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(31): Show |
88 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.353+3679T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184058542 | |||||||
| chr1:184058637 | G | A | 2 | a0001c0001t0005g0034 a0001c0001t0005g0056 |
3 | HG01099.hp1 HG01109.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.353+3774G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184058637 | |||||||
| chr1:184058811 | G | T | 1 | a0001c0001t0001g0111 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.353+3948G>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184058811 | |||||||
| chr1:184058866 | T | G | 1 | a0002c0002t0001g0112 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.353+4003T>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184058866 | |||||||
| chr1:184058899 | T | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+4036T>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184058899 | |||||||
| chr1:184058930 | G | A | 5 | a0001c0001t0001g0033 a0001c0001t0001g0126 a0001c0001t0001g0127 others(2): Show |
7 | HG02258.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.353+4067G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184058930 | |||||||
| chr1:184058982 | A | T | 1 | a0001c0001t0001g0070 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.353+4119A>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184058982 | |||||||
| chr1:184059022 | T | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+4159T>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184059022 | |||||||
| chr1:184059032 | C | CT | 26 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(23): Show |
67 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.353+4185dupT | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 184059032 | ||||||
| chr1:184059032 | CT | C | 9 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0126 others(6): Show |
12 | HG00558.hp1 HG00558.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.353+4185delT | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 184059032 | ||||||
| chr1:184059070 | T | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+4207T>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184059070 | |||||||
| chr1:184059141 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.353+4278G>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184059141 | |||||||
| chr1:184059157 | A | C | 1 | a0002c0002t0001g0048 | 2 | NA18964.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.353+4294A>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184059157 | |||||||
| chr1:184059302 | T | C | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+4439T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184059302 | |||||||
| chr1:184059562 | G | T | 3 | a0001c0001t0010g0135 a0001c0001t0010g0136 a0002c0002t0001g0106 |
3 | HG02486.hp2 NA18999.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.353+4699G>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184059562 | |||||||
| chr1:184059656 | C | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+4793C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184059656 | |||||||
| chr1:184059657 | G | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | HG01192.hp2 HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.353+4794G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184059657 | |||||||
| chr1:184059663 | C | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+4800C>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184059663 | |||||||
| chr1:184059690 | C | T | 1 | a0002c0002t0001g0105 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.353+4827C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184059690 | |||||||
| chr1:184059696 | A | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0053 a0001c0001t0001g0131 |
7 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.353+4833A>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184059696 | |||||||
| chr1:184059768 | G | A | 4 | a0001c0001t0005g0034 a0001c0001t0005g0056 a0001c0001t0010g0135 others(1): Show |
5 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.353+4905G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184059768 | |||||||
| chr1:184059778 | C | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+4915C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184059778 | |||||||
| chr1:184059790 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.353+4927C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184059790 | |||||||
| chr1:184059866 | T | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+5003T>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184059866 | |||||||
| chr1:184059937 | C | G | 1 | a0002c0002t0001g0104 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.353+5074C>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184059937 | |||||||
| chr1:184059997 | C | T | 2 | a0001c0001t0005g0034 a0001c0001t0005g0056 |
3 | HG01099.hp1 HG01109.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.353+5134C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184059997 | |||||||
| chr1:184060011 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.353+5148A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060011 | |||||||
| chr1:184060024 | A | T | 1 | a0001c0001t0001g0031 | 3 | HG02622.hp2 HG02896.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.353+5161A>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060024 | |||||||
| chr1:184060127 | T | C | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+5264T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060127 | |||||||
| chr1:184060202 | A | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+5339A>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060202 | |||||||
| chr1:184060219 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.353+5356T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060219 | |||||||
| chr1:184060296 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0110 |
5 | HG01884.hp1 HG01891.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.353+5433C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060296 | |||||||
| chr1:184060318 | C | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+5455C>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060318 | |||||||
| chr1:184060327 | G | A | 1 | a0001c0001t0001g0054 | 2 | HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.353+5464G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060327 | |||||||
| chr1:184060341 | C | T | 1 | a0001c0001t0001g0015 | 5 | HG01891.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.353+5478C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060341 | |||||||
| chr1:184060342 | G | A | 2 | a0001c0001t0005g0034 a0001c0001t0005g0056 |
3 | HG01099.hp1 HG01109.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.353+5479G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060342 | |||||||
| chr1:184060385 | G | C | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+5522G>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060385 | |||||||
| chr1:184060584 | A | G | 34 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(31): Show |
88 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.353+5721A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060584 | |||||||
| chr1:184060585 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.353+5722C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060585 | |||||||
| chr1:184060661 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0121 a0001c0001t0010g0135 others(1): Show |
10 | HG00741.hp2 HG01106.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.353+5798C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060661 | |||||||
| chr1:184060692 | C | T | 1 | a0002c0002t0001g0103 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.353+5829C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060692 | |||||||
| chr1:184060720 | C | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+5857C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060720 | |||||||
| chr1:184060732 | C | A | 1 | a0002c0002t0001g0086 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.353+5869C>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060732 | |||||||
| chr1:184060781 | CAGTT | C | 41 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(38): Show |
131 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.353+5921_353+5924d others(6): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 184060781 | ||||||
| chr1:184060816 | T | G | 2 | a0001c0001t0005g0034 a0001c0001t0005g0056 |
3 | HG01099.hp1 HG01109.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.353+5953T>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060816 | |||||||
| chr1:184060859 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(6): Show |
28 | HG00735.hp1 HG00741.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.353+5996C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060859 | |||||||
| chr1:184060898 | A | G | 1 | a0002c0002t0001g0095 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.353+6035A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060898 | |||||||
| chr1:184060963 | C | G | 1 | a0001c0001t0001g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.353+6100C>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060963 | |||||||
| chr1:184060982 | G | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+6119G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184060982 | |||||||
| chr1:184061012 | C | G | 1 | a0001c0001t0011g0138 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.353+6149C>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184061012 | |||||||
| chr1:184061038 | T | C | 1 | a0001c0001t0002g0108 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.353+6175T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184061038 | |||||||
| chr1:184061062 | A | T | 1 | a0002c0002t0001g0094 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.353+6199A>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184061062 | |||||||
| chr1:184061087 | T | C | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+6224T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184061087 | |||||||
| chr1:184061096 | G | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+6233G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184061096 | |||||||
| chr1:184061125 | T | C | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+6262T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184061125 | |||||||
| chr1:184061349 | A | G | 1 | a0002c0002t0001g0093 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.353+6486A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184061349 | |||||||
| chr1:184061384 | A | G | 2 | a0001c0001t0005g0034 a0001c0001t0005g0056 |
3 | HG01099.hp1 HG01109.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.353+6521A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184061384 | |||||||
| chr1:184061387 | C | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+6524C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184061387 | |||||||
| chr1:184061390 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.353+6527C>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184061390 | |||||||
| chr1:184061440 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.353+6577T>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184061440 | |||||||
| chr1:184061530 | C | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+6667C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184061530 | |||||||
| chr1:184061707 | A | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+6844A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184061707 | |||||||
| chr1:184061714 | G | C | 1 | a0002c0002t0001g0041 | 2 | HG01099.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.353+6851G>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184061714 | |||||||
| chr1:184061748 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.353+6885T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184061748 | |||||||
| chr1:184061759 | T | A | 1 | a0002c0002t0001g0112 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.353+6896T>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184061759 | |||||||
| chr1:184061921 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0004g0007 |
10 | HG02886.hp2 HG02896.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.353+7058C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184061921 | |||||||
| chr1:184061927 | G | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+7064G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184061927 | |||||||
| chr1:184061930 | T | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+7067T>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184061930 | |||||||
| chr1:184061936 | A | G | 4 | a0001c0001t0005g0034 a0001c0001t0005g0056 a0001c0001t0010g0135 others(1): Show |
5 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.353+7073A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184061936 | |||||||
| chr1:184062427 | A | C | 34 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(31): Show |
88 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.353+7564A>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184062427 | |||||||
| chr1:184062517 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.353+7654T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184062517 | |||||||
| chr1:184062566 | A | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+7703A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184062566 | |||||||
| chr1:184062756 | T | G | 5 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0050 others(2): Show |
10 | HG02004.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.353+7893T>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184062756 | |||||||
| chr1:184062787 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
4 | HG01168.hp1 HG01169.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.353+7924C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184062787 | |||||||
| chr1:184062860 | A | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.353+7997A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184062860 | |||||||
| chr1:184062887 | A | T | 1 | a0001c0001t0001g0068 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.353+8024A>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184062887 | |||||||
| chr1:184063123 | G | T | 1 | a0001c0001t0001g0067 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.353+8260G>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184063123 | |||||||
| chr1:184063124 | T | G | 1 | a0001c0001t0001g0067 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.353+8261T>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184063124 | |||||||
| chr1:184063126 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.353+8263C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184063126 | |||||||
| chr1:184063171 | C | T | 21 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(18): Show |
60 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.353+8308C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184063171 | |||||||
| chr1:184063269 | G | A | 119 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(116): Show |
303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.353+8406G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184063269 | |||||||
| chr1:184063455 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.353+8592G>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184063455 | |||||||
| chr1:184063601 | C | T | 2 | a0001c0001t0005g0034 a0001c0001t0005g0056 |
3 | HG01099.hp1 HG01109.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.354-8556C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184063601 | |||||||
| chr1:184063733 | C | T | 1 | a0001c0001t0001g0052 | 2 | HG01175.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.354-8424C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184063733 | |||||||
| chr1:184063761 | C | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-8396C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184063761 | |||||||
| chr1:184063911 | T | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-8246T>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184063911 | |||||||
| chr1:184064060 | C | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-8097C>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184064060 | |||||||
| chr1:184064088 | A | G | 1 | a0002c0002t0001g0130 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.354-8069A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184064088 | |||||||
| chr1:184064356 | A | T | 1 | a0001c0001t0001g0129 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.354-7801A>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184064356 | |||||||
| chr1:184064467 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.354-7690G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184064467 | |||||||
| chr1:184064546 | A | AAAACAAA others(5): Show |
2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-7601_354-7590d others(14): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 184064546 | ||||||
| chr1:184064546 | AAAAC | A | 1 | a0001c0001t0002g0030 | 3 | HG02145.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.354-7593_354-7590d others(6): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 184064546 | ||||||
| chr1:184064562 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0110 a0001c0001t0001g0111 |
6 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.354-7595C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184064562 | |||||||
| chr1:184064571 | C | T | 26 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0016 others(23): Show |
60 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.354-7586C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184064571 | |||||||
| chr1:184064665 | C | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-7492C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184064665 | |||||||
| chr1:184064898 | C | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-7259C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184064898 | |||||||
| chr1:184065024 | G | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-7133G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184065024 | |||||||
| chr1:184065041 | G | T | 34 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(31): Show |
88 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.354-7116G>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184065041 | |||||||
| chr1:184065067 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.354-7090G>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184065067 | |||||||
| chr1:184065104 | G | A | 1 | a0002c0002t0001g0094 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.354-7053G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184065104 | |||||||
| chr1:184065183 | T | TAC | 33 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(30): Show |
84 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.354-6953_354-6952d others(4): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 184065183 | ||||||
| chr1:184065183 | T | TACAC | 4 | a0001c0001t0001g0054 a0001c0001t0001g0059 a0001c0001t0002g0030 others(1): Show |
7 | HG02145.hp1 HG02602.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.354-6955_354-6952d others(6): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 184065183 | ||||||
| chr1:184065183 | T | TACACACA others(3): Show |
2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-6967_354-6966i others(12): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 184065183 | ||||||
| chr1:184065305 | A | G | 1 | a0001c0001t0014g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.354-6852A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184065305 | |||||||
| chr1:184065446 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.354-6711T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184065446 | |||||||
| chr1:184065604 | C | G | 1 | a0001c0001t0001g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.354-6553C>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184065604 | |||||||
| chr1:184065657 | A | G | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0016 others(30): Show |
70 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.354-6500A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184065657 | |||||||
| chr1:184065661 | C | T | 119 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(116): Show |
303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.354-6496C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184065661 | |||||||
| chr1:184065982 | A | G | 41 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(38): Show |
131 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.354-6175A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184065982 | |||||||
| chr1:184066060 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.354-6097A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184066060 | |||||||
| chr1:184066181 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.354-5976T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184066181 | |||||||
| chr1:184066286 | CTATT | C | 42 | a0001c0001t0011g0138 a0002c0002t0001g0002 a0002c0002t0001g0003 others(39): Show |
132 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.354-5867_354-5864d others(6): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 184066286 | ||||||
| chr1:184066342 | A | C | 26 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0016 others(23): Show |
60 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.354-5815A>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184066342 | |||||||
| chr1:184066388 | T | C | 1 | a0002c0002t0001g0112 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.354-5769T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184066388 | |||||||
| chr1:184066415 | T | G | 1 | a0001c0001t0006g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.354-5742T>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184066415 | |||||||
| chr1:184066530 | T | C | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-5627T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184066530 | |||||||
| chr1:184066550 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0008g0119 |
2 | HG02451.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.354-5607C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184066550 | |||||||
| chr1:184066649 | G | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-5508G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184066649 | |||||||
| chr1:184066698 | G | T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0126 a0001c0001t0001g0127 others(2): Show |
7 | HG02258.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.354-5459G>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184066698 | |||||||
| chr1:184066805 | C | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-5352C>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184066805 | |||||||
| chr1:184066988 | G | A | 2 | a0001c0001t0005g0034 a0001c0001t0005g0056 |
3 | HG01099.hp1 HG01109.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.354-5169G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184066988 | |||||||
| chr1:184067029 | G | A | 1 | a0001c0001t0001g0039 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.354-5128G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067029 | |||||||
| chr1:184067119 | C | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-5038C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067119 | |||||||
| chr1:184067150 | A | G | 1 | a0001c0001t0001g0045 | 2 | HG00280.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.354-5007A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067150 | |||||||
| chr1:184067196 | TG | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0042 a0001c0001t0001g0084 others(1): Show |
13 | HG02280.hp1 HG02630.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.354-4960delG | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067196 | |||||||
| chr1:184067231 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.354-4926A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067231 | |||||||
| chr1:184067425 | A | G | 1 | a0001c0001t0001g0038 | 2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.354-4732A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067425 | |||||||
| chr1:184067471 | C | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-4686C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067471 | |||||||
| chr1:184067778 | A | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-4379A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067778 | |||||||
| chr1:184067787 | T | C | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-4370T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067787 | |||||||
| chr1:184067828 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0018 |
9 | NA18951.hp1 NA18953.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.354-4329C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067828 | |||||||
| chr1:184067862 | G | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-4295G>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067862 | |||||||
| chr1:184067909 | C | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-4248C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067909 | |||||||
| chr1:184067924 | C | CA | 15 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0117 others(12): Show |
40 | HG00280.hp2 HG01943.hp2 HG02451.hp1 others(37): Show |
intron_variant | MODIFIER | c.354-4215dupA | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 184067924 | ||||||
| chr1:184067924 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0005g0056 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.354-4229_354-4215d others(17): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 184067924 | ||||||
| chr1:184067924 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0005g0034 | 2 | HG01099.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.354-4230_354-4215d others(18): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 184067924 | ||||||
| chr1:184067939 | AAAAT | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 |
6 | HG02258.hp1 HG02886.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.354-4216_354-4213d others(6): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 184067939 | ||||||
| chr1:184067940 | AAAT | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0060 others(3): Show |
9 | HG00558.hp1 HG00558.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.354-4215_354-4213d others(5): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 184067940 | ||||||
| chr1:184067941 | A | AT | 10 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(7): Show |
28 | HG00735.hp1 HG00741.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.354-4216_354-4215i others(3): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067941 | |||||||
| chr1:184067941 | A | ATAT | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0120 |
5 | HG01070.hp2 HG01106.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.354-4216_354-4215i others(5): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067941 | |||||||
| chr1:184067941 | A | T | 1 | a0001c0001t0001g0016 | 2 | NA18970.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.354-4216A>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067941 | |||||||
| chr1:184067941 | AAT | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(27): Show |
79 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.354-4187_354-4186d others(4): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 184067941 | ||||||
| chr1:184067941 | AATAT | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(14): Show |
63 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.354-4189_354-4186d others(6): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 184067941 | ||||||
| chr1:184067942 | AT | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0018 others(21): Show |
55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.354-4214delT | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067942 | |||||||
| chr1:184067942 | ATAT | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0047 others(3): Show |
7 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.354-4214_354-4212d others(5): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067942 | |||||||
| chr1:184067943 | T | A | 44 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0028 others(41): Show |
98 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.354-4214T>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067943 | |||||||
| chr1:184067945 | T | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0025 others(37): Show |
94 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.354-4212T>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067945 | |||||||
| chr1:184067947 | T | A | 17 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0061 others(14): Show |
27 | HG01069.hp2 HG01106.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.354-4210T>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067947 | |||||||
| chr1:184067949 | T | A | 5 | a0001c0001t0001g0055 a0001c0001t0001g0097 a0001c0001t0010g0135 others(2): Show |
7 | HG01069.hp2 HG02135.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.354-4208T>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067949 | |||||||
| chr1:184067951 | T | A | 1 | a0002c0002t0001g0089 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.354-4206T>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067951 | |||||||
| chr1:184067953 | T | C | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-4204T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067953 | |||||||
| chr1:184067956 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0010g0135 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.354-4197_354-4174d others(26): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 184067956 | ||||||
| chr1:184067990 | G | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-4167G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184067990 | |||||||
| chr1:184068085 | A | T | 1 | a0001c0001t0010g0135 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.354-4072A>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184068085 | |||||||
| chr1:184068200 | G | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-3957G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184068200 | |||||||
| chr1:184068269 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.354-3888C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184068269 | |||||||
| chr1:184068339 | C | A | 1 | a0001c0001t0001g0042 | 2 | HG02280.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.354-3818C>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184068339 | |||||||
| chr1:184068432 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.354-3725C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184068432 | |||||||
| chr1:184068503 | C | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0064 others(2): Show |
14 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.354-3654C>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184068503 | |||||||
| chr1:184068563 | C | T | 1 | a0002c0002t0001g0092 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.354-3594C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184068563 | |||||||
| chr1:184068620 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.354-3537G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184068620 | |||||||
| chr1:184068632 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.354-3525G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184068632 | |||||||
| chr1:184068935 | A | G | 3 | a0002c0002t0001g0019 a0002c0002t0001g0087 a0003c0003t0001g0085 |
6 | HG02559.hp2 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.354-3222A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184068935 | |||||||
| chr1:184068960 | C | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-3197C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184068960 | |||||||
| chr1:184069009 | A | C | 119 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(116): Show |
303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.354-3148A>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184069009 | |||||||
| chr1:184069017 | C | T | 119 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(116): Show |
303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.354-3140C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184069017 | |||||||
| chr1:184069463 | A | G | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-2694A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184069463 | |||||||
| chr1:184069647 | C | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-2510C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184069647 | |||||||
| chr1:184069727 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.354-2430A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184069727 | |||||||
| chr1:184069731 | T | C | 1 | a0001c0001t0001g0031 | 3 | HG02622.hp2 HG02896.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.354-2426T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184069731 | |||||||
| chr1:184069901 | T | C | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | HG01192.hp2 HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.354-2256T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184069901 | |||||||
| chr1:184070010 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.354-2147A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184070010 | |||||||
| chr1:184070137 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0042 a0001c0001t0001g0084 others(1): Show |
13 | HG02280.hp1 HG02630.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.354-2020T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184070137 | |||||||
| chr1:184070148 | T | A | 1 | a0001c0001t0001g0098 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.354-2009T>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184070148 | |||||||
| chr1:184070601 | T | A | 34 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(31): Show |
88 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.354-1556T>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184070601 | |||||||
| chr1:184070740 | A | G | 1 | a0001c0001t0010g0135 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.354-1417A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184070740 | |||||||
| chr1:184070747 | G | C | 1 | a0002c0002t0001g0090 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.354-1410G>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184070747 | |||||||
| chr1:184070761 | G | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-1396G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184070761 | |||||||
| chr1:184070777 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0042 a0001c0001t0001g0084 others(1): Show |
13 | HG02280.hp1 HG02630.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.354-1380A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184070777 | |||||||
| chr1:184070796 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.354-1361C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184070796 | |||||||
| chr1:184070803 | G | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-1354G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184070803 | |||||||
| chr1:184070835 | T | A | 2 | a0002c0002t0001g0024 a0002c0002t0001g0058 |
4 | NA18972.hp1 NA18975.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-1322T>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184070835 | |||||||
| chr1:184070974 | A | G | 1 | a0001c0001t0001g0037 | 2 | NA18975.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.354-1183A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184070974 | |||||||
| chr1:184071037 | A | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0061 |
2 | HG02602.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.354-1120A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071037 | |||||||
| chr1:184071160 | A | G | 1 | a0002c0002t0001g0088 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.354-997A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071160 | |||||||
| chr1:184071187 | T | C | 1 | a0001c0001t0001g0051 | 2 | HG01496.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.354-970T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071187 | |||||||
| chr1:184071198 | C | T | 1 | a0001c0001t0001g0012 | 6 | HG01261.hp2 HG01346.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.354-959C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071198 | |||||||
| chr1:184071257 | T | G | 4 | a0001c0001t0005g0034 a0001c0001t0005g0056 a0001c0001t0010g0135 others(1): Show |
5 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.354-900T>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071257 | |||||||
| chr1:184071396 | C | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-761C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071396 | |||||||
| chr1:184071438 | C | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-719C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071438 | |||||||
| chr1:184071496 | T | C | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-661T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071496 | |||||||
| chr1:184071554 | G | A | 1 | a0002c0002t0001g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.354-603G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071554 | |||||||
| chr1:184071589 | G | T | 1 | a0001c0001t0013g0080 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.354-568G>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071589 | |||||||
| chr1:184071836 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.354-321T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071836 | |||||||
| chr1:184071932 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-225A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071932 | |||||||
| chr1:184071934 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-223C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071934 | |||||||
| chr1:184071937 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-220T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071937 | |||||||
| chr1:184071941 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-216T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071941 | |||||||
| chr1:184071943 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-214T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071943 | |||||||
| chr1:184071947 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-210T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071947 | |||||||
| chr1:184071950 | C | CCCACCCC others(13): Show |
1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-207_354-206ins others(20): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071950 | |||||||
| chr1:184071951 | T | G | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-206T>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071951 | |||||||
| chr1:184071953 | C | G | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-204C>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071953 | |||||||
| chr1:184071963 | A | C | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-194A>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071963 | |||||||
| chr1:184071964 | A | C | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-193A>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071964 | |||||||
| chr1:184071967 | A | C | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-190A>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071967 | |||||||
| chr1:184071973 | A | C | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-184A>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071973 | |||||||
| chr1:184071973 | A | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-184A>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071973 | |||||||
| chr1:184071980 | A | T | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-177A>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071980 | |||||||
| chr1:184071981 | A | T | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-176A>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071981 | |||||||
| chr1:184071984 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-173T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071984 | |||||||
| chr1:184071988 | T | A | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-169T>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071988 | |||||||
| chr1:184071990 | A | T | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-167A>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071990 | |||||||
| chr1:184071992 | A | C | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-165A>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071992 | |||||||
| chr1:184071994 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-163T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071994 | |||||||
| chr1:184071998 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-159C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071998 | |||||||
| chr1:184071999 | C | G | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-158C>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184071999 | |||||||
| chr1:184072002 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-155A>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184072002 | |||||||
| chr1:184072005 | A | C | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354-152A>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184072005 | |||||||
| chr1:184072006 | C | A | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-151C>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184072006 | |||||||
| chr1:184072007 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-150T>C | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184072007 | |||||||
| chr1:184072008 | C | A | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-149C>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184072008 | |||||||
| chr1:184072012 | T | G | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-145T>G | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184072012 | |||||||
| chr1:184072014 | TTATTTTT others(28): Show |
T | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-142_354-108del others(35): Show |
TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184072014 | |||||||
| chr1:184072059 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.354-98C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184072059 | |||||||
| chr1:184072123 | G | A | 1 | a0002c0002t0001g0091 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.354-34G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 3/4 | chr1 | 184072123 | |||||||
| chr1:184072352 | G | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.495+54G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 4/4 | chr1 | 184072352 | |||||||
| chr1:184072439 | G | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.495+141G>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 4/4 | chr1 | 184072439 | |||||||
| chr1:184072495 | C | CA | 35 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(32): Show |
89 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.495+207dupA | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 184072495 | ||||||
| chr1:184072589 | G | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.496-238G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 4/4 | chr1 | 184072589 | |||||||
| chr1:184072592 | G | A | 5 | a0001c0001t0001g0033 a0001c0001t0001g0126 a0001c0001t0001g0127 others(2): Show |
7 | HG02258.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.496-235G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 4/4 | chr1 | 184072592 | |||||||
| chr1:184072626 | T | TA | 3 | a0001c0001t0001g0020 a0001c0001t0001g0067 a0001c0001t0001g0110 |
6 | HG01884.hp1 HG01891.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-194dupA | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 184072626 | ||||||
| chr1:184072634 | C | T | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.496-193C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 4/4 | chr1 | 184072634 | |||||||
| chr1:184072664 | C | T | 1 | a0001c0001t0013g0080 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.496-163C>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 4/4 | chr1 | 184072664 | |||||||
| chr1:184072785 | G | T | 1 | a0001c0001t0001g0035 | 2 | HG00099.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.496-42G>T | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 4/4 | chr1 | 184072785 | |||||||
| chr1:184072792 | G | A | 2 | a0001c0001t0010g0135 a0001c0001t0010g0136 |
2 | HG02486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.496-35G>A | TSEN15 | ENSG00000198860.14 | transcript | ENST00000645668.2 | protein_coding | 4/4 | chr1 | 184072792 |