Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55884 |
| ensemblid | ENSG00000176871.9 |
| hgncid | 19222 |
| symbol | WSB2 |
| name | WD repeat and SOCS box containing 2 |
| refseq_nuc | NM_018639.5 |
| refseq_prot | NP_061109.1 |
| ensembl_nuc | ENST00000315436.8 |
| ensembl_prot | ENSP00000319474.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 118032687 |
| end | 118061179 |
| strand | - |
| ver | v1.2 |
| region | chr12:118032687-118061179 |
| region5000 | chr12:118027687-118066179 |
| regionname0 | WSB2_chr12_118032687_118061179 |
| regionname5000 | WSB2_chr12_118027687_118066179 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 404 | 402 | 91 | 70 | 180 | 15 | 44 | 136 | WSB2_chr12_118027687_118066179 | WSB2 | MEAGE others(399): Show |
chr12 | 118027687 | 118066179 |
| a0002 | 0/0 | 404 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | MEAGE others(399): Show |
chr12 | 118027687 | 118066179 |
| a0003 | 0/0 | 404 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | MEAGE others(399): Show |
chr12 | 118027687 | 118066179 |
| a0004 | 0/0 | 404 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | MEAGE others(399): Show |
chr12 | 118027687 | 118066179 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1212 | 215 | 55 | 48 | 79 | 11 | 20 | WSB2_chr12_118027687_118066179 | WSB2 | ATGGA others(1207): Show |
chr12 | 118027687 | 118066179 | ||
| a0001c0002 | 0/0 | 1212 | 170 | 27 | 21 | 94 | 4 | 24 | WSB2_chr12_118027687_118066179 | WSB2 | ATGGA others(1207): Show |
chr12 | 118027687 | 118066179 | ||
| a0001c0003 | 0/0 | 1212 | 6 | 0 | 0 | 6 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | ATGGA others(1207): Show |
chr12 | 118027687 | 118066179 | ||
| a0001c0004 | 0/0 | 1212 | 6 | 6 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | ATGGA others(1207): Show |
chr12 | 118027687 | 118066179 | ||
| a0001c0006 | 0/0 | 1212 | 3 | 3 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | ATGGA others(1207): Show |
chr12 | 118027687 | 118066179 | ||
| a0001c0008 | 0/0 | 1212 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | ATGGA others(1207): Show |
chr12 | 118027687 | 118066179 | ||
| a0001c0009 | 0/0 | 1212 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | ATGGA others(1207): Show |
chr12 | 118027687 | 118066179 | ||
| a0002c0005 | 0/0 | 1212 | 6 | 6 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | ATGGA others(1207): Show |
chr12 | 118027687 | 118066179 | ||
| a0003c0010 | 0/0 | 1212 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | ATGGA others(1207): Show |
chr12 | 118027687 | 118066179 | ||
| a0004c0007 | 0/0 | 1212 | 1 | 0 | 0 | 0 | 1 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | ATGGA others(1207): Show |
chr12 | 118027687 | 118066179 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2855 | 151 | 22 | 41 | 60 | 9 | 17 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2850): Show |
chr12 | 118027687 | 118066179 |
| a0001c0001t0002 | 0/0 | 2855 | 13 | 6 | 1 | 6 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2850): Show |
chr12 | 118027687 | 118066179 |
| a0001c0001t0003 | 0/0 | 2851 | 16 | 15 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2846): Show |
chr12 | 118027687 | 118066179 |
| a0001c0001t0004 | 0/0 | 2856 | 4 | 2 | 0 | 2 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2851): Show |
chr12 | 118027687 | 118066179 |
| a0001c0001t0006 | 0/0 | 2852 | 7 | 1 | 5 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2847): Show |
chr12 | 118027687 | 118066179 |
| a0001c0001t0007 | 0/0 | 2854 | 10 | 0 | 0 | 9 | 1 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2849): Show |
chr12 | 118027687 | 118066179 |
| a0001c0001t0008 | 0/0 | 2856 | 2 | 2 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2851): Show |
chr12 | 118027687 | 118066179 |
| a0001c0001t0010 | 0/0 | 2856 | 3 | 3 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2851): Show |
chr12 | 118027687 | 118066179 |
| a0001c0001t0011 | 0/0 | 2855 | 1 | 0 | 0 | 0 | 1 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2850): Show |
chr12 | 118027687 | 118066179 |
| a0001c0001t0012 | 0/0 | 2855 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2850): Show |
chr12 | 118027687 | 118066179 |
| a0001c0001t0013 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2851): Show |
chr12 | 118027687 | 118066179 |
| a0001c0001t0014 | 0/0 | 2850 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2845): Show |
chr12 | 118027687 | 118066179 |
| a0001c0001t0016 | 0/0 | 2855 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2850): Show |
chr12 | 118027687 | 118066179 |
| a0001c0001t0017 | 0/0 | 2850 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2845): Show |
chr12 | 118027687 | 118066179 |
| a0001c0001t0018 | 0/0 | 2851 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2846): Show |
chr12 | 118027687 | 118066179 |
| a0001c0001t0019 | 0/0 | 2854 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2849): Show |
chr12 | 118027687 | 118066179 |
| a0001c0001t0020 | 0/0 | 2855 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2850): Show |
chr12 | 118027687 | 118066179 |
| a0001c0002t0001 | 0/0 | 2855 | 22 | 6 | 1 | 13 | 0 | 2 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2850): Show |
chr12 | 118027687 | 118066179 |
| a0001c0002t0002 | 0/0 | 2855 | 114 | 7 | 19 | 63 | 4 | 21 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2850): Show |
chr12 | 118027687 | 118066179 |
| a0001c0002t0004 | 0/0 | 2856 | 12 | 11 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2851): Show |
chr12 | 118027687 | 118066179 |
| a0001c0002t0005 | 0/0 | 2855 | 15 | 0 | 0 | 15 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2850): Show |
chr12 | 118027687 | 118066179 |
| a0001c0002t0008 | 0/0 | 2856 | 3 | 2 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2851): Show |
chr12 | 118027687 | 118066179 |
| a0001c0002t0009 | 0/0 | 2854 | 3 | 1 | 0 | 1 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2849): Show |
chr12 | 118027687 | 118066179 |
| a0001c0002t0021 | 0/0 | 2897 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2892): Show |
chr12 | 118027687 | 118066179 |
| a0001c0003t0002 | 0/0 | 2855 | 6 | 0 | 0 | 6 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2850): Show |
chr12 | 118027687 | 118066179 |
| a0001c0004t0006 | 0/0 | 2852 | 5 | 5 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2847): Show |
chr12 | 118027687 | 118066179 |
| a0001c0004t0015 | 0/0 | 2852 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2847): Show |
chr12 | 118027687 | 118066179 |
| a0001c0006t0002 | 0/0 | 2855 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2850): Show |
chr12 | 118027687 | 118066179 |
| a0001c0006t0006 | 0/0 | 2852 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2847): Show |
chr12 | 118027687 | 118066179 |
| a0001c0006t0008 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2851): Show |
chr12 | 118027687 | 118066179 |
| a0001c0008t0002 | 0/0 | 2855 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2850): Show |
chr12 | 118027687 | 118066179 |
| a0001c0009t0002 | 0/0 | 2855 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2850): Show |
chr12 | 118027687 | 118066179 |
| a0002c0005t0001 | 0/0 | 2855 | 6 | 6 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2850): Show |
chr12 | 118027687 | 118066179 |
| a0003c0010t0001 | 0/0 | 2855 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2850): Show |
chr12 | 118027687 | 118066179 |
| a0004c0007t0002 | 0/0 | 2855 | 1 | 0 | 0 | 0 | 1 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | AAGCA others(2850): Show |
chr12 | 118027687 | 118066179 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 15 | 0 | 2 | 7 | 2 | 4 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0002 | 0/0 | 10 | 0 | 7 | 3 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0003 | 0/0 | 8 | 5 | 0 | 0 | 2 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 4 | 1 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0124 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0003g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0003g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0006g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0007g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0007g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0007g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0007g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0007g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0007g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0007g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0007g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0007g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0008g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0010g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0010g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0010g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0011g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0012g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0013g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0014g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0016g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0017g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0018g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0019g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0001t0020g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0004 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0008 | 0/0 | 6 | 2 | 3 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0013 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0004g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0004g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0005g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0005g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0005g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0005g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0008g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0009g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0009g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0009g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0002t0021g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0003t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0003t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0004t0006g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0004t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0004t0015g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0006t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0006t0006g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0006t0008g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0008t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0001c0009t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0002c0005t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0002c0005t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0002c0005t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0003c0010t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| a0004c0007t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | GBR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0283 | EUR | GBR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0250 | EUR | GBR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0013 | EUR | FIN | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | FIN | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00323 | hp2 | a0001 | c0001 | t0007 | g0130 | EUR | FIN | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0225 | EAS | CHS | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | CHS | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0252 | EAS | CHS | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | CHS | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00544 | hp2 | a0001 | c0001 | t0020 | g0118 | EAS | CHS | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | CHS | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0259 | EAS | CHS | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0248 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0021 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0263 | EAS | CHS | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0041 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01168 | hp1 | a0001 | c0001 | t0006 | g0143 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0269 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0055 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0039 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01243 | hp2 | a0001 | c0002 | t0004 | g0289 | AMR | PUR | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0041 | AMR | CLM | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0204 | AMR | CLM | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0021 | AMR | CLM | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0021 | AMR | CLM | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0116 | AMR | CLM | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0219 | AMR | CLM | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | CLM | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0039 | AMR | CLM | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0230 | EUR | IBS | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | IBS | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0189 | EUR | IBS | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01517 | hp2 | a0001 | c0001 | t0011 | g0045 | EUR | IBS | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0215 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01891 | hp1 | a0001 | c0001 | t0018 | g0175 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0241 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0246 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0239 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0240 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0013 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0280 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02015 | hp1 | a0001 | c0003 | t0002 | g0236 | EAS | KHV | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0265 | EAS | KHV | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | KHV | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0140 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | KHV | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | KHV | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | KHV | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0214 | EAS | KHV | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02080 | hp2 | a0001 | c0003 | t0002 | g0037 | EAS | KHV | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02129 | hp1 | a0001 | c0001 | t0007 | g0160 | EAS | KHV | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | KHV | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0270 | EAS | KHV | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0062 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0235 | EAS | CDX | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02155 | hp2 | a0001 | c0002 | t0005 | g0014 | EAS | CDX | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0217 | EAS | CDX | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02257 | hp2 | a0003 | c0010 | t0001 | g0200 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02280 | hp1 | a0002 | c0005 | t0001 | g0009 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02280 | hp2 | a0001 | c0002 | t0004 | g0292 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02293 | hp1 | a0001 | c0008 | t0002 | g0255 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0049 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02451 | hp2 | a0001 | c0002 | t0004 | g0294 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0173 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02622 | hp2 | a0001 | c0004 | t0006 | g0012 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0139 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02647 | hp2 | a0001 | c0001 | t0013 | g0047 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0013 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02698 | hp1 | a0001 | c0001 | t0019 | g0137 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02698 | hp2 | a0001 | c0002 | t0009 | g0272 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02717 | hp1 | a0001 | c0002 | t0004 | g0044 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0052 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02723 | hp2 | a0001 | c0006 | t0008 | g0127 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0229 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02735 | hp2 | a0001 | c0001 | t0016 | g0128 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0059 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0206 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0244 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0223 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02818 | hp1 | a0001 | c0006 | t0002 | g0126 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02896 | hp1 | a0002 | c0005 | t0001 | g0123 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02896 | hp2 | a0001 | c0004 | t0006 | g0012 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02897 | hp1 | a0001 | c0004 | t0006 | g0012 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | ESN | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02965 | hp1 | a0001 | c0002 | t0004 | g0287 | AFR | ESN | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02965 | hp2 | a0001 | c0002 | t0004 | g0291 | AFR | ESN | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | ESN | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0201 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0114 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03041 | hp2 | a0001 | c0002 | t0004 | g0288 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03098 | hp1 | a0001 | c0002 | t0004 | g0284 | AFR | MSL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03098 | hp2 | a0002 | c0005 | t0001 | g0136 | AFR | MSL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03130 | hp1 | a0001 | c0002 | t0004 | g0044 | AFR | ESN | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | ESN | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0060 | AFR | ESN | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0181 | AFR | ESN | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03195 | hp2 | a0002 | c0005 | t0001 | g0009 | AFR | ESN | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | MSL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | MSL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03225 | hp1 | a0002 | c0005 | t0001 | g0009 | AFR | MSL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0138 | AFR | MSL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0268 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03453 | hp1 | a0001 | c0002 | t0004 | g0293 | AFR | MSL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0134 | AFR | MSL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | MSL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0253 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0243 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0040 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0040 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0180 | AFR | ESN | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | ESN | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03540 | hp2 | a0001 | c0002 | t0008 | g0185 | AFR | GWD | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | MSL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03579 | hp2 | a0001 | c0006 | t0006 | g0177 | AFR | MSL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0211 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0048 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03669 | hp1 | a0001 | c0001 | t0006 | g0144 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | STU | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0271 | SAS | STU | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0257 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0251 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0182 | SAS | BEB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0233 | SAS | BEB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0221 | SAS | BEB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0033 | SAS | BEB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0190 | SAS | BEB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0191 | SAS | BEB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | STU | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0273 | SAS | STU | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18522 | hp1 | a0001 | c0004 | t0015 | g0178 | AFR | YRI | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18747 | hp1 | a0001 | c0002 | t0005 | g0247 | EAS | CHB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18906 | hp2 | a0001 | c0002 | t0004 | g0285 | AFR | YRI | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18946 | hp1 | a0001 | c0002 | t0005 | g0261 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18952 | hp2 | a0001 | c0002 | t0005 | g0014 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18960 | hp2 | a0001 | c0002 | t0005 | g0256 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18961 | hp2 | a0001 | c0002 | t0021 | g0275 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18963 | hp2 | a0001 | c0002 | t0005 | g0042 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18972 | hp2 | a0001 | c0002 | t0009 | g0238 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18975 | hp1 | a0001 | c0001 | t0007 | g0086 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0281 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18980 | hp2 | a0001 | c0002 | t0005 | g0042 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18981 | hp2 | a0001 | c0001 | t0007 | g0088 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18989 | hp2 | a0001 | c0002 | t0005 | g0014 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18991 | hp1 | a0001 | c0001 | t0007 | g0073 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0258 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18993 | hp1 | a0001 | c0002 | t0005 | g0277 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18995 | hp1 | a0001 | c0002 | t0005 | g0276 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18997 | hp1 | a0001 | c0001 | t0007 | g0119 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18997 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18998 | hp1 | a0001 | c0002 | t0005 | g0278 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19002 | hp1 | a0001 | c0002 | t0005 | g0014 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19003 | hp2 | a0001 | c0003 | t0002 | g0037 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19005 | hp2 | a0001 | c0002 | t0005 | g0051 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19006 | hp2 | a0001 | c0002 | t0005 | g0279 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19007 | hp2 | a0001 | c0003 | t0002 | g0023 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19009 | hp1 | a0001 | c0001 | t0007 | g0153 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19011 | hp1 | a0001 | c0001 | t0007 | g0095 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0286 | AFR | LWK | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0184 | AFR | LWK | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0260 | AFR | LWK | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19062 | hp1 | a0001 | c0001 | t0007 | g0074 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19062 | hp2 | a0001 | c0001 | t0007 | g0071 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19065 | hp1 | a0001 | c0003 | t0002 | g0023 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19065 | hp2 | a0001 | c0001 | t0012 | g0046 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19067 | hp2 | a0001 | c0002 | t0008 | g0192 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19074 | hp2 | a0001 | c0003 | t0002 | g0023 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19077 | hp2 | a0001 | c0009 | t0002 | g0234 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19079 | hp1 | a0001 | c0002 | t0005 | g0274 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0254 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA19240 | hp2 | a0001 | c0004 | t0006 | g0012 | AFR | YRI | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA20129 | hp1 | a0001 | c0001 | t0017 | g0131 | AFR | ASW | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA20129 | hp2 | a0001 | c0001 | t0014 | g0167 | AFR | ASW | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA20752 | hp1 | a0004 | c0007 | t0002 | g0054 | EUR | TSI | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | TSI | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | GIH | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | GIH | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0141 | AMR | CLM | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0245 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02486 | hp1 | a0001 | c0004 | t0006 | g0179 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02559 | hp1 | a0002 | c0005 | t0001 | g0009 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0203 | AFR | ACB | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0056 | AFR | USA | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | USA | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | USA | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA21309 | hp1 | a0001 | c0002 | t0008 | g0176 | AFR | LWK | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| NA21309 | hp2 | a0001 | c0002 | t0009 | g0290 | AFR | LWK | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0135 | REF | REF | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0124 | REF | REF | WSB2_chr12_118027687_118066179 | WSB2 | chr12 | 118027687 | 118066179 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:118042916 | T | C | 1 | a0002 | 6 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(3): Show |
missense_variant | MODERATE | c.484A>G | p.Thr162Ala | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/9 | 615/2855 | 484/1215 | 162/404 | chr12 | 118042916 | |||
| chr12:118043202 | C | T | 1 | a0004 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.358G>A | p.Asp120Asn | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 3/9 | 489/2855 | 358/1215 | 120/404 | chr12 | 118043202 | |||
| chr12:118043322 | G | A | 1 | a0003 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.238C>T | p.Arg80Trp | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 3/9 | 369/2855 | 238/1215 | 80/404 | chr12 | 118043322 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:118034246 | G | A | 1 | a0001c0003 | 6 | HG02015.hp1 HG02080.hp2 NA19003.hp2 others(3): Show |
synonymous_variant | LOW | c.1165C>T | p.Leu389Leu | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 9/9 | 1296/2855 | 1165/1215 | 389/404 | chr12 | 118034246 | |||
| chr12:118034304 | C | T | 1 | a0001c0008 | 1 | HG02293.hp1 | synonymous_variant | LOW | c.1107G>A | p.Leu369Leu | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 9/9 | 1238/2855 | 1107/1215 | 369/404 | chr12 | 118034304 | |||
| chr12:118035222 | T | G | 1 | a0001c0006 | 3 | HG02723.hp2 HG02818.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.936A>C | p.Ala312Ala | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 7/9 | 1067/2855 | 936/1215 | 312/404 | chr12 | 118035222 | |||
| chr12:118035249 | T | C | 6 | a0001c0002 a0001c0003 a0001c0006 others(3): Show |
182 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
synonymous_variant | LOW | c.909A>G | p.Pro303Pro | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 7/9 | 1040/2855 | 909/1215 | 303/404 | chr12 | 118035249 | |||
| chr12:118036427 | G | A | 1 | a0001c0009 | 1 | NA19077.hp2 | synonymous_variant | LOW | c.744C>T | p.Ser248Ser | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 6/9 | 875/2855 | 744/1215 | 248/404 | chr12 | 118036427 | |||
| chr12:118036433 | G | A | 1 | a0001c0004 | 6 | HG02486.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
synonymous_variant | LOW | c.738C>T | p.Asp246Asp | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 6/9 | 869/2855 | 738/1215 | 246/404 | chr12 | 118036433 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:118032696 | CTATT | C | 8 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0014 others(5): Show |
33 | HG00639.hp2 HG01123.hp2 HG01168.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1496_*1499delAATA | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 9/9 | 1496 | chr12 | 118032696 | ||||||
| chr12:118032726 | T | C | 1 | a0001c0001t0010 | 3 | HG02055.hp2 HG02630.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1470A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 9/9 | 1470 | chr12 | 118032726 | ||||||
| chr12:118033305 | C | A | 1 | a0001c0002t0021 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*891G>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 9/9 | 891 | chr12 | 118033305 | ||||||
| chr12:118033306 | A | C | 1 | a0001c0002t0021 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*890T>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 9/9 | 890 | chr12 | 118033306 | ||||||
| chr12:118033310 | A | ATATTATT others(35): Show |
1 | a0001c0002t0021 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*885_*886insAAAAAA others(36): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 9/9 | 885 | chr12 | 118033310 | ||||||
| chr12:118033313 | C | T | 1 | a0001c0002t0021 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*883G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 9/9 | 883 | chr12 | 118033313 | ||||||
| chr12:118033314 | T | C | 1 | a0001c0002t0021 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*882A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 9/9 | 882 | chr12 | 118033314 | ||||||
| chr12:118033514 | A | G | 1 | a0001c0004t0015 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*682T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 9/9 | 682 | chr12 | 118033514 | ||||||
| chr12:118033547 | T | TA | 11 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0008 others(8): Show |
40 | HG00639.hp2 HG01123.hp2 HG01168.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*648dupT | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 9/9 | 648 | chr12 | 118033547 | ||||||
| chr12:118033547 | TA | T | 5 | a0001c0001t0007 a0001c0001t0014 a0001c0001t0017 others(2): Show |
16 | HG00323.hp2 HG02129.hp1 HG02698.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*648delT | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 9/9 | 648 | chr12 | 118033547 | ||||||
| chr12:118033577 | G | A | 1 | a0001c0001t0019 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*619C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 9/9 | 619 | chr12 | 118033577 | ||||||
| chr12:118033585 | C | G | 1 | a0001c0001t0016 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*611G>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 9/9 | 611 | chr12 | 118033585 | ||||||
| chr12:118033651 | T | C | 1 | a0001c0001t0020 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*545A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 9/9 | 545 | chr12 | 118033651 | ||||||
| chr12:118033955 | A | G | 21 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(18): Show |
197 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*241T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 9/9 | 241 | chr12 | 118033955 | ||||||
| chr12:118033979 | G | A | 2 | a0001c0002t0005 a0001c0002t0021 |
16 | HG02155.hp2 NA18747.hp1 NA18946.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*217C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 9/9 | 217 | chr12 | 118033979 | ||||||
| chr12:118061102 | C | T | 1 | a0001c0001t0013 | 1 | HG02647.hp2 | 5_prime_UTR_variant | MODIFIER | c.-54G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/9 | 54 | chr12 | 118061102 | ||||||
| chr12:118061159 | C | G | 1 | a0001c0001t0012 | 1 | NA19065.hp2 | 5_prime_UTR_variant | MODIFIER | c.-111G>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/9 | 111 | chr12 | 118061159 | ||||||
| chr12:118061159 | C | T | 1 | a0001c0001t0011 | 1 | HG01517.hp2 | 5_prime_UTR_variant | MODIFIER | c.-111G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/9 | 111 | chr12 | 118061159 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:118034549 | C | G | 1 | a0001c0002t0005g0279 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1053-191G>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034549 | |||||||
| chr12:118034574 | G | GCT | 4 | a0001c0001t0006g0049 a0001c0004t0006g0012 a0001c0004t0006g0179 others(1): Show |
7 | HG02451.hp1 HG02486.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1053-218_1053-217d others(4): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034574 | |||||||
| chr12:118034574 | G | GCTCT | 14 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0004g0044 others(11): Show |
15 | HG01243.hp2 HG01884.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1053-220_1053-217d others(6): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034574 | |||||||
| chr12:118034574 | G | GCTCTCT | 4 | a0001c0001t0003g0171 a0001c0001t0008g0052 a0001c0001t0008g0184 others(1): Show |
4 | HG02723.hp1 HG02723.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053-222_1053-217d others(8): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034574 | |||||||
| chr12:118034574 | G | GCTCTCTC others(1): Show |
6 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0169 others(3): Show |
6 | HG02145.hp2 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1053-224_1053-217d others(10): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034574 | |||||||
| chr12:118034574 | G | GCTCTCTC others(3): Show |
2 | a0001c0001t0003g0172 a0001c0001t0010g0140 |
2 | HG01243.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1053-217_1053-216i others(12): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034574 | |||||||
| chr12:118034574 | G | GCTCTCTC others(5): Show |
5 | a0001c0001t0003g0011 a0001c0001t0003g0032 a0001c0001t0003g0165 others(2): Show |
9 | HG02257.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1053-217_1053-216i others(14): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034574 | |||||||
| chr12:118034574 | G | GCTCTCTC others(15): Show |
1 | a0001c0002t0002g0041 | 2 | HG01099.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1053-217_1053-216i others(24): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034574 | |||||||
| chr12:118034574 | G | GCTCTCTC others(17): Show |
1 | a0001c0002t0002g0246 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1053-217_1053-216i others(26): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034574 | |||||||
| chr12:118034574 | G | GCTCTCTC others(13): Show |
1 | a0001c0002t0005g0277 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1053-217_1053-216i others(22): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034574 | |||||||
| chr12:118034574 | G | GCTCTCTC others(15): Show |
18 | a0001c0002t0002g0040 a0001c0002t0002g0043 a0001c0002t0002g0048 others(15): Show |
21 | HG01168.hp2 HG02015.hp2 HG02135.hp1 others(18): Show |
intron_variant | MODIFIER | c.1053-217_1053-216i others(24): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034574 | |||||||
| chr12:118034574 | G | GCTCTCTC others(17): Show |
11 | a0001c0002t0002g0024 a0001c0002t0002g0248 a0001c0002t0002g0251 others(8): Show |
16 | HG00639.hp1 HG02155.hp2 HG02698.hp2 others(13): Show |
intron_variant | MODIFIER | c.1053-217_1053-216i others(26): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034574 | |||||||
| chr12:118034574 | G | GCTCTCTC others(19): Show |
6 | a0001c0002t0002g0250 a0001c0002t0002g0263 a0001c0002t0002g0271 others(3): Show |
6 | HG00140.hp1 HG00673.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1053-217_1053-216i others(28): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034574 | |||||||
| chr12:118034574 | G | GCTCTCTC others(21): Show |
1 | a0001c0002t0002g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1053-217_1053-216i others(30): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034574 | |||||||
| chr12:118034583 | G | C | 78 | a0001c0001t0003g0011 a0001c0001t0003g0032 a0001c0001t0003g0163 others(75): Show |
95 | HG00140.hp1 HG00639.hp1 HG00673.hp1 others(92): Show |
intron_variant | MODIFIER | c.1053-225C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034583 | |||||||
| chr12:118034583 | G | GTC | 87 | a0001c0001t0002g0065 a0001c0001t0002g0087 a0001c0001t0002g0093 others(84): Show |
117 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1053-227_1053-226d others(4): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034583 | |||||||
| chr12:118034584 | T | TCTCTCTC others(32): Show |
2 | a0001c0002t0002g0056 a0004c0007t0002g0054 |
2 | HG06807.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1053-227_1053-226i others(41): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034584 | |||||||
| chr12:118034584 | T | TCTCTCTC others(34): Show |
1 | a0001c0002t0002g0055 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1053-227_1053-226i others(43): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034584 | |||||||
| chr12:118034617 | C | A | 7 | a0001c0002t0002g0248 a0001c0002t0002g0251 a0001c0002t0002g0268 others(4): Show |
7 | HG00639.hp1 HG01168.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.1053-259G>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034617 | |||||||
| chr12:118034617 | C | T | 1 | a0001c0002t0002g0228 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1053-259G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034617 | |||||||
| chr12:118034659 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0097 |
4 | HG00735.hp2 HG01081.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053-301G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034659 | |||||||
| chr12:118034734 | T | C | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1052+252A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034734 | |||||||
| chr12:118034826 | C | T | 2 | a0001c0001t0017g0131 a0001c0001t0018g0175 |
2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1052+160G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034826 | |||||||
| chr12:118034890 | T | C | 14 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0002t0004g0044 others(11): Show |
15 | HG01243.hp2 HG02145.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1052+96A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 8/8 | chr12 | 118034890 | |||||||
| chr12:118035188 | C | G | 4 | a0001c0002t0004g0293 a0001c0006t0002g0126 a0001c0006t0006g0177 others(1): Show |
4 | HG02723.hp2 HG02818.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.944+26G>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 7/8 | chr12 | 118035188 | |||||||
| chr12:118035512 | G | A | 2 | a0001c0001t0008g0052 a0001c0001t0008g0184 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.834-188C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 6/8 | chr12 | 118035512 | |||||||
| chr12:118036007 | G | C | 43 | a0001c0002t0001g0252 a0001c0002t0002g0024 a0001c0002t0002g0040 others(40): Show |
52 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.833+331C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 6/8 | chr12 | 118036007 | |||||||
| chr12:118036034 | T | G | 1 | a0001c0002t0002g0060 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.833+304A>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 6/8 | chr12 | 118036034 | |||||||
| chr12:118036095 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0091 |
2 | NA18612.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.833+243C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 6/8 | chr12 | 118036095 | |||||||
| chr12:118036212 | C | G | 3 | a0001c0004t0006g0012 a0001c0004t0006g0179 a0001c0004t0015g0178 |
6 | HG02486.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.833+126G>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 6/8 | chr12 | 118036212 | |||||||
| chr12:118036582 | G | A | 3 | a0001c0002t0002g0055 a0001c0002t0002g0056 a0004c0007t0002g0054 |
3 | HG01175.hp2 HG06807.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.661-72C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118036582 | |||||||
| chr12:118036682 | T | C | 47 | a0001c0002t0001g0252 a0001c0002t0002g0024 a0001c0002t0002g0040 others(44): Show |
56 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.661-172A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118036682 | |||||||
| chr12:118036794 | ACTTCTGA others(5): Show |
A | 1 | a0001c0001t0001g0091 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.661-296_661-285del others(12): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118036794 | |||||||
| chr12:118036802 | G | A | 1 | a0001c0001t0003g0171 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.661-292C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118036802 | |||||||
| chr12:118036837 | C | A | 17 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0004g0044 others(14): Show |
18 | HG01243.hp2 HG01884.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.661-327G>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118036837 | |||||||
| chr12:118036893 | T | G | 156 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(153): Show |
203 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.661-383A>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118036893 | |||||||
| chr12:118036989 | T | C | 65 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0252 others(62): Show |
75 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.661-479A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118036989 | |||||||
| chr12:118037001 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.661-491C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118037001 | |||||||
| chr12:118037126 | G | C | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.661-616C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118037126 | |||||||
| chr12:118037139 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.661-629C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118037139 | |||||||
| chr12:118037214 | G | A | 3 | a0001c0004t0006g0012 a0001c0004t0006g0179 a0001c0004t0015g0178 |
6 | HG02486.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-704C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118037214 | |||||||
| chr12:118037419 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.660+869G>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118037419 | |||||||
| chr12:118037593 | G | A | 44 | a0001c0002t0001g0252 a0001c0002t0002g0024 a0001c0002t0002g0040 others(41): Show |
53 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.660+695C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118037593 | |||||||
| chr12:118037599 | C | T | 1 | a0001c0002t0002g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.660+689G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118037599 | |||||||
| chr12:118037645 | G | A | 3 | a0001c0002t0002g0055 a0001c0002t0002g0056 a0004c0007t0002g0054 |
3 | HG01175.hp2 HG06807.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.660+643C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118037645 | |||||||
| chr12:118037664 | G | T | 1 | a0001c0001t0001g0079 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.660+624C>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118037664 | |||||||
| chr12:118037667 | T | TA | 45 | a0001c0001t0001g0079 a0001c0001t0002g0063 a0001c0001t0008g0052 others(42): Show |
54 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.660+620dupT | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118037667 | |||||||
| chr12:118037667 | TA | T | 6 | a0001c0001t0001g0028 a0001c0001t0010g0138 a0001c0002t0002g0218 others(3): Show |
10 | HG02486.hp1 HG02622.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.660+620delT | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118037667 | |||||||
| chr12:118037668 | A | T | 85 | a0001c0001t0001g0212 a0001c0001t0002g0166 a0001c0001t0003g0011 others(82): Show |
119 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.660+620T>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118037668 | |||||||
| chr12:118037669 | A | T | 1 | a0001c0002t0002g0218 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.660+619T>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118037669 | |||||||
| chr12:118037675 | A | T | 1 | a0001c0001t0007g0160 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.660+613T>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118037675 | |||||||
| chr12:118037681 | AAG | A | 18 | a0001c0001t0018g0175 a0001c0002t0001g0173 a0001c0002t0001g0174 others(15): Show |
19 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.660+605_660+606del others(2): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118037681 | |||||||
| chr12:118037795 | C | T | 1 | a0001c0002t0002g0231 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.660+493G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118037795 | |||||||
| chr12:118037949 | T | TA | 19 | a0001c0001t0018g0175 a0001c0002t0001g0173 a0001c0002t0001g0174 others(16): Show |
20 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.660+338_660+339ins others(1): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118037949 | |||||||
| chr12:118037951 | G | C | 19 | a0001c0001t0018g0175 a0001c0002t0001g0173 a0001c0002t0001g0174 others(16): Show |
20 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.660+337C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118037951 | |||||||
| chr12:118038162 | T | C | 72 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0008g0052 others(69): Show |
82 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.660+126A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118038162 | |||||||
| chr12:118038182 | T | C | 1 | a0001c0002t0004g0284 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.660+106A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118038182 | |||||||
| chr12:118038250 | T | G | 1 | a0001c0001t0008g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.660+38A>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118038250 | |||||||
| chr12:118038274 | C | T | 62 | a0001c0001t0018g0175 a0001c0002t0001g0173 a0001c0002t0001g0174 others(59): Show |
72 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.660+14G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 5/8 | chr12 | 118038274 | |||||||
| chr12:118038463 | T | A | 1 | a0001c0001t0003g0171 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.560-75A>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118038463 | |||||||
| chr12:118038597 | A | G | 3 | a0001c0002t0002g0055 a0001c0002t0002g0056 a0004c0007t0002g0054 |
3 | HG01175.hp2 HG06807.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.560-209T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118038597 | |||||||
| chr12:118038640 | A | G | 1 | a0001c0002t0002g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.560-252T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118038640 | |||||||
| chr12:118038741 | C | T | 1 | a0001c0006t0006g0177 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.560-353G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118038741 | |||||||
| chr12:118038987 | G | A | 1 | a0001c0002t0002g0193 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.560-599C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118038987 | |||||||
| chr12:118039011 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0006g0049 |
3 | HG02451.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.560-623A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118039011 | |||||||
| chr12:118039143 | C | T | 1 | a0001c0002t0004g0293 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.560-755G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118039143 | |||||||
| chr12:118039293 | T | C | 19 | a0001c0001t0018g0175 a0001c0002t0001g0173 a0001c0002t0001g0174 others(16): Show |
20 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.560-905A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118039293 | |||||||
| chr12:118039354 | A | G | 1 | a0003c0010t0001g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.560-966T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118039354 | |||||||
| chr12:118039377 | G | T | 69 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0018g0175 others(66): Show |
79 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.560-989C>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118039377 | |||||||
| chr12:118039601 | G | A | 1 | a0001c0002t0008g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.560-1213C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118039601 | |||||||
| chr12:118039664 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.560-1276G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118039664 | |||||||
| chr12:118039665 | G | A | 1 | a0001c0002t0002g0053 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.560-1277C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118039665 | |||||||
| chr12:118039668 | T | C | 2 | a0001c0001t0008g0052 a0001c0001t0008g0184 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.560-1280A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118039668 | |||||||
| chr12:118039706 | C | T | 1 | a0001c0002t0002g0225 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.560-1318G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118039706 | |||||||
| chr12:118039707 | G | A | 1 | a0001c0002t0001g0224 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.560-1319C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118039707 | |||||||
| chr12:118039930 | G | A | 1 | a0001c0002t0002g0228 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.560-1542C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118039930 | |||||||
| chr12:118039980 | G | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(54): Show |
89 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.560-1592C>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118039980 | |||||||
| chr12:118039989 | G | A | 1 | a0001c0002t0002g0241 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.560-1601C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118039989 | |||||||
| chr12:118040005 | C | G | 1 | a0001c0002t0002g0217 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.560-1617G>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118040005 | |||||||
| chr12:118040122 | G | A | 4 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0002t0008g0185 others(1): Show |
4 | HG02257.hp2 HG02572.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-1734C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118040122 | |||||||
| chr12:118040156 | C | T | 1 | a0001c0002t0004g0292 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.560-1768G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118040156 | |||||||
| chr12:118040192 | T | C | 7 | a0001c0002t0002g0024 a0001c0002t0002g0062 a0001c0002t0002g0249 others(4): Show |
9 | HG00673.hp1 HG02015.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.560-1804A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118040192 | |||||||
| chr12:118040224 | G | A | 1 | a0001c0002t0002g0240 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.560-1836C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118040224 | |||||||
| chr12:118040273 | T | G | 156 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0212 others(153): Show |
200 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.560-1885A>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118040273 | |||||||
| chr12:118040325 | T | C | 1 | a0001c0002t0002g0055 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.560-1937A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118040325 | |||||||
| chr12:118040332 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.560-1944G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118040332 | |||||||
| chr12:118040340 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.560-1952G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118040340 | |||||||
| chr12:118040420 | G | A | 2 | a0001c0001t0008g0052 a0001c0001t0008g0184 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.560-2032C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118040420 | |||||||
| chr12:118040438 | C | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(71): Show |
120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.560-2050G>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118040438 | |||||||
| chr12:118040484 | A | G | 1 | a0001c0003t0002g0236 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.560-2096T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118040484 | |||||||
| chr12:118040487 | G | A | 16 | a0001c0001t0018g0175 a0001c0002t0001g0173 a0001c0002t0001g0174 others(13): Show |
17 | HG01884.hp1 HG01891.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.560-2099C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118040487 | |||||||
| chr12:118040654 | C | CA | 45 | a0001c0001t0001g0020 a0001c0001t0001g0097 a0001c0001t0002g0093 others(42): Show |
56 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.559+2186dupT | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118040654 | |||||||
| chr12:118040654 | CA | C | 22 | a0001c0001t0001g0084 a0001c0001t0001g0159 a0001c0001t0001g0186 others(19): Show |
26 | HG01243.hp1 HG01257.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.559+2186delT | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118040654 | |||||||
| chr12:118040692 | T | C | 4 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0002t0008g0185 others(1): Show |
4 | HG02257.hp2 HG02572.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.559+2149A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118040692 | |||||||
| chr12:118040723 | G | T | 1 | a0001c0001t0001g0159 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.559+2118C>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118040723 | |||||||
| chr12:118040800 | C | A | 1 | a0001c0002t0005g0276 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.559+2041G>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118040800 | |||||||
| chr12:118040965 | C | G | 1 | a0001c0006t0006g0177 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.559+1876G>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118040965 | |||||||
| chr12:118041004 | G | A | 1 | a0001c0001t0018g0175 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.559+1837C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118041004 | |||||||
| chr12:118041058 | C | A | 4 | a0001c0002t0002g0182 a0001c0002t0002g0189 a0001c0002t0002g0229 others(1): Show |
4 | HG01515.hp1 HG01517.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.559+1783G>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118041058 | |||||||
| chr12:118041121 | T | C | 1 | a0001c0001t0007g0119 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.559+1720A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118041121 | |||||||
| chr12:118041128 | T | C | 1 | a0001c0002t0002g0211 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.559+1713A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118041128 | |||||||
| chr12:118041173 | C | T | 1 | a0001c0002t0008g0192 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.559+1668G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118041173 | |||||||
| chr12:118041196 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.559+1645T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118041196 | |||||||
| chr12:118041620 | C | A | 1 | a0001c0001t0018g0175 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.559+1221G>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118041620 | |||||||
| chr12:118041648 | T | C | 2 | a0001c0001t0008g0052 a0001c0001t0008g0184 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.559+1193A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118041648 | |||||||
| chr12:118041713 | G | A | 59 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(56): Show |
72 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.559+1128C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118041713 | |||||||
| chr12:118041748 | C | CT | 30 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0072 others(27): Show |
33 | HG00438.hp1 HG00673.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.559+1092dupA | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118041748 | |||||||
| chr12:118041748 | C | CTTT | 5 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0110 others(2): Show |
8 | HG00621.hp1 NA18964.hp2 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.559+1090_559+1092d others(5): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118041748 | |||||||
| chr12:118041748 | CT | C | 27 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0212 others(24): Show |
35 | HG00408.hp1 HG00544.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.559+1092delA | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118041748 | |||||||
| chr12:118041748 | CTT | C | 60 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0002g0166 others(57): Show |
73 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.559+1091_559+1092d others(4): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118041748 | |||||||
| chr12:118041899 | C | T | 12 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(9): Show |
16 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.559+942G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118041899 | |||||||
| chr12:118041912 | G | A | 1 | a0001c0002t0002g0228 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.559+929C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118041912 | |||||||
| chr12:118041937 | G | A | 11 | a0001c0002t0004g0044 a0001c0002t0004g0284 a0001c0002t0004g0285 others(8): Show |
12 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.559+904C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118041937 | |||||||
| chr12:118041984 | G | C | 2 | a0001c0001t0008g0052 a0001c0001t0008g0184 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.559+857C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118041984 | |||||||
| chr12:118042035 | C | T | 1 | a0001c0001t0004g0102 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.559+806G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118042035 | |||||||
| chr12:118042136 | T | C | 1 | a0001c0001t0007g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.559+705A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118042136 | |||||||
| chr12:118042253 | C | G | 1 | a0001c0001t0001g0082 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.559+588G>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118042253 | |||||||
| chr12:118042260 | A | G | 1 | a0001c0002t0001g0174 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.559+581T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118042260 | |||||||
| chr12:118042397 | G | C | 1 | a0001c0002t0008g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.559+444C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118042397 | |||||||
| chr12:118042414 | T | C | 2 | a0001c0001t0006g0021 a0001c0001t0006g0141 |
4 | HG00639.hp2 HG01123.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.559+427A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118042414 | |||||||
| chr12:118042429 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.559+412A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118042429 | |||||||
| chr12:118042477 | CAG | C | 3 | a0001c0001t0006g0144 a0001c0001t0008g0052 a0001c0001t0008g0184 |
3 | HG02723.hp1 HG03669.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.559+362_559+363del others(2): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118042477 | |||||||
| chr12:118042561 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.559+280G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118042561 | |||||||
| chr12:118042590 | A | G | 12 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(9): Show |
16 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.559+251T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118042590 | |||||||
| chr12:118042600 | G | A | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0003c0010t0001g0200 |
3 | HG02257.hp2 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.559+241C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118042600 | |||||||
| chr12:118042639 | G | A | 2 | a0001c0002t0002g0189 a0001c0002t0002g0230 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.559+202C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118042639 | |||||||
| chr12:118042678 | G | A | 4 | a0001c0001t0002g0109 a0001c0001t0002g0111 a0001c0001t0002g0113 others(1): Show |
4 | HG01891.hp2 HG02109.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.559+163C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118042678 | |||||||
| chr12:118042826 | C | G | 1 | a0001c0001t0010g0139 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.559+15G>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 4/8 | chr12 | 118042826 | |||||||
| chr12:118042982 | G | A | 1 | a0001c0002t0002g0191 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.428-10C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 3/8 | chr12 | 118042982 | |||||||
| chr12:118043069 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(72): Show |
121 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.427+64C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 3/8 | chr12 | 118043069 | |||||||
| chr12:118043445 | A | G | 1 | a0001c0002t0002g0221 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.183-68T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118043445 | |||||||
| chr12:118043494 | G | T | 9 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(6): Show |
13 | HG01243.hp1 HG02257.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.183-117C>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118043494 | |||||||
| chr12:118043623 | T | C | 1 | a0001c0002t0001g0180 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.183-246A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118043623 | |||||||
| chr12:118043642 | T | C | 3 | a0001c0001t0001g0075 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG00558.hp2 NA18612.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.183-265A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118043642 | |||||||
| chr12:118043683 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.183-306C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118043683 | |||||||
| chr12:118043729 | A | G | 173 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0133 others(170): Show |
224 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.183-352T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118043729 | |||||||
| chr12:118043783 | C | T | 2 | a0001c0001t0008g0052 a0001c0001t0008g0184 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.183-406G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118043783 | |||||||
| chr12:118043839 | A | G | 4 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0002t0008g0185 others(1): Show |
4 | HG02257.hp2 HG02572.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.183-462T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118043839 | |||||||
| chr12:118043896 | C | T | 1 | a0001c0001t0003g0164 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.183-519G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118043896 | |||||||
| chr12:118043988 | G | A | 3 | a0001c0002t0002g0055 a0001c0002t0002g0056 a0004c0007t0002g0054 |
3 | HG01175.hp2 HG06807.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.183-611C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118043988 | |||||||
| chr12:118044034 | G | C | 30 | a0001c0002t0001g0243 a0001c0002t0002g0004 a0001c0002t0002g0034 others(27): Show |
44 | HG00408.hp2 HG00597.hp1 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.183-657C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118044034 | |||||||
| chr12:118044074 | G | A | 1 | a0001c0002t0002g0250 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.183-697C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118044074 | |||||||
| chr12:118044115 | A | G | 161 | a0001c0001t0001g0028 a0001c0001t0001g0186 a0001c0001t0001g0187 others(158): Show |
209 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.183-738T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118044115 | |||||||
| chr12:118044169 | A | G | 12 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(9): Show |
16 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.183-792T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118044169 | |||||||
| chr12:118044200 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.183-823G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118044200 | |||||||
| chr12:118044208 | G | A | 4 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0002t0008g0185 others(1): Show |
4 | HG02257.hp2 HG02572.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.183-831C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118044208 | |||||||
| chr12:118044495 | T | C | 1 | a0001c0002t0002g0265 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.183-1118A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118044495 | |||||||
| chr12:118044547 | G | A | 47 | a0001c0002t0001g0252 a0001c0002t0002g0024 a0001c0002t0002g0040 others(44): Show |
56 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.183-1170C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118044547 | |||||||
| chr12:118044793 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.183-1416C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118044793 | |||||||
| chr12:118045084 | G | T | 1 | a0001c0001t0001g0133 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.183-1707C>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118045084 | |||||||
| chr12:118045098 | C | T | 1 | a0001c0002t0002g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.183-1721G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118045098 | |||||||
| chr12:118045180 | C | T | 1 | a0001c0001t0003g0171 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.183-1803G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118045180 | |||||||
| chr12:118045223 | G | C | 1 | a0001c0002t0001g0116 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.183-1846C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118045223 | |||||||
| chr12:118045236 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0133 |
3 | HG00741.hp2 HG01074.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.183-1859A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118045236 | |||||||
| chr12:118045272 | G | A | 12 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(9): Show |
16 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.183-1895C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118045272 | |||||||
| chr12:118045282 | G | A | 6 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0002t0001g0173 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.183-1905C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118045282 | |||||||
| chr12:118045296 | C | T | 6 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0002t0001g0173 others(3): Show |
6 | HG01884.hp1 HG02257.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.183-1919G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118045296 | |||||||
| chr12:118045319 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0006g0049 |
3 | HG02451.hp1 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.183-1942G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118045319 | |||||||
| chr12:118045364 | C | CA | 13 | a0001c0001t0002g0093 a0001c0002t0002g0269 a0001c0002t0004g0044 others(10): Show |
14 | HG01168.hp2 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.183-1988dupT | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118045364 | |||||||
| chr12:118045364 | C | CAA | 58 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(55): Show |
74 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.183-1989_183-1988d others(4): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118045364 | |||||||
| chr12:118045425 | C | T | 1 | a0001c0001t0003g0171 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.183-2048G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118045425 | |||||||
| chr12:118045500 | C | G | 2 | a0001c0002t0002g0208 a0001c0002t0002g0209 |
2 | NA18947.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.183-2123G>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118045500 | |||||||
| chr12:118045524 | C | T | 1 | a0001c0002t0001g0173 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.183-2147G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118045524 | |||||||
| chr12:118045525 | C | G | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.183-2148G>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118045525 | |||||||
| chr12:118045548 | A | C | 2 | a0001c0001t0008g0052 a0001c0001t0008g0184 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.183-2171T>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118045548 | |||||||
| chr12:118045581 | G | A | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0003c0010t0001g0200 |
3 | HG02257.hp2 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.183-2204C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118045581 | |||||||
| chr12:118045714 | GA | G | 14 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(11): Show |
18 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.183-2338delT | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118045714 | |||||||
| chr12:118045714 | GAA | G | 5 | a0001c0001t0003g0171 a0001c0004t0006g0012 a0001c0004t0006g0179 others(2): Show |
8 | HG02486.hp1 HG02622.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.183-2339_183-2338d others(4): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118045714 | |||||||
| chr12:118045790 | T | C | 12 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(9): Show |
16 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.183-2413A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118045790 | |||||||
| chr12:118046006 | T | A | 1 | a0001c0001t0001g0094 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.183-2629A>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118046006 | |||||||
| chr12:118046113 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.183-2736G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118046113 | |||||||
| chr12:118046355 | C | T | 32 | a0001c0002t0001g0243 a0001c0002t0002g0004 a0001c0002t0002g0034 others(29): Show |
46 | HG00408.hp2 HG00597.hp1 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.183-2978G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118046355 | |||||||
| chr12:118046394 | C | T | 1 | a0001c0001t0003g0171 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.183-3017G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118046394 | |||||||
| chr12:118046466 | CA | C | 103 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0050 others(100): Show |
147 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.183-3090delT | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118046466 | |||||||
| chr12:118046466 | CAA | C | 70 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(67): Show |
84 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.183-3091_183-3090d others(4): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118046466 | |||||||
| chr12:118046657 | T | C | 12 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(9): Show |
16 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.183-3280A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118046657 | |||||||
| chr12:118046665 | A | C | 1 | a0001c0002t0002g0060 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.183-3288T>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118046665 | |||||||
| chr12:118046709 | T | G | 3 | a0001c0002t0001g0243 a0001c0002t0002g0227 a0001c0002t0002g0228 |
3 | HG00408.hp2 HG03491.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.183-3332A>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118046709 | |||||||
| chr12:118046780 | G | T | 4 | a0001c0001t0018g0175 a0001c0004t0006g0012 a0001c0004t0006g0179 others(1): Show |
7 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.183-3403C>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118046780 | |||||||
| chr12:118046808 | G | C | 1 | a0001c0002t0002g0267 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.183-3431C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118046808 | |||||||
| chr12:118047264 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.183-3887C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118047264 | |||||||
| chr12:118047344 | C | T | 12 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(9): Show |
16 | HG01243.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.183-3967G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118047344 | |||||||
| chr12:118047349 | C | T | 1 | a0001c0006t0006g0177 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.183-3972G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118047349 | |||||||
| chr12:118047350 | G | A | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0003c0010t0001g0200 |
3 | HG02257.hp2 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.183-3973C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118047350 | |||||||
| chr12:118047517 | C | T | 1 | a0001c0002t0009g0290 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.183-4140G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118047517 | |||||||
| chr12:118047617 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.183-4240C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118047617 | |||||||
| chr12:118047635 | A | G | 88 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0266 others(85): Show |
105 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.183-4258T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118047635 | |||||||
| chr12:118047722 | A | G | 1 | a0001c0001t0007g0071 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.183-4345T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118047722 | |||||||
| chr12:118047771 | G | A | 1 | a0001c0002t0004g0284 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.183-4394C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118047771 | |||||||
| chr12:118047959 | T | C | 88 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0266 others(85): Show |
105 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.182+4351A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118047959 | |||||||
| chr12:118048024 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.182+4286C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118048024 | |||||||
| chr12:118048100 | A | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0030 |
4 | HG02258.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.182+4210T>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118048100 | |||||||
| chr12:118048218 | C | T | 1 | a0001c0001t0003g0171 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.182+4092G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118048218 | |||||||
| chr12:118048462 | C | T | 1 | a0001c0001t0003g0171 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.182+3848G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118048462 | |||||||
| chr12:118048463 | G | A | 4 | a0001c0002t0002g0182 a0001c0002t0002g0189 a0001c0002t0002g0229 others(1): Show |
4 | HG01515.hp1 HG01517.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.182+3847C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118048463 | |||||||
| chr12:118048582 | C | CA | 28 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(25): Show |
33 | HG01243.hp1 HG01884.hp1 HG02145.hp2 others(30): Show |
intron_variant | MODIFIER | c.182+3727dupT | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118048582 | |||||||
| chr12:118048582 | C | CAA | 7 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0003g0171 others(4): Show |
7 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.182+3726_182+3727d others(4): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118048582 | |||||||
| chr12:118048582 | CA | C | 50 | a0001c0001t0001g0068 a0001c0001t0001g0266 a0001c0002t0001g0252 others(47): Show |
59 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.182+3727delT | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118048582 | |||||||
| chr12:118048681 | GA | G | 13 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0003g0171 others(10): Show |
13 | HG01884.hp1 HG02055.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.182+3628delT | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118048681 | |||||||
| chr12:118048696 | A | T | 1 | a0001c0002t0005g0256 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.182+3614T>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118048696 | |||||||
| chr12:118048836 | G | A | 71 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0266 others(68): Show |
87 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.182+3474C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118048836 | |||||||
| chr12:118048837 | T | A | 1 | a0001c0002t0005g0256 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.182+3473A>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118048837 | |||||||
| chr12:118048854 | C | T | 3 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0244 |
3 | HG02145.hp2 HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.182+3456G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118048854 | |||||||
| chr12:118048886 | G | A | 1 | a0001c0001t0006g0143 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.182+3424C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118048886 | |||||||
| chr12:118048929 | T | G | 3 | a0001c0004t0006g0012 a0001c0004t0006g0179 a0001c0004t0015g0178 |
6 | HG02486.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.182+3381A>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118048929 | |||||||
| chr12:118049105 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
7 | HG01109.hp1 HG02055.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.182+3205A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118049105 | |||||||
| chr12:118049230 | C | T | 64 | a0001c0001t0001g0266 a0001c0001t0002g0166 a0001c0001t0003g0011 others(61): Show |
80 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.182+3080G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118049230 | |||||||
| chr12:118049298 | G | A | 2 | a0001c0001t0007g0074 a0001c0001t0007g0095 |
2 | NA19011.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.182+3012C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118049298 | |||||||
| chr12:118049406 | A | AT | 16 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0003g0171 others(13): Show |
16 | HG01884.hp1 HG01934.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.182+2903dupA | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118049406 | |||||||
| chr12:118049455 | G | A | 1 | a0001c0001t0004g0134 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.182+2855C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118049455 | |||||||
| chr12:118049504 | C | T | 1 | a0001c0001t0006g0143 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.182+2806G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118049504 | |||||||
| chr12:118049692 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.182+2618G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118049692 | |||||||
| chr12:118049693 | G | A | 1 | a0001c0002t0002g0196 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.182+2617C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118049693 | |||||||
| chr12:118049819 | G | A | 9 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0003g0171 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.182+2491C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118049819 | |||||||
| chr12:118049835 | A | G | 9 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0003g0171 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.182+2475T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118049835 | |||||||
| chr12:118049934 | G | A | 9 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0003g0171 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.182+2376C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118049934 | |||||||
| chr12:118049981 | C | T | 1 | a0001c0002t0002g0197 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.182+2329G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118049981 | |||||||
| chr12:118050061 | G | A | 1 | a0001c0002t0008g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.182+2249C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118050061 | |||||||
| chr12:118050068 | C | T | 1 | a0001c0006t0006g0177 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.182+2242G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118050068 | |||||||
| chr12:118050085 | A | G | 13 | a0001c0002t0002g0060 a0001c0002t0004g0044 a0001c0002t0004g0284 others(10): Show |
14 | HG01243.hp2 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.182+2225T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118050085 | |||||||
| chr12:118050180 | A | T | 3 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0244 |
3 | HG02145.hp2 HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.182+2130T>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118050180 | |||||||
| chr12:118050419 | C | T | 8 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0003g0171 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.182+1891G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118050419 | |||||||
| chr12:118050542 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.182+1768C>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118050542 | |||||||
| chr12:118050631 | C | T | 1 | a0001c0001t0018g0175 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.182+1679G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118050631 | |||||||
| chr12:118050643 | T | A | 2 | a0001c0001t0010g0139 a0001c0001t0010g0140 |
2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.182+1667A>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118050643 | |||||||
| chr12:118050644 | C | A | 2 | a0001c0001t0010g0139 a0001c0001t0010g0140 |
2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.182+1666G>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118050644 | |||||||
| chr12:118050771 | G | A | 16 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(13): Show |
23 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.182+1539C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118050771 | |||||||
| chr12:118050843 | G | C | 1 | a0001c0006t0006g0177 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.182+1467C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118050843 | |||||||
| chr12:118050849 | T | C | 73 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0266 others(70): Show |
89 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.182+1461A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118050849 | |||||||
| chr12:118050921 | A | G | 1 | a0001c0001t0003g0171 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.182+1389T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118050921 | |||||||
| chr12:118051112 | A | C | 1 | a0001c0001t0018g0175 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.182+1198T>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118051112 | |||||||
| chr12:118051121 | C | T | 8 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0003g0171 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.182+1189G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118051121 | |||||||
| chr12:118051201 | G | A | 48 | a0001c0001t0001g0266 a0001c0002t0001g0252 a0001c0002t0002g0024 others(45): Show |
57 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.182+1109C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118051201 | |||||||
| chr12:118051376 | A | C | 64 | a0001c0001t0001g0266 a0001c0001t0002g0166 a0001c0001t0003g0011 others(61): Show |
80 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.182+934T>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118051376 | |||||||
| chr12:118051386 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.182+924T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118051386 | |||||||
| chr12:118051565 | A | C | 8 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0003g0171 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.182+745T>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118051565 | |||||||
| chr12:118051639 | C | T | 1 | a0001c0002t0002g0254 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.182+671G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118051639 | |||||||
| chr12:118051749 | G | C | 12 | a0001c0002t0002g0060 a0001c0002t0004g0044 a0001c0002t0004g0284 others(9): Show |
13 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.182+561C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118051749 | |||||||
| chr12:118051831 | A | T | 72 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0266 others(69): Show |
88 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.182+479T>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118051831 | |||||||
| chr12:118051945 | G | C | 1 | a0001c0001t0008g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.182+365C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118051945 | |||||||
| chr12:118052277 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.182+33G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 2/8 | chr12 | 118052277 | |||||||
| chr12:118052499 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.14-21G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118052499 | |||||||
| chr12:118052561 | T | C | 2 | a0001c0001t0001g0027 a0001c0001t0006g0049 |
3 | HG02451.hp1 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.14-83A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118052561 | |||||||
| chr12:118052616 | G | T | 47 | a0001c0001t0001g0266 a0001c0002t0001g0252 a0001c0002t0002g0024 others(44): Show |
56 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.14-138C>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118052616 | |||||||
| chr12:118052703 | C | T | 12 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(9): Show |
19 | HG01243.hp1 HG02257.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.14-225G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118052703 | |||||||
| chr12:118052730 | G | C | 1 | a0001c0002t0002g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.14-252C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118052730 | |||||||
| chr12:118052802 | C | T | 10 | a0001c0001t0003g0142 a0001c0001t0006g0021 a0001c0001t0006g0141 others(7): Show |
12 | HG00639.hp2 HG01123.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.14-324G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118052802 | |||||||
| chr12:118052820 | C | G | 3 | a0001c0002t0004g0286 a0001c0002t0004g0287 a0001c0002t0004g0288 |
3 | HG02965.hp1 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.14-342G>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118052820 | |||||||
| chr12:118052835 | T | C | 11 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0003g0169 others(8): Show |
11 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.14-357A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118052835 | |||||||
| chr12:118052887 | A | G | 1 | a0001c0002t0002g0251 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.14-409T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118052887 | |||||||
| chr12:118053041 | C | T | 1 | a0001c0002t0004g0287 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.14-563G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118053041 | |||||||
| chr12:118053073 | C | T | 11 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0003g0169 others(8): Show |
11 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.14-595G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118053073 | |||||||
| chr12:118053096 | C | A | 12 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(9): Show |
19 | HG01243.hp1 HG02257.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.14-618G>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118053096 | |||||||
| chr12:118053133 | T | C | 1 | a0001c0001t0008g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.14-655A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118053133 | |||||||
| chr12:118053144 | C | G | 1 | a0001c0002t0001g0201 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.14-666G>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118053144 | |||||||
| chr12:118053235 | C | A | 11 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0003g0169 others(8): Show |
11 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.14-757G>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118053235 | |||||||
| chr12:118053288 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.14-810T>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118053288 | |||||||
| chr12:118053424 | G | A | 4 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0171 others(1): Show |
4 | HG02145.hp2 HG02809.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-946C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118053424 | |||||||
| chr12:118053600 | GA | G | 74 | a0001c0001t0001g0212 a0001c0002t0001g0005 a0001c0002t0001g0180 others(71): Show |
104 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.14-1123delT | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118053600 | |||||||
| chr12:118053632 | T | C | 2 | a0001c0002t0002g0189 a0001c0002t0002g0230 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.14-1154A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118053632 | |||||||
| chr12:118053742 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.14-1264G>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118053742 | |||||||
| chr12:118053759 | A | G | 1 | a0001c0002t0002g0253 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.14-1281T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118053759 | |||||||
| chr12:118053856 | C | A | 2 | a0001c0002t0001g0180 a0001c0002t0001g0181 |
2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.14-1378G>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118053856 | |||||||
| chr12:118053862 | G | C | 9 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(6): Show |
13 | HG01243.hp1 HG02257.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.14-1384C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118053862 | |||||||
| chr12:118053912 | T | C | 47 | a0001c0001t0001g0266 a0001c0002t0001g0252 a0001c0002t0002g0024 others(44): Show |
56 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.14-1434A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118053912 | |||||||
| chr12:118054141 | G | A | 47 | a0001c0001t0001g0266 a0001c0002t0001g0252 a0001c0002t0002g0024 others(44): Show |
56 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.14-1663C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054141 | |||||||
| chr12:118054215 | T | TA | 40 | a0001c0001t0001g0018 a0001c0001t0001g0075 a0001c0001t0001g0097 others(37): Show |
52 | HG00280.hp2 HG00544.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.14-1738_14-1737ins others(1): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054215 | |||||||
| chr12:118054216 | C | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.14-1738G>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054216 | |||||||
| chr12:118054217 | C | A | 40 | a0001c0001t0001g0018 a0001c0001t0001g0075 a0001c0001t0001g0097 others(37): Show |
52 | HG00280.hp2 HG00544.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.14-1739G>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054217 | |||||||
| chr12:118054217 | C | CAA | 66 | a0001c0001t0001g0154 a0001c0001t0003g0163 a0001c0001t0003g0168 others(63): Show |
87 | HG00408.hp1 HG00408.hp2 HG01071.hp2 others(84): Show |
intron_variant | MODIFIER | c.14-1741_14-1740dup others(2): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054217 | |||||||
| chr12:118054217 | C | CAAA | 51 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0266 others(48): Show |
66 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.14-1742_14-1740dup others(3): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054217 | |||||||
| chr12:118054217 | C | CAAAA | 15 | a0001c0001t0003g0032 a0001c0002t0002g0248 a0001c0002t0002g0249 others(12): Show |
16 | HG00639.hp1 HG01168.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.14-1743_14-1740dup others(4): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054217 | |||||||
| chr12:118054339 | C | T | 86 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0212 others(83): Show |
116 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.14-1861G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054339 | |||||||
| chr12:118054427 | T | C | 12 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(9): Show |
19 | HG01243.hp1 HG02257.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.14-1949A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054427 | |||||||
| chr12:118054441 | C | T | 2 | a0001c0002t0002g0250 a0001c0002t0002g0280 |
2 | HG00140.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.14-1963G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054441 | |||||||
| chr12:118054527 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.14-2049C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054527 | |||||||
| chr12:118054538 | C | T | 2 | a0002c0005t0001g0009 a0002c0005t0001g0123 |
5 | HG02280.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.14-2060G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054538 | |||||||
| chr12:118054573 | G | C | 1 | a0001c0001t0004g0102 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.14-2095C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054573 | |||||||
| chr12:118054617 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.14-2139G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054617 | |||||||
| chr12:118054681 | A | AAAT | 12 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0068 others(9): Show |
14 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.14-2206_14-2204dup others(3): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054681 | |||||||
| chr12:118054681 | A | AAATAAT | 7 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0076 others(4): Show |
10 | HG00621.hp1 NA18964.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.14-2209_14-2204dup others(6): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054681 | |||||||
| chr12:118054681 | A | T | 1 | a0001c0001t0008g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.14-2203T>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054681 | |||||||
| chr12:118054681 | AAAT | A | 93 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0212 others(90): Show |
124 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.14-2206_14-2204del others(3): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054681 | |||||||
| chr12:118054681 | AAATAAT | A | 12 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(9): Show |
19 | HG01243.hp1 HG02257.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.14-2209_14-2204del others(6): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054681 | |||||||
| chr12:118054681 | AAATAATA others(5): Show |
A | 47 | a0001c0001t0001g0266 a0001c0002t0001g0252 a0001c0002t0002g0024 others(44): Show |
56 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.14-2215_14-2204del others(12): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054681 | |||||||
| chr12:118054687 | T | A | 74 | a0001c0001t0001g0212 a0001c0002t0001g0005 a0001c0002t0001g0180 others(71): Show |
104 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.14-2209A>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054687 | |||||||
| chr12:118054690 | T | A | 5 | a0001c0002t0001g0180 a0001c0002t0001g0181 a0001c0002t0001g0245 others(2): Show |
5 | HG02109.hp1 HG03195.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.14-2212A>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054690 | |||||||
| chr12:118054825 | C | T | 71 | a0001c0001t0001g0212 a0001c0002t0001g0005 a0001c0002t0001g0201 others(68): Show |
101 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.14-2347G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054825 | |||||||
| chr12:118054841 | G | T | 25 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(22): Show |
33 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.14-2363C>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054841 | |||||||
| chr12:118054907 | G | A | 1 | a0001c0001t0018g0175 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.14-2429C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118054907 | |||||||
| chr12:118055015 | T | TA | 109 | a0001c0001t0001g0156 a0001c0001t0001g0186 a0001c0001t0001g0187 others(106): Show |
147 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.14-2538dupT | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118055015 | |||||||
| chr12:118055062 | T | C | 9 | a0001c0001t0002g0166 a0001c0001t0003g0011 a0001c0001t0003g0032 others(6): Show |
13 | HG01243.hp1 HG02257.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.14-2584A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118055062 | |||||||
| chr12:118055607 | C | CT | 38 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0027 others(35): Show |
46 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.14-3130dupA | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118055607 | |||||||
| chr12:118055607 | C | CTT | 61 | a0001c0001t0001g0068 a0001c0001t0001g0107 a0001c0001t0001g0108 others(58): Show |
88 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.14-3131_14-3130dup others(2): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118055607 | |||||||
| chr12:118055607 | C | CTTT | 18 | a0001c0002t0002g0033 a0001c0002t0002g0034 a0001c0002t0002g0035 others(15): Show |
21 | HG00597.hp1 HG01517.hp1 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.14-3132_14-3130dup others(3): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118055607 | |||||||
| chr12:118055607 | C | CTTTT | 8 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0003g0169 others(5): Show |
8 | HG02145.hp2 HG02572.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.14-3133_14-3130dup others(4): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118055607 | |||||||
| chr12:118055607 | CT | C | 21 | a0001c0001t0001g0152 a0001c0001t0002g0101 a0001c0001t0004g0102 others(18): Show |
22 | HG01243.hp2 HG01891.hp1 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.14-3130delA | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118055607 | |||||||
| chr12:118055607 | CTT | C | 51 | a0001c0001t0001g0266 a0001c0001t0002g0166 a0001c0001t0003g0011 others(48): Show |
67 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.14-3131_14-3130del others(2): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118055607 | |||||||
| chr12:118055683 | C | T | 1 | a0001c0006t0006g0177 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.14-3205G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118055683 | |||||||
| chr12:118055717 | A | C | 86 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0212 others(83): Show |
116 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.14-3239T>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118055717 | |||||||
| chr12:118055778 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.14-3300G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118055778 | |||||||
| chr12:118055807 | T | C | 1 | a0001c0002t0008g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.14-3329A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118055807 | |||||||
| chr12:118055858 | G | A | 1 | a0001c0003t0002g0236 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.14-3380C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118055858 | |||||||
| chr12:118055885 | G | A | 47 | a0001c0001t0001g0266 a0001c0002t0001g0252 a0001c0002t0002g0024 others(44): Show |
56 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.14-3407C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118055885 | |||||||
| chr12:118055911 | GT | G | 81 | a0001c0001t0001g0266 a0001c0001t0002g0166 a0001c0001t0003g0011 others(78): Show |
100 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.14-3434delA | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118055911 | |||||||
| chr12:118056076 | C | A | 5 | a0001c0001t0003g0142 a0001c0001t0006g0021 a0001c0001t0006g0141 others(2): Show |
7 | HG00639.hp2 HG01123.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.14-3598G>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118056076 | |||||||
| chr12:118056088 | C | T | 1 | a0001c0001t0008g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.14-3610G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118056088 | |||||||
| chr12:118056100 | T | C | 1 | a0001c0002t0005g0277 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.14-3622A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118056100 | |||||||
| chr12:118056164 | G | C | 5 | a0001c0002t0005g0042 a0001c0002t0005g0274 a0001c0002t0005g0276 others(2): Show |
6 | NA18961.hp2 NA18963.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.14-3686C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118056164 | |||||||
| chr12:118056245 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.14-3767G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118056245 | |||||||
| chr12:118056252 | C | T | 1 | a0001c0002t0002g0182 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.14-3774G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118056252 | |||||||
| chr12:118056350 | G | C | 47 | a0001c0001t0001g0266 a0001c0002t0001g0252 a0001c0002t0002g0024 others(44): Show |
56 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.14-3872C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118056350 | |||||||
| chr12:118056391 | C | T | 47 | a0001c0001t0001g0266 a0001c0002t0001g0252 a0001c0002t0002g0024 others(44): Show |
56 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.14-3913G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118056391 | |||||||
| chr12:118056548 | G | A | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.14-4070C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118056548 | |||||||
| chr12:118056680 | C | G | 1 | a0001c0002t0008g0185 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.14-4202G>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118056680 | |||||||
| chr12:118056704 | C | T | 1 | a0001c0001t0001g0025 | 2 | HG00621.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.14-4226G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118056704 | |||||||
| chr12:118056716 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.14-4238G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118056716 | |||||||
| chr12:118056793 | C | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0106 a0001c0001t0001g0147 |
4 | HG03942.hp2 HG04199.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.13+4243G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118056793 | |||||||
| chr12:118056808 | G | A | 3 | a0001c0001t0001g0103 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG00735.hp1 HG01261.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.13+4228C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118056808 | |||||||
| chr12:118056891 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.13+4145T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118056891 | |||||||
| chr12:118056902 | A | C | 86 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0212 others(83): Show |
116 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.13+4134T>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118056902 | |||||||
| chr12:118057080 | C | A | 12 | a0001c0002t0004g0044 a0001c0002t0004g0284 a0001c0002t0004g0285 others(9): Show |
13 | HG01243.hp2 HG02280.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.13+3956G>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057080 | |||||||
| chr12:118057086 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.13+3950C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057086 | |||||||
| chr12:118057107 | G | A | 2 | a0001c0002t0005g0278 a0001c0002t0005g0279 |
2 | NA18998.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.13+3929C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057107 | |||||||
| chr12:118057132 | G | A | 6 | a0001c0002t0002g0039 a0001c0002t0002g0237 a0001c0002t0002g0239 others(3): Show |
7 | HG01192.hp1 HG01496.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.13+3904C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057132 | |||||||
| chr12:118057162 | A | T | 47 | a0001c0001t0001g0266 a0001c0002t0001g0252 a0001c0002t0002g0024 others(44): Show |
56 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.13+3874T>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057162 | |||||||
| chr12:118057313 | T | C | 138 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0212 others(135): Show |
181 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.13+3723A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057313 | |||||||
| chr12:118057350 | T | C | 91 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0212 others(88): Show |
125 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.13+3686A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057350 | |||||||
| chr12:118057400 | G | A | 4 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0168 others(1): Show |
4 | HG01243.hp1 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.13+3636C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057400 | |||||||
| chr12:118057495 | G | A | 79 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0212 others(76): Show |
109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.13+3541C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057495 | |||||||
| chr12:118057639 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.13+3397A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057639 | |||||||
| chr12:118057685 | A | G | 1 | a0001c0001t0008g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.13+3351T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057685 | |||||||
| chr12:118057776 | G | GT | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(99): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.13+3259dupA | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057776 | |||||||
| chr12:118057776 | G | GTT | 6 | a0001c0001t0001g0066 a0001c0001t0002g0065 a0001c0002t0002g0048 others(3): Show |
6 | HG01934.hp2 HG02738.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.13+3258_13+3259dup others(2): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057776 | |||||||
| chr12:118057776 | GT | G | 10 | a0001c0001t0001g0147 a0001c0001t0003g0169 a0001c0001t0003g0170 others(7): Show |
10 | HG01243.hp1 HG01884.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.13+3259delA | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057776 | |||||||
| chr12:118057825 | G | A | 1 | a0001c0006t0006g0177 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.13+3211C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057825 | |||||||
| chr12:118057871 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0148 a0001c0001t0001g0149 |
6 | HG01109.hp1 HG02055.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.13+3165C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057871 | |||||||
| chr12:118057920 | C | CT | 156 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0212 others(153): Show |
203 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.13+3115_13+3116ins others(1): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057920 | |||||||
| chr12:118057920 | C | T | 2 | a0001c0001t0002g0063 a0001c0001t0002g0064 |
2 | HG01975.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.13+3116G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057920 | |||||||
| chr12:118057921 | A | T | 159 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0212 others(156): Show |
206 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.13+3115T>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057921 | |||||||
| chr12:118057921 | AT | A | 6 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0150 others(3): Show |
9 | HG01943.hp2 HG02080.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.13+3114delA | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057921 | |||||||
| chr12:118057938 | A | C | 159 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0212 others(156): Show |
206 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.13+3098T>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118057938 | |||||||
| chr12:118058122 | C | G | 3 | a0001c0002t0001g0180 a0001c0002t0001g0181 a0001c0002t0001g0245 |
3 | HG02109.hp1 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.13+2914G>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118058122 | |||||||
| chr12:118058397 | G | C | 1 | a0001c0001t0007g0153 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.13+2639C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118058397 | |||||||
| chr12:118058416 | C | T | 93 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0212 others(90): Show |
127 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.13+2620G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118058416 | |||||||
| chr12:118058465 | C | T | 1 | a0001c0001t0008g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.13+2571G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118058465 | |||||||
| chr12:118058494 | A | G | 160 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0212 others(157): Show |
207 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.13+2542T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118058494 | |||||||
| chr12:118058512 | G | A | 3 | a0001c0002t0001g0180 a0001c0002t0001g0181 a0001c0002t0001g0245 |
3 | HG02109.hp1 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.13+2524C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118058512 | |||||||
| chr12:118058617 | G | T | 1 | a0004c0007t0002g0054 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.13+2419C>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118058617 | |||||||
| chr12:118058630 | G | A | 3 | a0001c0004t0006g0012 a0001c0004t0006g0179 a0001c0004t0015g0178 |
6 | HG02486.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.13+2406C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118058630 | |||||||
| chr12:118058653 | T | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0154 a0001c0001t0001g0155 |
4 | HG02080.hp1 NA18979.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.13+2383A>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118058653 | |||||||
| chr12:118058700 | C | CT | 65 | a0001c0001t0001g0061 a0001c0001t0001g0161 a0001c0001t0001g0266 others(62): Show |
75 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.13+2335dupA | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118058700 | |||||||
| chr12:118058731 | T | C | 64 | a0001c0001t0001g0266 a0001c0001t0018g0175 a0001c0002t0001g0252 others(61): Show |
77 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.13+2305A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118058731 | |||||||
| chr12:118058891 | T | G | 1 | a0001c0001t0008g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.13+2145A>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118058891 | |||||||
| chr12:118058903 | T | C | 1 | a0001c0001t0018g0175 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.13+2133A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118058903 | |||||||
| chr12:118058988 | G | A | 5 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
5 | HG00438.hp1 HG02129.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.13+2048C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118058988 | |||||||
| chr12:118058990 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.13+2046G>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118058990 | |||||||
| chr12:118058993 | A | G | 160 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0212 others(157): Show |
207 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.13+2043T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118058993 | |||||||
| chr12:118059050 | T | G | 1 | a0001c0006t0006g0177 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.13+1986A>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118059050 | |||||||
| chr12:118059159 | T | G | 1 | a0001c0001t0011g0045 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.13+1877A>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118059159 | |||||||
| chr12:118059160 | G | A | 3 | a0001c0004t0006g0012 a0001c0004t0006g0179 a0001c0004t0015g0178 |
6 | HG02486.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.13+1876C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118059160 | |||||||
| chr12:118059204 | C | CA | 4 | a0001c0001t0004g0162 a0001c0004t0006g0012 a0001c0004t0006g0179 others(1): Show |
7 | HG02486.hp1 HG02622.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.13+1831dupT | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118059204 | |||||||
| chr12:118059219 | AACATT | A | 160 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0212 others(157): Show |
207 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.13+1812_13+1816del others(5): Show |
WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118059219 | |||||||
| chr12:118059261 | T | C | 2 | a0001c0002t0002g0043 a0001c0002t0002g0281 |
3 | NA18950.hp1 NA18951.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.13+1775A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118059261 | |||||||
| chr12:118059277 | T | C | 1 | a0001c0001t0008g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.13+1759A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118059277 | |||||||
| chr12:118059356 | G | A | 3 | a0001c0002t0001g0180 a0001c0002t0001g0181 a0001c0002t0001g0245 |
3 | HG02109.hp1 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.13+1680C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118059356 | |||||||
| chr12:118059383 | G | C | 76 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0212 others(73): Show |
106 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.13+1653C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118059383 | |||||||
| chr12:118059505 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.13+1531T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118059505 | |||||||
| chr12:118059580 | C | G | 1 | a0001c0001t0001g0057 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.13+1456G>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118059580 | |||||||
| chr12:118059670 | G | C | 1 | a0001c0001t0003g0244 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.13+1366C>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118059670 | |||||||
| chr12:118059672 | T | C | 1 | a0001c0001t0003g0244 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.13+1364A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118059672 | |||||||
| chr12:118059677 | T | A | 1 | a0001c0001t0003g0244 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.13+1359A>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118059677 | |||||||
| chr12:118059685 | G | T | 70 | a0001c0001t0001g0212 a0001c0002t0001g0005 a0001c0002t0001g0201 others(67): Show |
99 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.13+1351C>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118059685 | |||||||
| chr12:118060282 | T | G | 47 | a0001c0001t0001g0266 a0001c0002t0001g0252 a0001c0002t0002g0024 others(44): Show |
56 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.13+754A>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118060282 | |||||||
| chr12:118060297 | G | A | 48 | a0001c0001t0001g0266 a0001c0002t0001g0245 a0001c0002t0001g0252 others(45): Show |
57 | HG00140.hp1 HG00438.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.13+739C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118060297 | |||||||
| chr12:118060345 | C | G | 3 | a0001c0002t0002g0055 a0001c0002t0002g0056 a0004c0007t0002g0054 |
3 | HG01175.hp2 HG06807.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.13+691G>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118060345 | |||||||
| chr12:118060552 | A | G | 1 | a0001c0002t0002g0053 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.13+484T>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118060552 | |||||||
| chr12:118060722 | C | T | 1 | a0001c0001t0008g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.13+314G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118060722 | |||||||
| chr12:118060749 | C | T | 2 | a0001c0001t0001g0025 a0001c0002t0005g0051 |
3 | HG00621.hp1 NA19005.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.13+287G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118060749 | |||||||
| chr12:118060811 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.13+225G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118060811 | |||||||
| chr12:118060836 | T | C | 1 | a0001c0002t0002g0282 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.13+200A>G | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118060836 | |||||||
| chr12:118060893 | C | A | 1 | a0001c0001t0001g0283 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.13+143G>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118060893 | |||||||
| chr12:118060908 | G | A | 12 | a0001c0002t0004g0044 a0001c0002t0004g0284 a0001c0002t0004g0285 others(9): Show |
13 | HG01243.hp2 HG02280.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.13+128C>T | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118060908 | |||||||
| chr12:118060955 | C | G | 1 | a0001c0001t0006g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.13+81G>C | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118060955 | |||||||
| chr12:118060968 | C | T | 1 | a0001c0002t0002g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.13+68G>A | WSB2 | ENSG00000176871.9 | transcript | ENST00000315436.8 | protein_coding | 1/8 | chr12 | 118060968 |