Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51032 |
| ensemblid | ENSG00000215704.10 |
| hgncid | 29995 |
| symbol | CELA2B |
| name | chymotrypsin like elastase 2B |
| refseq_nuc | NM_015849.3 |
| refseq_prot | NP_056933.3 |
| ensembl_nuc | ENST00000375910.8 |
| ensembl_prot | ENSP00000365075.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 15476104 |
| end | 15491395 |
| strand | + |
| ver | v1.2 |
| region | chr1:15476104-15491395 |
| region5000 | chr1:15471104-15496395 |
| regionname0 | CELA2B_chr1_15476104_15491395 |
| regionname5000 | CELA2B_chr1_15471104_15496395 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 269 | 245 | 55 | 52 | 89 | 11 | 37 | 74 | CELA2B_chr1_15471104_15496395 | CELA2B | MIRTL others(264): Show |
chr1 | 15471104 | 15496395 |
| a0002 | 0/0 | 269 | 152 | 32 | 26 | 86 | 3 | 5 | 66 | CELA2B_chr1_15471104_15496395 | CELA2B | MIRTL others(264): Show |
chr1 | 15471104 | 15496395 |
| a0003 | 1/0 | 269 | 6 | 5 | 0 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | MIRTL others(264): Show |
chr1 | 15471104 | 15496395 |
| a0004 | 0/0 | 269 | 6 | 0 | 3 | 3 | 0 | 0 | 2 | CELA2B_chr1_15471104_15496395 | CELA2B | MIRTL others(264): Show |
chr1 | 15471104 | 15496395 |
| a0005 | 0/0 | 269 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | MIRTL others(264): Show |
chr1 | 15471104 | 15496395 |
| a0006 | 0/0 | 269 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | MIRTL others(264): Show |
chr1 | 15471104 | 15496395 |
| a0007 | 0/0 | 269 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | MIRTL others(264): Show |
chr1 | 15471104 | 15496395 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 807 | 225 | 45 | 51 | 80 | 11 | 37 | CELA2B_chr1_15471104_15496395 | CELA2B | ATGAT others(802): Show |
chr1 | 15471104 | 15496395 | ||
| a0001c0003 | 0/0 | 807 | 7 | 6 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ATGAT others(802): Show |
chr1 | 15471104 | 15496395 | ||
| a0001c0006 | 0/0 | 807 | 4 | 0 | 0 | 4 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ATGAT others(802): Show |
chr1 | 15471104 | 15496395 | ||
| a0001c0007 | 0/0 | 807 | 4 | 3 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ATGAT others(802): Show |
chr1 | 15471104 | 15496395 | ||
| a0001c0008 | 0/0 | 807 | 3 | 0 | 0 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ATGAT others(802): Show |
chr1 | 15471104 | 15496395 | ||
| a0001c0011 | 0/0 | 807 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ATGAT others(802): Show |
chr1 | 15471104 | 15496395 | ||
| a0001c0014 | 0/0 | 807 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ATGAT others(802): Show |
chr1 | 15471104 | 15496395 | ||
| a0002c0002 | 0/0 | 807 | 151 | 32 | 26 | 85 | 3 | 5 | CELA2B_chr1_15471104_15496395 | CELA2B | ATGAT others(802): Show |
chr1 | 15471104 | 15496395 | ||
| a0002c0013 | 0/0 | 807 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ATGAT others(802): Show |
chr1 | 15471104 | 15496395 | ||
| a0003c0005 | 1/0 | 807 | 6 | 5 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ATGAT others(802): Show |
chr1 | 15471104 | 15496395 | ||
| a0004c0004 | 0/0 | 807 | 6 | 0 | 3 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ATGAT others(802): Show |
chr1 | 15471104 | 15496395 | ||
| a0005c0010 | 0/0 | 807 | 2 | 0 | 0 | 0 | 2 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ATGAT others(802): Show |
chr1 | 15471104 | 15496395 | ||
| a0006c0009 | 0/0 | 807 | 2 | 0 | 1 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ATGAT others(802): Show |
chr1 | 15471104 | 15496395 | ||
| a0007c0012 | 0/0 | 807 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ATGAT others(802): Show |
chr1 | 15471104 | 15496395 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 915 | 216 | 40 | 51 | 77 | 11 | 36 | CELA2B_chr1_15471104_15496395 | CELA2B | ACAGA others(910): Show |
chr1 | 15471104 | 15496395 |
| a0001c0001t0002 | 0/0 | 915 | 6 | 3 | 0 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ACAGA others(910): Show |
chr1 | 15471104 | 15496395 |
| a0001c0001t0003 | 0/0 | 915 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ACAGA others(910): Show |
chr1 | 15471104 | 15496395 |
| a0001c0001t0004 | 0/0 | 915 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | ACAGA others(910): Show |
chr1 | 15471104 | 15496395 |
| a0001c0003t0001 | 0/0 | 915 | 7 | 6 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ACAGA others(910): Show |
chr1 | 15471104 | 15496395 |
| a0001c0006t0001 | 0/0 | 915 | 4 | 0 | 0 | 4 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ACAGA others(910): Show |
chr1 | 15471104 | 15496395 |
| a0001c0007t0001 | 0/0 | 915 | 4 | 3 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ACAGA others(910): Show |
chr1 | 15471104 | 15496395 |
| a0001c0008t0001 | 0/0 | 915 | 3 | 0 | 0 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ACAGA others(910): Show |
chr1 | 15471104 | 15496395 |
| a0001c0011t0001 | 0/0 | 915 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ACAGA others(910): Show |
chr1 | 15471104 | 15496395 |
| a0001c0014t0001 | 0/0 | 915 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ACAGA others(910): Show |
chr1 | 15471104 | 15496395 |
| a0002c0002t0001 | 0/0 | 915 | 151 | 32 | 26 | 85 | 3 | 5 | CELA2B_chr1_15471104_15496395 | CELA2B | ACAGA others(910): Show |
chr1 | 15471104 | 15496395 |
| a0002c0013t0001 | 0/0 | 915 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ACAGA others(910): Show |
chr1 | 15471104 | 15496395 |
| a0003c0005t0001 | 1/0 | 915 | 6 | 5 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ACAGA others(910): Show |
chr1 | 15471104 | 15496395 |
| a0004c0004t0001 | 0/0 | 915 | 6 | 0 | 3 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ACAGA others(910): Show |
chr1 | 15471104 | 15496395 |
| a0005c0010t0001 | 0/0 | 915 | 2 | 0 | 0 | 0 | 2 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ACAGA others(910): Show |
chr1 | 15471104 | 15496395 |
| a0006c0009t0001 | 0/0 | 915 | 2 | 0 | 1 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ACAGA others(910): Show |
chr1 | 15471104 | 15496395 |
| a0007c0012t0001 | 0/0 | 915 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | ACAGA others(910): Show |
chr1 | 15471104 | 15496395 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 24 | 0 | 8 | 11 | 2 | 3 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0003 | 0/0 | 20 | 0 | 3 | 10 | 3 | 4 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0005 | 0/0 | 15 | 3 | 6 | 0 | 1 | 5 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 2 | 0 | 4 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0011 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0014 | 0/0 | 5 | 1 | 1 | 0 | 0 | 3 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0022 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0023 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0024 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0031 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0052 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0056 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0057 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0080 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0002g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0003g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0001t0004g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0003t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0003t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0003t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0003t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0006t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0006t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0006t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0007t0001g0021 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0008t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0008t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0011t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0001c0014t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0001 | 0/0 | 36 | 8 | 11 | 14 | 0 | 3 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0004 | 0/0 | 22 | 5 | 2 | 14 | 1 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0026 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0028 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0002c0013t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0003c0005t0001g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0003c0005t0001g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0004c0004t0001g0010 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0004c0004t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0005c0010t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0006c0009t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0006c0009t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| a0007c0012t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | GBR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0044 | EUR | GBR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0004 | EUR | FIN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | FIN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | FIN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | CHS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00544 | hp2 | a0001 | c0011 | t0001 | g0003 | EAS | CHS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | CHS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | CHS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | CHS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00642 | hp2 | a0001 | c0007 | t0001 | g0021 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | CHS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | CHS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0120 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0121 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0028 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0104 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0049 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01496 | hp2 | a0004 | c0004 | t0001 | g0010 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0132 | EUR | IBS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01516 | hp2 | a0005 | c0010 | t0001 | g0018 | EUR | IBS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01517 | hp2 | a0005 | c0010 | t0001 | g0018 | EUR | IBS | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0028 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01934 | hp2 | a0004 | c0004 | t0001 | g0116 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0124 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0043 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01952 | hp1 | a0006 | c0009 | t0001 | g0010 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0049 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01978 | hp1 | a0004 | c0004 | t0001 | g0010 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0138 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0048 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0048 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02071 | hp1 | a0004 | c0004 | t0001 | g0010 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0158 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CDX | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CDX | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CDX | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0043 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0054 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0099 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02615 | hp1 | a0001 | c0007 | t0001 | g0021 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0103 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02723 | hp1 | a0001 | c0007 | t0001 | g0021 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02895 | hp1 | a0003 | c0005 | t0001 | g0016 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0045 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02897 | hp1 | a0003 | c0005 | t0001 | g0016 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0087 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0162 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03130 | hp1 | a0001 | c0014 | t0001 | g0176 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03195 | hp2 | a0001 | c0007 | t0001 | g0021 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03225 | hp1 | a0003 | c0005 | t0001 | g0016 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0054 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0159 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0136 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0044 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0141 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | STU | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | BEB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | STU | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | STU | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | YRI | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | YRI | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18941 | hp2 | a0001 | c0006 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18944 | hp1 | a0007 | c0012 | t0001 | g0041 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18953 | hp1 | a0001 | c0006 | t0001 | g0003 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18957 | hp1 | a0002 | c0013 | t0001 | g0101 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18964 | hp1 | a0004 | c0004 | t0001 | g0010 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18966 | hp2 | a0001 | c0006 | t0001 | g0006 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18968 | hp1 | a0004 | c0004 | t0001 | g0010 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18972 | hp1 | a0001 | c0006 | t0001 | g0003 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18994 | hp1 | a0001 | c0008 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19005 | hp1 | a0006 | c0009 | t0001 | g0117 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0167 | AFR | LWK | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | LWK | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | LWK | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19072 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19074 | hp1 | a0001 | c0008 | t0001 | g0035 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19088 | hp1 | a0001 | c0008 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | YRI | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0045 | AFR | YRI | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA20129 | hp1 | a0003 | c0005 | t0001 | g0016 | AFR | ASW | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | ASW | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | GIH | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | USA | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0040 | AFR | USA | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA18955 | hp2 | a0001 | c0003 | t0001 | g0085 | EAS | JPT | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0040 | AFR | USA | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA21309 | hp1 | a0003 | c0005 | t0001 | g0016 | AFR | LWK | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0080 | REF | REF | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| homoSapiens | grch38p0 | a0003 | c0005 | t0001 | g0003 | REF | REF | CELA2B_chr1_15471104_15496395 | CELA2B | chr1 | 15471104 | 15496395 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:15481125 | C | A | 1 | a0007 | 1 | NA18944.hp1 | missense_variant | MODERATE | c.157C>A | p.Gln53Lys | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/8 | 179/915 | 157/810 | 53/269 | chr1 | 15481125 | |||
| chr1:15482272 | G | A | 4 | a0002 a0004 a0006 others(1): Show |
161 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(158): Show |
missense_variant | MODERATE | c.235G>A | p.Gly79Arg | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/8 | 257/915 | 235/810 | 79/269 | chr1 | 15482272 | |||
| chr1:15482377 | G | A | 2 | a0002 a0007 |
153 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(150): Show |
missense_variant | MODERATE | c.340G>A | p.Asp114Asn | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/8 | 362/915 | 340/810 | 114/269 | chr1 | 15482377 | |||
| chr1:15485937 | A | G | 6 | a0001 a0002 a0004 others(3): Show |
407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
missense_variant | MODERATE | c.530A>G | p.Gln177Arg | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/8 | 552/915 | 530/810 | 177/269 | chr1 | 15485937 | |||
| chr1:15487348 | G | A | 1 | a0004 | 6 | HG01496.hp2 HG01934.hp2 HG01978.hp1 others(3): Show |
missense_variant | MODERATE | c.703G>A | p.Gly235Ser | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/8 | 725/915 | 703/810 | 235/269 | chr1 | 15487348 | |||
| chr1:15487349 | G | T | 1 | a0005 | 2 | HG01516.hp2 HG01517.hp2 |
missense_variant | MODERATE | c.704G>T | p.Gly235Val | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/8 | 726/915 | 704/810 | 235/269 | chr1 | 15487349 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:15476131 | T | A | 1 | a0001c0006 | 4 | NA18941.hp2 NA18953.hp1 NA18966.hp2 others(1): Show |
synonymous_variant | LOW | c.6T>A | p.Ile2Ile | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 1/8 | 28/915 | 6/810 | 2/269 | chr1 | 15476131 | |||
| chr1:15476137 | C | G | 1 | a0001c0006 | 4 | NA18941.hp2 NA18953.hp1 NA18966.hp2 others(1): Show |
synonymous_variant | LOW | c.12C>G | p.Thr4Thr | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 1/8 | 34/915 | 12/810 | 4/269 | chr1 | 15476137 | |||
| chr1:15476521 | G | A | 1 | a0001c0011 | 1 | HG00544.hp2 | synonymous_variant | LOW | c.105G>A | p.Ala35Ala | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/8 | 127/915 | 105/810 | 35/269 | chr1 | 15476521 | |||
| chr1:15483381 | G | A | 7 | a0001c0003 a0001c0014 a0002c0002 others(4): Show |
169 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(166): Show |
synonymous_variant | LOW | c.474G>A | p.Thr158Thr | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/8 | 496/915 | 474/810 | 158/269 | chr1 | 15483381 | |||
| chr1:15485905 | C | T | 1 | a0001c0008 | 3 | NA18994.hp1 NA19074.hp1 NA19088.hp1 |
synonymous_variant | LOW | c.498C>T | p.Asn166Asn | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/8 | 520/915 | 498/810 | 166/269 | chr1 | 15485905 | |||
| chr1:15487341 | T | C | 3 | a0001c0007 a0001c0014 a0002c0013 |
6 | HG00642.hp2 HG02615.hp1 HG02723.hp1 others(3): Show |
synonymous_variant | LOW | c.696T>C | p.His232His | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/8 | 718/915 | 696/810 | 232/269 | chr1 | 15487341 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:15476116 | C | T | 1 | a0001c0001t0003 | 2 | HG02486.hp2 HG02965.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-10C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 1/8 | chr1 | 15476116 | |||||||
| chr1:15491350 | G | A | 1 | a0001c0001t0004 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*38G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 8/8 | 38 | chr1 | 15491350 | ||||||
| chr1:15491368 | A | G | 1 | a0001c0001t0002 | 6 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*56A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 8/8 | 56 | chr1 | 15491368 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:15476293 | C | T | 1 | a0001c0014t0001g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.40+128C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 1/7 | chr1 | 15476293 | |||||||
| chr1:15476430 | G | T | 13 | a0001c0001t0001g0018 a0001c0001t0001g0056 a0001c0001t0001g0057 others(10): Show |
18 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.41-27G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 1/7 | chr1 | 15476430 | |||||||
| chr1:15476599 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.129+54C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15476599 | |||||||
| chr1:15476622 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.129+77C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15476622 | |||||||
| chr1:15476843 | A | G | 123 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(120): Show |
271 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.129+298A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15476843 | |||||||
| chr1:15476874 | C | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0094 others(1): Show |
6 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+329C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15476874 | |||||||
| chr1:15476892 | G | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG03927.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.129+347G>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15476892 | |||||||
| chr1:15476965 | AAG | A | 3 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 |
3 | NA18989.hp2 NA18993.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.129+426_129+427del others(2): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15476965 | ||||||
| chr1:15476990 | G | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0057 a0001c0001t0001g0169 others(7): Show |
14 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.129+445G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15476990 | |||||||
| chr1:15477063 | A | G | 21 | a0001c0001t0001g0018 a0001c0001t0001g0056 a0001c0001t0001g0057 others(18): Show |
28 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.129+518A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15477063 | |||||||
| chr1:15477135 | T | G | 1 | a0002c0002t0001g0099 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.129+590T>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15477135 | |||||||
| chr1:15477178 | C | T | 18 | a0001c0001t0001g0018 a0001c0001t0001g0056 a0001c0001t0001g0057 others(15): Show |
24 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.129+633C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15477178 | |||||||
| chr1:15477292 | T | A | 1 | a0002c0002t0001g0100 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.129+747T>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15477292 | |||||||
| chr1:15477356 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0001g0161 others(1): Show |
10 | HG01884.hp1 HG02257.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.129+811C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15477356 | |||||||
| chr1:15477524 | T | C | 14 | a0001c0001t0001g0018 a0001c0001t0001g0056 a0001c0001t0001g0057 others(11): Show |
20 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.129+979T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15477524 | |||||||
| chr1:15477913 | G | A | 1 | a0002c0013t0001g0101 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.129+1368G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15477913 | |||||||
| chr1:15478165 | G | A | 2 | a0001c0001t0002g0055 a0001c0001t0002g0163 |
3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.129+1620G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478165 | |||||||
| chr1:15478201 | C | CATATATA others(3): Show |
2 | a0001c0001t0001g0164 a0001c0001t0002g0098 |
2 | HG02486.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.129+1663_129+1672d others(12): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478201 | ||||||
| chr1:15478201 | C | CATATATA others(5): Show |
2 | a0001c0001t0002g0096 a0001c0001t0002g0097 |
2 | NA18993.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.129+1661_129+1672d others(14): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478201 | ||||||
| chr1:15478201 | C | CATATATA others(7): Show |
1 | a0001c0003t0001g0054 | 2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.129+1659_129+1672d others(16): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478201 | ||||||
| chr1:15478201 | C | CATATATA others(9): Show |
1 | a0001c0003t0001g0162 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.129+1657_129+1672d others(18): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478201 | ||||||
| chr1:15478209 | TATATATA others(5): Show |
T | 2 | a0001c0001t0002g0055 a0001c0001t0002g0163 |
3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.129+1672_129+1683d others(14): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478209 | ||||||
| chr1:15478213 | TATATTGG others(1): Show |
T | 5 | a0001c0003t0001g0040 a0004c0004t0001g0010 a0004c0004t0001g0116 others(2): Show |
10 | HG01496.hp2 HG01934.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+1673_129+1680d others(10): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478213 | ||||||
| chr1:15478215 | TATTGGG | T | 93 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(90): Show |
213 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.129+1673_129+1678d others(8): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478215 | ||||||
| chr1:15478217 | T | TATATATA others(18): Show |
1 | a0001c0014t0001g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.129+1672_129+1673i others(27): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478217 | |||||||
| chr1:15478217 | TTGGG | T | 8 | a0001c0001t0001g0005 a0001c0007t0001g0021 a0002c0002t0001g0001 others(5): Show |
17 | HG01891.hp1 HG02027.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.129+1673_129+1676d others(6): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478217 | |||||||
| chr1:15478218 | T | A | 6 | a0001c0001t0001g0164 a0001c0001t0002g0096 a0001c0001t0002g0097 others(3): Show |
7 | HG02451.hp2 HG02486.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.129+1673T>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478218 | |||||||
| chr1:15478219 | G | T | 6 | a0001c0001t0001g0164 a0001c0001t0002g0096 a0001c0001t0002g0097 others(3): Show |
7 | HG02451.hp2 HG02486.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.129+1674G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478219 | |||||||
| chr1:15478220 | G | A | 8 | a0001c0001t0001g0164 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
9 | HG00642.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.129+1675G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478220 | |||||||
| chr1:15478221 | G | T | 8 | a0001c0001t0001g0164 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
9 | HG00642.hp2 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.129+1676G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478221 | |||||||
| chr1:15478229 | G | T | 3 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 |
3 | NA18989.hp2 NA18993.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.129+1684G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478229 | |||||||
| chr1:15478230 | T | A | 3 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 |
3 | NA18989.hp2 NA18993.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.129+1685T>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478230 | |||||||
| chr1:15478232 | T | A | 3 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 |
3 | NA18989.hp2 NA18993.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.129+1687T>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478232 | |||||||
| chr1:15478299 | A | G | 2 | a0002c0002t0001g0158 a0002c0002t0001g0159 |
2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.129+1754A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478299 | |||||||
| chr1:15478369 | T | G | 6 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0096 others(3): Show |
7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.129+1824T>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478369 | |||||||
| chr1:15478471 | G | A | 1 | a0002c0002t0001g0102 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.129+1926G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478471 | |||||||
| chr1:15478490 | G | T | 4 | a0001c0001t0001g0164 a0001c0001t0002g0096 a0001c0001t0002g0097 others(1): Show |
4 | HG02486.hp1 NA18989.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+1945G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478490 | |||||||
| chr1:15478511 | G | A | 1 | a0001c0003t0001g0040 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.129+1966G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478511 | |||||||
| chr1:15478565 | A | AT | 7 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
8 | HG01169.hp2 HG02451.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.129+2037dupT | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478565 | ||||||
| chr1:15478565 | AT | A | 37 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(34): Show |
83 | HG00323.hp2 HG00423.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.129+2037delT | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478565 | ||||||
| chr1:15478565 | ATT | A | 76 | a0001c0001t0001g0018 a0001c0001t0001g0050 a0001c0001t0001g0056 others(73): Show |
174 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.129+2036_129+2037d others(4): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478565 | ||||||
| chr1:15478565 | ATTT | A | 5 | a0001c0001t0001g0168 a0001c0001t0002g0055 a0001c0001t0002g0163 others(2): Show |
6 | HG01109.hp2 HG02698.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+2035_129+2037d others(5): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478565 | ||||||
| chr1:15478633 | T | A | 2 | a0001c0001t0002g0055 a0001c0001t0002g0163 |
3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.129+2088T>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478633 | |||||||
| chr1:15478789 | AC | A | 3 | a0001c0003t0001g0054 a0001c0003t0001g0162 a0001c0014t0001g0176 |
4 | HG02451.hp2 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+2245delC | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478789 | |||||||
| chr1:15478911 | C | A | 6 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0096 others(3): Show |
7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.130-2187C>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15478911 | |||||||
| chr1:15478993 | CG | C | 9 | a0002c0002t0001g0020 a0002c0002t0001g0041 a0002c0002t0001g0105 others(6): Show |
12 | HG00673.hp1 NA18939.hp2 NA18944.hp1 others(9): Show |
intron_variant | MODIFIER | c.130-2098delG | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15478993 | ||||||
| chr1:15479052 | G | A | 1 | a0001c0007t0001g0021 | 4 | HG00642.hp2 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-2046G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15479052 | |||||||
| chr1:15479080 | G | A | 1 | a0001c0001t0001g0051 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.130-2018G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15479080 | |||||||
| chr1:15479129 | G | C | 4 | a0001c0001t0001g0164 a0001c0001t0002g0096 a0001c0001t0002g0097 others(1): Show |
4 | HG02486.hp1 NA18989.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-1969G>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15479129 | |||||||
| chr1:15479167 | C | T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(26): Show |
75 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.130-1931C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15479167 | |||||||
| chr1:15479227 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(26): Show |
75 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.130-1871G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15479227 | |||||||
| chr1:15479397 | T | C | 9 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0096 others(6): Show |
11 | HG02451.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.130-1701T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15479397 | |||||||
| chr1:15479607 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.130-1491C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15479607 | |||||||
| chr1:15479634 | A | G | 2 | a0002c0002t0001g0028 a0002c0002t0001g0141 |
4 | HG01099.hp1 HG01891.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-1464A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15479634 | |||||||
| chr1:15479726 | T | G | 1 | a0001c0001t0001g0090 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.130-1372T>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15479726 | |||||||
| chr1:15479749 | T | C | 5 | a0002c0002t0001g0042 a0002c0002t0001g0102 a0002c0002t0001g0110 others(2): Show |
6 | HG00597.hp1 NA18966.hp1 NA18997.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-1349T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15479749 | |||||||
| chr1:15480252 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.130-846C>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15480252 | |||||||
| chr1:15480277 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.130-821G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15480277 | |||||||
| chr1:15480337 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
8 | NA18951.hp1 NA18954.hp1 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.130-761G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15480337 | |||||||
| chr1:15480504 | G | T | 1 | a0001c0001t0002g0098 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.130-594G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15480504 | |||||||
| chr1:15480507 | G | A | 1 | a0001c0003t0001g0040 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.130-591G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15480507 | |||||||
| chr1:15480556 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.130-542C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15480556 | |||||||
| chr1:15480645 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.130-453A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15480645 | |||||||
| chr1:15480647 | T | C | 30 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(27): Show |
76 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.130-451T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15480647 | |||||||
| chr1:15480798 | G | A | 1 | a0002c0002t0001g0112 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.130-300G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15480798 | |||||||
| chr1:15480885 | C | A | 1 | a0001c0003t0001g0040 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.130-213C>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15480885 | |||||||
| chr1:15480898 | A | AT | 34 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(31): Show |
71 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.130-186dupT | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 15480898 | ||||||
| chr1:15481026 | G | A | 4 | a0002c0002t0001g0009 a0002c0002t0001g0113 a0002c0002t0001g0114 others(1): Show |
9 | HG00673.hp2 HG02040.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.130-72G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 2/7 | chr1 | 15481026 | |||||||
| chr1:15481235 | C | T | 1 | a0001c0001t0001g0030 | 3 | HG00323.hp2 HG01069.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.227+40C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15481235 | |||||||
| chr1:15481285 | G | A | 6 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0096 others(3): Show |
7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.227+90G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15481285 | |||||||
| chr1:15481318 | G | A | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0166 |
3 | HG02723.hp2 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.227+123G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15481318 | |||||||
| chr1:15481366 | T | C | 1 | a0001c0001t0003g0053 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.227+171T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15481366 | |||||||
| chr1:15481488 | A | G | 6 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0096 others(3): Show |
7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.227+293A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15481488 | |||||||
| chr1:15481703 | C | T | 64 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0007 others(61): Show |
147 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.227+508C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15481703 | |||||||
| chr1:15481709 | C | G | 1 | a0002c0002t0001g0137 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.227+514C>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15481709 | |||||||
| chr1:15481747 | C | T | 6 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0096 others(3): Show |
7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.228-518C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15481747 | |||||||
| chr1:15481794 | C | T | 79 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0096 others(76): Show |
171 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.228-471C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15481794 | |||||||
| chr1:15481881 | G | A | 6 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0096 others(3): Show |
7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.228-384G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15481881 | |||||||
| chr1:15482011 | TAG | T | 71 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0007 others(68): Show |
161 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.228-251_228-250del others(2): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 15482011 | ||||||
| chr1:15482014 | A | G | 1 | a0002c0002t0001g0137 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.228-251A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15482014 | |||||||
| chr1:15482159 | G | C | 1 | a0002c0002t0001g0118 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.228-106G>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15482159 | |||||||
| chr1:15482163 | A | T | 1 | a0002c0002t0001g0118 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.228-102A>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15482163 | |||||||
| chr1:15482207 | C | T | 67 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0007 others(64): Show |
153 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.228-58C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15482207 | |||||||
| chr1:15482250 | A | C | 6 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0096 others(3): Show |
7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.228-15A>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 3/7 | chr1 | 15482250 | |||||||
| chr1:15482428 | T | C | 1 | a0002c0002t0001g0119 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.356+35T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15482428 | |||||||
| chr1:15482502 | G | C | 1 | a0001c0001t0001g0064 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.356+109G>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15482502 | |||||||
| chr1:15482541 | G | A | 73 | a0001c0003t0001g0040 a0001c0003t0001g0087 a0002c0002t0001g0001 others(70): Show |
164 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.356+148G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15482541 | |||||||
| chr1:15482646 | G | A | 1 | a0002c0002t0001g0120 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.356+253G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15482646 | |||||||
| chr1:15482705 | C | T | 1 | a0002c0002t0001g0109 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.356+312C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15482705 | |||||||
| chr1:15482826 | C | G | 1 | a0002c0002t0001g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.356+433C>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15482826 | |||||||
| chr1:15482867 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.357-397G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15482867 | |||||||
| chr1:15482871 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.357-393C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15482871 | |||||||
| chr1:15482933 | C | T | 72 | a0001c0003t0001g0085 a0002c0002t0001g0001 a0002c0002t0001g0004 others(69): Show |
162 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.357-331C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15482933 | |||||||
| chr1:15482941 | A | AC | 113 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(110): Show |
252 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.357-322dupC | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 15482941 | ||||||
| chr1:15483051 | TGCTGGCA others(6): Show |
T | 3 | a0001c0001t0001g0057 a0001c0001t0001g0065 a0001c0001t0001g0170 |
4 | HG01167.hp1 HG01175.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.357-184_357-172del others(13): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 15483051 | ||||||
| chr1:15483097 | G | A | 2 | a0002c0002t0001g0044 a0002c0002t0001g0121 |
3 | HG00140.hp1 HG00741.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.357-167G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15483097 | |||||||
| chr1:15483106 | C | T | 30 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(27): Show |
76 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.357-158C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15483106 | |||||||
| chr1:15483211 | T | C | 113 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(110): Show |
252 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.357-53T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15483211 | |||||||
| chr1:15483246 | G | A | 3 | a0002c0002t0001g0007 a0002c0002t0001g0045 a0002c0002t0001g0099 |
10 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.357-18G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 4/7 | chr1 | 15483246 | |||||||
| chr1:15483470 | C | T | 1 | a0002c0002t0001g0140 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.493+70C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483470 | |||||||
| chr1:15483511 | G | C | 1 | a0001c0003t0001g0087 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.493+111G>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483511 | |||||||
| chr1:15483656 | G | A | 1 | a0001c0014t0001g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.493+256G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483656 | |||||||
| chr1:15483677 | C | T | 31 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(28): Show |
78 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.493+277C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483677 | |||||||
| chr1:15483695 | A | G | 1 | a0002c0002t0001g0102 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.493+295A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483695 | |||||||
| chr1:15483704 | G | C | 1 | a0002c0002t0001g0122 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.493+304G>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483704 | |||||||
| chr1:15483713 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.493+313A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483713 | |||||||
| chr1:15483757 | G | A | 72 | a0001c0003t0001g0085 a0002c0002t0001g0001 a0002c0002t0001g0004 others(69): Show |
162 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.493+357G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483757 | |||||||
| chr1:15483782 | C | T | 6 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0096 others(3): Show |
7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.493+382C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483782 | |||||||
| chr1:15483801 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.493+401C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483801 | |||||||
| chr1:15483803 | C | G | 3 | a0001c0003t0001g0054 a0001c0003t0001g0162 a0001c0014t0001g0176 |
4 | HG02451.hp2 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+403C>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483803 | |||||||
| chr1:15483827 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.493+427C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483827 | |||||||
| chr1:15483851 | T | C | 125 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(122): Show |
269 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.493+451T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15483851 | |||||||
| chr1:15483929 | CA | C | 37 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(34): Show |
84 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.493+541delA | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 15483929 | ||||||
| chr1:15484021 | G | A | 1 | a0002c0002t0001g0046 | 2 | NA18974.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.493+621G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484021 | |||||||
| chr1:15484120 | A | G | 8 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0146 others(5): Show |
17 | HG01975.hp2 HG01981.hp1 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.493+720A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484120 | |||||||
| chr1:15484129 | T | C | 107 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(104): Show |
245 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.493+729T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484129 | |||||||
| chr1:15484158 | A | G | 2 | a0001c0003t0001g0054 a0001c0003t0001g0162 |
3 | HG02451.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.493+758A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484158 | |||||||
| chr1:15484193 | C | T | 66 | a0001c0003t0001g0085 a0002c0002t0001g0001 a0002c0002t0001g0004 others(63): Show |
150 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.493+793C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484193 | |||||||
| chr1:15484243 | C | T | 6 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0096 others(3): Show |
7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.493+843C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484243 | |||||||
| chr1:15484301 | A | C | 3 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 |
3 | NA18989.hp2 NA18993.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.493+901A>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484301 | |||||||
| chr1:15484343 | A | T | 6 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0096 others(3): Show |
7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.493+943A>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484343 | |||||||
| chr1:15484498 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.493+1098G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484498 | |||||||
| chr1:15484570 | G | A | 2 | a0002c0002t0001g0028 a0002c0002t0001g0141 |
4 | HG01099.hp1 HG01891.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+1170G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484570 | |||||||
| chr1:15484641 | C | A | 117 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(114): Show |
260 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.493+1241C>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484641 | |||||||
| chr1:15484701 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.494-1200T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484701 | |||||||
| chr1:15484728 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0064 a0001c0001t0001g0083 others(1): Show |
8 | NA18942.hp1 NA18948.hp2 NA18979.hp2 others(5): Show |
intron_variant | MODIFIER | c.494-1173C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484728 | |||||||
| chr1:15484772 | CA | C | 6 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0096 others(3): Show |
7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.494-1128delA | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484772 | |||||||
| chr1:15484828 | G | T | 1 | a0001c0003t0001g0087 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.494-1073G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484828 | |||||||
| chr1:15484848 | T | C | 6 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0096 others(3): Show |
7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.494-1053T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484848 | |||||||
| chr1:15484851 | C | T | 83 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0096 others(80): Show |
176 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.494-1050C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484851 | |||||||
| chr1:15484901 | A | ATT | 7 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0096 others(4): Show |
9 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.494-987_494-986dup others(2): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 15484901 | ||||||
| chr1:15484901 | AT | A | 6 | a0001c0001t0001g0022 a0001c0001t0001g0146 a0002c0002t0001g0113 others(3): Show |
9 | HG00741.hp1 HG01106.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.494-986delT | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 15484901 | ||||||
| chr1:15484937 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0091 |
3 | HG01168.hp1 HG01169.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.494-964G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484937 | |||||||
| chr1:15484986 | C | T | 6 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0096 others(3): Show |
7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.494-915C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15484986 | |||||||
| chr1:15485085 | G | A | 6 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0096 others(3): Show |
7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.494-816G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15485085 | |||||||
| chr1:15485197 | C | T | 73 | a0001c0001t0001g0082 a0001c0003t0001g0085 a0002c0002t0001g0001 others(70): Show |
163 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.494-704C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15485197 | |||||||
| chr1:15485325 | C | T | 1 | a0002c0002t0001g0134 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.494-576C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15485325 | |||||||
| chr1:15485366 | G | C | 1 | a0001c0001t0001g0094 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.494-535G>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15485366 | |||||||
| chr1:15485383 | A | AGATAAGT others(1): Show |
78 | a0001c0001t0001g0082 a0001c0003t0001g0040 a0001c0003t0001g0054 others(75): Show |
170 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.494-517_494-510dup others(8): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 15485383 | ||||||
| chr1:15485417 | CA | C | 77 | a0001c0003t0001g0040 a0001c0003t0001g0054 a0001c0003t0001g0085 others(74): Show |
169 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.494-477delA | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 15485417 | ||||||
| chr1:15485499 | A | G | 6 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0096 others(3): Show |
7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.494-402A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15485499 | |||||||
| chr1:15485641 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.494-260G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15485641 | |||||||
| chr1:15485801 | G | A | 4 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 others(1): Show |
5 | HG02132.hp2 NA18967.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-100G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 5/7 | chr1 | 15485801 | |||||||
| chr1:15486170 | G | T | 24 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(21): Show |
61 | HG00323.hp2 HG00423.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.639+124G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15486170 | |||||||
| chr1:15486383 | G | T | 1 | a0001c0014t0001g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.639+337G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15486383 | |||||||
| chr1:15486453 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0070 |
6 | HG00099.hp1 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.639+407T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15486453 | |||||||
| chr1:15486472 | C | CA | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0083 others(3): Show |
6 | HG02976.hp1 NA18950.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.639+435dupA | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 15486472 | ||||||
| chr1:15486593 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.639+547G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15486593 | |||||||
| chr1:15486898 | A | G | 2 | a0002c0002t0001g0027 a0002c0002t0001g0100 |
4 | NA18952.hp1 NA18975.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.640-387A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15486898 | |||||||
| chr1:15487108 | G | A | 1 | a0002c0002t0001g0106 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.640-177G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15487108 | |||||||
| chr1:15487115 | A | T | 6 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0096 others(3): Show |
7 | HG02486.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.640-170A>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15487115 | |||||||
| chr1:15487239 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.640-46G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15487239 | |||||||
| chr1:15487258 | A | C | 4 | a0004c0004t0001g0010 a0004c0004t0001g0116 a0006c0009t0001g0010 others(1): Show |
8 | HG01496.hp2 HG01934.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.640-27A>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15487258 | |||||||
| chr1:15487261 | C | G | 4 | a0004c0004t0001g0010 a0004c0004t0001g0116 a0006c0009t0001g0010 others(1): Show |
8 | HG01496.hp2 HG01934.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.640-24C>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 6/7 | chr1 | 15487261 | |||||||
| chr1:15487474 | A | C | 137 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(134): Show |
289 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.792+37A>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15487474 | |||||||
| chr1:15487491 | C | T | 1 | a0001c0007t0001g0021 | 4 | HG00642.hp2 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+54C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15487491 | |||||||
| chr1:15487676 | G | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0146 |
6 | NA18954.hp1 NA18969.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+239G>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15487676 | |||||||
| chr1:15487691 | C | T | 124 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(121): Show |
270 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.792+254C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15487691 | |||||||
| chr1:15487883 | C | A | 3 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 |
3 | NA18989.hp2 NA18993.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.792+446C>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15487883 | |||||||
| chr1:15487980 | C | CCT | 135 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(132): Show |
286 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.792+543_792+544ins others(2): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15487980 | |||||||
| chr1:15488078 | C | T | 5 | a0001c0001t0002g0055 a0001c0001t0002g0096 a0001c0001t0002g0097 others(2): Show |
6 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+641C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15488078 | |||||||
| chr1:15488165 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.792+728T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15488165 | |||||||
| chr1:15488172 | A | G | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG01069.hp2 HG01071.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.792+735A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15488172 | |||||||
| chr1:15488228 | A | AT | 12 | a0001c0001t0001g0018 a0001c0001t0001g0056 a0001c0001t0001g0057 others(9): Show |
18 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.792+802dupT | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15488228 | ||||||
| chr1:15488466 | GA | G | 5 | a0001c0001t0002g0055 a0001c0001t0002g0096 a0001c0001t0002g0097 others(2): Show |
6 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+1031delA | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15488466 | ||||||
| chr1:15488542 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0071 |
8 | HG02074.hp2 NA18952.hp2 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.792+1105G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15488542 | |||||||
| chr1:15488583 | T | TCA | 5 | a0001c0001t0002g0055 a0001c0001t0002g0096 a0001c0001t0002g0097 others(2): Show |
6 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+1146_792+1147i others(4): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15488583 | |||||||
| chr1:15488609 | T | A | 1 | a0001c0001t0001g0156 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.792+1172T>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15488609 | |||||||
| chr1:15488694 | A | G | 5 | a0001c0001t0002g0055 a0001c0001t0002g0096 a0001c0001t0002g0097 others(2): Show |
6 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+1257A>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15488694 | |||||||
| chr1:15488789 | G | A | 3 | a0004c0004t0001g0010 a0004c0004t0001g0116 a0006c0009t0001g0010 |
7 | HG01496.hp2 HG01934.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.792+1352G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15488789 | |||||||
| chr1:15488974 | C | T | 2 | a0001c0001t0002g0055 a0001c0001t0002g0163 |
3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.792+1537C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15488974 | |||||||
| chr1:15489055 | A | C | 1 | a0001c0001t0001g0076 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.792+1618A>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489055 | |||||||
| chr1:15489084 | G | A | 83 | a0001c0001t0001g0014 a0001c0001t0001g0061 a0001c0001t0001g0066 others(80): Show |
178 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.792+1647G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489084 | |||||||
| chr1:15489107 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.792+1670C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489107 | |||||||
| chr1:15489225 | G | GTCCCAGC others(9): Show |
3 | a0004c0004t0001g0010 a0004c0004t0001g0116 a0006c0009t0001g0010 |
7 | HG01496.hp2 HG01934.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.792+1812_792+1827d others(18): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15489225 | ||||||
| chr1:15489304 | C | T | 1 | a0002c0002t0001g0132 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.792+1867C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489304 | |||||||
| chr1:15489410 | G | GT | 3 | a0004c0004t0001g0010 a0004c0004t0001g0116 a0006c0009t0001g0010 |
7 | HG01496.hp2 HG01934.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.793-1884dupT | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15489410 | ||||||
| chr1:15489427 | G | A | 76 | a0001c0001t0001g0014 a0001c0001t0001g0061 a0001c0001t0001g0066 others(73): Show |
169 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.793-1868G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489427 | |||||||
| chr1:15489478 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.793-1817G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489478 | |||||||
| chr1:15489487 | G | A | 1 | a0002c0002t0001g0126 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.793-1808G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489487 | |||||||
| chr1:15489546 | C | T | 1 | a0002c0002t0001g0104 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.793-1749C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489546 | |||||||
| chr1:15489570 | A | C | 1 | a0001c0003t0001g0040 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.793-1725A>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489570 | |||||||
| chr1:15489726 | A | T | 1 | a0002c0002t0001g0141 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.793-1569A>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489726 | |||||||
| chr1:15489800 | G | A | 3 | a0004c0004t0001g0010 a0004c0004t0001g0116 a0006c0009t0001g0010 |
7 | HG01496.hp2 HG01934.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.793-1495G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489800 | |||||||
| chr1:15489937 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.793-1358G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15489937 | |||||||
| chr1:15490018 | C | G | 1 | a0001c0001t0001g0079 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.793-1277C>G | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490018 | |||||||
| chr1:15490037 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.793-1258C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490037 | |||||||
| chr1:15490067 | T | C | 31 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(28): Show |
77 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.793-1228T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490067 | |||||||
| chr1:15490220 | A | ATATC | 30 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0025 others(27): Show |
68 | HG00099.hp1 HG00280.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.793-1039_793-1036d others(6): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15490220 | ||||||
| chr1:15490220 | A | ATATCTAT others(1): Show |
7 | a0001c0001t0001g0006 a0001c0001t0001g0039 a0001c0001t0001g0069 others(4): Show |
13 | HG00544.hp1 HG00673.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.793-1043_793-1036d others(10): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15490220 | ||||||
| chr1:15490220 | A | ATATCTAT others(5): Show |
1 | a0002c0002t0001g0131 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.793-1047_793-1036d others(14): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15490220 | ||||||
| chr1:15490220 | ATATC | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0068 |
4 | HG02622.hp2 HG02698.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-1039_793-1036d others(6): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15490220 | ||||||
| chr1:15490220 | ATATCTAT others(1): Show |
A | 35 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(32): Show |
87 | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.793-1043_793-1036d others(10): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15490220 | ||||||
| chr1:15490220 | ATATCTAT others(9): Show |
A | 3 | a0001c0003t0001g0054 a0001c0003t0001g0162 a0001c0014t0001g0176 |
4 | HG02451.hp2 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-1051_793-1036d others(18): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15490220 | ||||||
| chr1:15490256 | CTATA | C | 4 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 others(1): Show |
4 | HG03540.hp2 NA18989.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-1036_793-1033d others(6): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15490256 | ||||||
| chr1:15490258 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.793-1037A>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490258 | |||||||
| chr1:15490260 | A | C | 41 | a0001c0001t0001g0078 a0001c0001t0001g0093 a0001c0001t0001g0164 others(38): Show |
81 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.793-1035A>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490260 | |||||||
| chr1:15490263 | C | T | 39 | a0001c0001t0001g0078 a0001c0001t0001g0164 a0002c0002t0001g0004 others(36): Show |
78 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.793-1032C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490263 | |||||||
| chr1:15490265 | C | T | 39 | a0001c0001t0001g0078 a0001c0001t0001g0164 a0002c0002t0001g0004 others(36): Show |
78 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.793-1030C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490265 | |||||||
| chr1:15490267 | C | T | 1 | a0002c0002t0001g0108 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.793-1028C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490267 | |||||||
| chr1:15490273 | CACAT | C | 37 | a0001c0001t0001g0014 a0001c0001t0001g0061 a0001c0001t0001g0066 others(34): Show |
91 | HG00140.hp1 HG00597.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.793-1020_793-1017d others(6): Show |
CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15490273 | ||||||
| chr1:15490277 | T | C | 39 | a0001c0001t0001g0078 a0001c0001t0001g0164 a0002c0002t0001g0004 others(36): Show |
78 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.793-1018T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490277 | |||||||
| chr1:15490462 | T | C | 3 | a0002c0002t0001g0041 a0002c0002t0001g0105 a0007c0012t0001g0041 |
3 | NA18939.hp2 NA18944.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.793-833T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490462 | |||||||
| chr1:15490499 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0146 a0001c0001t0001g0147 |
7 | NA18951.hp1 NA18954.hp1 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.793-796C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490499 | |||||||
| chr1:15490547 | G | A | 5 | a0001c0001t0002g0055 a0001c0001t0002g0096 a0001c0001t0002g0097 others(2): Show |
6 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.793-748G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490547 | |||||||
| chr1:15490595 | C | T | 71 | a0001c0001t0001g0014 a0001c0001t0001g0061 a0001c0001t0001g0066 others(68): Show |
158 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.793-700C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490595 | |||||||
| chr1:15490596 | G | A | 1 | a0001c0003t0001g0040 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.793-699G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490596 | |||||||
| chr1:15490638 | C | T | 3 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 |
3 | NA18989.hp2 NA18993.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.793-657C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490638 | |||||||
| chr1:15490682 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.793-613A>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490682 | |||||||
| chr1:15490737 | G | T | 5 | a0001c0001t0002g0055 a0001c0001t0002g0096 a0001c0001t0002g0097 others(2): Show |
6 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.793-558G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490737 | |||||||
| chr1:15490760 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.793-535C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490760 | |||||||
| chr1:15490792 | C | T | 1 | a0004c0004t0001g0116 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.793-503C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490792 | |||||||
| chr1:15490823 | A | T | 35 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(32): Show |
79 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.793-472A>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490823 | |||||||
| chr1:15490824 | T | C | 38 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(35): Show |
83 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.793-471T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490824 | |||||||
| chr1:15490839 | G | A | 74 | a0001c0001t0001g0014 a0001c0001t0001g0061 a0001c0001t0001g0066 others(71): Show |
166 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.793-456G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15490839 | |||||||
| chr1:15490865 | CA | C | 16 | a0001c0001t0001g0035 a0001c0001t0001g0069 a0001c0001t0001g0072 others(13): Show |
18 | HG01069.hp2 HG01109.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.793-413delA | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15490865 | ||||||
| chr1:15491002 | G | A | 2 | a0001c0001t0001g0025 a0002c0002t0001g0128 |
4 | HG01928.hp2 HG01975.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-293G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15491002 | |||||||
| chr1:15491012 | C | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0156 a0001c0007t0001g0021 |
8 | HG00642.hp2 HG01928.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.793-283C>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15491012 | |||||||
| chr1:15491024 | AG | A | 26 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(23): Show |
60 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.793-266delG | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 15491024 | ||||||
| chr1:15491033 | G | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0174 |
2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.793-262G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15491033 | |||||||
| chr1:15491044 | G | A | 2 | a0001c0001t0001g0160 a0001c0003t0001g0040 |
3 | HG06807.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.793-251G>A | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15491044 | |||||||
| chr1:15491045 | A | C | 2 | a0001c0001t0001g0160 a0001c0003t0001g0040 |
3 | HG06807.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.793-250A>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15491045 | |||||||
| chr1:15491136 | C | T | 3 | a0001c0001t0001g0066 a0002c0002t0001g0047 a0002c0002t0001g0129 |
4 | HG02132.hp2 NA18956.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-159C>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15491136 | |||||||
| chr1:15491168 | T | C | 1 | a0002c0002t0001g0127 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.793-127T>C | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15491168 | |||||||
| chr1:15491229 | G | T | 1 | a0001c0007t0001g0021 | 4 | HG00642.hp2 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-66G>T | CELA2B | ENSG00000215704.10 | transcript | ENST00000375910.8 | protein_coding | 7/7 | chr1 | 15491229 |