Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3034 |
| ensemblid | ENSG00000084110.11 |
| hgncid | 4806 |
| symbol | HAL |
| name | histidine ammonia-lyase |
| refseq_nuc | NM_002108.4 |
| refseq_prot | NP_002099.1 |
| ensembl_nuc | ENST00000261208.8 |
| ensembl_prot | ENSP00000261208.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 95972662 |
| end | 95996344 |
| strand | - |
| ver | v1.2 |
| region | chr12:95972662-95996344 |
| region5000 | chr12:95967662-96001344 |
| regionname0 | HAL_chr12_95972662_95996344 |
| regionname5000 | HAL_chr12_95967662_96001344 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 657 | 378 | 88 | 58 | 176 | 12 | 43 | 137 | HAL_chr12_95967662_96001344 | HAL | MPRYT others(652): Show |
chr12 | 95967662 | 96001344 |
| a0002 | 1/0 | 657 | 31 | 1 | 14 | 7 | 5 | 3 | 4 | HAL_chr12_95967662_96001344 | HAL | MPRYT others(652): Show |
chr12 | 95967662 | 96001344 |
| a0003 | 0/0 | 657 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | MPRYT others(652): Show |
chr12 | 95967662 | 96001344 |
| a0004 | 0/0 | 657 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | HAL_chr12_95967662_96001344 | HAL | MPRYT others(652): Show |
chr12 | 95967662 | 96001344 |
| a0005 | 0/0 | 657 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | MPRYT others(652): Show |
chr12 | 95967662 | 96001344 |
| a0006 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | MPRYT others(652): Show |
chr12 | 95967662 | 96001344 |
| a0007 | 0/0 | 657 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | MPRYT others(652): Show |
chr12 | 95967662 | 96001344 |
| a0008 | 0/0 | 657 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | MPRYT others(652): Show |
chr12 | 95967662 | 96001344 |
| a0009 | 0/0 | 657 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | MPRYT others(652): Show |
chr12 | 95967662 | 96001344 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1971 | 232 | 52 | 51 | 92 | 7 | 29 | HAL_chr12_95967662_96001344 | HAL | ATGCC others(1966): Show |
chr12 | 95967662 | 96001344 | ||
| a0001c0002 | 0/0 | 1971 | 74 | 8 | 4 | 50 | 3 | 9 | HAL_chr12_95967662_96001344 | HAL | ATGCC others(1966): Show |
chr12 | 95967662 | 96001344 | ||
| a0001c0003 | 0/0 | 1971 | 47 | 18 | 3 | 21 | 1 | 4 | HAL_chr12_95967662_96001344 | HAL | ATGCC others(1966): Show |
chr12 | 95967662 | 96001344 | ||
| a0001c0005 | 0/0 | 1971 | 11 | 5 | 0 | 5 | 1 | 0 | HAL_chr12_95967662_96001344 | HAL | ATGCC others(1966): Show |
chr12 | 95967662 | 96001344 | ||
| a0001c0006 | 0/0 | 1971 | 5 | 5 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | ATGCC others(1966): Show |
chr12 | 95967662 | 96001344 | ||
| a0001c0007 | 0/0 | 1971 | 5 | 0 | 0 | 5 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | ATGCC others(1966): Show |
chr12 | 95967662 | 96001344 | ||
| a0001c0008 | 0/0 | 1971 | 3 | 0 | 0 | 2 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | ATGCC others(1966): Show |
chr12 | 95967662 | 96001344 | ||
| a0001c0015 | 0/0 | 1971 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | ATGCC others(1966): Show |
chr12 | 95967662 | 96001344 | ||
| a0002c0004 | 1/0 | 1971 | 31 | 1 | 14 | 7 | 5 | 3 | HAL_chr12_95967662_96001344 | HAL | ATGCC others(1966): Show |
chr12 | 95967662 | 96001344 | ||
| a0003c0010 | 0/0 | 1971 | 2 | 2 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | ATGCC others(1966): Show |
chr12 | 95967662 | 96001344 | ||
| a0004c0009 | 0/0 | 1971 | 2 | 0 | 0 | 2 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | ATGCC others(1966): Show |
chr12 | 95967662 | 96001344 | ||
| a0005c0012 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 1 | 0 | HAL_chr12_95967662_96001344 | HAL | ATGCC others(1966): Show |
chr12 | 95967662 | 96001344 | ||
| a0006c0011 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | ATGCC others(1966): Show |
chr12 | 95967662 | 96001344 | ||
| a0007c0014 | 0/0 | 1971 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | ATGCC others(1966): Show |
chr12 | 95967662 | 96001344 | ||
| a0008c0013 | 0/0 | 1971 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | ATGCC others(1966): Show |
chr12 | 95967662 | 96001344 | ||
| a0009c0016 | 0/0 | 1971 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | ATGCC others(1966): Show |
chr12 | 95967662 | 96001344 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3892 | 105 | 4 | 23 | 68 | 3 | 7 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0002 | 0/1 | 3891 | 41 | 3 | 13 | 6 | 2 | 16 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3886): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0003 | 0/0 | 3892 | 12 | 11 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0004 | 0/0 | 3892 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0005 | 0/0 | 3895 | 4 | 0 | 0 | 1 | 0 | 3 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3890): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0006 | 0/0 | 3892 | 13 | 13 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0007 | 0/0 | 3896 | 10 | 0 | 7 | 0 | 1 | 2 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3891): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0008 | 0/0 | 3892 | 7 | 0 | 0 | 6 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0009 | 0/0 | 3895 | 7 | 6 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3890): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0010 | 0/0 | 3891 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3886): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0011 | 0/0 | 3891 | 6 | 6 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3886): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0014 | 0/0 | 3892 | 4 | 0 | 0 | 4 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0015 | 0/0 | 3895 | 4 | 3 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3890): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0016 | 0/0 | 3891 | 3 | 1 | 2 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3886): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0019 | 0/0 | 3891 | 2 | 0 | 1 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3886): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0022 | 0/0 | 3891 | 2 | 1 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3886): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0025 | 0/0 | 3892 | 2 | 2 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0026 | 0/0 | 3891 | 2 | 0 | 1 | 0 | 1 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3886): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0031 | 0/0 | 3892 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0036 | 0/0 | 3896 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3891): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0039 | 0/0 | 3891 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3886): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0041 | 0/0 | 3892 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0042 | 0/0 | 3892 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0001t0043 | 0/0 | 3892 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0002t0001 | 0/0 | 3892 | 6 | 0 | 0 | 2 | 0 | 4 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0002t0002 | 0/0 | 3891 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3886): Show |
chr12 | 95967662 | 96001344 |
| a0001c0002t0003 | 0/0 | 3892 | 11 | 0 | 3 | 5 | 2 | 1 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0002t0004 | 0/0 | 3892 | 39 | 7 | 1 | 28 | 0 | 3 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0002t0010 | 0/0 | 3891 | 5 | 1 | 0 | 4 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3886): Show |
chr12 | 95967662 | 96001344 |
| a0001c0002t0016 | 0/0 | 3891 | 1 | 0 | 0 | 0 | 1 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3886): Show |
chr12 | 95967662 | 96001344 |
| a0001c0002t0020 | 0/0 | 3892 | 3 | 0 | 0 | 3 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0002t0021 | 0/0 | 3892 | 3 | 0 | 0 | 3 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0002t0024 | 0/0 | 3892 | 2 | 0 | 0 | 2 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0002t0029 | 0/0 | 3892 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0002t0038 | 0/0 | 3891 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3886): Show |
chr12 | 95967662 | 96001344 |
| a0001c0002t0040 | 0/0 | 3892 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0003t0005 | 0/0 | 3895 | 34 | 11 | 3 | 15 | 1 | 4 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3890): Show |
chr12 | 95967662 | 96001344 |
| a0001c0003t0012 | 0/0 | 3895 | 5 | 5 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3890): Show |
chr12 | 95967662 | 96001344 |
| a0001c0003t0017 | 0/0 | 3892 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0003t0018 | 0/0 | 3895 | 2 | 0 | 0 | 2 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3890): Show |
chr12 | 95967662 | 96001344 |
| a0001c0003t0027 | 0/0 | 3895 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3890): Show |
chr12 | 95967662 | 96001344 |
| a0001c0003t0030 | 0/0 | 3895 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3890): Show |
chr12 | 95967662 | 96001344 |
| a0001c0003t0033 | 0/0 | 3892 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0003t0034 | 0/0 | 3892 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0003t0035 | 0/0 | 3895 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3890): Show |
chr12 | 95967662 | 96001344 |
| a0001c0005t0001 | 0/0 | 3892 | 3 | 2 | 0 | 0 | 1 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0005t0002 | 0/0 | 3891 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3886): Show |
chr12 | 95967662 | 96001344 |
| a0001c0005t0004 | 0/0 | 3892 | 2 | 0 | 0 | 2 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0005t0006 | 0/0 | 3892 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0005t0017 | 0/0 | 3892 | 3 | 0 | 0 | 3 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0005t0032 | 0/0 | 3892 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0006t0013 | 0/0 | 3892 | 5 | 5 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0007t0001 | 0/0 | 3892 | 4 | 0 | 0 | 4 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0007t0019 | 0/0 | 3891 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3886): Show |
chr12 | 95967662 | 96001344 |
| a0001c0008t0001 | 0/0 | 3892 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0008t0008 | 0/0 | 3892 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0001c0008t0018 | 0/0 | 3895 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3890): Show |
chr12 | 95967662 | 96001344 |
| a0001c0015t0005 | 0/0 | 3895 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3890): Show |
chr12 | 95967662 | 96001344 |
| a0002c0004t0002 | 0/0 | 3891 | 3 | 0 | 2 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3886): Show |
chr12 | 95967662 | 96001344 |
| a0002c0004t0003 | 1/0 | 3892 | 24 | 1 | 12 | 3 | 5 | 2 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0002c0004t0004 | 0/0 | 3892 | 3 | 0 | 0 | 3 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0002c0004t0028 | 0/0 | 3892 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0003c0010t0023 | 0/0 | 3892 | 2 | 2 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0004c0009t0001 | 0/0 | 3892 | 2 | 0 | 0 | 2 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0005c0012t0002 | 0/0 | 3891 | 1 | 0 | 0 | 0 | 1 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3886): Show |
chr12 | 95967662 | 96001344 |
| a0006c0011t0037 | 0/0 | 3891 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3886): Show |
chr12 | 95967662 | 96001344 |
| a0007c0014t0001 | 0/0 | 3892 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0008c0013t0001 | 0/0 | 3892 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| a0009c0016t0001 | 0/0 | 3892 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | AGATA others(3887): Show |
chr12 | 95967662 | 96001344 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 37 | 2 | 11 | 19 | 2 | 3 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0004 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0005 | 0/0 | 8 | 1 | 5 | 0 | 0 | 2 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0015 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0003g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0003g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0006g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0006g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0007g0010 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0007g0023 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0007g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0007g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0008g0011 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0008g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0008g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0009g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0009g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0009g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0009g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0010g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0011g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0011g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0011g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0011g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0011g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0014g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0015g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0015g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0015g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0015g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0016g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0016g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0016g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0019g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0019g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0022g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0022g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0025g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0025g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0026g0058 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0031g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0036g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0039g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0041g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0042g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0001t0043g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0001g0012 | 0/0 | 5 | 0 | 0 | 1 | 0 | 4 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0003g0025 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0003g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0004g0002 | 0/0 | 12 | 5 | 0 | 6 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0004g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0004g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0004g0050 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0010g0049 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0010g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0010g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0010g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0016g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0020g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0020g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0020g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0021g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0021g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0021g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0024g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0029g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0038g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0002t0040g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0006 | 0/0 | 7 | 1 | 0 | 5 | 1 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0012g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0017g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0018g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0018g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0027g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0030g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0033g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0034g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0003t0035g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0005t0001g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0005t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0005t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0005t0004g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0005t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0005t0017g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0005t0017g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0005t0032g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0006t0013g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0006t0013g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0006t0013g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0007t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0007t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0007t0019g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0008t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0008t0008g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0008t0018g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0001c0015t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0002c0004t0002g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0002c0004t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0002c0004t0003g0008 | 0/0 | 6 | 0 | 2 | 2 | 0 | 2 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0002c0004t0003g0027 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0002c0004t0003g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0002c0004t0003g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0002c0004t0003g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0002c0004t0003g0054 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0002c0004t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0002c0004t0003g0133 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0002c0004t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0002c0004t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0002c0004t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0002c0004t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0002c0004t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0002c0004t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0002c0004t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0002c0004t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0002c0004t0028g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0003c0010t0023g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0004c0009t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0004c0009t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0005c0012t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0006c0011t0037g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0007c0014t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0008c0013t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| a0009c0016t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0005 | g0006 | EUR | GBR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | GBR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00140 | hp1 | a0001 | c0001 | t0007 | g0112 | EUR | GBR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00140 | hp2 | a0001 | c0001 | t0026 | g0058 | EUR | GBR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00280 | hp1 | a0005 | c0012 | t0002 | g0142 | EUR | FIN | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0156 | EUR | FIN | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00323 | hp2 | a0001 | c0002 | t0016 | g0199 | EUR | FIN | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00408 | hp2 | a0001 | c0003 | t0005 | g0006 | EAS | CHS | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | CHS | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00423 | hp2 | a0001 | c0001 | t0008 | g0168 | EAS | CHS | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00438 | hp1 | a0001 | c0003 | t0005 | g0118 | EAS | CHS | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00544 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | CHS | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00558 | hp1 | a0002 | c0004 | t0004 | g0220 | EAS | CHS | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00621 | hp1 | a0002 | c0004 | t0003 | g0008 | EAS | CHS | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00621 | hp2 | a0001 | c0002 | t0004 | g0179 | EAS | CHS | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00642 | hp1 | a0001 | c0001 | t0007 | g0010 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00642 | hp2 | a0001 | c0003 | t0005 | g0042 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00733 | hp2 | a0001 | c0003 | t0005 | g0042 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00735 | hp2 | a0002 | c0004 | t0003 | g0054 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00738 | hp2 | a0001 | c0001 | t0036 | g0111 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00741 | hp1 | a0001 | c0001 | t0007 | g0010 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01069 | hp1 | a0002 | c0004 | t0003 | g0051 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01071 | hp2 | a0002 | c0004 | t0003 | g0051 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01074 | hp1 | a0002 | c0004 | t0003 | g0008 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01081 | hp1 | a0001 | c0001 | t0009 | g0034 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01081 | hp2 | a0001 | c0002 | t0003 | g0025 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0205 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0010 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01167 | hp2 | a0001 | c0001 | t0022 | g0068 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01168 | hp1 | a0002 | c0004 | t0003 | g0052 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01169 | hp2 | a0002 | c0004 | t0003 | g0052 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01175 | hp2 | a0002 | c0004 | t0003 | g0027 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01192 | hp1 | a0002 | c0004 | t0003 | g0213 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01192 | hp2 | a0001 | c0001 | t0015 | g0070 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01243 | hp1 | a0001 | c0003 | t0005 | g0037 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01255 | hp1 | a0001 | c0002 | t0004 | g0195 | AMR | CLM | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01255 | hp2 | a0002 | c0004 | t0003 | g0219 | AMR | CLM | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01256 | hp1 | a0002 | c0004 | t0002 | g0053 | AMR | CLM | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01256 | hp2 | a0001 | c0001 | t0007 | g0098 | AMR | CLM | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01258 | hp2 | a0002 | c0004 | t0002 | g0053 | AMR | CLM | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0023 | AMR | CLM | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01261 | hp2 | a0001 | c0001 | t0007 | g0010 | AMR | CLM | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01361 | hp1 | a0001 | c0001 | t0007 | g0023 | AMR | CLM | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0025 | AMR | CLM | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | CLM | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01496 | hp1 | a0001 | c0001 | t0016 | g0149 | AMR | CLM | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01515 | hp1 | a0002 | c0004 | t0003 | g0038 | EUR | IBS | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0150 | EUR | IBS | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01516 | hp1 | a0002 | c0004 | t0003 | g0225 | EUR | IBS | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01516 | hp2 | a0001 | c0002 | t0003 | g0187 | EUR | IBS | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01517 | hp1 | a0001 | c0002 | t0003 | g0025 | EUR | IBS | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01517 | hp2 | a0002 | c0004 | t0003 | g0038 | EUR | IBS | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01884 | hp2 | a0001 | c0001 | t0011 | g0176 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01891 | hp2 | a0001 | c0002 | t0004 | g0002 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01934 | hp2 | a0002 | c0004 | t0003 | g0008 | AMR | PEL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01943 | hp2 | a0002 | c0004 | t0003 | g0076 | AMR | PEL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01975 | hp2 | a0001 | c0001 | t0016 | g0155 | AMR | PEL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02015 | hp1 | a0002 | c0004 | t0003 | g0008 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02015 | hp2 | a0001 | c0003 | t0017 | g0087 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02040 | hp1 | a0001 | c0002 | t0021 | g0196 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02055 | hp1 | a0001 | c0001 | t0015 | g0067 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02055 | hp2 | a0001 | c0001 | t0015 | g0064 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02071 | hp1 | a0001 | c0008 | t0008 | g0182 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02071 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02074 | hp1 | a0001 | c0002 | t0021 | g0198 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02074 | hp2 | a0001 | c0001 | t0042 | g0137 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02080 | hp1 | a0001 | c0008 | t0001 | g0183 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02080 | hp2 | a0001 | c0001 | t0008 | g0011 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02129 | hp1 | a0001 | c0002 | t0021 | g0193 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02129 | hp2 | a0001 | c0001 | t0043 | g0243 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02135 | hp1 | a0001 | c0003 | t0005 | g0082 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02135 | hp2 | a0001 | c0003 | t0005 | g0031 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02145 | hp1 | a0001 | c0003 | t0005 | g0037 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02145 | hp2 | a0001 | c0001 | t0016 | g0144 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02148 | hp1 | a0002 | c0004 | t0003 | g0027 | AMR | PEL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02155 | hp2 | a0001 | c0002 | t0040 | g0197 | EAS | CDX | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CDX | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02165 | hp2 | a0001 | c0001 | t0010 | g0140 | EAS | CDX | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02257 | hp1 | a0001 | c0002 | t0004 | g0002 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02257 | hp2 | a0001 | c0001 | t0009 | g0056 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02258 | hp1 | a0001 | c0002 | t0004 | g0209 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02280 | hp1 | a0001 | c0003 | t0005 | g0018 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0057 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02451 | hp2 | a0001 | c0003 | t0012 | g0009 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02523 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0244 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0200 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02602 | hp2 | a0001 | c0002 | t0004 | g0210 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02615 | hp1 | a0001 | c0003 | t0005 | g0081 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02615 | hp2 | a0001 | c0001 | t0011 | g0145 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0102 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02630 | hp1 | a0001 | c0003 | t0005 | g0104 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0153 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02647 | hp2 | a0001 | c0003 | t0005 | g0018 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02683 | hp2 | a0001 | c0001 | t0007 | g0023 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02723 | hp1 | a0001 | c0005 | t0002 | g0105 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02723 | hp2 | a0001 | c0003 | t0005 | g0018 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02735 | hp1 | a0001 | c0001 | t0007 | g0010 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02738 | hp1 | a0002 | c0004 | t0002 | g0224 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0237 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0043 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02818 | hp1 | a0001 | c0006 | t0013 | g0107 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02818 | hp2 | a0001 | c0001 | t0022 | g0066 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0229 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0245 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02896 | hp1 | a0001 | c0001 | t0011 | g0151 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02897 | hp1 | a0001 | c0001 | t0011 | g0046 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0246 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02922 | hp1 | a0003 | c0010 | t0023 | g0030 | AFR | ESN | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02922 | hp2 | a0001 | c0002 | t0004 | g0002 | AFR | ESN | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0101 | AFR | ESN | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02965 | hp2 | a0001 | c0003 | t0034 | g0080 | AFR | ESN | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02970 | hp1 | a0001 | c0002 | t0004 | g0002 | AFR | ESN | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02970 | hp2 | a0001 | c0003 | t0012 | g0009 | AFR | ESN | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0103 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03098 | hp1 | a0006 | c0011 | t0037 | g0071 | AFR | MSL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | MSL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03130 | hp1 | a0003 | c0010 | t0023 | g0030 | AFR | ESN | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03139 | hp1 | a0001 | c0006 | t0013 | g0106 | AFR | ESN | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03139 | hp2 | a0001 | c0001 | t0011 | g0046 | AFR | ESN | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03195 | hp1 | a0001 | c0001 | t0025 | g0241 | AFR | ESN | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | ESN | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03209 | hp1 | a0001 | c0003 | t0005 | g0236 | AFR | MSL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | MSL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0100 | AFR | MSL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0043 | AFR | MSL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03239 | hp1 | a0001 | c0002 | t0004 | g0002 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03453 | hp1 | a0001 | c0005 | t0001 | g0057 | AFR | MSL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0056 | AFR | MSL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03486 | hp1 | a0001 | c0003 | t0012 | g0009 | AFR | MSL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | MSL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03491 | hp1 | a0001 | c0003 | t0005 | g0033 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03492 | hp1 | a0001 | c0003 | t0005 | g0033 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0238 | AFR | ESN | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03516 | hp2 | a0001 | c0003 | t0005 | g0006 | AFR | ESN | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03540 | hp1 | a0001 | c0002 | t0004 | g0201 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | GWD | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03579 | hp1 | a0001 | c0002 | t0004 | g0002 | AFR | MSL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03688 | hp1 | a0001 | c0001 | t0005 | g0228 | SAS | STU | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | STU | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0113 | SAS | PJL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | BEB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0012 | SAS | BEB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03834 | hp2 | a0002 | c0004 | t0003 | g0008 | SAS | BEB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03927 | hp1 | a0001 | c0002 | t0004 | g0050 | SAS | BEB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03927 | hp2 | a0002 | c0004 | t0003 | g0008 | SAS | BEB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03942 | hp1 | a0001 | c0001 | t0008 | g0011 | SAS | BEB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | BEB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | STU | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | STU | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0227 | SAS | BEB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG04184 | hp2 | a0001 | c0003 | t0005 | g0232 | SAS | BEB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | STU | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG04199 | hp2 | a0001 | c0008 | t0018 | g0180 | SAS | STU | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG04228 | hp1 | a0001 | c0002 | t0003 | g0202 | SAS | STU | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | YRI | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18522 | hp2 | a0001 | c0002 | t0010 | g0049 | AFR | YRI | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18612 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | CHB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0048 | EAS | CHB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18906 | hp1 | a0001 | c0001 | t0041 | g0231 | AFR | YRI | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18906 | hp2 | a0001 | c0005 | t0006 | g0077 | AFR | YRI | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18940 | hp1 | a0001 | c0002 | t0029 | g0060 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18942 | hp1 | a0001 | c0002 | t0038 | g0190 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18942 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18943 | hp2 | a0001 | c0002 | t0003 | g0194 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18945 | hp1 | a0002 | c0004 | t0028 | g0061 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18945 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18946 | hp1 | a0001 | c0002 | t0003 | g0206 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18946 | hp2 | a0001 | c0003 | t0005 | g0032 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18949 | hp1 | a0002 | c0004 | t0004 | g0217 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18949 | hp2 | a0001 | c0007 | t0001 | g0239 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18951 | hp2 | a0001 | c0003 | t0005 | g0006 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18952 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18953 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18953 | hp2 | a0001 | c0005 | t0004 | g0039 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18954 | hp1 | a0004 | c0009 | t0001 | g0141 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18956 | hp1 | a0001 | c0003 | t0033 | g0088 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18957 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18959 | hp2 | a0001 | c0003 | t0018 | g0086 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18960 | hp1 | a0001 | c0002 | t0004 | g0177 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18962 | hp1 | a0001 | c0002 | t0010 | g0049 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18963 | hp1 | a0001 | c0002 | t0004 | g0026 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18964 | hp1 | a0001 | c0003 | t0005 | g0006 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18965 | hp1 | a0001 | c0002 | t0020 | g0186 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18967 | hp1 | a0001 | c0002 | t0003 | g0204 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18969 | hp1 | a0001 | c0002 | t0004 | g0050 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18969 | hp2 | a0007 | c0014 | t0001 | g0072 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18971 | hp1 | a0001 | c0007 | t0001 | g0028 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18971 | hp2 | a0001 | c0003 | t0027 | g0059 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18972 | hp1 | a0001 | c0002 | t0004 | g0026 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18972 | hp2 | a0001 | c0003 | t0005 | g0032 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18977 | hp1 | a0001 | c0001 | t0008 | g0011 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18977 | hp2 | a0001 | c0005 | t0017 | g0035 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18978 | hp1 | a0001 | c0003 | t0005 | g0119 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18979 | hp2 | a0001 | c0001 | t0014 | g0014 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18980 | hp1 | a0001 | c0007 | t0019 | g0240 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18980 | hp2 | a0001 | c0002 | t0004 | g0208 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18981 | hp1 | a0001 | c0005 | t0017 | g0165 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18981 | hp2 | a0001 | c0001 | t0014 | g0014 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18984 | hp1 | a0001 | c0002 | t0024 | g0047 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18984 | hp2 | a0001 | c0005 | t0017 | g0035 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18985 | hp1 | a0001 | c0001 | t0008 | g0011 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18985 | hp2 | a0002 | c0004 | t0004 | g0218 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18986 | hp2 | a0001 | c0001 | t0008 | g0011 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18987 | hp1 | a0001 | c0003 | t0005 | g0006 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18988 | hp2 | a0001 | c0002 | t0004 | g0188 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18989 | hp2 | a0001 | c0002 | t0010 | g0184 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18990 | hp2 | a0001 | c0002 | t0004 | g0185 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18991 | hp2 | a0001 | c0003 | t0035 | g0084 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18994 | hp1 | a0001 | c0002 | t0020 | g0191 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18994 | hp2 | a0001 | c0001 | t0008 | g0136 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18995 | hp2 | a0001 | c0002 | t0004 | g0203 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19001 | hp1 | a0001 | c0001 | t0005 | g0097 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19003 | hp2 | a0001 | c0005 | t0004 | g0039 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19011 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19012 | hp2 | a0008 | c0013 | t0001 | g0129 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | LWK | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0034 | AFR | LWK | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19043 | hp1 | a0001 | c0001 | t0031 | g0069 | AFR | LWK | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19043 | hp2 | a0001 | c0003 | t0030 | g0062 | AFR | LWK | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19057 | hp1 | a0001 | c0001 | t0039 | g0128 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19057 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19058 | hp1 | a0001 | c0002 | t0003 | g0048 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19062 | hp2 | a0001 | c0007 | t0001 | g0028 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19063 | hp1 | a0001 | c0002 | t0020 | g0192 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19065 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19065 | hp2 | a0009 | c0016 | t0001 | g0173 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19066 | hp1 | a0001 | c0003 | t0018 | g0114 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19067 | hp1 | a0001 | c0002 | t0004 | g0026 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19067 | hp2 | a0001 | c0002 | t0004 | g0181 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19068 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19072 | hp1 | a0002 | c0004 | t0003 | g0216 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19072 | hp2 | a0001 | c0002 | t0010 | g0189 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19074 | hp1 | a0001 | c0003 | t0005 | g0091 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19074 | hp2 | a0004 | c0009 | t0001 | g0074 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19076 | hp1 | a0001 | c0002 | t0010 | g0230 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19079 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19080 | hp2 | a0001 | c0001 | t0014 | g0014 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19081 | hp1 | a0001 | c0001 | t0019 | g0172 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19081 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19083 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19084 | hp1 | a0001 | c0003 | t0005 | g0006 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19085 | hp1 | a0001 | c0003 | t0005 | g0085 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19086 | hp1 | a0001 | c0003 | t0005 | g0031 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19089 | hp1 | a0001 | c0003 | t0005 | g0092 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19089 | hp2 | a0001 | c0002 | t0024 | g0047 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19090 | hp1 | a0001 | c0007 | t0001 | g0028 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19091 | hp1 | a0001 | c0001 | t0014 | g0014 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19091 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19240 | hp1 | a0001 | c0006 | t0013 | g0020 | AFR | YRI | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA19240 | hp2 | a0001 | c0003 | t0005 | g0090 | AFR | YRI | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA20752 | hp1 | a0002 | c0004 | t0003 | g0027 | EUR | TSI | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA20752 | hp2 | a0002 | c0004 | t0003 | g0054 | EUR | TSI | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA20805 | hp2 | a0001 | c0005 | t0001 | g0116 | EUR | TSI | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA20905 | hp1 | a0001 | c0003 | t0005 | g0233 | SAS | GIH | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01123 | hp1 | a0001 | c0001 | t0026 | g0058 | AMR | CLM | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG01123 | hp2 | a0001 | c0001 | t0019 | g0158 | AMR | CLM | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02109 | hp1 | a0001 | c0005 | t0032 | g0063 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02109 | hp2 | a0001 | c0003 | t0005 | g0211 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02486 | hp1 | a0001 | c0003 | t0005 | g0089 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02486 | hp2 | a0001 | c0003 | t0012 | g0009 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02559 | hp1 | a0001 | c0006 | t0013 | g0020 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG02559 | hp2 | a0001 | c0001 | t0015 | g0065 | AFR | ACB | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03471 | hp1 | a0001 | c0006 | t0013 | g0020 | AFR | MSL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG03471 | hp2 | a0001 | c0003 | t0012 | g0009 | AFR | MSL | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG06807 | hp1 | a0002 | c0004 | t0003 | g0215 | AFR | USA | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0099 | AFR | USA | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA18955 | hp2 | a0001 | c0015 | t0005 | g0178 | EAS | JPT | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0078 | AFR | LWK | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| NA21309 | hp2 | a0001 | c0001 | t0025 | g0242 | AFR | LWK | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0115 | REF | REF | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| homoSapiens | grch38p0 | a0002 | c0004 | t0003 | g0133 | REF | REF | HAL_chr12_95967662_96001344 | HAL | chr12 | 95967662 | 96001344 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:95974273 | G | A | 1 | a0008 | 1 | NA19012.hp2 | missense_variant | MODERATE | c.1933C>T | p.His645Tyr | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 21/21 | 2281/3892 | 1933/1974 | 645/657 | chr12 | 95974273 | |||
| chr12:95978015 | G | A | 1 | a0007 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.1583C>T | p.Thr528Met | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/21 | 1931/3892 | 1583/1974 | 528/657 | chr12 | 95978015 | |||
| chr12:95980697 | T | G | 1 | a0003 | 2 | HG02922.hp1 HG03130.hp1 |
missense_variant | MODERATE | c.1378A>C | p.Ile460Leu | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/21 | 1726/3892 | 1378/1974 | 460/657 | chr12 | 95980697 | |||
| chr12:95980836 | C | T | 8 | a0001 a0003 a0004 others(5): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
missense_variant | MODERATE | c.1315G>A | p.Val439Ile | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 16/21 | 1663/3892 | 1315/1974 | 439/657 | chr12 | 95980836 | |||
| chr12:95985945 | C | T | 1 | a0004 | 2 | NA18954.hp1 NA19074.hp2 |
missense_variant | MODERATE | c.1169G>A | p.Arg390His | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/21 | 1517/3892 | 1169/1974 | 390/657 | chr12 | 95985945 | |||
| chr12:95990407 | C | T | 1 | a0005 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.841G>A | p.Ala281Thr | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/21 | 1189/3892 | 841/1974 | 281/657 | chr12 | 95990407 | |||
| chr12:95993989 | T | C | 1 | a0009 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.421A>G | p.Thr141Ala | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 6/21 | 769/3892 | 421/1974 | 141/657 | chr12 | 95993989 | |||
| chr12:95995673 | C | T | 1 | a0006 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.238G>A | p.Val80Met | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 2/21 | 586/3892 | 238/1974 | 80/657 | chr12 | 95995673 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:95987197 | A | G | 2 | a0001c0003 a0001c0015 |
48 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(45): Show |
synonymous_variant | LOW | c.921T>C | p.Asn307Asn | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 12/21 | 1269/3892 | 921/1974 | 307/657 | chr12 | 95987197 | |||
| chr12:95990471 | T | C | 2 | a0001c0002 a0001c0005 |
85 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(82): Show |
synonymous_variant | LOW | c.777A>G | p.Pro259Pro | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/21 | 1125/3892 | 777/1974 | 259/657 | chr12 | 95990471 | |||
| chr12:95993831 | G | A | 1 | a0001c0006 | 5 | HG02559.hp1 HG02818.hp1 HG03139.hp1 others(2): Show |
synonymous_variant | LOW | c.492C>T | p.Tyr164Tyr | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 7/21 | 840/3892 | 492/1974 | 164/657 | chr12 | 95993831 | |||
| chr12:95993987 | T | A | 3 | a0001c0002 a0001c0008 a0001c0015 |
78 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(75): Show |
synonymous_variant | LOW | c.423A>T | p.Thr141Thr | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 6/21 | 771/3892 | 423/1974 | 141/657 | chr12 | 95993987 | |||
| chr12:95995878 | T | C | 1 | a0001c0007 | 5 | NA18949.hp2 NA18971.hp1 NA18980.hp1 others(2): Show |
synonymous_variant | LOW | c.33A>G | p.Glu11Glu | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 2/21 | 381/3892 | 33/1974 | 11/657 | chr12 | 95995878 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:95972733 | T | C | 16 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0010 others(13): Show |
72 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1499A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 21/21 | 1499 | chr12 | 95972733 | ||||||
| chr12:95972870 | C | T | 1 | a0006c0011t0037 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1362G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 21/21 | 1362 | chr12 | 95972870 | ||||||
| chr12:95972920 | G | A | 21 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 others(18): Show |
158 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*1312C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 21/21 | 1312 | chr12 | 95972920 | ||||||
| chr12:95972991 | T | G | 31 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(28): Show |
201 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*1241A>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 21/21 | 1241 | chr12 | 95972991 | ||||||
| chr12:95973071 | G | A | 1 | a0001c0003t0035 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1161C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 21/21 | 1161 | chr12 | 95973071 | ||||||
| chr12:95973232 | A | C | 1 | a0003c0010t0023 | 2 | HG02922.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1000T>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 21/21 | 1000 | chr12 | 95973232 | ||||||
| chr12:95973318 | A | G | 1 | a0001c0006t0013 | 5 | HG02559.hp1 HG02818.hp1 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*914T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 21/21 | 914 | chr12 | 95973318 | ||||||
| chr12:95973396 | G | A | 3 | a0001c0002t0021 a0001c0002t0024 a0001c0002t0040 |
6 | HG02040.hp1 HG02074.hp1 HG02129.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*836C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 21/21 | 836 | chr12 | 95973396 | ||||||
| chr12:95973476 | G | A | 1 | a0001c0001t0041 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*756C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 21/21 | 756 | chr12 | 95973476 | ||||||
| chr12:95973615 | C | T | 2 | a0001c0003t0017 a0001c0005t0017 |
4 | HG02015.hp2 NA18977.hp2 NA18981.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*617G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 21/21 | 617 | chr12 | 95973615 | ||||||
| chr12:95973702 | A | C | 2 | a0001c0001t0016 a0001c0002t0016 |
4 | HG00323.hp2 HG01496.hp1 HG01975.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*530T>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 21/21 | 530 | chr12 | 95973702 | ||||||
| chr12:95973823 | T | TAAA | 11 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0015 others(8): Show |
61 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*406_*408dupTTT | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 21/21 | 408 | chr12 | 95973823 | ||||||
| chr12:95973823 | T | TAAAA | 2 | a0001c0001t0007 a0001c0001t0036 |
11 | HG00140.hp1 HG00642.hp1 HG00738.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*405_*408dupTTTT | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 21/21 | 408 | chr12 | 95973823 | ||||||
| chr12:95973823 | TA | T | 17 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0011 others(14): Show |
72 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*408delT | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 21/21 | 408 | chr12 | 95973823 | ||||||
| chr12:95973952 | T | G | 1 | a0001c0001t0042 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*280A>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 21/21 | 280 | chr12 | 95973952 | ||||||
| chr12:95974041 | G | A | 1 | a0001c0001t0025 | 2 | HG03195.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*191C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 21/21 | 191 | chr12 | 95974041 | ||||||
| chr12:95974120 | A | T | 1 | a0001c0003t0033 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*112T>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 21/21 | 112 | chr12 | 95974120 | ||||||
| chr12:95974122 | G | T | 15 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0009 others(12): Show |
74 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*110C>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 21/21 | 110 | chr12 | 95974122 | ||||||
| chr12:95995948 | G | A | 1 | a0001c0001t0025 | 2 | HG03195.hp1 NA21309.hp2 |
5_prime_UTR_variant | MODIFIER | c.-38C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 2/21 | 38 | chr12 | 95995948 | ||||||
| chr12:95995979 | G | A | 1 | a0001c0001t0043 | 1 | HG02129.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-69C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 2/21 | chr12 | 95995979 | |||||||
| chr12:95996103 | C | T | 1 | a0001c0003t0030 | 1 | NA19043.hp2 | 5_prime_UTR_variant | MODIFIER | c.-107G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 1/21 | 193 | chr12 | 95996103 | ||||||
| chr12:95996123 | G | T | 5 | a0001c0001t0015 a0001c0001t0022 a0001c0001t0031 others(2): Show |
13 | HG01167.hp2 HG01192.hp2 HG02055.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-127C>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 1/21 | 213 | chr12 | 95996123 | ||||||
| chr12:95996132 | C | T | 1 | a0001c0003t0030 | 1 | NA19043.hp2 | 5_prime_UTR_variant | MODIFIER | c.-136G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 1/21 | 222 | chr12 | 95996132 | ||||||
| chr12:95996212 | T | G | 1 | a0001c0001t0026 | 2 | HG00140.hp2 HG01123.hp1 |
5_prime_UTR_variant | MODIFIER | c.-216A>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 1/21 | 302 | chr12 | 95996212 | ||||||
| chr12:95996318 | A | G | 4 | a0001c0001t0014 a0001c0002t0029 a0001c0003t0027 others(1): Show |
7 | NA18940.hp1 NA18945.hp1 NA18971.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-322T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 1/21 | 408 | chr12 | 95996318 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:95974477 | A | G | 47 | a0001c0001t0005g0097 a0001c0001t0005g0113 a0001c0001t0005g0227 others(44): Show |
68 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1834-105T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95974477 | |||||||
| chr12:95974482 | C | T | 1 | a0001c0002t0003g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1834-110G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95974482 | |||||||
| chr12:95974720 | GT | G | 29 | a0001c0003t0005g0006 a0001c0003t0005g0018 a0001c0003t0005g0031 others(26): Show |
46 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1834-349delA | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95974720 | |||||||
| chr12:95974871 | C | T | 1 | a0001c0002t0010g0189 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1834-499G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95974871 | |||||||
| chr12:95974937 | A | G | 44 | a0001c0001t0005g0097 a0001c0001t0005g0113 a0001c0001t0005g0227 others(41): Show |
63 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1834-565T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95974937 | |||||||
| chr12:95975032 | A | G | 1 | a0006c0011t0037g0071 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1834-660T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95975032 | |||||||
| chr12:95975157 | C | T | 2 | a0001c0001t0002g0152 a0001c0001t0002g0156 |
2 | HG00323.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1834-785G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95975157 | |||||||
| chr12:95975165 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(69): Show |
148 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1834-793C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95975165 | |||||||
| chr12:95975298 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1834-926G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95975298 | |||||||
| chr12:95975346 | T | C | 1 | a0001c0003t0033g0088 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1834-974A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95975346 | |||||||
| chr12:95975347 | C | CT | 44 | a0001c0001t0001g0127 a0001c0001t0002g0160 a0001c0001t0005g0097 others(41): Show |
62 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1834-976dupA | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95975347 | |||||||
| chr12:95975347 | C | CTTT | 20 | a0001c0001t0003g0099 a0001c0001t0006g0019 a0001c0001t0006g0043 others(17): Show |
29 | HG00140.hp1 HG00642.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1834-978_1834-976d others(5): Show |
HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95975347 | |||||||
| chr12:95975347 | C | T | 1 | a0001c0003t0033g0088 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1834-975G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95975347 | |||||||
| chr12:95975347 | CTTTTTTT | C | 4 | a0001c0001t0001g0130 a0001c0006t0013g0020 a0001c0006t0013g0106 others(1): Show |
6 | HG00558.hp2 HG02559.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1834-982_1834-976d others(9): Show |
HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95975347 | |||||||
| chr12:95975354 | T | C | 1 | a0001c0001t0003g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1834-982A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95975354 | |||||||
| chr12:95975520 | A | AT | 48 | a0001c0001t0005g0097 a0001c0001t0005g0113 a0001c0001t0005g0227 others(45): Show |
69 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1833+908dupA | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95975520 | |||||||
| chr12:95975521 | T | A | 1 | a0006c0011t0037g0071 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1833+908A>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95975521 | |||||||
| chr12:95975521 | T | C | 1 | a0003c0010t0023g0030 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1833+908A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95975521 | |||||||
| chr12:95975588 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1833+841T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95975588 | |||||||
| chr12:95975604 | C | G | 47 | a0001c0001t0005g0097 a0001c0001t0005g0113 a0001c0001t0005g0227 others(44): Show |
68 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1833+825G>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95975604 | |||||||
| chr12:95975662 | G | T | 41 | a0001c0001t0003g0148 a0001c0002t0001g0012 a0001c0002t0001g0207 others(38): Show |
75 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.1833+767C>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95975662 | |||||||
| chr12:95975862 | A | G | 1 | a0001c0001t0002g0222 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1833+567T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95975862 | |||||||
| chr12:95975972 | C | T | 7 | a0001c0001t0003g0099 a0001c0001t0006g0019 a0001c0001t0006g0043 others(4): Show |
10 | HG02622.hp1 HG02622.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1833+457G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95975972 | |||||||
| chr12:95976015 | G | A | 2 | a0001c0001t0006g0019 a0001c0001t0006g0103 |
4 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1833+414C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95976015 | |||||||
| chr12:95976288 | G | A | 3 | a0001c0006t0013g0020 a0001c0006t0013g0106 a0001c0006t0013g0107 |
5 | HG02559.hp1 HG02818.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1833+141C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95976288 | |||||||
| chr12:95976364 | C | T | 1 | a0001c0001t0007g0023 | 3 | HG01261.hp1 HG01361.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1833+65G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 20/20 | chr12 | 95976364 | |||||||
| chr12:95976502 | C | A | 2 | a0001c0001t0006g0019 a0001c0001t0006g0103 |
4 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1764-4G>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 19/20 | chr12 | 95976502 | |||||||
| chr12:95976545 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1764-47G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 19/20 | chr12 | 95976545 | |||||||
| chr12:95976755 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0175 |
2 | HG02165.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1655-49C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95976755 | |||||||
| chr12:95976845 | C | T | 1 | a0001c0002t0003g0194 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1655-139G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95976845 | |||||||
| chr12:95976850 | G | C | 1 | a0001c0001t0001g0131 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1655-144C>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95976850 | |||||||
| chr12:95976863 | A | C | 1 | a0001c0001t0001g0124 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1655-157T>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95976863 | |||||||
| chr12:95976892 | A | G | 45 | a0001c0001t0005g0097 a0001c0001t0005g0113 a0001c0001t0005g0227 others(42): Show |
64 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1655-186T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95976892 | |||||||
| chr12:95976963 | A | G | 39 | a0001c0001t0002g0005 a0001c0001t0002g0013 a0001c0001t0002g0015 others(36): Show |
57 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.1655-257T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95976963 | |||||||
| chr12:95977043 | G | A | 1 | a0001c0002t0020g0186 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1655-337C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977043 | |||||||
| chr12:95977043 | GT | G | 3 | a0001c0006t0013g0020 a0001c0006t0013g0106 a0001c0006t0013g0107 |
5 | HG02559.hp1 HG02818.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1655-338delA | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977043 | |||||||
| chr12:95977181 | G | A | 1 | a0002c0004t0003g0213 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1655-475C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977181 | |||||||
| chr12:95977227 | C | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(70): Show |
147 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1655-521G>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977227 | |||||||
| chr12:95977385 | T | TA | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(76): Show |
155 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1654+558dupT | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977385 | |||||||
| chr12:95977422 | C | T | 3 | a0001c0006t0013g0020 a0001c0006t0013g0106 a0001c0006t0013g0107 |
5 | HG02559.hp1 HG02818.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1654+522G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977422 | |||||||
| chr12:95977454 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0175 |
2 | HG02165.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1654+490C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977454 | |||||||
| chr12:95977642 | C | CA | 69 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(66): Show |
141 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1654+301dupT | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977642 | |||||||
| chr12:95977642 | C | CAAA | 41 | a0001c0001t0005g0097 a0001c0001t0005g0113 a0001c0001t0005g0227 others(38): Show |
56 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1654+299_1654+301d others(5): Show |
HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977642 | |||||||
| chr12:95977642 | C | CAAAA | 57 | a0001c0001t0003g0099 a0001c0001t0006g0019 a0001c0001t0006g0043 others(54): Show |
99 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.1654+298_1654+301d others(6): Show |
HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977642 | |||||||
| chr12:95977642 | C | CAAAAA | 12 | a0001c0001t0003g0017 a0001c0001t0006g0238 a0001c0001t0007g0010 others(9): Show |
22 | HG00140.hp1 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1654+297_1654+301d others(7): Show |
HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977642 | |||||||
| chr12:95977642 | C | CAAAAAA | 3 | a0001c0001t0003g0212 a0001c0003t0005g0018 a0001c0003t0005g0037 |
6 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1654+296_1654+301d others(8): Show |
HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977642 | |||||||
| chr12:95977642 | CAAAAAA | C | 36 | a0001c0001t0002g0005 a0001c0001t0002g0013 a0001c0001t0002g0015 others(33): Show |
54 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.1654+296_1654+301d others(8): Show |
HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977642 | |||||||
| chr12:95977656 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1654+288T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977656 | |||||||
| chr12:95977658 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1654+286T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977658 | |||||||
| chr12:95977710 | T | C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(222): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.1654+234A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977710 | |||||||
| chr12:95977749 | G | A | 1 | a0001c0001t0010g0140 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1654+195C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977749 | |||||||
| chr12:95977755 | G | C | 2 | a0001c0001t0025g0241 a0001c0001t0025g0242 |
2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1654+189C>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977755 | |||||||
| chr12:95977769 | G | A | 39 | a0001c0001t0001g0159 a0001c0001t0002g0005 a0001c0001t0002g0013 others(36): Show |
57 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.1654+175C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977769 | |||||||
| chr12:95977790 | G | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(109): Show |
204 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1654+154C>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977790 | |||||||
| chr12:95977861 | T | C | 4 | a0001c0001t0002g0013 a0001c0001t0002g0146 a0001c0001t0002g0160 others(1): Show |
8 | HG03209.hp2 HG03831.hp2 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1654+83A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977861 | |||||||
| chr12:95977892 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(66): Show |
141 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1654+52C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977892 | |||||||
| chr12:95977908 | C | G | 1 | a0001c0003t0005g0104 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1654+36G>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 18/20 | chr12 | 95977908 | |||||||
| chr12:95978116 | C | T | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(223): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.1520-38G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95978116 | |||||||
| chr12:95978129 | C | T | 1 | a0002c0004t0003g0052 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1520-51G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95978129 | |||||||
| chr12:95978149 | A | T | 1 | a0001c0001t0002g0154 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1520-71T>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95978149 | |||||||
| chr12:95978248 | A | AT | 186 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(183): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1520-171dupA | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95978248 | |||||||
| chr12:95978280 | A | G | 3 | a0001c0005t0001g0057 a0001c0005t0017g0035 a0001c0005t0017g0165 |
5 | HG02451.hp1 HG03453.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1520-202T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95978280 | |||||||
| chr12:95978354 | G | A | 1 | a0001c0003t0005g0033 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1520-276C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95978354 | |||||||
| chr12:95978431 | G | A | 1 | a0001c0006t0013g0107 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1520-353C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95978431 | |||||||
| chr12:95978595 | G | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(67): Show |
142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1520-517C>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95978595 | |||||||
| chr12:95978713 | C | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(67): Show |
142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1520-635G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95978713 | |||||||
| chr12:95978747 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1520-669T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95978747 | |||||||
| chr12:95978856 | G | C | 53 | a0001c0001t0009g0056 a0001c0001t0009g0244 a0001c0001t0009g0245 others(50): Show |
90 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.1520-778C>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95978856 | |||||||
| chr12:95978862 | G | T | 9 | a0001c0001t0009g0056 a0001c0001t0009g0244 a0001c0001t0009g0245 others(6): Show |
10 | HG01192.hp2 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1520-784C>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95978862 | |||||||
| chr12:95978983 | A | G | 9 | a0001c0001t0009g0056 a0001c0001t0009g0244 a0001c0001t0009g0245 others(6): Show |
10 | HG01192.hp2 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1520-905T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95978983 | |||||||
| chr12:95979117 | A | G | 1 | a0001c0001t0002g0162 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1520-1039T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95979117 | |||||||
| chr12:95979296 | C | T | 1 | a0001c0002t0004g0209 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1520-1218G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95979296 | |||||||
| chr12:95979343 | C | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.1519+1213G>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95979343 | |||||||
| chr12:95979439 | C | T | 11 | a0001c0001t0009g0056 a0001c0001t0009g0244 a0001c0001t0009g0245 others(8): Show |
12 | HG01192.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1519+1117G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95979439 | |||||||
| chr12:95979452 | G | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(240): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.1519+1104C>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95979452 | |||||||
| chr12:95979528 | G | T | 1 | a0001c0001t0022g0066 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1519+1028C>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95979528 | |||||||
| chr12:95979631 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.1519+925A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95979631 | |||||||
| chr12:95979652 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1519+904C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95979652 | |||||||
| chr12:95979788 | A | G | 1 | a0001c0001t0011g0153 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1519+768T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95979788 | |||||||
| chr12:95979871 | A | C | 41 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(38): Show |
75 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1519+685T>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95979871 | |||||||
| chr12:95980243 | TGG | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.1519+311_1519+312d others(4): Show |
HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95980243 | |||||||
| chr12:95980279 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(173): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1519+277A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95980279 | |||||||
| chr12:95980481 | T | A | 9 | a0001c0001t0009g0056 a0001c0001t0009g0244 a0001c0001t0009g0245 others(6): Show |
10 | HG01192.hp2 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1519+75A>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 17/20 | chr12 | 95980481 | |||||||
| chr12:95980755 | T | A | 1 | a0001c0002t0003g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1354-34A>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 16/20 | chr12 | 95980755 | |||||||
| chr12:95980776 | G | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(223): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.1353+22C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 16/20 | chr12 | 95980776 | |||||||
| chr12:95980785 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.1353+13A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 16/20 | chr12 | 95980785 | |||||||
| chr12:95980883 | C | T | 16 | a0001c0002t0003g0048 a0001c0002t0003g0204 a0001c0002t0003g0206 others(13): Show |
29 | HG00544.hp2 HG00621.hp2 HG02071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1288-20G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95980883 | |||||||
| chr12:95980894 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.1288-31A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95980894 | |||||||
| chr12:95980905 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(172): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1288-42G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95980905 | |||||||
| chr12:95980972 | G | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(126): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1288-109C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95980972 | |||||||
| chr12:95981110 | T | C | 1 | a0001c0002t0010g0189 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1288-247A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95981110 | |||||||
| chr12:95981190 | TA | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(173): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1288-328delT | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95981190 | |||||||
| chr12:95981221 | G | A | 9 | a0001c0001t0009g0056 a0001c0001t0009g0244 a0001c0001t0009g0245 others(6): Show |
10 | HG01192.hp2 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1288-358C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95981221 | |||||||
| chr12:95981380 | A | G | 9 | a0001c0001t0009g0056 a0001c0001t0009g0244 a0001c0001t0009g0245 others(6): Show |
10 | HG01192.hp2 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1288-517T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95981380 | |||||||
| chr12:95981680 | G | A | 3 | a0001c0005t0001g0057 a0001c0005t0017g0035 a0001c0005t0017g0165 |
5 | HG02451.hp1 HG03453.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1288-817C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95981680 | |||||||
| chr12:95981717 | C | T | 2 | a0002c0004t0003g0213 a0002c0004t0003g0215 |
2 | HG01192.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1288-854G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95981717 | |||||||
| chr12:95981756 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(223): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.1288-893T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95981756 | |||||||
| chr12:95981849 | A | C | 41 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(38): Show |
75 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1288-986T>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95981849 | |||||||
| chr12:95981904 | T | C | 115 | a0001c0001t0001g0159 a0001c0001t0002g0005 a0001c0001t0002g0013 others(112): Show |
184 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1288-1041A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95981904 | |||||||
| chr12:95981984 | C | G | 1 | a0002c0004t0003g0051 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1288-1121G>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95981984 | |||||||
| chr12:95982007 | G | A | 18 | a0002c0004t0002g0053 a0002c0004t0002g0224 a0002c0004t0003g0008 others(15): Show |
30 | HG00558.hp1 HG00621.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1288-1144C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95982007 | |||||||
| chr12:95982038 | T | C | 3 | a0001c0001t0006g0229 a0001c0001t0006g0237 a0001c0001t0006g0238 |
3 | HG02809.hp1 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1288-1175A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95982038 | |||||||
| chr12:95982152 | A | G | 1 | a0005c0012t0002g0142 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1288-1289T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95982152 | |||||||
| chr12:95982202 | G | A | 2 | a0001c0001t0003g0017 a0001c0001t0003g0212 |
5 | HG01891.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1288-1339C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95982202 | |||||||
| chr12:95982313 | T | C | 3 | a0001c0006t0013g0020 a0001c0006t0013g0106 a0001c0006t0013g0107 |
5 | HG02559.hp1 HG02818.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1288-1450A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95982313 | |||||||
| chr12:95982481 | C | T | 18 | a0002c0004t0002g0053 a0002c0004t0002g0224 a0002c0004t0003g0008 others(15): Show |
30 | HG00558.hp1 HG00621.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1287+1430G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95982481 | |||||||
| chr12:95982504 | T | C | 1 | a0001c0001t0006g0238 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1287+1407A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95982504 | |||||||
| chr12:95982506 | G | C | 1 | a0003c0010t0023g0030 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1287+1405C>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95982506 | |||||||
| chr12:95982555 | G | A | 18 | a0002c0004t0002g0053 a0002c0004t0002g0224 a0002c0004t0003g0008 others(15): Show |
30 | HG00558.hp1 HG00621.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1287+1356C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95982555 | |||||||
| chr12:95982611 | T | TA | 6 | a0001c0001t0005g0097 a0001c0001t0005g0113 a0001c0001t0005g0227 others(3): Show |
7 | HG01081.hp1 HG03688.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1287+1299dupT | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95982611 | |||||||
| chr12:95982615 | G | A | 39 | a0001c0001t0001g0159 a0001c0001t0002g0005 a0001c0001t0002g0013 others(36): Show |
57 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.1287+1296C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95982615 | |||||||
| chr12:95982689 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
4 | HG02040.hp2 NA18967.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1287+1222T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95982689 | |||||||
| chr12:95982985 | C | T | 18 | a0002c0004t0002g0053 a0002c0004t0002g0224 a0002c0004t0003g0008 others(15): Show |
30 | HG00558.hp1 HG00621.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1287+926G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95982985 | |||||||
| chr12:95983079 | G | A | 2 | a0001c0001t0001g0134 a0001c0005t0002g0105 |
2 | HG02723.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1287+832C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95983079 | |||||||
| chr12:95983160 | G | A | 1 | a0001c0002t0004g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1287+751C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95983160 | |||||||
| chr12:95983222 | T | C | 2 | a0001c0001t0006g0019 a0001c0001t0006g0103 |
4 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1287+689A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95983222 | |||||||
| chr12:95983245 | A | G | 11 | a0001c0001t0009g0056 a0001c0001t0009g0244 a0001c0001t0009g0245 others(8): Show |
12 | HG01192.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1287+666T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95983245 | |||||||
| chr12:95983396 | C | CA | 10 | a0001c0001t0009g0056 a0001c0001t0009g0244 a0001c0001t0009g0245 others(7): Show |
11 | HG01192.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1287+514dupT | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95983396 | |||||||
| chr12:95983396 | CA | C | 52 | a0001c0001t0003g0017 a0001c0001t0003g0099 a0001c0001t0003g0147 others(49): Show |
83 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.1287+514delT | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95983396 | |||||||
| chr12:95983400 | A | C | 18 | a0002c0004t0002g0053 a0002c0004t0002g0224 a0002c0004t0003g0008 others(15): Show |
30 | HG00558.hp1 HG00621.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1287+511T>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 15/20 | chr12 | 95983400 | |||||||
| chr12:95984083 | G | C | 2 | a0001c0002t0003g0202 a0001c0002t0003g0205 |
2 | HG01099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1207-92C>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95984083 | |||||||
| chr12:95984087 | T | C | 2 | a0001c0005t0006g0077 a0001c0005t0032g0063 |
2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1207-96A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95984087 | |||||||
| chr12:95984116 | T | A | 1 | a0001c0002t0004g0203 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1207-125A>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95984116 | |||||||
| chr12:95984133 | A | ATACTATG others(5): Show |
29 | a0001c0001t0009g0056 a0001c0001t0009g0244 a0001c0001t0009g0245 others(26): Show |
42 | HG00558.hp1 HG00621.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1207-143_1207-142i others(14): Show |
HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95984133 | |||||||
| chr12:95984463 | G | A | 2 | a0001c0005t0006g0077 a0001c0005t0032g0063 |
2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1207-472C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95984463 | |||||||
| chr12:95984481 | C | T | 94 | a0001c0001t0001g0159 a0001c0001t0002g0005 a0001c0001t0002g0013 others(91): Show |
149 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1207-490G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95984481 | |||||||
| chr12:95984524 | G | C | 11 | a0001c0001t0009g0056 a0001c0001t0009g0244 a0001c0001t0009g0245 others(8): Show |
12 | HG01192.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1207-533C>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95984524 | |||||||
| chr12:95984720 | G | T | 1 | a0003c0010t0023g0030 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1207-729C>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95984720 | |||||||
| chr12:95984721 | A | G | 1 | a0001c0001t0007g0023 | 3 | HG01261.hp1 HG01361.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1207-730T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95984721 | |||||||
| chr12:95984814 | A | G | 1 | a0001c0002t0004g0208 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1207-823T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95984814 | |||||||
| chr12:95984922 | T | A | 2 | a0001c0005t0006g0077 a0001c0005t0032g0063 |
2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1207-931A>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95984922 | |||||||
| chr12:95984940 | C | T | 9 | a0001c0001t0009g0056 a0001c0001t0009g0244 a0001c0001t0009g0245 others(6): Show |
10 | HG01192.hp2 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1207-949G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95984940 | |||||||
| chr12:95984980 | A | C | 11 | a0001c0001t0009g0056 a0001c0001t0009g0244 a0001c0001t0009g0245 others(8): Show |
12 | HG01192.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1206+928T>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95984980 | |||||||
| chr12:95984993 | C | T | 115 | a0001c0001t0001g0159 a0001c0001t0002g0005 a0001c0001t0002g0013 others(112): Show |
184 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1206+915G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95984993 | |||||||
| chr12:95985029 | C | T | 83 | a0001c0001t0001g0159 a0001c0001t0002g0005 a0001c0001t0002g0013 others(80): Show |
137 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.1206+879G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95985029 | |||||||
| chr12:95985149 | G | A | 39 | a0001c0001t0001g0159 a0001c0001t0002g0005 a0001c0001t0002g0013 others(36): Show |
57 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.1206+759C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95985149 | |||||||
| chr12:95985320 | G | T | 1 | a0003c0010t0023g0030 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1206+588C>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95985320 | |||||||
| chr12:95985456 | G | A | 1 | a0001c0001t0006g0102 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1206+452C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95985456 | |||||||
| chr12:95985488 | G | T | 9 | a0001c0001t0009g0056 a0001c0001t0009g0244 a0001c0001t0009g0245 others(6): Show |
10 | HG01192.hp2 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1206+420C>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95985488 | |||||||
| chr12:95985549 | C | G | 44 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(41): Show |
80 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.1206+359G>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95985549 | |||||||
| chr12:95985579 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1206+329C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95985579 | |||||||
| chr12:95985624 | C | CA | 42 | a0001c0001t0001g0041 a0001c0001t0001g0096 a0001c0001t0001g0120 others(39): Show |
76 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1206+283dupT | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95985624 | |||||||
| chr12:95985624 | CA | C | 89 | a0001c0001t0001g0109 a0001c0001t0001g0117 a0001c0001t0001g0121 others(86): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1206+283delT | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95985624 | |||||||
| chr12:95985624 | CAA | C | 24 | a0001c0001t0002g0150 a0001c0001t0002g0152 a0001c0001t0006g0078 others(21): Show |
36 | HG00621.hp1 HG00735.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1206+282_1206+283d others(4): Show |
HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95985624 | |||||||
| chr12:95985749 | T | C | 1 | a0001c0001t0006g0101 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1206+159A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95985749 | |||||||
| chr12:95985885 | C | CT | 8 | a0001c0001t0009g0056 a0001c0001t0009g0244 a0001c0001t0015g0064 others(5): Show |
9 | HG01192.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1206+22dupA | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 14/20 | chr12 | 95985885 | |||||||
| chr12:95986028 | G | A | 109 | a0001c0001t0001g0159 a0001c0001t0002g0005 a0001c0001t0002g0013 others(106): Show |
176 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1147+37C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 13/20 | chr12 | 95986028 | |||||||
| chr12:95986268 | A | G | 18 | a0002c0004t0002g0053 a0002c0004t0002g0224 a0002c0004t0003g0008 others(15): Show |
30 | HG00558.hp1 HG00621.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1052-108T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 12/20 | chr12 | 95986268 | |||||||
| chr12:95986347 | T | A | 2 | a0001c0001t0003g0017 a0001c0001t0003g0212 |
5 | HG01891.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1052-187A>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 12/20 | chr12 | 95986347 | |||||||
| chr12:95986353 | C | T | 28 | a0001c0001t0009g0056 a0001c0001t0009g0244 a0001c0001t0009g0245 others(25): Show |
41 | HG00558.hp1 HG00621.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1052-193G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 12/20 | chr12 | 95986353 | |||||||
| chr12:95986573 | C | T | 3 | a0001c0001t0006g0229 a0001c0001t0006g0237 a0001c0001t0006g0238 |
3 | HG02809.hp1 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1052-413G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 12/20 | chr12 | 95986573 | |||||||
| chr12:95986591 | C | T | 1 | a0001c0005t0017g0165 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1052-431G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 12/20 | chr12 | 95986591 | |||||||
| chr12:95986636 | G | A | 1 | a0001c0001t0042g0137 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1051+431C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 12/20 | chr12 | 95986636 | |||||||
| chr12:95986660 | A | G | 18 | a0002c0004t0002g0053 a0002c0004t0002g0224 a0002c0004t0003g0008 others(15): Show |
30 | HG00558.hp1 HG00621.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1051+407T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 12/20 | chr12 | 95986660 | |||||||
| chr12:95986664 | C | T | 18 | a0002c0004t0002g0053 a0002c0004t0002g0224 a0002c0004t0003g0008 others(15): Show |
30 | HG00558.hp1 HG00621.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1051+403G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 12/20 | chr12 | 95986664 | |||||||
| chr12:95986860 | G | A | 1 | a0001c0001t0006g0237 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1051+207C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 12/20 | chr12 | 95986860 | |||||||
| chr12:95986875 | T | C | 1 | a0001c0001t0006g0101 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1051+192A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 12/20 | chr12 | 95986875 | |||||||
| chr12:95986964 | C | A | 1 | a0001c0005t0002g0105 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1051+103G>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 12/20 | chr12 | 95986964 | |||||||
| chr12:95986971 | C | A | 1 | a0001c0001t0001g0138 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1051+96G>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 12/20 | chr12 | 95986971 | |||||||
| chr12:95986975 | C | T | 17 | a0001c0001t0001g0214 a0002c0004t0002g0053 a0002c0004t0002g0224 others(14): Show |
28 | HG00558.hp1 HG00621.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.1051+92G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 12/20 | chr12 | 95986975 | |||||||
| chr12:95986981 | C | T | 3 | a0001c0003t0005g0211 a0001c0003t0005g0236 a0001c0003t0012g0009 |
7 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1051+86G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 12/20 | chr12 | 95986981 | |||||||
| chr12:95987009 | C | A | 1 | a0002c0004t0002g0224 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1051+58G>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 12/20 | chr12 | 95987009 | |||||||
| chr12:95987454 | A | C | 181 | a0001c0001t0001g0159 a0001c0001t0001g0214 a0001c0001t0002g0005 others(178): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.904-240T>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 11/20 | chr12 | 95987454 | |||||||
| chr12:95987714 | T | C | 31 | a0001c0003t0005g0006 a0001c0003t0005g0018 a0001c0003t0005g0031 others(28): Show |
48 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.903+479A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 11/20 | chr12 | 95987714 | |||||||
| chr12:95987887 | T | A | 44 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(41): Show |
80 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.903+306A>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 11/20 | chr12 | 95987887 | |||||||
| chr12:95987894 | G | T | 3 | a0001c0001t0006g0229 a0001c0001t0006g0237 a0001c0001t0006g0238 |
3 | HG02809.hp1 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.903+299C>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 11/20 | chr12 | 95987894 | |||||||
| chr12:95987897 | C | CG | 62 | a0001c0001t0001g0016 a0001c0001t0001g0108 a0001c0001t0001g0120 others(59): Show |
105 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.903+295dupC | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 11/20 | chr12 | 95987897 | |||||||
| chr12:95987898 | G | C | 5 | a0001c0003t0005g0091 a0001c0003t0005g0092 a0001c0003t0005g0118 others(2): Show |
5 | HG00438.hp1 NA18955.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.903+295C>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 11/20 | chr12 | 95987898 | |||||||
| chr12:95987904 | G | C | 1 | a0001c0001t0006g0102 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.903+289C>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 11/20 | chr12 | 95987904 | |||||||
| chr12:95987978 | C | G | 1 | a0001c0001t0036g0111 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.903+215G>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 11/20 | chr12 | 95987978 | |||||||
| chr12:95988010 | C | A | 34 | a0001c0001t0002g0029 a0001c0001t0002g0083 a0001c0001t0026g0058 others(31): Show |
53 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.903+183G>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 11/20 | chr12 | 95988010 | |||||||
| chr12:95988301 | A | G | 2 | a0001c0001t0025g0241 a0001c0001t0025g0242 |
2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.856-61T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95988301 | |||||||
| chr12:95988376 | T | A | 1 | a0001c0001t0015g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.856-136A>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95988376 | |||||||
| chr12:95988447 | AT | A | 3 | a0001c0003t0005g0211 a0001c0003t0005g0236 a0001c0003t0012g0009 |
7 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.856-208delA | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95988447 | |||||||
| chr12:95988476 | G | T | 34 | a0001c0001t0002g0029 a0001c0001t0002g0083 a0001c0001t0026g0058 others(31): Show |
53 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.856-236C>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95988476 | |||||||
| chr12:95988529 | T | C | 47 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(44): Show |
84 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.856-289A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95988529 | |||||||
| chr12:95988534 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0139 |
4 | NA18954.hp2 NA18988.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.856-294A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95988534 | |||||||
| chr12:95988537 | C | G | 43 | a0001c0001t0001g0159 a0001c0001t0002g0005 a0001c0001t0002g0013 others(40): Show |
60 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.856-297G>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95988537 | |||||||
| chr12:95988647 | A | AG | 2 | a0001c0001t0001g0024 a0001c0001t0019g0172 |
4 | NA18943.hp1 NA18952.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.856-408dupC | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95988647 | |||||||
| chr12:95988822 | C | G | 41 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(38): Show |
75 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.856-582G>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95988822 | |||||||
| chr12:95988866 | A | G | 42 | a0001c0001t0001g0159 a0001c0001t0002g0005 a0001c0001t0002g0013 others(39): Show |
59 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.856-626T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95988866 | |||||||
| chr12:95988885 | G | A | 1 | a0001c0001t0010g0140 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.856-645C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95988885 | |||||||
| chr12:95988888 | A | G | 47 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(44): Show |
84 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.856-648T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95988888 | |||||||
| chr12:95988924 | C | T | 182 | a0001c0001t0001g0159 a0001c0001t0001g0214 a0001c0001t0001g0226 others(179): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.856-684G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95988924 | |||||||
| chr12:95988951 | C | G | 1 | a0001c0001t0002g0222 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.856-711G>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95988951 | |||||||
| chr12:95988977 | T | C | 2 | a0001c0005t0006g0077 a0001c0005t0032g0063 |
2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.856-737A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95988977 | |||||||
| chr12:95989039 | G | C | 47 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(44): Show |
84 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.856-799C>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95989039 | |||||||
| chr12:95989160 | C | T | 74 | a0001c0001t0003g0017 a0001c0001t0003g0099 a0001c0001t0003g0212 others(71): Show |
124 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.856-920G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95989160 | |||||||
| chr12:95989177 | G | A | 1 | a0001c0002t0004g0208 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.856-937C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95989177 | |||||||
| chr12:95989389 | C | A | 2 | a0001c0005t0006g0077 a0001c0005t0032g0063 |
2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.855+1004G>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95989389 | |||||||
| chr12:95989389 | C | G | 45 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(42): Show |
82 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.855+1004G>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95989389 | |||||||
| chr12:95989496 | T | C | 1 | a0001c0001t0001g0164 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.855+897A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95989496 | |||||||
| chr12:95989748 | C | T | 1 | a0001c0001t0006g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.855+645G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95989748 | |||||||
| chr12:95989934 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.855+459T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95989934 | |||||||
| chr12:95990230 | G | T | 1 | a0001c0002t0010g0184 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.855+163C>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95990230 | |||||||
| chr12:95990253 | C | T | 43 | a0001c0001t0002g0029 a0001c0001t0002g0083 a0001c0001t0004g0093 others(40): Show |
65 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.855+140G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95990253 | |||||||
| chr12:95990254 | G | A | 1 | a0001c0001t0002g0166 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.855+139C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95990254 | |||||||
| chr12:95990285 | A | G | 47 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(44): Show |
83 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.855+108T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95990285 | |||||||
| chr12:95990322 | C | T | 15 | a0001c0001t0003g0099 a0001c0001t0006g0019 a0001c0001t0006g0078 others(12): Show |
18 | HG01192.hp2 HG02109.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.855+71G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95990322 | |||||||
| chr12:95990344 | T | C | 51 | a0001c0001t0001g0007 a0001c0002t0001g0012 a0001c0002t0001g0207 others(48): Show |
92 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.855+49A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95990344 | |||||||
| chr12:95990361 | T | C | 49 | a0001c0001t0005g0228 a0001c0002t0001g0012 a0001c0002t0001g0207 others(46): Show |
85 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.855+32A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95990361 | |||||||
| chr12:95990384 | G | A | 2 | a0001c0001t0006g0019 a0001c0001t0006g0103 |
4 | HG02622.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.855+9C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 10/20 | chr12 | 95990384 | |||||||
| chr12:95990567 | T | C | 97 | a0001c0001t0001g0004 a0001c0001t0001g0159 a0001c0001t0001g0163 others(94): Show |
159 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.716-35A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95990567 | |||||||
| chr12:95990612 | G | A | 1 | a0001c0001t0002g0166 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.716-80C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95990612 | |||||||
| chr12:95990659 | A | T | 14 | a0001c0001t0003g0017 a0001c0001t0003g0212 a0001c0001t0005g0097 others(11): Show |
22 | HG00140.hp1 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.716-127T>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95990659 | |||||||
| chr12:95990687 | C | T | 1 | a0001c0002t0004g0181 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.716-155G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95990687 | |||||||
| chr12:95990719 | T | G | 51 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(48): Show |
87 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.716-187A>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95990719 | |||||||
| chr12:95990764 | A | G | 146 | a0001c0001t0001g0214 a0001c0001t0001g0221 a0001c0001t0001g0226 others(143): Show |
231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.716-232T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95990764 | |||||||
| chr12:95990832 | A | G | 6 | a0001c0003t0030g0062 a0001c0005t0001g0057 a0001c0005t0002g0105 others(3): Show |
8 | HG02109.hp1 HG02451.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.716-300T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95990832 | |||||||
| chr12:95990863 | A | G | 49 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(46): Show |
84 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.716-331T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95990863 | |||||||
| chr12:95990875 | C | T | 1 | a0001c0001t0006g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.716-343G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95990875 | |||||||
| chr12:95990886 | T | G | 1 | a0002c0004t0002g0224 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.716-354A>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95990886 | |||||||
| chr12:95990891 | C | G | 9 | a0001c0001t0003g0099 a0001c0001t0006g0019 a0001c0001t0006g0078 others(6): Show |
12 | HG02622.hp1 HG02622.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.716-359G>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95990891 | |||||||
| chr12:95990924 | A | G | 48 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(45): Show |
83 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.716-392T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95990924 | |||||||
| chr12:95991034 | C | T | 1 | a0001c0003t0005g0082 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.716-502G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95991034 | |||||||
| chr12:95991064 | T | C | 49 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(46): Show |
84 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.716-532A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95991064 | |||||||
| chr12:95991122 | G | T | 1 | a0001c0001t0006g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.716-590C>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95991122 | |||||||
| chr12:95991140 | C | A | 1 | a0001c0001t0006g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.716-608G>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95991140 | |||||||
| chr12:95991246 | GT | G | 39 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0002g0015 others(36): Show |
61 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.716-715delA | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95991246 | |||||||
| chr12:95991456 | G | A | 23 | a0001c0001t0001g0214 a0001c0001t0001g0221 a0001c0001t0001g0226 others(20): Show |
34 | HG00558.hp1 HG00621.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.716-924C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95991456 | |||||||
| chr12:95991498 | C | T | 1 | a0001c0001t0015g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.716-966G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95991498 | |||||||
| chr12:95991569 | C | G | 4 | a0001c0001t0001g0021 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
6 | HG02027.hp2 HG02083.hp1 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.716-1037G>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95991569 | |||||||
| chr12:95991571 | A | T | 4 | a0001c0003t0005g0018 a0001c0003t0005g0081 a0001c0003t0005g0104 others(1): Show |
6 | HG02280.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.716-1039T>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95991571 | |||||||
| chr12:95991581 | C | T | 32 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0002g0015 others(29): Show |
52 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.716-1049G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95991581 | |||||||
| chr12:95991661 | G | A | 23 | a0001c0001t0001g0214 a0001c0001t0001g0221 a0001c0001t0001g0226 others(20): Show |
34 | HG00558.hp1 HG00621.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.715+1019C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95991661 | |||||||
| chr12:95991678 | A | G | 99 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0002g0015 others(96): Show |
157 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.715+1002T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95991678 | |||||||
| chr12:95991756 | T | G | 10 | a0001c0001t0002g0079 a0001c0001t0009g0056 a0001c0001t0009g0244 others(7): Show |
11 | HG01192.hp2 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.715+924A>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95991756 | |||||||
| chr12:95991791 | AG | A | 2 | a0001c0001t0007g0010 a0001c0001t0007g0098 |
6 | HG00642.hp1 HG00741.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.715+888delC | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95991791 | |||||||
| chr12:95991802 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.715+878G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95991802 | |||||||
| chr12:95992038 | G | C | 1 | a0001c0001t0001g0167 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.715+642C>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95992038 | |||||||
| chr12:95992046 | G | C | 1 | a0001c0001t0008g0168 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.715+634C>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95992046 | |||||||
| chr12:95992081 | A | G | 1 | a0001c0001t0001g0036 | 2 | NA18747.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.715+599T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95992081 | |||||||
| chr12:95992118 | C | T | 2 | a0001c0001t0006g0237 a0001c0003t0005g0236 |
2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.715+562G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95992118 | |||||||
| chr12:95992353 | C | T | 3 | a0001c0001t0001g0226 a0002c0004t0003g0054 a0002c0004t0003g0225 |
4 | HG00735.hp2 HG01516.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.715+327G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95992353 | |||||||
| chr12:95992360 | A | G | 140 | a0001c0001t0001g0055 a0001c0001t0001g0095 a0001c0001t0001g0096 others(137): Show |
221 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.715+320T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95992360 | |||||||
| chr12:95992379 | T | G | 50 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(47): Show |
85 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.715+301A>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95992379 | |||||||
| chr12:95992457 | AG | A | 7 | a0001c0001t0003g0099 a0001c0001t0006g0019 a0001c0001t0006g0100 others(4): Show |
9 | HG02622.hp1 HG02622.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.715+222delC | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95992457 | |||||||
| chr12:95992495 | C | T | 50 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(47): Show |
85 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.715+185G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95992495 | |||||||
| chr12:95992502 | G | A | 1 | a0001c0003t0005g0104 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.715+178C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95992502 | |||||||
| chr12:95992607 | T | C | 1 | a0001c0001t0002g0169 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.715+73A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95992607 | |||||||
| chr12:95992655 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.715+25A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95992655 | |||||||
| chr12:95992671 | T | C | 1 | a0001c0001t0002g0171 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.715+9A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 9/20 | chr12 | 95992671 | |||||||
| chr12:95992852 | T | C | 50 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(47): Show |
85 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.590-47A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 8/20 | chr12 | 95992852 | |||||||
| chr12:95992868 | G | GCCCT | 50 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(47): Show |
85 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.590-67_590-64dupAG others(2): Show |
HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 8/20 | chr12 | 95992868 | |||||||
| chr12:95992868 | G | GCCCTCCC others(1): Show |
63 | a0001c0001t0001g0055 a0001c0001t0001g0095 a0001c0001t0001g0096 others(60): Show |
95 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.590-71_590-64dupAG others(6): Show |
HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 8/20 | chr12 | 95992868 | |||||||
| chr12:95992928 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.590-123C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 8/20 | chr12 | 95992928 | |||||||
| chr12:95993054 | C | T | 1 | a0001c0002t0010g0230 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.590-249G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 8/20 | chr12 | 95993054 | |||||||
| chr12:95993080 | G | A | 52 | a0001c0001t0001g0055 a0001c0001t0001g0095 a0001c0001t0001g0096 others(49): Show |
83 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.590-275C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 8/20 | chr12 | 95993080 | |||||||
| chr12:95993202 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0019g0172 |
4 | NA18943.hp1 NA18952.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+249A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 8/20 | chr12 | 95993202 | |||||||
| chr12:95993213 | G | C | 47 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(44): Show |
82 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.589+238C>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 8/20 | chr12 | 95993213 | |||||||
| chr12:95993234 | T | C | 47 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(44): Show |
82 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.589+217A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 8/20 | chr12 | 95993234 | |||||||
| chr12:95993294 | G | A | 46 | a0001c0002t0001g0012 a0001c0002t0001g0207 a0001c0002t0002g0200 others(43): Show |
81 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.589+157C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 8/20 | chr12 | 95993294 | |||||||
| chr12:95993321 | G | A | 2 | a0001c0001t0003g0017 a0001c0001t0003g0212 |
5 | HG01891.hp1 HG02280.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.589+130C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 8/20 | chr12 | 95993321 | |||||||
| chr12:95993550 | G | A | 3 | a0001c0005t0001g0057 a0001c0005t0002g0105 a0001c0005t0017g0035 |
5 | HG02451.hp1 HG02723.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.552-62C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 7/20 | chr12 | 95993550 | |||||||
| chr12:95993705 | C | T | 1 | a0001c0002t0004g0177 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.551+67G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 7/20 | chr12 | 95993705 | |||||||
| chr12:95993843 | A | G | 141 | a0001c0001t0001g0055 a0001c0001t0001g0073 a0001c0001t0001g0095 others(138): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
splice_region_variant&intron_variant | LOW | c.485-5T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 6/20 | chr12 | 95993843 | |||||||
| chr12:95994017 | G | T | 3 | a0001c0003t0030g0062 a0001c0005t0006g0077 a0001c0005t0032g0063 |
3 | HG02109.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.412-19C>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 5/20 | chr12 | 95994017 | |||||||
| chr12:95994051 | A | G | 20 | a0001c0001t0001g0214 a0001c0001t0001g0221 a0001c0001t0001g0234 others(17): Show |
30 | HG00558.hp1 HG00621.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.411+39T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 5/20 | chr12 | 95994051 | |||||||
| chr12:95994274 | G | A | 47 | a0001c0001t0001g0175 a0001c0001t0011g0176 a0001c0002t0001g0012 others(44): Show |
80 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.337-110C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 4/20 | chr12 | 95994274 | |||||||
| chr12:95994288 | T | C | 1 | a0001c0001t0002g0174 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.337-124A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 4/20 | chr12 | 95994288 | |||||||
| chr12:95994305 | T | G | 48 | a0001c0001t0001g0175 a0001c0001t0011g0176 a0001c0002t0001g0012 others(45): Show |
81 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.337-141A>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 4/20 | chr12 | 95994305 | |||||||
| chr12:95994321 | G | A | 3 | a0001c0001t0003g0017 a0001c0001t0003g0212 a0001c0003t0005g0211 |
6 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.337-157C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 4/20 | chr12 | 95994321 | |||||||
| chr12:95994404 | T | G | 30 | a0001c0001t0001g0055 a0001c0001t0001g0214 a0001c0001t0001g0221 others(27): Show |
42 | HG00558.hp1 HG00621.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.337-240A>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 4/20 | chr12 | 95994404 | |||||||
| chr12:95994410 | T | C | 1 | a0001c0001t0041g0231 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.337-246A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 4/20 | chr12 | 95994410 | |||||||
| chr12:95994435 | G | C | 1 | a0001c0001t0002g0013 | 5 | NA18948.hp1 NA18961.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.337-271C>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 4/20 | chr12 | 95994435 | |||||||
| chr12:95994755 | G | A | 1 | a0001c0001t0015g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.336+43C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 4/20 | chr12 | 95994755 | |||||||
| chr12:95995024 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.248-31T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 2/20 | chr12 | 95995024 | |||||||
| chr12:95995065 | C | T | 1 | a0004c0009t0001g0074 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.248-72G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 2/20 | chr12 | 95995065 | |||||||
| chr12:95995312 | T | C | 7 | a0001c0001t0006g0237 a0001c0001t0006g0238 a0001c0001t0025g0241 others(4): Show |
7 | HG02809.hp1 HG03195.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.248-319A>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 2/20 | chr12 | 95995312 | |||||||
| chr12:95995325 | A | C | 2 | a0001c0001t0001g0073 a0001c0001t0002g0029 |
3 | HG00099.hp2 HG01109.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.248-332T>G | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 2/20 | chr12 | 95995325 | |||||||
| chr12:95995544 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.247+120C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 2/20 | chr12 | 95995544 | |||||||
| chr12:95995553 | C | T | 2 | a0001c0003t0030g0062 a0001c0005t0032g0063 |
2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.247+111G>A | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 2/20 | chr12 | 95995553 | |||||||
| chr12:95995589 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.247+75C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 2/20 | chr12 | 95995589 | |||||||
| chr12:95995619 | A | G | 1 | a0007c0014t0001g0072 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.247+45T>C | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 2/20 | chr12 | 95995619 | |||||||
| chr12:95995641 | G | A | 3 | a0001c0001t0006g0237 a0001c0001t0006g0238 a0001c0003t0005g0236 |
3 | HG02809.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.247+23C>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 2/20 | chr12 | 95995641 | |||||||
| chr12:95996027 | C | A | 5 | a0001c0001t0009g0056 a0001c0001t0009g0244 a0001c0001t0009g0245 others(2): Show |
7 | HG02257.hp2 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-81-36G>T | HAL | ENSG00000084110.11 | transcript | ENST00000261208.8 | protein_coding | 1/20 | chr12 | 95996027 |