Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23436 |
| ensemblid | ENSG00000219073.8 |
| hgncid | 15945 |
| symbol | CELA3B |
| name | chymotrypsin like elastase 3B |
| refseq_nuc | NM_007352.4 |
| refseq_prot | NP_031378.1 |
| ensembl_nuc | ENST00000337107.11 |
| ensembl_prot | ENSP00000338369.6 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 21977022 |
| end | 21989354 |
| strand | + |
| ver | v1.2 |
| region | chr1:21977022-21989354 |
| region5000 | chr1:21972022-21994354 |
| regionname0 | CELA3B_chr1_21977022_21989354 |
| regionname5000 | CELA3B_chr1_21972022_21994354 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 270 | 323 | 61 | 73 | 133 | 15 | 40 | 100 | CELA3B_chr1_21972022_21994354 | CELA3B | MMLRL others(265): Show |
chr1 | 21972022 | 21994354 |
| a0002 | 1/0 | 270 | 86 | 24 | 2 | 55 | 1 | 3 | 43 | CELA3B_chr1_21972022_21994354 | CELA3B | MMLRL others(265): Show |
chr1 | 21972022 | 21994354 |
| a0003 | 0/0 | 270 | 9 | 0 | 0 | 6 | 0 | 3 | 5 | CELA3B_chr1_21972022_21994354 | CELA3B | MMLRL others(265): Show |
chr1 | 21972022 | 21994354 |
| a0004 | 0/0 | 247 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | MMLRL others(242): Show |
chr1 | 21972022 | 21994354 |
| a0005 | 0/0 | 270 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | MMLRL others(265): Show |
chr1 | 21972022 | 21994354 |
| a0006 | 0/0 | 270 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | MMLRL others(265): Show |
chr1 | 21972022 | 21994354 |
| a0007 | 0/0 | 270 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | MMLRL others(265): Show |
chr1 | 21972022 | 21994354 |
| a0008 | 0/0 | 270 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | MMLRL others(265): Show |
chr1 | 21972022 | 21994354 |
| a0009 | 0/0 | 270 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | MMLRL others(265): Show |
chr1 | 21972022 | 21994354 |
| a0010 | 0/0 | 270 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | MMLRL others(265): Show |
chr1 | 21972022 | 21994354 |
| a0011 | 0/0 | 270 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | MMLRL others(265): Show |
chr1 | 21972022 | 21994354 |
| a0012 | 0/0 | 270 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | MMLRL others(265): Show |
chr1 | 21972022 | 21994354 |
| a0013 | 0/0 | 270 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | MMLRL others(265): Show |
chr1 | 21972022 | 21994354 |
| a0014 | 0/0 | 270 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | MMLRL others(265): Show |
chr1 | 21972022 | 21994354 |
| a0015 | 0/0 | 266 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | MMLRL others(261): Show |
chr1 | 21972022 | 21994354 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 810 | 262 | 48 | 70 | 92 | 13 | 39 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(805): Show |
chr1 | 21972022 | 21994354 | ||
| a0001c0003 | 0/0 | 810 | 53 | 13 | 1 | 38 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(805): Show |
chr1 | 21972022 | 21994354 | ||
| a0001c0011 | 0/0 | 810 | 2 | 0 | 1 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(805): Show |
chr1 | 21972022 | 21994354 | ||
| a0001c0013 | 0/0 | 810 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(805): Show |
chr1 | 21972022 | 21994354 | ||
| a0001c0014 | 0/0 | 810 | 2 | 0 | 1 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(805): Show |
chr1 | 21972022 | 21994354 | ||
| a0001c0018 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(805): Show |
chr1 | 21972022 | 21994354 | ||
| a0001c0021 | 0/1 | 810 | 1 | 0 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(805): Show |
chr1 | 21972022 | 21994354 | ||
| a0002c0002 | 1/0 | 810 | 82 | 20 | 2 | 55 | 1 | 3 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(805): Show |
chr1 | 21972022 | 21994354 | ||
| a0002c0006 | 0/0 | 810 | 4 | 4 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(805): Show |
chr1 | 21972022 | 21994354 | ||
| a0003c0004 | 0/0 | 810 | 9 | 0 | 0 | 6 | 0 | 3 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(805): Show |
chr1 | 21972022 | 21994354 | ||
| a0004c0005 | 0/0 | 742 | 5 | 4 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(737): Show |
chr1 | 21972022 | 21994354 | ||
| a0005c0007 | 0/0 | 810 | 4 | 1 | 3 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(805): Show |
chr1 | 21972022 | 21994354 | ||
| a0006c0008 | 0/0 | 810 | 3 | 0 | 2 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(805): Show |
chr1 | 21972022 | 21994354 | ||
| a0007c0009 | 0/0 | 810 | 3 | 3 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(805): Show |
chr1 | 21972022 | 21994354 | ||
| a0008c0010 | 0/0 | 810 | 2 | 0 | 0 | 0 | 2 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(805): Show |
chr1 | 21972022 | 21994354 | ||
| a0009c0015 | 0/0 | 810 | 2 | 0 | 0 | 1 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(805): Show |
chr1 | 21972022 | 21994354 | ||
| a0010c0012 | 0/0 | 810 | 2 | 2 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(805): Show |
chr1 | 21972022 | 21994354 | ||
| a0011c0017 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(805): Show |
chr1 | 21972022 | 21994354 | ||
| a0012c0022 | 0/0 | 810 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(805): Show |
chr1 | 21972022 | 21994354 | ||
| a0013c0019 | 0/0 | 810 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(805): Show |
chr1 | 21972022 | 21994354 | ||
| a0014c0016 | 0/0 | 810 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(805): Show |
chr1 | 21972022 | 21994354 | ||
| a0015c0020 | 0/0 | 829 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | ATGAT others(824): Show |
chr1 | 21972022 | 21994354 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 906 | 262 | 48 | 70 | 92 | 13 | 39 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(901): Show |
chr1 | 21972022 | 21994354 |
| a0001c0003t0001 | 0/0 | 906 | 53 | 13 | 1 | 38 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(901): Show |
chr1 | 21972022 | 21994354 |
| a0001c0011t0001 | 0/0 | 906 | 2 | 0 | 1 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(901): Show |
chr1 | 21972022 | 21994354 |
| a0001c0013t0001 | 0/0 | 906 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(901): Show |
chr1 | 21972022 | 21994354 |
| a0001c0014t0001 | 0/0 | 906 | 2 | 0 | 1 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(901): Show |
chr1 | 21972022 | 21994354 |
| a0001c0018t0001 | 0/0 | 906 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(901): Show |
chr1 | 21972022 | 21994354 |
| a0001c0021t0001 | 0/1 | 906 | 1 | 0 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(901): Show |
chr1 | 21972022 | 21994354 |
| a0002c0002t0001 | 1/0 | 906 | 82 | 20 | 2 | 55 | 1 | 3 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(901): Show |
chr1 | 21972022 | 21994354 |
| a0002c0006t0001 | 0/0 | 906 | 4 | 4 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(901): Show |
chr1 | 21972022 | 21994354 |
| a0003c0004t0001 | 0/0 | 906 | 9 | 0 | 0 | 6 | 0 | 3 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(901): Show |
chr1 | 21972022 | 21994354 |
| a0004c0005t0002 | 0/0 | 760 | 5 | 4 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(755): Show |
chr1 | 21972022 | 21994354 |
| a0005c0007t0001 | 0/0 | 906 | 4 | 1 | 3 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(901): Show |
chr1 | 21972022 | 21994354 |
| a0006c0008t0001 | 0/0 | 906 | 3 | 0 | 2 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(901): Show |
chr1 | 21972022 | 21994354 |
| a0007c0009t0001 | 0/0 | 906 | 3 | 3 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(901): Show |
chr1 | 21972022 | 21994354 |
| a0008c0010t0001 | 0/0 | 906 | 2 | 0 | 0 | 0 | 2 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(901): Show |
chr1 | 21972022 | 21994354 |
| a0009c0015t0001 | 0/0 | 906 | 2 | 0 | 0 | 1 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(901): Show |
chr1 | 21972022 | 21994354 |
| a0010c0012t0001 | 0/0 | 906 | 2 | 2 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(901): Show |
chr1 | 21972022 | 21994354 |
| a0011c0017t0001 | 0/0 | 906 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(901): Show |
chr1 | 21972022 | 21994354 |
| a0012c0022t0001 | 0/0 | 906 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(901): Show |
chr1 | 21972022 | 21994354 |
| a0013c0019t0001 | 0/0 | 906 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(901): Show |
chr1 | 21972022 | 21994354 |
| a0014c0016t0001 | 0/0 | 906 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(901): Show |
chr1 | 21972022 | 21994354 |
| a0015c0020t0001 | 0/0 | 925 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | CCTAT others(920): Show |
chr1 | 21972022 | 21994354 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 38 | 0 | 8 | 29 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0003 | 0/0 | 24 | 2 | 6 | 5 | 5 | 6 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0004 | 0/0 | 17 | 0 | 11 | 0 | 0 | 6 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0005 | 0/0 | 18 | 6 | 4 | 2 | 0 | 6 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 4 | 0 | 1 | 2 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0009 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0010 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0011 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0012 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0014 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0015 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0017 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0028 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0003t0001g0006 | 0/0 | 16 | 0 | 0 | 16 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0003t0001g0008 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0003t0001g0016 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0003t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0003t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0003t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0003t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0003t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0011t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0013t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0014t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0014t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0018t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0001c0021t0001g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0001 | 0/0 | 39 | 0 | 1 | 35 | 1 | 2 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0013 | 1/0 | 7 | 6 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0018 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0019 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0026 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0006t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0006t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0002c0006t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0003c0004t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0003c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0003c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0003c0004t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0003c0004t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0003c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0003c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0004c0005t0002g0027 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0004c0005t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0004c0005t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0005c0007t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0005c0007t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0005c0007t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0006c0008t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0007c0009t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0007c0009t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0007c0009t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0008c0010t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0009c0015t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0009c0015t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0010c0012t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0011c0017t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0012c0022t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0013c0019t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0014c0016t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| a0015c0020t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | GBR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | GBR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00140 | hp2 | a0001 | c0003 | t0001 | g0063 | EUR | GBR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00280 | hp1 | a0001 | c0011 | t0001 | g0007 | EUR | FIN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | FIN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00438 | hp1 | a0001 | c0003 | t0001 | g0103 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00597 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00609 | hp1 | a0011 | c0017 | t0001 | g0160 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00735 | hp2 | a0005 | c0007 | t0001 | g0030 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01109 | hp2 | a0001 | c0014 | t0001 | g0007 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0166 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01175 | hp1 | a0001 | c0011 | t0001 | g0007 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01243 | hp1 | a0004 | c0005 | t0002 | g0027 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01243 | hp2 | a0005 | c0007 | t0001 | g0054 | AMR | PUR | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01255 | hp1 | a0005 | c0007 | t0001 | g0030 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0026 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01346 | hp2 | a0006 | c0008 | t0001 | g0004 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01496 | hp1 | a0006 | c0008 | t0001 | g0004 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01515 | hp2 | a0008 | c0010 | t0001 | g0044 | EUR | IBS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01517 | hp1 | a0008 | c0010 | t0001 | g0044 | EUR | IBS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01891 | hp1 | a0007 | c0009 | t0001 | g0136 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02004 | hp2 | a0012 | c0022 | t0001 | g0065 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02040 | hp1 | a0003 | c0004 | t0001 | g0024 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02056 | hp2 | a0001 | c0013 | t0001 | g0010 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02074 | hp1 | a0001 | c0013 | t0001 | g0010 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0064 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02135 | hp2 | a0009 | c0015 | t0001 | g0061 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02145 | hp2 | a0010 | c0012 | t0001 | g0012 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | CDX | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CDX | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CDX | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02257 | hp2 | a0004 | c0005 | t0002 | g0027 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02280 | hp1 | a0002 | c0006 | t0001 | g0043 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0124 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02572 | hp2 | a0002 | c0006 | t0001 | g0128 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0053 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02630 | hp1 | a0007 | c0009 | t0001 | g0135 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0117 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02886 | hp2 | a0014 | c0016 | t0001 | g0132 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0020 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0052 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02970 | hp2 | a0010 | c0012 | t0001 | g0012 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02976 | hp1 | a0015 | c0020 | t0001 | g0165 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03017 | hp1 | a0009 | c0015 | t0001 | g0079 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03098 | hp1 | a0004 | c0005 | t0002 | g0027 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03139 | hp2 | a0004 | c0005 | t0002 | g0131 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0051 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0020 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0126 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0127 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03491 | hp2 | a0003 | c0004 | t0001 | g0094 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0125 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ESN | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03579 | hp2 | a0007 | c0009 | t0001 | g0050 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | STU | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03704 | hp2 | a0003 | c0004 | t0001 | g0090 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03710 | hp2 | a0001 | c0014 | t0001 | g0139 | SAS | PJL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03834 | hp1 | a0003 | c0004 | t0001 | g0095 | SAS | BEB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | BEB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | STU | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG04204 | hp1 | a0006 | c0008 | t0001 | g0004 | SAS | STU | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18522 | hp1 | a0005 | c0007 | t0001 | g0055 | AFR | YRI | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18522 | hp2 | a0004 | c0005 | t0002 | g0130 | AFR | YRI | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | YRI | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | YRI | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18945 | hp2 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18947 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18950 | hp1 | a0001 | c0003 | t0001 | g0113 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18951 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18951 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18954 | hp1 | a0003 | c0004 | t0001 | g0097 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18959 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18962 | hp1 | a0003 | c0004 | t0001 | g0106 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18963 | hp1 | a0001 | c0018 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18965 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18969 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18974 | hp2 | a0001 | c0003 | t0001 | g0062 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18975 | hp1 | a0003 | c0004 | t0001 | g0024 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18978 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18980 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18984 | hp2 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18986 | hp2 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18990 | hp2 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18995 | hp2 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18997 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18999 | hp2 | a0003 | c0004 | t0001 | g0099 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19009 | hp2 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0060 | AFR | LWK | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19054 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19055 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19057 | hp2 | a0001 | c0003 | t0001 | g0157 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19058 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19060 | hp2 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19062 | hp2 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19066 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19068 | hp2 | a0001 | c0003 | t0001 | g0158 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19074 | hp1 | a0003 | c0004 | t0001 | g0024 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19074 | hp2 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19077 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19084 | hp2 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19087 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19087 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19090 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19091 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | YRI | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | YRI | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0020 | AFR | ASW | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | TSI | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02109 | hp2 | a0002 | c0006 | t0001 | g0043 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02486 | hp2 | a0013 | c0019 | t0001 | g0088 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | USA | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | USA | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18955 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA18955 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | USA | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | LWK | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| NA21309 | hp2 | a0002 | c0006 | t0001 | g0129 | AFR | LWK | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| homoSapiens | chm13v2 | a0001 | c0021 | t0001 | g0137 | REF | REF | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0013 | REF | REF | CELA3B_chr1_21972022_21994354 | CELA3B | chr1 | 21972022 | 21994354 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:21978396 | G | A | 1 | a0006 | 3 | HG01346.hp2 HG01496.hp1 HG04204.hp1 |
missense_variant | MODERATE | c.71G>A | p.Arg24His | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/8 | 89/906 | 71/813 | 24/270 | chr1 | 21978396 | |||
| chr1:21978398 | C | T | 1 | a0006 | 3 | HG01346.hp2 HG01496.hp1 HG04204.hp1 |
missense_variant | MODERATE | c.73C>T | p.Pro25Ser | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/8 | 91/906 | 73/813 | 25/270 | chr1 | 21978398 | |||
| chr1:21978416 | A | C | 2 | a0006 a0009 |
5 | HG01346.hp2 HG01496.hp1 HG02135.hp2 others(2): Show |
missense_variant | MODERATE | c.91A>C | p.Asn31His | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/8 | 109/906 | 91/813 | 31/270 | chr1 | 21978416 | |||
| chr1:21981045 | C | T | 12 | a0001 a0003 a0005 others(9): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
missense_variant | MODERATE | c.235C>T | p.Arg79Trp | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/8 | 253/906 | 235/813 | 79/270 | chr1 | 21981045 | |||
| chr1:21981049 | C | A | 1 | a0011 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.239C>A | p.Thr80Asn | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/8 | 257/906 | 239/813 | 80/270 | chr1 | 21981049 | |||
| chr1:21981089 | G | T | 1 | a0010 | 2 | HG02145.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.279G>T | p.Lys93Asn | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/8 | 297/906 | 279/813 | 93/270 | chr1 | 21981089 | |||
| chr1:21983722 | C | T | 1 | a0003 | 9 | HG02040.hp1 HG03491.hp2 HG03704.hp2 others(6): Show |
missense_variant | MODERATE | c.391C>T | p.Arg131Cys | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/8 | 409/906 | 391/813 | 131/270 | chr1 | 21983722 | |||
| chr1:21983732 | A | T | 1 | a0005 | 4 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(1): Show |
missense_variant | MODERATE | c.401A>T | p.Gln134Leu | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/8 | 419/906 | 401/813 | 134/270 | chr1 | 21983732 | |||
| chr1:21984218 | G | C | 1 | a0014 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.529G>C | p.Glu177Gln | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/8 | 547/906 | 529/813 | 177/270 | chr1 | 21984218 | |||
| chr1:21984278 | T | A | 1 | a0013 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.589T>A | p.Ser197Thr | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/8 | 607/906 | 589/813 | 197/270 | chr1 | 21984278 | |||
| chr1:21984314 | A | G | 1 | a0012 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.625A>G | p.Ile209Val | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/8 | 643/906 | 625/813 | 209/270 | chr1 | 21984314 | |||
| chr1:21984318 | G | A | 2 | a0007 a0008 |
5 | HG01515.hp2 HG01517.hp1 HG01891.hp1 others(2): Show |
missense_variant | MODERATE | c.629G>A | p.Arg210His | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/8 | 647/906 | 629/813 | 210/270 | chr1 | 21984318 | |||
| chr1:21986599 | C | CTTTGTTT others(12): Show |
1 | a0015 | 1 | HG02976.hp1 | frameshift_variant | HIGH | c.725_726insCAGCTTTT others(11): Show |
p.Gly243fs | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/8 | 744/906 | 726/813 | 242/270 | INFO_REALIGN_3_PRIME | chr1 | 21986599 | ||
| chr1:21986610 | C | G | 1 | a0008 | 2 | HG01515.hp2 HG01517.hp1 |
missense_variant | MODERATE | c.722C>G | p.Ala241Gly | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/8 | 740/906 | 722/813 | 241/270 | chr1 | 21986610 | |||
| chr1:21986630 | AGGAAGCC others(7717): Show |
A | 1 | a0004 | 5 | HG01243.hp1 HG02257.hp2 HG03098.hp1 others(2): Show |
exon_loss_variant | HIGH | c.743_*5075del | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 8/8 | 761/906 | chr1 | 21986630 | ||||||
| chr1:21989153 | TCCTCTCC others(5194): Show |
T | 1 | a0008 | 1 | HG01517.hp1 | exon_loss_variant&splice_acceptor_variant&3_prime_UTR_truncation&exon_loss_variant&splice_region_variant&intron_variant | HIGH | c.796-103_*5080del | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 21989153 | ||||||
| chr1:21989262 | ACCATAGC others(5085): Show |
A | 1 | a0008 | 1 | HG01515.hp2 | stop_lost&3_prime_UTR_truncation&exon_loss_variant&conservative_inframe_deletion&splice_region_variant | HIGH | c.799_*5077del | p.Ile267_Ter271del | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 8/8 | 817/906 | 799/813 | 267/270 | INFO_REALIGN_3_PRIME | chr1 | 21989262 | ||
| chr1:21989266 | T | C | 1 | a0001 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.800T>C | p.Ile267Thr | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 8/8 | 818/906 | 800/813 | 267/270 | chr1 | 21989266 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:21980847 | C | T | 14 | a0001c0001 a0001c0003 a0001c0011 others(11): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
synonymous_variant | LOW | c.153C>T | p.Ser51Ser | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 3/8 | 171/906 | 153/813 | 51/270 | chr1 | 21980847 | |||
| chr1:21980865 | C | G | 14 | a0001c0001 a0001c0003 a0001c0011 others(11): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
synonymous_variant | LOW | c.171C>G | p.Thr57Thr | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 3/8 | 189/906 | 171/813 | 57/270 | chr1 | 21980865 | |||
| chr1:21980883 | C | T | 1 | a0001c0014 | 2 | HG01109.hp2 HG03710.hp2 |
synonymous_variant | LOW | c.189C>T | p.Ile63Ile | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 3/8 | 207/906 | 189/813 | 63/270 | chr1 | 21980883 | |||
| chr1:21980892 | C | T | 1 | a0001c0013 | 2 | HG02056.hp2 HG02074.hp1 |
synonymous_variant | LOW | c.198C>T | p.Asp66Asp | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 3/8 | 216/906 | 198/813 | 66/270 | chr1 | 21980892 | |||
| chr1:21983697 | T | C | 2 | a0001c0003 a0001c0018 |
54 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(51): Show |
synonymous_variant | LOW | c.366T>C | p.Asn122Asn | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/8 | 384/906 | 366/813 | 122/270 | chr1 | 21983697 | |||
| chr1:21983742 | C | T | 1 | a0002c0006 | 4 | HG02109.hp2 HG02280.hp1 HG02572.hp2 others(1): Show |
synonymous_variant | LOW | c.411C>T | p.Asp137Asp | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/8 | 429/906 | 411/813 | 137/270 | chr1 | 21983742 | |||
| chr1:21983769 | G | C | 16 | a0001c0001 a0001c0003 a0001c0011 others(13): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
synonymous_variant | LOW | c.438G>C | p.Pro146Pro | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/8 | 456/906 | 438/813 | 146/270 | chr1 | 21983769 | |||
| chr1:21983790 | C | T | 1 | a0001c0018 | 1 | NA18963.hp1 | synonymous_variant | LOW | c.459C>T | p.Asn153Asn | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/8 | 477/906 | 459/813 | 153/270 | chr1 | 21983790 | |||
| chr1:21984208 | C | T | 1 | a0001c0011 | 2 | HG00280.hp1 HG01175.hp1 |
synonymous_variant | LOW | c.519C>T | p.Asp173Asp | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/8 | 537/906 | 519/813 | 173/270 | chr1 | 21984208 | |||
| chr1:21984232 | G | C | 13 | a0001c0001 a0001c0003 a0001c0011 others(10): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
synonymous_variant | LOW | c.543G>C | p.Pro181Pro | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/8 | 561/906 | 543/813 | 181/270 | chr1 | 21984232 | |||
| chr1:21984331 | T | C | 17 | a0001c0001 a0001c0003 a0001c0011 others(14): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
splice_region_variant&synonymous_variant | LOW | c.642T>C | p.Asn214Asn | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/8 | 660/906 | 642/813 | 214/270 | chr1 | 21984331 | |||
| chr1:21986668 | T | C | 16 | a0001c0001 a0001c0003 a0001c0011 others(13): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
synonymous_variant | LOW | c.780T>C | p.Ile260Ile | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/8 | 798/906 | 780/813 | 260/270 | chr1 | 21986668 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:21989302 | C | T | 1 | a0001c0001t0001 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*23C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 8/8 | 23 | chr1 | 21989302 | ||||||
| chr1:21989307 | C | T | 1 | a0002c0002t0001 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 8/8 | 28 | chr1 | 21989307 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:21977092 | C | A | 1 | a0007c0009t0001g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.43+10C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977092 | |||||||
| chr1:21977100 | G | C | 7 | a0001c0003t0001g0020 a0001c0003t0001g0051 a0001c0003t0001g0052 others(4): Show |
10 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+18G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977100 | |||||||
| chr1:21977209 | C | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(80): Show |
201 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.43+127C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977209 | |||||||
| chr1:21977226 | G | A | 1 | a0002c0002t0001g0018 | 5 | HG02109.hp1 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.43+144G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977226 | |||||||
| chr1:21977339 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.43+257G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977339 | |||||||
| chr1:21977353 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.43+271G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977353 | |||||||
| chr1:21977354 | C | A | 1 | a0001c0001t0001g0031 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.43+272C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977354 | |||||||
| chr1:21977428 | C | G | 31 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(28): Show |
53 | HG00438.hp1 HG00673.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.43+346C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977428 | |||||||
| chr1:21977474 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0057 a0001c0001t0001g0058 others(1): Show |
6 | HG01943.hp2 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+392G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977474 | |||||||
| chr1:21977511 | G | A | 2 | a0001c0001t0001g0111 a0013c0019t0001g0088 |
2 | HG01106.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.43+429G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977511 | |||||||
| chr1:21977603 | T | C | 1 | a0002c0002t0001g0112 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.43+521T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977603 | |||||||
| chr1:21977649 | T | A | 18 | a0001c0001t0001g0031 a0001c0003t0001g0006 a0001c0003t0001g0016 others(15): Show |
44 | HG00140.hp2 HG00597.hp2 HG02004.hp2 others(41): Show |
intron_variant | MODIFIER | c.43+567T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977649 | |||||||
| chr1:21977736 | T | C | 17 | a0001c0001t0001g0031 a0001c0003t0001g0006 a0001c0003t0001g0016 others(14): Show |
43 | HG00140.hp2 HG00597.hp2 HG02080.hp2 others(40): Show |
intron_variant | MODIFIER | c.44-633T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977736 | |||||||
| chr1:21977771 | C | T | 1 | a0001c0003t0001g0064 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.44-598C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977771 | |||||||
| chr1:21977779 | G | T | 58 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(55): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.44-590G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977779 | |||||||
| chr1:21977790 | T | C | 69 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(66): Show |
162 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.44-579T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977790 | |||||||
| chr1:21977914 | GC | G | 68 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(65): Show |
161 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.44-452delC | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 21977914 | ||||||
| chr1:21977935 | C | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.44-434C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977935 | |||||||
| chr1:21977936 | C | T | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.44-433C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977936 | |||||||
| chr1:21977938 | G | C | 17 | a0001c0001t0001g0031 a0001c0003t0001g0006 a0001c0003t0001g0016 others(14): Show |
43 | HG00140.hp2 HG00597.hp2 HG02080.hp2 others(40): Show |
intron_variant | MODIFIER | c.44-431G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977938 | |||||||
| chr1:21977961 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.44-408G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977961 | |||||||
| chr1:21977970 | A | G | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.44-399A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21977970 | |||||||
| chr1:21978092 | T | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(90): Show |
220 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.44-277T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21978092 | |||||||
| chr1:21978175 | G | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(65): Show |
161 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.44-194G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21978175 | |||||||
| chr1:21978178 | T | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(65): Show |
161 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.44-191T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21978178 | |||||||
| chr1:21978219 | A | G | 70 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(67): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.44-150A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21978219 | |||||||
| chr1:21978248 | G | A | 1 | a0001c0001t0001g0045 | 2 | HG00642.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.44-121G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21978248 | |||||||
| chr1:21978290 | C | T | 33 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(30): Show |
55 | HG00438.hp1 HG00673.hp2 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.44-79C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21978290 | |||||||
| chr1:21978297 | G | C | 1 | a0001c0001t0001g0034 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.44-72G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21978297 | |||||||
| chr1:21978338 | C | A | 44 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(41): Show |
92 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.44-31C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 1/7 | chr1 | 21978338 | |||||||
| chr1:21978487 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.129+33C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978487 | |||||||
| chr1:21978519 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.129+65G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978519 | |||||||
| chr1:21978604 | C | T | 3 | a0002c0006t0001g0043 a0002c0006t0001g0128 a0002c0006t0001g0129 |
4 | HG02109.hp2 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+150C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978604 | |||||||
| chr1:21978605 | G | A | 19 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0002c0002t0001g0001 others(16): Show |
67 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.129+151G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978605 | |||||||
| chr1:21978635 | C | G | 1 | a0012c0022t0001g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.129+181C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978635 | |||||||
| chr1:21978661 | G | T | 1 | a0001c0003t0001g0040 | 2 | NA18995.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.129+207G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978661 | |||||||
| chr1:21978682 | A | G | 1 | a0012c0022t0001g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.129+228A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978682 | |||||||
| chr1:21978722 | C | A | 4 | a0001c0003t0001g0020 a0001c0003t0001g0051 a0001c0003t0001g0052 others(1): Show |
6 | HG02615.hp1 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+268C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978722 | |||||||
| chr1:21978737 | A | C | 1 | a0007c0009t0001g0136 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.129+283A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978737 | |||||||
| chr1:21978784 | A | T | 1 | a0002c0002t0001g0123 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.129+330A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978784 | |||||||
| chr1:21978793 | A | T | 1 | a0002c0002t0001g0123 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.129+339A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978793 | |||||||
| chr1:21978796 | G | A | 1 | a0002c0002t0001g0123 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.129+342G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978796 | |||||||
| chr1:21978825 | T | C | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.129+371T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978825 | |||||||
| chr1:21978857 | G | A | 1 | a0001c0003t0001g0051 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.129+403G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978857 | |||||||
| chr1:21978874 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.129+420G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978874 | |||||||
| chr1:21978903 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG00099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.129+449C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978903 | |||||||
| chr1:21978909 | C | T | 4 | a0001c0003t0001g0020 a0001c0003t0001g0051 a0001c0003t0001g0052 others(1): Show |
6 | HG02615.hp1 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+455C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21978909 | |||||||
| chr1:21979001 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.129+547C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979001 | |||||||
| chr1:21979014 | T | A | 1 | a0001c0001t0001g0046 | 2 | HG03017.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.129+560T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979014 | |||||||
| chr1:21979047 | C | CA | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.129+602dupA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979047 | ||||||
| chr1:21979133 | C | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.129+679C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979133 | |||||||
| chr1:21979134 | A | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.129+680A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979134 | |||||||
| chr1:21979135 | C | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.129+681C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979135 | |||||||
| chr1:21979136 | A | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.129+682A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979136 | |||||||
| chr1:21979144 | C | T | 1 | a0002c0006t0001g0043 | 2 | HG02109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.129+690C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979144 | |||||||
| chr1:21979158 | T | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.129+704T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979158 | |||||||
| chr1:21979159 | G | A | 35 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(32): Show |
106 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.129+705G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979159 | |||||||
| chr1:21979165 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.129+711C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979165 | |||||||
| chr1:21979215 | G | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.129+761G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979215 | |||||||
| chr1:21979219 | T | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.129+765T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979219 | |||||||
| chr1:21979232 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.129+778C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979232 | |||||||
| chr1:21979241 | T | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(38): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.129+787T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979241 | |||||||
| chr1:21979298 | G | T | 7 | a0005c0007t0001g0030 a0005c0007t0001g0054 a0005c0007t0001g0055 others(4): Show |
9 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.129+844G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979298 | |||||||
| chr1:21979352 | G | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
10 | HG00609.hp1 HG03041.hp1 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.129+898G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979352 | |||||||
| chr1:21979372 | G | A | 8 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0045 others(5): Show |
24 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.129+918G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979372 | |||||||
| chr1:21979394 | T | C | 1 | a0002c0002t0001g0124 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.129+940T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979394 | |||||||
| chr1:21979413 | C | T | 7 | a0005c0007t0001g0030 a0005c0007t0001g0054 a0005c0007t0001g0055 others(4): Show |
9 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.129+959C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979413 | |||||||
| chr1:21979415 | G | A | 3 | a0004c0005t0002g0027 a0004c0005t0002g0130 a0004c0005t0002g0131 |
5 | HG01243.hp1 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+961G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979415 | |||||||
| chr1:21979422 | C | T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(38): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.129+968C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979422 | |||||||
| chr1:21979443 | CTTTTCTT others(6): Show |
C | 1 | a0001c0001t0001g0089 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.129+994_129+1006de others(14): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979443 | ||||||
| chr1:21979446 | TTCTTTTC | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0038 a0001c0001t0001g0087 others(3): Show |
6 | HG02055.hp2 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+994_129+1000de others(8): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979446 | ||||||
| chr1:21979447 | TCTTTTC | T | 28 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(25): Show |
45 | HG00438.hp1 HG00673.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.129+994_129+999del others(6): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979447 | |||||||
| chr1:21979448 | CTTTTCT | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0161 others(2): Show |
11 | HG00609.hp1 HG03041.hp1 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.129+999_129+1004de others(7): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979448 | ||||||
| chr1:21979448 | CTTTTCTT others(7): Show |
C | 1 | a0001c0001t0001g0078 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.129+999_129+1012de others(15): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979448 | ||||||
| chr1:21979449 | TTTTC | T | 4 | a0001c0003t0001g0020 a0001c0003t0001g0051 a0001c0003t0001g0052 others(1): Show |
6 | HG02615.hp1 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+999_129+1002de others(5): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979449 | ||||||
| chr1:21979450 | TTTC | T | 7 | a0001c0001t0001g0031 a0001c0003t0001g0006 a0001c0003t0001g0016 others(4): Show |
13 | HG02080.hp2 HG02135.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.129+999_129+1001de others(4): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979450 | ||||||
| chr1:21979451 | TTC | T | 9 | a0001c0001t0001g0071 a0001c0003t0001g0006 a0001c0003t0001g0032 others(6): Show |
25 | HG00140.hp2 HG00597.hp2 NA18950.hp1 others(22): Show |
intron_variant | MODIFIER | c.129+999_129+1000de others(3): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979451 | ||||||
| chr1:21979452 | TC | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(29): Show |
102 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.129+999delC | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979452 | |||||||
| chr1:21979453 | C | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0084 others(1): Show |
5 | HG02004.hp2 HG03195.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+999C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979453 | |||||||
| chr1:21979453 | CT | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(63): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.129+1016delT | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979453 | ||||||
| chr1:21979453 | CTT | C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0153 a0002c0002t0001g0026 others(7): Show |
13 | HG00597.hp1 HG01167.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.129+1015_129+1016d others(4): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979453 | ||||||
| chr1:21979453 | CTTT | C | 5 | a0001c0001t0001g0142 a0005c0007t0001g0030 a0005c0007t0001g0054 others(2): Show |
7 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.129+1014_129+1016d others(5): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 21979453 | ||||||
| chr1:21979468 | T | G | 1 | a0002c0002t0001g0125 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.129+1014T>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979468 | |||||||
| chr1:21979477 | G | A | 1 | a0015c0020t0001g0165 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.129+1023G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979477 | |||||||
| chr1:21979478 | G | A | 1 | a0003c0004t0001g0090 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.129+1024G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979478 | |||||||
| chr1:21979516 | A | G | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.129+1062A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979516 | |||||||
| chr1:21979549 | T | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.129+1095T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979549 | |||||||
| chr1:21979551 | C | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.129+1097C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979551 | |||||||
| chr1:21979558 | T | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.129+1104T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979558 | |||||||
| chr1:21979566 | C | T | 1 | a0001c0001t0001g0049 | 2 | NA18963.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.129+1112C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979566 | |||||||
| chr1:21979601 | T | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.129+1147T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979601 | |||||||
| chr1:21979666 | C | G | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.130-1158C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979666 | |||||||
| chr1:21979700 | T | C | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.130-1124T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979700 | |||||||
| chr1:21979715 | C | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.130-1109C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979715 | |||||||
| chr1:21979743 | C | T | 13 | a0001c0001t0001g0031 a0001c0003t0001g0006 a0001c0003t0001g0016 others(10): Show |
37 | HG00140.hp2 HG00597.hp2 HG02080.hp2 others(34): Show |
intron_variant | MODIFIER | c.130-1081C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979743 | |||||||
| chr1:21979855 | C | T | 7 | a0005c0007t0001g0030 a0005c0007t0001g0054 a0005c0007t0001g0055 others(4): Show |
9 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.130-969C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979855 | |||||||
| chr1:21979885 | T | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.130-939T>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979885 | |||||||
| chr1:21979978 | A | G | 1 | a0008c0010t0001g0044 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.130-846A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979978 | |||||||
| chr1:21979988 | G | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.130-836G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21979988 | |||||||
| chr1:21980014 | A | AC | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.130-810_130-809ins others(1): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980014 | |||||||
| chr1:21980015 | A | C | 1 | a0001c0001t0001g0084 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.130-809A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980015 | |||||||
| chr1:21980040 | C | G | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.130-784C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980040 | |||||||
| chr1:21980059 | C | T | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.130-765C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980059 | |||||||
| chr1:21980062 | A | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.130-762A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980062 | |||||||
| chr1:21980131 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.130-693C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980131 | |||||||
| chr1:21980134 | G | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0057 others(6): Show |
18 | HG01943.hp2 HG01952.hp1 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.130-690G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980134 | |||||||
| chr1:21980195 | G | C | 1 | a0001c0003t0001g0032 | 2 | NA18986.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.130-629G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980195 | |||||||
| chr1:21980210 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.130-614T>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980210 | |||||||
| chr1:21980217 | C | T | 49 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(46): Show |
97 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.130-607C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980217 | |||||||
| chr1:21980240 | G | A | 8 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0045 others(5): Show |
24 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.130-584G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980240 | |||||||
| chr1:21980277 | C | T | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.130-547C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980277 | |||||||
| chr1:21980297 | T | C | 30 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(27): Show |
51 | HG00438.hp1 HG00673.hp2 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.130-527T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980297 | |||||||
| chr1:21980309 | G | C | 2 | a0002c0002t0001g0025 a0002c0002t0001g0114 |
4 | HG02083.hp2 NA19067.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-515G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980309 | |||||||
| chr1:21980316 | C | T | 17 | a0001c0001t0001g0031 a0001c0003t0001g0006 a0001c0003t0001g0016 others(14): Show |
43 | HG00140.hp2 HG00597.hp2 HG02080.hp2 others(40): Show |
intron_variant | MODIFIER | c.130-508C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980316 | |||||||
| chr1:21980330 | T | C | 2 | a0002c0002t0001g0019 a0014c0016t0001g0132 |
6 | HG01891.hp2 HG02886.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-494T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980330 | |||||||
| chr1:21980339 | C | T | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.130-485C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980339 | |||||||
| chr1:21980344 | C | T | 1 | a0001c0003t0001g0166 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.130-480C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980344 | |||||||
| chr1:21980345 | G | C | 1 | a0012c0022t0001g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.130-479G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980345 | |||||||
| chr1:21980364 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.130-460A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980364 | |||||||
| chr1:21980376 | G | A | 1 | a0002c0002t0001g0114 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.130-448G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980376 | |||||||
| chr1:21980456 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(33): Show |
108 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.130-368G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980456 | |||||||
| chr1:21980462 | A | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.130-362A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980462 | |||||||
| chr1:21980465 | A | G | 1 | a0002c0006t0001g0129 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.130-359A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980465 | |||||||
| chr1:21980484 | C | A | 1 | a0002c0002t0001g0041 | 2 | HG00558.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.130-340C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980484 | |||||||
| chr1:21980492 | G | C | 1 | a0002c0002t0001g0041 | 2 | HG00558.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.130-332G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980492 | |||||||
| chr1:21980510 | C | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0028 others(7): Show |
28 | HG00609.hp1 HG00642.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.130-314C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980510 | |||||||
| chr1:21980511 | G | A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0028 others(7): Show |
28 | HG00609.hp1 HG00642.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.130-313G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980511 | |||||||
| chr1:21980539 | C | G | 47 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(44): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.130-285C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980539 | |||||||
| chr1:21980541 | C | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(44): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.130-283C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980541 | |||||||
| chr1:21980546 | A | G | 47 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(44): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.130-278A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980546 | |||||||
| chr1:21980567 | G | C | 4 | a0001c0003t0001g0020 a0001c0003t0001g0051 a0001c0003t0001g0052 others(1): Show |
6 | HG02615.hp1 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-257G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980567 | |||||||
| chr1:21980589 | G | C | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.130-235G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980589 | |||||||
| chr1:21980666 | A | G | 1 | a0001c0014t0001g0139 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.130-158A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980666 | |||||||
| chr1:21980692 | TC | T | 1 | a0001c0001t0001g0022 | 3 | HG00673.hp1 HG02135.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.130-131delC | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980692 | |||||||
| chr1:21980696 | T | A | 31 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0028 others(28): Show |
84 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.130-128T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980696 | |||||||
| chr1:21980706 | T | C | 36 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(33): Show |
60 | HG00438.hp1 HG00673.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.130-118T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980706 | |||||||
| chr1:21980713 | C | A | 65 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(62): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.130-111C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980713 | |||||||
| chr1:21980714 | G | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(98): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.130-110G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980714 | |||||||
| chr1:21980723 | G | C | 1 | a0008c0010t0001g0044 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.130-101G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980723 | |||||||
| chr1:21980730 | C | A | 23 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0037 others(20): Show |
37 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.130-94C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980730 | |||||||
| chr1:21980759 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(33): Show |
108 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.130-65G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 2/7 | chr1 | 21980759 | |||||||
| chr1:21980985 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.228-53G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 3/7 | chr1 | 21980985 | |||||||
| chr1:21981030 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18990.hp1 | splice_region_variant&intron_variant | LOW | c.228-8G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 3/7 | chr1 | 21981030 | |||||||
| chr1:21981183 | G | C | 1 | a0001c0001t0001g0028 | 3 | HG01069.hp1 HG01071.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.362+11G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981183 | |||||||
| chr1:21981187 | C | T | 1 | a0008c0010t0001g0044 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.362+15C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981187 | |||||||
| chr1:21981215 | C | T | 13 | a0001c0003t0001g0006 a0001c0003t0001g0008 a0001c0003t0001g0032 others(10): Show |
40 | HG00140.hp2 HG00597.hp2 HG02080.hp2 others(37): Show |
intron_variant | MODIFIER | c.362+43C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981215 | |||||||
| chr1:21981216 | A | G | 13 | a0001c0003t0001g0006 a0001c0003t0001g0008 a0001c0003t0001g0032 others(10): Show |
40 | HG00140.hp2 HG00597.hp2 HG02080.hp2 others(37): Show |
intron_variant | MODIFIER | c.362+44A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981216 | |||||||
| chr1:21981250 | T | C | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.362+78T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981250 | |||||||
| chr1:21981262 | G | GTAGGACG others(8): Show |
1 | a0001c0001t0001g0084 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.362+91_362+92insAG others(13): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21981262 | ||||||
| chr1:21981264 | T | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.362+92T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981264 | |||||||
| chr1:21981270 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.362+98G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981270 | |||||||
| chr1:21981270 | G | GTAGGGAC others(9): Show |
136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.362+105_362+106ins others(16): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21981270 | ||||||
| chr1:21981278 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.362+106G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981278 | |||||||
| chr1:21981288 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.362+116G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981288 | |||||||
| chr1:21981336 | A | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.362+164A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981336 | |||||||
| chr1:21981382 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.362+210G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981382 | |||||||
| chr1:21981406 | C | T | 1 | a0015c0020t0001g0165 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.362+234C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981406 | |||||||
| chr1:21981422 | G | A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0028 others(7): Show |
28 | HG00609.hp1 HG00642.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.362+250G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981422 | |||||||
| chr1:21981475 | A | T | 1 | a0001c0001t0001g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.362+303A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981475 | |||||||
| chr1:21981477 | G | T | 1 | a0001c0001t0001g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.362+305G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981477 | |||||||
| chr1:21981479 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.362+307C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981479 | |||||||
| chr1:21981543 | C | A | 11 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0028 others(8): Show |
29 | HG00609.hp1 HG00642.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.362+371C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981543 | |||||||
| chr1:21981667 | C | T | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.362+495C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981667 | |||||||
| chr1:21981671 | C | T | 3 | a0004c0005t0002g0027 a0004c0005t0002g0130 a0004c0005t0002g0131 |
5 | HG01243.hp1 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.362+499C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981671 | |||||||
| chr1:21981672 | G | T | 15 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0101 others(12): Show |
25 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.362+500G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981672 | |||||||
| chr1:21981685 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.362+513G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981685 | |||||||
| chr1:21981691 | G | A | 1 | a0012c0022t0001g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.362+519G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981691 | |||||||
| chr1:21981720 | A | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.362+548A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981720 | |||||||
| chr1:21981728 | CT | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.362+571delT | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21981728 | ||||||
| chr1:21981728 | CTT | C | 7 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0091 others(4): Show |
13 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.362+570_362+571del others(2): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21981728 | ||||||
| chr1:21981842 | C | T | 1 | a0003c0004t0001g0097 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.362+670C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981842 | |||||||
| chr1:21981870 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.362+698C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981870 | |||||||
| chr1:21981875 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.362+703G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981875 | |||||||
| chr1:21981919 | G | A | 1 | a0011c0017t0001g0160 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.362+747G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981919 | |||||||
| chr1:21981927 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.362+755G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981927 | |||||||
| chr1:21981938 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.362+766G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981938 | |||||||
| chr1:21981942 | A | G | 19 | a0001c0001t0001g0057 a0001c0001t0001g0070 a0001c0001t0001g0092 others(16): Show |
21 | HG00099.hp2 HG00438.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.362+770A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981942 | |||||||
| chr1:21981946 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.362+774C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981946 | |||||||
| chr1:21981947 | G | A | 7 | a0001c0001t0001g0057 a0001c0001t0001g0070 a0001c0003t0001g0020 others(4): Show |
9 | HG02300.hp1 HG02615.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.362+775G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981947 | |||||||
| chr1:21981960 | C | T | 3 | a0001c0001t0001g0087 a0002c0002t0001g0019 a0014c0016t0001g0132 |
7 | HG01891.hp2 HG02886.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.362+788C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981960 | |||||||
| chr1:21981967 | T | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0087 others(1): Show |
4 | HG02056.hp1 HG03017.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.362+795T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981967 | |||||||
| chr1:21981976 | C | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.362+804C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981976 | |||||||
| chr1:21981993 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.362+821A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21981993 | |||||||
| chr1:21982000 | C | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.362+828C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982000 | |||||||
| chr1:21982005 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0087 |
8 | HG00738.hp1 HG01167.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.362+833A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982005 | |||||||
| chr1:21982016 | C | T | 3 | a0007c0009t0001g0050 a0007c0009t0001g0135 a0007c0009t0001g0136 |
3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.362+844C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982016 | |||||||
| chr1:21982023 | C | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.362+851C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982023 | |||||||
| chr1:21982054 | A | C | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.362+882A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982054 | |||||||
| chr1:21982095 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.362+923G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982095 | |||||||
| chr1:21982148 | G | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.362+976G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982148 | |||||||
| chr1:21982163 | C | A | 1 | a0001c0001t0001g0134 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.362+991C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982163 | |||||||
| chr1:21982179 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.362+1007G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982179 | |||||||
| chr1:21982211 | A | G | 65 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(62): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.362+1039A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982211 | |||||||
| chr1:21982215 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.362+1043G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982215 | |||||||
| chr1:21982217 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.362+1045C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982217 | |||||||
| chr1:21982279 | C | T | 1 | a0003c0004t0001g0090 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.362+1107C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982279 | |||||||
| chr1:21982301 | G | A | 1 | a0002c0002t0001g0116 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.362+1129G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982301 | |||||||
| chr1:21982314 | A | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.362+1142A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982314 | |||||||
| chr1:21982360 | C | T | 9 | a0001c0003t0001g0020 a0001c0003t0001g0051 a0005c0007t0001g0030 others(6): Show |
13 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.362+1188C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982360 | |||||||
| chr1:21982439 | TA | T | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.363-1247delA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21982439 | ||||||
| chr1:21982440 | A | T | 2 | a0004c0005t0002g0027 a0004c0005t0002g0130 |
3 | HG01243.hp1 HG02257.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.363-1254A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982440 | |||||||
| chr1:21982441 | A | T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0028 others(9): Show |
31 | HG00609.hp1 HG00642.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.363-1253A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982441 | |||||||
| chr1:21982465 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.363-1229C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982465 | |||||||
| chr1:21982490 | T | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(36): Show |
111 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.363-1204T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982490 | |||||||
| chr1:21982498 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.363-1196G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982498 | |||||||
| chr1:21982545 | C | T | 3 | a0004c0005t0002g0027 a0004c0005t0002g0130 a0004c0005t0002g0131 |
5 | HG01243.hp1 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.363-1149C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982545 | |||||||
| chr1:21982596 | C | CA | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.363-1089dupA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21982596 | ||||||
| chr1:21982771 | A | G | 31 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(28): Show |
53 | HG00673.hp2 HG01069.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.363-923A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982771 | |||||||
| chr1:21982791 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.363-903C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982791 | |||||||
| chr1:21982803 | G | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.363-891G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982803 | |||||||
| chr1:21982827 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.363-867G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982827 | |||||||
| chr1:21982844 | AT | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.363-842delT | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21982844 | ||||||
| chr1:21982944 | C | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0031 others(7): Show |
27 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.363-750C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982944 | |||||||
| chr1:21982973 | G | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.363-721G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21982973 | |||||||
| chr1:21983075 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.363-619C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983075 | |||||||
| chr1:21983077 | C | T | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.363-617C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983077 | |||||||
| chr1:21983121 | G | A | 3 | a0005c0007t0001g0030 a0005c0007t0001g0054 a0005c0007t0001g0055 |
4 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-573G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983121 | |||||||
| chr1:21983197 | T | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.363-497T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983197 | |||||||
| chr1:21983213 | A | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.363-481A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983213 | |||||||
| chr1:21983216 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.363-478G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983216 | |||||||
| chr1:21983232 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.363-462G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983232 | |||||||
| chr1:21983312 | G | A | 12 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0028 others(9): Show |
31 | HG00609.hp1 HG00642.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.363-382G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983312 | |||||||
| chr1:21983315 | A | G | 38 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(35): Show |
110 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.363-379A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983315 | |||||||
| chr1:21983354 | CA | C | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.363-329delA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21983354 | ||||||
| chr1:21983374 | T | A | 7 | a0005c0007t0001g0030 a0005c0007t0001g0054 a0005c0007t0001g0055 others(4): Show |
9 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.363-320T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983374 | |||||||
| chr1:21983381 | T | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.363-313T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983381 | |||||||
| chr1:21983392 | C | T | 1 | a0002c0002t0001g0042 | 2 | NA18942.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.363-302C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983392 | |||||||
| chr1:21983445 | T | C | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.363-249T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983445 | |||||||
| chr1:21983464 | T | C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(62): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.363-230T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983464 | |||||||
| chr1:21983524 | T | C | 1 | a0012c0022t0001g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.363-170T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983524 | |||||||
| chr1:21983525 | G | C | 1 | a0012c0022t0001g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.363-169G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983525 | |||||||
| chr1:21983548 | A | AATG | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.363-129_363-127dup others(3): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21983548 | ||||||
| chr1:21983548 | A | AATGATGA others(2): Show |
3 | a0007c0009t0001g0050 a0007c0009t0001g0135 a0007c0009t0001g0136 |
3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.363-135_363-127dup others(9): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21983548 | ||||||
| chr1:21983548 | A | AATGATGA others(5): Show |
1 | a0008c0010t0001g0044 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.363-138_363-127dup others(12): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 21983548 | ||||||
| chr1:21983587 | G | A | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.363-107G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983587 | |||||||
| chr1:21983634 | G | A | 6 | a0005c0007t0001g0030 a0005c0007t0001g0054 a0005c0007t0001g0055 others(3): Show |
7 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.363-60G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983634 | |||||||
| chr1:21983646 | T | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.363-48T>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983646 | |||||||
| chr1:21983652 | C | T | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.363-42C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983652 | |||||||
| chr1:21983671 | C | T | 1 | a0002c0002t0001g0121 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.363-23C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 4/7 | chr1 | 21983671 | |||||||
| chr1:21983911 | C | T | 3 | a0004c0005t0002g0027 a0004c0005t0002g0130 a0004c0005t0002g0131 |
5 | HG01243.hp1 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.499+81C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21983911 | |||||||
| chr1:21983918 | A | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.499+88A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21983918 | |||||||
| chr1:21983920 | A | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.499+90A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21983920 | |||||||
| chr1:21983973 | C | G | 1 | a0002c0002t0001g0120 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.499+143C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21983973 | |||||||
| chr1:21983977 | A | C | 1 | a0001c0001t0001g0089 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.499+147A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21983977 | |||||||
| chr1:21983981 | C | T | 1 | a0001c0003t0001g0033 | 2 | NA18990.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.499+151C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21983981 | |||||||
| chr1:21984014 | T | A | 1 | a0001c0001t0001g0161 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.500-175T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21984014 | |||||||
| chr1:21984026 | G | A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0031 others(7): Show |
27 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.500-163G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21984026 | |||||||
| chr1:21984049 | A | G | 1 | a0001c0001t0001g0038 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.500-140A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21984049 | |||||||
| chr1:21984095 | A | G | 1 | a0015c0020t0001g0165 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.500-94A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21984095 | |||||||
| chr1:21984113 | C | T | 3 | a0007c0009t0001g0050 a0007c0009t0001g0135 a0007c0009t0001g0136 |
3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.500-76C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21984113 | |||||||
| chr1:21984168 | C | A | 1 | a0002c0002t0001g0117 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.500-21C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21984168 | |||||||
| chr1:21984169 | G | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.500-20G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21984169 | |||||||
| chr1:21984181 | C | T | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
splice_region_variant&intron_variant | LOW | c.500-8C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 5/7 | chr1 | 21984181 | |||||||
| chr1:21984354 | G | C | 1 | a0012c0022t0001g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.642+23G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984354 | |||||||
| chr1:21984440 | C | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.642+109C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984440 | |||||||
| chr1:21984502 | G | C | 3 | a0007c0009t0001g0050 a0007c0009t0001g0135 a0007c0009t0001g0136 |
3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.642+171G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984502 | |||||||
| chr1:21984518 | G | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.642+187G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984518 | |||||||
| chr1:21984544 | A | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0096 |
9 | HG01070.hp2 HG01071.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.642+213A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984544 | |||||||
| chr1:21984566 | G | C | 99 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(96): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.642+235G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984566 | |||||||
| chr1:21984590 | C | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0110 |
5 | HG00099.hp1 HG00741.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.642+259C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984590 | |||||||
| chr1:21984622 | C | A | 1 | a0008c0010t0001g0044 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.642+291C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984622 | |||||||
| chr1:21984634 | G | T | 2 | a0001c0003t0001g0040 a0001c0003t0001g0113 |
3 | NA18950.hp1 NA18995.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.642+303G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984634 | |||||||
| chr1:21984747 | G | C | 7 | a0005c0007t0001g0030 a0005c0007t0001g0054 a0005c0007t0001g0055 others(4): Show |
9 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.642+416G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984747 | |||||||
| chr1:21984816 | C | T | 4 | a0001c0003t0001g0020 a0001c0003t0001g0051 a0001c0003t0001g0052 others(1): Show |
6 | HG02615.hp1 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.642+485C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984816 | |||||||
| chr1:21984855 | G | A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0029 others(18): Show |
56 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.642+524G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984855 | |||||||
| chr1:21984866 | G | C | 1 | a0001c0001t0001g0028 | 3 | HG01069.hp1 HG01071.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.642+535G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984866 | |||||||
| chr1:21984920 | C | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.642+589C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984920 | |||||||
| chr1:21984925 | C | T | 1 | a0012c0022t0001g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.642+594C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984925 | |||||||
| chr1:21984947 | A | C | 2 | a0001c0003t0001g0016 a0001c0003t0001g0060 |
7 | HG02615.hp2 HG02723.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.642+616A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984947 | |||||||
| chr1:21984953 | A | T | 1 | a0002c0002t0001g0127 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.642+622A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21984953 | |||||||
| chr1:21985016 | A | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.642+685A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985016 | |||||||
| chr1:21985061 | C | T | 1 | a0001c0003t0001g0166 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.642+730C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985061 | |||||||
| chr1:21985063 | T | C | 4 | a0007c0009t0001g0050 a0007c0009t0001g0135 a0007c0009t0001g0136 others(1): Show |
5 | HG01515.hp2 HG01517.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.642+732T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985063 | |||||||
| chr1:21985130 | T | A | 68 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(65): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.642+799T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985130 | |||||||
| chr1:21985149 | G | A | 4 | a0007c0009t0001g0050 a0007c0009t0001g0135 a0007c0009t0001g0136 others(1): Show |
5 | HG01515.hp2 HG01517.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.642+818G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985149 | |||||||
| chr1:21985153 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.642+822C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985153 | |||||||
| chr1:21985163 | G | T | 16 | a0001c0003t0001g0006 a0001c0003t0001g0008 a0001c0003t0001g0016 others(13): Show |
48 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.642+832G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985163 | |||||||
| chr1:21985183 | T | C | 3 | a0007c0009t0001g0050 a0007c0009t0001g0135 a0007c0009t0001g0136 |
3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.642+852T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985183 | |||||||
| chr1:21985189 | G | T | 1 | a0001c0001t0001g0049 | 2 | NA18963.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.642+858G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985189 | |||||||
| chr1:21985274 | T | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.642+943T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985274 | |||||||
| chr1:21985275 | G | A | 17 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0037 others(14): Show |
31 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.642+944G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985275 | |||||||
| chr1:21985280 | C | CT | 60 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(57): Show |
135 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.642+964dupT | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 21985280 | ||||||
| chr1:21985280 | C | CTT | 66 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(63): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.642+963_642+964dup others(2): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 21985280 | ||||||
| chr1:21985280 | CT | C | 6 | a0001c0003t0001g0020 a0001c0003t0001g0051 a0001c0003t0001g0052 others(3): Show |
8 | HG02615.hp1 HG02895.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+964delT | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 21985280 | ||||||
| chr1:21985306 | C | T | 36 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(33): Show |
60 | HG00673.hp2 HG01069.hp2 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.642+975C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985306 | |||||||
| chr1:21985319 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.642+988C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985319 | |||||||
| chr1:21985327 | C | G | 1 | a0001c0001t0001g0151 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.642+996C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985327 | |||||||
| chr1:21985338 | C | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0057 others(6): Show |
18 | HG01943.hp2 HG01952.hp1 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.642+1007C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985338 | |||||||
| chr1:21985383 | T | C | 3 | a0007c0009t0001g0050 a0007c0009t0001g0135 a0007c0009t0001g0136 |
3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.642+1052T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985383 | |||||||
| chr1:21985389 | C | A | 3 | a0007c0009t0001g0050 a0007c0009t0001g0135 a0007c0009t0001g0136 |
3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.642+1058C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985389 | |||||||
| chr1:21985405 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0093 |
3 | HG02818.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.642+1074G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985405 | |||||||
| chr1:21985415 | G | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
253 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(250): Show |
intron_variant | MODIFIER | c.642+1084G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985415 | |||||||
| chr1:21985477 | C | T | 34 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(31): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.643-1054C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985477 | |||||||
| chr1:21985546 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.643-985G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985546 | |||||||
| chr1:21985578 | A | G | 2 | a0002c0002t0001g0025 a0002c0002t0001g0114 |
4 | HG02083.hp2 NA19067.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-953A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985578 | |||||||
| chr1:21985595 | G | GA | 39 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(36): Show |
112 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.643-923dupA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 21985595 | ||||||
| chr1:21985595 | GA | G | 5 | a0001c0003t0001g0157 a0002c0002t0001g0114 a0002c0002t0001g0119 others(2): Show |
6 | HG00735.hp2 HG01255.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-923delA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 21985595 | ||||||
| chr1:21985613 | C | T | 4 | a0004c0005t0002g0027 a0004c0005t0002g0130 a0004c0005t0002g0131 others(1): Show |
6 | HG01243.hp1 HG02004.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-918C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985613 | |||||||
| chr1:21985618 | T | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.643-913T>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985618 | |||||||
| chr1:21985619 | T | C | 1 | a0008c0010t0001g0044 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.643-912T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985619 | |||||||
| chr1:21985638 | T | A | 2 | a0008c0010t0001g0044 a0012c0022t0001g0065 |
3 | HG01515.hp2 HG01517.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.643-893T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985638 | |||||||
| chr1:21985658 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.643-873G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985658 | |||||||
| chr1:21985662 | C | T | 3 | a0007c0009t0001g0050 a0007c0009t0001g0135 a0007c0009t0001g0136 |
3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.643-869C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985662 | |||||||
| chr1:21985666 | C | T | 3 | a0005c0007t0001g0030 a0005c0007t0001g0054 a0005c0007t0001g0055 |
4 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-865C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985666 | |||||||
| chr1:21985676 | G | A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0031 others(7): Show |
27 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.643-855G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985676 | |||||||
| chr1:21985694 | A | G | 38 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(35): Show |
110 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.643-837A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985694 | |||||||
| chr1:21985708 | T | G | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.643-823T>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985708 | |||||||
| chr1:21985726 | C | G | 1 | a0004c0005t0002g0130 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.643-805C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985726 | |||||||
| chr1:21985771 | G | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(35): Show |
110 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.643-760G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985771 | |||||||
| chr1:21985781 | C | T | 3 | a0007c0009t0001g0050 a0007c0009t0001g0135 a0007c0009t0001g0136 |
3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.643-750C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985781 | |||||||
| chr1:21985783 | C | T | 3 | a0005c0007t0001g0030 a0005c0007t0001g0054 a0005c0007t0001g0055 |
4 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-748C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985783 | |||||||
| chr1:21985794 | G | A | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.643-737G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985794 | |||||||
| chr1:21985807 | T | C | 3 | a0004c0005t0002g0027 a0004c0005t0002g0130 a0004c0005t0002g0131 |
5 | HG01243.hp1 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.643-724T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985807 | |||||||
| chr1:21985814 | C | G | 35 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(32): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.643-717C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985814 | |||||||
| chr1:21985832 | C | A | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.643-699C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985832 | |||||||
| chr1:21985848 | G | A | 1 | a0012c0022t0001g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.643-683G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985848 | |||||||
| chr1:21985851 | C | A | 6 | a0004c0005t0002g0027 a0004c0005t0002g0130 a0004c0005t0002g0131 others(3): Show |
8 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.643-680C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985851 | |||||||
| chr1:21985867 | G | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.643-664G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985867 | |||||||
| chr1:21985869 | C | T | 3 | a0007c0009t0001g0050 a0007c0009t0001g0135 a0007c0009t0001g0136 |
3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.643-662C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985869 | |||||||
| chr1:21985877 | C | T | 34 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(31): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.643-654C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985877 | |||||||
| chr1:21985892 | GA | G | 3 | a0004c0005t0002g0027 a0004c0005t0002g0130 a0004c0005t0002g0131 |
5 | HG01243.hp1 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.643-630delA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 21985892 | ||||||
| chr1:21985921 | C | CATT | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.643-610_643-609ins others(3): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985921 | |||||||
| chr1:21985921 | C | T | 1 | a0002c0002t0001g0117 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.643-610C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985921 | |||||||
| chr1:21985926 | T | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.643-605T>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985926 | |||||||
| chr1:21985931 | T | C | 3 | a0004c0005t0002g0027 a0004c0005t0002g0130 a0004c0005t0002g0131 |
5 | HG01243.hp1 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.643-600T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985931 | |||||||
| chr1:21985952 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.643-579A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985952 | |||||||
| chr1:21985962 | T | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.643-569T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985962 | |||||||
| chr1:21985983 | C | T | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.643-548C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985983 | |||||||
| chr1:21985984 | T | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.643-547T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21985984 | |||||||
| chr1:21986009 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.643-522C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986009 | |||||||
| chr1:21986100 | G | A | 3 | a0007c0009t0001g0050 a0007c0009t0001g0135 a0007c0009t0001g0136 |
3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.643-431G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986100 | |||||||
| chr1:21986115 | C | T | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.643-416C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986115 | |||||||
| chr1:21986118 | A | G | 1 | a0001c0003t0001g0166 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.643-413A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986118 | |||||||
| chr1:21986124 | T | G | 34 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(31): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.643-407T>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986124 | |||||||
| chr1:21986174 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(136): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.643-357A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986174 | |||||||
| chr1:21986221 | T | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.643-310T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986221 | |||||||
| chr1:21986225 | T | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.643-306T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986225 | |||||||
| chr1:21986242 | A | G | 1 | a0002c0002t0001g0019 | 5 | HG01891.hp2 HG02922.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-289A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986242 | |||||||
| chr1:21986262 | A | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.643-269A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986262 | |||||||
| chr1:21986300 | C | T | 1 | a0012c0022t0001g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.643-231C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986300 | |||||||
| chr1:21986307 | C | T | 3 | a0007c0009t0001g0050 a0007c0009t0001g0135 a0007c0009t0001g0136 |
3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.643-224C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986307 | |||||||
| chr1:21986308 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.643-223G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986308 | |||||||
| chr1:21986330 | A | T | 65 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(62): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.643-201A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986330 | |||||||
| chr1:21986333 | T | G | 32 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(29): Show |
56 | HG00673.hp2 HG01069.hp2 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.643-198T>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986333 | |||||||
| chr1:21986356 | A | G | 1 | a0001c0001t0001g0029 | 3 | HG01081.hp2 HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.643-175A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986356 | |||||||
| chr1:21986357 | G | C | 5 | a0001c0001t0001g0029 a0004c0005t0002g0027 a0004c0005t0002g0130 others(2): Show |
9 | HG01081.hp2 HG01243.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.643-174G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986357 | |||||||
| chr1:21986440 | T | C | 2 | a0007c0009t0001g0135 a0007c0009t0001g0136 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.643-91T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986440 | |||||||
| chr1:21986505 | C | T | 1 | a0012c0022t0001g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.643-26C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986505 | |||||||
| chr1:21986512 | A | T | 1 | a0001c0001t0001g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.643-19A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986512 | |||||||
| chr1:21986524 | G | T | 20 | a0001c0001t0001g0007 a0001c0001t0001g0138 a0001c0003t0001g0006 others(17): Show |
59 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(56): Show |
splice_region_variant&intron_variant | LOW | c.643-7G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 6/7 | chr1 | 21986524 | |||||||
| chr1:21986704 | C | A | 97 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(94): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.795+21C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21986704 | |||||||
| chr1:21986705 | G | A | 3 | a0005c0007t0001g0030 a0005c0007t0001g0054 a0005c0007t0001g0055 |
4 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.795+22G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21986705 | |||||||
| chr1:21986810 | G | GGGGACGA others(42): Show |
1 | a0002c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.795+132_795+133ins others(49): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21986810 | ||||||
| chr1:21986867 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.795+184T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21986867 | |||||||
| chr1:21986878 | G | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(36): Show |
111 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.795+195G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21986878 | |||||||
| chr1:21986976 | G | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
244 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.795+293G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21986976 | |||||||
| chr1:21987028 | G | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(37): Show |
117 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.795+345G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987028 | |||||||
| chr1:21987051 | C | T | 1 | a0001c0001t0001g0004 | 2 | HG02300.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.795+368C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987051 | |||||||
| chr1:21987067 | A | C | 1 | a0015c0020t0001g0165 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.795+384A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987067 | |||||||
| chr1:21987068 | G | A | 1 | a0015c0020t0001g0165 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.795+385G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987068 | |||||||
| chr1:21987115 | A | G | 1 | a0001c0001t0001g0003 | 2 | HG02027.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.795+432A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987115 | |||||||
| chr1:21987119 | C | A | 1 | a0001c0001t0001g0003 | 2 | HG02027.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.795+436C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987119 | |||||||
| chr1:21987122 | A | G | 1 | a0001c0001t0001g0003 | 2 | HG02027.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.795+439A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987122 | |||||||
| chr1:21987143 | A | C | 1 | a0001c0001t0001g0003 | 2 | HG02027.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.795+460A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987143 | |||||||
| chr1:21987153 | G | A | 4 | a0001c0001t0001g0002 a0007c0009t0001g0050 a0007c0009t0001g0135 others(1): Show |
4 | HG00323.hp2 HG01891.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.795+470G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987153 | |||||||
| chr1:21987153 | GA | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.795+481delA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21987153 | ||||||
| chr1:21987154 | A | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0071 a0001c0001t0001g0147 |
3 | HG00323.hp2 HG01255.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.795+471A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987154 | |||||||
| chr1:21987155 | A | G | 3 | a0007c0009t0001g0050 a0007c0009t0001g0135 a0007c0009t0001g0136 |
3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.795+472A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987155 | |||||||
| chr1:21987163 | A | G | 1 | a0001c0001t0001g0003 | 2 | HG02027.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.795+480A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987163 | |||||||
| chr1:21987184 | A | C | 1 | a0001c0001t0001g0003 | 2 | HG02027.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.795+501A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987184 | |||||||
| chr1:21987185 | G | A | 1 | a0001c0001t0001g0003 | 2 | HG02027.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.795+502G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987185 | |||||||
| chr1:21987196 | A | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.795+513A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987196 | |||||||
| chr1:21987237 | A | G | 2 | a0001c0001t0001g0003 a0012c0022t0001g0065 |
3 | HG02004.hp2 HG02027.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.795+554A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987237 | |||||||
| chr1:21987242 | C | T | 2 | a0001c0001t0001g0003 a0012c0022t0001g0065 |
3 | HG02004.hp2 HG02027.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.795+559C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987242 | |||||||
| chr1:21987332 | A | T | 1 | a0001c0001t0001g0144 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.795+649A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987332 | |||||||
| chr1:21987365 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.795+682C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987365 | |||||||
| chr1:21987427 | A | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.795+744A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987427 | |||||||
| chr1:21987462 | A | T | 1 | a0015c0020t0001g0165 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.795+779A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987462 | |||||||
| chr1:21987466 | AAAG | A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.795+785_795+787del others(3): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21987466 | ||||||
| chr1:21987467 | AAG | A | 20 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0015 others(17): Show |
42 | HG00609.hp1 HG00642.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.795+787_795+788del others(2): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21987467 | ||||||
| chr1:21987519 | T | C | 3 | a0001c0001t0001g0147 a0001c0001t0001g0163 a0001c0003t0001g0032 |
4 | HG01255.hp2 HG03098.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.795+836T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987519 | |||||||
| chr1:21987520 | G | C | 3 | a0001c0001t0001g0147 a0001c0001t0001g0163 a0001c0003t0001g0032 |
4 | HG01255.hp2 HG03098.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.795+837G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987520 | |||||||
| chr1:21987522 | GA | G | 41 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(38): Show |
121 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.795+840delA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987522 | |||||||
| chr1:21987541 | C | T | 1 | a0001c0001t0001g0007 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.795+858C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987541 | |||||||
| chr1:21987543 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.795+860G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987543 | |||||||
| chr1:21987579 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
10 | HG00609.hp1 HG03041.hp1 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.795+896C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987579 | |||||||
| chr1:21987585 | T | A | 14 | a0001c0003t0001g0006 a0001c0003t0001g0008 a0001c0003t0001g0016 others(11): Show |
37 | HG00438.hp1 HG00597.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.795+902T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987585 | |||||||
| chr1:21987594 | A | G | 1 | a0002c0002t0001g0126 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.795+911A>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987594 | |||||||
| chr1:21987609 | C | A | 9 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0031 others(6): Show |
26 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.795+926C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987609 | |||||||
| chr1:21987747 | A | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.795+1064A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987747 | |||||||
| chr1:21987768 | G | C | 5 | a0001c0001t0001g0049 a0001c0001t0001g0109 a0005c0007t0001g0030 others(2): Show |
7 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.795+1085G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987768 | |||||||
| chr1:21987796 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.795+1113C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987796 | |||||||
| chr1:21987797 | T | C | 35 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(32): Show |
58 | HG00673.hp2 HG01069.hp2 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.795+1114T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987797 | |||||||
| chr1:21987892 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.795+1209G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987892 | |||||||
| chr1:21987906 | G | C | 9 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0031 others(6): Show |
26 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.795+1223G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987906 | |||||||
| chr1:21987913 | T | A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0031 others(7): Show |
27 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.795+1230T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987913 | |||||||
| chr1:21987951 | A | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(85): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.795+1268A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987951 | |||||||
| chr1:21987977 | G | A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(43): Show |
135 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.796-1285G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987977 | |||||||
| chr1:21987982 | G | C | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(79): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.796-1280G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987982 | |||||||
| chr1:21987983 | T | C | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(79): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.796-1279T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21987983 | |||||||
| chr1:21988073 | G | A | 35 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(32): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.796-1189G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988073 | |||||||
| chr1:21988095 | C | G | 4 | a0007c0009t0001g0050 a0007c0009t0001g0135 a0007c0009t0001g0136 others(1): Show |
4 | HG01891.hp1 HG02004.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.796-1167C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988095 | |||||||
| chr1:21988157 | C | A | 1 | a0012c0022t0001g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.796-1105C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988157 | |||||||
| chr1:21988157 | C | T | 31 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(28): Show |
51 | HG00673.hp2 HG01069.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.796-1105C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988157 | |||||||
| chr1:21988235 | CA | C | 47 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(44): Show |
91 | HG00438.hp1 HG00597.hp2 HG00673.hp2 others(88): Show |
intron_variant | MODIFIER | c.796-1020delA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21988235 | ||||||
| chr1:21988242 | AC | A | 5 | a0001c0003t0001g0020 a0001c0003t0001g0051 a0001c0003t0001g0052 others(2): Show |
7 | HG02004.hp2 HG02615.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.796-1019delC | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988242 | |||||||
| chr1:21988297 | A | AT | 63 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(60): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.796-965_796-964ins others(1): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988297 | |||||||
| chr1:21988299 | T | A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(38): Show |
120 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.796-963T>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988299 | |||||||
| chr1:21988320 | G | A | 42 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(39): Show |
122 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.796-942G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988320 | |||||||
| chr1:21988341 | C | A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(38): Show |
121 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.796-921C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988341 | |||||||
| chr1:21988357 | C | T | 1 | a0012c0022t0001g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.796-905C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988357 | |||||||
| chr1:21988480 | A | T | 1 | a0001c0001t0001g0002 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.796-782A>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988480 | |||||||
| chr1:21988507 | C | T | 4 | a0001c0001t0001g0111 a0002c0006t0001g0043 a0002c0006t0001g0128 others(1): Show |
5 | HG01106.hp1 HG02109.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.796-755C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988507 | |||||||
| chr1:21988520 | G | A | 2 | a0001c0003t0001g0040 a0001c0003t0001g0113 |
3 | NA18950.hp1 NA18995.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.796-742G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988520 | |||||||
| chr1:21988552 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.796-710C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988552 | |||||||
| chr1:21988570 | G | C | 1 | a0015c0020t0001g0165 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.796-692G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988570 | |||||||
| chr1:21988586 | A | C | 1 | a0001c0001t0001g0086 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.796-676A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988586 | |||||||
| chr1:21988590 | TA | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.796-652delA | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21988590 | ||||||
| chr1:21988590 | TAA | T | 57 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(54): Show |
104 | HG00438.hp1 HG00597.hp2 HG01069.hp2 others(101): Show |
intron_variant | MODIFIER | c.796-653_796-652del others(2): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21988590 | ||||||
| chr1:21988614 | G | A | 9 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0031 others(6): Show |
26 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.796-648G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988614 | |||||||
| chr1:21988745 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.796-517C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988745 | |||||||
| chr1:21988762 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.796-500C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988762 | |||||||
| chr1:21988825 | G | C | 32 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(29): Show |
54 | HG00673.hp2 HG01069.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.796-437G>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988825 | |||||||
| chr1:21988844 | T | C | 1 | a0005c0007t0001g0054 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.796-418T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988844 | |||||||
| chr1:21988904 | C | A | 1 | a0015c0020t0001g0165 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.796-358C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988904 | |||||||
| chr1:21988905 | T | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
426 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(423): Show |
intron_variant | MODIFIER | c.796-357T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988905 | |||||||
| chr1:21988908 | A | C | 2 | a0002c0002t0001g0118 a0015c0020t0001g0165 |
2 | HG02976.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.796-354A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988908 | |||||||
| chr1:21988911 | A | AAT | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.796-344_796-343dup others(2): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21988911 | ||||||
| chr1:21988928 | TATAC | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
247 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.796-314_796-311del others(4): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21988928 | ||||||
| chr1:21988948 | C | CAT | 2 | a0001c0001t0001g0003 a0001c0001t0001g0143 |
3 | HG01258.hp1 HG01516.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.796-306_796-305dup others(2): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21988948 | ||||||
| chr1:21988948 | CAT | C | 3 | a0007c0009t0001g0050 a0007c0009t0001g0135 a0007c0009t0001g0136 |
3 | HG01891.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.796-306_796-305del others(2): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21988948 | ||||||
| chr1:21988960 | C | A | 1 | a0002c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.796-302C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988960 | |||||||
| chr1:21988961 | A | C | 1 | a0002c0002t0001g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.796-301A>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988961 | |||||||
| chr1:21988966 | G | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.796-296G>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988966 | |||||||
| chr1:21988969 | G | A | 13 | a0001c0003t0001g0006 a0001c0003t0001g0008 a0001c0003t0001g0016 others(10): Show |
36 | HG00438.hp1 HG00597.hp2 HG02080.hp2 others(33): Show |
intron_variant | MODIFIER | c.796-293G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21988969 | |||||||
| chr1:21988978 | TAC | T | 2 | a0002c0002t0001g0019 a0014c0016t0001g0132 |
6 | HG01891.hp2 HG02886.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.796-272_796-271del others(2): Show |
CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 21988978 | ||||||
| chr1:21989111 | C | G | 4 | a0001c0003t0001g0020 a0001c0003t0001g0051 a0001c0003t0001g0052 others(1): Show |
6 | HG02615.hp1 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.796-151C>G | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21989111 | |||||||
| chr1:21989153 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.796-109T>C | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21989153 | |||||||
| chr1:21989169 | C | T | 2 | a0005c0007t0001g0054 a0008c0010t0001g0044 |
2 | HG01243.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.796-93C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21989169 | |||||||
| chr1:21989191 | C | T | 9 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0031 others(6): Show |
26 | HG00609.hp1 HG00642.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.796-71C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21989191 | |||||||
| chr1:21989217 | G | A | 2 | a0005c0007t0001g0054 a0008c0010t0001g0044 |
2 | HG01243.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.796-45G>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21989217 | |||||||
| chr1:21989222 | C | T | 4 | a0001c0001t0001g0111 a0002c0006t0001g0043 a0002c0006t0001g0128 others(1): Show |
5 | HG01106.hp1 HG02109.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.796-40C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21989222 | |||||||
| chr1:21989245 | C | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.796-17C>T | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21989245 | |||||||
| chr1:21989249 | C | A | 2 | a0001c0003t0001g0020 a0001c0003t0001g0051 |
3 | HG02895.hp2 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.796-13C>A | CELA3B | ENSG00000219073.8 | transcript | ENST00000337107.11 | protein_coding | 7/7 | chr1 | 21989249 |