Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57703 |
| ensemblid | ENSG00000163510.14 |
| hgncid | 29322 |
| symbol | CWC22 |
| name | CWC22 spliceosome associated protein homolog |
| refseq_nuc | NM_020943.3 |
| refseq_prot | NP_065994.1 |
| ensembl_nuc | ENST00000410053.8 |
| ensembl_prot | ENSP00000387006.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 179944876 |
| end | 180007297 |
| strand | - |
| ver | v1.2 |
| region | chr2:179944876-180007297 |
| region5000 | chr2:179939876-180012297 |
| regionname0 | CWC22_chr2_179944876_180007297 |
| regionname5000 | CWC22_chr2_179939876_180012297 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 908 | 186 | 52 | 24 | 82 | 8 | 19 | 64 | CWC22_chr2_179939876_180012297 | CWC22 | MKSSV others(903): Show |
chr2 | 179939876 | 180012297 |
| a0002 | 0/0 | 908 | 82 | 14 | 17 | 44 | 1 | 6 | 37 | CWC22_chr2_179939876_180012297 | CWC22 | MKSSV others(903): Show |
chr2 | 179939876 | 180012297 |
| a0003 | 0/0 | 908 | 64 | 4 | 8 | 48 | 1 | 3 | 39 | CWC22_chr2_179939876_180012297 | CWC22 | MKSSV others(903): Show |
chr2 | 179939876 | 180012297 |
| a0004 | 1/0 | 908 | 29 | 13 | 8 | 0 | 3 | 4 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | MKSSV others(903): Show |
chr2 | 179939876 | 180012297 |
| a0005 | 0/0 | 908 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | MKSSV others(903): Show |
chr2 | 179939876 | 180012297 |
| a0006 | 0/0 | 908 | 3 | 0 | 0 | 2 | 0 | 1 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | MKSSV others(903): Show |
chr2 | 179939876 | 180012297 |
| a0007 | 0/0 | 908 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | MKSSV others(903): Show |
chr2 | 179939876 | 180012297 |
| a0008 | 0/0 | 908 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | MKSSV others(903): Show |
chr2 | 179939876 | 180012297 |
| a0009 | 0/0 | 908 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | MKSSV others(903): Show |
chr2 | 179939876 | 180012297 |
| a0010 | 0/0 | 908 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | MKSSV others(903): Show |
chr2 | 179939876 | 180012297 |
| a0011 | 0/0 | 908 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | MKSSV others(903): Show |
chr2 | 179939876 | 180012297 |
| a0012 | 0/0 | 908 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | MKSSV others(903): Show |
chr2 | 179939876 | 180012297 |
| a0013 | 0/0 | 529 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | MKSSV others(524): Show |
chr2 | 179939876 | 180012297 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2724 | 174 | 41 | 24 | 81 | 8 | 19 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0001c0005 | 0/0 | 2724 | 4 | 4 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0001c0008 | 0/0 | 2724 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0001c0011 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0001c0012 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0001c0014 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0001c0015 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0001c0017 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0001c0022 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0002c0002 | 0/0 | 2724 | 81 | 14 | 17 | 43 | 1 | 6 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0002c0013 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0003c0003 | 0/0 | 2724 | 64 | 4 | 8 | 48 | 1 | 3 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0004c0004 | 1/0 | 2724 | 28 | 12 | 8 | 0 | 3 | 4 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0004c0018 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0005c0007 | 0/0 | 2724 | 3 | 3 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0005c0020 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0006c0006 | 0/0 | 2724 | 3 | 0 | 0 | 2 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0007c0009 | 0/0 | 2724 | 2 | 0 | 2 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0008c0016 | 0/0 | 2724 | 1 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0009c0023 | 0/0 | 2724 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0010c0024 | 0/0 | 2724 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0011c0010 | 0/0 | 2724 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0012c0021 | 0/0 | 2724 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2719): Show |
chr2 | 179939876 | 180012297 | ||
| a0013c0019 | 0/0 | 2748 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | ATGAA others(2743): Show |
chr2 | 179939876 | 180012297 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3524 | 169 | 41 | 22 | 80 | 7 | 18 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0001c0001t0002 | 0/0 | 3524 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0001c0001t0003 | 0/0 | 3524 | 3 | 0 | 1 | 0 | 1 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0001c0001t0006 | 0/0 | 3524 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0001c0005t0001 | 0/0 | 3524 | 4 | 4 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0001c0008t0002 | 0/0 | 3524 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0001c0011t0001 | 0/0 | 3524 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0001c0012t0001 | 0/0 | 3524 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0001c0014t0002 | 0/0 | 3524 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0001c0015t0002 | 0/0 | 3524 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0001c0017t0009 | 0/0 | 3524 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0001c0022t0001 | 0/0 | 3524 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0002c0002t0002 | 0/0 | 3524 | 78 | 14 | 17 | 41 | 1 | 5 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0002c0002t0007 | 0/0 | 3524 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0002c0002t0008 | 0/0 | 3524 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0002c0002t0010 | 0/0 | 3524 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AGCTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0002c0013t0002 | 0/0 | 3524 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0003c0003t0002 | 0/0 | 3524 | 62 | 4 | 8 | 46 | 1 | 3 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0003c0003t0005 | 0/0 | 3524 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0004c0004t0001 | 1/0 | 3524 | 1 | 0 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0004c0004t0002 | 0/0 | 3524 | 25 | 10 | 8 | 0 | 3 | 4 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0004c0004t0004 | 0/0 | 3524 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0004c0018t0001 | 0/0 | 3524 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0005c0007t0002 | 0/0 | 3524 | 3 | 3 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0005c0020t0002 | 0/0 | 3524 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0006c0006t0001 | 0/0 | 3524 | 3 | 0 | 0 | 2 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0007c0009t0001 | 0/0 | 3524 | 2 | 0 | 2 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0008c0016t0001 | 0/0 | 3524 | 1 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0009c0023t0001 | 0/0 | 3524 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0010c0024t0002 | 0/0 | 3524 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0011c0010t0001 | 0/0 | 3524 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0012c0021t0001 | 0/0 | 3524 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3519): Show |
chr2 | 179939876 | 180012297 |
| a0013c0019t0001 | 0/0 | 3548 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | AACTT others(3543): Show |
chr2 | 179939876 | 180012297 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 3 | 1 | 2 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 5 | 2 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0005t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0005t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0005t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0005t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0008t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0008t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0011t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0012t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0014t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0015t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0017t0009g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0001c0022t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0001 | 0/0 | 9 | 0 | 6 | 3 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0005 | 0/0 | 7 | 0 | 1 | 5 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0007g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0008g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0002t0010g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0002c0013t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0014 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0034 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0003c0003t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0001g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0002g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0002g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0004t0004g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0004c0018t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0005c0007t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0005c0007t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0005c0020t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0006c0006t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0006c0006t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0007c0009t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0007c0009t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0008c0016t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0009c0023t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0010c0024t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0011c0010t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0012c0021t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| a0013c0019t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0003 | c0003 | t0002 | g0014 | EUR | GBR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00140 | hp2 | a0008 | c0016 | t0001 | g0060 | EUR | GBR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0173 | EUR | FIN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00280 | hp2 | a0004 | c0004 | t0002 | g0215 | EUR | FIN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | FIN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00408 | hp1 | a0003 | c0003 | t0002 | g0207 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00438 | hp1 | a0003 | c0003 | t0002 | g0198 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00544 | hp1 | a0003 | c0003 | t0002 | g0007 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00558 | hp2 | a0006 | c0006 | t0001 | g0106 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00597 | hp2 | a0003 | c0003 | t0002 | g0012 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0238 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00738 | hp1 | a0004 | c0004 | t0002 | g0214 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0259 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01069 | hp1 | a0001 | c0001 | t0006 | g0172 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01099 | hp1 | a0004 | c0004 | t0002 | g0038 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01106 | hp2 | a0003 | c0003 | t0002 | g0188 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01175 | hp1 | a0009 | c0023 | t0001 | g0068 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01175 | hp2 | a0003 | c0003 | t0002 | g0014 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01243 | hp1 | a0003 | c0003 | t0002 | g0183 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0261 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01256 | hp1 | a0007 | c0009 | t0001 | g0162 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01256 | hp2 | a0003 | c0003 | t0002 | g0211 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01258 | hp2 | a0007 | c0009 | t0001 | g0163 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01358 | hp1 | a0003 | c0003 | t0002 | g0195 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01361 | hp1 | a0004 | c0004 | t0002 | g0223 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0234 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01516 | hp1 | a0004 | c0004 | t0002 | g0220 | EUR | IBS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01934 | hp1 | a0003 | c0003 | t0002 | g0189 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0242 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01943 | hp1 | a0004 | c0004 | t0002 | g0017 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01975 | hp2 | a0004 | c0004 | t0002 | g0017 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01981 | hp1 | a0004 | c0004 | t0002 | g0037 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0240 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0258 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0245 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02027 | hp2 | a0003 | c0003 | t0002 | g0200 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0047 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02055 | hp2 | a0003 | c0003 | t0002 | g0014 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0244 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02074 | hp1 | a0003 | c0003 | t0002 | g0206 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02132 | hp1 | a0010 | c0024 | t0002 | g0255 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02132 | hp2 | a0003 | c0003 | t0002 | g0201 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02135 | hp1 | a0003 | c0003 | t0002 | g0035 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0228 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02148 | hp1 | a0003 | c0003 | t0002 | g0182 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0256 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CDX | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | CDX | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CDX | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02165 | hp2 | a0003 | c0003 | t0002 | g0199 | EAS | CDX | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02257 | hp1 | a0004 | c0004 | t0002 | g0271 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02280 | hp2 | a0004 | c0004 | t0002 | g0177 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02300 | hp1 | a0004 | c0004 | t0002 | g0038 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02300 | hp2 | a0004 | c0004 | t0002 | g0216 | AMR | PEL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02451 | hp1 | a0004 | c0004 | t0002 | g0033 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0232 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02615 | hp1 | a0001 | c0005 | t0001 | g0150 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0045 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0263 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0045 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02735 | hp2 | a0004 | c0004 | t0002 | g0017 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0264 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02809 | hp2 | a0001 | c0022 | t0001 | g0088 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0262 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02895 | hp1 | a0004 | c0004 | t0002 | g0179 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02896 | hp1 | a0004 | c0004 | t0004 | g0032 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02896 | hp2 | a0001 | c0005 | t0001 | g0151 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02897 | hp1 | a0004 | c0004 | t0004 | g0032 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02897 | hp2 | a0004 | c0004 | t0002 | g0178 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02965 | hp1 | a0003 | c0003 | t0002 | g0034 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02970 | hp1 | a0003 | c0003 | t0002 | g0186 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03017 | hp2 | a0004 | c0004 | t0002 | g0222 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03098 | hp2 | a0004 | c0004 | t0002 | g0270 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0047 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03139 | hp2 | a0004 | c0004 | t0002 | g0218 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03195 | hp1 | a0001 | c0012 | t0001 | g0055 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03195 | hp2 | a0005 | c0007 | t0002 | g0039 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03209 | hp1 | a0005 | c0007 | t0002 | g0039 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03209 | hp2 | a0004 | c0004 | t0002 | g0033 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0266 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03239 | hp1 | a0004 | c0004 | t0002 | g0217 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03453 | hp2 | a0001 | c0008 | t0002 | g0175 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03486 | hp2 | a0001 | c0005 | t0001 | g0149 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0040 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0044 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0040 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03540 | hp1 | a0001 | c0015 | t0002 | g0269 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03540 | hp2 | a0001 | c0008 | t0002 | g0180 | AFR | GWD | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03579 | hp2 | a0011 | c0010 | t0001 | g0118 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03654 | hp1 | a0002 | c0002 | t0008 | g0230 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03669 | hp1 | a0003 | c0003 | t0002 | g0212 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03688 | hp1 | a0012 | c0021 | t0001 | g0112 | SAS | STU | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0031 | SAS | STU | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03710 | hp1 | a0003 | c0003 | t0002 | g0034 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03834 | hp1 | a0006 | c0006 | t0001 | g0028 | SAS | BEB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03834 | hp2 | a0004 | c0004 | t0002 | g0221 | SAS | BEB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG04204 | hp2 | a0003 | c0003 | t0002 | g0210 | SAS | STU | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0044 | SAS | STU | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | STU | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18522 | hp1 | a0005 | c0007 | t0002 | g0226 | AFR | YRI | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | CHB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18941 | hp2 | a0003 | c0003 | t0002 | g0197 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18943 | hp1 | a0003 | c0003 | t0002 | g0208 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18946 | hp1 | a0006 | c0006 | t0001 | g0028 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18946 | hp2 | a0003 | c0003 | t0002 | g0190 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0235 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18952 | hp1 | a0003 | c0003 | t0002 | g0007 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18954 | hp1 | a0003 | c0003 | t0002 | g0012 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18957 | hp2 | a0003 | c0003 | t0002 | g0196 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18960 | hp2 | a0003 | c0003 | t0002 | g0036 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18961 | hp1 | a0003 | c0003 | t0002 | g0209 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18966 | hp1 | a0003 | c0003 | t0005 | g0275 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18967 | hp1 | a0003 | c0003 | t0002 | g0192 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18968 | hp1 | a0001 | c0011 | t0001 | g0073 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18970 | hp1 | a0003 | c0003 | t0002 | g0007 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18971 | hp2 | a0003 | c0003 | t0002 | g0018 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18973 | hp2 | a0002 | c0002 | t0010 | g0276 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18975 | hp1 | a0003 | c0003 | t0002 | g0203 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18978 | hp2 | a0003 | c0003 | t0002 | g0194 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18979 | hp1 | a0003 | c0003 | t0002 | g0035 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18980 | hp1 | a0003 | c0003 | t0002 | g0012 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18984 | hp2 | a0003 | c0003 | t0002 | g0015 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18987 | hp2 | a0003 | c0003 | t0002 | g0204 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18989 | hp1 | a0003 | c0003 | t0002 | g0015 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18990 | hp1 | a0003 | c0003 | t0002 | g0018 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18992 | hp1 | a0003 | c0003 | t0002 | g0202 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18998 | hp2 | a0003 | c0003 | t0002 | g0191 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA18999 | hp2 | a0003 | c0003 | t0002 | g0016 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19003 | hp1 | a0003 | c0003 | t0002 | g0018 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19004 | hp1 | a0003 | c0003 | t0002 | g0268 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19005 | hp1 | a0003 | c0003 | t0002 | g0205 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19009 | hp2 | a0003 | c0003 | t0002 | g0016 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19010 | hp2 | a0003 | c0003 | t0002 | g0012 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19011 | hp1 | a0003 | c0003 | t0005 | g0274 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19030 | hp1 | a0001 | c0005 | t0001 | g0135 | AFR | LWK | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0019 | AFR | LWK | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | LWK | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19056 | hp2 | a0003 | c0003 | t0002 | g0007 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19058 | hp1 | a0003 | c0003 | t0002 | g0016 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19060 | hp1 | a0003 | c0003 | t0002 | g0193 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19062 | hp1 | a0003 | c0003 | t0002 | g0015 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19068 | hp1 | a0003 | c0003 | t0002 | g0036 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19080 | hp1 | a0003 | c0003 | t0002 | g0224 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19081 | hp1 | a0013 | c0019 | t0001 | g0087 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19081 | hp2 | a0002 | c0013 | t0002 | g0265 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19082 | hp1 | a0003 | c0003 | t0002 | g0185 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19082 | hp2 | a0002 | c0002 | t0007 | g0174 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19085 | hp2 | a0003 | c0003 | t0002 | g0267 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0239 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0236 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19088 | hp2 | a0003 | c0003 | t0002 | g0007 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19089 | hp2 | a0003 | c0003 | t0002 | g0184 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0019 | AFR | YRI | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0005 | EUR | TSI | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA20752 | hp2 | a0004 | c0004 | t0002 | g0037 | EUR | TSI | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01123 | hp1 | a0003 | c0003 | t0002 | g0213 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02109 | hp1 | a0004 | c0004 | t0002 | g0219 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0227 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0260 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03471 | hp1 | a0004 | c0004 | t0002 | g0176 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG03471 | hp2 | a0003 | c0003 | t0002 | g0187 | AFR | MSL | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG06807 | hp1 | a0005 | c0020 | t0002 | g0225 | AFR | USA | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | USA | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA20300 | hp1 | a0004 | c0018 | t0001 | g0081 | AFR | USA | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | USA | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA21309 | hp1 | a0001 | c0017 | t0009 | g0273 | AFR | LWK | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| NA21309 | hp2 | a0001 | c0014 | t0002 | g0181 | AFR | LWK | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0103 | REF | REF | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| homoSapiens | grch38p0 | a0004 | c0004 | t0001 | g0147 | REF | REF | CWC22_chr2_179939876_180012297 | CWC22 | chr2 | 179939876 | 180012297 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:179945475 | C | T | 1 | a0003 | 64 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
missense_variant | MODERATE | c.2381G>A | p.Arg794Gln | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 20/20 | 2925/3524 | 2381/2727 | 794/908 | chr2 | 179945475 | |||
| chr2:179945537 | A | T | 12 | a0001 a0002 a0003 others(9): Show |
346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
missense_variant | MODERATE | c.2319T>A | p.Ser773Arg | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 20/20 | 2863/3524 | 2319/2727 | 773/908 | chr2 | 179945537 | |||
| chr2:179945631 | C | T | 2 | a0002 a0010 |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
missense_variant | MODERATE | c.2225G>A | p.Arg742Lys | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 20/20 | 2769/3524 | 2225/2727 | 742/908 | chr2 | 179945631 | |||
| chr2:179945634 | T | A | 1 | a0005 | 4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
missense_variant | MODERATE | c.2222A>T | p.Asp741Val | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 20/20 | 2766/3524 | 2222/2727 | 741/908 | chr2 | 179945634 | |||
| chr2:179950602 | C | T | 1 | a0006 | 3 | HG00558.hp2 HG03834.hp1 NA18946.hp1 |
missense_variant | MODERATE | c.2050G>A | p.Asp684Asn | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/20 | 2594/3524 | 2050/2727 | 684/908 | chr2 | 179950602 | |||
| chr2:179950686 | C | T | 1 | a0008 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.1966G>A | p.Ala656Thr | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/20 | 2510/3524 | 1966/2727 | 656/908 | chr2 | 179950686 | |||
| chr2:179954220 | A | AAAATTCC others(17): Show |
1 | a0013 | 1 | NA19081.hp1 | disruptive_inframe_insertion | MODERATE | c.1673_1674insGAATTT others(18): Show |
p.Asp558delinsGluAsn others(21): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2217/3524 | 1673/2727 | 558/908 | chr2 | 179954220 | |||
| chr2:179954224 | G | C | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1670C>G | p.Thr557Ser | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2214/3524 | 1670/2727 | 557/908 | chr2 | 179954224 | |||
| chr2:179954239 | G | C | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1655C>G | p.Ala552Gly | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2199/3524 | 1655/2727 | 552/908 | chr2 | 179954239 | |||
| chr2:179954246 | T | A | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1648A>T | p.Met550Leu | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2192/3524 | 1648/2727 | 550/908 | chr2 | 179954246 | |||
| chr2:179954248 | T | A | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1646A>T | p.Lys549Met | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2190/3524 | 1646/2727 | 549/908 | chr2 | 179954248 | |||
| chr2:179954252 | C | G | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1642G>C | p.Ala548Pro | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2186/3524 | 1642/2727 | 548/908 | chr2 | 179954252 | |||
| chr2:179954254 | A | C | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1640T>G | p.Val547Gly | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2184/3524 | 1640/2727 | 547/908 | chr2 | 179954254 | |||
| chr2:179954256 | A | T | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1638T>A | p.Asn546Lys | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2182/3524 | 1638/2727 | 546/908 | chr2 | 179954256 | |||
| chr2:179954258 | T | A | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1636A>T | p.Asn546Tyr | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2180/3524 | 1636/2727 | 546/908 | chr2 | 179954258 | |||
| chr2:179954263 | A | C | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1631T>G | p.Leu544Trp | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2175/3524 | 1631/2727 | 544/908 | chr2 | 179954263 | |||
| chr2:179954268 | G | C | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1626C>G | p.Asn542Lys | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2170/3524 | 1626/2727 | 542/908 | chr2 | 179954268 | |||
| chr2:179954270 | T | C | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1624A>G | p.Asn542Asp | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2168/3524 | 1624/2727 | 542/908 | chr2 | 179954270 | |||
| chr2:179954275 | T | A | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1619A>T | p.Glu540Val | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2163/3524 | 1619/2727 | 540/908 | chr2 | 179954275 | |||
| chr2:179954281 | C | T | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1613G>A | p.Arg538His | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2157/3524 | 1613/2727 | 538/908 | chr2 | 179954281 | |||
| chr2:179954282 | G | C | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1612C>G | p.Arg538Gly | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2156/3524 | 1612/2727 | 538/908 | chr2 | 179954282 | |||
| chr2:179954285 | G | T | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1609C>A | p.His537Asn | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2153/3524 | 1609/2727 | 537/908 | chr2 | 179954285 | |||
| chr2:179954287 | A | T | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1607T>A | p.Ile536Asn | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2151/3524 | 1607/2727 | 536/908 | chr2 | 179954287 | |||
| chr2:179954288 | T | G | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1606A>C | p.Ile536Leu | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2150/3524 | 1606/2727 | 536/908 | chr2 | 179954288 | |||
| chr2:179954292 | A | T | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1602T>A | p.Asp534Glu | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2146/3524 | 1602/2727 | 534/908 | chr2 | 179954292 | |||
| chr2:179954295 | A | C | 1 | a0013 | 1 | NA19081.hp1 | stop_gained | HIGH | c.1599T>G | p.Tyr533* | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2143/3524 | 1599/2727 | 533/908 | chr2 | 179954295 | |||
| chr2:179954296 | T | C | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1598A>G | p.Tyr533Cys | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2142/3524 | 1598/2727 | 533/908 | chr2 | 179954296 | |||
| chr2:179954305 | T | C | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1589A>G | p.Lys530Arg | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2133/3524 | 1589/2727 | 530/908 | chr2 | 179954305 | |||
| chr2:179954306 | T | A | 1 | a0013 | 1 | NA19081.hp1 | stop_gained | HIGH | c.1588A>T | p.Lys530* | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2132/3524 | 1588/2727 | 530/908 | chr2 | 179954306 | |||
| chr2:179954308 | A | C | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1586T>G | p.Phe529Cys | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2130/3524 | 1586/2727 | 529/908 | chr2 | 179954308 | |||
| chr2:179954310 | T | C | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1584A>G | p.Ile528Met | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2128/3524 | 1584/2727 | 528/908 | chr2 | 179954310 | |||
| chr2:179954315 | C | A | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1579G>T | p.Gly527Cys | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2123/3524 | 1579/2727 | 527/908 | chr2 | 179954315 | |||
| chr2:179954320 | A | T | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1574T>A | p.Phe525Tyr | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2118/3524 | 1574/2727 | 525/908 | chr2 | 179954320 | |||
| chr2:179954324 | A | T | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1570T>A | p.Ser524Thr | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2114/3524 | 1570/2727 | 524/908 | chr2 | 179954324 | |||
| chr2:179954326 | T | A | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1568A>T | p.Glu523Val | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2112/3524 | 1568/2727 | 523/908 | chr2 | 179954326 | |||
| chr2:179954328 | C | G | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1566G>C | p.Met522Ile | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2110/3524 | 1566/2727 | 522/908 | chr2 | 179954328 | |||
| chr2:179954329 | A | G | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1565T>C | p.Met522Thr | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2109/3524 | 1565/2727 | 522/908 | chr2 | 179954329 | |||
| chr2:179954333 | A | C | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1561T>G | p.Tyr521Asp | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2105/3524 | 1561/2727 | 521/908 | chr2 | 179954333 | |||
| chr2:179954337 | T | A | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1557A>T | p.Lys519Asn | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2101/3524 | 1557/2727 | 519/908 | chr2 | 179954337 | |||
| chr2:179954346 | C | G | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1548G>C | p.Met516Ile | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2092/3524 | 1548/2727 | 516/908 | chr2 | 179954346 | |||
| chr2:179954347 | A | T | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1547T>A | p.Met516Lys | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2091/3524 | 1547/2727 | 516/908 | chr2 | 179954347 | |||
| chr2:179954352 | A | C | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1542T>G | p.Phe514Leu | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2086/3524 | 1542/2727 | 514/908 | chr2 | 179954352 | |||
| chr2:179954354 | A | T | 1 | a0013 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1540T>A | p.Phe514Ile | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2084/3524 | 1540/2727 | 514/908 | chr2 | 179954354 | |||
| chr2:179954356 | C | T | 1 | a0013 | 1 | NA19081.hp1 | missense_variant&splice_region_variant | MODERATE | c.1538G>A | p.Arg513Gln | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2082/3524 | 1538/2727 | 513/908 | chr2 | 179954356 | |||
| chr2:179954357 | G | C | 1 | a0013 | 1 | NA19081.hp1 | missense_variant&splice_region_variant | MODERATE | c.1537C>G | p.Arg513Gly | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2081/3524 | 1537/2727 | 513/908 | chr2 | 179954357 | |||
| chr2:179970716 | C | G | 1 | a0007 | 2 | HG01256.hp1 HG01258.hp2 |
missense_variant | MODERATE | c.1081G>C | p.Glu361Gln | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 10/20 | 1625/3524 | 1081/2727 | 361/908 | chr2 | 179970716 | |||
| chr2:179970773 | C | A | 1 | a0012 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.1024G>T | p.Val342Leu | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 10/20 | 1568/3524 | 1024/2727 | 342/908 | chr2 | 179970773 | |||
| chr2:179986767 | T | C | 1 | a0009 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.134A>G | p.Tyr45Cys | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/20 | 678/3524 | 134/2727 | 45/908 | chr2 | 179986767 | |||
| chr2:179988629 | C | T | 1 | a0011 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.43G>A | p.Asp15Asn | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/20 | 587/3524 | 43/2727 | 15/908 | chr2 | 179988629 | |||
| chr2:179988635 | C | A | 1 | a0010 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.37G>T | p.Gly13Cys | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/20 | 581/3524 | 37/2727 | 13/908 | chr2 | 179988635 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:179945231 | G | A | 1 | a0001c0014 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.2625C>T | p.Ala875Ala | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 20/20 | 3169/3524 | 2625/2727 | 875/908 | chr2 | 179945231 | |||
| chr2:179945453 | C | T | 12 | a0001c0001 a0001c0005 a0001c0011 others(9): Show |
190 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(187): Show |
synonymous_variant | LOW | c.2403G>A | p.Ala801Ala | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 20/20 | 2947/3524 | 2403/2727 | 801/908 | chr2 | 179945453 | |||
| chr2:179954232 | A | G | 1 | a0013c0019 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.1662T>C | p.Leu554Leu | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2206/3524 | 1662/2727 | 554/908 | chr2 | 179954232 | |||
| chr2:179954253 | A | G | 1 | a0013c0019 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.1641T>C | p.Val547Val | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2185/3524 | 1641/2727 | 547/908 | chr2 | 179954253 | |||
| chr2:179954259 | T | G | 1 | a0013c0019 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.1635A>C | p.Arg545Arg | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2179/3524 | 1635/2727 | 545/908 | chr2 | 179954259 | |||
| chr2:179954271 | T | A | 1 | a0013c0019 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.1623A>T | p.Thr541Thr | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2167/3524 | 1623/2727 | 541/908 | chr2 | 179954271 | |||
| chr2:179954286 | G | T | 1 | a0013c0019 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.1608C>A | p.Ile536Ile | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/20 | 2152/3524 | 1608/2727 | 536/908 | chr2 | 179954286 | |||
| chr2:179964597 | T | C | 1 | a0005c0020 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.1347A>G | p.Glu449Glu | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/20 | 1891/3524 | 1347/2727 | 449/908 | chr2 | 179964597 | |||
| chr2:179970702 | T | C | 1 | a0001c0015 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.1095A>G | p.Gln365Gln | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 10/20 | 1639/3524 | 1095/2727 | 365/908 | chr2 | 179970702 | |||
| chr2:179971038 | G | C | 1 | a0001c0005 | 4 | HG02615.hp1 HG02896.hp2 HG03486.hp2 others(1): Show |
synonymous_variant | LOW | c.843C>G | p.Leu281Leu | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 9/20 | 1387/3524 | 843/2727 | 281/908 | chr2 | 179971038 | |||
| chr2:179971065 | T | A | 18 | a0001c0001 a0001c0005 a0001c0011 others(15): Show |
278 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(275): Show |
synonymous_variant | LOW | c.816A>T | p.Val272Val | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 9/20 | 1360/3524 | 816/2727 | 272/908 | chr2 | 179971065 | |||
| chr2:179971071 | G | A | 1 | a0001c0022 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.810C>T | p.His270His | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 9/20 | 1354/3524 | 810/2727 | 270/908 | chr2 | 179971071 | |||
| chr2:179978219 | C | T | 1 | a0001c0012 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.552G>A | p.Glu184Glu | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/20 | 1096/3524 | 552/2727 | 184/908 | chr2 | 179978219 | |||
| chr2:179978303 | C | T | 1 | a0001c0011 | 1 | NA18968.hp1 | synonymous_variant | LOW | c.468G>A | p.Arg156Arg | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/20 | 1012/3524 | 468/2727 | 156/908 | chr2 | 179978303 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:179993410 | C | T | 1 | a0002c0002t0008 | 1 | HG03654.hp1 | 5_prime_UTR_variant | MODIFIER | c.-69G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/20 | 69 | chr2 | 179993410 | ||||||
| chr2:180006897 | C | A | 1 | a0001c0001t0006 | 1 | HG01069.hp1 | 5_prime_UTR_variant | MODIFIER | c.-144G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/20 | 13556 | chr2 | 180006897 | ||||||
| chr2:180006908 | G | C | 1 | a0001c0001t0003 | 3 | HG00280.hp1 HG01069.hp2 HG03688.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-155C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/20 | chr2 | 180006908 | |||||||
| chr2:180007008 | G | A | 1 | a0001c0017t0009 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-255C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/20 | 13667 | chr2 | 180007008 | ||||||
| chr2:180007102 | C | T | 1 | a0004c0004t0004 | 2 | HG02896.hp1 HG02897.hp1 |
5_prime_UTR_variant | MODIFIER | c.-349G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/20 | 13761 | chr2 | 180007102 | ||||||
| chr2:180007192 | G | A | 1 | a0003c0003t0005 | 2 | NA18966.hp1 NA19011.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-439C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/20 | chr2 | 180007192 | |||||||
| chr2:180007259 | A | G | 1 | a0002c0002t0007 | 1 | NA19082.hp2 | 5_prime_UTR_variant | MODIFIER | c.-506T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/20 | 13918 | chr2 | 180007259 | ||||||
| chr2:180007267 | G | C | 17 | a0001c0001t0002 a0001c0008t0002 a0001c0014t0002 others(14): Show |
184 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(181): Show |
5_prime_UTR_variant | MODIFIER | c.-514C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/20 | 13926 | chr2 | 180007267 | ||||||
| chr2:180007296 | T | C | 1 | a0002c0002t0010 | 1 | NA18973.hp2 | 5_prime_UTR_variant | MODIFIER | c.-543A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/20 | 13955 | chr2 | 180007296 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:179945831 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2141-116T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179945831 | |||||||
| chr2:179945936 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0143 |
2 | NA18951.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.2141-221C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179945936 | |||||||
| chr2:179945940 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2141-225A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179945940 | |||||||
| chr2:179945969 | G | A | 1 | a0002c0002t0002g0243 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2141-254C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179945969 | |||||||
| chr2:179946097 | G | A | 1 | a0004c0018t0001g0081 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2141-382C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946097 | |||||||
| chr2:179946171 | C | G | 1 | a0004c0004t0004g0032 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2141-456G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946171 | |||||||
| chr2:179946213 | G | T | 1 | a0004c0004t0004g0032 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2141-498C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946213 | |||||||
| chr2:179946216 | G | A | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2141-501C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946216 | |||||||
| chr2:179946232 | T | C | 49 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(46): Show |
75 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.2141-517A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946232 | |||||||
| chr2:179946233 | T | C | 1 | a0001c0008t0002g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2141-518A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946233 | |||||||
| chr2:179946265 | C | T | 1 | a0003c0003t0002g0195 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2141-550G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946265 | |||||||
| chr2:179946266 | G | A | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2141-551C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946266 | |||||||
| chr2:179946418 | C | G | 1 | a0001c0001t0001g0153 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2141-703G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946418 | |||||||
| chr2:179946449 | C | CA | 81 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0048 others(78): Show |
111 | HG00597.hp1 HG00621.hp1 HG00642.hp1 others(108): Show |
intron_variant | MODIFIER | c.2141-735dupT | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946449 | |||||||
| chr2:179946449 | C | CAA | 7 | a0001c0014t0002g0181 a0002c0002t0002g0228 a0002c0002t0002g0244 others(4): Show |
8 | HG01175.hp1 HG02056.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2141-736_2141-735d others(4): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946449 | |||||||
| chr2:179946464 | A | AG | 28 | a0003c0003t0002g0007 a0003c0003t0002g0018 a0003c0003t0002g0034 others(25): Show |
36 | HG00280.hp2 HG00544.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.2141-750dupC | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946464 | |||||||
| chr2:179946464 | A | AGG | 28 | a0003c0003t0002g0012 a0003c0003t0002g0014 a0003c0003t0002g0016 others(25): Show |
39 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.2141-751_2141-750d others(4): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946464 | |||||||
| chr2:179946465 | G | A | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
248 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.2141-750C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946465 | |||||||
| chr2:179946466 | G | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(54): Show |
85 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.2141-751C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946466 | |||||||
| chr2:179946467 | G | C | 1 | a0002c0002t0002g0247 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2141-752C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946467 | |||||||
| chr2:179946468 | G | C | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.2141-753C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946468 | |||||||
| chr2:179946473 | G | T | 1 | a0001c0008t0002g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2141-758C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946473 | |||||||
| chr2:179946476 | A | G | 3 | a0005c0007t0002g0039 a0005c0007t0002g0226 a0005c0020t0002g0225 |
4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2141-761T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946476 | |||||||
| chr2:179946486 | G | A | 1 | a0003c0003t0002g0189 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2141-771C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946486 | |||||||
| chr2:179946487 | A | G | 1 | a0003c0003t0002g0189 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2141-772T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946487 | |||||||
| chr2:179946509 | T | C | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2141-794A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946509 | |||||||
| chr2:179946517 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2141-802G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946517 | |||||||
| chr2:179946539 | T | C | 1 | a0004c0018t0001g0081 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2141-824A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946539 | |||||||
| chr2:179946558 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02145.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.2141-843G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946558 | |||||||
| chr2:179946961 | A | G | 3 | a0005c0007t0002g0039 a0005c0007t0002g0226 a0005c0020t0002g0225 |
4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2141-1246T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179946961 | |||||||
| chr2:179947113 | T | C | 46 | a0003c0003t0002g0007 a0003c0003t0002g0012 a0003c0003t0002g0014 others(43): Show |
64 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.2141-1398A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179947113 | |||||||
| chr2:179947140 | T | C | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2141-1425A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179947140 | |||||||
| chr2:179947718 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2141-2003A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179947718 | |||||||
| chr2:179947849 | T | C | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | NA18947.hp2 NA18985.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.2141-2134A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179947849 | |||||||
| chr2:179947927 | T | C | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.2141-2212A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179947927 | |||||||
| chr2:179947971 | G | A | 1 | a0001c0008t0002g0180 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2141-2256C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179947971 | |||||||
| chr2:179948138 | T | C | 4 | a0001c0017t0009g0273 a0005c0007t0002g0039 a0005c0007t0002g0226 others(1): Show |
5 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.2140+2374A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179948138 | |||||||
| chr2:179948295 | CTAAA | C | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.2140+2213_2140+221 others(8): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179948295 | |||||||
| chr2:179948335 | T | C | 3 | a0001c0008t0002g0175 a0001c0008t0002g0180 a0001c0014t0002g0181 |
3 | HG03453.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2140+2177A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179948335 | |||||||
| chr2:179948396 | G | A | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.2140+2116C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179948396 | |||||||
| chr2:179948397 | A | AT | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.2140+2114dupA | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179948397 | |||||||
| chr2:179948403 | TA | T | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.2140+2108delT | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179948403 | |||||||
| chr2:179948409 | T | A | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.2140+2103A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179948409 | |||||||
| chr2:179948679 | C | T | 7 | a0002c0002t0002g0001 a0002c0002t0002g0234 a0002c0002t0002g0240 others(4): Show |
15 | HG00642.hp1 HG01258.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.2140+1833G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179948679 | |||||||
| chr2:179948918 | T | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.2140+1594A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179948918 | |||||||
| chr2:179948978 | T | C | 3 | a0001c0008t0002g0175 a0001c0008t0002g0180 a0001c0014t0002g0181 |
3 | HG03453.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2140+1534A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179948978 | |||||||
| chr2:179949133 | A | G | 1 | a0002c0002t0002g0045 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2140+1379T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949133 | |||||||
| chr2:179949184 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2140+1328A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949184 | |||||||
| chr2:179949233 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2140+1279A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949233 | |||||||
| chr2:179949350 | C | T | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.2140+1162G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949350 | |||||||
| chr2:179949360 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2140+1152A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949360 | |||||||
| chr2:179949440 | G | T | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2140+1072C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949440 | |||||||
| chr2:179949467 | G | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.2140+1045C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949467 | |||||||
| chr2:179949468 | C | T | 1 | a0003c0003t0002g0202 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2140+1044G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949468 | |||||||
| chr2:179949546 | A | C | 1 | a0002c0002t0002g0229 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2140+966T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949546 | |||||||
| chr2:179949861 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0160 |
3 | NA18967.hp2 NA18988.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2140+651G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949861 | |||||||
| chr2:179949892 | A | C | 1 | a0001c0001t0001g0075 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2140+620T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179949892 | |||||||
| chr2:179950130 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2140+382A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179950130 | |||||||
| chr2:179950345 | G | T | 1 | a0002c0002t0002g0043 | 2 | HG02080.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.2140+167C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 19/19 | chr2 | 179950345 | |||||||
| chr2:179950801 | A | T | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
190 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.1919+24T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 18/19 | chr2 | 179950801 | |||||||
| chr2:179951122 | A | C | 3 | a0005c0007t0002g0039 a0005c0007t0002g0226 a0005c0020t0002g0225 |
4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1818-196T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179951122 | |||||||
| chr2:179951144 | A | G | 3 | a0005c0007t0002g0039 a0005c0007t0002g0226 a0005c0020t0002g0225 |
4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1818-218T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179951144 | |||||||
| chr2:179951328 | T | A | 1 | a0002c0002t0002g0257 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1818-402A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179951328 | |||||||
| chr2:179951428 | AC | A | 48 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(45): Show |
74 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.1818-503delG | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179951428 | |||||||
| chr2:179951531 | A | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0115 a0001c0001t0001g0116 |
6 | HG01081.hp1 HG01123.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1818-605T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179951531 | |||||||
| chr2:179951542 | A | G | 3 | a0005c0007t0002g0039 a0005c0007t0002g0226 a0005c0020t0002g0225 |
4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1818-616T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179951542 | |||||||
| chr2:179951689 | A | C | 1 | a0002c0002t0002g0263 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1818-763T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179951689 | |||||||
| chr2:179951950 | A | G | 1 | a0003c0003t0002g0194 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1817+521T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179951950 | |||||||
| chr2:179951962 | G | T | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.1817+509C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179951962 | |||||||
| chr2:179952016 | C | T | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.1817+455G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179952016 | |||||||
| chr2:179952038 | G | A | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.1817+433C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179952038 | |||||||
| chr2:179952084 | T | C | 1 | a0004c0004t0002g0271 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1817+387A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179952084 | |||||||
| chr2:179952131 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1817+340A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179952131 | |||||||
| chr2:179952249 | T | C | 1 | a0002c0002t0002g0046 | 2 | NA18992.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1817+222A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179952249 | |||||||
| chr2:179952344 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1817+127A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 17/19 | chr2 | 179952344 | |||||||
| chr2:179953030 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1690-432A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/19 | chr2 | 179953030 | |||||||
| chr2:179953175 | A | AT | 13 | a0004c0004t0002g0017 a0004c0004t0002g0037 a0004c0004t0002g0038 others(10): Show |
17 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1690-578dupA | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/19 | chr2 | 179953175 | |||||||
| chr2:179953215 | C | A | 7 | a0002c0002t0002g0045 a0002c0002t0002g0047 a0002c0002t0002g0260 others(4): Show |
9 | HG02055.hp1 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1690-617G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/19 | chr2 | 179953215 | |||||||
| chr2:179953567 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1689+638G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/19 | chr2 | 179953567 | |||||||
| chr2:179953816 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1689+389T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/19 | chr2 | 179953816 | |||||||
| chr2:179953922 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1689+283T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/19 | chr2 | 179953922 | |||||||
| chr2:179954143 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1689+62G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 16/19 | chr2 | 179954143 | |||||||
| chr2:179954358 | C | T | 1 | a0013c0019t0001g0087 | 1 | NA19081.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.1537-1G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 15/19 | chr2 | 179954358 | |||||||
| chr2:179954359 | TAATAAAT others(6): Show |
T | 1 | a0013c0019t0001g0087 | 1 | NA19081.hp1 | splice_region_variant&intron_variant | LOW | c.1537-15_1537-3delT others(12): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 15/19 | chr2 | 179954359 | |||||||
| chr2:179954378 | A | T | 1 | a0013c0019t0001g0087 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1537-21T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 15/19 | chr2 | 179954378 | |||||||
| chr2:179954379 | C | A | 1 | a0013c0019t0001g0087 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1537-22G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 15/19 | chr2 | 179954379 | |||||||
| chr2:179954427 | A | T | 1 | a0002c0002t0002g0045 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1537-70T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 15/19 | chr2 | 179954427 | |||||||
| chr2:179954865 | A | G | 6 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(3): Show |
6 | HG01361.hp2 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1536+92T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 15/19 | chr2 | 179954865 | |||||||
| chr2:179955251 | T | G | 47 | a0002c0013t0002g0265 a0003c0003t0002g0007 a0003c0003t0002g0012 others(44): Show |
65 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1459-217A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179955251 | |||||||
| chr2:179955253 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1459-219G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179955253 | |||||||
| chr2:179955419 | T | C | 6 | a0002c0013t0002g0265 a0003c0003t0002g0016 a0003c0003t0002g0185 others(3): Show |
8 | NA18941.hp2 NA18957.hp2 NA18998.hp2 others(5): Show |
intron_variant | MODIFIER | c.1459-385A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179955419 | |||||||
| chr2:179955742 | C | T | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1459-708G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179955742 | |||||||
| chr2:179955777 | T | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
7 | HG02622.hp2 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1459-743A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179955777 | |||||||
| chr2:179955877 | C | A | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
190 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.1459-843G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179955877 | |||||||
| chr2:179956149 | T | A | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.1459-1115A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179956149 | |||||||
| chr2:179956384 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1459-1350A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179956384 | |||||||
| chr2:179956412 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1459-1378A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179956412 | |||||||
| chr2:179956582 | C | CTA | 3 | a0001c0017t0009g0273 a0005c0007t0002g0039 a0005c0007t0002g0226 |
4 | HG03195.hp2 HG03209.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1459-1550_1459-154 others(6): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179956582 | |||||||
| chr2:179956630 | A | C | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.1459-1596T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179956630 | |||||||
| chr2:179956773 | T | C | 1 | a0003c0003t0002g0198 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1459-1739A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179956773 | |||||||
| chr2:179956784 | C | CT | 48 | a0002c0002t0002g0259 a0002c0013t0002g0265 a0003c0003t0002g0007 others(45): Show |
66 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1459-1751dupA | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179956784 | |||||||
| chr2:179956918 | G | A | 1 | a0003c0003t0002g0192 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1459-1884C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179956918 | |||||||
| chr2:179957271 | A | G | 3 | a0001c0008t0002g0175 a0001c0008t0002g0180 a0001c0014t0002g0181 |
3 | HG03453.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1458+1751T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179957271 | |||||||
| chr2:179957293 | G | A | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
190 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.1458+1729C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179957293 | |||||||
| chr2:179957297 | T | A | 4 | a0001c0017t0009g0273 a0005c0007t0002g0039 a0005c0007t0002g0226 others(1): Show |
5 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1458+1725A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179957297 | |||||||
| chr2:179957545 | A | T | 2 | a0004c0004t0002g0215 a0004c0004t0002g0216 |
2 | HG00280.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1458+1477T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179957545 | |||||||
| chr2:179957748 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1458+1274G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179957748 | |||||||
| chr2:179957828 | T | C | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.1458+1194A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179957828 | |||||||
| chr2:179957839 | T | C | 3 | a0001c0008t0002g0175 a0001c0008t0002g0180 a0001c0014t0002g0181 |
3 | HG03453.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1458+1183A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179957839 | |||||||
| chr2:179957842 | GA | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
276 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1458+1179delT | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179957842 | |||||||
| chr2:179958106 | A | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
368 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.1458+916T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958106 | |||||||
| chr2:179958163 | G | T | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
281 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.1458+859C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958163 | |||||||
| chr2:179958330 | C | CA | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(149): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1458+691dupT | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958330 | |||||||
| chr2:179958330 | C | CAA | 8 | a0001c0001t0001g0056 a0001c0001t0001g0101 a0001c0001t0001g0156 others(5): Show |
8 | HG01169.hp1 HG01243.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.1458+690_1458+691d others(4): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958330 | |||||||
| chr2:179958350 | AG | A | 50 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(47): Show |
76 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.1458+671delC | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958350 | |||||||
| chr2:179958351 | G | A | 5 | a0002c0002t0002g0005 a0002c0002t0002g0235 a0002c0002t0002g0236 others(2): Show |
5 | HG01109.hp1 HG02056.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1458+671C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958351 | |||||||
| chr2:179958513 | A | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0072 others(11): Show |
21 | HG00558.hp1 HG01496.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.1458+509T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958513 | |||||||
| chr2:179958546 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1458+476A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958546 | |||||||
| chr2:179958547 | T | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0132 |
2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1458+475A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958547 | |||||||
| chr2:179958656 | T | C | 2 | a0003c0003t0002g0193 a0003c0003t0002g0201 |
2 | HG02132.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1458+366A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958656 | |||||||
| chr2:179958820 | A | C | 1 | a0002c0002t0002g0045 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1458+202T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958820 | |||||||
| chr2:179958856 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1458+166T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958856 | |||||||
| chr2:179958863 | C | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
102 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1458+159G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958863 | |||||||
| chr2:179958910 | T | C | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1458+112A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 14/19 | chr2 | 179958910 | |||||||
| chr2:179959138 | T | C | 2 | a0002c0002t0002g0047 a0002c0002t0002g0266 |
3 | HG02055.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1398-56A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959138 | |||||||
| chr2:179959447 | G | A | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1398-365C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959447 | |||||||
| chr2:179959507 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | NA18944.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1398-425T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959507 | |||||||
| chr2:179959681 | A | G | 1 | a0002c0002t0002g0045 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1398-599T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959681 | |||||||
| chr2:179959754 | A | T | 1 | a0001c0001t0001g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1398-672T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959754 | |||||||
| chr2:179959761 | G | C | 1 | a0001c0001t0001g0086 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1398-679C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959761 | |||||||
| chr2:179959772 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1398-690C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959772 | |||||||
| chr2:179959816 | T | C | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1398-734A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959816 | |||||||
| chr2:179959870 | T | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(20): Show |
39 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1398-788A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959870 | |||||||
| chr2:179959887 | G | A | 3 | a0005c0007t0002g0039 a0005c0007t0002g0226 a0005c0020t0002g0225 |
4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398-805C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959887 | |||||||
| chr2:179959933 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1398-851A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959933 | |||||||
| chr2:179959942 | A | T | 46 | a0002c0013t0002g0265 a0003c0003t0002g0007 a0003c0003t0002g0012 others(43): Show |
64 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1398-860T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179959942 | |||||||
| chr2:179960044 | T | A | 5 | a0003c0003t0002g0193 a0003c0003t0002g0199 a0003c0003t0002g0200 others(2): Show |
5 | HG00408.hp1 HG02027.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1398-962A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960044 | |||||||
| chr2:179960172 | T | C | 1 | a0001c0014t0002g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1398-1090A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960172 | |||||||
| chr2:179960436 | G | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1398-1354C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960436 | |||||||
| chr2:179960626 | T | C | 1 | a0002c0002t0002g0257 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1398-1544A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960626 | |||||||
| chr2:179960673 | T | C | 1 | a0003c0003t0002g0204 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1398-1591A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960673 | |||||||
| chr2:179960715 | T | C | 1 | a0001c0008t0002g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1398-1633A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960715 | |||||||
| chr2:179960775 | T | C | 47 | a0002c0013t0002g0265 a0003c0003t0002g0007 a0003c0003t0002g0012 others(44): Show |
65 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1398-1693A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960775 | |||||||
| chr2:179960913 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1398-1831A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960913 | |||||||
| chr2:179960957 | C | T | 1 | a0002c0002t0002g0045 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1398-1875G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960957 | |||||||
| chr2:179960958 | G | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(249): Show |
346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.1398-1876C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960958 | |||||||
| chr2:179960977 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1398-1895A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179960977 | |||||||
| chr2:179961280 | A | C | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.1398-2198T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179961280 | |||||||
| chr2:179961563 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1398-2481T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179961563 | |||||||
| chr2:179961603 | C | T | 1 | a0002c0002t0002g0260 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1398-2521G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179961603 | |||||||
| chr2:179961724 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(46): Show |
74 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.1398-2642C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179961724 | |||||||
| chr2:179961785 | C | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
368 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.1398-2703G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179961785 | |||||||
| chr2:179961897 | T | C | 1 | a0001c0008t0002g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1397+2650A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179961897 | |||||||
| chr2:179961903 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1397+2644A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179961903 | |||||||
| chr2:179961985 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1397+2562G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179961985 | |||||||
| chr2:179962007 | C | T | 3 | a0001c0008t0002g0175 a0001c0008t0002g0180 a0001c0014t0002g0181 |
3 | HG03453.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1397+2540G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962007 | |||||||
| chr2:179962054 | A | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.1397+2493T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962054 | |||||||
| chr2:179962061 | T | A | 1 | a0002c0002t0002g0258 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1397+2486A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962061 | |||||||
| chr2:179962250 | T | A | 3 | a0005c0007t0002g0039 a0005c0007t0002g0226 a0005c0020t0002g0225 |
4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397+2297A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962250 | |||||||
| chr2:179962329 | G | C | 1 | a0001c0014t0002g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1397+2218C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962329 | |||||||
| chr2:179962398 | C | G | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1397+2149G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962398 | |||||||
| chr2:179962404 | C | A | 1 | a0001c0001t0001g0144 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1397+2143G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962404 | |||||||
| chr2:179962475 | G | C | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1397+2072C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962475 | |||||||
| chr2:179962641 | A | AT | 7 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(4): Show |
7 | HG01361.hp2 HG01884.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1397+1905dupA | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962641 | |||||||
| chr2:179962819 | T | G | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1397+1728A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962819 | |||||||
| chr2:179962952 | A | G | 1 | a0003c0003t0002g0193 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1397+1595T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179962952 | |||||||
| chr2:179963052 | T | G | 1 | a0001c0008t0002g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1397+1495A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963052 | |||||||
| chr2:179963092 | C | T | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1397+1455G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963092 | |||||||
| chr2:179963107 | A | G | 1 | a0002c0002t0010g0276 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1397+1440T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963107 | |||||||
| chr2:179963219 | T | TG | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1397+1327dupC | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963219 | |||||||
| chr2:179963276 | A | C | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1397+1271T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963276 | |||||||
| chr2:179963284 | G | C | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1397+1263C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963284 | |||||||
| chr2:179963285 | A | G | 3 | a0005c0007t0002g0039 a0005c0007t0002g0226 a0005c0020t0002g0225 |
4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397+1262T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963285 | |||||||
| chr2:179963328 | T | G | 46 | a0003c0003t0002g0007 a0003c0003t0002g0012 a0003c0003t0002g0014 others(43): Show |
64 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1397+1219A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963328 | |||||||
| chr2:179963335 | C | CT | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
213 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.1397+1211dupA | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963335 | |||||||
| chr2:179963335 | C | CTT | 84 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0048 others(81): Show |
115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1397+1210_1397+121 others(6): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963335 | |||||||
| chr2:179963335 | C | CTTT | 16 | a0001c0001t0001g0138 a0002c0002t0002g0235 a0002c0002t0002g0237 others(13): Show |
17 | HG01243.hp2 HG01934.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.1397+1209_1397+121 others(7): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963335 | |||||||
| chr2:179963436 | A | G | 2 | a0004c0004t0002g0215 a0004c0004t0002g0216 |
2 | HG00280.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1397+1111T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963436 | |||||||
| chr2:179963447 | A | C | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1397+1100T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963447 | |||||||
| chr2:179963448 | T | C | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1397+1099A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963448 | |||||||
| chr2:179963457 | C | T | 1 | a0006c0006t0001g0028 | 2 | HG03834.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.1397+1090G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963457 | |||||||
| chr2:179963695 | T | A | 1 | a0002c0002t0002g0260 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1397+852A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963695 | |||||||
| chr2:179963705 | A | G | 2 | a0002c0002t0002g0046 a0002c0013t0002g0265 |
3 | NA18992.hp2 NA19002.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1397+842T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963705 | |||||||
| chr2:179963765 | A | G | 1 | a0005c0020t0002g0225 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1397+782T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179963765 | |||||||
| chr2:179964056 | CAA | C | 2 | a0002c0002t0002g0047 a0002c0002t0002g0266 |
3 | HG02055.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1397+489_1397+490d others(4): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179964056 | |||||||
| chr2:179964079 | A | C | 1 | a0001c0001t0001g0089 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1397+468T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179964079 | |||||||
| chr2:179964089 | C | A | 1 | a0004c0004t0002g0221 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1397+458G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179964089 | |||||||
| chr2:179964466 | G | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 |
3 | NA18947.hp2 NA18985.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1397+81C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179964466 | |||||||
| chr2:179964480 | T | C | 1 | a0002c0002t0002g0250 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1397+67A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 13/19 | chr2 | 179964480 | |||||||
| chr2:179964655 | A | G | 3 | a0005c0007t0002g0039 a0005c0007t0002g0226 a0005c0020t0002g0225 |
4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1316-27T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179964655 | |||||||
| chr2:179964731 | T | C | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1316-103A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179964731 | |||||||
| chr2:179964744 | A | C | 2 | a0002c0002t0002g0040 a0002c0002t0002g0239 |
3 | HG03490.hp2 HG03492.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1316-116T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179964744 | |||||||
| chr2:179964825 | G | C | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1316-197C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179964825 | |||||||
| chr2:179964977 | G | A | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1316-349C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179964977 | |||||||
| chr2:179965074 | C | G | 1 | a0002c0002t0002g0241 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1316-446G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179965074 | |||||||
| chr2:179965076 | CT | C | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1316-449delA | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179965076 | |||||||
| chr2:179965226 | G | A | 2 | a0004c0004t0002g0215 a0004c0004t0002g0216 |
2 | HG00280.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1316-598C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179965226 | |||||||
| chr2:179965248 | T | C | 1 | a0002c0002t0002g0260 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1316-620A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179965248 | |||||||
| chr2:179965371 | G | C | 1 | a0003c0003t0002g0209 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1315+507C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179965371 | |||||||
| chr2:179965430 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1315+448A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179965430 | |||||||
| chr2:179965438 | T | C | 2 | a0002c0002t0002g0231 a0002c0002t0002g0233 |
2 | NA18986.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1315+440A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179965438 | |||||||
| chr2:179965490 | T | C | 1 | a0001c0012t0001g0055 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1315+388A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179965490 | |||||||
| chr2:179965524 | A | G | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1315+354T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 12/19 | chr2 | 179965524 | |||||||
| chr2:179966178 | TG | T | 39 | a0003c0003t0002g0007 a0003c0003t0002g0012 a0003c0003t0002g0015 others(36): Show |
54 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1211-197delC | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966178 | |||||||
| chr2:179966231 | A | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.1211-249T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966231 | |||||||
| chr2:179966274 | G | C | 39 | a0003c0003t0002g0007 a0003c0003t0002g0012 a0003c0003t0002g0015 others(36): Show |
54 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1211-292C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966274 | |||||||
| chr2:179966296 | T | G | 1 | a0001c0008t0002g0180 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1211-314A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966296 | |||||||
| chr2:179966494 | A | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0050 a0001c0001t0001g0140 others(6): Show |
12 | HG02615.hp2 HG02622.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1211-512T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966494 | |||||||
| chr2:179966603 | T | C | 1 | a0001c0014t0002g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1211-621A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966603 | |||||||
| chr2:179966650 | T | C | 39 | a0003c0003t0002g0007 a0003c0003t0002g0012 a0003c0003t0002g0015 others(36): Show |
54 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1211-668A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966650 | |||||||
| chr2:179966672 | T | A | 3 | a0005c0007t0002g0039 a0005c0007t0002g0226 a0005c0020t0002g0225 |
4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1211-690A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966672 | |||||||
| chr2:179966687 | T | G | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1211-705A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966687 | |||||||
| chr2:179966898 | T | C | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1211-916A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966898 | |||||||
| chr2:179966996 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1211-1014C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179966996 | |||||||
| chr2:179967072 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1211-1090C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967072 | |||||||
| chr2:179967178 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1211-1196C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967178 | |||||||
| chr2:179967200 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1211-1218C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967200 | |||||||
| chr2:179967212 | T | C | 2 | a0007c0009t0001g0162 a0007c0009t0001g0163 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1211-1230A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967212 | |||||||
| chr2:179967337 | T | A | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
368 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.1211-1355A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967337 | |||||||
| chr2:179967373 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1211-1391C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967373 | |||||||
| chr2:179967719 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1211-1737A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967719 | |||||||
| chr2:179967746 | C | CAT | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
177 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.1211-1766_1211-176 others(6): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967746 | |||||||
| chr2:179967755 | A | G | 13 | a0004c0004t0002g0017 a0004c0004t0002g0037 a0004c0004t0002g0038 others(10): Show |
17 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1211-1773T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967755 | |||||||
| chr2:179967782 | C | T | 46 | a0003c0003t0002g0007 a0003c0003t0002g0012 a0003c0003t0002g0014 others(43): Show |
64 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1211-1800G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967782 | |||||||
| chr2:179967820 | A | G | 2 | a0003c0003t0002g0186 a0003c0003t0002g0187 |
2 | HG02970.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1211-1838T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967820 | |||||||
| chr2:179967883 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1211-1901G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967883 | |||||||
| chr2:179967945 | C | T | 16 | a0004c0004t0002g0017 a0004c0004t0002g0037 a0004c0004t0002g0038 others(13): Show |
21 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1211-1963G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967945 | |||||||
| chr2:179967948 | T | C | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.1211-1966A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967948 | |||||||
| chr2:179967977 | T | C | 3 | a0001c0008t0002g0175 a0001c0008t0002g0180 a0001c0014t0002g0181 |
3 | HG03453.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1211-1995A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179967977 | |||||||
| chr2:179968020 | A | G | 2 | a0004c0004t0002g0215 a0004c0004t0002g0216 |
2 | HG00280.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1211-2038T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968020 | |||||||
| chr2:179968027 | G | C | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1211-2045C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968027 | |||||||
| chr2:179968453 | A | G | 3 | a0002c0002t0002g0044 a0002c0002t0002g0232 a0002c0002t0008g0230 |
4 | HG02602.hp2 HG03491.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1210+2048T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968453 | |||||||
| chr2:179968478 | T | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
7 | HG02622.hp2 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1210+2023A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968478 | |||||||
| chr2:179968535 | C | T | 46 | a0003c0003t0002g0007 a0003c0003t0002g0012 a0003c0003t0002g0014 others(43): Show |
64 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1210+1966G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968535 | |||||||
| chr2:179968590 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1210+1911G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968590 | |||||||
| chr2:179968591 | G | A | 2 | a0001c0001t0003g0031 a0001c0001t0003g0173 |
3 | HG00280.hp1 HG01069.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1210+1910C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968591 | |||||||
| chr2:179968599 | G | A | 1 | a0002c0002t0002g0044 | 2 | HG03491.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1210+1902C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968599 | |||||||
| chr2:179968759 | G | A | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1210+1742C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968759 | |||||||
| chr2:179968788 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0095 a0005c0007t0002g0039 others(1): Show |
6 | HG03195.hp2 HG03209.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.1210+1713C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968788 | |||||||
| chr2:179968802 | G | A | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1210+1699C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968802 | |||||||
| chr2:179968808 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1210+1693G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968808 | |||||||
| chr2:179968861 | C | T | 1 | a0003c0003t0002g0207 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1210+1640G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179968861 | |||||||
| chr2:179969065 | C | T | 1 | a0004c0004t0002g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1210+1436G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179969065 | |||||||
| chr2:179969076 | G | C | 1 | a0003c0003t0002g0185 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1210+1425C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179969076 | |||||||
| chr2:179969103 | T | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(76): Show |
98 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.1210+1398A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179969103 | |||||||
| chr2:179969207 | C | T | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1210+1294G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179969207 | |||||||
| chr2:179969216 | T | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0065 |
2 | HG01169.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1210+1285A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179969216 | |||||||
| chr2:179969234 | G | C | 45 | a0002c0013t0002g0265 a0003c0003t0002g0007 a0003c0003t0002g0012 others(42): Show |
63 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1210+1267C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179969234 | |||||||
| chr2:179969354 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1210+1147C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179969354 | |||||||
| chr2:179969721 | C | T | 46 | a0003c0003t0002g0007 a0003c0003t0002g0012 a0003c0003t0002g0014 others(43): Show |
64 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1210+780G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179969721 | |||||||
| chr2:179969898 | C | T | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1210+603G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179969898 | |||||||
| chr2:179969919 | T | C | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.1210+582A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 11/19 | chr2 | 179969919 | |||||||
| chr2:179970647 | T | TA | 3 | a0005c0007t0002g0039 a0005c0007t0002g0226 a0005c0020t0002g0225 |
4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
splice_donor_variant&intron_variant | HIGH | c.1147+2dupT | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 10/19 | chr2 | 179970647 | |||||||
| chr2:179970862 | A | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
368 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(365): Show |
splice_region_variant&intron_variant | LOW | c.941-6T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 9/19 | chr2 | 179970862 | |||||||
| chr2:179971095 | A | T | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.805-19T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179971095 | |||||||
| chr2:179971265 | G | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(203): Show |
282 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.805-189C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179971265 | |||||||
| chr2:179971293 | T | C | 101 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(98): Show |
147 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.805-217A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179971293 | |||||||
| chr2:179971316 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.805-240A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179971316 | |||||||
| chr2:179971474 | C | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02615.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.805-398G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179971474 | |||||||
| chr2:179971538 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.805-462C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179971538 | |||||||
| chr2:179971698 | G | C | 1 | a0001c0001t0001g0154 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.805-622C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179971698 | |||||||
| chr2:179971753 | C | A | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.805-677G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179971753 | |||||||
| chr2:179972251 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.804+942G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179972251 | |||||||
| chr2:179972299 | A | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(76): Show |
98 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.804+894T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179972299 | |||||||
| chr2:179972342 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.804+851T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179972342 | |||||||
| chr2:179972376 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0054 |
2 | NA18985.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.804+817T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179972376 | |||||||
| chr2:179972640 | T | A | 1 | a0001c0001t0001g0066 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.804+553A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179972640 | |||||||
| chr2:179972723 | T | C | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.804+470A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179972723 | |||||||
| chr2:179972815 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG01081.hp2 HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.804+378C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179972815 | |||||||
| chr2:179972860 | C | A | 2 | a0005c0007t0002g0039 a0005c0007t0002g0226 |
3 | HG03195.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.804+333G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179972860 | |||||||
| chr2:179972886 | G | A | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.804+307C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179972886 | |||||||
| chr2:179972995 | T | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.804+198A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179972995 | |||||||
| chr2:179973049 | T | G | 47 | a0002c0013t0002g0265 a0003c0003t0002g0007 a0003c0003t0002g0012 others(44): Show |
65 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.804+144A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179973049 | |||||||
| chr2:179973079 | T | A | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.804+114A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179973079 | |||||||
| chr2:179973096 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.804+97A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179973096 | |||||||
| chr2:179973147 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.804+46C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 8/19 | chr2 | 179973147 | |||||||
| chr2:179973317 | C | T | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.751-71G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 7/19 | chr2 | 179973317 | |||||||
| chr2:179973332 | A | G | 1 | a0002c0002t0008g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.751-86T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 7/19 | chr2 | 179973332 | |||||||
| chr2:179973360 | T | C | 1 | a0004c0018t0001g0081 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.751-114A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 7/19 | chr2 | 179973360 | |||||||
| chr2:179973386 | A | C | 1 | a0001c0001t0001g0154 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.751-140T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 7/19 | chr2 | 179973386 | |||||||
| chr2:179973578 | C | A | 1 | a0001c0008t0002g0180 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.750+56G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 7/19 | chr2 | 179973578 | |||||||
| chr2:179973857 | C | G | 1 | a0001c0014t0002g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.582-55G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179973857 | |||||||
| chr2:179973857 | C | T | 1 | a0009c0023t0001g0068 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.582-55G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179973857 | |||||||
| chr2:179973924 | A | G | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.582-122T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179973924 | |||||||
| chr2:179973935 | G | A | 1 | a0001c0001t0001g0022 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.582-133C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179973935 | |||||||
| chr2:179973950 | A | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(48): Show |
76 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.582-148T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179973950 | |||||||
| chr2:179974031 | C | T | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.582-229G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974031 | |||||||
| chr2:179974281 | A | G | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.582-479T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974281 | |||||||
| chr2:179974382 | C | G | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.582-580G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974382 | |||||||
| chr2:179974514 | A | G | 55 | a0001c0015t0002g0269 a0002c0002t0002g0001 a0002c0002t0002g0005 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.582-712T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974514 | |||||||
| chr2:179974530 | A | G | 4 | a0001c0017t0009g0273 a0005c0007t0002g0039 a0005c0007t0002g0226 others(1): Show |
5 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.582-728T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974530 | |||||||
| chr2:179974762 | G | A | 1 | a0003c0003t0002g0203 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.582-960C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974762 | |||||||
| chr2:179974854 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.582-1052G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974854 | |||||||
| chr2:179974893 | T | C | 56 | a0001c0015t0002g0269 a0002c0002t0002g0001 a0002c0002t0002g0005 others(53): Show |
84 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.582-1091A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974893 | |||||||
| chr2:179974942 | T | G | 2 | a0001c0001t0001g0137 a0006c0006t0001g0106 |
2 | HG00558.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.582-1140A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974942 | |||||||
| chr2:179974980 | G | A | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(200): Show |
279 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.582-1178C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179974980 | |||||||
| chr2:179975065 | T | A | 1 | a0002c0002t0002g0239 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.582-1263A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179975065 | |||||||
| chr2:179975066 | T | A | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(200): Show |
279 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.582-1264A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179975066 | |||||||
| chr2:179975198 | T | C | 3 | a0002c0002t0002g0042 a0002c0002t0002g0246 a0002c0002t0002g0247 |
4 | NA18960.hp1 NA18999.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.582-1396A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179975198 | |||||||
| chr2:179975341 | C | T | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.582-1539G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179975341 | |||||||
| chr2:179975413 | C | T | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.582-1611G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179975413 | |||||||
| chr2:179975439 | G | C | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.582-1637C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179975439 | |||||||
| chr2:179975678 | T | C | 22 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(19): Show |
38 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.582-1876A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179975678 | |||||||
| chr2:179975695 | G | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(203): Show |
282 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.582-1893C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179975695 | |||||||
| chr2:179975752 | G | A | 55 | a0001c0015t0002g0269 a0002c0002t0002g0001 a0002c0002t0002g0005 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.582-1950C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179975752 | |||||||
| chr2:179975784 | T | C | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.582-1982A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179975784 | |||||||
| chr2:179976381 | A | C | 1 | a0001c0008t0002g0180 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.581+1809T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179976381 | |||||||
| chr2:179976506 | A | AC | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(200): Show |
279 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.581+1683dupG | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179976506 | |||||||
| chr2:179976597 | A | AACG | 106 | a0001c0015t0002g0269 a0001c0017t0009g0273 a0002c0002t0002g0001 others(103): Show |
153 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.581+1592_581+1593i others(5): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179976597 | |||||||
| chr2:179976687 | T | C | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.581+1503A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179976687 | |||||||
| chr2:179976710 | A | T | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.581+1480T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179976710 | |||||||
| chr2:179976728 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.581+1462C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179976728 | |||||||
| chr2:179976827 | T | G | 56 | a0001c0015t0002g0269 a0002c0002t0002g0001 a0002c0002t0002g0005 others(53): Show |
84 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.581+1363A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179976827 | |||||||
| chr2:179976947 | G | C | 1 | a0001c0001t0001g0077 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.581+1243C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179976947 | |||||||
| chr2:179976973 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.581+1217C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179976973 | |||||||
| chr2:179977118 | G | A | 1 | a0002c0002t0002g0260 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.581+1072C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179977118 | |||||||
| chr2:179977187 | T | G | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.581+1003A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179977187 | |||||||
| chr2:179977693 | T | C | 1 | a0003c0003t0002g0204 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.581+497A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179977693 | |||||||
| chr2:179977776 | T | C | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.581+414A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179977776 | |||||||
| chr2:179977817 | C | T | 1 | a0004c0004t0002g0223 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.581+373G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179977817 | |||||||
| chr2:179977899 | C | G | 1 | a0001c0001t0001g0155 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.581+291G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179977899 | |||||||
| chr2:179977900 | G | A | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
192 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.581+290C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179977900 | |||||||
| chr2:179978047 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.581+143T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 6/19 | chr2 | 179978047 | |||||||
| chr2:179978399 | C | T | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.453-81G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179978399 | |||||||
| chr2:179978483 | TC | T | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.453-166delG | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179978483 | |||||||
| chr2:179978681 | T | G | 2 | a0004c0004t0002g0176 a0004c0004t0002g0177 |
2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.453-363A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179978681 | |||||||
| chr2:179978806 | C | G | 1 | a0001c0001t0001g0144 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.453-488G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179978806 | |||||||
| chr2:179978809 | C | G | 1 | a0002c0002t0002g0240 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.453-491G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179978809 | |||||||
| chr2:179978862 | TTACC | T | 101 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(98): Show |
147 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.453-548_453-545del others(4): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179978862 | |||||||
| chr2:179979031 | T | C | 4 | a0001c0017t0009g0273 a0005c0007t0002g0039 a0005c0007t0002g0226 others(1): Show |
5 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.453-713A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979031 | |||||||
| chr2:179979148 | A | C | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.453-830T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979148 | |||||||
| chr2:179979282 | A | AAAC | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.453-967_453-965dup others(3): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979282 | |||||||
| chr2:179979300 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.453-982A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979300 | |||||||
| chr2:179979343 | C | T | 3 | a0005c0007t0002g0039 a0005c0007t0002g0226 a0005c0020t0002g0225 |
4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.453-1025G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979343 | |||||||
| chr2:179979436 | G | A | 1 | a0001c0008t0002g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.453-1118C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979436 | |||||||
| chr2:179979576 | T | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.453-1258A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979576 | |||||||
| chr2:179979631 | G | T | 3 | a0001c0008t0002g0175 a0001c0008t0002g0180 a0001c0014t0002g0181 |
3 | HG03453.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.453-1313C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979631 | |||||||
| chr2:179979655 | G | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.453-1337C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979655 | |||||||
| chr2:179979853 | T | C | 1 | a0002c0002t0002g0263 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.453-1535A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979853 | |||||||
| chr2:179979862 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.453-1544C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179979862 | |||||||
| chr2:179980055 | C | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(46): Show |
74 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.452+1697G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980055 | |||||||
| chr2:179980114 | C | T | 1 | a0002c0002t0002g0233 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.452+1638G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980114 | |||||||
| chr2:179980419 | A | AT | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
262 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.452+1332dupA | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980419 | |||||||
| chr2:179980419 | A | ATT | 10 | a0001c0001t0001g0092 a0001c0001t0001g0105 a0001c0001t0001g0155 others(7): Show |
12 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.452+1331_452+1332d others(4): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980419 | |||||||
| chr2:179980513 | G | C | 2 | a0002c0002t0002g0244 a0002c0002t0002g0245 |
2 | HG02027.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.452+1239C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980513 | |||||||
| chr2:179980518 | T | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
368 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.452+1234A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980518 | |||||||
| chr2:179980527 | T | C | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.452+1225A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980527 | |||||||
| chr2:179980637 | C | T | 1 | a0003c0003t0002g0182 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.452+1115G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980637 | |||||||
| chr2:179980661 | C | T | 3 | a0005c0007t0002g0039 a0005c0007t0002g0226 a0005c0020t0002g0225 |
4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.452+1091G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980661 | |||||||
| chr2:179980671 | C | T | 3 | a0001c0008t0002g0175 a0001c0008t0002g0180 a0001c0014t0002g0181 |
3 | HG03453.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.452+1081G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980671 | |||||||
| chr2:179980680 | T | C | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.452+1072A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980680 | |||||||
| chr2:179980833 | C | T | 1 | a0001c0001t0001g0013 | 3 | HG02486.hp2 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.452+919G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980833 | |||||||
| chr2:179980965 | T | C | 6 | a0002c0002t0002g0041 a0002c0002t0002g0043 a0002c0002t0002g0251 others(3): Show |
8 | HG02080.hp2 HG02155.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.452+787A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179980965 | |||||||
| chr2:179981053 | T | TA | 3 | a0002c0002t0002g0042 a0002c0002t0002g0246 a0002c0002t0002g0247 |
4 | NA18960.hp1 NA18999.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.452+698dupT | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179981053 | |||||||
| chr2:179981610 | T | C | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.452+142A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 5/19 | chr2 | 179981610 | |||||||
| chr2:179982016 | G | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(203): Show |
282 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.207-19C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179982016 | |||||||
| chr2:179982091 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.207-94G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179982091 | |||||||
| chr2:179982355 | A | G | 2 | a0005c0007t0002g0039 a0005c0007t0002g0226 |
3 | HG03195.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.207-358T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179982355 | |||||||
| chr2:179982720 | T | C | 3 | a0004c0004t0002g0270 a0004c0004t0002g0271 a0004c0004t0004g0032 |
4 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.207-723A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179982720 | |||||||
| chr2:179982862 | C | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0144 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.207-865G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179982862 | |||||||
| chr2:179983147 | T | G | 1 | a0002c0002t0002g0253 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.207-1150A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983147 | |||||||
| chr2:179983179 | T | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.207-1182A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983179 | |||||||
| chr2:179983309 | T | C | 4 | a0002c0002t0002g0020 a0002c0002t0002g0248 a0002c0002t0002g0249 others(1): Show |
6 | NA18747.hp1 NA18939.hp1 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.207-1312A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983309 | |||||||
| chr2:179983311 | T | A | 2 | a0001c0015t0002g0269 a0002c0002t0002g0045 |
3 | HG02630.hp1 HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.207-1314A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983311 | |||||||
| chr2:179983463 | A | G | 1 | a0002c0002t0002g0237 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.207-1466T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983463 | |||||||
| chr2:179983487 | C | T | 13 | a0004c0004t0002g0017 a0004c0004t0002g0037 a0004c0004t0002g0038 others(10): Show |
17 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.207-1490G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983487 | |||||||
| chr2:179983564 | T | C | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.207-1567A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983564 | |||||||
| chr2:179983758 | T | C | 1 | a0002c0002t0002g0259 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.207-1761A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983758 | |||||||
| chr2:179983761 | C | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(203): Show |
283 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.207-1764G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983761 | |||||||
| chr2:179983802 | A | G | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.207-1805T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983802 | |||||||
| chr2:179983924 | C | T | 13 | a0004c0004t0002g0017 a0004c0004t0002g0037 a0004c0004t0002g0038 others(10): Show |
17 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.207-1927G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983924 | |||||||
| chr2:179983961 | T | C | 3 | a0005c0007t0002g0039 a0005c0007t0002g0226 a0005c0020t0002g0225 |
4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.207-1964A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179983961 | |||||||
| chr2:179984055 | C | A | 4 | a0001c0017t0009g0273 a0004c0004t0002g0270 a0004c0004t0002g0271 others(1): Show |
5 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.207-2058G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984055 | |||||||
| chr2:179984165 | C | T | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.207-2168G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984165 | |||||||
| chr2:179984223 | T | C | 1 | a0002c0002t0002g0232 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.207-2226A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984223 | |||||||
| chr2:179984227 | T | C | 1 | a0001c0008t0002g0180 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.207-2230A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984227 | |||||||
| chr2:179984257 | C | T | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(145): Show |
196 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.207-2260G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984257 | |||||||
| chr2:179984363 | A | T | 58 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(55): Show |
87 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.206+2332T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984363 | |||||||
| chr2:179984472 | T | C | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.206+2223A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984472 | |||||||
| chr2:179984496 | T | C | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.206+2199A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984496 | |||||||
| chr2:179984539 | A | G | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.206+2156T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984539 | |||||||
| chr2:179984548 | G | A | 1 | a0001c0014t0002g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.206+2147C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984548 | |||||||
| chr2:179984775 | A | C | 1 | a0002c0002t0002g0251 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.206+1920T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984775 | |||||||
| chr2:179984935 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.206+1760A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984935 | |||||||
| chr2:179984978 | C | A | 1 | a0001c0001t0001g0138 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.206+1717G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179984978 | |||||||
| chr2:179985286 | T | C | 3 | a0001c0001t0001g0050 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02615.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.206+1409A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179985286 | |||||||
| chr2:179985353 | T | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.206+1342A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179985353 | |||||||
| chr2:179985539 | G | A | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.206+1156C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179985539 | |||||||
| chr2:179985820 | G | GTA | 66 | a0001c0001t0001g0054 a0001c0001t0001g0114 a0001c0008t0002g0175 others(63): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.206+873_206+874dup others(2): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179985820 | |||||||
| chr2:179985902 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.206+793C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179985902 | |||||||
| chr2:179985978 | T | C | 1 | a0001c0001t0001g0050 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.206+717A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179985978 | |||||||
| chr2:179986183 | G | T | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.206+512C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179986183 | |||||||
| chr2:179986386 | A | G | 3 | a0004c0004t0002g0270 a0004c0004t0002g0271 a0004c0004t0004g0032 |
4 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.206+309T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179986386 | |||||||
| chr2:179986389 | G | A | 1 | a0002c0002t0002g0263 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.206+306C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179986389 | |||||||
| chr2:179986434 | A | G | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.206+261T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179986434 | |||||||
| chr2:179986475 | A | T | 13 | a0004c0004t0002g0017 a0004c0004t0002g0037 a0004c0004t0002g0038 others(10): Show |
17 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.206+220T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 4/19 | chr2 | 179986475 | |||||||
| chr2:179987139 | T | C | 5 | a0002c0002t0002g0043 a0002c0002t0002g0251 a0002c0002t0002g0252 others(2): Show |
6 | HG02080.hp2 NA18965.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.96-334A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179987139 | |||||||
| chr2:179987223 | T | C | 47 | a0002c0013t0002g0265 a0003c0003t0002g0007 a0003c0003t0002g0012 others(44): Show |
65 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.96-418A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179987223 | |||||||
| chr2:179987450 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.96-645T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179987450 | |||||||
| chr2:179987555 | T | C | 1 | a0002c0002t0002g0233 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.96-750A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179987555 | |||||||
| chr2:179987646 | G | C | 1 | a0002c0002t0002g0254 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.96-841C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179987646 | |||||||
| chr2:179987692 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.95+885G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179987692 | |||||||
| chr2:179987700 | AT | A | 46 | a0003c0003t0002g0007 a0003c0003t0002g0012 a0003c0003t0002g0014 others(43): Show |
64 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.95+876delA | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179987700 | |||||||
| chr2:179988000 | T | C | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.95+577A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179988000 | |||||||
| chr2:179988040 | A | G | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.95+537T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179988040 | |||||||
| chr2:179988179 | G | A | 1 | a0001c0008t0002g0180 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.95+398C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179988179 | |||||||
| chr2:179988232 | C | A | 3 | a0004c0004t0002g0270 a0004c0004t0002g0271 a0004c0004t0004g0032 |
4 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95+345G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179988232 | |||||||
| chr2:179988281 | G | A | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.95+296C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179988281 | |||||||
| chr2:179988455 | T | C | 7 | a0001c0017t0009g0273 a0004c0004t0002g0270 a0004c0004t0002g0271 others(4): Show |
9 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.95+122A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 3/19 | chr2 | 179988455 | |||||||
| chr2:179988740 | A | C | 2 | a0003c0003t0002g0018 a0003c0003t0002g0224 |
4 | NA18971.hp2 NA18990.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-96T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179988740 | |||||||
| chr2:179988888 | T | G | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.28-244A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179988888 | |||||||
| chr2:179988940 | G | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
179 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.28-296C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179988940 | |||||||
| chr2:179989067 | C | G | 4 | a0001c0001t0001g0071 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
4 | HG01081.hp2 HG01884.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-423G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989067 | |||||||
| chr2:179989074 | C | G | 1 | a0001c0001t0001g0104 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.28-430G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989074 | |||||||
| chr2:179989115 | T | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
179 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.28-471A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989115 | |||||||
| chr2:179989241 | TATA | T | 264 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(261): Show |
362 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.28-600_28-598delTA others(1): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989241 | |||||||
| chr2:179989250 | A | T | 265 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(262): Show |
360 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.28-606T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989250 | |||||||
| chr2:179989284 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.28-640C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989284 | |||||||
| chr2:179989503 | C | T | 1 | a0003c0003t0002g0182 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.28-859G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989503 | |||||||
| chr2:179989590 | A | T | 2 | a0002c0002t0002g0235 a0002c0002t0002g0236 |
2 | NA18950.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.28-946T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989590 | |||||||
| chr2:179989710 | T | C | 1 | a0002c0002t0002g0260 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.28-1066A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989710 | |||||||
| chr2:179989893 | A | G | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.28-1249T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989893 | |||||||
| chr2:179989930 | T | C | 1 | a0002c0002t0002g0044 | 2 | HG03491.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.28-1286A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989930 | |||||||
| chr2:179989938 | G | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02615.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.28-1294C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989938 | |||||||
| chr2:179989984 | C | G | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.28-1340G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179989984 | |||||||
| chr2:179990317 | C | G | 1 | a0002c0002t0002g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.28-1673G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990317 | |||||||
| chr2:179990505 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.28-1861T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990505 | |||||||
| chr2:179990542 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0115 a0001c0001t0001g0116 |
6 | HG01081.hp1 HG01123.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-1898G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990542 | |||||||
| chr2:179990546 | C | CAG | 3 | a0001c0001t0001g0101 a0001c0001t0001g0140 a0004c0004t0002g0037 |
4 | HG01981.hp1 HG02922.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-1904_28-1903dup others(2): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990546 | |||||||
| chr2:179990546 | CAG | C | 35 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0051 others(32): Show |
41 | HG00558.hp2 HG02056.hp1 HG02074.hp2 others(38): Show |
intron_variant | MODIFIER | c.28-1904_28-1903del others(2): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990546 | |||||||
| chr2:179990546 | CAGAG | C | 214 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.28-1906_28-1903del others(4): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990546 | |||||||
| chr2:179990556 | G | C | 1 | a0001c0001t0001g0078 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.28-1912C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990556 | |||||||
| chr2:179990743 | G | A | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.28-2099C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990743 | |||||||
| chr2:179990773 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.28-2129A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990773 | |||||||
| chr2:179990830 | A | G | 1 | a0001c0001t0003g0173 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.28-2186T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990830 | |||||||
| chr2:179990874 | T | C | 2 | a0001c0001t0001g0139 a0001c0001t0001g0143 |
2 | NA18951.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.28-2230A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990874 | |||||||
| chr2:179990899 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.28-2255C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179990899 | |||||||
| chr2:179991136 | C | T | 47 | a0002c0013t0002g0265 a0003c0003t0002g0007 a0003c0003t0002g0012 others(44): Show |
65 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.27+2179G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991136 | |||||||
| chr2:179991169 | C | T | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
367 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(364): Show |
intron_variant | MODIFIER | c.27+2146G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991169 | |||||||
| chr2:179991266 | C | CT | 47 | a0002c0013t0002g0265 a0003c0003t0002g0007 a0003c0003t0002g0012 others(44): Show |
65 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.27+2048dupA | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991266 | |||||||
| chr2:179991319 | G | A | 1 | a0003c0003t0002g0205 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.27+1996C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991319 | |||||||
| chr2:179991345 | T | C | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.27+1970A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991345 | |||||||
| chr2:179991529 | G | A | 1 | a0005c0020t0002g0225 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.27+1786C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991529 | |||||||
| chr2:179991674 | G | A | 3 | a0002c0002t0002g0019 a0002c0002t0002g0227 a0002c0002t0002g0228 |
5 | HG02109.hp2 HG02145.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+1641C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991674 | |||||||
| chr2:179991687 | A | G | 1 | a0001c0008t0002g0180 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.27+1628T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991687 | |||||||
| chr2:179991729 | G | A | 11 | a0001c0001t0001g0011 a0001c0001t0001g0050 a0001c0001t0001g0140 others(8): Show |
14 | HG02145.hp2 HG02257.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.27+1586C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991729 | |||||||
| chr2:179991732 | T | C | 252 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(249): Show |
347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.27+1583A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991732 | |||||||
| chr2:179991789 | A | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | NA19079.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.27+1526T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991789 | |||||||
| chr2:179991931 | T | C | 5 | a0002c0002t0002g0021 a0002c0002t0002g0256 a0002c0002t0002g0257 others(2): Show |
7 | HG00733.hp1 HG00741.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.27+1384A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179991931 | |||||||
| chr2:179992149 | T | A | 22 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(19): Show |
38 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.27+1166A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179992149 | |||||||
| chr2:179992498 | C | A | 1 | a0001c0001t0001g0097 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.27+817G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179992498 | |||||||
| chr2:179992545 | T | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
368 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.27+770A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179992545 | |||||||
| chr2:179992548 | C | T | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.27+767G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179992548 | |||||||
| chr2:179992742 | A | G | 1 | a0002c0002t0002g0260 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.27+573T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179992742 | |||||||
| chr2:179992856 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27+459G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179992856 | |||||||
| chr2:179992869 | A | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.27+446T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179992869 | |||||||
| chr2:179992940 | T | G | 1 | a0001c0001t0001g0143 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.27+375A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179992940 | |||||||
| chr2:179992986 | C | T | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
190 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.27+329G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179992986 | |||||||
| chr2:179993004 | TAC | T | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
190 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.27+309_27+310delGT | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179993004 | |||||||
| chr2:179993004 | TACAC | T | 4 | a0001c0017t0009g0273 a0004c0004t0002g0270 a0004c0004t0002g0271 others(1): Show |
5 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+307_27+310delGT others(2): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179993004 | |||||||
| chr2:179993020 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG01081.hp2 HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.27+295G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179993020 | |||||||
| chr2:179993030 | C | T | 13 | a0004c0004t0002g0017 a0004c0004t0002g0037 a0004c0004t0002g0038 others(10): Show |
17 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.27+285G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179993030 | |||||||
| chr2:179993048 | T | G | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.27+267A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 2/19 | chr2 | 179993048 | |||||||
| chr2:179993465 | T | C | 1 | a0001c0014t0002g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-113-11A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179993465 | |||||||
| chr2:179993729 | A | G | 19 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0024 others(16): Show |
28 | HG00280.hp1 HG00558.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.-113-275T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179993729 | |||||||
| chr2:179994119 | G | A | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-113-665C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994119 | |||||||
| chr2:179994221 | CAAAAATA others(5): Show |
C | 1 | a0001c0022t0001g0088 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-113-779_-113-768d others(14): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994221 | |||||||
| chr2:179994255 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-113-801A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994255 | |||||||
| chr2:179994264 | T | C | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-113-810A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994264 | |||||||
| chr2:179994311 | GA | G | 43 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0020 others(40): Show |
67 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.-113-858delT | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994311 | |||||||
| chr2:179994546 | C | T | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 |
3 | HG01361.hp2 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-113-1092G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994546 | |||||||
| chr2:179994549 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-113-1095G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994549 | |||||||
| chr2:179994567 | G | A | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.-113-1113C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994567 | |||||||
| chr2:179994598 | T | G | 1 | a0003c0003t0002g0206 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-113-1144A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994598 | |||||||
| chr2:179994612 | T | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0001g0080 |
4 | HG00558.hp1 HG02135.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.-113-1158A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994612 | |||||||
| chr2:179994832 | C | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
367 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(364): Show |
intron_variant | MODIFIER | c.-113-1378G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994832 | |||||||
| chr2:179994901 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG02040.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.-113-1447C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994901 | |||||||
| chr2:179994940 | C | A | 1 | a0001c0014t0002g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-113-1486G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179994940 | |||||||
| chr2:179995005 | C | T | 1 | a0002c0002t0002g0229 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-113-1551G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179995005 | |||||||
| chr2:179995012 | G | A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(43): Show |
71 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.-113-1558C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179995012 | |||||||
| chr2:179995112 | C | T | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.-113-1658G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179995112 | |||||||
| chr2:179995113 | G | A | 1 | a0001c0008t0002g0180 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-113-1659C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179995113 | |||||||
| chr2:179995219 | T | C | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.-113-1765A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179995219 | |||||||
| chr2:179995588 | T | C | 1 | a0003c0003t0002g0207 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-113-2134A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179995588 | |||||||
| chr2:179995670 | A | C | 1 | a0003c0003t0002g0182 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-113-2216T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179995670 | |||||||
| chr2:179995761 | G | A | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.-113-2307C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179995761 | |||||||
| chr2:179996007 | T | C | 1 | a0003c0003t0002g0208 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-113-2553A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996007 | |||||||
| chr2:179996218 | A | G | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.-113-2764T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996218 | |||||||
| chr2:179996277 | A | T | 2 | a0003c0003t0002g0210 a0003c0003t0002g0211 |
2 | HG01256.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-113-2823T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996277 | |||||||
| chr2:179996312 | C | T | 3 | a0002c0002t0002g0019 a0002c0002t0002g0227 a0002c0002t0002g0228 |
5 | HG02109.hp2 HG02145.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-113-2858G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996312 | |||||||
| chr2:179996386 | A | C | 47 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(44): Show |
72 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.-113-2932T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996386 | |||||||
| chr2:179996725 | G | A | 13 | a0004c0004t0002g0017 a0004c0004t0002g0037 a0004c0004t0002g0038 others(10): Show |
17 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.-113-3271C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996725 | |||||||
| chr2:179996731 | G | C | 1 | a0004c0018t0001g0081 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-113-3277C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996731 | |||||||
| chr2:179996761 | A | G | 3 | a0001c0001t0001g0146 a0001c0001t0003g0031 a0001c0001t0003g0173 |
4 | HG00280.hp1 HG01069.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.-113-3307T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996761 | |||||||
| chr2:179996788 | G | C | 7 | a0001c0017t0009g0273 a0004c0004t0002g0270 a0004c0004t0002g0271 others(4): Show |
9 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-113-3334C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996788 | |||||||
| chr2:179996831 | T | TA | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
197 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.-113-3378dupT | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996831 | |||||||
| chr2:179996831 | T | TTA | 2 | a0005c0007t0002g0039 a0005c0007t0002g0226 |
3 | HG03195.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-113-3378_-113-337 others(6): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996831 | |||||||
| chr2:179996883 | C | CA | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.-113-3430dupT | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179996883 | |||||||
| chr2:179997259 | A | G | 1 | a0001c0008t0002g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-113-3805T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179997259 | |||||||
| chr2:179997337 | C | T | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-113-3883G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179997337 | |||||||
| chr2:179997406 | C | G | 13 | a0004c0004t0002g0017 a0004c0004t0002g0037 a0004c0004t0002g0038 others(10): Show |
17 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.-113-3952G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179997406 | |||||||
| chr2:179997468 | C | G | 1 | a0002c0002t0002g0227 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-113-4014G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179997468 | |||||||
| chr2:179997593 | T | G | 13 | a0004c0004t0002g0017 a0004c0004t0002g0037 a0004c0004t0002g0038 others(10): Show |
17 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.-113-4139A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179997593 | |||||||
| chr2:179997610 | T | C | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.-113-4156A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179997610 | |||||||
| chr2:179997879 | A | G | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(203): Show |
283 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.-113-4425T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179997879 | |||||||
| chr2:179997927 | C | G | 13 | a0004c0004t0002g0017 a0004c0004t0002g0037 a0004c0004t0002g0038 others(10): Show |
17 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.-113-4473G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179997927 | |||||||
| chr2:179998340 | C | T | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.-113-4886G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998340 | |||||||
| chr2:179998357 | T | G | 3 | a0001c0001t0001g0146 a0001c0001t0003g0031 a0001c0001t0003g0173 |
4 | HG00280.hp1 HG01069.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.-113-4903A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998357 | |||||||
| chr2:179998373 | A | C | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-113-4919T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998373 | |||||||
| chr2:179998441 | A | T | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
200 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.-113-4987T>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998441 | |||||||
| chr2:179998459 | T | G | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.-113-5005A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998459 | |||||||
| chr2:179998787 | T | A | 1 | a0002c0002t0002g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-113-5333A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998787 | |||||||
| chr2:179998793 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-113-5339C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998793 | |||||||
| chr2:179998829 | T | C | 1 | a0001c0014t0002g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-113-5375A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998829 | |||||||
| chr2:179998934 | T | C | 3 | a0001c0005t0001g0149 a0001c0005t0001g0150 a0001c0005t0001g0151 |
3 | HG02615.hp1 HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-113-5480A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998934 | |||||||
| chr2:179998946 | A | C | 7 | a0001c0001t0001g0071 a0001c0001t0001g0083 a0001c0001t0001g0089 others(4): Show |
7 | HG01081.hp2 HG01884.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-113-5492T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998946 | |||||||
| chr2:179998981 | G | A | 54 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(51): Show |
82 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.-113-5527C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179998981 | |||||||
| chr2:179999273 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-113-5819A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179999273 | |||||||
| chr2:179999382 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02145.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-113-5928G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179999382 | |||||||
| chr2:179999826 | C | A | 1 | a0003c0003t0002g0209 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-113-6372G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179999826 | |||||||
| chr2:179999954 | G | C | 4 | a0003c0003t0002g0210 a0003c0003t0002g0211 a0003c0003t0002g0212 others(1): Show |
4 | HG01123.hp1 HG01256.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.-113-6500C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 179999954 | |||||||
| chr2:180000069 | C | T | 2 | a0005c0007t0002g0039 a0005c0007t0002g0226 |
3 | HG03195.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-113-6615G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000069 | |||||||
| chr2:180000240 | A | G | 60 | a0002c0013t0002g0265 a0003c0003t0002g0007 a0003c0003t0002g0012 others(57): Show |
82 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.-114+6627T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000240 | |||||||
| chr2:180000244 | G | C | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-114+6623C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000244 | |||||||
| chr2:180000406 | T | G | 1 | a0001c0001t0001g0153 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-114+6461A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000406 | |||||||
| chr2:180000481 | G | T | 3 | a0004c0004t0002g0270 a0004c0004t0002g0271 a0004c0004t0004g0032 |
4 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-114+6386C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000481 | |||||||
| chr2:180000767 | G | C | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-114+6100C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000767 | |||||||
| chr2:180000770 | T | C | 1 | a0003c0003t0002g0224 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-114+6097A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000770 | |||||||
| chr2:180000820 | GAA | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0084 others(3): Show |
14 | NA18942.hp1 NA18948.hp1 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.-114+6045_-114+604 others(6): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000820 | |||||||
| chr2:180000872 | A | C | 2 | a0003c0003t0002g0267 a0003c0003t0002g0268 |
2 | NA19004.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-114+5995T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000872 | |||||||
| chr2:180000898 | T | G | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-114+5969A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000898 | |||||||
| chr2:180000940 | A | G | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-114+5927T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180000940 | |||||||
| chr2:180001006 | T | A | 1 | a0001c0001t0001g0154 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-114+5861A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001006 | |||||||
| chr2:180001037 | C | T | 3 | a0004c0004t0002g0270 a0004c0004t0002g0271 a0004c0004t0004g0032 |
4 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-114+5830G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001037 | |||||||
| chr2:180001048 | C | A | 1 | a0005c0020t0002g0225 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-114+5819G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001048 | |||||||
| chr2:180001157 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-114+5710A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001157 | |||||||
| chr2:180001420 | G | T | 3 | a0004c0004t0002g0270 a0004c0004t0002g0271 a0004c0004t0004g0032 |
4 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-114+5447C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001420 | |||||||
| chr2:180001519 | G | A | 8 | a0001c0008t0002g0175 a0001c0008t0002g0180 a0001c0014t0002g0181 others(5): Show |
9 | HG02280.hp2 HG02451.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-114+5348C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001519 | |||||||
| chr2:180001519 | G | T | 2 | a0005c0007t0002g0039 a0005c0007t0002g0226 |
3 | HG03195.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-114+5348C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001519 | |||||||
| chr2:180001527 | G | A | 22 | a0001c0008t0002g0175 a0001c0008t0002g0180 a0001c0014t0002g0181 others(19): Show |
27 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.-114+5340C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001527 | |||||||
| chr2:180001634 | G | T | 1 | a0001c0001t0001g0025 | 2 | NA18948.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-114+5233C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001634 | |||||||
| chr2:180001814 | C | T | 2 | a0003c0003t0002g0182 a0003c0003t0002g0183 |
2 | HG01243.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-114+5053G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001814 | |||||||
| chr2:180001894 | T | C | 2 | a0005c0007t0002g0039 a0005c0007t0002g0226 |
3 | HG03195.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-114+4973A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001894 | |||||||
| chr2:180001928 | C | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0165 |
2 | NA18972.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.-114+4939G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180001928 | |||||||
| chr2:180002024 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-114+4843G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180002024 | |||||||
| chr2:180002328 | A | G | 2 | a0003c0003t0005g0274 a0003c0003t0005g0275 |
2 | NA18966.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-114+4539T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180002328 | |||||||
| chr2:180002367 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-114+4500G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180002367 | |||||||
| chr2:180002469 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-114+4398A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180002469 | |||||||
| chr2:180002515 | G | T | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-114+4352C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180002515 | |||||||
| chr2:180002695 | T | C | 6 | a0001c0008t0002g0175 a0004c0004t0002g0033 a0004c0004t0002g0176 others(3): Show |
7 | HG02280.hp2 HG02451.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-114+4172A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180002695 | |||||||
| chr2:180002793 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
7 | HG02622.hp2 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-114+4074C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180002793 | |||||||
| chr2:180002847 | A | G | 1 | a0001c0015t0002g0269 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-114+4020T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180002847 | |||||||
| chr2:180002901 | A | C | 1 | a0004c0018t0001g0081 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-114+3966T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180002901 | |||||||
| chr2:180002919 | G | C | 7 | a0001c0017t0009g0273 a0004c0004t0002g0270 a0004c0004t0002g0271 others(4): Show |
9 | HG02257.hp1 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-114+3948C>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180002919 | |||||||
| chr2:180003063 | T | C | 1 | a0002c0002t0002g0046 | 2 | NA18992.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-114+3804A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180003063 | |||||||
| chr2:180003115 | G | A | 1 | a0002c0013t0002g0265 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-114+3752C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180003115 | |||||||
| chr2:180003176 | T | G | 1 | a0001c0001t0001g0069 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-114+3691A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180003176 | |||||||
| chr2:180003301 | C | A | 1 | a0004c0004t0002g0223 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-114+3566G>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180003301 | |||||||
| chr2:180003666 | C | T | 46 | a0003c0003t0002g0007 a0003c0003t0002g0012 a0003c0003t0002g0014 others(43): Show |
64 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.-114+3201G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180003666 | |||||||
| chr2:180003731 | A | G | 14 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0072 others(11): Show |
21 | HG00558.hp1 HG01496.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.-114+3136T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180003731 | |||||||
| chr2:180003759 | A | C | 1 | a0001c0001t0001g0071 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-114+3108T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180003759 | |||||||
| chr2:180003901 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-114+2966T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180003901 | |||||||
| chr2:180003915 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-114+2952T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180003915 | |||||||
| chr2:180004035 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-114+2832A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004035 | |||||||
| chr2:180004060 | G | T | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-114+2807C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004060 | |||||||
| chr2:180004111 | A | C | 131 | a0001c0001t0001g0069 a0001c0008t0002g0175 a0001c0008t0002g0180 others(128): Show |
184 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.-114+2756T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004111 | |||||||
| chr2:180004361 | T | G | 2 | a0002c0002t0002g0047 a0002c0002t0002g0266 |
3 | HG02055.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-114+2506A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004361 | |||||||
| chr2:180004418 | G | A | 68 | a0001c0008t0002g0175 a0001c0008t0002g0180 a0001c0014t0002g0181 others(65): Show |
91 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.-114+2449C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004418 | |||||||
| chr2:180004430 | C | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0056 others(16): Show |
26 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.-114+2437G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004430 | |||||||
| chr2:180004457 | G | T | 55 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0019 others(52): Show |
83 | HG00621.hp1 HG00642.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.-114+2410C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004457 | |||||||
| chr2:180004461 | A | G | 127 | a0001c0008t0002g0175 a0001c0008t0002g0180 a0001c0014t0002g0181 others(124): Show |
179 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.-114+2406T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004461 | |||||||
| chr2:180004500 | T | G | 3 | a0001c0001t0001g0161 a0007c0009t0001g0162 a0007c0009t0001g0163 |
3 | HG00738.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-114+2367A>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004500 | |||||||
| chr2:180004610 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-114+2257C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004610 | |||||||
| chr2:180004683 | C | G | 1 | a0001c0012t0001g0055 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-114+2184G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004683 | |||||||
| chr2:180004808 | A | G | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | NA18947.hp2 NA18985.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-114+2059T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004808 | |||||||
| chr2:180004822 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-114+2045C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004822 | |||||||
| chr2:180004841 | G | A | 1 | a0001c0001t0001g0013 | 3 | HG02486.hp2 HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-114+2026C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004841 | |||||||
| chr2:180004873 | G | T | 1 | a0001c0001t0001g0050 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-114+1994C>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004873 | |||||||
| chr2:180004893 | C | T | 8 | a0001c0008t0002g0175 a0001c0008t0002g0180 a0001c0014t0002g0181 others(5): Show |
9 | HG02280.hp2 HG02451.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-114+1974G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004893 | |||||||
| chr2:180004909 | G | A | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-114+1958C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180004909 | |||||||
| chr2:180005024 | A | G | 1 | a0001c0017t0009g0273 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-114+1843T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005024 | |||||||
| chr2:180005135 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-114+1732A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005135 | |||||||
| chr2:180005303 | A | C | 126 | a0001c0008t0002g0175 a0001c0008t0002g0180 a0001c0014t0002g0181 others(123): Show |
178 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.-114+1564T>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005303 | |||||||
| chr2:180005405 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-114+1462C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005405 | |||||||
| chr2:180005560 | A | G | 3 | a0005c0007t0002g0039 a0005c0007t0002g0226 a0005c0020t0002g0225 |
4 | HG03195.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-114+1307T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005560 | |||||||
| chr2:180005567 | C | G | 1 | a0001c0001t0001g0049 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-114+1300G>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005567 | |||||||
| chr2:180005742 | C | T | 6 | a0001c0008t0002g0175 a0004c0004t0002g0033 a0004c0004t0002g0176 others(3): Show |
7 | HG02280.hp2 HG02451.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-114+1125G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005742 | |||||||
| chr2:180005782 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02145.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-114+1085A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005782 | |||||||
| chr2:180005785 | A | G | 1 | a0001c0001t0001g0022 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-114+1082T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005785 | |||||||
| chr2:180005800 | G | A | 2 | a0003c0003t0002g0018 a0003c0003t0002g0224 |
4 | NA18971.hp2 NA18990.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.-114+1067C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005800 | |||||||
| chr2:180005863 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-114+1004G>A | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005863 | |||||||
| chr2:180005940 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-114+927A>G | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180005940 | |||||||
| chr2:180006166 | G | A | 65 | a0001c0008t0002g0175 a0001c0008t0002g0180 a0001c0014t0002g0181 others(62): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.-114+701C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180006166 | |||||||
| chr2:180006168 | GTC | G | 65 | a0001c0008t0002g0175 a0001c0008t0002g0180 a0001c0014t0002g0181 others(62): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.-114+697_-114+698d others(4): Show |
CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180006168 | |||||||
| chr2:180006331 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-114+536A>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180006331 | |||||||
| chr2:180006448 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-114+419C>T | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180006448 | |||||||
| chr2:180006668 | A | G | 130 | a0001c0008t0002g0175 a0001c0008t0002g0180 a0001c0014t0002g0181 others(127): Show |
183 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.-114+199T>C | CWC22 | ENSG00000163510.14 | transcript | ENST00000410053.8 | protein_coding | 1/19 | chr2 | 180006668 |