Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 255411 |
| ensemblid | ENSG00000257987.6 |
| hgncid | 48628 |
| symbol | TEX49 |
| name | sperm microtubule inner protein 11 |
| refseq_nuc | NM_001351123.2 |
| refseq_prot | NP_001338052.1 |
| ensembl_nuc | ENST00000548380.6 |
| ensembl_prot | ENSP00000489652.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 48727435 |
| end | 48765790 |
| strand | + |
| ver | v1.2 |
| region | chr12:48727435-48765790 |
| region5000 | chr12:48722435-48770790 |
| regionname0 | TEX49_chr12_48727435_48765790 |
| regionname5000 | TEX49_chr12_48722435_48770790 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 131 | 319 | 82 | 64 | 118 | 14 | 39 | 90 | TEX49_chr12_48722435_48770790 | TEX49 | MAFFN others(126): Show |
chr12 | 48722435 | 48770790 |
| a0002 | 0/0 | 131 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | MAFFN others(126): Show |
chr12 | 48722435 | 48770790 |
| a0003 | 0/0 | 131 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | MAFFN others(126): Show |
chr12 | 48722435 | 48770790 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 393 | 317 | 81 | 64 | 118 | 14 | 38 | TEX49_chr12_48722435_48770790 | TEX49 | ATGGC others(388): Show |
chr12 | 48722435 | 48770790 | ||
| a0001c0003 | 0/0 | 393 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | ATGGC others(388): Show |
chr12 | 48722435 | 48770790 | ||
| a0001c0004 | 0/0 | 393 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | ATGGC others(388): Show |
chr12 | 48722435 | 48770790 | ||
| a0002c0002 | 0/0 | 393 | 2 | 0 | 2 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | ATGGC others(388): Show |
chr12 | 48722435 | 48770790 | ||
| a0003c0005 | 0/0 | 393 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | ATGGC others(388): Show |
chr12 | 48722435 | 48770790 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 577 | 303 | 81 | 64 | 106 | 14 | 36 | TEX49_chr12_48722435_48770790 | TEX49 | AGTGC others(572): Show |
chr12 | 48722435 | 48770790 |
| a0001c0001t0002 | 0/0 | 577 | 11 | 0 | 0 | 10 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | AGTGC others(572): Show |
chr12 | 48722435 | 48770790 |
| a0001c0001t0003 | 0/0 | 577 | 2 | 0 | 0 | 2 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | AGTGC others(572): Show |
chr12 | 48722435 | 48770790 |
| a0001c0001t0004 | 0/0 | 577 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | AGTGC others(572): Show |
chr12 | 48722435 | 48770790 |
| a0001c0003t0001 | 0/0 | 577 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | AGTGC others(572): Show |
chr12 | 48722435 | 48770790 |
| a0001c0004t0001 | 0/0 | 577 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | AGTGC others(572): Show |
chr12 | 48722435 | 48770790 |
| a0002c0002t0001 | 0/0 | 577 | 2 | 0 | 2 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | AGTGC others(572): Show |
chr12 | 48722435 | 48770790 |
| a0003c0005t0001 | 0/0 | 577 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | AGTGC others(572): Show |
chr12 | 48722435 | 48770790 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0001c0004t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| a0003c0005t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | GBR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | GBR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | FIN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | FIN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | FIN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | CHS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0171 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0172 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | IBS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | IBS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0284 | EUR | IBS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | IBS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0298 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CDX | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0316 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | STU | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0287 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03710 | hp1 | a0003 | c0005 | t0001 | g0203 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | BEB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | BEB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0219 | SAS | STU | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | STU | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | STU | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | STU | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | STU | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | YRI | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | YRI | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | LWK | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ASW | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ASW | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | TSI | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | TSI | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | GIH | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | GIH | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | USA | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | USA | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | USA | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | LWK | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | LWK | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0059 | REF | REF | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0031 | REF | REF | TEX49_chr12_48722435_48770790 | TEX49 | chr12 | 48722435 | 48770790 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48759271 | G | A | 1 | a0002 | 2 | HG01257.hp1 HG01258.hp2 |
missense_variant | MODERATE | c.142G>A | p.Val48Met | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/4 | 188/577 | 142/396 | 48/131 | chr12 | 48759271 | |||
| chr12:48764916 | G | T | 1 | a0003 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.268G>T | p.Asp90Tyr | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 3/4 | 314/577 | 268/396 | 90/131 | chr12 | 48764916 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48759322 | T | C | 1 | a0001c0003 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.193T>C | p.Leu65Leu | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/4 | 239/577 | 193/396 | 65/131 | chr12 | 48759322 | |||
| chr12:48764987 | G | C | 1 | a0001c0004 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.339G>C | p.Ala113Ala | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 3/4 | 385/577 | 339/396 | 113/131 | chr12 | 48764987 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48727447 | T | C | 1 | a0001c0001t0003 | 2 | HG02071.hp1 HG02080.hp2 |
5_prime_UTR_variant | MODIFIER | c.-34T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/4 | 34 | chr12 | 48727447 | ||||||
| chr12:48765743 | A | G | 1 | a0001c0001t0004 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*88A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 4/4 | 88 | chr12 | 48765743 | ||||||
| chr12:48765752 | A | C | 1 | a0001c0001t0002 | 11 | HG00423.hp1 HG03654.hp2 NA18952.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*97A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 4/4 | 97 | chr12 | 48765752 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48727560 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
2 | HG01516.hp1 HG01517.hp2 |
splice_donor_variant&intron_variant | HIGH | c.79+1G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48727560 | |||||||
| chr12:48727733 | C | A | 1 | a0001c0001t0001g0008 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.79+174C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48727733 | |||||||
| chr12:48727737 | T | A | 1 | a0001c0001t0001g0009 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.79+178T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48727737 | |||||||
| chr12:48727895 | A | G | 7 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+336A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48727895 | |||||||
| chr12:48728038 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.79+479G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728038 | |||||||
| chr12:48728048 | CA | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
191 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.79+502delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48728048 | ||||||
| chr12:48728078 | A | C | 1 | a0001c0004t0001g0316 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.79+519A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728078 | |||||||
| chr12:48728109 | G | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
190 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.79+550G>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728109 | |||||||
| chr12:48728170 | C | CT | 11 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(8): Show |
11 | HG02027.hp1 NA18970.hp1 NA18984.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+612dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48728170 | ||||||
| chr12:48728237 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01257.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.79+678C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728237 | |||||||
| chr12:48728239 | A | G | 2 | a0001c0001t0003g0297 a0001c0001t0003g0298 |
2 | HG02071.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.79+680A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728239 | |||||||
| chr12:48728404 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79+845T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728404 | |||||||
| chr12:48728614 | A | G | 7 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(4): Show |
7 | HG02055.hp2 HG02735.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+1055A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728614 | |||||||
| chr12:48728633 | G | A | 1 | a0001c0001t0001g0011 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.79+1074G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728633 | |||||||
| chr12:48728653 | A | T | 1 | a0001c0001t0001g0296 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.79+1094A>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728653 | |||||||
| chr12:48728661 | T | G | 1 | a0001c0001t0001g0296 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.79+1102T>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728661 | |||||||
| chr12:48728662 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.79+1103C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728662 | |||||||
| chr12:48728707 | C | CA | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(5): Show |
8 | HG01978.hp2 HG02055.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+1172dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48728707 | ||||||
| chr12:48728707 | CA | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.79+1172delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48728707 | ||||||
| chr12:48728707 | CAA | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0288 a0001c0001t0001g0289 others(7): Show |
10 | HG01081.hp1 HG01346.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+1171_79+1172del others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48728707 | ||||||
| chr12:48728707 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79+1162_79+1172del others(11): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48728707 | ||||||
| chr12:48728806 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.79+1247T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728806 | |||||||
| chr12:48728994 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG00621.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.79+1435G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48728994 | |||||||
| chr12:48729046 | A | G | 6 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(3): Show |
6 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+1487A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729046 | |||||||
| chr12:48729123 | C | T | 1 | a0001c0003t0001g0287 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.79+1564C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729123 | |||||||
| chr12:48729130 | T | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
191 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.79+1571T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729130 | |||||||
| chr12:48729140 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.79+1581G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729140 | |||||||
| chr12:48729175 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0288 |
2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.79+1616G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729175 | |||||||
| chr12:48729244 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.79+1685A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729244 | |||||||
| chr12:48729254 | A | T | 6 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(3): Show |
6 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+1695A>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729254 | |||||||
| chr12:48729257 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.79+1698C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729257 | |||||||
| chr12:48729263 | C | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | HG02818.hp1 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.79+1704C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729263 | |||||||
| chr12:48729318 | A | G | 7 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+1759A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729318 | |||||||
| chr12:48729526 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.79+1967T>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729526 | |||||||
| chr12:48729533 | C | CA | 28 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(25): Show |
28 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.79+1984dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48729533 | ||||||
| chr12:48729576 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.79+2017G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729576 | |||||||
| chr12:48729624 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG00099.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.79+2065C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729624 | |||||||
| chr12:48729707 | T | TA | 12 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(9): Show |
12 | HG00741.hp2 HG01175.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+2168dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48729707 | ||||||
| chr12:48729707 | TA | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(91): Show |
95 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.79+2168delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48729707 | ||||||
| chr12:48729707 | TAA | T | 11 | a0001c0001t0001g0122 a0001c0001t0001g0128 a0001c0001t0001g0129 others(8): Show |
11 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+2167_79+2168del others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48729707 | ||||||
| chr12:48729738 | A | C | 1 | a0001c0004t0001g0316 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.79+2179A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729738 | |||||||
| chr12:48729874 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.79+2315T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48729874 | |||||||
| chr12:48730260 | G | A | 1 | a0001c0001t0002g0189 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.79+2701G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48730260 | |||||||
| chr12:48730308 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.79+2749G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48730308 | |||||||
| chr12:48730397 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.79+2838C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48730397 | |||||||
| chr12:48730429 | C | G | 2 | a0001c0001t0001g0281 a0001c0001t0002g0280 |
2 | NA18942.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.79+2870C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48730429 | |||||||
| chr12:48730551 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.79+2992G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48730551 | |||||||
| chr12:48730712 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.79+3153T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48730712 | |||||||
| chr12:48730724 | G | A | 1 | a0001c0001t0001g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79+3165G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48730724 | |||||||
| chr12:48730892 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.79+3333C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48730892 | |||||||
| chr12:48731092 | C | G | 1 | a0001c0001t0001g0286 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79+3533C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48731092 | |||||||
| chr12:48731141 | C | A | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.79+3582C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48731141 | |||||||
| chr12:48731244 | G | A | 42 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(39): Show |
42 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.79+3685G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48731244 | |||||||
| chr12:48731261 | C | G | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(48): Show |
51 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.79+3702C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48731261 | |||||||
| chr12:48731360 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
192 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.79+3801A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48731360 | |||||||
| chr12:48731451 | A | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0288 |
2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.79+3892A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48731451 | |||||||
| chr12:48731490 | C | CA | 10 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(7): Show |
10 | HG00733.hp2 HG00735.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+3944dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48731490 | ||||||
| chr12:48731631 | A | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+4072A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48731631 | |||||||
| chr12:48731674 | T | A | 1 | a0001c0001t0001g0296 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.79+4115T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48731674 | |||||||
| chr12:48731919 | C | T | 2 | a0001c0001t0001g0296 a0001c0001t0001g0311 |
2 | HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.79+4360C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48731919 | |||||||
| chr12:48732010 | G | A | 11 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+4451G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48732010 | |||||||
| chr12:48732110 | C | G | 7 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+4551C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48732110 | |||||||
| chr12:48732127 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
104 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.79+4568C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48732127 | |||||||
| chr12:48732146 | C | CA | 6 | a0001c0001t0001g0010 a0001c0001t0001g0070 a0001c0001t0001g0071 others(3): Show |
6 | HG00544.hp1 HG00673.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+4603dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48732146 | ||||||
| chr12:48732146 | CA | C | 8 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(5): Show |
8 | HG02818.hp1 HG02965.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+4603delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48732146 | ||||||
| chr12:48732146 | CAA | C | 7 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+4602_79+4603del others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48732146 | ||||||
| chr12:48732362 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.79+4803G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48732362 | |||||||
| chr12:48732643 | G | A | 7 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(4): Show |
7 | HG02818.hp1 HG02965.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+5084G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48732643 | |||||||
| chr12:48732685 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.79+5126G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48732685 | |||||||
| chr12:48732825 | G | A | 15 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(12): Show |
15 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.79+5266G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48732825 | |||||||
| chr12:48732979 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.79+5420G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48732979 | |||||||
| chr12:48733072 | C | CT | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
214 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.79+5534dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48733072 | ||||||
| chr12:48733072 | C | CTT | 76 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0018 others(73): Show |
77 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.79+5533_79+5534dup others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48733072 | ||||||
| chr12:48733072 | C | CTTT | 26 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(23): Show |
26 | HG00323.hp2 HG00621.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.79+5532_79+5534dup others(3): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48733072 | ||||||
| chr12:48733123 | G | A | 6 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0196 others(3): Show |
6 | HG00423.hp2 HG00558.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+5564G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48733123 | |||||||
| chr12:48733230 | C | A | 1 | a0001c0001t0001g0032 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.79+5671C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48733230 | |||||||
| chr12:48733381 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.79+5822G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48733381 | |||||||
| chr12:48733424 | C | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
192 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.79+5865C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48733424 | |||||||
| chr12:48733606 | T | C | 1 | a0001c0001t0001g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79+6047T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48733606 | |||||||
| chr12:48733764 | C | CT | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.79+6228dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48733764 | ||||||
| chr12:48733764 | C | CTT | 28 | a0001c0001t0001g0068 a0001c0001t0001g0074 a0001c0001t0001g0113 others(25): Show |
28 | HG00621.hp1 HG00621.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.79+6227_79+6228dup others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48733764 | ||||||
| chr12:48733764 | CT | C | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(33): Show |
36 | HG00323.hp2 HG01070.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.79+6228delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48733764 | ||||||
| chr12:48733852 | C | A | 1 | a0001c0001t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.79+6293C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48733852 | |||||||
| chr12:48733914 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.79+6355G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48733914 | |||||||
| chr12:48733924 | C | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0288 |
2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.79+6365C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48733924 | |||||||
| chr12:48734150 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.79+6591G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48734150 | |||||||
| chr12:48734478 | A | G | 29 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(26): Show |
29 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.79+6919A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48734478 | |||||||
| chr12:48734739 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0278 |
2 | HG01123.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.79+7180C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48734739 | |||||||
| chr12:48734796 | G | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0080 |
2 | HG03516.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.79+7237G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48734796 | |||||||
| chr12:48734799 | C | A | 1 | a0001c0001t0001g0081 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.79+7240C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48734799 | |||||||
| chr12:48734833 | C | A | 1 | a0001c0001t0001g0130 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.79+7274C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48734833 | |||||||
| chr12:48734998 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.79+7439T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48734998 | |||||||
| chr12:48735003 | C | CA | 125 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(122): Show |
126 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.79+7464dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48735003 | ||||||
| chr12:48735003 | C | CAA | 40 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(37): Show |
40 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.79+7463_79+7464dup others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48735003 | ||||||
| chr12:48735003 | C | CAAA | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
134 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.79+7462_79+7464dup others(3): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48735003 | ||||||
| chr12:48735003 | C | CAAAA | 16 | a0001c0001t0001g0008 a0001c0001t0001g0148 a0001c0001t0001g0154 others(13): Show |
16 | HG00642.hp2 HG00673.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.79+7461_79+7464dup others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48735003 | ||||||
| chr12:48735024 | G | A | 6 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(3): Show |
6 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+7465G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48735024 | |||||||
| chr12:48735025 | A | C | 1 | a0001c0001t0001g0211 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.79+7466A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48735025 | |||||||
| chr12:48735330 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79+7771G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48735330 | |||||||
| chr12:48735456 | G | A | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | HG01346.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.79+7897G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48735456 | |||||||
| chr12:48735534 | G | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0282 a0001c0001t0001g0294 others(1): Show |
4 | HG01346.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+7975G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48735534 | |||||||
| chr12:48735582 | T | C | 7 | a0001c0001t0001g0125 a0001c0001t0001g0310 a0001c0001t0001g0311 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+8023T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48735582 | |||||||
| chr12:48735587 | A | AAAAT | 12 | a0001c0001t0001g0010 a0001c0001t0001g0125 a0001c0001t0001g0282 others(9): Show |
12 | HG01109.hp2 HG01346.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+8042_79+8045dup others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48735587 | ||||||
| chr12:48735666 | G | A | 28 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(25): Show |
28 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.79+8107G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48735666 | |||||||
| chr12:48735713 | G | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0186 a0001c0001t0001g0226 others(11): Show |
15 | HG02056.hp1 HG02080.hp1 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.79+8154G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48735713 | |||||||
| chr12:48735831 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79+8272C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48735831 | |||||||
| chr12:48735863 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.79+8304G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48735863 | |||||||
| chr12:48736126 | C | A | 1 | a0001c0001t0001g0296 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.79+8567C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48736126 | |||||||
| chr12:48736156 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0288 |
2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.79+8597G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48736156 | |||||||
| chr12:48736208 | A | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0282 a0001c0001t0001g0294 others(2): Show |
5 | HG01346.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+8649A>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48736208 | |||||||
| chr12:48736244 | G | C | 52 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(49): Show |
52 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.79+8685G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48736244 | |||||||
| chr12:48736413 | C | CA | 23 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0063 others(20): Show |
23 | HG00621.hp2 HG00733.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.79+8876dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48736413 | ||||||
| chr12:48736413 | CA | C | 42 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(39): Show |
42 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.79+8876delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48736413 | ||||||
| chr12:48736695 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.79+9136G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48736695 | |||||||
| chr12:48736699 | G | GT | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
155 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.79+9153dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48736699 | ||||||
| chr12:48736758 | T | C | 4 | a0001c0001t0001g0310 a0001c0001t0001g0312 a0001c0001t0001g0313 others(1): Show |
4 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+9199T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48736758 | |||||||
| chr12:48737012 | A | C | 52 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(49): Show |
52 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.79+9453A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737012 | |||||||
| chr12:48737053 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.79+9494G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737053 | |||||||
| chr12:48737100 | C | G | 29 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(26): Show |
29 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.79+9541C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737100 | |||||||
| chr12:48737243 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.79+9684G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737243 | |||||||
| chr12:48737281 | G | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0086 a0001c0001t0001g0115 |
3 | HG00738.hp1 HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.79+9722G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737281 | |||||||
| chr12:48737415 | A | AT | 13 | a0001c0001t0001g0010 a0001c0001t0001g0061 a0001c0001t0001g0062 others(10): Show |
13 | HG00642.hp2 HG01070.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.79+9872dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48737415 | ||||||
| chr12:48737415 | AT | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0162 a0001c0001t0001g0267 others(3): Show |
6 | HG01884.hp1 HG02970.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+9872delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48737415 | ||||||
| chr12:48737483 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.79+9924C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737483 | |||||||
| chr12:48737544 | A | T | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG01433.hp2 HG01496.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.79+9985A>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737544 | |||||||
| chr12:48737568 | C | A | 28 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(25): Show |
28 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.79+10009C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737568 | |||||||
| chr12:48737575 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
193 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.79+10016T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737575 | |||||||
| chr12:48737616 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.79+10057T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737616 | |||||||
| chr12:48737677 | A | C | 7 | a0001c0001t0001g0125 a0001c0001t0001g0310 a0001c0001t0001g0311 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+10118A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737677 | |||||||
| chr12:48737697 | G | A | 7 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(4): Show |
7 | HG02818.hp1 HG02965.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+10138G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737697 | |||||||
| chr12:48737702 | A | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0288 |
2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.79+10143A>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737702 | |||||||
| chr12:48737831 | C | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0125 a0001c0001t0001g0282 others(9): Show |
12 | HG01109.hp2 HG01346.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+10272C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737831 | |||||||
| chr12:48737888 | T | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0282 a0001c0001t0001g0294 others(1): Show |
4 | HG01346.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+10329T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737888 | |||||||
| chr12:48737906 | C | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0125 a0001c0001t0001g0282 others(9): Show |
12 | HG01109.hp2 HG01346.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+10347C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737906 | |||||||
| chr12:48737925 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0302 |
2 | HG02818.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.79+10366C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48737925 | |||||||
| chr12:48738013 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.79+10454C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48738013 | |||||||
| chr12:48738014 | G | A | 7 | a0001c0001t0001g0125 a0001c0001t0001g0310 a0001c0001t0001g0311 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+10455G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48738014 | |||||||
| chr12:48738028 | T | C | 1 | a0001c0004t0001g0316 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.79+10469T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48738028 | |||||||
| chr12:48738350 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
188 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.79+10791T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48738350 | |||||||
| chr12:48738369 | CATATAAT others(8): Show |
C | 7 | a0001c0001t0001g0125 a0001c0001t0001g0310 a0001c0001t0001g0311 others(4): Show |
7 | HG01109.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+10813_79+10827d others(17): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48738369 | ||||||
| chr12:48738512 | T | C | 1 | a0001c0001t0004g0219 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.79+10953T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48738512 | |||||||
| chr12:48738539 | CT | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
141 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.79+10993delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48738539 | ||||||
| chr12:48738620 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.79+11061C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48738620 | |||||||
| chr12:48738858 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0060 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.79+11299C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48738858 | |||||||
| chr12:48738924 | C | CT | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
178 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.79+11377dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48738924 | ||||||
| chr12:48738974 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
142 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.79+11415C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48738974 | |||||||
| chr12:48739015 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0306 |
2 | NA18967.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.79+11456C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739015 | |||||||
| chr12:48739084 | C | T | 1 | a0001c0001t0001g0300 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.79+11525C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739084 | |||||||
| chr12:48739339 | G | A | 4 | a0001c0001t0001g0310 a0001c0001t0001g0312 a0001c0001t0001g0313 others(1): Show |
4 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+11780G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739339 | |||||||
| chr12:48739366 | A | T | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | HG00733.hp2 HG00735.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.79+11807A>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739366 | |||||||
| chr12:48739499 | A | C | 3 | a0001c0001t0001g0079 a0001c0001t0001g0086 a0001c0001t0001g0115 |
3 | HG00738.hp1 HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.79+11940A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739499 | |||||||
| chr12:48739500 | ATTAC | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0086 a0001c0001t0001g0115 |
3 | HG00738.hp1 HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.79+11942_79+11945d others(6): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739500 | |||||||
| chr12:48739505 | C | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0086 a0001c0001t0001g0115 |
3 | HG00738.hp1 HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.79+11946C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739505 | |||||||
| chr12:48739567 | G | A | 1 | a0001c0001t0001g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79+12008G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739567 | |||||||
| chr12:48739571 | G | A | 2 | a0001c0001t0001g0238 a0001c0001t0002g0285 |
2 | NA19065.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.79+12012G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739571 | |||||||
| chr12:48739574 | T | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0036 others(11): Show |
14 | HG01346.hp2 HG02559.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.79+12015T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739574 | |||||||
| chr12:48739578 | C | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
192 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.79+12019C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739578 | |||||||
| chr12:48739595 | A | C | 1 | a0001c0001t0001g0150 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.79+12036A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739595 | |||||||
| chr12:48739708 | A | G | 1 | a0001c0001t0002g0264 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.79+12149A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739708 | |||||||
| chr12:48739734 | A | G | 3 | a0001c0001t0001g0282 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG01346.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.79+12175A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739734 | |||||||
| chr12:48739735 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.79+12176C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739735 | |||||||
| chr12:48739822 | C | T | 10 | a0001c0001t0001g0186 a0001c0001t0001g0226 a0001c0001t0001g0227 others(7): Show |
10 | HG02129.hp2 NA18944.hp2 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.79+12263C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739822 | |||||||
| chr12:48739901 | C | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0179 others(1): Show |
4 | HG01175.hp1 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+12342C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739901 | |||||||
| chr12:48739942 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
153 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.79+12383C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48739942 | |||||||
| chr12:48740051 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0282 a0001c0001t0001g0294 others(1): Show |
4 | HG01346.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+12492T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48740051 | |||||||
| chr12:48740451 | A | G | 1 | a0001c0001t0001g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79+12892A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48740451 | |||||||
| chr12:48740493 | CT | C | 14 | a0001c0001t0001g0032 a0001c0001t0001g0084 a0001c0001t0001g0087 others(11): Show |
14 | HG00323.hp1 HG01256.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.79+12951delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48740493 | ||||||
| chr12:48740495 | T | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
90 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.79+12936T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48740495 | |||||||
| chr12:48740496 | T | C | 4 | a0001c0001t0001g0032 a0001c0001t0001g0239 a0001c0001t0001g0240 others(1): Show |
4 | HG02647.hp1 NA18950.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+12937T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48740496 | |||||||
| chr12:48740521 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.79+12962C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48740521 | |||||||
| chr12:48740549 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.79+12990T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48740549 | |||||||
| chr12:48740660 | C | CT | 6 | a0001c0001t0001g0144 a0001c0001t0001g0156 a0001c0001t0001g0157 others(3): Show |
6 | HG00741.hp2 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+13116dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48740660 | ||||||
| chr12:48740703 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.79+13144G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48740703 | |||||||
| chr12:48740881 | T | C | 291 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(288): Show |
296 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.79+13322T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48740881 | |||||||
| chr12:48740917 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0288 |
2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.79+13358G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48740917 | |||||||
| chr12:48741069 | C | CT | 13 | a0001c0001t0001g0034 a0001c0001t0001g0114 a0001c0001t0001g0140 others(10): Show |
13 | HG00423.hp2 HG00741.hp1 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.79+13531dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48741069 | ||||||
| chr12:48741069 | CT | C | 50 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0037 others(47): Show |
50 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.79+13531delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48741069 | ||||||
| chr12:48741183 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
141 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.79+13624C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48741183 | |||||||
| chr12:48741468 | C | CCGATATG others(3): Show |
8 | a0001c0001t0001g0010 a0001c0001t0001g0162 a0001c0001t0001g0163 others(5): Show |
8 | HG01346.hp2 HG01884.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+13909_79+13910i others(12): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48741468 | |||||||
| chr12:48741469 | G | A | 27 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(24): Show |
27 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.79+13910G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48741469 | |||||||
| chr12:48741619 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.79+14060T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48741619 | |||||||
| chr12:48741647 | C | CT | 11 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0088 others(8): Show |
11 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.79+14105dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48741647 | ||||||
| chr12:48741775 | G | A | 6 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+14216G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48741775 | |||||||
| chr12:48741886 | G | A | 5 | a0001c0001t0001g0144 a0001c0001t0001g0156 a0001c0001t0001g0157 others(2): Show |
5 | HG02818.hp1 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+14327G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48741886 | |||||||
| chr12:48741987 | T | C | 6 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(3): Show |
6 | HG02615.hp1 HG02717.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+14428T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48741987 | |||||||
| chr12:48742021 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0038 |
2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.79+14462T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742021 | |||||||
| chr12:48742081 | T | A | 11 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+14522T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742081 | |||||||
| chr12:48742082 | T | A | 18 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(15): Show |
18 | HG01167.hp2 HG01169.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.79+14523T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742082 | |||||||
| chr12:48742204 | A | C | 1 | a0001c0001t0001g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79+14645A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742204 | |||||||
| chr12:48742276 | TC | T | 11 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0077 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+14719delC | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48742276 | ||||||
| chr12:48742277 | C | CT | 14 | a0001c0001t0001g0119 a0001c0001t0001g0145 a0001c0001t0001g0146 others(11): Show |
14 | HG00642.hp2 HG01256.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.79+14718_79+14719i others(3): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742277 | |||||||
| chr12:48742277 | C | CTT | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
121 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.79+14718_79+14719i others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742277 | |||||||
| chr12:48742277 | C | CTTT | 7 | a0001c0001t0001g0140 a0001c0001t0001g0155 a0001c0001t0001g0211 others(4): Show |
7 | HG01361.hp2 HG02080.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+14718_79+14719i others(5): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742277 | |||||||
| chr12:48742278 | C | T | 303 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(300): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.79+14719C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742278 | |||||||
| chr12:48742281 | T | TC | 3 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0288 |
3 | HG02486.hp2 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.79+14722_79+14723i others(3): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742281 | |||||||
| chr12:48742282 | T | C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0027 others(3): Show |
6 | HG01884.hp2 HG02451.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+14723T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742282 | |||||||
| chr12:48742285 | T | C | 1 | a0001c0001t0001g0011 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.79+14726T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742285 | |||||||
| chr12:48742285 | T | TTC | 7 | a0001c0001t0001g0187 a0001c0001t0001g0212 a0001c0001t0001g0215 others(4): Show |
7 | HG00639.hp2 HG00741.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+14727_79+14728i others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48742285 | ||||||
| chr12:48742358 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0296 |
3 | HG02559.hp2 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.79+14799C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742358 | |||||||
| chr12:48742442 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.79+14883C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742442 | |||||||
| chr12:48742478 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.79+14919T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742478 | |||||||
| chr12:48742522 | T | A | 1 | a0001c0001t0001g0093 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.79+14963T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742522 | |||||||
| chr12:48742568 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | HG01255.hp1 HG03654.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.79+15009G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742568 | |||||||
| chr12:48742682 | G | C | 3 | a0001c0001t0001g0310 a0001c0001t0001g0312 a0001c0001t0001g0313 |
3 | HG02109.hp2 HG02258.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.79+15123G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742682 | |||||||
| chr12:48742986 | C | T | 1 | a0001c0004t0001g0316 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.79+15427C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48742986 | |||||||
| chr12:48743154 | T | C | 6 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+15595T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48743154 | |||||||
| chr12:48743180 | G | C | 3 | a0001c0001t0001g0282 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG01346.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.79+15621G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48743180 | |||||||
| chr12:48743230 | T | TA | 7 | a0001c0001t0001g0114 a0001c0001t0001g0118 a0001c0001t0001g0187 others(4): Show |
7 | HG00741.hp2 HG01346.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+15688dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48743230 | ||||||
| chr12:48743255 | G | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(54): Show |
59 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.79+15696G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48743255 | |||||||
| chr12:48743591 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0241 a0001c0001t0001g0242 others(3): Show |
6 | HG01496.hp2 HG01978.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-15618G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48743591 | |||||||
| chr12:48743669 | C | T | 8 | a0001c0001t0001g0144 a0001c0001t0001g0156 a0001c0001t0001g0157 others(5): Show |
8 | HG01346.hp2 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-15540C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48743669 | |||||||
| chr12:48743792 | C | A | 13 | a0001c0001t0001g0144 a0001c0001t0001g0156 a0001c0001t0001g0157 others(10): Show |
13 | HG01346.hp2 HG01884.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.80-15417C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48743792 | |||||||
| chr12:48743909 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.80-15300G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48743909 | |||||||
| chr12:48743933 | C | CA | 24 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(21): Show |
24 | HG00323.hp1 HG00741.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.80-15246dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48743933 | ||||||
| chr12:48743933 | C | CAA | 12 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0046 others(9): Show |
12 | HG00280.hp1 HG01167.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-15247_80-15246d others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48743933 | ||||||
| chr12:48743933 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0288 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.80-15257_80-15246d others(14): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48743933 | ||||||
| chr12:48743933 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0311 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.80-15258_80-15246d others(15): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48743933 | ||||||
| chr12:48743933 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.80-15262_80-15246d others(19): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48743933 | ||||||
| chr12:48743933 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0125 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.80-15263_80-15246d others(20): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48743933 | ||||||
| chr12:48743933 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0162 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.80-15264_80-15246d others(21): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48743933 | ||||||
| chr12:48743933 | CA | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
166 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.80-15246delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48743933 | ||||||
| chr12:48743933 | CAA | C | 10 | a0001c0001t0001g0065 a0001c0001t0001g0074 a0001c0001t0001g0080 others(7): Show |
10 | HG01346.hp2 HG01515.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-15247_80-15246d others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48743933 | ||||||
| chr12:48743990 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0296 |
3 | HG02559.hp2 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.80-15219G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48743990 | |||||||
| chr12:48744014 | G | A | 3 | a0001c0001t0001g0282 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG01346.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.80-15195G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744014 | |||||||
| chr12:48744248 | CA | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
177 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.80-14942delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48744248 | ||||||
| chr12:48744248 | CAA | C | 7 | a0001c0001t0001g0144 a0001c0001t0001g0156 a0001c0001t0001g0157 others(4): Show |
7 | HG01978.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-14943_80-14942d others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48744248 | ||||||
| chr12:48744283 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0288 |
2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.80-14926G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744283 | |||||||
| chr12:48744385 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.80-14824G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744385 | |||||||
| chr12:48744435 | G | C | 5 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(2): Show |
5 | HG01167.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-14774G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744435 | |||||||
| chr12:48744590 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.80-14619T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744590 | |||||||
| chr12:48744650 | C | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0311 |
2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.80-14559C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744650 | |||||||
| chr12:48744663 | C | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0296 |
3 | HG02559.hp2 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.80-14546C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744663 | |||||||
| chr12:48744698 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
176 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.80-14511G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744698 | |||||||
| chr12:48744739 | T | A | 2 | a0001c0001t0001g0216 a0001c0003t0001g0287 |
2 | HG03669.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.80-14470T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744739 | |||||||
| chr12:48744740 | A | G | 2 | a0001c0001t0001g0216 a0001c0003t0001g0287 |
2 | HG03669.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.80-14469A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744740 | |||||||
| chr12:48744813 | GGAA | G | 34 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0190 others(31): Show |
35 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.80-14383_80-14381d others(5): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48744813 | ||||||
| chr12:48744817 | G | A | 6 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-14392G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744817 | |||||||
| chr12:48744838 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.80-14371A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744838 | |||||||
| chr12:48744993 | G | A | 37 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(34): Show |
37 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.80-14216G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48744993 | |||||||
| chr12:48745008 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.80-14201C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745008 | |||||||
| chr12:48745033 | A | G | 16 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0144 others(13): Show |
16 | HG01346.hp2 HG01884.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.80-14176A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745033 | |||||||
| chr12:48745041 | C | T | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0111 |
3 | NA18975.hp1 NA18977.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.80-14168C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745041 | |||||||
| chr12:48745140 | G | C | 1 | a0001c0001t0001g0286 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.80-14069G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745140 | |||||||
| chr12:48745144 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.80-14065G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745144 | |||||||
| chr12:48745175 | G | A | 37 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(34): Show |
37 | HG00323.hp2 HG01099.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.80-14034G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745175 | |||||||
| chr12:48745220 | G | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0296 |
3 | HG02559.hp2 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.80-13989G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745220 | |||||||
| chr12:48745222 | G | A | 3 | a0001c0001t0001g0282 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG01346.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.80-13987G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745222 | |||||||
| chr12:48745462 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.80-13747C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745462 | |||||||
| chr12:48745477 | C | A | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG02970.hp2 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.80-13732C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745477 | |||||||
| chr12:48745493 | C | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0241 a0001c0001t0001g0242 others(2): Show |
5 | HG01496.hp2 HG01978.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-13716C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745493 | |||||||
| chr12:48745538 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.80-13671G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745538 | |||||||
| chr12:48745646 | C | T | 6 | a0001c0001t0001g0088 a0001c0001t0001g0107 a0001c0001t0001g0108 others(3): Show |
6 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-13563C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745646 | |||||||
| chr12:48745731 | T | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
256 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.80-13478T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745731 | |||||||
| chr12:48745908 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.80-13301G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745908 | |||||||
| chr12:48745922 | T | C | 4 | a0001c0001t0001g0144 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
4 | HG02818.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-13287T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48745922 | |||||||
| chr12:48746029 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0288 |
2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.80-13180C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746029 | |||||||
| chr12:48746168 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.80-13041A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746168 | |||||||
| chr12:48746360 | C | CT | 20 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(17): Show |
20 | HG01175.hp2 HG01192.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.80-12825dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48746360 | ||||||
| chr12:48746360 | CT | C | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(33): Show |
36 | HG00323.hp1 HG01099.hp1 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.80-12825delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48746360 | ||||||
| chr12:48746397 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.80-12812C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746397 | |||||||
| chr12:48746565 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.80-12644C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746565 | |||||||
| chr12:48746660 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.80-12549C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746660 | |||||||
| chr12:48746691 | T | C | 4 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0286 others(1): Show |
4 | HG01884.hp1 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-12518T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746691 | |||||||
| chr12:48746747 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.80-12462C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746747 | |||||||
| chr12:48746817 | G | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0144 others(4): Show |
7 | HG02559.hp2 HG02647.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-12392G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746817 | |||||||
| chr12:48746857 | T | G | 7 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0144 others(4): Show |
7 | HG02559.hp2 HG02647.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-12352T>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746857 | |||||||
| chr12:48746868 | C | G | 1 | a0001c0001t0001g0240 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.80-12341C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746868 | |||||||
| chr12:48746933 | A | T | 3 | a0001c0001t0001g0227 a0001c0001t0001g0233 a0001c0001t0001g0234 |
3 | NA18944.hp2 NA18975.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.80-12276A>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746933 | |||||||
| chr12:48746951 | T | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0144 others(6): Show |
9 | HG02559.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-12258T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48746951 | |||||||
| chr12:48747001 | C | A | 4 | a0001c0001t0001g0090 a0001c0001t0001g0095 a0001c0001t0001g0098 others(1): Show |
4 | HG03834.hp1 NA18950.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-12208C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747001 | |||||||
| chr12:48747056 | A | G | 2 | a0001c0001t0001g0315 a0001c0004t0001g0316 |
2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.80-12153A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747056 | |||||||
| chr12:48747057 | T | A | 1 | a0001c0001t0001g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.80-12152T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747057 | |||||||
| chr12:48747058 | T | C | 3 | a0001c0001t0001g0282 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG01346.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.80-12151T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747058 | |||||||
| chr12:48747076 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
193 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.80-12133A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747076 | |||||||
| chr12:48747231 | C | G | 2 | a0001c0001t0001g0315 a0001c0004t0001g0316 |
2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.80-11978C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747231 | |||||||
| chr12:48747407 | A | C | 1 | a0001c0001t0001g0263 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.80-11802A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747407 | |||||||
| chr12:48747412 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
185 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.80-11797T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747412 | |||||||
| chr12:48747431 | A | G | 1 | a0001c0001t0001g0305 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.80-11778A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747431 | |||||||
| chr12:48747445 | T | G | 4 | a0001c0001t0001g0144 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
4 | HG02818.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-11764T>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747445 | |||||||
| chr12:48747581 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.80-11628T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747581 | |||||||
| chr12:48747596 | T | C | 3 | a0001c0001t0001g0282 a0001c0001t0001g0294 a0001c0001t0001g0295 |
3 | HG01346.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.80-11613T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747596 | |||||||
| chr12:48747647 | CTTGGCTA others(13): Show |
C | 2 | a0001c0001t0001g0163 a0001c0001t0003g0297 |
2 | HG02080.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.80-11539_80-11520d others(22): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48747647 | ||||||
| chr12:48747803 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.80-11406G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747803 | |||||||
| chr12:48747830 | T | C | 7 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(4): Show |
7 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-11379T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747830 | |||||||
| chr12:48747860 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.80-11349C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747860 | |||||||
| chr12:48747947 | G | A | 5 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0040 others(2): Show |
5 | HG01167.hp1 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-11262G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48747947 | |||||||
| chr12:48748271 | A | G | 4 | a0001c0001t0001g0088 a0001c0001t0001g0107 a0001c0001t0001g0110 others(1): Show |
4 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-10938A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48748271 | |||||||
| chr12:48748314 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.80-10895C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48748314 | |||||||
| chr12:48748469 | G | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
146 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.80-10740G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48748469 | |||||||
| chr12:48748488 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
144 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.80-10721C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48748488 | |||||||
| chr12:48748497 | GA | G | 6 | a0001c0001t0001g0142 a0001c0001t0001g0156 a0001c0001t0001g0157 others(3): Show |
6 | HG02818.hp1 HG02965.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-10698delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48748497 | ||||||
| chr12:48748555 | A | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-10654A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48748555 | |||||||
| chr12:48748622 | G | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-10587G>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48748622 | |||||||
| chr12:48748669 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.80-10540C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48748669 | |||||||
| chr12:48748889 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.80-10320A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48748889 | |||||||
| chr12:48748902 | T | C | 6 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-10307T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48748902 | |||||||
| chr12:48748919 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.80-10290C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48748919 | |||||||
| chr12:48749177 | G | A | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(46): Show |
49 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.80-10032G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749177 | |||||||
| chr12:48749261 | C | CA | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
134 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.80-9933dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48749261 | ||||||
| chr12:48749313 | T | C | 50 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(47): Show |
50 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.80-9896T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749313 | |||||||
| chr12:48749323 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.80-9886G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749323 | |||||||
| chr12:48749333 | G | C | 1 | a0001c0001t0001g0299 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.80-9876G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749333 | |||||||
| chr12:48749356 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.80-9853C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749356 | |||||||
| chr12:48749496 | C | T | 1 | a0001c0001t0001g0303 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.80-9713C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749496 | |||||||
| chr12:48749497 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.80-9712G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749497 | |||||||
| chr12:48749603 | C | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
145 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.80-9606C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749603 | |||||||
| chr12:48749629 | C | T | 5 | a0001c0001t0001g0196 a0001c0001t0001g0246 a0001c0001t0001g0301 others(2): Show |
5 | NA18953.hp1 NA19058.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-9580C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749629 | |||||||
| chr12:48749635 | CA | C | 8 | a0001c0001t0001g0052 a0001c0001t0001g0116 a0001c0001t0001g0131 others(5): Show |
8 | HG00735.hp2 HG01099.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-9548delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48749635 | ||||||
| chr12:48749635 | CAA | C | 47 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0020 others(44): Show |
47 | HG00544.hp1 HG00621.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.80-9549_80-9548del others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48749635 | ||||||
| chr12:48749635 | CAAA | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.80-9550_80-9548del others(3): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48749635 | ||||||
| chr12:48749635 | CAAAA | C | 6 | a0001c0001t0001g0099 a0001c0001t0001g0118 a0001c0001t0001g0127 others(3): Show |
6 | HG01169.hp1 HG02451.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-9551_80-9548del others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48749635 | ||||||
| chr12:48749635 | CAAAAAAA | C | 45 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(42): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.80-9554_80-9548del others(7): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48749635 | ||||||
| chr12:48749635 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0117 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.80-9559_80-9548del others(12): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48749635 | ||||||
| chr12:48749683 | G | GTTC | 41 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(38): Show |
41 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.80-9514_80-9512dup others(3): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48749683 | ||||||
| chr12:48749695 | C | CTTCT | 7 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-9512_80-9511ins others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48749695 | ||||||
| chr12:48749841 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.80-9368G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749841 | |||||||
| chr12:48749849 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.80-9360G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749849 | |||||||
| chr12:48749933 | C | T | 16 | a0001c0001t0001g0125 a0001c0001t0001g0144 a0001c0001t0001g0145 others(13): Show |
16 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.80-9276C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48749933 | |||||||
| chr12:48750118 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.80-9091G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48750118 | |||||||
| chr12:48750196 | C | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
139 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.80-9013C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48750196 | |||||||
| chr12:48750220 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.80-8989G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48750220 | |||||||
| chr12:48750620 | C | T | 4 | a0001c0001t0001g0144 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
4 | HG02818.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-8589C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48750620 | |||||||
| chr12:48750696 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.80-8513C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48750696 | |||||||
| chr12:48750749 | C | A | 1 | a0001c0004t0001g0316 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.80-8460C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48750749 | |||||||
| chr12:48750851 | C | T | 6 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-8358C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48750851 | |||||||
| chr12:48751349 | C | A | 1 | a0001c0001t0001g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.80-7860C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751349 | |||||||
| chr12:48751354 | C | T | 50 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(47): Show |
50 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.80-7855C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751354 | |||||||
| chr12:48751367 | A | G | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(46): Show |
49 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.80-7842A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751367 | |||||||
| chr12:48751372 | G | A | 50 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(47): Show |
50 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.80-7837G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751372 | |||||||
| chr12:48751383 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.80-7826G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751383 | |||||||
| chr12:48751562 | C | T | 50 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(47): Show |
50 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.80-7647C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751562 | |||||||
| chr12:48751736 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.80-7473A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751736 | |||||||
| chr12:48751796 | G | T | 1 | a0001c0001t0001g0310 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.80-7413G>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751796 | |||||||
| chr12:48751963 | A | C | 1 | a0001c0001t0001g0215 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.80-7246A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751963 | |||||||
| chr12:48751975 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0127 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.80-7234G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751975 | |||||||
| chr12:48751985 | C | T | 15 | a0001c0001t0001g0125 a0001c0001t0001g0144 a0001c0001t0001g0145 others(12): Show |
15 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.80-7224C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48751985 | |||||||
| chr12:48752002 | G | A | 50 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(47): Show |
50 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.80-7207G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752002 | |||||||
| chr12:48752066 | C | CA | 37 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(34): Show |
37 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.80-7130dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48752066 | ||||||
| chr12:48752066 | C | CAA | 6 | a0001c0001t0001g0047 a0001c0001t0001g0169 a0001c0001t0001g0217 others(3): Show |
6 | HG01106.hp1 HG01175.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-7131_80-7130dup others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48752066 | ||||||
| chr12:48752076 | A | C | 1 | a0001c0001t0001g0299 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.80-7133A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752076 | |||||||
| chr12:48752079 | AC | A | 12 | a0001c0001t0001g0125 a0001c0001t0001g0144 a0001c0001t0001g0146 others(9): Show |
12 | HG02257.hp2 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.80-7129delC | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752079 | |||||||
| chr12:48752080 | C | A | 53 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(50): Show |
53 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.80-7129C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752080 | |||||||
| chr12:48752084 | C | A | 1 | a0001c0004t0001g0316 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.80-7125C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752084 | |||||||
| chr12:48752257 | G | A | 15 | a0001c0001t0001g0125 a0001c0001t0001g0144 a0001c0001t0001g0145 others(12): Show |
15 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.80-6952G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752257 | |||||||
| chr12:48752269 | A | G | 10 | a0001c0001t0001g0125 a0001c0001t0001g0145 a0001c0001t0001g0146 others(7): Show |
10 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-6940A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752269 | |||||||
| chr12:48752338 | G | T | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(46): Show |
49 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.80-6871G>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752338 | |||||||
| chr12:48752396 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.80-6813A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752396 | |||||||
| chr12:48752477 | A | C | 1 | a0001c0001t0001g0286 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.80-6732A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752477 | |||||||
| chr12:48752669 | CT | C | 31 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0033 others(28): Show |
31 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.80-6519delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48752669 | ||||||
| chr12:48752669 | CTT | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
120 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.80-6520_80-6519del others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48752669 | ||||||
| chr12:48752669 | CTTT | C | 6 | a0001c0001t0001g0144 a0001c0001t0001g0156 a0001c0001t0001g0157 others(3): Show |
6 | HG02683.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-6521_80-6519del others(3): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48752669 | ||||||
| chr12:48752767 | G | A | 15 | a0001c0001t0001g0125 a0001c0001t0001g0144 a0001c0001t0001g0145 others(12): Show |
15 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.80-6442G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752767 | |||||||
| chr12:48752872 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.80-6337G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752872 | |||||||
| chr12:48752883 | G | T | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(46): Show |
49 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.80-6326G>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752883 | |||||||
| chr12:48752913 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.80-6296C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752913 | |||||||
| chr12:48752967 | A | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
205 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.80-6242A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752967 | |||||||
| chr12:48752970 | C | T | 15 | a0001c0001t0001g0125 a0001c0001t0001g0144 a0001c0001t0001g0145 others(12): Show |
15 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.80-6239C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48752970 | |||||||
| chr12:48753063 | C | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.80-6146C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753063 | |||||||
| chr12:48753152 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.80-6057T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753152 | |||||||
| chr12:48753164 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
138 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.80-6045G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753164 | |||||||
| chr12:48753544 | C | A | 3 | a0001c0001t0001g0310 a0001c0001t0001g0312 a0001c0001t0001g0313 |
3 | HG02109.hp2 HG02258.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.80-5665C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753544 | |||||||
| chr12:48753547 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0096 |
2 | NA18974.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.80-5662G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753547 | |||||||
| chr12:48753566 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0034 |
2 | HG00741.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.80-5643T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753566 | |||||||
| chr12:48753664 | G | T | 58 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0044 others(55): Show |
59 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.80-5545G>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753664 | |||||||
| chr12:48753672 | T | G | 1 | a0001c0004t0001g0316 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.80-5537T>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753672 | |||||||
| chr12:48753691 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.80-5518T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753691 | |||||||
| chr12:48753691 | TC | T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0025 others(4): Show |
7 | HG01891.hp1 HG02559.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-5517delC | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753691 | |||||||
| chr12:48753692 | C | CT | 72 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0020 others(69): Show |
72 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.80-5497dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48753692 | ||||||
| chr12:48753692 | C | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0125 a0001c0001t0001g0145 others(11): Show |
14 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.80-5517C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753692 | |||||||
| chr12:48753692 | CT | C | 6 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0064 others(3): Show |
6 | HG00323.hp1 HG01070.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-5497delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48753692 | ||||||
| chr12:48753693 | T | C | 13 | a0001c0001t0001g0013 a0001c0001t0001g0125 a0001c0001t0001g0145 others(10): Show |
13 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.80-5516T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753693 | |||||||
| chr12:48753694 | T | C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0025 others(4): Show |
7 | HG01891.hp1 HG02559.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-5515T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753694 | |||||||
| chr12:48753697 | T | C | 7 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(4): Show |
7 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-5512T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753697 | |||||||
| chr12:48753698 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.80-5511T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753698 | |||||||
| chr12:48753763 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.80-5446G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753763 | |||||||
| chr12:48753777 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.80-5432C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753777 | |||||||
| chr12:48753796 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.80-5413G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753796 | |||||||
| chr12:48753891 | C | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.80-5318C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753891 | |||||||
| chr12:48753950 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.80-5259G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753950 | |||||||
| chr12:48753984 | T | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.80-5225T>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48753984 | |||||||
| chr12:48754017 | A | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0288 |
2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.80-5192A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48754017 | |||||||
| chr12:48754127 | G | A | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(46): Show |
49 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.80-5082G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48754127 | |||||||
| chr12:48754544 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
142 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.80-4665G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48754544 | |||||||
| chr12:48754697 | G | A | 8 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | HG00642.hp2 HG02055.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-4512G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48754697 | |||||||
| chr12:48754700 | T | C | 9 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(6): Show |
9 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.80-4509T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48754700 | |||||||
| chr12:48754861 | T | TTCAGCCT others(38): Show |
4 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0042 others(1): Show |
4 | HG01167.hp1 HG02630.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-4337_80-4293dup others(45): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48754861 | ||||||
| chr12:48754875 | T | TA | 3 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0183 |
3 | HG01099.hp2 HG01123.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.80-4333dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48754875 | ||||||
| chr12:48755126 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.80-4083G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755126 | |||||||
| chr12:48755127 | G | C | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(48): Show |
51 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.80-4082G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755127 | |||||||
| chr12:48755477 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.80-3732C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755477 | |||||||
| chr12:48755498 | C | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0122 |
2 | HG02300.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.80-3711C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755498 | |||||||
| chr12:48755586 | T | A | 5 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0261 others(2): Show |
5 | HG02451.hp2 HG02572.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-3623T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755586 | |||||||
| chr12:48755638 | G | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0076 others(5): Show |
9 | HG01361.hp1 HG02004.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.80-3571G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755638 | |||||||
| chr12:48755642 | C | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
192 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.80-3567C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755642 | |||||||
| chr12:48755681 | T | C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-3528T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755681 | |||||||
| chr12:48755769 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.80-3440C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755769 | |||||||
| chr12:48755814 | A | G | 50 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(47): Show |
50 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.80-3395A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755814 | |||||||
| chr12:48755875 | C | CT | 15 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0058 others(12): Show |
15 | HG00544.hp1 HG00738.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.80-3314dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48755875 | ||||||
| chr12:48755875 | CT | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.80-3314delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48755875 | ||||||
| chr12:48755880 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.80-3329T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48755880 | |||||||
| chr12:48756036 | C | G | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.80-3173C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48756036 | |||||||
| chr12:48756124 | C | A | 1 | a0001c0001t0001g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.80-3085C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48756124 | |||||||
| chr12:48756134 | C | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
133 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.80-3075C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48756134 | |||||||
| chr12:48756248 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.80-2961C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48756248 | |||||||
| chr12:48756320 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.80-2889G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48756320 | |||||||
| chr12:48756404 | G | A | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG00544.hp1 HG00673.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.80-2805G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48756404 | |||||||
| chr12:48756618 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.80-2591C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48756618 | |||||||
| chr12:48756757 | A | G | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
205 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.80-2452A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48756757 | |||||||
| chr12:48756771 | C | CTT | 7 | a0001c0001t0001g0125 a0001c0001t0001g0146 a0001c0001t0001g0147 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-2432_80-2431dup others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48756771 | ||||||
| chr12:48756773 | T | TTC | 38 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(35): Show |
39 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.80-2435_80-2434ins others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48756773 | ||||||
| chr12:48756779 | C | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(46): Show |
50 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.80-2430C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48756779 | |||||||
| chr12:48757137 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0076 a0001c0001t0001g0096 others(2): Show |
5 | HG01361.hp1 HG02004.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-2072G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757137 | |||||||
| chr12:48757314 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
196 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.80-1895A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757314 | |||||||
| chr12:48757373 | C | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
136 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.80-1836C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757373 | |||||||
| chr12:48757423 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.80-1786G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757423 | |||||||
| chr12:48757507 | G | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0055 a0001c0001t0001g0144 others(4): Show |
7 | HG02559.hp2 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-1702G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757507 | |||||||
| chr12:48757519 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.80-1690G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757519 | |||||||
| chr12:48757581 | T | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
160 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.80-1628T>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757581 | |||||||
| chr12:48757610 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0315 |
2 | HG02970.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.80-1599C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757610 | |||||||
| chr12:48757651 | AAT | A | 37 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(34): Show |
38 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.80-1556_80-1555del others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48757651 | ||||||
| chr12:48757652 | AT | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(143): Show |
149 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.80-1556delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757652 | |||||||
| chr12:48757653 | T | A | 13 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0025 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.80-1556T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757653 | |||||||
| chr12:48757657 | AAT | A | 6 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0204 others(3): Show |
6 | HG00323.hp1 HG00642.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-1550_80-1549del others(2): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48757657 | ||||||
| chr12:48757659 | T | A | 1 | a0001c0001t0001g0271 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.80-1550T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757659 | |||||||
| chr12:48757659 | TA | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
153 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.80-1545delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr12 | 48757659 | ||||||
| chr12:48757660 | A | T | 6 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0204 others(3): Show |
6 | HG00323.hp1 HG00642.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-1549A>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757660 | |||||||
| chr12:48757783 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.80-1426C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48757783 | |||||||
| chr12:48758053 | G | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(46): Show |
50 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.80-1156G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758053 | |||||||
| chr12:48758060 | C | T | 5 | a0001c0001t0001g0144 a0001c0001t0001g0156 a0001c0001t0001g0157 others(2): Show |
5 | HG02559.hp2 HG02818.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-1149C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758060 | |||||||
| chr12:48758065 | C | T | 4 | a0001c0001t0001g0144 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
4 | HG02818.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-1144C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758065 | |||||||
| chr12:48758082 | C | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(5): Show |
8 | HG01891.hp1 HG02055.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-1127C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758082 | |||||||
| chr12:48758253 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
208 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.80-956A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758253 | |||||||
| chr12:48758282 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80-927A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758282 | |||||||
| chr12:48758417 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.80-792C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758417 | |||||||
| chr12:48758428 | G | T | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.80-781G>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758428 | |||||||
| chr12:48758433 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.80-776C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758433 | |||||||
| chr12:48758650 | A | G | 25 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0016 others(22): Show |
25 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.80-559A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758650 | |||||||
| chr12:48758805 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.80-404T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48758805 | |||||||
| chr12:48759097 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.80-112T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48759097 | |||||||
| chr12:48759133 | T | G | 6 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0125 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-76T>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 1/3 | chr12 | 48759133 | |||||||
| chr12:48759374 | T | C | 13 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(10): Show |
13 | HG02055.hp1 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.202+43T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759374 | |||||||
| chr12:48759415 | T | G | 21 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0055 others(18): Show |
21 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.202+84T>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759415 | |||||||
| chr12:48759416 | T | C | 21 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0055 others(18): Show |
21 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.202+85T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759416 | |||||||
| chr12:48759455 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.202+124G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759455 | |||||||
| chr12:48759493 | C | T | 3 | a0001c0001t0001g0179 a0001c0001t0001g0202 a0001c0001t0001g0284 |
3 | HG01516.hp2 HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.202+162C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759493 | |||||||
| chr12:48759582 | GA | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+252delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759582 | |||||||
| chr12:48759584 | G | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+253G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759584 | |||||||
| chr12:48759585 | G | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+254G>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759585 | |||||||
| chr12:48759586 | C | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+255C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759586 | |||||||
| chr12:48759700 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0127 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.202+369G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759700 | |||||||
| chr12:48759716 | A | C | 1 | a0001c0001t0001g0011 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.202+385A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759716 | |||||||
| chr12:48759725 | G | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(158): Show |
162 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.202+394G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759725 | |||||||
| chr12:48759817 | T | A | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.202+486T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759817 | |||||||
| chr12:48759820 | T | C | 11 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0030 others(8): Show |
11 | HG01884.hp2 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.202+489T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759820 | |||||||
| chr12:48759867 | G | C | 28 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(25): Show |
28 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.202+536G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759867 | |||||||
| chr12:48759953 | C | T | 24 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0016 others(21): Show |
24 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.202+622C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48759953 | |||||||
| chr12:48760232 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.202+901G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48760232 | |||||||
| chr12:48760471 | C | G | 9 | a0001c0001t0001g0094 a0001c0001t0001g0096 a0001c0001t0001g0196 others(6): Show |
9 | NA18953.hp1 NA18953.hp2 NA19058.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+1140C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48760471 | |||||||
| chr12:48760599 | C | T | 10 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0030 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.202+1268C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48760599 | |||||||
| chr12:48760767 | T | C | 6 | a0001c0001t0001g0186 a0001c0001t0001g0230 a0001c0001t0001g0232 others(3): Show |
6 | HG02129.hp2 NA18944.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.202+1436T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48760767 | |||||||
| chr12:48760792 | G | A | 1 | a0001c0001t0001g0292 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.202+1461G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48760792 | |||||||
| chr12:48761365 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.202+2034C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48761365 | |||||||
| chr12:48761445 | C | CA | 30 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0022 others(27): Show |
30 | HG00621.hp2 HG01433.hp2 HG01928.hp1 others(27): Show |
intron_variant | MODIFIER | c.202+2132dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48761445 | ||||||
| chr12:48761445 | CA | C | 34 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0030 others(31): Show |
35 | HG01891.hp1 HG02056.hp2 HG02071.hp1 others(32): Show |
intron_variant | MODIFIER | c.202+2132delA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48761445 | ||||||
| chr12:48761445 | CAA | C | 30 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0026 others(27): Show |
30 | HG00558.hp2 HG00621.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.202+2131_202+2132d others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48761445 | ||||||
| chr12:48761594 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 |
3 | HG02055.hp1 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.202+2263A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48761594 | |||||||
| chr12:48761612 | T | A | 1 | a0001c0001t0001g0274 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.202+2281T>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48761612 | |||||||
| chr12:48761612 | T | TA | 10 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0058 others(7): Show |
10 | HG00738.hp1 HG00738.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.202+2296dupA | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48761612 | ||||||
| chr12:48761651 | T | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0036 others(3): Show |
6 | HG02257.hp1 HG02647.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.202+2320T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48761651 | |||||||
| chr12:48761719 | C | CT | 49 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0022 others(46): Show |
49 | HG00639.hp1 HG00735.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.202+2412dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48761719 | ||||||
| chr12:48761719 | C | CTT | 9 | a0001c0001t0001g0051 a0001c0001t0001g0055 a0001c0001t0001g0068 others(6): Show |
9 | HG01192.hp1 HG01243.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.202+2411_202+2412d others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48761719 | ||||||
| chr12:48761719 | CT | C | 9 | a0001c0001t0001g0016 a0001c0001t0001g0139 a0001c0001t0001g0148 others(6): Show |
9 | HG00099.hp2 HG00642.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+2412delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48761719 | ||||||
| chr12:48761840 | A | G | 1 | a0001c0001t0001g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.202+2509A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48761840 | |||||||
| chr12:48761904 | A | T | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.202+2573A>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48761904 | |||||||
| chr12:48761982 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.202+2651G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48761982 | |||||||
| chr12:48762014 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.202+2683T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762014 | |||||||
| chr12:48762047 | C | CT | 81 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(78): Show |
82 | HG00639.hp1 HG00642.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.202+2741dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48762047 | ||||||
| chr12:48762047 | C | CTT | 13 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0097 others(10): Show |
13 | HG00621.hp2 HG00735.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.202+2740_202+2741d others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48762047 | ||||||
| chr12:48762047 | CT | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0061 a0001c0001t0001g0175 others(3): Show |
6 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.202+2741delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48762047 | ||||||
| chr12:48762094 | T | G | 1 | a0001c0001t0001g0269 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.203-2757T>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762094 | |||||||
| chr12:48762122 | G | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.203-2729G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762122 | |||||||
| chr12:48762159 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.203-2692T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762159 | |||||||
| chr12:48762215 | T | C | 4 | a0001c0001t0001g0055 a0001c0001t0001g0109 a0001c0001t0001g0147 others(1): Show |
4 | HG02886.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-2636T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762215 | |||||||
| chr12:48762338 | G | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0108 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.203-2513G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762338 | |||||||
| chr12:48762356 | C | CT | 74 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(71): Show |
76 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.203-2466dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48762356 | ||||||
| chr12:48762356 | C | CTT | 18 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0025 others(15): Show |
18 | HG00558.hp2 HG00735.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.203-2467_203-2466d others(4): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48762356 | ||||||
| chr12:48762356 | C | CTTT | 9 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0193 others(6): Show |
9 | HG00733.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.203-2468_203-2466d others(5): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48762356 | ||||||
| chr12:48762356 | C | CTTTT | 17 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0024 others(14): Show |
17 | HG01243.hp2 HG01884.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.203-2469_203-2466d others(6): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48762356 | ||||||
| chr12:48762356 | C | CTTTTT | 8 | a0001c0001t0001g0030 a0001c0001t0001g0109 a0001c0001t0001g0125 others(5): Show |
8 | HG01109.hp2 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.203-2470_203-2466d others(7): Show |
TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48762356 | ||||||
| chr12:48762356 | CT | C | 6 | a0001c0001t0001g0028 a0001c0001t0001g0052 a0001c0001t0001g0165 others(3): Show |
6 | HG01099.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.203-2466delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48762356 | ||||||
| chr12:48762357 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.203-2494T>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762357 | |||||||
| chr12:48762431 | G | A | 1 | a0001c0001t0004g0219 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.203-2420G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762431 | |||||||
| chr12:48762437 | G | A | 21 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0030 others(18): Show |
21 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.203-2414G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762437 | |||||||
| chr12:48762471 | G | A | 12 | a0001c0001t0001g0022 a0001c0001t0001g0045 a0001c0001t0001g0082 others(9): Show |
12 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.203-2380G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762471 | |||||||
| chr12:48762559 | G | T | 1 | a0001c0001t0001g0131 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.203-2292G>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762559 | |||||||
| chr12:48762621 | G | C | 21 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0030 others(18): Show |
21 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.203-2230G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762621 | |||||||
| chr12:48762779 | G | C | 21 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0030 others(18): Show |
21 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.203-2072G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48762779 | |||||||
| chr12:48763318 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.203-1533C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48763318 | |||||||
| chr12:48763355 | G | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0108 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.203-1496G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48763355 | |||||||
| chr12:48763414 | A | G | 4 | a0001c0001t0001g0055 a0001c0001t0001g0109 a0001c0001t0001g0147 others(1): Show |
4 | HG02886.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-1437A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48763414 | |||||||
| chr12:48763561 | A | T | 1 | a0001c0001t0001g0295 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.203-1290A>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48763561 | |||||||
| chr12:48763681 | C | CT | 28 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0035 others(25): Show |
28 | HG00673.hp1 HG00673.hp2 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.203-1153dupT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48763681 | ||||||
| chr12:48763681 | CT | C | 11 | a0001c0001t0001g0055 a0001c0001t0001g0072 a0001c0001t0001g0109 others(8): Show |
11 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(8): Show |
intron_variant | MODIFIER | c.203-1153delT | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr12 | 48763681 | ||||||
| chr12:48763710 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.203-1141G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48763710 | |||||||
| chr12:48763813 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.203-1038C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48763813 | |||||||
| chr12:48763839 | C | G | 8 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0108 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.203-1012C>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48763839 | |||||||
| chr12:48763946 | G | A | 10 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.203-905G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48763946 | |||||||
| chr12:48764216 | C | T | 22 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0030 others(19): Show |
22 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.203-635C>T | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48764216 | |||||||
| chr12:48764614 | G | C | 1 | a0001c0001t0001g0039 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.203-237G>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48764614 | |||||||
| chr12:48764689 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.203-162G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48764689 | |||||||
| chr12:48764707 | G | A | 22 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0030 others(19): Show |
22 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.203-144G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48764707 | |||||||
| chr12:48764721 | C | A | 1 | a0001c0001t0001g0301 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.203-130C>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48764721 | |||||||
| chr12:48764756 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.203-95G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 2/3 | chr12 | 48764756 | |||||||
| chr12:48765151 | A | G | 5 | a0001c0001t0001g0078 a0001c0001t0001g0144 a0001c0001t0001g0157 others(2): Show |
5 | HG01891.hp1 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.347+156A>G | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 3/3 | chr12 | 48765151 | |||||||
| chr12:48765346 | A | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0127 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.348-261A>C | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 3/3 | chr12 | 48765346 | |||||||
| chr12:48765482 | G | A | 4 | a0001c0001t0001g0049 a0001c0001t0001g0170 a0001c0001t0001g0173 others(1): Show |
4 | HG01099.hp2 HG01243.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.348-125G>A | TEX49 | ENSG00000257987.6 | transcript | ENST00000548380.6 | protein_coding | 3/3 | chr12 | 48765482 |