Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2487 |
| ensemblid | ENSG00000162998.5 |
| hgncid | 3959 |
| symbol | FRZB |
| name | frizzled related protein |
| refseq_nuc | NM_001463.4 |
| refseq_prot | NP_001454.2 |
| ensembl_nuc | ENST00000295113.5 |
| ensembl_prot | ENSP00000295113.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 182833275 |
| end | 182866637 |
| strand | - |
| ver | v1.2 |
| region | chr2:182833275-182866637 |
| region5000 | chr2:182828275-182871637 |
| regionname0 | FRZB_chr2_182833275_182866637 |
| regionname5000 | FRZB_chr2_182828275_182871637 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 325 | 321 | 65 | 53 | 160 | 8 | 34 | 123 | FRZB_chr2_182828275_182871637 | FRZB | MVCGS others(320): Show |
chr2 | 182828275 | 182871637 |
| a0002 | 0/1 | 325 | 33 | 26 | 1 | 2 | 3 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | MVCGS others(320): Show |
chr2 | 182828275 | 182871637 |
| a0003 | 0/0 | 325 | 9 | 1 | 6 | 0 | 1 | 1 | 0 | FRZB_chr2_182828275_182871637 | FRZB | MVCGS others(320): Show |
chr2 | 182828275 | 182871637 |
| a0004 | 0/0 | 325 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | MVCGS others(320): Show |
chr2 | 182828275 | 182871637 |
| a0005 | 0/0 | 325 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | MVCGS others(320): Show |
chr2 | 182828275 | 182871637 |
| a0006 | 0/0 | 325 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | MVCGS others(320): Show |
chr2 | 182828275 | 182871637 |
| a0007 | 0/0 | 325 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | MVCGS others(320): Show |
chr2 | 182828275 | 182871637 |
| a0008 | 0/0 | 325 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FRZB_chr2_182828275_182871637 | FRZB | MVCGS others(320): Show |
chr2 | 182828275 | 182871637 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 975 | 316 | 60 | 53 | 160 | 8 | 34 | FRZB_chr2_182828275_182871637 | FRZB | ATGGT others(970): Show |
chr2 | 182828275 | 182871637 | ||
| a0001c0004 | 0/0 | 975 | 5 | 5 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ATGGT others(970): Show |
chr2 | 182828275 | 182871637 | ||
| a0002c0002 | 0/1 | 975 | 31 | 25 | 1 | 1 | 3 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ATGGT others(970): Show |
chr2 | 182828275 | 182871637 | ||
| a0002c0008 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ATGGT others(970): Show |
chr2 | 182828275 | 182871637 | ||
| a0002c0010 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ATGGT others(970): Show |
chr2 | 182828275 | 182871637 | ||
| a0003c0003 | 0/0 | 975 | 8 | 0 | 6 | 0 | 1 | 1 | FRZB_chr2_182828275_182871637 | FRZB | ATGGT others(970): Show |
chr2 | 182828275 | 182871637 | ||
| a0003c0009 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ATGGT others(970): Show |
chr2 | 182828275 | 182871637 | ||
| a0004c0005 | 0/0 | 975 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ATGGT others(970): Show |
chr2 | 182828275 | 182871637 | ||
| a0005c0006 | 0/0 | 975 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ATGGT others(970): Show |
chr2 | 182828275 | 182871637 | ||
| a0006c0012 | 0/0 | 975 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ATGGT others(970): Show |
chr2 | 182828275 | 182871637 | ||
| a0007c0007 | 0/0 | 975 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ATGGT others(970): Show |
chr2 | 182828275 | 182871637 | ||
| a0008c0011 | 0/0 | 975 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | ATGGT others(970): Show |
chr2 | 182828275 | 182871637 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2637 | 219 | 40 | 18 | 137 | 3 | 20 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2632): Show |
chr2 | 182828275 | 182871637 |
| a0001c0001t0002 | 0/0 | 2637 | 74 | 8 | 30 | 20 | 5 | 11 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2632): Show |
chr2 | 182828275 | 182871637 |
| a0001c0001t0004 | 0/0 | 2637 | 5 | 5 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2632): Show |
chr2 | 182828275 | 182871637 |
| a0001c0001t0005 | 0/0 | 2636 | 4 | 1 | 0 | 3 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2631): Show |
chr2 | 182828275 | 182871637 |
| a0001c0001t0006 | 0/0 | 2636 | 4 | 0 | 1 | 0 | 0 | 3 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2631): Show |
chr2 | 182828275 | 182871637 |
| a0001c0001t0007 | 0/0 | 2637 | 3 | 2 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2632): Show |
chr2 | 182828275 | 182871637 |
| a0001c0001t0008 | 0/0 | 2637 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2632): Show |
chr2 | 182828275 | 182871637 |
| a0001c0001t0009 | 0/0 | 2637 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2632): Show |
chr2 | 182828275 | 182871637 |
| a0001c0001t0010 | 0/0 | 2637 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2632): Show |
chr2 | 182828275 | 182871637 |
| a0001c0001t0011 | 0/0 | 2637 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2632): Show |
chr2 | 182828275 | 182871637 |
| a0001c0004t0001 | 0/0 | 2637 | 3 | 3 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2632): Show |
chr2 | 182828275 | 182871637 |
| a0001c0004t0004 | 0/0 | 2637 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2632): Show |
chr2 | 182828275 | 182871637 |
| a0002c0002t0001 | 0/1 | 2637 | 1 | 0 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2632): Show |
chr2 | 182828275 | 182871637 |
| a0002c0002t0003 | 0/0 | 2636 | 30 | 25 | 1 | 1 | 3 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2631): Show |
chr2 | 182828275 | 182871637 |
| a0002c0008t0002 | 0/0 | 2637 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2632): Show |
chr2 | 182828275 | 182871637 |
| a0002c0010t0003 | 0/0 | 2636 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2631): Show |
chr2 | 182828275 | 182871637 |
| a0003c0003t0001 | 0/0 | 2637 | 4 | 0 | 2 | 0 | 1 | 1 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2632): Show |
chr2 | 182828275 | 182871637 |
| a0003c0003t0002 | 0/0 | 2637 | 4 | 0 | 4 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2632): Show |
chr2 | 182828275 | 182871637 |
| a0003c0009t0004 | 0/0 | 2637 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2632): Show |
chr2 | 182828275 | 182871637 |
| a0004c0005t0003 | 0/0 | 2636 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2631): Show |
chr2 | 182828275 | 182871637 |
| a0005c0006t0003 | 0/0 | 2636 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2631): Show |
chr2 | 182828275 | 182871637 |
| a0006c0012t0001 | 0/0 | 2637 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2632): Show |
chr2 | 182828275 | 182871637 |
| a0007c0007t0002 | 0/0 | 2637 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2632): Show |
chr2 | 182828275 | 182871637 |
| a0008c0011t0001 | 0/0 | 2637 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | ACTTG others(2632): Show |
chr2 | 182828275 | 182871637 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 20 | 2 | 1 | 17 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0002 | 0/0 | 16 | 0 | 5 | 9 | 0 | 2 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0005 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0008 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0018 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0003 | 0/0 | 15 | 3 | 6 | 2 | 1 | 3 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0004 | 0/0 | 9 | 0 | 7 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0006g0020 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0006g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0007g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0007g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0008g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0009g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0010g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0001t0011g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0004t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0004t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0001c0004t0004g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0001g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0048 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0002t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0008t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0002c0010t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0003c0003t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0003c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0003c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0003c0003t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0003c0003t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0003c0003t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0003c0003t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0003c0009t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0004c0005t0003g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0005c0006t0003g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0006c0012t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0007c0007t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| a0008c0011t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00099 | hp2 | a0003 | c0003 | t0001 | g0132 | EUR | GBR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0135 | EUR | GBR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0016 | EUR | GBR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | FIN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00597 | hp1 | a0002 | c0002 | t0003 | g0145 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0199 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00642 | hp2 | a0003 | c0003 | t0002 | g0052 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00735 | hp1 | a0003 | c0003 | t0002 | g0125 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01071 | hp1 | a0003 | c0003 | t0002 | g0131 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01081 | hp1 | a0001 | c0001 | t0007 | g0150 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01099 | hp2 | a0006 | c0012 | t0001 | g0221 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0022 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01169 | hp2 | a0003 | c0003 | t0002 | g0053 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01192 | hp1 | a0004 | c0005 | t0003 | g0023 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01243 | hp1 | a0007 | c0007 | t0002 | g0062 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01261 | hp2 | a0002 | c0002 | t0003 | g0074 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01346 | hp1 | a0004 | c0005 | t0003 | g0023 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01358 | hp1 | a0005 | c0006 | t0003 | g0051 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01361 | hp1 | a0005 | c0006 | t0003 | g0051 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01361 | hp2 | a0001 | c0001 | t0011 | g0122 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0047 | EUR | IBS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01515 | hp2 | a0002 | c0002 | t0003 | g0048 | EUR | IBS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01517 | hp1 | a0002 | c0002 | t0003 | g0048 | EUR | IBS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0030 | EUR | IBS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01884 | hp2 | a0001 | c0004 | t0004 | g0037 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01978 | hp1 | a0003 | c0003 | t0001 | g0054 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01981 | hp2 | a0001 | c0001 | t0010 | g0040 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02145 | hp1 | a0002 | c0002 | t0003 | g0070 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02148 | hp1 | a0001 | c0001 | t0010 | g0040 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02257 | hp1 | a0002 | c0002 | t0003 | g0167 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0137 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0038 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02280 | hp1 | a0003 | c0009 | t0004 | g0178 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02451 | hp1 | a0002 | c0002 | t0003 | g0075 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0083 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02572 | hp2 | a0002 | c0002 | t0003 | g0127 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02622 | hp2 | a0002 | c0002 | t0003 | g0024 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0096 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0141 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02818 | hp1 | a0002 | c0002 | t0003 | g0176 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02886 | hp1 | a0002 | c0002 | t0003 | g0175 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0045 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0059 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0045 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02897 | hp2 | a0002 | c0002 | t0003 | g0064 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02965 | hp1 | a0002 | c0002 | t0003 | g0139 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02965 | hp2 | a0002 | c0002 | t0003 | g0065 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02976 | hp1 | a0002 | c0002 | t0003 | g0179 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03017 | hp1 | a0003 | c0003 | t0001 | g0022 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03041 | hp1 | a0002 | c0002 | t0003 | g0069 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03041 | hp2 | a0002 | c0002 | t0003 | g0060 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03098 | hp1 | a0001 | c0004 | t0004 | g0037 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03130 | hp1 | a0002 | c0002 | t0003 | g0143 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03195 | hp2 | a0002 | c0002 | t0003 | g0140 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0038 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03453 | hp2 | a0002 | c0002 | t0003 | g0174 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03486 | hp2 | a0002 | c0002 | t0003 | g0072 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03490 | hp1 | a0001 | c0001 | t0006 | g0020 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03492 | hp2 | a0001 | c0001 | t0006 | g0020 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03540 | hp2 | a0002 | c0010 | t0003 | g0063 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0099 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03579 | hp2 | a0002 | c0002 | t0003 | g0066 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | BEB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | BEB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | STU | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | STU | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | STU | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG04204 | hp2 | a0001 | c0001 | t0006 | g0020 | SAS | STU | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG04228 | hp1 | a0008 | c0011 | t0001 | g0220 | SAS | STU | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | STU | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | YRI | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18906 | hp1 | a0002 | c0002 | t0003 | g0068 | AFR | YRI | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18985 | hp2 | a0001 | c0001 | t0005 | g0200 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0097 | AFR | LWK | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19067 | hp2 | a0001 | c0001 | t0005 | g0214 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19084 | hp2 | a0001 | c0001 | t0005 | g0194 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19085 | hp1 | a0002 | c0008 | t0002 | g0184 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ASW | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ASW | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | TSI | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA20752 | hp2 | a0002 | c0002 | t0003 | g0119 | EUR | TSI | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | GIH | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | GIH | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02109 | hp1 | a0002 | c0002 | t0003 | g0061 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02486 | hp2 | a0002 | c0002 | t0003 | g0173 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02559 | hp1 | a0002 | c0002 | t0003 | g0154 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03471 | hp1 | a0002 | c0002 | t0003 | g0152 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG06807 | hp1 | a0002 | c0002 | t0003 | g0067 | AFR | USA | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | USA | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA20300 | hp1 | a0002 | c0002 | t0003 | g0024 | AFR | USA | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0142 | AFR | LWK | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0195 | REF | REF | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0018 | REF | REF | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:182834856 | C | T | 1 | a0002 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.971G>A | p.Arg324His | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 1056/2637 | 971/978 | 324/325 | chr2 | 182834856 | |||
| chr2:182834857 | G | C | 3 | a0002 a0004 a0005 |
35 | HG00597.hp1 HG01192.hp1 HG01261.hp2 others(32): Show |
missense_variant | MODERATE | c.970C>G | p.Arg324Gly | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 1055/2637 | 970/978 | 324/325 | chr2 | 182834857 | |||
| chr2:182838419 | C | T | 1 | a0007 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.787G>A | p.Glu263Lys | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 4/6 | 872/2637 | 787/978 | 263/325 | chr2 | 182838419 | |||
| chr2:182838608 | G | A | 2 | a0003 a0004 |
11 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(8): Show |
missense_variant | MODERATE | c.598C>T | p.Arg200Trp | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 4/6 | 683/2637 | 598/978 | 200/325 | chr2 | 182838608 | |||
| chr2:182866405 | T | C | 1 | a0008 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.148A>G | p.Met50Val | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/6 | 233/2637 | 148/978 | 50/325 | chr2 | 182866405 | |||
| chr2:182866465 | C | A | 2 | a0005 a0006 |
3 | HG01099.hp2 HG01358.hp1 HG01361.hp1 |
missense_variant | MODERATE | c.88G>T | p.Ala30Ser | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/6 | 173/2637 | 88/978 | 30/325 | chr2 | 182866465 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:182837963 | G | A | 1 | a0003c0009 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.846C>T | p.Leu282Leu | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/6 | 931/2637 | 846/978 | 282/325 | chr2 | 182837963 | |||
| chr2:182842533 | T | C | 1 | a0002c0010 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.537A>G | p.Lys179Lys | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/6 | 622/2637 | 537/978 | 179/325 | chr2 | 182842533 | |||
| chr2:182858811 | G | A | 1 | a0001c0004 | 5 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
synonymous_variant | LOW | c.501C>T | p.Asn167Asn | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/6 | 586/2637 | 501/978 | 167/325 | chr2 | 182858811 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:182833364 | A | G | 5 | a0001c0001t0002 a0001c0001t0005 a0002c0008t0002 others(2): Show |
84 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1485T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 1485 | chr2 | 182833364 | ||||||
| chr2:182833427 | C | T | 3 | a0001c0001t0004 a0001c0004t0004 a0003c0009t0004 |
8 | HG01884.hp2 HG02109.hp2 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1422G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 1422 | chr2 | 182833427 | ||||||
| chr2:182833506 | T | A | 4 | a0001c0001t0004 a0001c0001t0008 a0001c0004t0004 others(1): Show |
10 | HG01884.hp2 HG02109.hp2 HG02280.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1343A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 1343 | chr2 | 182833506 | ||||||
| chr2:182833520 | T | C | 1 | a0001c0001t0011 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1329A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 1329 | chr2 | 182833520 | ||||||
| chr2:182833834 | C | T | 1 | a0001c0001t0009 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1015G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 1015 | chr2 | 182833834 | ||||||
| chr2:182833858 | CA | C | 2 | a0001c0001t0005 a0001c0001t0006 |
8 | HG00639.hp1 HG03490.hp1 HG03492.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*990delT | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 990 | chr2 | 182833858 | ||||||
| chr2:182833872 | T | C | 4 | a0002c0002t0003 a0002c0010t0003 a0004c0005t0003 others(1): Show |
35 | HG00597.hp1 HG01192.hp1 HG01261.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*977A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 977 | chr2 | 182833872 | ||||||
| chr2:182833964 | G | A | 4 | a0002c0002t0003 a0002c0010t0003 a0004c0005t0003 others(1): Show |
35 | HG00597.hp1 HG01192.hp1 HG01261.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*885C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 885 | chr2 | 182833964 | ||||||
| chr2:182833970 | A | G | 1 | a0001c0001t0007 | 3 | HG01081.hp1 HG02896.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*879T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 879 | chr2 | 182833970 | ||||||
| chr2:182834000 | GA | G | 4 | a0002c0002t0003 a0002c0010t0003 a0004c0005t0003 others(1): Show |
35 | HG00597.hp1 HG01192.hp1 HG01261.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*848delT | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 848 | chr2 | 182834000 | ||||||
| chr2:182834453 | A | G | 1 | a0001c0001t0008 | 2 | HG02647.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*396T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 396 | chr2 | 182834453 | ||||||
| chr2:182834637 | C | T | 4 | a0002c0002t0003 a0002c0010t0003 a0004c0005t0003 others(1): Show |
35 | HG00597.hp1 HG01192.hp1 HG01261.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*212G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 212 | chr2 | 182834637 | ||||||
| chr2:182834684 | G | A | 1 | a0001c0001t0010 | 2 | HG01981.hp2 HG02148.hp1 |
3_prime_UTR_variant | MODIFIER | c.*165C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 165 | chr2 | 182834684 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:182834983 | G | A | 2 | a0001c0001t0002g0092 a0001c0001t0002g0136 |
2 | HG02040.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.862-18C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182834983 | |||||||
| chr2:182835041 | G | A | 19 | a0001c0001t0001g0009 a0001c0001t0001g0036 a0001c0001t0001g0041 others(16): Show |
29 | HG00408.hp1 HG00597.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.862-76C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835041 | |||||||
| chr2:182835079 | C | G | 4 | a0001c0001t0001g0058 a0001c0001t0001g0128 a0001c0004t0001g0038 others(1): Show |
5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.862-114G>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835079 | |||||||
| chr2:182835225 | T | C | 2 | a0001c0001t0008g0096 a0001c0001t0008g0099 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.862-260A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835225 | |||||||
| chr2:182835227 | T | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0055 others(23): Show |
36 | HG00609.hp2 HG00621.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.862-262A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835227 | |||||||
| chr2:182835328 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.862-363G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835328 | |||||||
| chr2:182835365 | C | T | 14 | a0001c0001t0001g0089 a0001c0001t0001g0118 a0001c0001t0001g0126 others(11): Show |
14 | HG00642.hp2 HG00673.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.862-400G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835365 | |||||||
| chr2:182835447 | T | TG | 19 | a0001c0001t0001g0009 a0001c0001t0001g0036 a0001c0001t0001g0041 others(16): Show |
28 | HG00408.hp1 HG00597.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.862-483dupC | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835447 | |||||||
| chr2:182835538 | A | T | 1 | a0001c0001t0002g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.862-573T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835538 | |||||||
| chr2:182835539 | A | T | 1 | a0001c0001t0002g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.862-574T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835539 | |||||||
| chr2:182835568 | AC | A | 48 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(45): Show |
98 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.862-604delG | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835568 | |||||||
| chr2:182835703 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.862-738C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835703 | |||||||
| chr2:182835913 | G | A | 2 | a0001c0001t0002g0187 a0005c0006t0003g0051 |
3 | HG01358.hp1 HG01361.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.862-948C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835913 | |||||||
| chr2:182835935 | A | T | 2 | a0002c0002t0003g0175 a0002c0002t0003g0176 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.862-970T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835935 | |||||||
| chr2:182836059 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.862-1094A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836059 | |||||||
| chr2:182836076 | C | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0012 others(50): Show |
96 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.862-1111G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836076 | |||||||
| chr2:182836139 | T | A | 15 | a0001c0001t0001g0170 a0001c0001t0002g0187 a0001c0001t0004g0083 others(12): Show |
18 | HG01261.hp2 HG01358.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.862-1174A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836139 | |||||||
| chr2:182836155 | C | T | 9 | a0001c0001t0001g0117 a0003c0003t0001g0022 a0003c0003t0001g0054 others(6): Show |
11 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.862-1190G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836155 | |||||||
| chr2:182836173 | T | C | 15 | a0001c0001t0001g0170 a0001c0001t0002g0187 a0001c0001t0004g0083 others(12): Show |
18 | HG01261.hp2 HG01358.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.862-1208A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836173 | |||||||
| chr2:182836232 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.862-1267A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836232 | |||||||
| chr2:182836286 | T | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0103 others(5): Show |
15 | HG03688.hp2 NA18747.hp1 NA18747.hp2 others(12): Show |
intron_variant | MODIFIER | c.862-1321A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836286 | |||||||
| chr2:182836459 | C | T | 1 | a0001c0001t0001g0046 | 2 | HG00323.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.861+1489G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836459 | |||||||
| chr2:182836510 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.861+1438C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836510 | |||||||
| chr2:182836580 | C | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0026 others(15): Show |
33 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.861+1368G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836580 | |||||||
| chr2:182836860 | A | G | 136 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(133): Show |
209 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.861+1088T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836860 | |||||||
| chr2:182836979 | A | T | 4 | a0001c0001t0001g0170 a0001c0004t0001g0038 a0001c0004t0001g0137 others(1): Show |
6 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.861+969T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836979 | |||||||
| chr2:182837054 | T | C | 1 | a0001c0001t0006g0199 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.861+894A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182837054 | |||||||
| chr2:182837199 | A | T | 1 | a0001c0001t0001g0206 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.861+749T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182837199 | |||||||
| chr2:182837344 | T | C | 1 | a0001c0001t0002g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.861+604A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182837344 | |||||||
| chr2:182837505 | TG | T | 19 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0073 others(16): Show |
26 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.861+442delC | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182837505 | |||||||
| chr2:182837541 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0005g0142 a0002c0002t0003g0139 others(2): Show |
9 | HG02257.hp1 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.861+407G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182837541 | |||||||
| chr2:182837729 | T | A | 1 | a0002c0002t0003g0140 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.861+219A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182837729 | |||||||
| chr2:182837780 | A | C | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.861+168T>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182837780 | |||||||
| chr2:182837824 | C | T | 1 | a0005c0006t0003g0051 | 2 | HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.861+124G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182837824 | |||||||
| chr2:182838102 | T | C | 19 | a0001c0001t0001g0058 a0001c0001t0001g0171 a0001c0001t0002g0169 others(16): Show |
20 | HG01243.hp1 HG01358.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.798-91A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 4/5 | chr2 | 182838102 | |||||||
| chr2:182838164 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.798-153G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 4/5 | chr2 | 182838164 | |||||||
| chr2:182838236 | G | A | 8 | a0003c0003t0001g0022 a0003c0003t0001g0054 a0003c0003t0001g0132 others(5): Show |
10 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.797+173C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 4/5 | chr2 | 182838236 | |||||||
| chr2:182838958 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.593-345C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182838958 | |||||||
| chr2:182838966 | A | C | 1 | a0001c0001t0002g0113 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.593-353T>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182838966 | |||||||
| chr2:182839057 | C | T | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.593-444G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839057 | |||||||
| chr2:182839136 | G | A | 3 | a0002c0002t0003g0174 a0002c0002t0003g0175 a0002c0002t0003g0176 |
3 | HG02818.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.593-523C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839136 | |||||||
| chr2:182839321 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.593-708T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839321 | |||||||
| chr2:182839356 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(69): Show |
146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.593-743T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839356 | |||||||
| chr2:182839409 | T | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(63): Show |
114 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.593-796A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839409 | |||||||
| chr2:182839433 | C | G | 1 | a0001c0001t0007g0150 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.593-820G>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839433 | |||||||
| chr2:182839444 | C | T | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.593-831G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839444 | |||||||
| chr2:182839517 | T | C | 1 | a0003c0009t0004g0178 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.593-904A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839517 | |||||||
| chr2:182839534 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.593-921G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839534 | |||||||
| chr2:182839761 | C | A | 3 | a0001c0001t0001g0171 a0001c0001t0002g0169 a0002c0002t0003g0173 |
3 | HG02486.hp2 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.593-1148G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839761 | |||||||
| chr2:182839855 | T | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(55): Show |
105 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.593-1242A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839855 | |||||||
| chr2:182839891 | A | G | 4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0169 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.593-1278T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839891 | |||||||
| chr2:182839911 | T | C | 1 | a0001c0001t0001g0029 | 2 | NA18962.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.593-1298A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839911 | |||||||
| chr2:182839913 | T | C | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.593-1300A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839913 | |||||||
| chr2:182839931 | T | C | 5 | a0003c0003t0001g0022 a0003c0003t0001g0054 a0003c0003t0002g0052 others(2): Show |
7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.593-1318A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839931 | |||||||
| chr2:182839953 | C | G | 22 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0073 others(19): Show |
31 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-1340G>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839953 | |||||||
| chr2:182839991 | C | T | 21 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0026 others(18): Show |
36 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.593-1378G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839991 | |||||||
| chr2:182840469 | A | G | 7 | a0001c0001t0001g0058 a0001c0001t0007g0059 a0002c0002t0003g0060 others(4): Show |
7 | HG01243.hp1 HG02109.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.593-1856T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182840469 | |||||||
| chr2:182841047 | G | C | 2 | a0003c0003t0001g0022 a0003c0003t0001g0054 |
3 | HG01109.hp2 HG01978.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.592+1431C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841047 | |||||||
| chr2:182841090 | C | T | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.592+1388G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841090 | |||||||
| chr2:182841129 | A | G | 1 | a0001c0001t0002g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.592+1349T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841129 | |||||||
| chr2:182841410 | G | A | 1 | a0001c0001t0002g0185 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.592+1068C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841410 | |||||||
| chr2:182841437 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(186): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.592+1041A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841437 | |||||||
| chr2:182841540 | C | T | 1 | a0007c0007t0002g0062 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.592+938G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841540 | |||||||
| chr2:182841713 | A | C | 4 | a0001c0001t0001g0041 a0001c0001t0001g0155 a0001c0001t0001g0158 others(1): Show |
5 | NA18969.hp1 NA18972.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+765T>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841713 | |||||||
| chr2:182841726 | T | A | 1 | a0001c0001t0002g0161 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.592+752A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841726 | |||||||
| chr2:182841784 | G | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(75): Show |
140 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.592+694C>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841784 | |||||||
| chr2:182841792 | T | C | 12 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0073 others(9): Show |
17 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.592+686A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841792 | |||||||
| chr2:182841827 | A | G | 3 | a0001c0004t0001g0038 a0001c0004t0001g0137 a0001c0004t0004g0037 |
5 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+651T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841827 | |||||||
| chr2:182841948 | C | T | 1 | a0001c0001t0002g0210 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.592+530G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841948 | |||||||
| chr2:182842076 | T | G | 5 | a0003c0003t0001g0022 a0003c0003t0001g0054 a0003c0003t0002g0052 others(2): Show |
7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.592+402A>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182842076 | |||||||
| chr2:182842098 | T | C | 2 | a0001c0001t0001g0107 a0001c0001t0002g0104 |
2 | NA18969.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.592+380A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182842098 | |||||||
| chr2:182842127 | G | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(78): Show |
145 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.592+351C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182842127 | |||||||
| chr2:182842129 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.592+349T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182842129 | |||||||
| chr2:182842200 | T | A | 5 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0169 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+278A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182842200 | |||||||
| chr2:182842302 | T | C | 2 | a0002c0002t0003g0074 a0002c0002t0003g0075 |
2 | HG01261.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.592+176A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182842302 | |||||||
| chr2:182842445 | C | A | 1 | a0001c0001t0001g0205 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.592+33G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182842445 | |||||||
| chr2:182842972 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(113): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.527-429A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182842972 | |||||||
| chr2:182843077 | G | C | 3 | a0001c0001t0002g0157 a0001c0001t0002g0162 a0001c0001t0002g0166 |
3 | HG01993.hp1 HG01993.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.527-534C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843077 | |||||||
| chr2:182843080 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(68): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.527-537C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843080 | |||||||
| chr2:182843468 | T | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(196): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.527-925A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843468 | |||||||
| chr2:182843511 | C | A | 1 | a0001c0001t0001g0171 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.527-968G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843511 | |||||||
| chr2:182843528 | G | T | 33 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0026 others(30): Show |
50 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.527-985C>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843528 | |||||||
| chr2:182843656 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0002g0056 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.527-1113G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843656 | |||||||
| chr2:182843676 | A | G | 1 | a0001c0001t0004g0141 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.527-1133T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843676 | |||||||
| chr2:182843761 | G | A | 1 | a0002c0002t0003g0072 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.527-1218C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843761 | |||||||
| chr2:182843797 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.527-1254C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843797 | |||||||
| chr2:182843799 | C | T | 1 | a0001c0001t0002g0192 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.527-1256G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843799 | |||||||
| chr2:182843800 | G | A | 1 | a0003c0009t0004g0178 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.527-1257C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843800 | |||||||
| chr2:182843880 | A | C | 1 | a0002c0002t0003g0069 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.527-1337T>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843880 | |||||||
| chr2:182844507 | T | C | 1 | a0001c0001t0002g0033 | 2 | HG01346.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.527-1964A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182844507 | |||||||
| chr2:182844803 | C | G | 12 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0073 others(9): Show |
17 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.527-2260G>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182844803 | |||||||
| chr2:182845005 | C | T | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.527-2462G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182845005 | |||||||
| chr2:182845258 | T | C | 3 | a0001c0004t0001g0038 a0001c0004t0001g0137 a0001c0004t0004g0037 |
5 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.527-2715A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182845258 | |||||||
| chr2:182845269 | C | CT | 3 | a0001c0001t0004g0172 a0005c0006t0003g0051 a0006c0012t0001g0221 |
4 | HG01099.hp2 HG01358.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.527-2727dupA | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182845269 | |||||||
| chr2:182845409 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(109): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.527-2866G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182845409 | |||||||
| chr2:182845562 | GA | G | 13 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0134 others(10): Show |
24 | HG00423.hp1 HG00558.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.527-3020delT | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182845562 | |||||||
| chr2:182845711 | C | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(68): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.527-3168G>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182845711 | |||||||
| chr2:182845951 | C | G | 1 | a0001c0001t0001g0043 | 2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.527-3408G>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182845951 | |||||||
| chr2:182846170 | T | C | 5 | a0003c0003t0001g0022 a0003c0003t0001g0054 a0003c0003t0002g0052 others(2): Show |
7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.527-3627A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846170 | |||||||
| chr2:182846200 | A | G | 1 | a0001c0001t0002g0190 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.527-3657T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846200 | |||||||
| chr2:182846216 | A | C | 1 | a0001c0001t0002g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.527-3673T>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846216 | |||||||
| chr2:182846223 | T | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(193): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.527-3680A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846223 | |||||||
| chr2:182846262 | A | C | 1 | a0003c0009t0004g0178 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.527-3719T>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846262 | |||||||
| chr2:182846325 | T | A | 1 | a0002c0002t0003g0048 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.527-3782A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846325 | |||||||
| chr2:182846414 | T | C | 1 | a0002c0002t0003g0048 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.527-3871A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846414 | |||||||
| chr2:182846499 | A | G | 1 | a0001c0001t0008g0096 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.527-3956T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846499 | |||||||
| chr2:182846689 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(209): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.527-4146C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846689 | |||||||
| chr2:182846709 | T | C | 1 | a0002c0002t0003g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.527-4166A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846709 | |||||||
| chr2:182846800 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.527-4257G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846800 | |||||||
| chr2:182846920 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.527-4377A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846920 | |||||||
| chr2:182847021 | T | C | 20 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0026 others(17): Show |
33 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.527-4478A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182847021 | |||||||
| chr2:182847155 | T | C | 17 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0058 others(14): Show |
18 | HG01099.hp2 HG01243.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.527-4612A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182847155 | |||||||
| chr2:182847242 | C | G | 5 | a0003c0003t0001g0022 a0003c0003t0001g0054 a0003c0003t0002g0052 others(2): Show |
7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.527-4699G>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182847242 | |||||||
| chr2:182847251 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(104): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.527-4708A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182847251 | |||||||
| chr2:182847412 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0002g0056 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.527-4869C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182847412 | |||||||
| chr2:182847432 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.527-4889C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182847432 | |||||||
| chr2:182847444 | T | G | 5 | a0003c0003t0001g0022 a0003c0003t0001g0054 a0003c0003t0002g0052 others(2): Show |
7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.527-4901A>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182847444 | |||||||
| chr2:182847620 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(109): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.527-5077C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182847620 | |||||||
| chr2:182847796 | T | C | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.527-5253A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182847796 | |||||||
| chr2:182847867 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.527-5324C>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182847867 | |||||||
| chr2:182848070 | T | TA | 19 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0026 others(16): Show |
31 | HG00621.hp2 HG01884.hp1 HG02056.hp2 others(28): Show |
intron_variant | MODIFIER | c.527-5528dupT | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182848070 | |||||||
| chr2:182848070 | TA | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(112): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.527-5528delT | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182848070 | |||||||
| chr2:182848083 | A | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(99): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.527-5540T>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182848083 | |||||||
| chr2:182848360 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(109): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.527-5817G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182848360 | |||||||
| chr2:182848551 | C | A | 3 | a0001c0004t0001g0038 a0001c0004t0001g0137 a0001c0004t0004g0037 |
5 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.527-6008G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182848551 | |||||||
| chr2:182848584 | A | G | 1 | a0001c0001t0002g0169 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.527-6041T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182848584 | |||||||
| chr2:182848598 | T | C | 1 | a0002c0002t0003g0145 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.527-6055A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182848598 | |||||||
| chr2:182848616 | C | T | 7 | a0001c0001t0001g0058 a0001c0001t0007g0059 a0002c0002t0003g0060 others(4): Show |
7 | HG01243.hp1 HG02109.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.527-6073G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182848616 | |||||||
| chr2:182848709 | C | T | 1 | a0001c0001t0002g0112 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.527-6166G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182848709 | |||||||
| chr2:182848963 | C | T | 1 | a0002c0002t0003g0068 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.527-6420G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182848963 | |||||||
| chr2:182849009 | C | T | 3 | a0002c0002t0003g0066 a0002c0002t0003g0179 a0003c0009t0004g0178 |
3 | HG02280.hp1 HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.527-6466G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849009 | |||||||
| chr2:182849088 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.527-6545C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849088 | |||||||
| chr2:182849097 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(104): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.527-6554T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849097 | |||||||
| chr2:182849155 | G | C | 5 | a0003c0003t0001g0022 a0003c0003t0001g0054 a0003c0003t0002g0052 others(2): Show |
7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.527-6612C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849155 | |||||||
| chr2:182849227 | A | AAAAT | 8 | a0001c0001t0001g0019 a0001c0001t0001g0155 a0001c0001t0001g0189 others(5): Show |
10 | HG01261.hp2 HG02015.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.527-6688_527-6685d others(6): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849227 | |||||||
| chr2:182849227 | A | AAAATAAA others(5): Show |
1 | a0001c0001t0009g0045 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.527-6696_527-6685d others(14): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849227 | |||||||
| chr2:182849227 | AAAAT | A | 40 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(37): Show |
65 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.527-6688_527-6685d others(6): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849227 | |||||||
| chr2:182849227 | AAAATAAA others(1): Show |
A | 12 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0058 others(9): Show |
15 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.527-6692_527-6685d others(10): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849227 | |||||||
| chr2:182849227 | AAAATAAA others(5): Show |
A | 6 | a0001c0001t0001g0027 a0001c0001t0001g0076 a0002c0002t0003g0024 others(3): Show |
9 | HG01192.hp1 HG01346.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.527-6696_527-6685d others(14): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849227 | |||||||
| chr2:182849227 | AAAATAAA others(9): Show |
A | 1 | a0002c0002t0003g0064 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.527-6700_527-6685d others(18): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849227 | |||||||
| chr2:182849227 | AAAATAAA others(13): Show |
A | 3 | a0001c0001t0001g0079 a0001c0001t0002g0133 a0003c0003t0001g0054 |
3 | HG01978.hp1 HG02074.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.527-6704_527-6685d others(22): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849227 | |||||||
| chr2:182849227 | AAAATAAA others(17): Show |
A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(78): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.527-6708_527-6685d others(26): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849227 | |||||||
| chr2:182849748 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.527-7205T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849748 | |||||||
| chr2:182849797 | A | G | 13 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0058 others(10): Show |
13 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.527-7254T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849797 | |||||||
| chr2:182850185 | TTA | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(112): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.527-7644_527-7643d others(4): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850185 | |||||||
| chr2:182850225 | G | T | 4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0169 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.527-7682C>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850225 | |||||||
| chr2:182850266 | G | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0073 others(9): Show |
17 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.527-7723C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850266 | |||||||
| chr2:182850400 | T | A | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.527-7857A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850400 | |||||||
| chr2:182850544 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(96): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.527-8001T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850544 | |||||||
| chr2:182850560 | C | CT | 16 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0169 others(13): Show |
19 | HG00642.hp2 HG01099.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.527-8018dupA | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850560 | |||||||
| chr2:182850690 | G | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
12 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.526+8096C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850690 | |||||||
| chr2:182850876 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.526+7910G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850876 | |||||||
| chr2:182850883 | G | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0026 others(8): Show |
22 | HG00621.hp2 HG02056.hp2 HG02074.hp2 others(19): Show |
intron_variant | MODIFIER | c.526+7903C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850883 | |||||||
| chr2:182850982 | T | G | 3 | a0002c0002t0003g0066 a0002c0002t0003g0179 a0003c0009t0004g0178 |
3 | HG02280.hp1 HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.526+7804A>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850982 | |||||||
| chr2:182850988 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(216): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.526+7798T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850988 | |||||||
| chr2:182850991 | T | C | 1 | a0002c0002t0003g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.526+7795A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850991 | |||||||
| chr2:182851213 | G | C | 1 | a0001c0001t0002g0129 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.526+7573C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182851213 | |||||||
| chr2:182851259 | C | T | 2 | a0001c0001t0004g0083 a0001c0001t0004g0141 |
2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.526+7527G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182851259 | |||||||
| chr2:182851306 | G | A | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.526+7480C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182851306 | |||||||
| chr2:182851458 | C | A | 1 | a0001c0001t0002g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.526+7328G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182851458 | |||||||
| chr2:182851645 | G | C | 5 | a0003c0003t0001g0022 a0003c0003t0001g0054 a0003c0003t0002g0052 others(2): Show |
7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.526+7141C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182851645 | |||||||
| chr2:182851654 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.526+7132A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182851654 | |||||||
| chr2:182851851 | C | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0073 others(9): Show |
17 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.526+6935G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182851851 | |||||||
| chr2:182852079 | T | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(67): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.526+6707A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182852079 | |||||||
| chr2:182852172 | C | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(111): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.526+6614G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182852172 | |||||||
| chr2:182852246 | T | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0219 |
2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.526+6540A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182852246 | |||||||
| chr2:182852323 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.526+6463C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182852323 | |||||||
| chr2:182852373 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(109): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.526+6413C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182852373 | |||||||
| chr2:182852377 | G | A | 5 | a0003c0003t0001g0022 a0003c0003t0001g0054 a0003c0003t0002g0052 others(2): Show |
7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.526+6409C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182852377 | |||||||
| chr2:182852689 | T | C | 10 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0058 others(7): Show |
10 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.526+6097A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182852689 | |||||||
| chr2:182852883 | T | C | 1 | a0002c0002t0003g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.526+5903A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182852883 | |||||||
| chr2:182852944 | C | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0073 others(7): Show |
15 | HG02145.hp1 HG02559.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.526+5842G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182852944 | |||||||
| chr2:182853043 | AC | A | 13 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0058 others(10): Show |
13 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.526+5742delG | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853043 | |||||||
| chr2:182853150 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.526+5636C>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853150 | |||||||
| chr2:182853332 | C | T | 3 | a0001c0001t0004g0172 a0005c0006t0003g0051 a0006c0012t0001g0221 |
4 | HG01099.hp2 HG01358.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+5454G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853332 | |||||||
| chr2:182853400 | A | C | 4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0169 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+5386T>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853400 | |||||||
| chr2:182853421 | A | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0111 |
2 | NA18944.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.526+5365T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853421 | |||||||
| chr2:182853430 | C | A | 8 | a0001c0001t0001g0039 a0001c0001t0001g0138 a0001c0001t0001g0147 others(5): Show |
10 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.526+5356G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853430 | |||||||
| chr2:182853441 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.526+5345C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853441 | |||||||
| chr2:182853577 | T | A | 1 | a0001c0001t0001g0188 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.526+5209A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853577 | |||||||
| chr2:182853579 | A | T | 1 | a0001c0001t0001g0188 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.526+5207T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853579 | |||||||
| chr2:182853588 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.526+5198A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853588 | |||||||
| chr2:182853620 | C | A | 1 | a0001c0001t0001g0188 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.526+5166G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853620 | |||||||
| chr2:182853622 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.526+5164A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853622 | |||||||
| chr2:182853625 | G | T | 1 | a0001c0001t0001g0188 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.526+5161C>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853625 | |||||||
| chr2:182853772 | C | A | 1 | a0001c0001t0002g0207 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.526+5014G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853772 | |||||||
| chr2:182853817 | G | C | 3 | a0002c0002t0003g0066 a0002c0002t0003g0179 a0003c0009t0004g0178 |
3 | HG02280.hp1 HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.526+4969C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853817 | |||||||
| chr2:182853849 | C | T | 13 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0058 others(10): Show |
13 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.526+4937G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853849 | |||||||
| chr2:182853879 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.526+4907C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853879 | |||||||
| chr2:182854106 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.526+4680A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182854106 | |||||||
| chr2:182854151 | G | T | 1 | a0002c0002t0003g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.526+4635C>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182854151 | |||||||
| chr2:182854205 | A | G | 1 | a0001c0001t0007g0059 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.526+4581T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182854205 | |||||||
| chr2:182854232 | T | C | 12 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0073 others(9): Show |
17 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.526+4554A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182854232 | |||||||
| chr2:182854361 | A | G | 2 | a0001c0001t0004g0083 a0001c0001t0004g0141 |
2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.526+4425T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182854361 | |||||||
| chr2:182854411 | T | G | 1 | a0001c0001t0002g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.526+4375A>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182854411 | |||||||
| chr2:182854519 | G | A | 2 | a0005c0006t0003g0051 a0006c0012t0001g0221 |
3 | HG01099.hp2 HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.526+4267C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182854519 | |||||||
| chr2:182854720 | G | A | 10 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0058 others(7): Show |
10 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.526+4066C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182854720 | |||||||
| chr2:182854744 | T | C | 1 | a0002c0002t0003g0140 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.526+4042A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182854744 | |||||||
| chr2:182854992 | A | G | 2 | a0005c0006t0003g0051 a0006c0012t0001g0221 |
3 | HG01099.hp2 HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.526+3794T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182854992 | |||||||
| chr2:182855025 | C | T | 3 | a0001c0004t0001g0038 a0001c0004t0001g0137 a0001c0004t0004g0037 |
5 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.526+3761G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182855025 | |||||||
| chr2:182855070 | T | C | 2 | a0003c0003t0001g0132 a0003c0003t0002g0131 |
2 | HG00099.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.526+3716A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182855070 | |||||||
| chr2:182855304 | G | GA | 3 | a0001c0004t0001g0038 a0001c0004t0001g0137 a0001c0004t0004g0037 |
5 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.526+3481dupT | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182855304 | |||||||
| chr2:182855947 | A | G | 12 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0073 others(9): Show |
17 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.526+2839T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182855947 | |||||||
| chr2:182856138 | C | T | 3 | a0001c0001t0004g0153 a0002c0002t0003g0152 a0002c0002t0003g0154 |
3 | HG02559.hp1 HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.526+2648G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856138 | |||||||
| chr2:182856147 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.526+2639C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856147 | |||||||
| chr2:182856262 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.526+2524C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856262 | |||||||
| chr2:182856373 | A | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(67): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.526+2413T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856373 | |||||||
| chr2:182856375 | A | T | 1 | a0001c0001t0001g0086 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.526+2411T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856375 | |||||||
| chr2:182856385 | A | G | 1 | a0001c0001t0002g0151 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.526+2401T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856385 | |||||||
| chr2:182856396 | C | T | 3 | a0001c0004t0001g0038 a0001c0004t0001g0137 a0001c0004t0004g0037 |
5 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.526+2390G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856396 | |||||||
| chr2:182856593 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0219 |
2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.526+2193G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856593 | |||||||
| chr2:182856669 | C | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.526+2117G>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856669 | |||||||
| chr2:182856731 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(111): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.526+2055T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856731 | |||||||
| chr2:182856800 | G | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(67): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.526+1986C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856800 | |||||||
| chr2:182856980 | G | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(67): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.526+1806C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856980 | |||||||
| chr2:182857073 | A | G | 1 | a0002c0002t0003g0145 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.526+1713T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182857073 | |||||||
| chr2:182857206 | A | G | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0002g0056 |
3 | HG02145.hp2 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.526+1580T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182857206 | |||||||
| chr2:182857419 | G | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(67): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.526+1367C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182857419 | |||||||
| chr2:182857472 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(95): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.526+1314A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182857472 | |||||||
| chr2:182857541 | C | T | 1 | a0001c0001t0007g0150 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.526+1245G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182857541 | |||||||
| chr2:182857616 | C | CA | 9 | a0001c0001t0001g0209 a0001c0001t0001g0211 a0001c0001t0002g0210 others(6): Show |
11 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.526+1169dupT | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182857616 | |||||||
| chr2:182857774 | T | C | 1 | a0001c0001t0002g0166 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.526+1012A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182857774 | |||||||
| chr2:182858149 | T | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(95): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.526+637A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858149 | |||||||
| chr2:182858201 | A | G | 13 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0058 others(10): Show |
13 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.526+585T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858201 | |||||||
| chr2:182858223 | G | A | 3 | a0002c0002t0003g0174 a0002c0002t0003g0175 a0002c0002t0003g0176 |
3 | HG02818.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.526+563C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858223 | |||||||
| chr2:182858224 | C | T | 1 | a0002c0002t0003g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.526+562G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858224 | |||||||
| chr2:182858238 | T | C | 16 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0169 others(13): Show |
19 | HG00642.hp2 HG01099.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.526+548A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858238 | |||||||
| chr2:182858292 | A | G | 10 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0058 others(7): Show |
10 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.526+494T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858292 | |||||||
| chr2:182858378 | G | A | 3 | a0002c0002t0003g0066 a0002c0002t0003g0179 a0003c0009t0004g0178 |
3 | HG02280.hp1 HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.526+408C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858378 | |||||||
| chr2:182858401 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(111): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.526+385G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858401 | |||||||
| chr2:182858410 | G | T | 1 | a0001c0001t0002g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.526+376C>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858410 | |||||||
| chr2:182858509 | G | A | 5 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0169 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.526+277C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858509 | |||||||
| chr2:182858739 | A | T | 1 | a0001c0001t0001g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.526+47T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858739 | |||||||
| chr2:182858952 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.479-119A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182858952 | |||||||
| chr2:182858967 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.479-134C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182858967 | |||||||
| chr2:182858994 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(111): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.479-161T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182858994 | |||||||
| chr2:182859211 | T | G | 20 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0026 others(17): Show |
33 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.479-378A>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182859211 | |||||||
| chr2:182859220 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.479-387C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182859220 | |||||||
| chr2:182859510 | G | A | 13 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0058 others(10): Show |
13 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.479-677C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182859510 | |||||||
| chr2:182859523 | C | T | 5 | a0001c0001t0001g0044 a0001c0001t0001g0186 a0001c0001t0001g0213 others(2): Show |
6 | HG00423.hp2 HG00544.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.479-690G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182859523 | |||||||
| chr2:182859700 | G | T | 5 | a0003c0003t0001g0022 a0003c0003t0001g0054 a0003c0003t0002g0052 others(2): Show |
7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.479-867C>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182859700 | |||||||
| chr2:182859723 | A | G | 8 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0169 others(5): Show |
8 | HG02280.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.479-890T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182859723 | |||||||
| chr2:182859810 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(194): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.479-977G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182859810 | |||||||
| chr2:182859824 | C | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0073 others(9): Show |
17 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.479-991G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182859824 | |||||||
| chr2:182859884 | A | T | 5 | a0003c0003t0001g0022 a0003c0003t0001g0054 a0003c0003t0002g0052 others(2): Show |
7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.479-1051T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182859884 | |||||||
| chr2:182859894 | A | G | 3 | a0001c0001t0004g0172 a0005c0006t0003g0051 a0006c0012t0001g0221 |
4 | HG01099.hp2 HG01358.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-1061T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182859894 | |||||||
| chr2:182860017 | C | T | 28 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0073 others(25): Show |
36 | HG00642.hp2 HG01099.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.479-1184G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860017 | |||||||
| chr2:182860179 | A | T | 3 | a0001c0004t0001g0038 a0001c0004t0001g0137 a0001c0004t0004g0037 |
5 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.479-1346T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860179 | |||||||
| chr2:182860260 | C | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0073 others(9): Show |
17 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.479-1427G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860260 | |||||||
| chr2:182860493 | A | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(83): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.479-1660T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860493 | |||||||
| chr2:182860784 | T | A | 1 | a0002c0002t0003g0167 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.479-1951A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860784 | |||||||
| chr2:182860823 | C | T | 1 | a0002c0002t0003g0140 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.479-1990G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860823 | |||||||
| chr2:182860864 | C | CA | 13 | a0001c0001t0001g0081 a0001c0001t0001g0098 a0001c0001t0001g0108 others(10): Show |
13 | HG00423.hp1 HG00544.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.479-2032dupT | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860864 | |||||||
| chr2:182860864 | C | CAA | 13 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0058 others(10): Show |
13 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.479-2033_479-2032d others(4): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860864 | |||||||
| chr2:182860864 | CA | C | 17 | a0001c0001t0001g0032 a0001c0001t0001g0109 a0001c0001t0001g0170 others(14): Show |
20 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.479-2032delT | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860864 | |||||||
| chr2:182860959 | G | C | 4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG00609.hp1 HG02040.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.479-2126C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860959 | |||||||
| chr2:182860990 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.479-2157C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860990 | |||||||
| chr2:182861261 | A | G | 1 | a0003c0009t0004g0178 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.479-2428T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182861261 | |||||||
| chr2:182861303 | T | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(67): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.479-2470A>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182861303 | |||||||
| chr2:182861316 | A | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(83): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.479-2483T>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182861316 | |||||||
| chr2:182861352 | C | T | 28 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0073 others(25): Show |
36 | HG00642.hp2 HG01099.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.479-2519G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182861352 | |||||||
| chr2:182861407 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.479-2574T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182861407 | |||||||
| chr2:182861480 | G | T | 2 | a0005c0006t0003g0051 a0006c0012t0001g0221 |
3 | HG01099.hp2 HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.479-2647C>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182861480 | |||||||
| chr2:182861500 | T | C | 1 | a0001c0001t0002g0100 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.479-2667A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182861500 | |||||||
| chr2:182861957 | C | T | 1 | a0001c0001t0001g0043 | 2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.479-3124G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182861957 | |||||||
| chr2:182861973 | C | T | 4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0169 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-3140G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182861973 | |||||||
| chr2:182861985 | C | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(67): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.479-3152G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182861985 | |||||||
| chr2:182862201 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(111): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.479-3368T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182862201 | |||||||
| chr2:182862773 | CTT | C | 28 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0073 others(25): Show |
36 | HG00642.hp2 HG01099.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.478+3300_478+3301d others(4): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182862773 | |||||||
| chr2:182862773 | CTTT | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(83): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.478+3299_478+3301d others(5): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182862773 | |||||||
| chr2:182862808 | G | A | 2 | a0001c0001t0001g0182 a0001c0001t0001g0219 |
2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.478+3267C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182862808 | |||||||
| chr2:182862951 | G | A | 1 | a0001c0001t0002g0135 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.478+3124C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182862951 | |||||||
| chr2:182863202 | C | T | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.478+2873G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863202 | |||||||
| chr2:182863212 | C | CT | 5 | a0003c0003t0001g0022 a0003c0003t0001g0054 a0003c0003t0002g0052 others(2): Show |
7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.478+2862_478+2863i others(3): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863212 | |||||||
| chr2:182863213 | C | T | 5 | a0003c0003t0001g0022 a0003c0003t0001g0054 a0003c0003t0002g0052 others(2): Show |
7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.478+2862G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863213 | |||||||
| chr2:182863271 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.478+2804T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863271 | |||||||
| chr2:182863328 | T | C | 3 | a0002c0002t0003g0174 a0002c0002t0003g0175 a0002c0002t0003g0176 |
3 | HG02818.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.478+2747A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863328 | |||||||
| chr2:182863393 | C | G | 7 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0106 others(4): Show |
8 | HG00733.hp2 HG01192.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.478+2682G>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863393 | |||||||
| chr2:182863417 | C | A | 1 | a0001c0001t0001g0101 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.478+2658G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863417 | |||||||
| chr2:182863483 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.478+2592T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863483 | |||||||
| chr2:182863562 | C | T | 28 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0073 others(25): Show |
36 | HG00642.hp2 HG01099.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.478+2513G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863562 | |||||||
| chr2:182863625 | T | C | 2 | a0002c0002t0003g0179 a0003c0009t0004g0178 |
2 | HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.478+2450A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863625 | |||||||
| chr2:182863685 | G | GA | 47 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0032 others(44): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.478+2389dupT | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863685 | |||||||
| chr2:182863686 | A | T | 1 | a0002c0002t0003g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.478+2389T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863686 | |||||||
| chr2:182863690 | A | C | 1 | a0001c0001t0001g0182 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.478+2385T>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863690 | |||||||
| chr2:182863858 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0002g0136 |
5 | HG02040.hp1 NA18950.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.478+2217C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863858 | |||||||
| chr2:182863906 | C | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(86): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.478+2169G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863906 | |||||||
| chr2:182863980 | C | T | 1 | a0002c0002t0003g0065 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.478+2095G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863980 | |||||||
| chr2:182864122 | T | G | 2 | a0002c0002t0003g0179 a0003c0009t0004g0178 |
2 | HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.478+1953A>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864122 | |||||||
| chr2:182864129 | A | T | 3 | a0001c0004t0001g0038 a0001c0004t0001g0137 a0001c0004t0004g0037 |
5 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.478+1946T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864129 | |||||||
| chr2:182864194 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.478+1881G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864194 | |||||||
| chr2:182864236 | C | T | 20 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0073 others(17): Show |
26 | HG01099.hp2 HG01261.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.478+1839G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864236 | |||||||
| chr2:182864347 | A | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(68): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.478+1728T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864347 | |||||||
| chr2:182864469 | C | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(68): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.478+1606G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864469 | |||||||
| chr2:182864697 | C | T | 20 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0073 others(17): Show |
26 | HG01099.hp2 HG01261.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.478+1378G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864697 | |||||||
| chr2:182864785 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(106): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.478+1290G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864785 | |||||||
| chr2:182864805 | A | G | 4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0169 others(1): Show |
4 | HG02486.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.478+1270T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864805 | |||||||
| chr2:182864854 | T | G | 2 | a0002c0002t0003g0179 a0003c0009t0004g0178 |
2 | HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.478+1221A>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864854 | |||||||
| chr2:182864873 | G | C | 1 | a0002c0002t0003g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.478+1202C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864873 | |||||||
| chr2:182864893 | G | C | 20 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0073 others(17): Show |
26 | HG01099.hp2 HG01261.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.478+1182C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864893 | |||||||
| chr2:182864896 | A | G | 1 | a0001c0001t0004g0083 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.478+1179T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864896 | |||||||
| chr2:182865042 | A | G | 12 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0025 others(9): Show |
24 | HG00621.hp2 HG02056.hp2 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.478+1033T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182865042 | |||||||
| chr2:182865229 | G | A | 16 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0058 others(13): Show |
16 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.478+846C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182865229 | |||||||
| chr2:182865252 | C | T | 13 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0073 others(10): Show |
18 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.478+823G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182865252 | |||||||
| chr2:182865359 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.478+716A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182865359 | |||||||
| chr2:182865381 | A | G | 10 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0058 others(7): Show |
10 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.478+694T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182865381 | |||||||
| chr2:182865701 | A | G | 5 | a0003c0003t0001g0022 a0003c0003t0001g0054 a0003c0003t0002g0052 others(2): Show |
7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.478+374T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182865701 | |||||||
| chr2:182865799 | T | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(52): Show |
102 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.478+276A>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182865799 |