Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26061 |
| ensemblid | ENSG00000131373.15 |
| hgncid | 17856 |
| symbol | HACL1 |
| name | 2-hydroxyacyl-CoA lyase 1 |
| refseq_nuc | NM_012260.4 |
| refseq_prot | NP_036392.2 |
| ensembl_nuc | ENST00000321169.10 |
| ensembl_prot | ENSP00000323811.5 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 15560699 |
| end | 15601569 |
| strand | - |
| ver | v1.2 |
| region | chr3:15560699-15601569 |
| region5000 | chr3:15555699-15606569 |
| regionname0 | HACL1_chr3_15560699_15601569 |
| regionname5000 | HACL1_chr3_15555699_15606569 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 578 | 418 | 94 | 73 | 194 | 8 | 47 | 150 | HACL1_chr3_15555699_15606569 | HACL1 | MPDSN others(573): Show |
chr3 | 15555699 | 15606569 |
| a0002 | 0/0 | 578 | 4 | 0 | 1 | 0 | 2 | 1 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | MPDSN others(573): Show |
chr3 | 15555699 | 15606569 |
| a0003 | 0/0 | 578 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | MPDSN others(573): Show |
chr3 | 15555699 | 15606569 |
| a0004 | 0/0 | 578 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | MPDSN others(573): Show |
chr3 | 15555699 | 15606569 |
| a0005 | 0/0 | 578 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | MPDSN others(573): Show |
chr3 | 15555699 | 15606569 |
| a0006 | 0/0 | 578 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | MPDSN others(573): Show |
chr3 | 15555699 | 15606569 |
| a0007 | 0/0 | 578 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | MPDSN others(573): Show |
chr3 | 15555699 | 15606569 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1734 | 350 | 83 | 65 | 152 | 7 | 41 | HACL1_chr3_15555699_15606569 | HACL1 | ATGCC others(1729): Show |
chr3 | 15555699 | 15606569 | ||
| a0001c0002 | 0/0 | 1734 | 51 | 3 | 6 | 36 | 1 | 5 | HACL1_chr3_15555699_15606569 | HACL1 | ATGCC others(1729): Show |
chr3 | 15555699 | 15606569 | ||
| a0001c0003 | 0/0 | 1734 | 7 | 7 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | ATGCC others(1729): Show |
chr3 | 15555699 | 15606569 | ||
| a0001c0004 | 0/0 | 1734 | 6 | 0 | 1 | 5 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | ATGCC others(1729): Show |
chr3 | 15555699 | 15606569 | ||
| a0001c0007 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | ATGCC others(1729): Show |
chr3 | 15555699 | 15606569 | ||
| a0001c0008 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | ATGCC others(1729): Show |
chr3 | 15555699 | 15606569 | ||
| a0001c0013 | 0/0 | 1734 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | ATGCC others(1729): Show |
chr3 | 15555699 | 15606569 | ||
| a0001c0014 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | ATGCC others(1729): Show |
chr3 | 15555699 | 15606569 | ||
| a0002c0005 | 0/0 | 1734 | 3 | 0 | 1 | 0 | 1 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | ATGCC others(1729): Show |
chr3 | 15555699 | 15606569 | ||
| a0002c0015 | 0/0 | 1734 | 1 | 0 | 0 | 0 | 1 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | ATGCC others(1729): Show |
chr3 | 15555699 | 15606569 | ||
| a0003c0006 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | ATGCC others(1729): Show |
chr3 | 15555699 | 15606569 | ||
| a0004c0009 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | ATGCC others(1729): Show |
chr3 | 15555699 | 15606569 | ||
| a0005c0010 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | ATGCC others(1729): Show |
chr3 | 15555699 | 15606569 | ||
| a0006c0011 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | ATGCC others(1729): Show |
chr3 | 15555699 | 15606569 | ||
| a0007c0012 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | ATGCC others(1729): Show |
chr3 | 15555699 | 15606569 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2009 | 339 | 83 | 60 | 149 | 7 | 39 | HACL1_chr3_15555699_15606569 | HACL1 | AGAGG others(2004): Show |
chr3 | 15555699 | 15606569 |
| a0001c0001t0002 | 1/0 | 2009 | 11 | 0 | 5 | 3 | 0 | 2 | HACL1_chr3_15555699_15606569 | HACL1 | AGAGG others(2004): Show |
chr3 | 15555699 | 15606569 |
| a0001c0002t0001 | 0/0 | 2009 | 51 | 3 | 6 | 36 | 1 | 5 | HACL1_chr3_15555699_15606569 | HACL1 | AGAGG others(2004): Show |
chr3 | 15555699 | 15606569 |
| a0001c0003t0001 | 0/0 | 2009 | 4 | 4 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | AGAGG others(2004): Show |
chr3 | 15555699 | 15606569 |
| a0001c0003t0003 | 0/0 | 2004 | 3 | 3 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | AGAGG others(1999): Show |
chr3 | 15555699 | 15606569 |
| a0001c0004t0001 | 0/0 | 2009 | 6 | 0 | 1 | 5 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | AGAGG others(2004): Show |
chr3 | 15555699 | 15606569 |
| a0001c0007t0001 | 0/0 | 2009 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | AGAGG others(2004): Show |
chr3 | 15555699 | 15606569 |
| a0001c0008t0001 | 0/0 | 2009 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | AGAGG others(2004): Show |
chr3 | 15555699 | 15606569 |
| a0001c0013t0001 | 0/0 | 2009 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | AGAGG others(2004): Show |
chr3 | 15555699 | 15606569 |
| a0001c0014t0001 | 0/0 | 2009 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | AGAGG others(2004): Show |
chr3 | 15555699 | 15606569 |
| a0002c0005t0001 | 0/0 | 2009 | 3 | 0 | 1 | 0 | 1 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | AGAGG others(2004): Show |
chr3 | 15555699 | 15606569 |
| a0002c0015t0001 | 0/0 | 2009 | 1 | 0 | 0 | 0 | 1 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | AGAGG others(2004): Show |
chr3 | 15555699 | 15606569 |
| a0003c0006t0001 | 0/0 | 2009 | 2 | 2 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | AGAGG others(2004): Show |
chr3 | 15555699 | 15606569 |
| a0004c0009t0004 | 0/0 | 2009 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | AGAGG others(2004): Show |
chr3 | 15555699 | 15606569 |
| a0005c0010t0001 | 0/0 | 2009 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | AGAGG others(2004): Show |
chr3 | 15555699 | 15606569 |
| a0006c0011t0001 | 0/0 | 2009 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | AGAGG others(2004): Show |
chr3 | 15555699 | 15606569 |
| a0007c0012t0001 | 0/0 | 2009 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | AGAGG others(2004): Show |
chr3 | 15555699 | 15606569 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0007 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0010 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0335 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0002g0039 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0002g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0002g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0001t0002g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0004 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0002t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0003t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0003t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0003t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0003t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0004t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0004t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0007t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0008t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0013t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0001c0014t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0002c0005t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0002c0005t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0002c0005t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0002c0015t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0003c0006t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0004c0009t0004g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0005c0010t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0006c0011t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| a0007c0012t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | GBR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00099 | hp2 | a0002 | c0005 | t0001 | g0276 | EUR | GBR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0270 | EUR | GBR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0307 | EUR | FIN | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00280 | hp2 | a0002 | c0015 | t0001 | g0286 | EUR | FIN | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | CHS | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00735 | hp2 | a0002 | c0005 | t0001 | g0200 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0360 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01069 | hp1 | a0001 | c0004 | t0001 | g0157 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0288 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0324 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0363 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0331 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0357 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0299 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0365 | AMR | CLM | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0309 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01978 | hp2 | a0001 | c0014 | t0001 | g0285 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0358 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0321 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0329 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0298 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0305 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0301 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0325 | EAS | CDX | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CDX | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CDX | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0316 | EAS | KHV | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0364 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0204 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0323 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0348 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0349 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02965 | hp1 | a0004 | c0009 | t0004 | g0356 | AFR | ESN | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | ESN | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | ESN | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03017 | hp1 | a0002 | c0005 | t0001 | g0277 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | MSL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | MSL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03130 | hp2 | a0003 | c0006 | t0001 | g0036 | AFR | ESN | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03139 | hp1 | a0001 | c0003 | t0003 | g0069 | AFR | ESN | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03195 | hp1 | a0001 | c0003 | t0003 | g0070 | AFR | ESN | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03195 | hp2 | a0003 | c0006 | t0001 | g0036 | AFR | ESN | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0352 | AFR | MSL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03209 | hp2 | a0005 | c0010 | t0001 | g0078 | AFR | MSL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0354 | AFR | MSL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | ESN | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0303 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | STU | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | STU | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0359 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | BEB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0327 | SAS | BEB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0332 | SAS | STU | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | STU | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG04199 | hp2 | a0001 | c0013 | t0001 | g0145 | SAS | STU | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | STU | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | YRI | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18612 | hp1 | a0001 | c0004 | t0001 | g0138 | EAS | CHB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | YRI | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | YRI | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18948 | hp2 | a0006 | c0011 | t0001 | g0133 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0319 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18959 | hp1 | a0001 | c0004 | t0001 | g0148 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18960 | hp1 | a0001 | c0004 | t0001 | g0147 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18975 | hp1 | a0001 | c0004 | t0001 | g0137 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0322 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19007 | hp1 | a0001 | c0007 | t0001 | g0313 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | LWK | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19043 | hp1 | a0001 | c0008 | t0001 | g0076 | AFR | LWK | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19054 | hp1 | a0007 | c0012 | t0001 | g0278 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0333 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0362 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0317 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0328 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0361 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19091 | hp1 | a0001 | c0004 | t0001 | g0149 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0062 | AFR | YRI | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | YRI | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ASW | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ASW | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | TSI | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | TSI | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | TSI | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | TSI | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0312 | SAS | GIH | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0293 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | USA | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | USA | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | USA | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | USA | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | LWK | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| NA21309 | hp2 | a0001 | c0003 | t0003 | g0071 | AFR | LWK | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0335 | REF | REF | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0039 | REF | REF | HACL1_chr3_15555699_15606569 | HACL1 | chr3 | 15555699 | 15606569 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:15563430 | C | G | 1 | a0006 | 1 | NA18948.hp2 | missense_variant | MODERATE | c.1632G>C | p.Gln544His | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/17 | 1738/2009 | 1632/1737 | 544/578 | chr3 | 15563430 | |||
| chr3:15563507 | C | T | 1 | a0005 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1555G>A | p.Glu519Lys | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/17 | 1661/2009 | 1555/1737 | 519/578 | chr3 | 15563507 | |||
| chr3:15568478 | T | C | 1 | a0007 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.1204A>G | p.Met402Val | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 13/17 | 1310/2009 | 1204/1737 | 402/578 | chr3 | 15568478 | |||
| chr3:15582883 | C | T | 1 | a0004 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.661G>A | p.Gly221Arg | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/17 | 767/2009 | 661/1737 | 221/578 | chr3 | 15582883 | |||
| chr3:15586533 | T | A | 1 | a0002 | 4 | HG00099.hp2 HG00280.hp2 HG00735.hp2 others(1): Show |
missense_variant | MODERATE | c.451A>T | p.Ile151Phe | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 6/17 | 557/2009 | 451/1737 | 151/578 | chr3 | 15586533 | |||
| chr3:15586557 | T | C | 1 | a0003 | 2 | HG03130.hp2 HG03195.hp2 |
missense_variant | MODERATE | c.427A>G | p.Ser143Gly | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 6/17 | 533/2009 | 427/1737 | 143/578 | chr3 | 15586557 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:15563448 | G | A | 1 | a0001c0008 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.1614C>T | p.Leu538Leu | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/17 | 1720/2009 | 1614/1737 | 538/578 | chr3 | 15563448 | |||
| chr3:15568533 | A | G | 1 | a0001c0004 | 6 | HG01069.hp1 NA18612.hp1 NA18959.hp1 others(3): Show |
synonymous_variant | LOW | c.1149T>C | p.His383His | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 13/17 | 1255/2009 | 1149/1737 | 383/578 | chr3 | 15568533 | |||
| chr3:15568563 | C | T | 3 | a0001c0002 a0001c0007 a0003c0006 |
54 | HG00280.hp1 HG00544.hp1 HG01069.hp2 others(51): Show |
synonymous_variant | LOW | c.1119G>A | p.Leu373Leu | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 13/17 | 1225/2009 | 1119/1737 | 373/578 | chr3 | 15568563 | |||
| chr3:15571749 | T | C | 1 | a0001c0013 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.1014A>G | p.Lys338Lys | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/17 | 1120/2009 | 1014/1737 | 338/578 | chr3 | 15571749 | |||
| chr3:15582929 | C | T | 2 | a0001c0003 a0001c0008 |
8 | HG02647.hp1 HG02970.hp1 HG02976.hp2 others(5): Show |
synonymous_variant | LOW | c.615G>A | p.Thr205Thr | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/17 | 721/2009 | 615/1737 | 205/578 | chr3 | 15582929 | |||
| chr3:15585337 | C | T | 1 | a0001c0007 | 1 | NA19007.hp1 | synonymous_variant | LOW | c.465G>A | p.Val155Val | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/17 | 571/2009 | 465/1737 | 155/578 | chr3 | 15585337 | |||
| chr3:15596407 | G | A | 2 | a0001c0014 a0002c0015 |
2 | HG00280.hp2 HG01978.hp2 |
synonymous_variant | LOW | c.204C>T | p.Ser68Ser | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/17 | 310/2009 | 204/1737 | 68/578 | chr3 | 15596407 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:15560757 | GTTTAT | G | 1 | a0001c0003t0003 | 3 | HG03139.hp1 HG03195.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*103_*107delATAAA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 17/17 | 103 | chr3 | 15560757 | ||||||
| chr3:15601481 | T | C | 1 | a0004c0009t0004 | 1 | HG02965.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-18A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 1/17 | chr3 | 15601481 | |||||||
| chr3:15601536 | A | G | 16 | a0001c0001t0001 a0001c0002t0001 a0001c0003t0001 others(13): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
5_prime_UTR_variant | MODIFIER | c.-73T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 1/17 | 73 | chr3 | 15601536 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:15560997 | A | G | 1 | a0001c0003t0003g0069 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1705-100T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15560997 | |||||||
| chr3:15561067 | A | C | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1705-170T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15561067 | |||||||
| chr3:15561294 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1705-397A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15561294 | |||||||
| chr3:15561315 | T | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0340 others(8): Show |
15 | HG01109.hp1 HG01168.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1705-418A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15561315 | |||||||
| chr3:15561411 | G | C | 2 | a0001c0001t0002g0359 a0001c0002t0001g0189 |
2 | HG03704.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1705-514C>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15561411 | |||||||
| chr3:15561444 | AAAAT | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0172 others(4): Show |
11 | HG01192.hp2 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1705-551_1705-548d others(6): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15561444 | |||||||
| chr3:15561520 | G | A | 1 | a0001c0001t0002g0364 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1705-623C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15561520 | |||||||
| chr3:15561668 | T | C | 1 | a0005c0010t0001g0078 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1705-771A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15561668 | |||||||
| chr3:15561689 | T | G | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1705-792A>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15561689 | |||||||
| chr3:15561749 | T | TA | 31 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(28): Show |
37 | HG00423.hp2 HG00639.hp2 HG01928.hp1 others(34): Show |
intron_variant | MODIFIER | c.1705-853dupT | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15561749 | |||||||
| chr3:15561843 | G | A | 1 | a0001c0003t0003g0069 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1705-946C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15561843 | |||||||
| chr3:15562004 | G | A | 13 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(10): Show |
13 | HG01175.hp2 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1705-1107C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15562004 | |||||||
| chr3:15562040 | C | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1705-1143G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15562040 | |||||||
| chr3:15562143 | T | C | 3 | a0001c0001t0001g0308 a0001c0001t0001g0311 a0001c0001t0001g0330 |
3 | HG00733.hp1 HG01943.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1704+1215A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15562143 | |||||||
| chr3:15562413 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1704+945A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15562413 | |||||||
| chr3:15562457 | C | G | 1 | a0001c0008t0001g0076 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1704+901G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15562457 | |||||||
| chr3:15562521 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01081.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1704+837A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15562521 | |||||||
| chr3:15562541 | T | C | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG00544.hp2 HG02735.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1704+817A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15562541 | |||||||
| chr3:15562548 | T | C | 1 | a0001c0002t0001g0323 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1704+810A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15562548 | |||||||
| chr3:15562622 | C | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(12): Show |
21 | HG00639.hp2 HG01928.hp1 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.1704+736G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15562622 | |||||||
| chr3:15562840 | C | G | 13 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(10): Show |
13 | HG01175.hp2 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1704+518G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15562840 | |||||||
| chr3:15562882 | A | G | 6 | a0001c0001t0002g0357 a0001c0001t0002g0358 a0001c0001t0002g0359 others(3): Show |
6 | HG00738.hp1 HG01099.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.1704+476T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15562882 | |||||||
| chr3:15562951 | C | T | 2 | a0001c0002t0001g0287 a0001c0002t0001g0304 |
2 | NA19009.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1704+407G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15562951 | |||||||
| chr3:15562968 | CTCT | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(97): Show |
119 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.1704+387_1704+389d others(5): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15562968 | |||||||
| chr3:15562991 | C | A | 1 | a0001c0001t0001g0265 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1704+367G>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15562991 | |||||||
| chr3:15563245 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1704+113C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 16/16 | chr3 | 15563245 | |||||||
| chr3:15563609 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1518-65A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 15/16 | chr3 | 15563609 | |||||||
| chr3:15563924 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1518-380T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 15/16 | chr3 | 15563924 | |||||||
| chr3:15563957 | A | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01081.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1518-413T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 15/16 | chr3 | 15563957 | |||||||
| chr3:15563977 | A | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0340 others(8): Show |
15 | HG01109.hp1 HG01168.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1518-433T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 15/16 | chr3 | 15563977 | |||||||
| chr3:15564108 | C | T | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG00544.hp2 HG02735.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1517+443G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 15/16 | chr3 | 15564108 | |||||||
| chr3:15564194 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1517+357T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 15/16 | chr3 | 15564194 | |||||||
| chr3:15564208 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1517+343C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 15/16 | chr3 | 15564208 | |||||||
| chr3:15564316 | T | G | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 |
3 | HG00544.hp2 NA18957.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1517+235A>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 15/16 | chr3 | 15564316 | |||||||
| chr3:15564476 | CA | C | 8 | a0001c0001t0001g0142 a0001c0001t0001g0150 a0001c0001t0001g0151 others(5): Show |
8 | HG02145.hp2 HG02886.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1517+74delT | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 15/16 | chr3 | 15564476 | |||||||
| chr3:15564671 | T | C | 1 | a0001c0003t0003g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1410-13A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15564671 | |||||||
| chr3:15564873 | G | C | 14 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0040 others(11): Show |
16 | HG00597.hp2 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1410-215C>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15564873 | |||||||
| chr3:15564941 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1410-283G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15564941 | |||||||
| chr3:15565089 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1410-431G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15565089 | |||||||
| chr3:15565168 | A | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01081.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1410-510T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15565168 | |||||||
| chr3:15565264 | G | A | 34 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(31): Show |
40 | HG00423.hp2 HG00639.hp2 HG01928.hp1 others(37): Show |
intron_variant | MODIFIER | c.1410-606C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15565264 | |||||||
| chr3:15565290 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1410-632A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15565290 | |||||||
| chr3:15565327 | G | A | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
16 | HG01175.hp2 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1410-669C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15565327 | |||||||
| chr3:15565409 | C | T | 34 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(31): Show |
40 | HG00423.hp2 HG00639.hp2 HG01928.hp1 others(37): Show |
intron_variant | MODIFIER | c.1410-751G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15565409 | |||||||
| chr3:15565433 | C | T | 1 | a0002c0005t0001g0276 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1410-775G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15565433 | |||||||
| chr3:15565495 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(83): Show |
101 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1410-837T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15565495 | |||||||
| chr3:15565574 | T | C | 1 | a0001c0003t0001g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1410-916A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15565574 | |||||||
| chr3:15565574 | T | G | 11 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0340 others(8): Show |
15 | HG01109.hp1 HG01168.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1410-916A>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15565574 | |||||||
| chr3:15565813 | G | T | 2 | a0001c0003t0001g0015 a0001c0003t0001g0062 |
3 | HG02970.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1410-1155C>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15565813 | |||||||
| chr3:15565858 | G | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0340 others(8): Show |
15 | HG01109.hp1 HG01168.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1410-1200C>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15565858 | |||||||
| chr3:15565987 | A | G | 1 | a0001c0002t0001g0297 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1410-1329T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15565987 | |||||||
| chr3:15566038 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0172 others(4): Show |
11 | HG01192.hp2 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1410-1380C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15566038 | |||||||
| chr3:15566137 | C | A | 1 | a0001c0001t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1410-1479G>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15566137 | |||||||
| chr3:15566193 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1410-1535T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15566193 | |||||||
| chr3:15566270 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1409+1574T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15566270 | |||||||
| chr3:15566279 | C | G | 2 | a0001c0003t0001g0204 a0001c0008t0001g0076 |
2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1409+1565G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15566279 | |||||||
| chr3:15566378 | G | A | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG01175.hp2 HG01891.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1409+1466C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15566378 | |||||||
| chr3:15566479 | C | T | 27 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(24): Show |
33 | HG00423.hp2 HG00639.hp2 HG01928.hp1 others(30): Show |
intron_variant | MODIFIER | c.1409+1365G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15566479 | |||||||
| chr3:15566559 | G | A | 3 | a0001c0001t0001g0223 a0001c0001t0001g0232 a0001c0001t0001g0235 |
3 | HG00642.hp2 HG01109.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1409+1285C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15566559 | |||||||
| chr3:15566699 | T | C | 1 | a0001c0001t0001g0342 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1409+1145A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15566699 | |||||||
| chr3:15566734 | C | CT | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(166): Show |
200 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.1409+1109dupA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15566734 | |||||||
| chr3:15566745 | T | TC | 52 | a0001c0001t0001g0249 a0001c0001t0001g0308 a0001c0001t0001g0310 others(49): Show |
58 | HG00280.hp1 HG00544.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.1409+1098dupG | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15566745 | |||||||
| chr3:15566771 | T | C | 1 | a0001c0003t0003g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1409+1073A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15566771 | |||||||
| chr3:15566815 | C | CT | 37 | a0001c0001t0001g0012 a0001c0001t0001g0052 a0001c0001t0001g0083 others(34): Show |
39 | HG00544.hp2 HG00673.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1409+1028dupA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15566815 | |||||||
| chr3:15566815 | CT | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(96): Show |
117 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1409+1028delA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15566815 | |||||||
| chr3:15566815 | CTT | C | 13 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(10): Show |
14 | HG01175.hp2 HG01891.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1409+1027_1409+102 others(6): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15566815 | |||||||
| chr3:15566841 | T | C | 54 | a0001c0001t0001g0035 a0001c0001t0001g0249 a0001c0001t0001g0283 others(51): Show |
61 | HG00280.hp1 HG00544.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.1409+1003A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15566841 | |||||||
| chr3:15566900 | A | C | 355 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(352): Show |
417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.1409+944T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15566900 | |||||||
| chr3:15566995 | T | C | 5 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(2): Show |
5 | HG00544.hp2 HG01257.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1409+849A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15566995 | |||||||
| chr3:15567095 | C | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0172 others(5): Show |
12 | HG01192.hp2 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1409+749G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15567095 | |||||||
| chr3:15567206 | C | CT | 80 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(77): Show |
93 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1409+637dupA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15567206 | |||||||
| chr3:15567206 | C | CTT | 9 | a0001c0001t0001g0049 a0001c0001t0001g0249 a0001c0001t0001g0281 others(6): Show |
9 | HG02071.hp1 HG02135.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.1409+636_1409+637d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15567206 | |||||||
| chr3:15567206 | CT | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(75): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.1409+637delA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15567206 | |||||||
| chr3:15567206 | CTTTTT | C | 11 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0056 others(8): Show |
11 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1409+633_1409+637d others(7): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15567206 | |||||||
| chr3:15567266 | A | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1409+578T>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15567266 | |||||||
| chr3:15567274 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1409+570C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15567274 | |||||||
| chr3:15567292 | C | G | 5 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
5 | HG01256.hp2 HG02300.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1409+552G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15567292 | |||||||
| chr3:15567295 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1409+549G>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15567295 | |||||||
| chr3:15567376 | AT | A | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
16 | HG01175.hp2 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1409+467delA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15567376 | |||||||
| chr3:15567533 | TC | T | 24 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0054 others(21): Show |
26 | HG01081.hp1 HG01175.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1409+310delG | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15567533 | |||||||
| chr3:15567684 | G | A | 26 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0019 others(23): Show |
31 | HG00423.hp2 HG00639.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.1409+160C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15567684 | |||||||
| chr3:15567689 | T | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0034 others(26): Show |
38 | HG00140.hp2 HG00408.hp2 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.1409+155A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 14/16 | chr3 | 15567689 | |||||||
| chr3:15568153 | C | T | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG01175.hp2 HG01891.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1251-151G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 13/16 | chr3 | 15568153 | |||||||
| chr3:15568175 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1251-173A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 13/16 | chr3 | 15568175 | |||||||
| chr3:15568404 | C | G | 2 | a0001c0002t0001g0288 a0001c0002t0001g0324 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1250+28G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 13/16 | chr3 | 15568404 | |||||||
| chr3:15568405 | G | A | 2 | a0001c0002t0001g0288 a0001c0002t0001g0324 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1250+27C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 13/16 | chr3 | 15568405 | |||||||
| chr3:15568693 | G | A | 3 | a0001c0001t0001g0222 a0001c0001t0001g0229 a0001c0001t0001g0230 |
3 | HG02056.hp2 HG02132.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1096-107C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15568693 | |||||||
| chr3:15568737 | T | C | 3 | a0001c0001t0001g0336 a0001c0001t0001g0337 a0001c0001t0001g0338 |
3 | HG00733.hp2 HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1096-151A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15568737 | |||||||
| chr3:15568770 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0183 a0001c0001t0001g0184 |
4 | HG02257.hp1 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-184A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15568770 | |||||||
| chr3:15568810 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0272 |
2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1096-224C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15568810 | |||||||
| chr3:15568814 | A | T | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG00544.hp2 HG02735.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096-228T>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15568814 | |||||||
| chr3:15568907 | A | G | 13 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0187 others(10): Show |
20 | HG00140.hp2 HG01261.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1096-321T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15568907 | |||||||
| chr3:15568947 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1096-361C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15568947 | |||||||
| chr3:15569014 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1096-428A>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15569014 | |||||||
| chr3:15569064 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1096-478G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15569064 | |||||||
| chr3:15569280 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1096-694C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15569280 | |||||||
| chr3:15569381 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1096-795G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15569381 | |||||||
| chr3:15569424 | G | A | 1 | a0001c0001t0001g0338 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1096-838C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15569424 | |||||||
| chr3:15569442 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1096-856A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15569442 | |||||||
| chr3:15569456 | C | T | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG01175.hp2 HG01891.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1096-870G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15569456 | |||||||
| chr3:15569467 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG01081.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1096-881G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15569467 | |||||||
| chr3:15569556 | T | C | 27 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(24): Show |
33 | HG00423.hp2 HG00639.hp2 HG01928.hp1 others(30): Show |
intron_variant | MODIFIER | c.1096-970A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15569556 | |||||||
| chr3:15569561 | C | A | 2 | a0001c0001t0001g0227 a0001c0001t0001g0234 |
2 | HG02015.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.1096-975G>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15569561 | |||||||
| chr3:15569588 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1096-1002C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15569588 | |||||||
| chr3:15569691 | C | T | 1 | a0001c0001t0001g0350 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1096-1105G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15569691 | |||||||
| chr3:15569859 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(167): Show |
201 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.1096-1273T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15569859 | |||||||
| chr3:15569993 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1096-1407T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15569993 | |||||||
| chr3:15570053 | T | G | 1 | a0001c0002t0001g0323 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1096-1467A>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15570053 | |||||||
| chr3:15570091 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1096-1505G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15570091 | |||||||
| chr3:15570119 | G | A | 1 | a0001c0003t0001g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1096-1533C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15570119 | |||||||
| chr3:15570195 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1095+1473G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15570195 | |||||||
| chr3:15570196 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0272 |
2 | HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1095+1472C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15570196 | |||||||
| chr3:15570343 | A | C | 1 | a0001c0001t0001g0311 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1095+1325T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15570343 | |||||||
| chr3:15570409 | C | A | 2 | a0001c0003t0001g0015 a0001c0003t0001g0062 |
3 | HG02970.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1095+1259G>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15570409 | |||||||
| chr3:15570441 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1095+1227T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15570441 | |||||||
| chr3:15570513 | T | C | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0056 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1095+1155A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15570513 | |||||||
| chr3:15570585 | T | TA | 16 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0040 others(13): Show |
18 | HG00597.hp2 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.1095+1082dupT | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15570585 | |||||||
| chr3:15570634 | G | GCA | 82 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(79): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.1095+1032_1095+103 others(6): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15570634 | |||||||
| chr3:15570706 | T | C | 52 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(49): Show |
61 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(58): Show |
intron_variant | MODIFIER | c.1095+962A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15570706 | |||||||
| chr3:15570772 | A | C | 1 | a0001c0001t0001g0336 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1095+896T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15570772 | |||||||
| chr3:15570790 | G | A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01081.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1095+878C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15570790 | |||||||
| chr3:15570806 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1095+862G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15570806 | |||||||
| chr3:15570981 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1095+687A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15570981 | |||||||
| chr3:15570994 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1095+674A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15570994 | |||||||
| chr3:15571112 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1095+556T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15571112 | |||||||
| chr3:15571119 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1095+549G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15571119 | |||||||
| chr3:15571147 | C | CT | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
16 | HG01175.hp2 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1095+520dupA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15571147 | |||||||
| chr3:15571149 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1095+519A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15571149 | |||||||
| chr3:15571264 | T | A | 1 | a0001c0008t0001g0076 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1095+404A>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15571264 | |||||||
| chr3:15571277 | C | T | 7 | a0001c0001t0001g0031 a0001c0001t0001g0253 a0001c0001t0001g0254 others(4): Show |
8 | NA18942.hp2 NA18966.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.1095+391G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15571277 | |||||||
| chr3:15571419 | C | T | 1 | a0001c0001t0001g0024 | 2 | HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1095+249G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15571419 | |||||||
| chr3:15571660 | G | A | 3 | a0001c0003t0003g0069 a0001c0003t0003g0070 a0001c0003t0003g0071 |
3 | HG03139.hp1 HG03195.hp1 NA21309.hp2 |
splice_region_variant&intron_variant | LOW | c.1095+8C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 12/16 | chr3 | 15571660 | |||||||
| chr3:15571772 | T | A | 1 | a0001c0001t0001g0101 | 1 | NA19082.hp2 | splice_region_variant&intron_variant | LOW | c.994-3A>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15571772 | |||||||
| chr3:15571772 | T | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(83): Show |
101 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(98): Show |
splice_region_variant&intron_variant | LOW | c.994-3A>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15571772 | |||||||
| chr3:15571772 | T | TA | 51 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(48): Show |
60 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(57): Show |
splice_region_variant&intron_variant | LOW | c.994-4dupT | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15571772 | |||||||
| chr3:15571773 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA19076.hp2 | splice_region_variant&intron_variant | LOW | c.994-4T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15571773 | |||||||
| chr3:15571784 | A | AC | 6 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0182 others(3): Show |
8 | HG01255.hp1 HG01255.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.994-16_994-15insG | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15571784 | |||||||
| chr3:15571784 | A | ACAC | 31 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(28): Show |
37 | HG00423.hp2 HG00639.hp2 HG01928.hp1 others(34): Show |
intron_variant | MODIFIER | c.994-16_994-15insGT others(1): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15571784 | |||||||
| chr3:15571784 | A | C | 2 | a0001c0001t0001g0266 a0001c0001t0001g0275 |
2 | HG03130.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.994-15T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15571784 | |||||||
| chr3:15571829 | C | CT | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(112): Show |
139 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.994-61dupA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15571829 | |||||||
| chr3:15571829 | C | CTT | 32 | a0001c0001t0001g0007 a0001c0001t0001g0051 a0001c0001t0001g0065 others(29): Show |
35 | HG00280.hp2 HG00423.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.994-62_994-61dupAA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15571829 | |||||||
| chr3:15571829 | C | CTTT | 6 | a0001c0001t0001g0038 a0001c0001t0001g0131 a0001c0001t0001g0341 others(3): Show |
7 | HG01109.hp1 HG02055.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-63_994-61dupAA others(1): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15571829 | |||||||
| chr3:15571829 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0072 |
2 | NA18978.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.994-60G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15571829 | |||||||
| chr3:15571829 | CT | C | 57 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0045 others(54): Show |
63 | HG00280.hp1 HG00597.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.994-61delA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15571829 | |||||||
| chr3:15571829 | CTT | C | 16 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0053 others(13): Show |
17 | HG01169.hp2 HG01175.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.994-62_994-61delAA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15571829 | |||||||
| chr3:15571829 | CTTTTTTT | C | 10 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0172 others(7): Show |
14 | HG00642.hp2 HG01109.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.994-67_994-61delAA others(5): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15571829 | |||||||
| chr3:15571829 | CTTTTTTT others(13): Show |
C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01081.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.994-80_994-61delAA others(18): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15571829 | |||||||
| chr3:15571835 | T | C | 1 | a0001c0002t0001g0333 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.994-66A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15571835 | |||||||
| chr3:15571842 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.994-73A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15571842 | |||||||
| chr3:15571843 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.994-74A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15571843 | |||||||
| chr3:15571927 | TCTCCCAG others(25): Show |
T | 1 | a0001c0001t0001g0011 | 3 | NA18957.hp2 NA18975.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.994-190_994-159del others(32): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15571927 | |||||||
| chr3:15572007 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.994-238A>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15572007 | |||||||
| chr3:15572087 | GTCTCGGC others(4): Show |
G | 1 | a0001c0001t0001g0220 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.994-329_994-319del others(11): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15572087 | |||||||
| chr3:15572333 | T | C | 1 | a0001c0003t0003g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.994-564A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15572333 | |||||||
| chr3:15572621 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.993+538T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15572621 | |||||||
| chr3:15572634 | T | A | 1 | a0001c0001t0001g0073 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.993+525A>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15572634 | |||||||
| chr3:15572642 | A | C | 6 | a0001c0002t0001g0314 a0001c0002t0001g0315 a0001c0002t0001g0317 others(3): Show |
6 | NA18944.hp1 NA18952.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.993+517T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15572642 | |||||||
| chr3:15572741 | T | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0340 others(8): Show |
15 | HG01109.hp1 HG01168.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.993+418A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15572741 | |||||||
| chr3:15572803 | C | T | 1 | a0004c0009t0004g0356 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.993+356G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15572803 | |||||||
| chr3:15572832 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(85): Show |
103 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.993+327T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15572832 | |||||||
| chr3:15573104 | A | G | 1 | a0001c0003t0003g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.993+55T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 11/16 | chr3 | 15573104 | |||||||
| chr3:15573416 | T | C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.910-174A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 10/16 | chr3 | 15573416 | |||||||
| chr3:15573483 | C | T | 15 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
16 | HG01175.hp2 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.910-241G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 10/16 | chr3 | 15573483 | |||||||
| chr3:15573675 | T | C | 3 | a0001c0003t0003g0069 a0001c0003t0003g0070 a0001c0003t0003g0071 |
3 | HG03139.hp1 HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.910-433A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 10/16 | chr3 | 15573675 | |||||||
| chr3:15573728 | C | T | 1 | a0001c0008t0001g0076 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.910-486G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 10/16 | chr3 | 15573728 | |||||||
| chr3:15573836 | C | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0233 |
2 | NA18956.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.910-594G>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 10/16 | chr3 | 15573836 | |||||||
| chr3:15573862 | G | A | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 |
3 | HG00544.hp2 NA18957.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.910-620C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 10/16 | chr3 | 15573862 | |||||||
| chr3:15574293 | G | T | 1 | a0001c0001t0001g0212 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.909+684C>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 10/16 | chr3 | 15574293 | |||||||
| chr3:15574494 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01081.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.909+483A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 10/16 | chr3 | 15574494 | |||||||
| chr3:15574550 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.909+427C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 10/16 | chr3 | 15574550 | |||||||
| chr3:15574626 | C | T | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG00544.hp2 HG02735.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+351G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 10/16 | chr3 | 15574626 | |||||||
| chr3:15574771 | G | GAAGTA | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(166): Show |
200 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.909+205_909+206ins others(5): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 10/16 | chr3 | 15574771 | |||||||
| chr3:15574892 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.909+85T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 10/16 | chr3 | 15574892 | |||||||
| chr3:15575215 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.804-133A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15575215 | |||||||
| chr3:15575337 | T | G | 53 | a0001c0001t0001g0249 a0001c0001t0001g0308 a0001c0001t0001g0310 others(50): Show |
59 | HG00280.hp1 HG00544.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.804-255A>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15575337 | |||||||
| chr3:15575541 | C | CT | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(135): Show |
163 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.804-460dupA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15575541 | |||||||
| chr3:15575548 | T | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0052 a0001c0001t0001g0279 others(1): Show |
6 | HG00673.hp2 NA18962.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.804-466A>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15575548 | |||||||
| chr3:15575676 | G | A | 2 | a0001c0002t0001g0307 a0001c0002t0001g0327 |
2 | HG00280.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.804-594C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15575676 | |||||||
| chr3:15575696 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.804-614A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15575696 | |||||||
| chr3:15575765 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.804-683A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15575765 | |||||||
| chr3:15575867 | T | C | 1 | a0001c0001t0002g0363 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.804-785A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15575867 | |||||||
| chr3:15575926 | G | C | 31 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(28): Show |
37 | HG00423.hp2 HG00639.hp2 HG01928.hp1 others(34): Show |
intron_variant | MODIFIER | c.804-844C>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15575926 | |||||||
| chr3:15576064 | A | G | 4 | a0001c0001t0001g0350 a0001c0001t0001g0351 a0001c0001t0001g0352 others(1): Show |
4 | HG03098.hp2 HG03209.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.804-982T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15576064 | |||||||
| chr3:15576077 | G | A | 363 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(360): Show |
425 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(422): Show |
intron_variant | MODIFIER | c.804-995C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15576077 | |||||||
| chr3:15576104 | C | T | 1 | a0001c0003t0003g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.804-1022G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15576104 | |||||||
| chr3:15576154 | C | CA | 53 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0019 others(50): Show |
59 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.804-1073dupT | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15576154 | |||||||
| chr3:15576154 | C | CAA | 7 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0083 others(4): Show |
9 | HG00639.hp2 HG01928.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-1074_804-1073d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15576154 | |||||||
| chr3:15576154 | CA | C | 18 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0048 others(15): Show |
19 | HG01106.hp1 HG01167.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.804-1073delT | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15576154 | |||||||
| chr3:15576154 | CAA | C | 28 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(25): Show |
34 | HG00597.hp2 HG01168.hp1 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.804-1074_804-1073d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15576154 | |||||||
| chr3:15576154 | CAAA | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(77): Show |
95 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.804-1075_804-1073d others(5): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15576154 | |||||||
| chr3:15576210 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.804-1128G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15576210 | |||||||
| chr3:15576352 | T | C | 5 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0247 others(2): Show |
5 | HG02015.hp1 HG02129.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.804-1270A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15576352 | |||||||
| chr3:15576401 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.804-1319A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15576401 | |||||||
| chr3:15576709 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.804-1627G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15576709 | |||||||
| chr3:15576735 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.804-1653A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15576735 | |||||||
| chr3:15576752 | C | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0259 a0001c0001t0001g0260 |
4 | NA18942.hp2 NA18971.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.804-1670G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15576752 | |||||||
| chr3:15576791 | C | G | 11 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0340 others(8): Show |
15 | HG01109.hp1 HG01168.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.804-1709G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15576791 | |||||||
| chr3:15576824 | A | G | 1 | a0001c0002t0001g0316 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.804-1742T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15576824 | |||||||
| chr3:15576887 | C | A | 1 | a0001c0001t0001g0143 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.804-1805G>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15576887 | |||||||
| chr3:15576945 | A | C | 2 | a0001c0001t0001g0240 a0001c0001t0001g0272 |
2 | HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.804-1863T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15576945 | |||||||
| chr3:15576985 | T | C | 31 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(28): Show |
37 | HG00423.hp2 HG00639.hp2 HG01928.hp1 others(34): Show |
intron_variant | MODIFIER | c.804-1903A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15576985 | |||||||
| chr3:15577260 | G | C | 2 | a0001c0002t0001g0314 a0001c0002t0001g0315 |
2 | NA18944.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.804-2178C>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15577260 | |||||||
| chr3:15577283 | G | C | 1 | a0001c0001t0001g0064 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.804-2201C>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15577283 | |||||||
| chr3:15577347 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.804-2265T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15577347 | |||||||
| chr3:15577409 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.804-2327T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15577409 | |||||||
| chr3:15577528 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.803+2382A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15577528 | |||||||
| chr3:15577551 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.803+2359C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15577551 | |||||||
| chr3:15577574 | T | C | 1 | a0001c0008t0001g0076 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.803+2336A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15577574 | |||||||
| chr3:15577603 | C | G | 1 | a0001c0003t0003g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.803+2307G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15577603 | |||||||
| chr3:15577604 | A | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0172 others(4): Show |
11 | HG01192.hp2 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.803+2306T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15577604 | |||||||
| chr3:15577608 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0172 others(4): Show |
11 | HG01192.hp2 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.803+2302G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15577608 | |||||||
| chr3:15577611 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.803+2299A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15577611 | |||||||
| chr3:15577806 | A | C | 1 | a0001c0001t0001g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.803+2104T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15577806 | |||||||
| chr3:15577870 | G | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0340 others(8): Show |
15 | HG01109.hp1 HG01168.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.803+2040C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15577870 | |||||||
| chr3:15578013 | G | C | 1 | a0001c0001t0001g0268 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.803+1897C>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15578013 | |||||||
| chr3:15578092 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.803+1818G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15578092 | |||||||
| chr3:15578097 | C | CA | 30 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0113 others(27): Show |
30 | HG00423.hp1 HG00642.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.803+1812dupT | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15578097 | |||||||
| chr3:15578097 | CA | C | 54 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0014 others(51): Show |
62 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.803+1812delT | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15578097 | |||||||
| chr3:15578097 | CAA | C | 12 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0054 others(9): Show |
13 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.803+1811_803+1812d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15578097 | |||||||
| chr3:15578290 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.803+1620A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15578290 | |||||||
| chr3:15578541 | G | A | 1 | a0001c0002t0001g0323 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.803+1369C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15578541 | |||||||
| chr3:15578582 | G | A | 4 | a0001c0001t0001g0208 a0001c0001t0001g0239 a0001c0001t0001g0269 others(1): Show |
4 | HG00140.hp1 HG00741.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.803+1328C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15578582 | |||||||
| chr3:15578584 | A | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG01081.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.803+1326T>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15578584 | |||||||
| chr3:15578729 | C | T | 2 | a0001c0002t0001g0299 a0001c0002t0001g0332 |
2 | HG01243.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.803+1181G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15578729 | |||||||
| chr3:15578817 | A | G | 1 | a0005c0010t0001g0078 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.803+1093T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15578817 | |||||||
| chr3:15578901 | G | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0252 |
2 | HG02015.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.803+1009C>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15578901 | |||||||
| chr3:15578987 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.803+923A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15578987 | |||||||
| chr3:15578987 | T | G | 1 | a0001c0002t0001g0306 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.803+923A>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15578987 | |||||||
| chr3:15579058 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.803+852A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15579058 | |||||||
| chr3:15579249 | A | G | 13 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(10): Show |
13 | HG01175.hp2 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.803+661T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15579249 | |||||||
| chr3:15579259 | A | C | 1 | a0005c0010t0001g0078 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.803+651T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15579259 | |||||||
| chr3:15579373 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.803+537A>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15579373 | |||||||
| chr3:15579477 | A | C | 1 | a0001c0001t0001g0330 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.803+433T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15579477 | |||||||
| chr3:15579495 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.803+415C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15579495 | |||||||
| chr3:15579497 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.803+413A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15579497 | |||||||
| chr3:15579636 | G | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(166): Show |
200 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.803+274C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15579636 | |||||||
| chr3:15579807 | C | T | 1 | a0001c0003t0003g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.803+103G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 9/16 | chr3 | 15579807 | |||||||
| chr3:15580252 | C | T | 1 | a0005c0010t0001g0078 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.668-207G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15580252 | |||||||
| chr3:15580295 | T | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0283 |
3 | HG02615.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.668-250A>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15580295 | |||||||
| chr3:15580630 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.668-585C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15580630 | |||||||
| chr3:15580822 | T | C | 1 | a0001c0001t0001g0029 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.668-777A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15580822 | |||||||
| chr3:15580971 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0272 |
2 | HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.668-926C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15580971 | |||||||
| chr3:15581005 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.668-960C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15581005 | |||||||
| chr3:15581045 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.668-1000C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15581045 | |||||||
| chr3:15581046 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.668-1001G>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15581046 | |||||||
| chr3:15581181 | C | T | 1 | a0001c0002t0001g0314 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.668-1136G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15581181 | |||||||
| chr3:15581264 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(114): Show |
141 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.668-1219A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15581264 | |||||||
| chr3:15581477 | A | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0172 others(4): Show |
11 | HG01192.hp2 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.667+1400T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15581477 | |||||||
| chr3:15581564 | G | T | 4 | a0001c0003t0001g0204 a0001c0003t0003g0069 a0001c0003t0003g0071 others(1): Show |
4 | HG02647.hp1 HG03139.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.667+1313C>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15581564 | |||||||
| chr3:15581960 | A | G | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.667+917T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15581960 | |||||||
| chr3:15582004 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.667+873T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15582004 | |||||||
| chr3:15582016 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.667+861G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15582016 | |||||||
| chr3:15582041 | C | T | 1 | a0001c0001t0001g0330 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.667+836G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15582041 | |||||||
| chr3:15582109 | C | G | 31 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(28): Show |
37 | HG00423.hp2 HG00639.hp2 HG01928.hp1 others(34): Show |
intron_variant | MODIFIER | c.667+768G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15582109 | |||||||
| chr3:15582213 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01081.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.667+664A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15582213 | |||||||
| chr3:15582255 | C | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(165): Show |
199 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.667+622G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15582255 | |||||||
| chr3:15582339 | C | A | 13 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(10): Show |
13 | HG01175.hp2 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.667+538G>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15582339 | |||||||
| chr3:15582553 | T | C | 31 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(28): Show |
37 | HG00423.hp2 HG00639.hp2 HG01928.hp1 others(34): Show |
intron_variant | MODIFIER | c.667+324A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 8/16 | chr3 | 15582553 | |||||||
| chr3:15583033 | T | C | 2 | a0001c0001t0001g0274 a0001c0001t0001g0290 |
2 | NA18995.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.555-44A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15583033 | |||||||
| chr3:15583463 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.555-474T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15583463 | |||||||
| chr3:15583638 | CTTT | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0180 others(4): Show |
8 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.555-652_555-650del others(3): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15583638 | |||||||
| chr3:15583691 | T | G | 18 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(15): Show |
24 | HG00423.hp2 HG00639.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.555-702A>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15583691 | |||||||
| chr3:15583692 | C | CT | 11 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0340 others(8): Show |
15 | HG01109.hp1 HG01168.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.555-704dupA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15583692 | |||||||
| chr3:15583716 | G | A | 7 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0180 others(4): Show |
8 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.555-727C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15583716 | |||||||
| chr3:15583760 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.555-771G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15583760 | |||||||
| chr3:15583763 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.555-774A>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15583763 | |||||||
| chr3:15583782 | T | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0180 others(4): Show |
8 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.555-793A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15583782 | |||||||
| chr3:15584054 | A | T | 2 | a0001c0002t0001g0188 a0001c0002t0001g0189 |
2 | NA18942.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.555-1065T>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15584054 | |||||||
| chr3:15584082 | T | C | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG00544.hp2 HG02735.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.555-1093A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15584082 | |||||||
| chr3:15584317 | C | T | 1 | a0001c0008t0001g0076 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.554+931G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15584317 | |||||||
| chr3:15584322 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.554+926C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15584322 | |||||||
| chr3:15584397 | G | A | 1 | a0001c0001t0001g0284 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.554+851C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15584397 | |||||||
| chr3:15584503 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
5 | HG02257.hp1 HG02559.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+745C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15584503 | |||||||
| chr3:15584694 | A | G | 3 | a0001c0001t0001g0350 a0001c0001t0001g0351 a0001c0001t0001g0352 |
3 | HG03209.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.554+554T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15584694 | |||||||
| chr3:15584842 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0040 others(1): Show |
6 | HG01891.hp2 HG02647.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.554+406A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15584842 | |||||||
| chr3:15584846 | A | G | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG00544.hp2 HG02735.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.554+402T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15584846 | |||||||
| chr3:15584864 | G | C | 13 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(10): Show |
13 | HG01175.hp2 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.554+384C>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15584864 | |||||||
| chr3:15584970 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+278C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15584970 | |||||||
| chr3:15584984 | T | A | 7 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0180 others(4): Show |
8 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.554+264A>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15584984 | |||||||
| chr3:15585136 | T | C | 2 | a0001c0003t0001g0015 a0001c0003t0001g0062 |
3 | HG02970.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.554+112A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15585136 | |||||||
| chr3:15585188 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.554+60C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 7/16 | chr3 | 15585188 | |||||||
| chr3:15585437 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.460-95A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 6/16 | chr3 | 15585437 | |||||||
| chr3:15585543 | TAAG | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0172 others(4): Show |
11 | HG01192.hp2 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.460-204_460-202del others(3): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 6/16 | chr3 | 15585543 | |||||||
| chr3:15585547 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(86): Show |
104 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.460-205T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 6/16 | chr3 | 15585547 | |||||||
| chr3:15585597 | G | T | 13 | a0001c0001t0001g0034 a0001c0001t0001g0197 a0001c0001t0001g0198 others(10): Show |
14 | HG00408.hp2 HG02015.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.460-255C>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 6/16 | chr3 | 15585597 | |||||||
| chr3:15585726 | T | G | 13 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(10): Show |
13 | HG01175.hp2 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.460-384A>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 6/16 | chr3 | 15585726 | |||||||
| chr3:15585754 | A | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0340 others(8): Show |
15 | HG01109.hp1 HG01168.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.460-412T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 6/16 | chr3 | 15585754 | |||||||
| chr3:15585994 | T | C | 3 | a0001c0001t0001g0067 a0001c0001t0001g0100 a0001c0001t0001g0110 |
3 | HG02738.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.459+531A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 6/16 | chr3 | 15585994 | |||||||
| chr3:15586156 | T | C | 3 | a0001c0002t0001g0288 a0001c0002t0001g0312 a0001c0002t0001g0324 |
3 | HG01069.hp2 HG01071.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.459+369A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 6/16 | chr3 | 15586156 | |||||||
| chr3:15586159 | C | T | 7 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0180 others(4): Show |
8 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.459+366G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 6/16 | chr3 | 15586159 | |||||||
| chr3:15586321 | C | T | 5 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
5 | HG01256.hp2 HG02300.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+204G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 6/16 | chr3 | 15586321 | |||||||
| chr3:15586744 | A | T | 11 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0340 others(8): Show |
15 | HG01109.hp1 HG01168.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.382-142T>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15586744 | |||||||
| chr3:15586884 | A | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0172 others(4): Show |
11 | HG01192.hp2 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.382-282T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15586884 | |||||||
| chr3:15586894 | T | A | 3 | a0001c0001t0001g0350 a0001c0001t0001g0351 a0001c0001t0001g0352 |
3 | HG03209.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.382-292A>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15586894 | |||||||
| chr3:15587074 | C | A | 7 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0180 others(4): Show |
8 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-472G>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15587074 | |||||||
| chr3:15587154 | G | A | 7 | a0001c0001t0001g0074 a0001c0003t0001g0015 a0001c0003t0001g0062 others(4): Show |
8 | HG02886.hp1 HG02970.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-552C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15587154 | |||||||
| chr3:15587228 | G | C | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG00544.hp2 HG02735.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-626C>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15587228 | |||||||
| chr3:15587301 | T | TAAATTTG others(21): Show |
1 | a0001c0002t0001g0325 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.382-727_382-700dup others(28): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15587301 | |||||||
| chr3:15587370 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.382-768A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15587370 | |||||||
| chr3:15587375 | T | C | 1 | a0001c0001t0001g0349 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.382-773A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15587375 | |||||||
| chr3:15587411 | T | C | 4 | a0002c0005t0001g0200 a0002c0005t0001g0276 a0002c0005t0001g0277 others(1): Show |
4 | HG00099.hp2 HG00280.hp2 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-809A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15587411 | |||||||
| chr3:15587535 | C | T | 3 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01081.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.382-933G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15587535 | |||||||
| chr3:15587679 | T | G | 1 | a0001c0001t0001g0050 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.382-1077A>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15587679 | |||||||
| chr3:15587789 | T | C | 20 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0054 others(17): Show |
21 | HG01081.hp1 HG01175.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.382-1187A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15587789 | |||||||
| chr3:15587830 | T | C | 4 | a0001c0001t0001g0066 a0001c0001t0001g0099 a0001c0001t0001g0103 others(1): Show |
4 | HG01981.hp2 HG01993.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-1228A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15587830 | |||||||
| chr3:15587957 | G | A | 35 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(32): Show |
41 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.382-1355C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15587957 | |||||||
| chr3:15587964 | G | C | 1 | a0001c0002t0001g0326 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.382-1362C>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15587964 | |||||||
| chr3:15588022 | T | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0052 a0001c0001t0001g0279 others(1): Show |
6 | HG00673.hp2 NA18962.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-1420A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15588022 | |||||||
| chr3:15588136 | T | A | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 |
3 | HG00544.hp2 NA18957.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.381+1404A>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15588136 | |||||||
| chr3:15588143 | T | C | 10 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0209 others(7): Show |
12 | HG00642.hp1 HG01071.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.381+1397A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15588143 | |||||||
| chr3:15588337 | T | C | 1 | a0001c0002t0001g0332 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.381+1203A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15588337 | |||||||
| chr3:15588339 | A | T | 35 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(32): Show |
41 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.381+1201T>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15588339 | |||||||
| chr3:15588398 | G | T | 5 | a0001c0003t0001g0015 a0001c0003t0001g0062 a0001c0003t0003g0069 others(2): Show |
6 | HG02970.hp1 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+1142C>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15588398 | |||||||
| chr3:15588462 | G | A | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG00544.hp2 HG02735.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+1078C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15588462 | |||||||
| chr3:15588501 | G | C | 1 | a0001c0008t0001g0076 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.381+1039C>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15588501 | |||||||
| chr3:15588546 | C | T | 7 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0180 others(4): Show |
8 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+994G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15588546 | |||||||
| chr3:15588581 | A | G | 13 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(10): Show |
13 | HG01175.hp2 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.381+959T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15588581 | |||||||
| chr3:15588648 | T | A | 1 | a0001c0001t0001g0094 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.381+892A>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15588648 | |||||||
| chr3:15588725 | A | G | 1 | a0001c0001t0001g0026 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.381+815T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15588725 | |||||||
| chr3:15588788 | T | TTTCAAGT others(34): Show |
1 | a0001c0002t0001g0327 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.381+751_381+752ins others(41): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15588788 | |||||||
| chr3:15588788 | T | TTTCAAGT others(76): Show |
1 | a0001c0002t0001g0307 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.381+751_381+752ins others(83): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15588788 | |||||||
| chr3:15588948 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG01081.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.381+592G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15588948 | |||||||
| chr3:15589388 | T | G | 1 | a0001c0001t0001g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.381+152A>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15589388 | |||||||
| chr3:15589404 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.381+136C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 5/16 | chr3 | 15589404 | |||||||
| chr3:15589895 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0172 others(4): Show |
11 | HG01192.hp2 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.309-283G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15589895 | |||||||
| chr3:15589927 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(165): Show |
199 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.309-315A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15589927 | |||||||
| chr3:15590060 | T | TAAAAAAT others(299): Show |
1 | a0001c0001t0001g0096 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.309-449_309-448ins others(306): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15590060 | |||||||
| chr3:15590060 | T | TAAAAAAT others(307): Show |
1 | a0005c0010t0001g0078 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.309-449_309-448ins others(314): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15590060 | |||||||
| chr3:15590060 | T | TAAAAAAT others(321): Show |
1 | a0001c0001t0001g0080 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.309-449_309-448ins others(328): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15590060 | |||||||
| chr3:15590060 | T | TAAAAAAT others(322): Show |
7 | a0001c0001t0001g0017 a0001c0001t0001g0077 a0001c0001t0001g0079 others(4): Show |
8 | HG02083.hp2 HG03942.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-449_309-448ins others(329): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15590060 | |||||||
| chr3:15590060 | T | TAAAAAAT others(323): Show |
12 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0065 others(9): Show |
15 | HG00423.hp2 HG00639.hp2 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.309-449_309-448ins others(330): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15590060 | |||||||
| chr3:15590060 | T | TAAAAAAT others(324): Show |
5 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0092 others(2): Show |
7 | HG01928.hp1 HG01952.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.309-449_309-448ins others(331): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15590060 | |||||||
| chr3:15590060 | T | TAAAAAAT others(325): Show |
1 | a0001c0001t0001g0130 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.309-449_309-448ins others(332): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15590060 | |||||||
| chr3:15590060 | T | TAAAAAAT others(328): Show |
1 | a0001c0001t0001g0095 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.309-449_309-448ins others(335): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15590060 | |||||||
| chr3:15590060 | T | TAAAAAAT others(322): Show |
1 | a0004c0009t0004g0356 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.309-449_309-448ins others(329): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15590060 | |||||||
| chr3:15590067 | T | TATCTGGC others(321): Show |
1 | a0001c0001t0001g0097 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.309-456_309-455ins others(328): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15590067 | |||||||
| chr3:15590164 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01081.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.309-552A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15590164 | |||||||
| chr3:15590195 | T | A | 1 | a0001c0004t0001g0149 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.309-583A>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15590195 | |||||||
| chr3:15590692 | T | G | 7 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0180 others(4): Show |
8 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.308+908A>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15590692 | |||||||
| chr3:15590721 | A | C | 1 | a0001c0001t0001g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.308+879T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15590721 | |||||||
| chr3:15590820 | C | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0172 others(4): Show |
11 | HG01192.hp2 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.308+780G>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15590820 | |||||||
| chr3:15590894 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.308+706T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15590894 | |||||||
| chr3:15591055 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.308+545A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15591055 | |||||||
| chr3:15591086 | G | T | 2 | a0001c0003t0001g0015 a0001c0003t0001g0062 |
3 | HG02970.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.308+514C>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15591086 | |||||||
| chr3:15591151 | T | A | 1 | a0001c0001t0001g0280 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.308+449A>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15591151 | |||||||
| chr3:15591176 | C | T | 6 | a0001c0003t0001g0015 a0001c0003t0001g0062 a0001c0003t0003g0069 others(3): Show |
7 | HG02970.hp1 HG02976.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.308+424G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15591176 | |||||||
| chr3:15591232 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.308+368G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15591232 | |||||||
| chr3:15591277 | CT | C | 18 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0191 others(15): Show |
20 | HG00408.hp2 HG02015.hp1 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.308+322delA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15591277 | |||||||
| chr3:15591291 | A | G | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 |
3 | HG00544.hp2 NA18957.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.308+309T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15591291 | |||||||
| chr3:15591450 | C | T | 1 | a0001c0004t0001g0157 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.308+150G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15591450 | |||||||
| chr3:15591452 | C | G | 1 | a0001c0002t0001g0312 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.308+148G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15591452 | |||||||
| chr3:15591492 | GT | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(129): Show |
157 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.308+107delA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 4/16 | chr3 | 15591492 | |||||||
| chr3:15591706 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.228-26T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15591706 | |||||||
| chr3:15591781 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.228-101G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15591781 | |||||||
| chr3:15591885 | C | CGTATATA others(17): Show |
1 | a0001c0001t0001g0340 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.228-229_228-206dup others(24): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15591885 | |||||||
| chr3:15591886 | G | A | 1 | a0001c0003t0003g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.228-206C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15591886 | |||||||
| chr3:15591886 | GTATA | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01081.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.228-210_228-207del others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15591886 | |||||||
| chr3:15591909 | T | C | 3 | a0001c0001t0001g0097 a0001c0001t0001g0345 a0001c0001t0001g0346 |
3 | HG02896.hp1 HG02897.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.228-229A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15591909 | |||||||
| chr3:15591916 | AGTGTATA others(13): Show |
A | 1 | a0001c0002t0001g0328 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.228-256_228-237del others(20): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15591916 | |||||||
| chr3:15591929 | G | C | 1 | a0001c0001t0001g0097 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.228-249C>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15591929 | |||||||
| chr3:15591948 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.228-268G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15591948 | |||||||
| chr3:15592005 | T | TATACGTA others(16): Show |
1 | a0001c0001t0001g0284 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.228-348_228-326dup others(23): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592005 | |||||||
| chr3:15592028 | C | CATACGTA others(3): Show |
7 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0180 others(4): Show |
8 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.228-358_228-349dup others(10): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592028 | |||||||
| chr3:15592028 | CATACGTA others(40): Show |
C | 1 | a0001c0001t0001g0097 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.228-395_228-349del others(47): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592028 | |||||||
| chr3:15592031 | A | G | 52 | a0001c0001t0001g0308 a0001c0001t0001g0310 a0001c0001t0001g0311 others(49): Show |
58 | HG00280.hp1 HG00544.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.228-351T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592031 | |||||||
| chr3:15592033 | GTATA | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(84): Show |
102 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.228-357_228-354del others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592033 | |||||||
| chr3:15592048 | C | CTATATAC others(3): Show |
4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-378_228-369dup others(10): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592048 | |||||||
| chr3:15592051 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0172 others(4): Show |
11 | HG01192.hp2 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.228-371A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592051 | |||||||
| chr3:15592060 | ATATACGT others(7): Show |
A | 5 | a0001c0001t0001g0072 a0001c0001t0001g0096 a0001c0001t0001g0112 others(2): Show |
5 | HG00673.hp1 HG02486.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-394_228-381del others(14): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592060 | |||||||
| chr3:15592061 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01081.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.228-381A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592061 | |||||||
| chr3:15592065 | C | CACA | 5 | a0001c0001t0001g0065 a0001c0003t0001g0015 a0001c0003t0001g0062 others(2): Show |
6 | HG02965.hp1 HG02970.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.228-386_228-385ins others(3): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592065 | |||||||
| chr3:15592066 | G | C | 5 | a0001c0001t0001g0065 a0001c0003t0001g0015 a0001c0003t0001g0062 others(2): Show |
6 | HG02965.hp1 HG02970.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.228-386C>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592066 | |||||||
| chr3:15592072 | A | ATACACAC others(2): Show |
84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(81): Show |
99 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.228-393_228-392ins others(9): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592072 | |||||||
| chr3:15592073 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(85): Show |
103 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.228-393G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592073 | |||||||
| chr3:15592074 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(81): Show |
99 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.228-394C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592074 | |||||||
| chr3:15592074 | G | GTATA | 266 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(263): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.228-398_228-395dup others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592074 | |||||||
| chr3:15592075 | T | TATAC | 3 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01081.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.228-399_228-396dup others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592075 | |||||||
| chr3:15592080 | G | A | 5 | a0001c0001t0001g0065 a0001c0003t0001g0015 a0001c0003t0001g0062 others(2): Show |
6 | HG02965.hp1 HG02970.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.228-400C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592080 | |||||||
| chr3:15592083 | T | C | 5 | a0001c0001t0001g0065 a0001c0003t0001g0015 a0001c0003t0001g0062 others(2): Show |
6 | HG02965.hp1 HG02970.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.228-403A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592083 | |||||||
| chr3:15592084 | A | G | 5 | a0001c0001t0001g0065 a0001c0003t0001g0015 a0001c0003t0001g0062 others(2): Show |
6 | HG02965.hp1 HG02970.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.228-404T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592084 | |||||||
| chr3:15592085 | TATACACA others(2): Show |
T | 5 | a0001c0001t0001g0065 a0001c0003t0001g0015 a0001c0003t0001g0062 others(2): Show |
6 | HG02965.hp1 HG02970.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.228-414_228-406del others(9): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592085 | |||||||
| chr3:15592087 | TAC | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(81): Show |
99 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.228-409_228-408del others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592087 | |||||||
| chr3:15592089 | C | CGT | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-410_228-409ins others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592089 | |||||||
| chr3:15592091 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-411G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592091 | |||||||
| chr3:15592093 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-413G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592093 | |||||||
| chr3:15592095 | C | CGTA | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-416_228-415ins others(3): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592095 | |||||||
| chr3:15592095 | C | G | 5 | a0001c0001t0001g0065 a0001c0003t0001g0015 a0001c0003t0001g0062 others(2): Show |
6 | HG02965.hp1 HG02970.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.228-415G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592095 | |||||||
| chr3:15592102 | C | T | 5 | a0001c0001t0001g0065 a0001c0003t0001g0015 a0001c0003t0001g0062 others(2): Show |
6 | HG02965.hp1 HG02970.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.228-422G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592102 | |||||||
| chr3:15592103 | G | A | 43 | a0001c0002t0001g0004 a0001c0002t0001g0037 a0001c0002t0001g0188 others(40): Show |
48 | HG00280.hp1 HG00544.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.228-423C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592103 | |||||||
| chr3:15592105 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.228-425T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592105 | |||||||
| chr3:15592107 | A | ACATACGT others(9): Show |
87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(84): Show |
102 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.228-428_228-427ins others(16): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592107 | |||||||
| chr3:15592108 | T | C | 5 | a0001c0001t0001g0065 a0001c0003t0001g0015 a0001c0003t0001g0062 others(2): Show |
6 | HG02965.hp1 HG02970.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.228-428A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592108 | |||||||
| chr3:15592110 | T | TAC | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-432_228-431dup others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592110 | |||||||
| chr3:15592112 | CACA | C | 5 | a0001c0001t0001g0065 a0001c0003t0001g0015 a0001c0003t0001g0062 others(2): Show |
6 | HG02965.hp1 HG02970.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.228-435_228-433del others(3): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592112 | |||||||
| chr3:15592114 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(84): Show |
102 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.228-434G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592114 | |||||||
| chr3:15592116 | C | CG | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(84): Show |
102 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.228-437_228-436ins others(1): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592116 | |||||||
| chr3:15592116 | C | G | 5 | a0001c0001t0001g0065 a0001c0003t0001g0015 a0001c0003t0001g0062 others(2): Show |
6 | HG02965.hp1 HG02970.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.228-436G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592116 | |||||||
| chr3:15592132 | A | ACGTGTAT others(31): Show |
1 | a0001c0001t0001g0173 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.228-490_228-453dup others(38): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592132 | |||||||
| chr3:15592132 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(89): Show |
108 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.228-452T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592132 | |||||||
| chr3:15592134 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(86): Show |
105 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.228-454C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592134 | |||||||
| chr3:15592134 | G | GTGTATAT others(31): Show |
12 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0072 others(9): Show |
16 | HG00673.hp1 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.228-492_228-455dup others(38): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592134 | |||||||
| chr3:15592170 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.228-490C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592170 | |||||||
| chr3:15592172 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.228-492T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592172 | |||||||
| chr3:15592172 | A | G | 13 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0065 others(10): Show |
14 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.228-492T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592172 | |||||||
| chr3:15592183 | T | G | 1 | a0001c0001t0001g0097 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.228-503A>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592183 | |||||||
| chr3:15592186 | A | C | 1 | a0001c0001t0001g0097 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.228-506T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592186 | |||||||
| chr3:15592188 | ATACGTAT others(35): Show |
A | 1 | a0001c0001t0001g0097 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.228-550_228-509del others(42): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592188 | |||||||
| chr3:15592190 | A | G | 11 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0340 others(8): Show |
15 | HG01109.hp1 HG01168.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.228-510T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592190 | |||||||
| chr3:15592199 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(164): Show |
198 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.228-519A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592199 | |||||||
| chr3:15592201 | T | TATACATG others(69): Show |
1 | a0001c0001t0001g0125 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.228-522_228-521ins others(76): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592201 | |||||||
| chr3:15592203 | T | C | 52 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(49): Show |
61 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(58): Show |
intron_variant | MODIFIER | c.228-523A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592203 | |||||||
| chr3:15592208 | G | A | 2 | a0001c0001t0001g0065 a0004c0009t0004g0356 |
2 | HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.228-528C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592208 | |||||||
| chr3:15592209 | C | T | 5 | a0001c0001t0001g0079 a0001c0001t0001g0176 a0001c0001t0001g0177 others(2): Show |
5 | HG00544.hp2 HG02735.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.228-529G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592209 | |||||||
| chr3:15592219 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.228-539A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592219 | |||||||
| chr3:15592221 | T | G | 9 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0065 others(6): Show |
10 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.228-541A>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592221 | |||||||
| chr3:15592224 | A | C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0065 others(6): Show |
10 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.228-544T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592224 | |||||||
| chr3:15592226 | ATACG | A | 9 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0065 others(6): Show |
10 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.228-550_228-547del others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592226 | |||||||
| chr3:15592237 | C | T | 3 | a0001c0001t0001g0065 a0001c0001t0001g0097 a0004c0009t0004g0356 |
3 | HG02965.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.228-557G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592237 | |||||||
| chr3:15592239 | T | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(108): Show |
132 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.228-559A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592239 | |||||||
| chr3:15592239 | T | TATACATA others(27): Show |
27 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0053 others(24): Show |
31 | HG00544.hp2 HG01109.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.228-560_228-559ins others(34): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592239 | |||||||
| chr3:15592239 | T | TATACATA others(27): Show |
27 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(24): Show |
33 | HG00423.hp2 HG00639.hp2 HG01928.hp1 others(30): Show |
intron_variant | MODIFIER | c.228-560_228-559ins others(34): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592239 | |||||||
| chr3:15592239 | T | TATACATA others(25): Show |
1 | a0001c0001t0001g0098 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.228-560_228-559ins others(32): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592239 | |||||||
| chr3:15592246 | A | G | 1 | a0001c0002t0001g0329 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.228-566T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592246 | |||||||
| chr3:15592253 | T | G | 1 | a0001c0001t0001g0191 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.228-573A>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592253 | |||||||
| chr3:15592262 | C | CCATATAT others(7): Show |
3 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01081.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.228-596_228-583dup others(14): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592262 | |||||||
| chr3:15592272 | G | GCATACAT others(27): Show |
1 | a0001c0001t0001g0347 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.228-593_228-592ins others(34): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592272 | |||||||
| chr3:15592273 | T | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(98): Show |
121 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.228-593A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592273 | |||||||
| chr3:15592277 | C | CATAT | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-598_228-597ins others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592277 | |||||||
| chr3:15592281 | C | T | 3 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01081.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.228-601G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592281 | |||||||
| chr3:15592283 | T | TATACATA others(35): Show |
4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-604_228-603ins others(42): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592283 | |||||||
| chr3:15592284 | G | A | 7 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0180 others(4): Show |
8 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.228-604C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592284 | |||||||
| chr3:15592295 | C | CATACGTA others(25): Show |
1 | a0001c0001t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.228-647_228-616dup others(32): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592295 | |||||||
| chr3:15592295 | C | T | 11 | a0001c0001t0001g0025 a0001c0001t0001g0105 a0001c0001t0001g0116 others(8): Show |
12 | HG02074.hp2 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.228-615G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592295 | |||||||
| chr3:15592297 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0172 others(4): Show |
11 | HG01192.hp2 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.228-617A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592297 | |||||||
| chr3:15592301 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.228-621A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592301 | |||||||
| chr3:15592360 | A | ATGTATAC others(25): Show |
1 | a0001c0001t0001g0150 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.228-712_228-681dup others(32): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592360 | |||||||
| chr3:15592370 | A | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0182 others(2): Show |
6 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.228-690T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592370 | |||||||
| chr3:15592371 | C | CAGACACA others(25): Show |
1 | a0001c0001t0001g0169 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.228-723_228-692dup others(32): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592371 | |||||||
| chr3:15592371 | C | CAGACACA others(57): Show |
11 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0340 others(8): Show |
15 | HG01109.hp1 HG01168.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.228-692_228-691ins others(64): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592371 | |||||||
| chr3:15592371 | C | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0182 others(2): Show |
6 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.228-691G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592371 | |||||||
| chr3:15592398 | A | ACATGTAG others(23): Show |
5 | a0001c0002t0001g0295 a0001c0003t0001g0015 a0001c0003t0001g0062 others(2): Show |
6 | HG02970.hp1 HG02976.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.228-748_228-719dup others(30): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592398 | |||||||
| chr3:15592423 | C | CGT | 7 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0180 others(4): Show |
8 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.228-745_228-744dup others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592423 | |||||||
| chr3:15592428 | G | A | 7 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0180 others(4): Show |
8 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.228-748C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592428 | |||||||
| chr3:15592433 | T | C | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | NA18966.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.228-753A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592433 | |||||||
| chr3:15592441 | C | T | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.228-761G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592441 | |||||||
| chr3:15592447 | CAT | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-769_228-768del others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592447 | |||||||
| chr3:15592448 | A | ACACACGT others(7): Show |
4 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
4 | HG01081.hp1 HG01884.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-769_228-768ins others(14): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592448 | |||||||
| chr3:15592449 | T | C | 1 | a0003c0006t0001g0036 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.228-769A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592449 | |||||||
| chr3:15592451 | C | G | 4 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
4 | HG01081.hp1 HG01884.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-771G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592451 | |||||||
| chr3:15592456 | A | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-776T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592456 | |||||||
| chr3:15592456 | A | T | 1 | a0001c0001t0001g0168 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.228-776T>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592456 | |||||||
| chr3:15592457 | C | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0182 others(2): Show |
6 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.228-777G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592457 | |||||||
| chr3:15592464 | A | ATG | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-785_228-784ins others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592464 | |||||||
| chr3:15592467 | C | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-787G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592467 | |||||||
| chr3:15592467 | CACACACG others(7): Show |
C | 7 | a0001c0001t0001g0074 a0001c0001t0001g0084 a0001c0001t0001g0098 others(4): Show |
7 | HG02074.hp2 HG02083.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.228-801_228-788del others(14): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592467 | |||||||
| chr3:15592481 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-801A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592481 | |||||||
| chr3:15592481 | T | TAC | 332 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(329): Show |
392 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(389): Show |
intron_variant | MODIFIER | c.228-803_228-802dup others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592481 | |||||||
| chr3:15592481 | T | TACACACA others(11): Show |
13 | a0001c0001t0001g0031 a0001c0001t0001g0042 a0001c0001t0001g0050 others(10): Show |
14 | HG00597.hp2 HG00639.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.228-802_228-801ins others(18): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592481 | |||||||
| chr3:15592483 | CACTTGTA others(7): Show |
C | 1 | a0001c0001t0001g0195 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.228-817_228-804del others(14): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592483 | |||||||
| chr3:15592485 | CTT | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-807_228-806del others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592485 | |||||||
| chr3:15592486 | T | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0063 a0001c0001t0001g0180 others(3): Show |
6 | HG01081.hp1 HG01884.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.228-806A>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592486 | |||||||
| chr3:15592487 | T | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0063 a0001c0001t0001g0180 others(3): Show |
6 | HG01081.hp1 HG01884.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.228-807A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592487 | |||||||
| chr3:15592487 | T | G | 1 | a0001c0001t0001g0268 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.228-807A>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592487 | |||||||
| chr3:15592491 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.228-811A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592491 | |||||||
| chr3:15592492 | A | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-812T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592492 | |||||||
| chr3:15592493 | C | T | 1 | a0005c0010t0001g0078 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.228-813G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592493 | |||||||
| chr3:15592493 | CATATACA others(5): Show |
C | 1 | a0001c0001t0001g0338 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.228-825_228-814del others(12): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592493 | |||||||
| chr3:15592494 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.228-814T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592494 | |||||||
| chr3:15592494 | ATATACAC others(1): Show |
A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-822_228-815del others(8): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592494 | |||||||
| chr3:15592497 | T | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0063 a0001c0001t0001g0180 others(3): Show |
6 | HG01081.hp1 HG01884.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.228-817A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592497 | |||||||
| chr3:15592502 | T | A | 3 | a0001c0001t0001g0289 a0001c0002t0001g0329 a0005c0010t0001g0078 |
3 | HG01943.hp2 HG02040.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.228-822A>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592502 | |||||||
| chr3:15592503 | T | C | 2 | a0001c0001t0001g0289 a0001c0002t0001g0329 |
2 | HG01943.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.228-823A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592503 | |||||||
| chr3:15592505 | T | TATAC | 5 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 others(2): Show |
5 | HG01081.hp1 HG01884.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-826_228-825ins others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592505 | |||||||
| chr3:15592506 | A | ACGCACGT others(33): Show |
1 | a0005c0010t0001g0078 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.228-827_228-826ins others(40): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592506 | |||||||
| chr3:15592507 | T | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-827A>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592507 | |||||||
| chr3:15592509 | T | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(4): Show |
8 | HG01943.hp2 HG02004.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.228-829A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592509 | |||||||
| chr3:15592511 | C | A | 1 | a0001c0001t0001g0199 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.228-831G>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592511 | |||||||
| chr3:15592512 | ACTTGTAT others(149): Show |
A | 1 | a0001c0001t0001g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.228-988_228-833del | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592512 | |||||||
| chr3:15592513 | CTT | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-835_228-834del others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592513 | |||||||
| chr3:15592514 | T | A | 2 | a0002c0005t0001g0200 a0005c0010t0001g0078 |
2 | HG00735.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.228-834A>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592514 | |||||||
| chr3:15592517 | T | A | 1 | a0001c0001t0001g0021 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.228-837A>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592517 | |||||||
| chr3:15592519 | T | C | 2 | a0002c0005t0001g0200 a0005c0010t0001g0078 |
2 | HG00735.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.228-839A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592519 | |||||||
| chr3:15592520 | A | G | 1 | a0005c0010t0001g0078 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.228-840T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592520 | |||||||
| chr3:15592523 | T | C | 1 | a0005c0010t0001g0078 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.228-843A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592523 | |||||||
| chr3:15592524 | A | G | 2 | a0002c0005t0001g0200 a0005c0010t0001g0078 |
2 | HG00735.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.228-844T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592524 | |||||||
| chr3:15592525 | T | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0182 others(4): Show |
8 | HG01943.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.228-845A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592525 | |||||||
| chr3:15592526 | A | G | 2 | a0002c0005t0001g0200 a0005c0010t0001g0078 |
2 | HG00735.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.228-846T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592526 | |||||||
| chr3:15592527 | C | T | 2 | a0002c0005t0001g0200 a0005c0010t0001g0078 |
2 | HG00735.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.228-847G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592527 | |||||||
| chr3:15592528 | A | ACATGTAT others(21): Show |
1 | a0001c0001t0001g0275 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.228-876_228-849dup others(28): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592528 | |||||||
| chr3:15592528 | A | ACGTGTAT others(49): Show |
2 | a0001c0001t0001g0035 a0001c0001t0001g0283 |
3 | HG02615.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.228-849_228-848ins others(56): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592528 | |||||||
| chr3:15592528 | A | G | 2 | a0002c0005t0001g0200 a0005c0010t0001g0078 |
2 | HG00735.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.228-848T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592528 | |||||||
| chr3:15592530 | A | ATGTACGC others(39): Show |
1 | a0001c0001t0002g0359 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.228-851_228-850ins others(46): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592530 | |||||||
| chr3:15592530 | A | ATGTACGC others(67): Show |
1 | a0001c0002t0001g0004 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.228-851_228-850ins others(74): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592530 | |||||||
| chr3:15592530 | A | ATGTACGC others(95): Show |
1 | a0001c0002t0001g0323 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.228-851_228-850ins others(102): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592530 | |||||||
| chr3:15592530 | A | ATGTATAC others(105): Show |
1 | a0001c0001t0001g0330 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.228-851_228-850ins others(112): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592530 | |||||||
| chr3:15592530 | A | ATGTATAC others(133): Show |
1 | a0001c0001t0001g0308 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.228-851_228-850ins others(140): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592530 | |||||||
| chr3:15592530 | A | ATGTATAC others(217): Show |
1 | a0001c0001t0001g0311 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.228-851_228-850ins others(224): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592530 | |||||||
| chr3:15592530 | A | ATGTATAC others(21): Show |
23 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0206 others(20): Show |
24 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.228-878_228-851dup others(28): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592530 | |||||||
| chr3:15592530 | A | ATGTATAC others(49): Show |
20 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0052 others(17): Show |
20 | HG00140.hp1 HG00673.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.228-906_228-851dup others(56): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592530 | |||||||
| chr3:15592530 | A | ATGTATAC others(77): Show |
8 | a0001c0001t0001g0031 a0001c0001t0001g0262 a0001c0002t0001g0193 others(5): Show |
8 | HG02027.hp2 HG02523.hp1 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.228-934_228-851dup others(84): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592530 | |||||||
| chr3:15592530 | A | ATGTATAC others(105): Show |
3 | a0001c0001t0001g0012 a0001c0001t0001g0268 a0001c0001t0001g0281 |
3 | NA18945.hp2 NA19005.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.228-962_228-851dup others(112): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592530 | |||||||
| chr3:15592530 | A | ATGTATAC others(133): Show |
2 | a0001c0001t0001g0011 a0001c0001t0001g0256 |
3 | HG03688.hp2 NA18957.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.228-990_228-851dup others(140): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592530 | |||||||
| chr3:15592530 | A | ATGTATAC others(161): Show |
1 | a0001c0001t0001g0011 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.228-1018_228-851du others(169): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592530 | |||||||
| chr3:15592530 | A | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0283 a0002c0005t0001g0200 others(1): Show |
5 | HG00735.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-850T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592530 | |||||||
| chr3:15592530 | A | T | 1 | a0001c0002t0001g0329 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.228-850T>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592530 | |||||||
| chr3:15592530 | ATGTATAC others(21): Show |
A | 1 | a0001c0001t0002g0364 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.228-878_228-851del others(28): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592530 | |||||||
| chr3:15592530 | ATGTATAC others(77): Show |
A | 1 | a0001c0001t0002g0039 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.228-934_228-851del others(84): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592530 | |||||||
| chr3:15592531 | T | C | 5 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
6 | HG01943.hp2 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.228-851A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592531 | |||||||
| chr3:15592537 | C | T | 1 | a0001c0002t0001g0329 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.228-857G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592537 | |||||||
| chr3:15592538 | ACATG | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
6 | HG01943.hp2 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.228-862_228-859del others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592538 | |||||||
| chr3:15592543 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01081.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.228-863A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592543 | |||||||
| chr3:15592543 | T | TACGCACA others(21): Show |
1 | a0001c0001t0001g0210 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.228-864_228-863ins others(28): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592543 | |||||||
| chr3:15592546 | G | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
6 | HG01943.hp2 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.228-866C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592546 | |||||||
| chr3:15592549 | CAT | C | 28 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(25): Show |
34 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.228-871_228-870del others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592549 | |||||||
| chr3:15592549 | CATGTGTG others(23): Show |
C | 3 | a0001c0001t0001g0101 a0001c0001t0001g0119 a0001c0001t0001g0169 |
3 | NA18965.hp2 NA19057.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.228-899_228-870del others(30): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592549 | |||||||
| chr3:15592549 | CATGTGTG others(51): Show |
C | 4 | a0001c0001t0001g0117 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
4 | HG02132.hp1 NA18962.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-927_228-870del others(58): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592549 | |||||||
| chr3:15592549 | CATGTGTG others(79): Show |
C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0022 others(4): Show |
8 | HG00621.hp1 HG01952.hp1 HG04204.hp2 others(5): Show |
intron_variant | MODIFIER | c.228-955_228-870del others(86): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592549 | |||||||
| chr3:15592549 | CATGTGTG others(107): Show |
C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0022 others(6): Show |
12 | HG00408.hp1 HG01433.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.228-983_228-870del | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592549 | |||||||
| chr3:15592549 | CATGTGTG others(135): Show |
C | 18 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0066 others(15): Show |
19 | HG00423.hp1 HG01099.hp2 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.228-1011_228-870de others(1): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592549 | |||||||
| chr3:15592549 | CATGTGTG others(163): Show |
C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0105 others(2): Show |
5 | NA18945.hp1 NA18972.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-1039_228-870de others(1): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592549 | |||||||
| chr3:15592549 | CATGTGTG others(219): Show |
C | 1 | a0001c0001t0001g0129 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.228-1095_228-870de others(1): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592549 | |||||||
| chr3:15592549 | CATGTGTG others(247): Show |
C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0123 |
2 | NA18960.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.228-1123_228-870de others(1): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592549 | |||||||
| chr3:15592549 | CATGTGTG others(275): Show |
C | 1 | a0001c0001t0001g0084 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.228-1151_228-870de others(1): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592549 | |||||||
| chr3:15592549 | CATGTGTG others(303): Show |
C | 3 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0083 |
3 | HG01978.hp1 NA18986.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.228-1179_228-870de others(1): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592549 | |||||||
| chr3:15592549 | CATGTGTG others(387): Show |
C | 1 | a0001c0001t0001g0082 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.228-1263_228-870de others(1): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592549 | |||||||
| chr3:15592550 | A | T | 2 | a0001c0001t0001g0289 a0001c0002t0001g0329 |
2 | HG01943.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.228-870T>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592550 | |||||||
| chr3:15592550 | ATGTGTGC others(309): Show |
A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0182 |
2 | HG02258.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.228-1186_228-871de others(1): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592550 | |||||||
| chr3:15592550 | ATGTGTGC others(337): Show |
A | 1 | a0001c0001t0001g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.228-1214_228-871de others(1): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592550 | |||||||
| chr3:15592551 | T | C | 22 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0030 others(19): Show |
22 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.228-871A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592551 | |||||||
| chr3:15592554 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0184 a0001c0001t0001g0289 others(1): Show |
4 | HG01943.hp2 HG02040.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.228-874C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592554 | |||||||
| chr3:15592556 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0184 a0001c0001t0001g0289 others(1): Show |
4 | HG01943.hp2 HG02040.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.228-876C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592556 | |||||||
| chr3:15592558 | G | A | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG00544.hp2 HG02735.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.228-878C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592558 | |||||||
| chr3:15592560 | G | A | 2 | a0001c0001t0001g0289 a0001c0002t0001g0329 |
2 | HG01943.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.228-880C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592560 | |||||||
| chr3:15592568 | ATGTACGC others(95): Show |
A | 1 | a0001c0001t0001g0289 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.228-990_228-889del | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592568 | |||||||
| chr3:15592568 | ATGTACGC others(289): Show |
A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0184 |
2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.228-1184_228-889de others(1): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592568 | |||||||
| chr3:15592571 | T | C | 4 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
4 | HG00621.hp2 HG01081.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-891A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592571 | |||||||
| chr3:15592574 | GCACATGT others(123): Show |
G | 1 | a0001c0001t0001g0114 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.228-1024_228-895de others(1): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592574 | |||||||
| chr3:15592577 | CAT | C | 27 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(24): Show |
33 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.228-899_228-898del others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592577 | |||||||
| chr3:15592577 | CATGTGTG others(163): Show |
C | 1 | a0001c0001t0001g0127 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.228-1067_228-898de others(1): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592577 | |||||||
| chr3:15592577 | CATGTGTG others(191): Show |
C | 1 | a0001c0001t0001g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.228-1095_228-898de others(1): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592577 | |||||||
| chr3:15592579 | T | C | 23 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0033 others(20): Show |
25 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.228-899A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592579 | |||||||
| chr3:15592599 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.228-919A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592599 | |||||||
| chr3:15592605 | CAT | C | 28 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(25): Show |
34 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.228-927_228-926del others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592605 | |||||||
| chr3:15592607 | T | C | 20 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0033 others(17): Show |
22 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.228-927A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592607 | |||||||
| chr3:15592614 | G | A | 1 | a0001c0001t0002g0364 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.228-934C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592614 | |||||||
| chr3:15592627 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.228-947A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592627 | |||||||
| chr3:15592628 | ACGCACAT others(383): Show |
A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01081.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.228-1338_228-949de others(1): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592628 | |||||||
| chr3:15592633 | CAT | C | 32 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(29): Show |
38 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.228-955_228-954del others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592633 | |||||||
| chr3:15592634 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.228-954T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592634 | |||||||
| chr3:15592635 | T | C | 21 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0033 others(18): Show |
23 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.228-955A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592635 | |||||||
| chr3:15592655 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.228-975A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592655 | |||||||
| chr3:15592661 | CAT | C | 34 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(31): Show |
40 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.228-983_228-982del others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592661 | |||||||
| chr3:15592663 | T | C | 20 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0033 others(17): Show |
22 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.228-983A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592663 | |||||||
| chr3:15592670 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.228-990C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592670 | |||||||
| chr3:15592683 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.228-1003A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592683 | |||||||
| chr3:15592684 | ACGCACAT others(327): Show |
A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0060 others(8): Show |
15 | HG01109.hp1 HG01168.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.228-1338_228-1005d others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592684 | |||||||
| chr3:15592689 | CAT | C | 35 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(32): Show |
41 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.228-1011_228-1010d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592689 | |||||||
| chr3:15592690 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.228-1010T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592690 | |||||||
| chr3:15592691 | T | C | 20 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0033 others(17): Show |
22 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.228-1011A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592691 | |||||||
| chr3:15592695 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.228-1015A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592695 | |||||||
| chr3:15592700 | GTATACAC others(327): Show |
G | 6 | a0001c0001t0001g0019 a0001c0001t0001g0065 a0001c0001t0001g0085 others(3): Show |
6 | HG02965.hp1 HG03486.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.228-1354_228-1021d others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592700 | |||||||
| chr3:15592711 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.228-1031A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592711 | |||||||
| chr3:15592712 | ACGCACAT others(299): Show |
A | 1 | a0001c0001t0001g0348 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.228-1338_228-1033d others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592712 | |||||||
| chr3:15592717 | CAT | C | 45 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(42): Show |
54 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.228-1039_228-1038d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592717 | |||||||
| chr3:15592719 | T | C | 20 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0033 others(17): Show |
22 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.228-1039A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592719 | |||||||
| chr3:15592728 | GTATACAC others(299): Show |
G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG00639.hp2 HG02273.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.228-1354_228-1049d others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592728 | |||||||
| chr3:15592740 | ACGCACAT others(271): Show |
A | 6 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.228-1338_228-1061d others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592740 | |||||||
| chr3:15592745 | CAT | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(46): Show |
59 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.228-1067_228-1066d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592745 | |||||||
| chr3:15592747 | T | C | 20 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0033 others(17): Show |
22 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.228-1067A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592747 | |||||||
| chr3:15592752 | G | C | 1 | a0001c0001t0001g0034 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.228-1072C>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592752 | |||||||
| chr3:15592756 | GTATACAC others(271): Show |
G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG01952.hp2 NA19003.hp2 NA19055.hp1 others(3): Show |
intron_variant | MODIFIER | c.228-1354_228-1077d others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592756 | |||||||
| chr3:15592761 | C | G | 1 | a0001c0001t0001g0338 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.228-1081G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592761 | |||||||
| chr3:15592768 | ACGCACAT others(243): Show |
A | 13 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0059 others(10): Show |
16 | HG01175.hp2 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.228-1338_228-1089d others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592768 | |||||||
| chr3:15592773 | CAT | C | 48 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(45): Show |
59 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.228-1095_228-1094d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592773 | |||||||
| chr3:15592775 | T | C | 20 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0033 others(17): Show |
22 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.228-1095A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592775 | |||||||
| chr3:15592784 | GTATACAC others(243): Show |
G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0020 others(6): Show |
10 | HG00423.hp2 HG01928.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.228-1354_228-1105d others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592784 | |||||||
| chr3:15592789 | C | G | 2 | a0001c0001t0001g0336 a0001c0001t0001g0337 |
2 | HG00733.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.228-1109G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592789 | |||||||
| chr3:15592796 | ACGCACAT others(215): Show |
A | 10 | a0001c0001t0001g0024 a0001c0001t0001g0142 a0001c0001t0001g0176 others(7): Show |
10 | HG00544.hp2 HG02109.hp1 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.228-1338_228-1117d others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592796 | |||||||
| chr3:15592801 | CAT | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0016 others(38): Show |
48 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.228-1123_228-1122d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592801 | |||||||
| chr3:15592801 | CATGTGTG others(217): Show |
C | 1 | a0001c0001t0001g0013 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.228-1345_228-1122d others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592801 | |||||||
| chr3:15592803 | T | C | 20 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0033 others(17): Show |
22 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.228-1123A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592803 | |||||||
| chr3:15592812 | GTATACAC others(215): Show |
G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0098 |
3 | HG02083.hp2 NA18964.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.228-1354_228-1133d others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592812 | |||||||
| chr3:15592824 | ACGCACAT others(187): Show |
A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0152 a0001c0001t0001g0158 others(1): Show |
4 | HG03453.hp2 HG03579.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-1338_228-1145d others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592824 | |||||||
| chr3:15592829 | CAT | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0021 others(36): Show |
43 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.228-1151_228-1150d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592829 | |||||||
| chr3:15592829 | CATGTGTG others(189): Show |
C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0046 others(3): Show |
7 | HG01106.hp2 HG01243.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.228-1345_228-1150d others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592829 | |||||||
| chr3:15592831 | T | C | 20 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0033 others(17): Show |
22 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.228-1151A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592831 | |||||||
| chr3:15592852 | ACGCACAT others(159): Show |
A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0067 a0001c0001t0001g0100 others(8): Show |
11 | HG01069.hp1 HG02080.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.228-1338_228-1173d others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592852 | |||||||
| chr3:15592857 | CAT | C | 36 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0021 others(33): Show |
37 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.228-1179_228-1178d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592857 | |||||||
| chr3:15592857 | CATGTGTG others(107): Show |
C | 1 | a0001c0001t0001g0272 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.228-1291_228-1178d others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592857 | |||||||
| chr3:15592857 | CATGTGTG others(161): Show |
C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0027 others(6): Show |
9 | HG00597.hp2 HG01109.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.228-1345_228-1178d others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592857 | |||||||
| chr3:15592859 | T | C | 18 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0033 others(15): Show |
20 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.228-1179A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592859 | |||||||
| chr3:15592866 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0184 |
2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.228-1186C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592866 | |||||||
| chr3:15592867 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0184 |
4 | HG02257.hp1 HG02258.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-1187A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592867 | |||||||
| chr3:15592874 | ACATG | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0184 |
4 | HG02257.hp1 HG02258.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-1198_228-1195d others(6): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592874 | |||||||
| chr3:15592880 | ACGCACAT others(131): Show |
A | 18 | a0001c0001t0001g0073 a0001c0001t0001g0109 a0001c0001t0001g0135 others(15): Show |
18 | HG00597.hp1 HG02071.hp2 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.228-1338_228-1201d others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592880 | |||||||
| chr3:15592882 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0184 |
4 | HG02257.hp1 HG02258.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-1202C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592882 | |||||||
| chr3:15592885 | CAT | C | 20 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(17): Show |
20 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.228-1207_228-1206d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592885 | |||||||
| chr3:15592885 | CATGTGTG others(133): Show |
C | 10 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0027 others(7): Show |
11 | HG01255.hp1 HG02056.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.228-1345_228-1206d others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592885 | |||||||
| chr3:15592886 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.228-1206T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592886 | |||||||
| chr3:15592886 | A | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0184 |
4 | HG02257.hp1 HG02258.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-1206T>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592886 | |||||||
| chr3:15592887 | T | C | 15 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0186 others(12): Show |
17 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.228-1207A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592887 | |||||||
| chr3:15592890 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0184 |
4 | HG02257.hp1 HG02258.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-1210C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592890 | |||||||
| chr3:15592892 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0184 |
4 | HG02257.hp1 HG02258.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-1212C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592892 | |||||||
| chr3:15592893 | CGT | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0184 |
4 | HG02257.hp1 HG02258.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-1215_228-1214d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592893 | |||||||
| chr3:15592895 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.228-1215A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592895 | |||||||
| chr3:15592896 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0184 |
4 | HG02257.hp1 HG02258.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-1216C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592896 | |||||||
| chr3:15592904 | A | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0184 |
4 | HG02257.hp1 HG02258.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-1224T>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592904 | |||||||
| chr3:15592908 | ACG | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0184 |
4 | HG02257.hp1 HG02258.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-1230_228-1229d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592908 | |||||||
| chr3:15592908 | ACGCACAT others(103): Show |
A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0134 a0001c0001t0001g0153 others(3): Show |
9 | HG01167.hp1 HG01169.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.228-1338_228-1229d others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592908 | |||||||
| chr3:15592910 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.228-1230C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592910 | |||||||
| chr3:15592911 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0184 |
4 | HG02257.hp1 HG02258.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-1231G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592911 | |||||||
| chr3:15592913 | CAT | C | 13 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0072 others(10): Show |
13 | HG00621.hp1 HG01978.hp1 HG03209.hp2 others(10): Show |
intron_variant | MODIFIER | c.228-1235_228-1234d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592913 | |||||||
| chr3:15592913 | CATGTGTG others(105): Show |
C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0026 others(18): Show |
24 | HG00099.hp1 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.228-1345_228-1234d others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592913 | |||||||
| chr3:15592914 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.228-1234T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592914 | |||||||
| chr3:15592914 | A | T | 1 | a0001c0001t0001g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.228-1234T>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592914 | |||||||
| chr3:15592915 | T | C | 12 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0186 others(9): Show |
14 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.228-1235A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592915 | |||||||
| chr3:15592916 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0184 |
4 | HG02257.hp1 HG02258.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-1236C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592916 | |||||||
| chr3:15592918 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-1238C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592918 | |||||||
| chr3:15592919 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0184 |
4 | HG02257.hp1 HG02258.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-1239A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592919 | |||||||
| chr3:15592920 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-1240C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592920 | |||||||
| chr3:15592922 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0184 |
4 | HG02257.hp1 HG02258.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-1242C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592922 | |||||||
| chr3:15592924 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.228-1244C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592924 | |||||||
| chr3:15592932 | A | T | 1 | a0001c0001t0001g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.228-1252T>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592932 | |||||||
| chr3:15592935 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0184 |
4 | HG02257.hp1 HG02258.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-1255A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592935 | |||||||
| chr3:15592936 | ACGCACAT others(75): Show |
A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0143 a0001c0001t0001g0156 |
3 | HG02572.hp1 NA18981.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.228-1338_228-1257d others(84): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592936 | |||||||
| chr3:15592939 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.228-1259G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592939 | |||||||
| chr3:15592941 | CAT | C | 6 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
6 | HG01978.hp1 NA18949.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.228-1263_228-1262d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592941 | |||||||
| chr3:15592941 | CATGTGTG others(77): Show |
C | 20 | a0001c0001t0001g0029 a0001c0001t0001g0045 a0001c0001t0001g0207 others(17): Show |
21 | HG00280.hp1 HG00733.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.228-1345_228-1262d others(86): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592941 | |||||||
| chr3:15592942 | A | G | 2 | a0001c0001t0001g0074 a0005c0010t0001g0078 |
2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.228-1262T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592942 | |||||||
| chr3:15592943 | T | C | 14 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0033 others(11): Show |
17 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.228-1263A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592943 | |||||||
| chr3:15592944 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.228-1264C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592944 | |||||||
| chr3:15592946 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.228-1266C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592946 | |||||||
| chr3:15592947 | T | C | 2 | a0001c0001t0001g0183 a0005c0010t0001g0078 |
2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.228-1267A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592947 | |||||||
| chr3:15592948 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.228-1268C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592948 | |||||||
| chr3:15592950 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.228-1270C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592950 | |||||||
| chr3:15592963 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-1283A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592963 | |||||||
| chr3:15592969 | CAT | C | 6 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
6 | HG01978.hp1 HG02148.hp1 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.228-1291_228-1290d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592969 | |||||||
| chr3:15592969 | CATGTGTG others(49): Show |
C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(21): Show |
24 | HG00140.hp2 HG00735.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.228-1345_228-1290d others(58): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592969 | |||||||
| chr3:15592970 | A | G | 2 | a0001c0001t0001g0074 a0005c0010t0001g0078 |
2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.228-1290T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592970 | |||||||
| chr3:15592971 | T | C | 12 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0033 others(9): Show |
14 | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.228-1291A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592971 | |||||||
| chr3:15592975 | T | C | 1 | a0005c0010t0001g0078 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.228-1295A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592975 | |||||||
| chr3:15592991 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.228-1311A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592991 | |||||||
| chr3:15592992 | ACGCACAT others(19): Show |
A | 1 | a0001c0001t0001g0139 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.228-1338_228-1313d others(28): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592992 | |||||||
| chr3:15592997 | CAT | C | 6 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
6 | HG01978.hp1 HG02148.hp1 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.228-1319_228-1318d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592997 | |||||||
| chr3:15592997 | CATGTGTG others(21): Show |
C | 27 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0191 others(24): Show |
29 | HG00642.hp1 HG00642.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.228-1345_228-1318d others(30): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592997 | |||||||
| chr3:15592998 | A | G | 2 | a0001c0001t0001g0074 a0005c0010t0001g0078 |
2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.228-1318T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592998 | |||||||
| chr3:15592999 | T | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0183 others(4): Show |
9 | HG00733.hp1 HG01943.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.228-1319A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15592999 | |||||||
| chr3:15593003 | T | C | 1 | a0005c0010t0001g0078 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.228-1323A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593003 | |||||||
| chr3:15593020 | ACG | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(80): Show |
97 | HG00544.hp2 HG00597.hp1 HG01069.hp1 others(94): Show |
intron_variant | MODIFIER | c.228-1342_228-1341d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593020 | |||||||
| chr3:15593021 | C | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0016 others(50): Show |
64 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.228-1341G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593021 | |||||||
| chr3:15593022 | G | A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0016 others(50): Show |
64 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.228-1342C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593022 | |||||||
| chr3:15593025 | T | C | 86 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0031 others(83): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.228-1345A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593025 | |||||||
| chr3:15593026 | A | G | 7 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(4): Show |
7 | HG01978.hp1 HG02148.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.228-1346T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593026 | |||||||
| chr3:15593027 | T | C | 1 | a0001c0001t0001g0330 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.228-1347A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593027 | |||||||
| chr3:15593030 | A | G | 7 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(4): Show |
7 | HG01978.hp1 HG02148.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.228-1350T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593030 | |||||||
| chr3:15593032 | A | G | 7 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(4): Show |
7 | HG01978.hp1 HG02148.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.228-1352T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593032 | |||||||
| chr3:15593034 | A | G | 7 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(4): Show |
7 | HG01978.hp1 HG02148.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.228-1354T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593034 | |||||||
| chr3:15593048 | AGAGT | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0340 others(8): Show |
15 | HG01109.hp1 HG01168.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.228-1372_228-1369d others(6): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593048 | |||||||
| chr3:15593057 | T | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0180 others(4): Show |
8 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.228-1377A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593057 | |||||||
| chr3:15593072 | A | AGTGTATA others(27): Show |
4 | a0001c0001t0001g0111 a0001c0002t0001g0295 a0001c0002t0001g0296 others(1): Show |
4 | HG02698.hp1 NA19011.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.228-1426_228-1393d others(36): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593072 | |||||||
| chr3:15593072 | A | AGTGTATA others(61): Show |
1 | a0001c0002t0001g0294 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.228-1393_228-1392i others(70): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593072 | |||||||
| chr3:15593076 | T | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0173 others(3): Show |
10 | HG01192.hp2 HG01884.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.228-1396A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593076 | |||||||
| chr3:15593094 | TACATATA others(85): Show |
T | 1 | a0001c0001t0001g0139 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.228-1506_228-1415d others(94): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593094 | |||||||
| chr3:15593096 | CAT | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0340 others(8): Show |
15 | HG01109.hp1 HG01168.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.228-1418_228-1417d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593096 | |||||||
| chr3:15593118 | C | CACACACA others(29): Show |
1 | a0001c0001t0001g0126 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.228-1439_228-1438i others(38): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593118 | |||||||
| chr3:15593124 | CAT | C | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 |
3 | HG00544.hp2 NA18957.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.228-1446_228-1445d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593124 | |||||||
| chr3:15593128 | C | T | 4 | a0001c0001t0001g0223 a0001c0001t0001g0232 a0001c0001t0001g0235 others(1): Show |
4 | HG00642.hp2 HG01109.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.228-1448G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593128 | |||||||
| chr3:15593137 | G | GTA | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(156): Show |
189 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(186): Show |
intron_variant | MODIFIER | c.228-1459_228-1458d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593137 | |||||||
| chr3:15593146 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-1466G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593146 | |||||||
| chr3:15593152 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-1472A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593152 | |||||||
| chr3:15593154 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-1474G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593154 | |||||||
| chr3:15593158 | C | CAT | 3 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01081.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.228-1480_228-1479d others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593158 | |||||||
| chr3:15593158 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-1478G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593158 | |||||||
| chr3:15593222 | C | CT | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(164): Show |
198 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.228-1543dupA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593222 | |||||||
| chr3:15593320 | C | G | 1 | a0001c0003t0003g0069 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.228-1640G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593320 | |||||||
| chr3:15593517 | C | G | 1 | a0001c0002t0001g0293 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.228-1837G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593517 | |||||||
| chr3:15593536 | C | T | 31 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(28): Show |
37 | HG00423.hp2 HG00639.hp2 HG01928.hp1 others(34): Show |
intron_variant | MODIFIER | c.228-1856G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593536 | |||||||
| chr3:15593609 | C | T | 2 | a0001c0003t0001g0015 a0001c0003t0001g0062 |
3 | HG02970.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.228-1929G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593609 | |||||||
| chr3:15593687 | G | GT | 10 | a0001c0001t0001g0054 a0001c0001t0001g0077 a0001c0001t0001g0203 others(7): Show |
10 | HG00621.hp2 HG01192.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.228-2008dupA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593687 | |||||||
| chr3:15593687 | G | T | 2 | a0001c0001t0001g0115 a0001c0013t0001g0145 |
2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.228-2007C>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593687 | |||||||
| chr3:15593782 | G | GT | 17 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(14): Show |
17 | HG01175.hp2 HG01891.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.228-2103dupA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593782 | |||||||
| chr3:15593782 | GT | G | 8 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0180 others(5): Show |
9 | HG01081.hp1 HG01167.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.228-2103delA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593782 | |||||||
| chr3:15593792 | T | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(83): Show |
101 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.228-2112A>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593792 | |||||||
| chr3:15593794 | G | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(83): Show |
101 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.228-2114C>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593794 | |||||||
| chr3:15593795 | TC | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(80): Show |
98 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.228-2116delG | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593795 | |||||||
| chr3:15593796 | C | CT | 8 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0233 others(5): Show |
8 | HG00140.hp1 HG02738.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.228-2117dupA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593796 | |||||||
| chr3:15593796 | C | T | 3 | a0001c0001t0001g0131 a0001c0001t0001g0135 a0001c0013t0001g0145 |
3 | HG02135.hp2 HG04199.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.228-2116G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593796 | |||||||
| chr3:15593796 | CT | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0180 others(3): Show |
6 | HG01081.hp1 HG01884.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.228-2117delA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593796 | |||||||
| chr3:15593827 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.228-2147G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15593827 | |||||||
| chr3:15594028 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.228-2348C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15594028 | |||||||
| chr3:15594051 | GGCCTCCC others(1805): Show |
G | 1 | a0001c0001t0001g0201 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.227+521_227+2332de others(1): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15594051 | |||||||
| chr3:15594088 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0172 others(4): Show |
11 | HG01192.hp2 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.227+2296G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15594088 | |||||||
| chr3:15594089 | G | A | 1 | a0001c0002t0001g0327 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.227+2295C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15594089 | |||||||
| chr3:15594150 | G | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0340 others(8): Show |
15 | HG01109.hp1 HG01168.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.227+2234C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15594150 | |||||||
| chr3:15594314 | G | A | 1 | a0001c0003t0003g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.227+2070C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15594314 | |||||||
| chr3:15594321 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.227+2063C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15594321 | |||||||
| chr3:15594510 | C | T | 7 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0180 others(4): Show |
8 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.227+1874G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15594510 | |||||||
| chr3:15594613 | T | C | 27 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(24): Show |
33 | HG00423.hp2 HG00639.hp2 HG01928.hp1 others(30): Show |
intron_variant | MODIFIER | c.227+1771A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15594613 | |||||||
| chr3:15594655 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.227+1729C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15594655 | |||||||
| chr3:15594696 | G | A | 4 | a0001c0001t0001g0350 a0001c0001t0001g0351 a0001c0001t0001g0352 others(1): Show |
4 | HG03098.hp2 HG03209.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.227+1688C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15594696 | |||||||
| chr3:15594761 | A | G | 7 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0180 others(4): Show |
8 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.227+1623T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15594761 | |||||||
| chr3:15594867 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | NA19055.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.227+1517G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15594867 | |||||||
| chr3:15594912 | G | C | 1 | a0001c0001t0001g0284 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.227+1472C>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15594912 | |||||||
| chr3:15595028 | G | A | 31 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(28): Show |
37 | HG00423.hp2 HG00639.hp2 HG01928.hp1 others(34): Show |
intron_variant | MODIFIER | c.227+1356C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15595028 | |||||||
| chr3:15595029 | A | G | 31 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(28): Show |
37 | HG00423.hp2 HG00639.hp2 HG01928.hp1 others(34): Show |
intron_variant | MODIFIER | c.227+1355T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15595029 | |||||||
| chr3:15595462 | CAT | C | 30 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(27): Show |
36 | HG00423.hp2 HG00639.hp2 HG01928.hp1 others(33): Show |
intron_variant | MODIFIER | c.227+920_227+921del others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15595462 | |||||||
| chr3:15595466 | T | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0180 others(4): Show |
8 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.227+918A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15595466 | |||||||
| chr3:15595604 | C | CT | 18 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(15): Show |
18 | HG00140.hp1 HG00673.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.227+779dupA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15595604 | |||||||
| chr3:15595604 | CT | C | 82 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(79): Show |
92 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.227+779delA | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15595604 | |||||||
| chr3:15595604 | CTT | C | 14 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0063 others(11): Show |
15 | HG00423.hp1 HG00423.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.227+778_227+779del others(2): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15595604 | |||||||
| chr3:15595604 | CTTT | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(41): Show |
50 | HG00639.hp2 HG01928.hp1 HG01952.hp1 others(47): Show |
intron_variant | MODIFIER | c.227+777_227+779del others(3): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15595604 | |||||||
| chr3:15595604 | CTTTT | C | 63 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(60): Show |
79 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.227+776_227+779del others(4): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15595604 | |||||||
| chr3:15595604 | CTTTTT | C | 51 | a0001c0001t0001g0001 a0001c0001t0001g0051 a0001c0001t0001g0053 others(48): Show |
56 | HG00597.hp1 HG01069.hp1 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.227+775_227+779del others(5): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15595604 | |||||||
| chr3:15595639 | T | C | 17 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0033 others(14): Show |
19 | HG00642.hp1 HG00642.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.227+745A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15595639 | |||||||
| chr3:15595667 | T | C | 2 | a0001c0002t0001g0307 a0001c0002t0001g0327 |
2 | HG00280.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.227+717A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15595667 | |||||||
| chr3:15595673 | A | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.227+711T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15595673 | |||||||
| chr3:15595696 | G | A | 1 | a0001c0007t0001g0313 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.227+688C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15595696 | |||||||
| chr3:15595901 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.227+483C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15595901 | |||||||
| chr3:15595938 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01081.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.227+446A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15595938 | |||||||
| chr3:15595970 | T | A | 1 | a0001c0001t0001g0353 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.227+414A>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15595970 | |||||||
| chr3:15596054 | C | G | 3 | a0001c0001t0001g0336 a0001c0001t0001g0337 a0001c0001t0001g0338 |
3 | HG00733.hp2 HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.227+330G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15596054 | |||||||
| chr3:15596116 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.227+268C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 3/16 | chr3 | 15596116 | |||||||
| chr3:15596494 | T | C | 1 | a0001c0002t0001g0332 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.187-70A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15596494 | |||||||
| chr3:15596664 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.187-240A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15596664 | |||||||
| chr3:15596753 | G | A | 30 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(27): Show |
36 | HG00423.hp2 HG00639.hp2 HG01928.hp1 others(33): Show |
intron_variant | MODIFIER | c.187-329C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15596753 | |||||||
| chr3:15596791 | T | C | 1 | a0001c0001t0001g0348 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.187-367A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15596791 | |||||||
| chr3:15596823 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(85): Show |
103 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.187-399G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15596823 | |||||||
| chr3:15597002 | G | T | 1 | a0001c0001t0001g0349 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.187-578C>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597002 | |||||||
| chr3:15597130 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.187-706G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597130 | |||||||
| chr3:15597161 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.187-737T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597161 | |||||||
| chr3:15597186 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.187-762A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597186 | |||||||
| chr3:15597200 | TC | T | 7 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0180 others(4): Show |
8 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.187-777delG | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597200 | |||||||
| chr3:15597280 | T | C | 1 | a0002c0015t0001g0286 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.187-856A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597280 | |||||||
| chr3:15597446 | A | G | 1 | a0003c0006t0001g0036 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.187-1022T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597446 | |||||||
| chr3:15597524 | C | CTCATTTC others(300): Show |
3 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01081.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.187-1101_187-1100i others(309): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597524 | |||||||
| chr3:15597524 | C | CTCATTTC others(303): Show |
4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.187-1101_187-1100i others(312): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597524 | |||||||
| chr3:15597632 | GA | G | 7 | a0001c0004t0001g0137 a0001c0004t0001g0138 a0001c0004t0001g0147 others(4): Show |
7 | HG00735.hp2 HG01069.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.187-1209delT | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597632 | |||||||
| chr3:15597633 | A | G | 5 | a0001c0003t0001g0015 a0001c0003t0001g0062 a0001c0003t0003g0069 others(2): Show |
6 | HG02970.hp1 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.187-1209T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597633 | |||||||
| chr3:15597657 | T | TGGATCAT others(309): Show |
1 | a0001c0001t0001g0146 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.187-1234_187-1233i others(318): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(310): Show |
1 | a0001c0001t0001g0136 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.187-1234_187-1233i others(319): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(307): Show |
3 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | HG02965.hp2 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.187-1234_187-1233i others(316): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(320): Show |
1 | a0001c0001t0001g0161 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.187-1234_187-1233i others(329): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(291): Show |
1 | a0001c0001t0001g0171 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.187-1234_187-1233i others(300): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(292): Show |
1 | a0001c0001t0001g0170 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.187-1234_187-1233i others(301): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(297): Show |
2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG04204.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.187-1234_187-1233i others(306): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(299): Show |
1 | a0001c0001t0001g0167 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.187-1234_187-1233i others(308): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(301): Show |
1 | a0001c0001t0001g0166 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.187-1234_187-1233i others(310): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(302): Show |
1 | a0001c0001t0001g0165 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.187-1234_187-1233i others(311): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(306): Show |
1 | a0001c0001t0001g0160 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.187-1234_187-1233i others(315): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(307): Show |
3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0004t0001g0157 |
3 | HG01069.hp1 HG01167.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.187-1234_187-1233i others(316): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(308): Show |
11 | a0001c0001t0001g0051 a0001c0001t0001g0150 a0001c0001t0001g0151 others(8): Show |
11 | HG02145.hp2 HG02572.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.187-1234_187-1233i others(317): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(309): Show |
11 | a0001c0001t0001g0001 a0001c0001t0001g0139 a0001c0001t0001g0140 others(8): Show |
16 | HG00597.hp1 HG01943.hp2 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.187-1234_187-1233i others(318): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(310): Show |
4 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | HG02135.hp2 HG03927.hp2 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.187-1234_187-1233i others(319): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(311): Show |
10 | a0001c0001t0001g0002 a0001c0001t0001g0123 a0001c0001t0001g0124 others(7): Show |
14 | HG01928.hp2 HG01952.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.187-1234_187-1233i others(320): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(312): Show |
11 | a0001c0001t0001g0009 a0001c0001t0001g0068 a0001c0001t0001g0115 others(8): Show |
13 | HG00408.hp1 HG01099.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.187-1234_187-1233i others(321): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(313): Show |
6 | a0001c0001t0001g0023 a0001c0001t0001g0067 a0001c0001t0001g0111 others(3): Show |
7 | HG00423.hp1 HG00621.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.187-1234_187-1233i others(322): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(314): Show |
2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG03492.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.187-1234_187-1233i others(323): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(315): Show |
7 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0072 others(4): Show |
9 | HG02293.hp2 NA18950.hp1 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.187-1234_187-1233i others(324): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(316): Show |
2 | a0001c0001t0001g0021 a0001c0001t0001g0106 |
3 | NA18972.hp1 NA18993.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.187-1234_187-1233i others(325): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(317): Show |
5 | a0001c0001t0001g0066 a0001c0001t0001g0102 a0001c0001t0001g0103 others(2): Show |
5 | HG01993.hp2 HG02735.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.187-1234_187-1233i others(326): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(318): Show |
1 | a0001c0001t0001g0101 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.187-1234_187-1233i others(327): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(321): Show |
1 | a0001c0001t0001g0100 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.187-1234_187-1233i others(330): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597657 | T | TGGATCAT others(337): Show |
1 | a0001c0001t0001g0099 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.187-1234_187-1233i others(346): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597657 | |||||||
| chr3:15597937 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(164): Show |
198 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.187-1513G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15597937 | |||||||
| chr3:15598020 | TG | T | 18 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(15): Show |
24 | HG00423.hp2 HG00639.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.187-1597delC | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15598020 | |||||||
| chr3:15598021 | G | T | 14 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0203 others(11): Show |
18 | HG01109.hp1 HG01168.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.187-1597C>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15598021 | |||||||
| chr3:15598039 | A | G | 20 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0054 others(17): Show |
21 | HG01081.hp1 HG01175.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.187-1615T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15598039 | |||||||
| chr3:15598394 | A | C | 1 | a0001c0001t0001g0073 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.187-1970T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15598394 | |||||||
| chr3:15598409 | T | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(230): Show |
272 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.187-1985A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15598409 | |||||||
| chr3:15598410 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0172 others(4): Show |
11 | HG01192.hp2 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.187-1986C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15598410 | |||||||
| chr3:15598433 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.187-2009C>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15598433 | |||||||
| chr3:15598773 | T | C | 5 | a0001c0003t0001g0015 a0001c0003t0001g0062 a0001c0003t0003g0069 others(2): Show |
6 | HG02970.hp1 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.186+2317A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15598773 | |||||||
| chr3:15598941 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.186+2149G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15598941 | |||||||
| chr3:15598969 | T | C | 20 | a0001c0001t0001g0025 a0001c0001t0001g0053 a0001c0001t0001g0054 others(17): Show |
21 | HG01081.hp1 HG01175.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.186+2121A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15598969 | |||||||
| chr3:15599131 | C | G | 1 | a0001c0001t0001g0072 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.186+1959G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15599131 | |||||||
| chr3:15599400 | G | T | 2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | NA18952.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.186+1690C>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15599400 | |||||||
| chr3:15599463 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.186+1627G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15599463 | |||||||
| chr3:15599510 | T | TA | 56 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(53): Show |
62 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.186+1579dupT | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15599510 | |||||||
| chr3:15599510 | TA | T | 16 | a0001c0001t0001g0016 a0001c0001t0001g0053 a0001c0001t0001g0063 others(13): Show |
18 | HG00099.hp1 HG01081.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.186+1579delT | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15599510 | |||||||
| chr3:15599535 | T | C | 1 | a0001c0002t0001g0333 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.186+1555A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15599535 | |||||||
| chr3:15599554 | C | T | 3 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG01081.hp1 HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.186+1536G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15599554 | |||||||
| chr3:15599656 | C | T | 1 | a0001c0002t0001g0193 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.186+1434G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15599656 | |||||||
| chr3:15599689 | T | C | 1 | a0001c0001t0001g0334 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.186+1401A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15599689 | |||||||
| chr3:15599696 | A | G | 1 | a0001c0002t0001g0192 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.186+1394T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15599696 | |||||||
| chr3:15599715 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.186+1375T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15599715 | |||||||
| chr3:15599728 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.186+1362A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15599728 | |||||||
| chr3:15599914 | A | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.186+1176T>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15599914 | |||||||
| chr3:15599939 | T | C | 3 | a0001c0001t0001g0336 a0001c0001t0001g0337 a0001c0001t0001g0338 |
3 | HG00733.hp2 HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.186+1151A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15599939 | |||||||
| chr3:15600068 | G | GATAAAGA others(10): Show |
4 | a0001c0001t0001g0063 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
4 | HG01081.hp1 HG01884.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.186+1005_186+1021d others(19): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15600068 | |||||||
| chr3:15600068 | G | GATAAAGA others(27): Show |
4 | a0001c0001t0001g0025 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.186+988_186+1021du others(35): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15600068 | |||||||
| chr3:15600068 | GATAAAGA others(10): Show |
G | 4 | a0001c0001t0001g0187 a0001c0002t0001g0188 a0001c0002t0001g0189 others(1): Show |
4 | HG00544.hp1 HG01261.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.186+1005_186+1021d others(19): Show |
HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15600068 | |||||||
| chr3:15600116 | T | A | 1 | a0001c0001t0001g0185 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.186+974A>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15600116 | |||||||
| chr3:15600152 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.186+938G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15600152 | |||||||
| chr3:15600464 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(164): Show |
198 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.186+626G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15600464 | |||||||
| chr3:15600508 | G | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0340 others(8): Show |
15 | HG01109.hp1 HG01168.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.186+582C>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15600508 | |||||||
| chr3:15600518 | T | C | 1 | a0001c0001t0001g0349 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.186+572A>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15600518 | |||||||
| chr3:15600640 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.186+450G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15600640 | |||||||
| chr3:15600665 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.186+425C>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15600665 | |||||||
| chr3:15601011 | C | A | 13 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(10): Show |
13 | HG01175.hp2 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.186+79G>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15601011 | |||||||
| chr3:15601024 | A | G | 2 | a0001c0003t0001g0015 a0001c0003t0001g0062 |
3 | HG02970.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.186+66T>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15601024 | |||||||
| chr3:15601078 | G | C | 1 | a0001c0002t0001g0354 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.186+12C>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 2/16 | chr3 | 15601078 | |||||||
| chr3:15601198 | A | C | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
9 | HG01175.hp2 HG01891.hp1 HG02145.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.82-4T>G | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 1/16 | chr3 | 15601198 | |||||||
| chr3:15601287 | C | G | 1 | a0001c0001t0001g0052 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.82-93G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 1/16 | chr3 | 15601287 | |||||||
| chr3:15601294 | C | G | 1 | a0001c0001t0001g0051 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.81+89G>C | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 1/16 | chr3 | 15601294 | |||||||
| chr3:15601328 | C | A | 1 | a0001c0001t0001g0355 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.81+55G>T | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 1/16 | chr3 | 15601328 | |||||||
| chr3:15601337 | C | T | 13 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0040 others(10): Show |
15 | HG00597.hp2 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.81+46G>A | HACL1 | ENSG00000131373.15 | transcript | ENST00000321169.10 | protein_coding | 1/16 | chr3 | 15601337 |