Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 794 |
| ensemblid | ENSG00000172137.19 |
| hgncid | 1435 |
| symbol | CALB2 |
| name | calbindin 2 |
| refseq_nuc | NM_001740.5 |
| refseq_prot | NP_001731.2 |
| ensembl_nuc | ENST00000302628.9 |
| ensembl_prot | ENSP00000307508.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 71358723 |
| end | 71390433 |
| strand | + |
| ver | v1.2 |
| region | chr16:71358723-71390433 |
| region5000 | chr16:71353723-71395433 |
| regionname0 | CALB2_chr16_71358723_71390433 |
| regionname5000 | CALB2_chr16_71353723_71395433 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 271 | 383 | 79 | 65 | 185 | 12 | 40 | 145 | CALB2_chr16_71353723_71395433 | CALB2 | MAGPQ others(266): Show |
chr16 | 71353723 | 71395433 |
| a0002 | 0/0 | 271 | 42 | 15 | 11 | 8 | 2 | 6 | 6 | CALB2_chr16_71353723_71395433 | CALB2 | MAGPQ others(266): Show |
chr16 | 71353723 | 71395433 |
| a0003 | 0/0 | 271 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | MAGPQ others(266): Show |
chr16 | 71353723 | 71395433 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 813 | 380 | 78 | 65 | 183 | 12 | 40 | CALB2_chr16_71353723_71395433 | CALB2 | ATGGC others(808): Show |
chr16 | 71353723 | 71395433 | ||
| a0001c0003 | 0/0 | 813 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | ATGGC others(808): Show |
chr16 | 71353723 | 71395433 | ||
| a0001c0004 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | ATGGC others(808): Show |
chr16 | 71353723 | 71395433 | ||
| a0002c0002 | 0/0 | 813 | 42 | 15 | 11 | 8 | 2 | 6 | CALB2_chr16_71353723_71395433 | CALB2 | ATGGC others(808): Show |
chr16 | 71353723 | 71395433 | ||
| a0003c0005 | 0/0 | 813 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | ATGGC others(808): Show |
chr16 | 71353723 | 71395433 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1454 | 267 | 60 | 57 | 112 | 8 | 29 | CALB2_chr16_71353723_71395433 | CALB2 | AGCGC others(1449): Show |
chr16 | 71353723 | 71395433 |
| a0001c0001t0002 | 1/0 | 1454 | 97 | 2 | 8 | 71 | 4 | 11 | CALB2_chr16_71353723_71395433 | CALB2 | AGCGC others(1449): Show |
chr16 | 71353723 | 71395433 |
| a0001c0001t0003 | 0/0 | 1453 | 16 | 16 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | AGCGC others(1448): Show |
chr16 | 71353723 | 71395433 |
| a0001c0003t0001 | 0/0 | 1454 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | AGCGC others(1449): Show |
chr16 | 71353723 | 71395433 |
| a0001c0004t0001 | 0/0 | 1454 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | AGCGC others(1449): Show |
chr16 | 71353723 | 71395433 |
| a0002c0002t0001 | 0/0 | 1454 | 7 | 3 | 2 | 0 | 0 | 2 | CALB2_chr16_71353723_71395433 | CALB2 | AGCGC others(1449): Show |
chr16 | 71353723 | 71395433 |
| a0002c0002t0002 | 0/0 | 1454 | 32 | 11 | 9 | 7 | 2 | 3 | CALB2_chr16_71353723_71395433 | CALB2 | AGCGC others(1449): Show |
chr16 | 71353723 | 71395433 |
| a0002c0002t0004 | 0/0 | 1454 | 3 | 1 | 0 | 1 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | AGCGC others(1449): Show |
chr16 | 71353723 | 71395433 |
| a0003c0005t0002 | 0/0 | 1454 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | AGCGC others(1449): Show |
chr16 | 71353723 | 71395433 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 13 | 1 | 5 | 7 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0003 | 0/0 | 9 | 1 | 2 | 3 | 0 | 3 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 4 | 3 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0130 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0001 | 0/0 | 22 | 0 | 0 | 20 | 0 | 2 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0266 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0003g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0003g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0001c0004t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0002c0002t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| a0003c0005t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0252 | EUR | GBR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | GBR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0195 | EUR | FIN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | FIN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | FIN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0193 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0042 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0042 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0198 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0041 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0041 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0200 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0196 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0040 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0040 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0229 | EUR | IBS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0021 | EUR | IBS | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0063 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0220 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0194 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | CDX | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02165 | hp2 | a0002 | c0002 | t0004 | g0214 | EAS | CDX | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0064 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02622 | hp1 | a0002 | c0002 | t0004 | g0062 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0205 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0288 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0065 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0263 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0207 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0189 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0024 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0024 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0066 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0202 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0067 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0140 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | GWD | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0208 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03669 | hp2 | a0002 | c0002 | t0004 | g0217 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | STU | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0179 | SAS | BEB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0163 | SAS | BEB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0256 | SAS | BEB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0201 | SAS | STU | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | STU | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | STU | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0241 | SAS | STU | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0048 | SAS | STU | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | YRI | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18974 | hp1 | a0001 | c0003 | t0001 | g0098 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18982 | hp2 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0060 | AFR | LWK | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0136 | AFR | LWK | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19066 | hp2 | a0003 | c0005 | t0002 | g0014 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | YRI | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | YRI | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ASW | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ASW | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0028 | EUR | TSI | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | TSI | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0203 | EUR | TSI | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | TSI | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0258 | SAS | GIH | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0209 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | MSL | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | USA | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | USA | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | USA | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0061 | AFR | LWK | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0130 | REF | REF | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0266 | REF | REF | CALB2_chr16_71353723_71395433 | CALB2 | chr16 | 71353723 | 71395433 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71377733 | G | A | 1 | a0002 | 42 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(39): Show |
missense_variant | MODERATE | c.328G>A | p.Ala110Thr | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/11 | 398/1454 | 328/816 | 110/271 | chr16 | 71377733 | |||
| chr16:71389825 | A | G | 1 | a0003 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.776A>G | p.Lys259Arg | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 11/11 | 846/1454 | 776/816 | 259/271 | chr16 | 71389825 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71382754 | C | T | 1 | a0001c0003 | 2 | NA18974.hp1 NA18982.hp2 |
synonymous_variant | LOW | c.378C>T | p.Tyr126Tyr | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 5/11 | 448/1454 | 378/816 | 126/271 | chr16 | 71382754 | |||
| chr16:71383411 | T | C | 1 | a0001c0004 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.444T>C | p.Asp148Asp | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 6/11 | 514/1454 | 444/816 | 148/271 | chr16 | 71383411 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71390003 | T | C | 6 | a0001c0001t0001 a0001c0001t0003 a0001c0003t0001 others(3): Show |
295 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*138T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 11/11 | 138 | chr16 | 71390003 | ||||||
| chr16:71390025 | TG | T | 1 | a0001c0001t0003 | 16 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*166delG | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 11/11 | 166 | INFO_REALIGN_3_PRIME | chr16 | 71390025 | |||||
| chr16:71390137 | C | T | 1 | a0002c0002t0004 | 3 | HG02165.hp2 HG02622.hp1 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*272C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 11/11 | 272 | chr16 | 71390137 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71359202 | C | G | 1 | a0001c0001t0001g0302 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.94+316C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71359202 | |||||||
| chr16:71359409 | C | A | 1 | a0001c0001t0001g0050 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.94+523C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71359409 | |||||||
| chr16:71359488 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0003g0051 |
3 | HG01515.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.94+602G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71359488 | |||||||
| chr16:71359633 | A | G | 1 | a0001c0001t0001g0301 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.94+747A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71359633 | |||||||
| chr16:71359660 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.94+774A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71359660 | |||||||
| chr16:71359787 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.94+901G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71359787 | |||||||
| chr16:71359840 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
5 | HG01433.hp2 HG02109.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+954G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71359840 | |||||||
| chr16:71360310 | G | C | 1 | a0001c0001t0001g0056 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.94+1424G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71360310 | |||||||
| chr16:71360391 | A | T | 1 | a0001c0001t0002g0299 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.94+1505A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71360391 | |||||||
| chr16:71360537 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.94+1651C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71360537 | |||||||
| chr16:71360692 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0295 a0001c0001t0001g0296 others(2): Show |
9 | HG02630.hp1 HG02647.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+1806A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71360692 | |||||||
| chr16:71360838 | G | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 others(6): Show |
16 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.94+1952G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71360838 | |||||||
| chr16:71360849 | T | G | 10 | a0001c0001t0001g0053 a0002c0002t0002g0024 a0002c0002t0002g0060 others(7): Show |
11 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+1963T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71360849 | |||||||
| chr16:71360956 | C | T | 1 | a0002c0002t0002g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.94+2070C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71360956 | |||||||
| chr16:71361010 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.94+2124C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361010 | |||||||
| chr16:71361011 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.94+2125G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361011 | |||||||
| chr16:71361043 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.94+2157A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361043 | |||||||
| chr16:71361229 | C | T | 4 | a0001c0001t0001g0049 a0001c0001t0001g0290 a0001c0001t0001g0291 others(1): Show |
5 | HG01943.hp1 HG01981.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+2343C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361229 | |||||||
| chr16:71361253 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.94+2367G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361253 | |||||||
| chr16:71361322 | C | G | 1 | a0001c0001t0001g0289 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.94+2436C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361322 | |||||||
| chr16:71361483 | C | T | 6 | a0002c0002t0002g0061 a0002c0002t0002g0063 a0002c0002t0002g0064 others(3): Show |
6 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+2597C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361483 | |||||||
| chr16:71361602 | A | G | 1 | a0001c0001t0002g0288 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.94+2716A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361602 | |||||||
| chr16:71361634 | T | C | 1 | a0001c0001t0003g0069 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.94+2748T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361634 | |||||||
| chr16:71361695 | G | A | 1 | a0001c0001t0003g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.94+2809G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361695 | |||||||
| chr16:71361901 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(91): Show |
137 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.94+3015G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361901 | |||||||
| chr16:71361992 | T | C | 223 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(220): Show |
314 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.94+3106T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71361992 | |||||||
| chr16:71362156 | A | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.94+3270A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362156 | |||||||
| chr16:71362163 | C | A | 1 | a0002c0002t0002g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.94+3277C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362163 | |||||||
| chr16:71362183 | C | G | 1 | a0001c0001t0001g0133 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.94+3297C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362183 | |||||||
| chr16:71362232 | A | G | 223 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(220): Show |
314 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.94+3346A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362232 | |||||||
| chr16:71362251 | C | T | 2 | a0001c0001t0001g0219 a0001c0001t0002g0218 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.94+3365C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362251 | |||||||
| chr16:71362269 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(108): Show |
161 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.94+3383A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362269 | |||||||
| chr16:71362370 | C | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 others(6): Show |
16 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.94+3484C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362370 | |||||||
| chr16:71362387 | A | G | 31 | a0001c0001t0001g0053 a0001c0001t0001g0199 a0001c0001t0001g0206 others(28): Show |
37 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.94+3501A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362387 | |||||||
| chr16:71362454 | G | A | 1 | a0002c0002t0002g0193 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.94+3568G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362454 | |||||||
| chr16:71362505 | G | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 others(6): Show |
16 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.94+3619G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362505 | |||||||
| chr16:71362581 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.94+3695C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362581 | |||||||
| chr16:71362758 | G | A | 17 | a0001c0001t0001g0199 a0002c0002t0001g0198 a0002c0002t0001g0200 others(14): Show |
22 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.94+3872G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362758 | |||||||
| chr16:71362759 | G | GCT | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(67): Show |
97 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.94+3880_94+3881dup others(2): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71362759 | ||||||
| chr16:71362774 | T | G | 11 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0053 others(8): Show |
18 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.94+3888T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362774 | |||||||
| chr16:71362943 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | NA18997.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.94+4057G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362943 | |||||||
| chr16:71362998 | A | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(93): Show |
139 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.94+4112A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71362998 | |||||||
| chr16:71363005 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0132 |
7 | HG01884.hp2 HG02965.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+4119C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363005 | |||||||
| chr16:71363011 | C | A | 3 | a0002c0002t0001g0207 a0002c0002t0001g0208 a0002c0002t0001g0209 |
3 | HG02559.hp1 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.94+4125C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363011 | |||||||
| chr16:71363018 | T | C | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(219): Show |
312 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.94+4132T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363018 | |||||||
| chr16:71363057 | G | A | 3 | a0002c0002t0002g0194 a0002c0002t0002g0195 a0002c0002t0002g0196 |
3 | HG00280.hp1 HG01255.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.94+4171G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363057 | |||||||
| chr16:71363200 | C | A | 1 | a0001c0001t0001g0294 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.94+4314C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363200 | |||||||
| chr16:71363342 | T | C | 3 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0002c0002t0002g0140 |
3 | HG03239.hp2 NA18612.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.94+4456T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363342 | |||||||
| chr16:71363440 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.94+4554G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363440 | |||||||
| chr16:71363575 | C | T | 1 | a0002c0002t0002g0205 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.94+4689C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363575 | |||||||
| chr16:71363580 | C | T | 9 | a0002c0002t0002g0024 a0002c0002t0002g0060 a0002c0002t0002g0061 others(6): Show |
10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+4694C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363580 | |||||||
| chr16:71363616 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.94+4730G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363616 | |||||||
| chr16:71363694 | G | C | 7 | a0001c0001t0001g0043 a0001c0001t0001g0221 a0001c0001t0001g0222 others(4): Show |
8 | HG00738.hp2 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.94+4808G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363694 | |||||||
| chr16:71363757 | A | G | 5 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(2): Show |
5 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+4871A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363757 | |||||||
| chr16:71363859 | CTGGGAAC others(6): Show |
C | 1 | a0001c0001t0002g0226 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.94+4975_94+4987del others(13): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71363859 | ||||||
| chr16:71363968 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.94+5082G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363968 | |||||||
| chr16:71363974 | C | T | 13 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0006 others(10): Show |
18 | HG01891.hp2 HG02109.hp2 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.94+5088C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71363974 | |||||||
| chr16:71364028 | C | T | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG00597.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.94+5142C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364028 | |||||||
| chr16:71364057 | C | T | 91 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(88): Show |
134 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.94+5171C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364057 | |||||||
| chr16:71364220 | T | A | 58 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(55): Show |
88 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.94+5334T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364220 | |||||||
| chr16:71364281 | T | A | 9 | a0002c0002t0002g0024 a0002c0002t0002g0060 a0002c0002t0002g0061 others(6): Show |
10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+5395T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364281 | |||||||
| chr16:71364282 | T | G | 9 | a0002c0002t0002g0024 a0002c0002t0002g0060 a0002c0002t0002g0061 others(6): Show |
10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+5396T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364282 | |||||||
| chr16:71364284 | A | G | 9 | a0002c0002t0002g0024 a0002c0002t0002g0060 a0002c0002t0002g0061 others(6): Show |
10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+5398A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364284 | |||||||
| chr16:71364285 | T | C | 9 | a0002c0002t0002g0024 a0002c0002t0002g0060 a0002c0002t0002g0061 others(6): Show |
10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+5399T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364285 | |||||||
| chr16:71364287 | T | G | 9 | a0002c0002t0002g0024 a0002c0002t0002g0060 a0002c0002t0002g0061 others(6): Show |
10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+5401T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364287 | |||||||
| chr16:71364288 | T | C | 9 | a0002c0002t0002g0024 a0002c0002t0002g0060 a0002c0002t0002g0061 others(6): Show |
10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+5402T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364288 | |||||||
| chr16:71364289 | G | T | 9 | a0002c0002t0002g0024 a0002c0002t0002g0060 a0002c0002t0002g0061 others(6): Show |
10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+5403G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364289 | |||||||
| chr16:71364290 | A | ACCAGCC | 9 | a0002c0002t0002g0024 a0002c0002t0002g0060 a0002c0002t0002g0061 others(6): Show |
10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+5405_94+5406ins others(6): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71364290 | ||||||
| chr16:71364300 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0107 |
5 | HG00544.hp1 NA18947.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+5414C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364300 | |||||||
| chr16:71364307 | C | A | 2 | a0001c0001t0001g0219 a0001c0001t0002g0218 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.94+5421C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364307 | |||||||
| chr16:71364492 | C | T | 1 | a0001c0001t0002g0283 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.94+5606C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71364492 | |||||||
| chr16:71365044 | C | T | 1 | a0002c0002t0002g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.94+6158C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365044 | |||||||
| chr16:71365289 | G | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(67): Show |
97 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.94+6403G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365289 | |||||||
| chr16:71365297 | C | T | 1 | a0001c0001t0002g0282 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.94+6411C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365297 | |||||||
| chr16:71365322 | G | C | 1 | a0001c0001t0001g0139 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.94+6436G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365322 | |||||||
| chr16:71365366 | G | A | 3 | a0002c0002t0002g0040 a0002c0002t0002g0041 a0002c0002t0002g0042 |
6 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+6480G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365366 | |||||||
| chr16:71365394 | C | G | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(75): Show |
107 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.94+6508C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365394 | |||||||
| chr16:71365676 | A | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(67): Show |
97 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.95-6477A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365676 | |||||||
| chr16:71365718 | C | G | 1 | a0002c0002t0002g0204 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.95-6435C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365718 | |||||||
| chr16:71365728 | T | A | 1 | a0001c0001t0001g0074 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.95-6425T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365728 | |||||||
| chr16:71365814 | G | A | 4 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0070 others(1): Show |
4 | HG02922.hp2 HG03209.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-6339G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365814 | |||||||
| chr16:71365947 | G | A | 2 | a0002c0002t0002g0197 a0002c0002t0002g0204 |
2 | NA18990.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.95-6206G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365947 | |||||||
| chr16:71365980 | G | A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0050 others(17): Show |
29 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.95-6173G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71365980 | |||||||
| chr16:71366006 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.95-6147T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366006 | |||||||
| chr16:71366020 | CTCTCT | C | 7 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0053 others(4): Show |
9 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-6131_95-6127del others(5): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366020 | ||||||
| chr16:71366022 | C | CTTTTT | 4 | a0001c0001t0001g0002 a0001c0001t0001g0095 a0001c0001t0001g0219 others(1): Show |
4 | HG02071.hp1 HG02165.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-6130_95-6129ins others(5): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | ||||||
| chr16:71366022 | C | CTTTTTTT others(2): Show |
27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(24): Show |
35 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.95-6130_95-6129ins others(9): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | ||||||
| chr16:71366022 | C | CTTTTTTT others(3): Show |
32 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(29): Show |
38 | HG00280.hp2 HG01123.hp2 HG01517.hp1 others(35): Show |
intron_variant | MODIFIER | c.95-6130_95-6129ins others(10): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | ||||||
| chr16:71366022 | C | CTTTTTTT others(4): Show |
11 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(8): Show |
17 | HG00423.hp1 HG00738.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.95-6130_95-6129ins others(11): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | ||||||
| chr16:71366022 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0286 |
3 | HG03688.hp2 NA18949.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.95-6130_95-6129ins others(12): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | ||||||
| chr16:71366022 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0143 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.95-6130_95-6129ins others(13): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | ||||||
| chr16:71366022 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0003g0211 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.95-6130_95-6129ins others(14): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | ||||||
| chr16:71366022 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0085 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.95-6130_95-6129ins others(18): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | ||||||
| chr16:71366022 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0081 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.95-6130_95-6129ins others(19): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | ||||||
| chr16:71366022 | C | CTTTTTTT others(13): Show |
13 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(10): Show |
17 | HG00544.hp1 HG00558.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-6130_95-6129ins others(20): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | ||||||
| chr16:71366022 | C | CTTTTTTT others(14): Show |
46 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(43): Show |
59 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.95-6130_95-6129ins others(21): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | ||||||
| chr16:71366022 | C | CTTTTTTT others(15): Show |
20 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(17): Show |
23 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.95-6130_95-6129ins others(22): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | ||||||
| chr16:71366022 | C | CTTTTTTT others(16): Show |
4 | a0001c0001t0001g0029 a0001c0001t0001g0083 a0001c0001t0001g0088 others(1): Show |
4 | HG01070.hp1 HG01168.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-6130_95-6129ins others(23): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | ||||||
| chr16:71366022 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0001g0074 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.95-6130_95-6129ins others(24): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | ||||||
| chr16:71366022 | C | CTTTTTTT others(18): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0076 a0001c0001t0001g0089 |
3 | HG02155.hp2 HG03688.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.95-6130_95-6129ins others(25): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | ||||||
| chr16:71366022 | C | CTTTTTTT others(20): Show |
1 | a0001c0001t0001g0027 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.95-6130_95-6129ins others(27): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | ||||||
| chr16:71366022 | C | CTTTTTTT others(21): Show |
1 | a0001c0001t0001g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.95-6130_95-6129ins others(28): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366022 | ||||||
| chr16:71366024 | C | CT | 4 | a0001c0001t0002g0001 a0001c0001t0002g0252 a0001c0001t0002g0263 others(1): Show |
6 | HG00140.hp1 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-6109dupT | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | ||||||
| chr16:71366024 | C | CTTTTT | 8 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 others(5): Show |
15 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.95-6113_95-6109dup others(5): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | ||||||
| chr16:71366024 | C | CTTTTTTT others(7): Show |
3 | a0001c0001t0001g0043 a0001c0001t0001g0221 a0001c0001t0001g0225 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-6122_95-6109dup others(14): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | ||||||
| chr16:71366024 | C | CTTTTTTT others(8): Show |
3 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0002c0002t0002g0220 |
3 | HG00738.hp2 HG02055.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.95-6123_95-6109dup others(15): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | ||||||
| chr16:71366024 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.95-6124_95-6109dup others(16): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | ||||||
| chr16:71366024 | C | CTTTTTTT others(14): Show |
6 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0025 others(3): Show |
6 | HG01884.hp2 HG02165.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-6109_95-6108ins others(21): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | ||||||
| chr16:71366024 | C | CTTTTTTT others(15): Show |
2 | a0001c0001t0001g0017 a0001c0001t0003g0006 |
3 | HG02896.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.95-6109_95-6108ins others(22): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | ||||||
| chr16:71366024 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0003g0006 | 3 | HG02258.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.95-6109_95-6108ins others(23): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | ||||||
| chr16:71366024 | C | CTTTTTTT others(17): Show |
3 | a0001c0001t0003g0006 a0001c0001t0003g0215 a0002c0002t0001g0207 |
4 | HG02818.hp1 HG02970.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-6109_95-6108ins others(24): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | ||||||
| chr16:71366024 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0003g0216 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.95-6109_95-6108ins others(25): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | ||||||
| chr16:71366024 | C | CTTTTTTT others(20): Show |
2 | a0001c0001t0001g0290 a0001c0001t0001g0291 |
2 | HG01943.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.95-6109_95-6108ins others(27): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | ||||||
| chr16:71366024 | C | CTTTTTTT others(21): Show |
3 | a0001c0001t0001g0049 a0002c0002t0001g0208 a0002c0002t0001g0209 |
3 | HG02293.hp2 HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.95-6109_95-6108ins others(28): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | ||||||
| chr16:71366024 | C | CTTTTTTT others(22): Show |
1 | a0001c0001t0001g0049 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.95-6109_95-6108ins others(29): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | ||||||
| chr16:71366024 | C | CTTTTTTT others(26): Show |
1 | a0001c0001t0001g0292 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.95-6109_95-6108ins others(33): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | ||||||
| chr16:71366024 | C | T | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
219 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.95-6129C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366024 | |||||||
| chr16:71366024 | CT | C | 6 | a0001c0001t0002g0039 a0001c0001t0002g0072 a0001c0001t0002g0228 others(3): Show |
6 | HG00673.hp1 HG01069.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-6109delT | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366024 | ||||||
| chr16:71366025 | T | TC | 25 | a0001c0001t0001g0199 a0002c0002t0001g0200 a0002c0002t0001g0201 others(22): Show |
31 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.95-6128_95-6127ins others(1): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366025 | |||||||
| chr16:71366026 | T | C | 1 | a0002c0002t0002g0061 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.95-6127T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366026 | |||||||
| chr16:71366027 | T | C | 1 | a0002c0002t0001g0198 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.95-6126T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366027 | |||||||
| chr16:71366127 | C | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 others(5): Show |
15 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.95-6026C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366127 | |||||||
| chr16:71366188 | G | A | 1 | a0002c0002t0004g0214 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.95-5965G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366188 | |||||||
| chr16:71366217 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.95-5936G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366217 | |||||||
| chr16:71366228 | G | A | 142 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(139): Show |
203 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.95-5925G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366228 | |||||||
| chr16:71366324 | C | CT | 23 | a0001c0001t0001g0182 a0001c0001t0001g0199 a0001c0001t0001g0274 others(20): Show |
26 | HG00280.hp1 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.95-5809dupT | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366324 | ||||||
| chr16:71366324 | C | CTT | 6 | a0002c0002t0002g0020 a0002c0002t0002g0042 a0002c0002t0002g0193 others(3): Show |
9 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-5810_95-5809dup others(2): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366324 | ||||||
| chr16:71366338 | T | G | 5 | a0001c0001t0002g0021 a0001c0001t0002g0227 a0001c0001t0002g0228 others(2): Show |
7 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-5815T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366338 | |||||||
| chr16:71366344 | TG | T | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
232 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.95-5808delG | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366344 | |||||||
| chr16:71366344 | TGA | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(15): Show |
27 | HG01109.hp1 HG01256.hp1 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.95-5797_95-5796del others(2): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71366344 | ||||||
| chr16:71366345 | G | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(37): Show |
48 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.95-5808G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366345 | |||||||
| chr16:71366346 | A | T | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
280 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.95-5807A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366346 | |||||||
| chr16:71366532 | T | C | 2 | a0002c0002t0002g0197 a0002c0002t0002g0204 |
2 | NA18990.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.95-5621T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366532 | |||||||
| chr16:71366630 | T | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 others(5): Show |
15 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.95-5523T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366630 | |||||||
| chr16:71366676 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.95-5477G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366676 | |||||||
| chr16:71366830 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.95-5323G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366830 | |||||||
| chr16:71366858 | G | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(86): Show |
132 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.95-5295G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71366858 | |||||||
| chr16:71367055 | G | A | 2 | a0001c0001t0001g0219 a0001c0001t0002g0218 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.95-5098G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367055 | |||||||
| chr16:71367117 | G | T | 5 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(2): Show |
5 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-5036G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367117 | |||||||
| chr16:71367124 | C | T | 19 | a0001c0001t0001g0199 a0002c0002t0001g0198 a0002c0002t0001g0200 others(16): Show |
24 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.95-5029C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367124 | |||||||
| chr16:71367139 | G | A | 1 | a0001c0001t0001g0037 | 2 | HG01517.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.95-5014G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367139 | |||||||
| chr16:71367165 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.95-4988G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367165 | |||||||
| chr16:71367168 | A | G | 7 | a0001c0001t0001g0043 a0001c0001t0001g0221 a0001c0001t0001g0222 others(4): Show |
8 | HG00738.hp2 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-4985A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367168 | |||||||
| chr16:71367274 | G | A | 1 | a0001c0001t0001g0025 | 2 | NA18960.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.95-4879G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367274 | |||||||
| chr16:71367291 | CGTCTTTA others(5): Show |
C | 1 | a0001c0001t0001g0158 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.95-4848_95-4837del others(12): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71367291 | ||||||
| chr16:71367434 | C | A | 1 | a0001c0001t0002g0226 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.95-4719C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367434 | |||||||
| chr16:71367565 | C | G | 1 | a0001c0001t0001g0105 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.95-4588C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367565 | |||||||
| chr16:71367602 | C | T | 4 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0003g0070 others(1): Show |
4 | HG02922.hp2 HG03209.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-4551C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367602 | |||||||
| chr16:71367651 | T | C | 50 | a0001c0001t0001g0183 a0001c0001t0001g0192 a0001c0001t0001g0231 others(47): Show |
75 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.95-4502T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367651 | |||||||
| chr16:71367752 | T | C | 50 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0053 others(47): Show |
63 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.95-4401T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367752 | |||||||
| chr16:71367821 | G | A | 5 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(2): Show |
5 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-4332G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367821 | |||||||
| chr16:71367890 | G | A | 12 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0053 others(9): Show |
14 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.95-4263G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71367890 | |||||||
| chr16:71368038 | G | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.95-4115G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368038 | |||||||
| chr16:71368161 | C | T | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0054 others(3): Show |
8 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-3992C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368161 | |||||||
| chr16:71368423 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.95-3730G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368423 | |||||||
| chr16:71368439 | A | G | 2 | a0001c0001t0001g0219 a0001c0001t0002g0218 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.95-3714A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368439 | |||||||
| chr16:71368506 | A | AAAAATAA others(3): Show |
8 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 others(5): Show |
15 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.95-3637_95-3628dup others(10): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71368506 | ||||||
| chr16:71368612 | G | A | 1 | a0002c0002t0002g0024 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.95-3541G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368612 | |||||||
| chr16:71368642 | G | A | 20 | a0001c0001t0001g0199 a0002c0002t0001g0198 a0002c0002t0001g0200 others(17): Show |
25 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.95-3511G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368642 | |||||||
| chr16:71368704 | T | C | 43 | a0001c0001t0001g0199 a0001c0001t0001g0212 a0001c0001t0001g0213 others(40): Show |
54 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.95-3449T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368704 | |||||||
| chr16:71368718 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.95-3435G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368718 | |||||||
| chr16:71368750 | G | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 others(5): Show |
15 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.95-3403G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368750 | |||||||
| chr16:71368851 | C | T | 2 | a0001c0001t0001g0219 a0001c0001t0002g0218 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.95-3302C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368851 | |||||||
| chr16:71368861 | G | A | 1 | a0001c0001t0001g0286 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.95-3292G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71368861 | |||||||
| chr16:71369025 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.95-3128C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369025 | |||||||
| chr16:71369038 | G | A | 4 | a0001c0001t0003g0006 a0001c0001t0003g0069 a0001c0001t0003g0215 others(1): Show |
9 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-3115G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369038 | |||||||
| chr16:71369096 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.95-3057A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369096 | |||||||
| chr16:71369180 | C | T | 91 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(88): Show |
134 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.95-2973C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369180 | |||||||
| chr16:71369194 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.95-2959G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369194 | |||||||
| chr16:71369332 | C | T | 45 | a0001c0001t0001g0199 a0001c0001t0001g0212 a0001c0001t0001g0213 others(42): Show |
56 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.95-2821C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369332 | |||||||
| chr16:71369399 | C | G | 1 | a0001c0001t0001g0053 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.95-2754C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369399 | |||||||
| chr16:71369422 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0160 a0001c0001t0001g0161 |
6 | NA18941.hp2 NA18946.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-2731G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369422 | |||||||
| chr16:71369561 | T | C | 2 | a0001c0001t0001g0231 a0001c0001t0002g0288 |
2 | HG02698.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.95-2592T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369561 | |||||||
| chr16:71369682 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.95-2471C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369682 | |||||||
| chr16:71369756 | C | A | 1 | a0001c0001t0001g0284 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.95-2397C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369756 | |||||||
| chr16:71369777 | C | CTGA | 9 | a0002c0002t0002g0024 a0002c0002t0002g0060 a0002c0002t0002g0061 others(6): Show |
10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-2376_95-2375ins others(3): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369777 | |||||||
| chr16:71369778 | C | CGAG | 214 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
303 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.95-2374_95-2372dup others(3): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71369778 | ||||||
| chr16:71369778 | C | G | 9 | a0002c0002t0002g0024 a0002c0002t0002g0060 a0002c0002t0002g0061 others(6): Show |
10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-2375C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369778 | |||||||
| chr16:71369915 | C | T | 1 | a0001c0001t0003g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.95-2238C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369915 | |||||||
| chr16:71369931 | A | C | 1 | a0001c0001t0002g0260 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.95-2222A>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369931 | |||||||
| chr16:71369972 | G | A | 4 | a0001c0001t0003g0006 a0001c0001t0003g0069 a0001c0001t0003g0215 others(1): Show |
9 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-2181G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71369972 | |||||||
| chr16:71370106 | A | G | 4 | a0001c0001t0003g0006 a0001c0001t0003g0069 a0001c0001t0003g0215 others(1): Show |
9 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-2047A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71370106 | |||||||
| chr16:71370267 | C | A | 2 | a0001c0001t0002g0039 a0001c0001t0002g0232 |
3 | NA18977.hp1 NA18994.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.95-1886C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71370267 | |||||||
| chr16:71370482 | TA | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 others(9): Show |
19 | HG00741.hp1 HG01109.hp1 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.95-1658delA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 71370482 | ||||||
| chr16:71370484 | A | G | 7 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0053 others(4): Show |
9 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-1669A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71370484 | |||||||
| chr16:71370605 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.95-1548C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71370605 | |||||||
| chr16:71370786 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.95-1367C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71370786 | |||||||
| chr16:71370877 | C | T | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(95): Show |
148 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.95-1276C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71370877 | |||||||
| chr16:71370901 | G | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0290 a0001c0001t0001g0292 |
4 | HG01981.hp2 HG01993.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-1252G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71370901 | |||||||
| chr16:71370940 | T | C | 7 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0053 others(4): Show |
9 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-1213T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71370940 | |||||||
| chr16:71370969 | G | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(84): Show |
130 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.95-1184G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71370969 | |||||||
| chr16:71371015 | C | A | 2 | a0001c0001t0001g0188 a0001c0004t0001g0189 |
2 | HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.95-1138C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71371015 | |||||||
| chr16:71371086 | G | T | 4 | a0001c0001t0003g0006 a0001c0001t0003g0069 a0001c0001t0003g0215 others(1): Show |
9 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-1067G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71371086 | |||||||
| chr16:71371095 | C | T | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(218): Show |
311 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.95-1058C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71371095 | |||||||
| chr16:71371141 | G | A | 1 | a0002c0002t0002g0194 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.95-1012G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71371141 | |||||||
| chr16:71371691 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.95-462C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71371691 | |||||||
| chr16:71371737 | G | T | 1 | a0001c0001t0001g0101 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.95-416G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71371737 | |||||||
| chr16:71371816 | G | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 others(6): Show |
16 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.95-337G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71371816 | |||||||
| chr16:71371881 | C | T | 65 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(62): Show |
92 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.95-272C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71371881 | |||||||
| chr16:71371917 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.95-236G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71371917 | |||||||
| chr16:71372121 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(97): Show |
150 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.95-32C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 1/10 | chr16 | 71372121 | |||||||
| chr16:71372244 | G | A | 1 | a0002c0002t0002g0203 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.171+15G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372244 | |||||||
| chr16:71372249 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.171+20C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372249 | |||||||
| chr16:71372285 | C | T | 5 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(2): Show |
5 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.171+56C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372285 | |||||||
| chr16:71372346 | A | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(78): Show |
115 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.171+117A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372346 | |||||||
| chr16:71372384 | G | A | 42 | a0001c0001t0001g0199 a0001c0001t0001g0212 a0001c0001t0001g0213 others(39): Show |
48 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.171+155G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372384 | |||||||
| chr16:71372425 | G | A | 6 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0219 others(3): Show |
6 | HG02809.hp1 HG02922.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.171+196G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372425 | |||||||
| chr16:71372458 | T | C | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(221): Show |
314 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.171+229T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372458 | |||||||
| chr16:71372478 | G | A | 3 | a0002c0002t0001g0207 a0002c0002t0001g0208 a0002c0002t0001g0209 |
3 | HG02559.hp1 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.171+249G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372478 | |||||||
| chr16:71372488 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.171+259C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372488 | |||||||
| chr16:71372640 | G | A | 31 | a0001c0001t0001g0199 a0002c0002t0001g0198 a0002c0002t0001g0200 others(28): Show |
37 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.171+411G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372640 | |||||||
| chr16:71372700 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(97): Show |
150 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.171+471C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372700 | |||||||
| chr16:71372743 | C | A | 1 | a0001c0001t0001g0079 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.171+514C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372743 | |||||||
| chr16:71372855 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.171+626C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372855 | |||||||
| chr16:71372876 | G | A | 7 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0053 others(4): Show |
9 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.171+647G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71372876 | |||||||
| chr16:71373090 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.171+861T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71373090 | |||||||
| chr16:71373120 | CTG | C | 4 | a0001c0001t0002g0045 a0001c0001t0002g0226 a0001c0001t0002g0261 others(1): Show |
5 | HG02135.hp2 NA19000.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+894_171+895del others(2): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 71373120 | ||||||
| chr16:71373214 | C | G | 1 | a0001c0001t0001g0180 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.171+985C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71373214 | |||||||
| chr16:71373239 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.171+1010C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71373239 | |||||||
| chr16:71373295 | G | A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(96): Show |
149 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.171+1066G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71373295 | |||||||
| chr16:71373408 | T | G | 1 | a0001c0001t0001g0162 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.171+1179T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71373408 | |||||||
| chr16:71373472 | G | C | 7 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0053 others(4): Show |
9 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.171+1243G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71373472 | |||||||
| chr16:71373479 | C | T | 9 | a0002c0002t0002g0024 a0002c0002t0002g0060 a0002c0002t0002g0061 others(6): Show |
10 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.171+1250C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71373479 | |||||||
| chr16:71373622 | T | C | 42 | a0001c0001t0001g0199 a0001c0001t0001g0212 a0001c0001t0001g0213 others(39): Show |
48 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.172-1123T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71373622 | |||||||
| chr16:71373627 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
266 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.172-1118A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71373627 | |||||||
| chr16:71373824 | C | A | 4 | a0001c0001t0003g0006 a0001c0001t0003g0069 a0001c0001t0003g0215 others(1): Show |
9 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-921C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71373824 | |||||||
| chr16:71374092 | G | A | 1 | a0001c0001t0002g0261 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.172-653G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71374092 | |||||||
| chr16:71374147 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0003g0051 |
3 | HG01515.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.172-598G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71374147 | |||||||
| chr16:71374214 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.172-531G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71374214 | |||||||
| chr16:71374384 | G | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(86): Show |
132 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.172-361G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71374384 | |||||||
| chr16:71374462 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.172-283G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71374462 | |||||||
| chr16:71374572 | T | G | 69 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(66): Show |
101 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.172-173T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71374572 | |||||||
| chr16:71374573 | T | G | 1 | a0001c0001t0001g0162 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.172-172T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71374573 | |||||||
| chr16:71374613 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.172-132A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71374613 | |||||||
| chr16:71374624 | A | G | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(73): Show |
108 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.172-121A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 2/10 | chr16 | 71374624 | |||||||
| chr16:71375037 | G | A | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(120): Show |
163 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.261+203G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375037 | |||||||
| chr16:71375066 | C | A | 1 | a0001c0001t0002g0163 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.261+232C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375066 | |||||||
| chr16:71375214 | C | T | 36 | a0002c0002t0001g0179 a0002c0002t0001g0198 a0002c0002t0001g0200 others(33): Show |
42 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.261+380C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375214 | |||||||
| chr16:71375235 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.261+401C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375235 | |||||||
| chr16:71375240 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG03688.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.261+406G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375240 | |||||||
| chr16:71375252 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.261+418T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375252 | |||||||
| chr16:71375306 | A | G | 6 | a0002c0002t0002g0061 a0002c0002t0002g0063 a0002c0002t0002g0064 others(3): Show |
6 | HG02055.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+472A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375306 | |||||||
| chr16:71375324 | G | A | 9 | a0001c0001t0001g0238 a0001c0001t0001g0274 a0001c0001t0002g0071 others(6): Show |
9 | NA18940.hp1 NA18942.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.261+490G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375324 | |||||||
| chr16:71375428 | G | A | 1 | a0001c0001t0003g0215 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.261+594G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375428 | |||||||
| chr16:71375434 | C | T | 8 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0053 others(5): Show |
10 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.261+600C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375434 | |||||||
| chr16:71375442 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.261+608A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375442 | |||||||
| chr16:71375475 | G | A | 1 | a0001c0001t0002g0239 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.261+641G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375475 | |||||||
| chr16:71375476 | C | T | 36 | a0002c0002t0001g0179 a0002c0002t0001g0198 a0002c0002t0001g0200 others(33): Show |
42 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.261+642C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375476 | |||||||
| chr16:71375575 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.261+741G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375575 | |||||||
| chr16:71375739 | G | A | 3 | a0002c0002t0001g0207 a0002c0002t0001g0208 a0002c0002t0001g0209 |
3 | HG02559.hp1 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.261+905G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375739 | |||||||
| chr16:71375893 | G | A | 2 | a0002c0002t0002g0136 a0002c0002t0002g0220 |
2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.261+1059G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71375893 | |||||||
| chr16:71376154 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.261+1320G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71376154 | |||||||
| chr16:71376217 | G | T | 61 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(58): Show |
88 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.261+1383G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71376217 | |||||||
| chr16:71376338 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.262-1329G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71376338 | |||||||
| chr16:71376348 | G | C | 1 | a0001c0001t0001g0289 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.262-1319G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71376348 | |||||||
| chr16:71376455 | G | A | 7 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0053 others(4): Show |
9 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.262-1212G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71376455 | |||||||
| chr16:71376507 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0177 |
5 | NA18965.hp2 NA18966.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.262-1160A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71376507 | |||||||
| chr16:71376535 | G | GCATCCAC others(183): Show |
6 | a0001c0001t0001g0043 a0001c0001t0001g0221 a0001c0001t0001g0222 others(3): Show |
7 | HG00738.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.262-1106_262-917du others(191): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 71376535 | ||||||
| chr16:71376616 | C | A | 1 | a0001c0001t0001g0289 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.262-1051C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71376616 | |||||||
| chr16:71376659 | C | A | 36 | a0002c0002t0001g0179 a0002c0002t0001g0198 a0002c0002t0001g0200 others(33): Show |
42 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.262-1008C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71376659 | |||||||
| chr16:71376714 | TACA | T | 4 | a0001c0001t0002g0021 a0001c0001t0002g0228 a0001c0001t0002g0229 others(1): Show |
6 | HG00735.hp1 HG01169.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.262-950_262-948del others(3): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 71376714 | ||||||
| chr16:71376738 | A | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0049 a0001c0001t0001g0100 others(2): Show |
7 | HG01981.hp2 HG01993.hp1 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.262-929A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71376738 | |||||||
| chr16:71376765 | A | G | 6 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0219 others(3): Show |
6 | HG02809.hp1 HG02922.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.262-902A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71376765 | |||||||
| chr16:71376770 | TACATGCA others(3): Show |
T | 7 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0053 others(4): Show |
9 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.262-889_262-880del others(10): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 71376770 | ||||||
| chr16:71377094 | G | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(58): Show |
88 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.262-573G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71377094 | |||||||
| chr16:71377343 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.262-324A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71377343 | |||||||
| chr16:71377543 | G | T | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
306 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.262-124G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 3/10 | chr16 | 71377543 | |||||||
| chr16:71377896 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.342+149G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71377896 | |||||||
| chr16:71377897 | G | T | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(95): Show |
148 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.342+150G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71377897 | |||||||
| chr16:71378117 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.342+370G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71378117 | |||||||
| chr16:71378383 | TA | T | 21 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
24 | HG01168.hp1 HG01168.hp2 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.342+651delA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71378383 | ||||||
| chr16:71378473 | C | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(86): Show |
132 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.342+726C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71378473 | |||||||
| chr16:71378480 | T | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(71): Show |
107 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.342+733T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71378480 | |||||||
| chr16:71378665 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.342+918T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71378665 | |||||||
| chr16:71378739 | G | A | 1 | a0001c0001t0003g0211 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.342+992G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71378739 | |||||||
| chr16:71378779 | C | T | 38 | a0001c0001t0001g0289 a0001c0001t0002g0236 a0001c0001t0002g0237 others(35): Show |
44 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.342+1032C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71378779 | |||||||
| chr16:71378825 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.342+1078T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71378825 | |||||||
| chr16:71378882 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.342+1135G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71378882 | |||||||
| chr16:71378928 | G | T | 1 | a0001c0001t0001g0159 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.342+1181G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71378928 | |||||||
| chr16:71378985 | T | C | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(80): Show |
116 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.342+1238T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71378985 | |||||||
| chr16:71379033 | T | C | 1 | a0001c0001t0002g0241 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.342+1286T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71379033 | |||||||
| chr16:71379074 | T | C | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
317 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.342+1327T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71379074 | |||||||
| chr16:71379232 | G | A | 2 | a0002c0002t0002g0136 a0002c0002t0002g0220 |
2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.342+1485G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71379232 | |||||||
| chr16:71379271 | T | TAATA | 14 | a0001c0001t0001g0058 a0001c0001t0001g0107 a0001c0001t0001g0126 others(11): Show |
15 | HG00544.hp1 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.342+1567_342+1570d others(6): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71379271 | ||||||
| chr16:71379271 | TAATA | T | 78 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0053 others(75): Show |
111 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.342+1567_342+1570d others(6): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71379271 | ||||||
| chr16:71379271 | TAATAAAT others(1): Show |
T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(71): Show |
105 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.342+1563_342+1570d others(10): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71379271 | ||||||
| chr16:71379271 | TAATAAAT others(5): Show |
T | 2 | a0001c0001t0002g0071 a0001c0001t0002g0072 |
2 | NA18961.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.342+1559_342+1570d others(14): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71379271 | ||||||
| chr16:71379402 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.342+1655T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71379402 | |||||||
| chr16:71379416 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.342+1669T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71379416 | |||||||
| chr16:71379580 | C | T | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(87): Show |
133 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.342+1833C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71379580 | |||||||
| chr16:71379649 | C | T | 5 | a0001c0001t0002g0047 a0001c0001t0002g0264 a0001c0001t0002g0272 others(2): Show |
6 | NA18943.hp2 NA18952.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.342+1902C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71379649 | |||||||
| chr16:71379771 | T | A | 3 | a0002c0002t0001g0207 a0002c0002t0001g0208 a0002c0002t0001g0209 |
3 | HG02559.hp1 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.342+2024T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71379771 | |||||||
| chr16:71379782 | GCAGA | G | 7 | a0001c0001t0001g0036 a0001c0001t0001g0068 a0001c0001t0001g0108 others(4): Show |
8 | HG00733.hp1 HG01074.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.342+2039_342+2042d others(6): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71379782 | ||||||
| chr16:71379789 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.342+2042G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71379789 | |||||||
| chr16:71379818 | G | C | 1 | a0001c0001t0001g0056 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.342+2071G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71379818 | |||||||
| chr16:71379939 | G | GACATTCT others(56): Show |
1 | a0001c0001t0001g0124 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.342+2193_342+2255d others(65): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71379939 | ||||||
| chr16:71380148 | C | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 others(5): Show |
15 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.342+2401C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380148 | |||||||
| chr16:71380148 | C | G | 35 | a0002c0002t0001g0198 a0002c0002t0001g0200 a0002c0002t0001g0201 others(32): Show |
41 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.342+2401C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380148 | |||||||
| chr16:71380156 | G | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(98): Show |
151 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.342+2409G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380156 | |||||||
| chr16:71380160 | G | C | 35 | a0002c0002t0001g0198 a0002c0002t0001g0200 a0002c0002t0001g0201 others(32): Show |
41 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.342+2413G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380160 | |||||||
| chr16:71380205 | T | A | 7 | a0001c0001t0003g0006 a0001c0001t0003g0046 a0001c0001t0003g0069 others(4): Show |
13 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.342+2458T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380205 | |||||||
| chr16:71380221 | T | A | 1 | a0001c0001t0002g0242 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.342+2474T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380221 | |||||||
| chr16:71380254 | ATTTCTTT others(2): Show |
A | 8 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0223 others(5): Show |
10 | HG00735.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.343-2453_343-2445d others(11): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380254 | ||||||
| chr16:71380268 | T | A | 1 | a0002c0002t0002g0220 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.343-2451T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380268 | |||||||
| chr16:71380287 | C | CT | 6 | a0001c0001t0001g0036 a0001c0001t0001g0068 a0001c0001t0001g0108 others(3): Show |
6 | HG00733.hp1 HG01074.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.343-2428dupT | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380287 | ||||||
| chr16:71380287 | CTTTTCTT others(3): Show |
C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0295 others(2): Show |
8 | HG02145.hp2 HG02486.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.343-2427_343-2418d others(12): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380287 | ||||||
| chr16:71380287 | CTTTTCTT others(4): Show |
C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 others(3): Show |
8 | HG01109.hp1 HG02976.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.343-2427_343-2417d others(13): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380287 | ||||||
| chr16:71380287 | CTTTTCTT others(6): Show |
C | 1 | a0001c0001t0001g0052 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.343-2427_343-2415d others(15): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380287 | ||||||
| chr16:71380287 | CTTTTCTT others(7): Show |
C | 12 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(9): Show |
16 | HG00544.hp1 HG00558.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.343-2427_343-2414d others(16): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380287 | ||||||
| chr16:71380287 | CTTTTCTT others(11): Show |
C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0053 others(3): Show |
8 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.343-2427_343-2410d others(20): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380287 | ||||||
| chr16:71380287 | CTTTTCTT others(12): Show |
C | 1 | a0001c0001t0003g0051 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.343-2427_343-2409d others(21): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380287 | ||||||
| chr16:71380288 | TTTTC | T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(27): Show |
32 | HG01069.hp2 HG01071.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.343-2427_343-2424d others(6): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380288 | ||||||
| chr16:71380289 | TTTC | T | 33 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(30): Show |
44 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.343-2427_343-2425d others(5): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380289 | ||||||
| chr16:71380290 | TTC | T | 13 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0031 others(10): Show |
16 | HG01123.hp1 HG01433.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.343-2427_343-2426d others(4): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380290 | ||||||
| chr16:71380291 | TC | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(3): Show |
9 | HG01884.hp2 HG02165.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.343-2427delC | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380291 | |||||||
| chr16:71380292 | C | CT | 16 | a0001c0001t0001g0213 a0001c0001t0001g0231 a0001c0001t0002g0014 others(13): Show |
18 | HG01192.hp1 HG01358.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.343-2392dupT | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | ||||||
| chr16:71380292 | C | T | 9 | a0001c0001t0001g0009 a0001c0001t0001g0036 a0001c0001t0001g0068 others(6): Show |
10 | HG00733.hp1 HG01074.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.343-2427C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380292 | |||||||
| chr16:71380292 | CT | C | 31 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0183 others(28): Show |
37 | HG00438.hp1 HG00544.hp2 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.343-2392delT | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | ||||||
| chr16:71380292 | CTT | C | 33 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0043 others(30): Show |
43 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.343-2393_343-2392d others(4): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | ||||||
| chr16:71380292 | CTTT | C | 28 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(25): Show |
40 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.343-2394_343-2392d others(5): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | ||||||
| chr16:71380292 | CTTTT | C | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(32): Show |
38 | HG00280.hp2 HG00408.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.343-2395_343-2392d others(6): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | ||||||
| chr16:71380292 | CTTTTT | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0155 others(3): Show |
6 | HG01517.hp1 HG02015.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.343-2396_343-2392d others(7): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | ||||||
| chr16:71380292 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0048 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.343-2404_343-2392d others(15): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | ||||||
| chr16:71380292 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0003 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.343-2407_343-2392d others(18): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | ||||||
| chr16:71380292 | CTTTTTTT others(10): Show |
C | 3 | a0002c0002t0002g0063 a0002c0002t0002g0194 a0002c0002t0002g0196 |
3 | HG01255.hp2 HG02055.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.343-2408_343-2392d others(19): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | ||||||
| chr16:71380292 | CTTTTTTT others(11): Show |
C | 29 | a0002c0002t0001g0198 a0002c0002t0001g0200 a0002c0002t0001g0201 others(26): Show |
35 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.343-2409_343-2392d others(20): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | ||||||
| chr16:71380292 | CTTTTTTT others(12): Show |
C | 3 | a0002c0002t0002g0064 a0002c0002t0004g0214 a0002c0002t0004g0217 |
3 | HG02165.hp2 HG02451.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.343-2410_343-2392d others(21): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380292 | ||||||
| chr16:71380387 | C | T | 35 | a0002c0002t0001g0198 a0002c0002t0001g0200 a0002c0002t0001g0201 others(32): Show |
41 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.343-2332C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380387 | |||||||
| chr16:71380456 | GCAC | G | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(87): Show |
133 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.343-2256_343-2254d others(5): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71380456 | ||||||
| chr16:71380536 | G | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(97): Show |
150 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.343-2183G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380536 | |||||||
| chr16:71380583 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG00741.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.343-2136C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380583 | |||||||
| chr16:71380676 | C | G | 35 | a0002c0002t0001g0198 a0002c0002t0001g0200 a0002c0002t0001g0201 others(32): Show |
41 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.343-2043C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380676 | |||||||
| chr16:71380676 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.343-2043C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380676 | |||||||
| chr16:71380706 | C | A | 35 | a0002c0002t0001g0198 a0002c0002t0001g0200 a0002c0002t0001g0201 others(32): Show |
41 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.343-2013C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71380706 | |||||||
| chr16:71381012 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0289 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.343-1707G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381012 | |||||||
| chr16:71381029 | G | A | 21 | a0002c0002t0001g0198 a0002c0002t0001g0200 a0002c0002t0001g0201 others(18): Show |
27 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.343-1690G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381029 | |||||||
| chr16:71381037 | G | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(133): Show |
192 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.343-1682G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381037 | |||||||
| chr16:71381209 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1510G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381209 | |||||||
| chr16:71381210 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1509G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381210 | |||||||
| chr16:71381213 | A | C | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1506A>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381213 | |||||||
| chr16:71381215 | G | C | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1504G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381215 | |||||||
| chr16:71381216 | TCATATTT others(56): Show |
T | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1502_343-1440d others(65): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381216 | |||||||
| chr16:71381282 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1437G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381282 | |||||||
| chr16:71381286 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1433T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381286 | |||||||
| chr16:71381288 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1431T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381288 | |||||||
| chr16:71381292 | A | T | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1427A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381292 | |||||||
| chr16:71381297 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1422G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381297 | |||||||
| chr16:71381303 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1416G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381303 | |||||||
| chr16:71381304 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1415G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381304 | |||||||
| chr16:71381307 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1412T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381307 | |||||||
| chr16:71381308 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1411T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381308 | |||||||
| chr16:71381310 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1409T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381310 | |||||||
| chr16:71381311 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1408T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381311 | |||||||
| chr16:71381313 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1406T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381313 | |||||||
| chr16:71381314 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1405G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381314 | |||||||
| chr16:71381319 | G | C | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1400G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381319 | |||||||
| chr16:71381320 | A | C | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1399A>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381320 | |||||||
| chr16:71381321 | A | T | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1398A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381321 | |||||||
| chr16:71381327 | A | T | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1392A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381327 | |||||||
| chr16:71381328 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0002g0260 |
2 | HG00639.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.343-1391C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381328 | |||||||
| chr16:71381329 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1390T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381329 | |||||||
| chr16:71381331 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1388T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381331 | |||||||
| chr16:71381333 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1386G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381333 | |||||||
| chr16:71381336 | A | T | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1383A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381336 | |||||||
| chr16:71381337 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1382T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381337 | |||||||
| chr16:71381342 | T | C | 2 | a0001c0001t0002g0243 a0001c0001t0002g0259 |
2 | NA18959.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.343-1377T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381342 | |||||||
| chr16:71381387 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-1332G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381387 | |||||||
| chr16:71381409 | C | CA | 46 | a0001c0001t0001g0043 a0001c0001t0001g0137 a0001c0001t0001g0145 others(43): Show |
53 | HG00280.hp1 HG00597.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.343-1294dupA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71381409 | ||||||
| chr16:71381409 | CA | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(95): Show |
148 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.343-1294delA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71381409 | ||||||
| chr16:71381491 | A | G | 35 | a0002c0002t0001g0198 a0002c0002t0001g0200 a0002c0002t0001g0201 others(32): Show |
41 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.343-1228A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381491 | |||||||
| chr16:71381496 | G | A | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(63): Show |
93 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.343-1223G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381496 | |||||||
| chr16:71381583 | G | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0221 a0001c0001t0001g0222 others(3): Show |
7 | HG00738.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.343-1136G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381583 | |||||||
| chr16:71381603 | A | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(156): Show |
223 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.343-1116A>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381603 | |||||||
| chr16:71381603 | A | T | 1 | a0001c0001t0001g0289 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.343-1116A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381603 | |||||||
| chr16:71381682 | G | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(87): Show |
133 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.343-1037G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381682 | |||||||
| chr16:71381691 | G | A | 4 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(1): Show |
4 | NA18942.hp2 NA18973.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-1028G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381691 | |||||||
| chr16:71381737 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.343-982G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381737 | |||||||
| chr16:71381748 | T | G | 35 | a0002c0002t0001g0198 a0002c0002t0001g0200 a0002c0002t0001g0201 others(32): Show |
41 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.343-971T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381748 | |||||||
| chr16:71381873 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.343-846C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381873 | |||||||
| chr16:71381905 | C | T | 15 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(12): Show |
21 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.343-814C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71381905 | |||||||
| chr16:71382016 | A | AGAGGAG | 18 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0050 others(15): Show |
27 | HG00738.hp1 HG00741.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.343-681_343-676dup others(6): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382016 | ||||||
| chr16:71382016 | A | AGAGGAGG others(2): Show |
41 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(38): Show |
59 | HG00408.hp1 HG00423.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.343-684_343-676dup others(9): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382016 | ||||||
| chr16:71382016 | A | AGAGGAGG others(5): Show |
4 | a0001c0001t0001g0165 a0001c0001t0001g0185 a0001c0001t0001g0186 others(1): Show |
4 | HG00597.hp1 HG00609.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-687_343-676dup others(12): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382016 | ||||||
| chr16:71382016 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.343-703A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382016 | |||||||
| chr16:71382016 | AGAG | A | 195 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(192): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.343-678_343-676del others(3): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382016 | ||||||
| chr16:71382026 | G | A | 1 | a0001c0001t0002g0245 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.343-693G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382026 | |||||||
| chr16:71382026 | GAGGAGGA others(11): Show |
G | 1 | a0001c0001t0001g0109 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.343-678_343-661del others(18): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382026 | ||||||
| chr16:71382032 | GAGGAGGA others(5): Show |
G | 2 | a0001c0001t0001g0188 a0001c0004t0001g0189 |
2 | HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.343-675_343-664del others(12): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382032 | ||||||
| chr16:71382041 | G | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 others(6): Show |
16 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.343-678G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382041 | |||||||
| chr16:71382041 | G | T | 2 | a0001c0001t0002g0071 a0001c0001t0002g0072 |
2 | NA18961.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.343-678G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382041 | |||||||
| chr16:71382044 | T | G | 5 | a0001c0001t0001g0056 a0001c0001t0001g0153 a0001c0001t0002g0071 others(2): Show |
5 | HG03225.hp1 NA18961.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-675T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382044 | |||||||
| chr16:71382050 | G | T | 1 | a0001c0001t0001g0153 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.343-669G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382050 | |||||||
| chr16:71382057 | A | G | 2 | a0001c0001t0002g0071 a0001c0001t0002g0072 |
2 | NA18961.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.343-662A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382057 | |||||||
| chr16:71382059 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.343-660A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382059 | |||||||
| chr16:71382060 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.343-659G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382060 | |||||||
| chr16:71382063 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.343-656G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382063 | |||||||
| chr16:71382069 | G | A | 2 | a0001c0001t0002g0039 a0001c0001t0002g0232 |
3 | NA18977.hp1 NA18994.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.343-650G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382069 | |||||||
| chr16:71382117 | G | C | 21 | a0002c0002t0001g0198 a0002c0002t0001g0200 a0002c0002t0001g0201 others(18): Show |
27 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.343-602G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382117 | |||||||
| chr16:71382122 | A | G | 4 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(1): Show |
4 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-597A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382122 | |||||||
| chr16:71382124 | A | AAAGGAAG others(9): Show |
9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0058 others(6): Show |
16 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.343-576_343-561dup others(16): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382124 | ||||||
| chr16:71382139 | A | AGAAG | 4 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0190 others(1): Show |
4 | HG02451.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-568_343-565dup others(4): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382139 | ||||||
| chr16:71382139 | A | AGAAGGAA others(27): Show |
1 | a0001c0001t0001g0153 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.343-561_343-560ins others(34): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382139 | ||||||
| chr16:71382139 | A | AGAAGGAA others(27): Show |
64 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(61): Show |
91 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.343-561_343-560ins others(34): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382139 | ||||||
| chr16:71382155 | A | AAGGAAGG others(47): Show |
4 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0219 others(1): Show |
4 | HG02809.hp1 NA19043.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-564_343-563ins others(54): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382155 | |||||||
| chr16:71382155 | A | AAGGAAGG others(11): Show |
127 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(124): Show |
176 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.343-564_343-563ins others(18): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382155 | |||||||
| chr16:71382155 | A | AGAAGGAA others(9): Show |
1 | a0001c0001t0001g0289 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.343-561_343-560ins others(16): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382155 | ||||||
| chr16:71382155 | A | AGAAGGAA others(13): Show |
5 | a0001c0001t0003g0006 a0001c0001t0003g0046 a0001c0001t0003g0069 others(2): Show |
11 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.343-561_343-560ins others(20): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382155 | ||||||
| chr16:71382155 | A | AGAAGGAA others(17): Show |
2 | a0001c0001t0003g0070 a0001c0001t0003g0211 |
2 | HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.343-561_343-560ins others(24): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 71382155 | ||||||
| chr16:71382155 | A | G | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0053 others(8): Show |
13 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.343-564A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382155 | |||||||
| chr16:71382161 | T | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(147): Show |
207 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.343-558T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382161 | |||||||
| chr16:71382162 | A | G | 5 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0219 others(2): Show |
5 | HG02809.hp1 HG03195.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-557A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382162 | |||||||
| chr16:71382173 | G | C | 1 | a0001c0001t0003g0216 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.343-546G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382173 | |||||||
| chr16:71382508 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.343-211C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382508 | |||||||
| chr16:71382528 | T | C | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
317 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(314): Show |
intron_variant | MODIFIER | c.343-191T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382528 | |||||||
| chr16:71382531 | C | T | 7 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0053 others(4): Show |
9 | HG01433.hp2 HG01515.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.343-188C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382531 | |||||||
| chr16:71382682 | C | T | 1 | a0001c0001t0002g0244 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.343-37C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 4/10 | chr16 | 71382682 | |||||||
| chr16:71382894 | C | A | 1 | a0001c0001t0001g0148 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.399+119C>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 5/10 | chr16 | 71382894 | |||||||
| chr16:71382934 | G | A | 1 | a0001c0001t0003g0191 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.399+159G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 5/10 | chr16 | 71382934 | |||||||
| chr16:71382966 | AT | A | 45 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(42): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.399+194delT | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 71382966 | ||||||
| chr16:71383003 | C | T | 2 | a0001c0001t0003g0057 a0001c0001t0003g0191 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.399+228C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 5/10 | chr16 | 71383003 | |||||||
| chr16:71383219 | G | A | 7 | a0001c0001t0003g0006 a0001c0001t0003g0046 a0001c0001t0003g0069 others(4): Show |
13 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.400-148G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 5/10 | chr16 | 71383219 | |||||||
| chr16:71383228 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.400-139G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 5/10 | chr16 | 71383228 | |||||||
| chr16:71383241 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.400-126T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 5/10 | chr16 | 71383241 | |||||||
| chr16:71383323 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.400-44G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 5/10 | chr16 | 71383323 | |||||||
| chr16:71383325 | A | ATGCACGA others(141): Show |
1 | a0002c0002t0002g0065 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.400-41_477+29dupTG others(146): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 71383325 | ||||||
| chr16:71383330 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.400-37C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 5/10 | chr16 | 71383330 | |||||||
| chr16:71383476 | G | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0190 |
2 | HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.477+32G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 6/10 | chr16 | 71383476 | |||||||
| chr16:71383492 | C | T | 2 | a0001c0001t0001g0289 a0001c0001t0001g0297 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.477+48C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 6/10 | chr16 | 71383492 | |||||||
| chr16:71383595 | C | T | 47 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(44): Show |
69 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.477+151C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 6/10 | chr16 | 71383595 | |||||||
| chr16:71383860 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(59): Show |
92 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.478-110A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 6/10 | chr16 | 71383860 | |||||||
| chr16:71383880 | C | T | 62 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(59): Show |
89 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.478-90C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 6/10 | chr16 | 71383880 | |||||||
| chr16:71383896 | C | T | 2 | a0002c0002t0004g0214 a0002c0002t0004g0217 |
2 | HG02165.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.478-74C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 6/10 | chr16 | 71383896 | |||||||
| chr16:71383939 | A | G | 4 | a0001c0001t0001g0111 a0002c0002t0001g0207 a0002c0002t0001g0208 others(1): Show |
4 | HG02559.hp1 HG02818.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-31A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 6/10 | chr16 | 71383939 | |||||||
| chr16:71384043 | G | A | 1 | a0001c0001t0002g0047 | 2 | NA18952.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.533+18G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 7/10 | chr16 | 71384043 | |||||||
| chr16:71384388 | T | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0037 others(15): Show |
28 | HG00738.hp1 HG00741.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.573+10T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | chr16 | 71384388 | |||||||
| chr16:71384524 | A | G | 1 | a0002c0002t0002g0195 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.573+146A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | chr16 | 71384524 | |||||||
| chr16:71384533 | A | C | 1 | a0001c0001t0001g0092 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.573+155A>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | chr16 | 71384533 | |||||||
| chr16:71384569 | TA | T | 4 | a0001c0001t0001g0111 a0002c0002t0001g0207 a0002c0002t0001g0208 others(1): Show |
4 | HG02559.hp1 HG02818.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+192delA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | chr16 | 71384569 | |||||||
| chr16:71384618 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.574-165C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | chr16 | 71384618 | |||||||
| chr16:71384659 | CCACA | C | 48 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(45): Show |
69 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.574-117_574-114del others(4): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384659 | ||||||
| chr16:71384669 | A | G | 59 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(56): Show |
86 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.574-114A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | chr16 | 71384669 | |||||||
| chr16:71384686 | T | G | 72 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(69): Show |
98 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.574-97T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | chr16 | 71384686 | |||||||
| chr16:71384687 | G | GCACACAC others(1292): Show |
1 | a0001c0001t0001g0092 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.574-78_574-77insCA others(1297): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1124): Show |
1 | a0002c0002t0002g0065 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1129): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1261): Show |
1 | a0001c0001t0002g0283 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1266): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1263): Show |
1 | a0002c0002t0002g0041 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1268): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1272): Show |
30 | a0001c0001t0001g0111 a0001c0001t0002g0163 a0002c0002t0001g0207 others(27): Show |
35 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1277): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1239): Show |
1 | a0001c0001t0002g0048 | 2 | HG03669.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1244): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1252): Show |
1 | a0001c0001t0002g0281 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1257): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1272): Show |
2 | a0001c0001t0002g0267 a0001c0001t0002g0279 |
2 | NA18971.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1277): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1272): Show |
60 | a0001c0001t0001g0250 a0001c0001t0001g0271 a0001c0001t0001g0276 others(57): Show |
92 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1277): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1261): Show |
1 | a0001c0001t0002g0252 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1266): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1286): Show |
1 | a0001c0001t0001g0284 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1291): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1270): Show |
1 | a0002c0002t0002g0203 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1275): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1272): Show |
1 | a0002c0002t0002g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1277): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1277): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0083 |
4 | NA18947.hp2 NA18967.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1282): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1285): Show |
1 | a0001c0001t0001g0297 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1290): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1272): Show |
1 | a0001c0001t0001g0289 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1277): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1240): Show |
2 | a0001c0001t0001g0166 a0001c0001t0001g0175 |
2 | HG02015.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1245): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1251): Show |
1 | a0001c0001t0001g0160 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1256): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1249): Show |
1 | a0001c0001t0001g0174 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1254): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1256): Show |
1 | a0001c0001t0001g0183 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1261): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1234): Show |
1 | a0001c0001t0001g0169 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1239): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1256): Show |
58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(55): Show |
84 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1261): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1258): Show |
2 | a0001c0001t0001g0167 a0002c0002t0001g0200 |
2 | HG01081.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1263): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1256): Show |
1 | a0001c0001t0001g0170 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1261): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1256): Show |
4 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0164 others(1): Show |
4 | NA18997.hp2 NA19002.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1261): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1286): Show |
2 | a0001c0001t0001g0117 a0001c0001t0001g0131 |
2 | HG00323.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1291): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1299): Show |
17 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0031 others(14): Show |
23 | HG01168.hp1 HG01169.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1304): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1299): Show |
1 | a0001c0001t0001g0290 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1304): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1297): Show |
1 | a0001c0001t0001g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1302): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1275): Show |
3 | a0001c0001t0001g0213 a0001c0001t0001g0219 a0001c0001t0002g0218 |
3 | HG02809.hp1 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1280): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1301): Show |
1 | a0001c0001t0001g0238 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1306): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1263): Show |
1 | a0001c0001t0001g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1268): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1277): Show |
1 | a0001c0001t0001g0015 | 3 | HG01256.hp1 HG01258.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1282): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1290): Show |
1 | a0001c0001t0001g0192 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1295): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1288): Show |
28 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0025 others(25): Show |
46 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1293): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1286): Show |
1 | a0001c0001t0001g0087 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1291): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1284): Show |
1 | a0001c0001t0001g0034 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1289): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1276): Show |
1 | a0001c0001t0003g0191 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1281): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1290): Show |
1 | a0001c0001t0003g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1295): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1288): Show |
2 | a0001c0001t0001g0187 a0001c0001t0001g0190 |
2 | HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1293): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1237): Show |
1 | a0001c0001t0001g0124 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1242): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1284): Show |
2 | a0001c0001t0001g0022 a0001c0001t0001g0210 |
3 | HG01515.hp2 HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1289): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1280): Show |
42 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(39): Show |
62 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1285): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1280): Show |
1 | a0001c0001t0001g0120 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1285): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1278): Show |
1 | a0001c0001t0001g0224 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1283): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1278): Show |
1 | a0001c0001t0001g0115 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1283): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1297): Show |
2 | a0001c0001t0001g0074 a0001c0001t0001g0080 |
2 | HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1302): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1288): Show |
2 | a0001c0001t0001g0030 a0001c0001t0001g0171 |
3 | NA19005.hp1 NA19010.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1293): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1252): Show |
1 | a0001c0001t0001g0186 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1257): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384687 | G | GCACACAC others(1297): Show |
1 | a0001c0001t0001g0091 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.574-83_574-82insTA others(1302): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384687 | ||||||
| chr16:71384692 | C | CACCACAC others(1240): Show |
1 | a0001c0001t0003g0211 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1245): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384692 | ||||||
| chr16:71384692 | C | CACCACAC others(1258): Show |
6 | a0001c0001t0003g0006 a0001c0001t0003g0046 a0001c0001t0003g0051 others(3): Show |
12 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.574-79_574-78insCA others(1263): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384692 | ||||||
| chr16:71384692 | C | CACCACAC others(1238): Show |
1 | a0001c0001t0003g0070 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1243): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384692 | ||||||
| chr16:71384694 | C | CCACACAC others(1286): Show |
1 | a0001c0001t0001g0270 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.574-79_574-78insCA others(1291): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 71384694 | ||||||
| chr16:71384856 | T | C | 2 | a0001c0001t0002g0267 a0001c0001t0002g0279 |
2 | NA18971.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.627+20T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71384856 | |||||||
| chr16:71384880 | C | T | 1 | a0001c0001t0002g0235 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.627+44C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71384880 | |||||||
| chr16:71384933 | G | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0164 others(1): Show |
4 | NA18997.hp2 NA19002.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+97G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71384933 | |||||||
| chr16:71384945 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.627+109C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71384945 | |||||||
| chr16:71385005 | G | A | 4 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0219 others(1): Show |
4 | HG02809.hp1 NA19043.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+169G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71385005 | |||||||
| chr16:71385013 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.627+177A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71385013 | |||||||
| chr16:71385096 | G | A | 19 | a0001c0001t0002g0163 a0002c0002t0002g0020 a0002c0002t0002g0024 others(16): Show |
25 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.627+260G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71385096 | |||||||
| chr16:71385126 | A | G | 2 | a0002c0002t0004g0214 a0002c0002t0004g0217 |
2 | HG02165.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.627+290A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71385126 | |||||||
| chr16:71385199 | T | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(200): Show |
286 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.627+363T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71385199 | |||||||
| chr16:71385204 | A | G | 1 | a0001c0001t0002g0299 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.627+368A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71385204 | |||||||
| chr16:71385246 | G | A | 2 | a0001c0001t0001g0289 a0001c0001t0001g0297 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.628-331G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71385246 | |||||||
| chr16:71385327 | T | C | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
324 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(321): Show |
intron_variant | MODIFIER | c.628-250T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71385327 | |||||||
| chr16:71385349 | C | T | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(68): Show |
97 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.628-228C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71385349 | |||||||
| chr16:71385466 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.628-111C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 9/10 | chr16 | 71385466 | |||||||
| chr16:71385691 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.699+43C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71385691 | |||||||
| chr16:71385692 | A | G | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
282 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.699+44A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71385692 | |||||||
| chr16:71385711 | G | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0131 |
3 | HG00323.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.699+63G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71385711 | |||||||
| chr16:71385795 | T | G | 1 | a0001c0001t0001g0296 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.699+147T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71385795 | |||||||
| chr16:71385932 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.699+284A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71385932 | |||||||
| chr16:71386264 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.699+616C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71386264 | |||||||
| chr16:71386293 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.699+645G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71386293 | |||||||
| chr16:71386296 | G | T | 2 | a0002c0002t0002g0136 a0002c0002t0002g0220 |
2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.699+648G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71386296 | |||||||
| chr16:71386367 | AAGAG | A | 4 | a0001c0001t0001g0111 a0002c0002t0001g0207 a0002c0002t0001g0208 others(1): Show |
4 | HG02559.hp1 HG02818.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.699+723_699+726del others(4): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71386367 | ||||||
| chr16:71386384 | A | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | NA18997.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.699+736A>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71386384 | |||||||
| chr16:71386639 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.699+991G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71386639 | |||||||
| chr16:71386674 | T | A | 63 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(60): Show |
92 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.699+1026T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71386674 | |||||||
| chr16:71386808 | C | T | 2 | a0001c0001t0001g0289 a0001c0001t0001g0297 |
2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.699+1160C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71386808 | |||||||
| chr16:71387022 | G | T | 1 | a0001c0001t0001g0238 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.699+1374G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71387022 | |||||||
| chr16:71387112 | T | C | 1 | a0001c0001t0001g0133 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.699+1464T>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71387112 | |||||||
| chr16:71387271 | G | T | 1 | a0001c0001t0002g0255 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.699+1623G>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71387271 | |||||||
| chr16:71387378 | G | A | 2 | a0001c0001t0003g0191 a0002c0002t0002g0202 |
2 | HG03017.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.699+1730G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71387378 | |||||||
| chr16:71387461 | C | CT | 6 | a0001c0001t0001g0178 a0001c0001t0001g0187 a0001c0001t0001g0190 others(3): Show |
6 | HG00639.hp1 HG02451.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.699+1826dupT | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71387461 | ||||||
| chr16:71387486 | T | A | 1 | a0001c0001t0001g0284 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.699+1838T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71387486 | |||||||
| chr16:71387486 | T | G | 66 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(63): Show |
96 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.699+1838T>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71387486 | |||||||
| chr16:71387672 | A | G | 70 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(67): Show |
100 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.699+2024A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71387672 | |||||||
| chr16:71387802 | G | A | 1 | a0002c0002t0002g0193 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.700-1947G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71387802 | |||||||
| chr16:71388124 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.700-1625G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71388124 | |||||||
| chr16:71388148 | G | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(63): Show |
96 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.700-1601G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71388148 | |||||||
| chr16:71388183 | G | GT | 67 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(64): Show |
97 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.700-1566_700-1565i others(3): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71388183 | |||||||
| chr16:71388334 | C | CA | 68 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(65): Show |
97 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.700-1398dupA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71388334 | ||||||
| chr16:71388334 | CA | C | 30 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(27): Show |
43 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.700-1398delA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71388334 | ||||||
| chr16:71388342 | AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0099 |
2 | HG01070.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.700-1401_700-1392d others(12): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71388342 | ||||||
| chr16:71388346 | A | AAAAAAG | 6 | a0001c0001t0003g0006 a0001c0001t0003g0046 a0001c0001t0003g0069 others(3): Show |
12 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.700-1379_700-1374d others(8): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71388346 | ||||||
| chr16:71388346 | A | AAG | 62 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(59): Show |
82 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.700-1402_700-1401i others(4): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71388346 | ||||||
| chr16:71388431 | C | G | 66 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(63): Show |
96 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.700-1318C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71388431 | |||||||
| chr16:71388600 | C | G | 72 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(69): Show |
98 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.700-1149C>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71388600 | |||||||
| chr16:71388707 | G | A | 2 | a0001c0001t0002g0245 a0001c0001t0002g0283 |
2 | NA18957.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.700-1042G>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71388707 | |||||||
| chr16:71388819 | T | TA | 9 | a0001c0001t0001g0099 a0001c0001t0001g0138 a0001c0001t0003g0006 others(6): Show |
15 | HG01168.hp2 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.700-915dupA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71388819 | ||||||
| chr16:71388819 | TA | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(63): Show |
96 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.700-915delA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71388819 | ||||||
| chr16:71388820 | A | T | 1 | a0002c0002t0002g0193 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.700-929A>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71388820 | |||||||
| chr16:71388997 | C | CA | 9 | a0001c0001t0002g0218 a0001c0001t0002g0233 a0001c0001t0002g0235 others(6): Show |
9 | HG00597.hp2 HG02055.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.700-732dupA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71388997 | ||||||
| chr16:71388997 | CA | C | 26 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0074 others(23): Show |
35 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.700-732delA | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71388997 | ||||||
| chr16:71388997 | CAA | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(183): Show |
260 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.700-733_700-732del others(2): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71388997 | ||||||
| chr16:71389055 | A | G | 214 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
297 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.700-694A>G | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71389055 | |||||||
| chr16:71389187 | C | CAAAATAA others(2): Show |
64 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(61): Show |
94 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.700-547_700-539dup others(9): Show |
CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 71389187 | ||||||
| chr16:71389254 | G | C | 1 | a0001c0001t0002g0248 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.700-495G>C | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71389254 | |||||||
| chr16:71389584 | C | T | 29 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0017 others(26): Show |
43 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.700-165C>T | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71389584 | |||||||
| chr16:71389657 | T | A | 1 | a0001c0001t0002g0249 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.700-92T>A | CALB2 | ENSG00000172137.19 | transcript | ENST00000302628.9 | protein_coding | 10/10 | chr16 | 71389657 |