Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 54682 |
|---|---|
| ensemblid | ENSG00000111261.14 |
| hgncid | 25505 |
| symbol | MANSC1 |
| name | MANSC domain containing 1 |
| refseq_nuc | NM_018050.4 |
| refseq_prot | NP_060520.2 |
| ensembl_nuc | ENST00000535902.6 |
| ensembl_prot | ENSP00000438205.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 12326056 |
| end | 12350242 |
| strand | - |
| ver | v1.2 |
| region | chr12:12326056-12350242 |
| region5000 | chr12:12321056-12355242 |
| regionname0 | MANSC1_chr12_12326056_12350242 |
| regionname5000 | MANSC1_chr12_12321056_12355242 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 431 | 293 | 49 | 59 | 151 | 8 | 24 | 112 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0002 | 0/0 | 431 | 21 | 0 | 7 | 8 | 4 | 2 | 7 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0003 | 0/0 | 431 | 4 | 0 | 0 | 4 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0004 | 0/0 | 431 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0005 | 0/0 | 139 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0006 | 0/0 | 431 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0007 | 0/0 | 431 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1296 | 144 | 20 | 20 | 90 | 2 | 11 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| c0002 | 0/1 | 1296 | 129 | 21 | 37 | 53 | 6 | 11 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| c0003 | 0/0 | 1296 | 18 | 0 | 7 | 5 | 4 | 2 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| c0004 | 0/0 | 1296 | 8 | 0 | 0 | 8 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| c0005 | 0/0 | 1296 | 7 | 6 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| c0006 | 0/0 | 1296 | 4 | 0 | 0 | 4 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| c0007 | 0/0 | 1296 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| c0008 | 0/0 | 1296 | 2 | 0 | 1 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| c0009 | 0/0 | 1296 | 2 | 2 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| c0010 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| c0011 | 0/0 | 1312 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| c0012 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| c0013 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| c0014 | 0/0 | 1296 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4244 | 30 | 0 | 9 | 14 | 1 | 6 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0002 | 0/0 | 4243 | 27 | 0 | 3 | 23 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0003 | 0/0 | 4244 | 20 | 0 | 3 | 16 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0004 | 0/0 | 4242 | 12 | 0 | 2 | 7 | 2 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0005 | 0/0 | 4246 | 10 | 4 | 0 | 6 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0006 | 0/0 | 4234 | 8 | 0 | 4 | 0 | 3 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0007 | 0/0 | 4246 | 7 | 0 | 0 | 7 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0008 | 0/0 | 4242 | 7 | 0 | 0 | 7 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0009 | 0/0 | 4240 | 6 | 0 | 2 | 4 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0010 | 0/0 | 4245 | 6 | 2 | 0 | 4 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0011 | 0/0 | 4242 | 5 | 0 | 0 | 4 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0012 | 0/0 | 4244 | 5 | 0 | 4 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0013 | 0/1 | 4246 | 5 | 0 | 3 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0014 | 0/0 | 4241 | 5 | 0 | 2 | 2 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0015 | 0/0 | 4244 | 5 | 0 | 1 | 3 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0016 | 0/0 | 4237 | 5 | 0 | 2 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0017 | 0/0 | 4242 | 4 | 0 | 1 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0018 | 0/0 | 4242 | 4 | 0 | 2 | 1 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0019 | 0/0 | 4248 | 4 | 1 | 1 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0020 | 0/0 | 4237 | 4 | 0 | 4 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0021 | 0/0 | 4242 | 4 | 0 | 0 | 3 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0022 | 0/0 | 4242 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0023 | 0/0 | 4245 | 3 | 3 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0024 | 0/0 | 4227 | 3 | 3 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0025 | 0/0 | 4247 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0026 | 0/0 | 4239 | 2 | 1 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0027 | 0/0 | 4240 | 2 | 0 | 2 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0028 | 0/0 | 4242 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0029 | 0/0 | 4244 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0030 | 0/0 | 4246 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0031 | 0/0 | 4248 | 2 | 0 | 0 | 1 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0032 | 0/0 | 4241 | 2 | 0 | 2 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0033 | 0/0 | 4243 | 2 | 2 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0034 | 0/0 | 4246 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0035 | 0/0 | 4242 | 2 | 2 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0036 | 0/0 | 4243 | 2 | 0 | 1 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0037 | 0/0 | 4248 | 2 | 0 | 1 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0038 | 0/0 | 4227 | 2 | 0 | 2 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0039 | 0/0 | 4242 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0040 | 0/0 | 4248 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0041 | 0/0 | 4243 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0042 | 0/0 | 4238 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0043 | 0/0 | 4240 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0044 | 0/0 | 4244 | 2 | 0 | 0 | 0 | 0 | 2 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0045 | 0/0 | 4246 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0046 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0047 | 0/0 | 4235 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0048 | 0/0 | 4237 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0049 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0050 | 0/0 | 4235 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0051 | 0/0 | 4237 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0052 | 0/0 | 4238 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0053 | 0/0 | 4238 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0054 | 0/0 | 4240 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0055 | 0/0 | 4239 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0056 | 0/0 | 4242 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0057 | 0/0 | 4240 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0058 | 0/0 | 4241 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0059 | 0/0 | 4242 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0060 | 0/0 | 4242 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0061 | 0/0 | 4242 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0062 | 0/0 | 4242 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0063 | 0/0 | 4242 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0064 | 0/0 | 4243 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0065 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0066 | 0/0 | 4242 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0067 | 0/0 | 4246 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0068 | 0/0 | 4243 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0069 | 0/0 | 4246 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0070 | 0/0 | 4244 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0071 | 0/0 | 4246 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0072 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0073 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0074 | 0/0 | 4244 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0075 | 0/0 | 4248 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0076 | 0/0 | 4248 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0077 | 0/0 | 4249 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0078 | 0/0 | 4247 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0079 | 0/0 | 4250 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0080 | 0/0 | 4248 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0081 | 0/0 | 4248 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0082 | 0/0 | 4250 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0083 | 0/0 | 4250 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0084 | 0/0 | 4243 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0085 | 0/0 | 4243 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0086 | 0/0 | 4245 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0087 | 0/0 | 4235 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0088 | 0/0 | 4238 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0089 | 0/0 | 4239 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0090 | 0/0 | 4242 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0091 | 0/0 | 4241 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0092 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0093 | 0/0 | 4244 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0094 | 0/0 | 4247 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0095 | 0/0 | 4250 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0096 | 0/0 | 4246 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0097 | 0/0 | 4249 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0098 | 0/0 | 4231 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0099 | 0/0 | 4227 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0100 | 0/0 | 4238 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0101 | 0/0 | 4237 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0102 | 1/0 | 4237 | 1 | 0 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0103 | 0/0 | 4239 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0104 | 0/0 | 4239 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0105 | 0/0 | 4239 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0106 | 0/0 | 4242 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0107 | 0/0 | 4241 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0108 | 0/0 | 4246 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0109 | 0/0 | 4244 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0110 | 0/0 | 4245 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0111 | 0/0 | 4245 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0112 | 0/0 | 4245 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0113 | 0/0 | 4247 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0114 | 0/0 | 4245 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0115 | 0/0 | 4248 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0116 | 0/0 | 4245 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0117 | 0/0 | 4247 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0118 | 0/0 | 4249 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0119 | 0/0 | 4250 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0120 | 0/0 | 4251 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0121 | 0/0 | 4243 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0122 | 0/0 | 4243 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0123 | 0/0 | 4237 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0124 | 0/0 | 4240 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0125 | 0/0 | 4235 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0126 | 0/0 | 4234 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0127 | 0/0 | 4237 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0128 | 0/0 | 4236 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0129 | 0/0 | 4238 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0130 | 0/0 | 4237 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0131 | 0/0 | 4237 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0132 | 0/0 | 4238 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| t0133 | 0/0 | 4241 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0002 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1296 | 144 | 20 | 20 | 90 | 2 | 11 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002 | 0/1 | 1296 | 129 | 21 | 37 | 53 | 6 | 11 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0004 | 0/0 | 1296 | 8 | 0 | 0 | 8 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0005 | 0/0 | 1296 | 7 | 6 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0008 | 0/0 | 1296 | 2 | 0 | 1 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0009 | 0/0 | 1296 | 2 | 2 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0014 | 0/0 | 1296 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0002c0003 | 0/0 | 1296 | 18 | 0 | 7 | 5 | 4 | 2 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0002c0007 | 0/0 | 1296 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0003c0006 | 0/0 | 1296 | 4 | 0 | 0 | 4 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0004c0010 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0005c0011 | 0/0 | 1312 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0006c0012 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0007c0013 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 5538 | 26 | 0 | 3 | 22 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0003 | 0/0 | 5539 | 20 | 0 | 3 | 16 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0005 | 0/0 | 5541 | 10 | 4 | 0 | 6 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0010 | 0/0 | 5540 | 5 | 2 | 0 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0014 | 0/0 | 5536 | 4 | 0 | 2 | 1 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0015 | 0/0 | 5539 | 5 | 0 | 1 | 3 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0016 | 0/0 | 5532 | 5 | 0 | 2 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0017 | 0/0 | 5537 | 4 | 0 | 1 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0018 | 0/0 | 5537 | 4 | 0 | 2 | 1 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0021 | 0/0 | 5537 | 2 | 0 | 0 | 1 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0022 | 0/0 | 5537 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0024 | 0/0 | 5522 | 3 | 3 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0025 | 0/0 | 5542 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0029 | 0/0 | 5539 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0030 | 0/0 | 5541 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0038 | 0/0 | 5522 | 2 | 0 | 2 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0039 | 0/0 | 5537 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0040 | 0/0 | 5543 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0041 | 0/0 | 5538 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0044 | 0/0 | 5539 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0054 | 0/0 | 5535 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0062 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0065 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0066 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0068 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0079 | 0/0 | 5545 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0080 | 0/0 | 5543 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0081 | 0/0 | 5543 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0098 | 0/0 | 5526 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0099 | 0/0 | 5522 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0100 | 0/0 | 5533 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0101 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0102 | 1/0 | 5532 | 1 | 0 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0103 | 0/0 | 5534 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0104 | 0/0 | 5534 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0105 | 0/0 | 5534 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0106 | 0/0 | 5537 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0107 | 0/0 | 5536 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0108 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0109 | 0/0 | 5539 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0110 | 0/0 | 5540 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0111 | 0/0 | 5540 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0112 | 0/0 | 5540 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0113 | 0/0 | 5542 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0114 | 0/0 | 5540 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0116 | 0/0 | 5540 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0117 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0118 | 0/0 | 5544 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0119 | 0/0 | 5545 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0120 | 0/0 | 5546 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0121 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0122 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0124 | 0/0 | 5535 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0125 | 0/0 | 5530 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0129 | 0/0 | 5533 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0130 | 0/0 | 5532 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0131 | 0/0 | 5532 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0001t0133 | 0/0 | 5536 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0001 | 0/0 | 5539 | 30 | 0 | 9 | 14 | 1 | 6 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0004 | 0/0 | 5537 | 12 | 0 | 2 | 7 | 2 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0007 | 0/0 | 5541 | 7 | 0 | 0 | 7 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0008 | 0/0 | 5537 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0009 | 0/0 | 5535 | 3 | 0 | 2 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0011 | 0/0 | 5537 | 5 | 0 | 0 | 4 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0012 | 0/0 | 5539 | 5 | 0 | 4 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0013 | 0/1 | 5541 | 3 | 0 | 2 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0019 | 0/0 | 5543 | 4 | 1 | 1 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0020 | 0/0 | 5532 | 4 | 0 | 4 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0023 | 0/0 | 5540 | 3 | 3 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0027 | 0/0 | 5535 | 2 | 0 | 2 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0028 | 0/0 | 5537 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0031 | 0/0 | 5543 | 2 | 0 | 0 | 1 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0032 | 0/0 | 5536 | 2 | 0 | 2 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0033 | 0/0 | 5538 | 2 | 2 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0035 | 0/0 | 5537 | 2 | 2 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0036 | 0/0 | 5538 | 2 | 0 | 1 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0037 | 0/0 | 5543 | 2 | 0 | 1 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0045 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0046 | 0/0 | 5539 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0047 | 0/0 | 5530 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0052 | 0/0 | 5533 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0053 | 0/0 | 5533 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0056 | 0/0 | 5537 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0057 | 0/0 | 5535 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0059 | 0/0 | 5537 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0060 | 0/0 | 5537 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0061 | 0/0 | 5537 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0063 | 0/0 | 5537 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0064 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0067 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0069 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0070 | 0/0 | 5539 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0071 | 0/0 | 5541 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0072 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0073 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0074 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0075 | 0/0 | 5543 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0076 | 0/0 | 5543 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0077 | 0/0 | 5544 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0078 | 0/0 | 5542 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0082 | 0/0 | 5545 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0083 | 0/0 | 5545 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0085 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0086 | 0/0 | 5540 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0087 | 0/0 | 5530 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0088 | 0/0 | 5533 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0089 | 0/0 | 5534 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0091 | 0/0 | 5536 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0092 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0093 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0094 | 0/0 | 5542 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0002t0096 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0004t0008 | 0/0 | 5537 | 5 | 0 | 0 | 5 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0004t0034 | 0/0 | 5541 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0004t0095 | 0/0 | 5545 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0005t0026 | 0/0 | 5534 | 2 | 1 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0005t0050 | 0/0 | 5530 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0005t0051 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0005t0055 | 0/0 | 5534 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0005t0058 | 0/0 | 5536 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0005t0084 | 0/0 | 5538 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0008t0013 | 0/0 | 5541 | 2 | 0 | 1 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0009t0048 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0009t0049 | 0/0 | 5531 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0001c0014t0090 | 0/0 | 5537 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0002c0003t0006 | 0/0 | 5529 | 8 | 0 | 4 | 0 | 3 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0002c0003t0021 | 0/0 | 5537 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0002c0003t0042 | 0/0 | 5533 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0002c0003t0043 | 0/0 | 5535 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0002c0003t0044 | 0/0 | 5539 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0002c0003t0126 | 0/0 | 5529 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0002c0003t0127 | 0/0 | 5532 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0002c0003t0128 | 0/0 | 5531 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0002c0003t0132 | 0/0 | 5533 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0002c0007t0009 | 0/0 | 5535 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0003c0006t0002 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0003c0006t0010 | 0/0 | 5540 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0003c0006t0014 | 0/0 | 5536 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0003c0006t0025 | 0/0 | 5542 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0004c0010t0042 | 0/0 | 5533 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0005c0011t0123 | 0/0 | 5548 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0006c0012t0097 | 0/0 | 5544 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| a0007c0013t0115 | 0/0 | 5543 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | copy fasta | chr12 | 12321056 | 12355242 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0005g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0010g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0010g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0010g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0010g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0010g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0014g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0014g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0014g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0014g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0015g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0015g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0015g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0015g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0016g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0016g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0016g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0016g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0016g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0017g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0017g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0017g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0017g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0018g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0018g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0018g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0018g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0021g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0021g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0022g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0022g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0022g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0024g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0024g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0024g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0025g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0025g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0029g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0029g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0030g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0030g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0038g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0038g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0039g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0039g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0040g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0040g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0041g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0041g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0044g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0054g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0062g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0065g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0066g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0068g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0079g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0080g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0081g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0098g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0099g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0100g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0101g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0102g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0103g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0104g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0105g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0106g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0107g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0108g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0109g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0110g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0111g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0112g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0113g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0114g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0116g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0117g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0118g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0119g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0120g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0121g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0122g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0124g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0125g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0129g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0130g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0131g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0001t0133g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0004g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0004g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0004g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0004g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0004g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0007g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0007g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0007g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0007g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0007g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0008g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0008g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0009g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0009g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0009g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0011g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0011g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0011g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0011g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0011g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0012g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0012g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0012g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0012g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0012g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0013g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0013g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0013g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0019g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0019g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0019g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0020g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0020g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0020g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0020g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0023g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0023g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0023g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0027g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0027g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0028g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0028g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0031g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0031g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0032g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0032g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0033g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0033g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0035g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0035g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0036g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0036g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0037g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0037g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0045g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0046g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0047g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0052g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0053g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0056g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0057g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0059g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0060g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0061g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0063g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0064g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0067g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0069g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0070g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0071g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0072g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0073g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0074g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0075g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0076g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0077g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0078g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0082g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0083g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0085g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0086g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0087g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0088g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0089g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0091g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0092g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0093g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0094g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0002t0096g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0004t0008g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0004t0008g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0004t0008g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0004t0008g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0004t0008g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0004t0034g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0004t0034g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0004t0095g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0005t0026g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0005t0026g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0005t0050g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0005t0051g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0005t0055g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0005t0058g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0005t0084g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0008t0013g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0008t0013g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0009t0048g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0009t0049g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0001c0014t0090g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0002c0003t0006g0001 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0002c0003t0006g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0002c0003t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0002c0003t0006g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0002c0003t0006g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0002c0003t0021g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0002c0003t0021g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0002c0003t0042g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0002c0003t0043g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0002c0003t0043g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0002c0003t0044g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0002c0003t0126g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0002c0003t0127g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0002c0003t0128g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0002c0003t0132g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0002c0007t0009g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0002c0007t0009g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0003c0006t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0003c0006t0010g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0003c0006t0014g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0003c0006t0025g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0004c0010t0042g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0005c0011t0123g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0006c0012t0097g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| a0007c0013t0115g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0003 | t0127 | g0042 | EUR | GBR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0123 | EUR | GBR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00280 | hp1 | a0001 | c0001 | t0018 | g0196 | EUR | FIN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00280 | hp2 | a0001 | c0002 | t0060 | g0032 | EUR | FIN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00323 | hp1 | a0001 | c0002 | t0004 | g0183 | EUR | FIN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0278 | EUR | FIN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00408 | hp1 | a0001 | c0002 | t0007 | g0152 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00408 | hp2 | a0001 | c0001 | t0017 | g0264 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00423 | hp1 | a0001 | c0002 | t0083 | g0185 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00423 | hp2 | a0001 | c0001 | t0068 | g0219 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00438 | hp1 | a0001 | c0001 | t0010 | g0207 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00438 | hp2 | a0001 | c0001 | t0025 | g0019 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00597 | hp1 | a0001 | c0002 | t0007 | g0138 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00597 | hp2 | a0003 | c0006 | t0002 | g0220 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00609 | hp1 | a0001 | c0001 | t0065 | g0290 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00609 | hp2 | a0001 | c0002 | t0082 | g0137 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00621 | hp1 | a0001 | c0001 | t0133 | g0070 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00639 | hp1 | a0001 | c0002 | t0061 | g0033 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00639 | hp2 | a0001 | c0002 | t0013 | g0180 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0114 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00642 | hp2 | a0001 | c0002 | t0020 | g0125 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00673 | hp1 | a0001 | c0001 | t0131 | g0282 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00673 | hp2 | a0003 | c0006 | t0025 | g0228 | EAS | CHS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00733 | hp1 | a0001 | c0002 | t0012 | g0175 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00733 | hp2 | a0001 | c0002 | t0063 | g0111 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00735 | hp1 | a0002 | c0003 | t0006 | g0040 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00735 | hp2 | a0002 | c0003 | t0006 | g0001 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00741 | hp1 | a0001 | c0002 | t0012 | g0188 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0085 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01069 | hp1 | a0001 | c0002 | t0027 | g0031 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01069 | hp2 | a0001 | c0002 | t0012 | g0189 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01081 | hp1 | a0001 | c0002 | t0059 | g0029 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01081 | hp2 | a0001 | c0002 | t0037 | g0133 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0127 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01099 | hp2 | a0001 | c0002 | t0032 | g0096 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01109 | hp1 | a0001 | c0002 | t0094 | g0082 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01109 | hp2 | a0002 | c0003 | t0006 | g0039 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01167 | hp1 | a0001 | c0002 | t0020 | g0126 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01167 | hp2 | a0001 | c0001 | t0038 | g0203 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01168 | hp1 | a0001 | c0002 | t0075 | g0170 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01168 | hp2 | a0001 | c0001 | t0018 | g0198 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01169 | hp1 | a0001 | c0001 | t0018 | g0197 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01169 | hp2 | a0001 | c0001 | t0038 | g0204 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0132 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01243 | hp2 | a0001 | c0001 | t0129 | g0263 | AMR | PUR | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01255 | hp1 | a0001 | c0002 | t0077 | g0184 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01255 | hp2 | a0002 | c0003 | t0128 | g0038 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01256 | hp1 | a0001 | c0002 | t0020 | g0106 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01256 | hp2 | a0001 | c0002 | t0004 | g0122 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0284 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01258 | hp2 | a0001 | c0002 | t0020 | g0109 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01261 | hp1 | a0002 | c0003 | t0132 | g0043 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01261 | hp2 | a0001 | c0001 | t0079 | g0164 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01346 | hp1 | a0001 | c0002 | t0027 | g0030 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0092 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0117 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0258 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01361 | hp1 | a0001 | c0002 | t0013 | g0172 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01361 | hp2 | a0002 | c0003 | t0126 | g0044 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01433 | hp1 | a0001 | c0002 | t0009 | g0088 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01433 | hp2 | a0001 | c0008 | t0013 | g0182 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01496 | hp1 | a0001 | c0001 | t0015 | g0157 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01516 | hp1 | a0002 | c0003 | t0006 | g0001 | EUR | IBS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01516 | hp2 | a0001 | c0002 | t0037 | g0072 | EUR | IBS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01517 | hp1 | a0001 | c0002 | t0004 | g0166 | EUR | IBS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01517 | hp2 | a0002 | c0003 | t0006 | g0001 | EUR | IBS | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01884 | hp1 | a0001 | c0002 | t0093 | g0080 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0067 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01891 | hp1 | a0001 | c0009 | t0049 | g0201 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01891 | hp2 | a0001 | c0005 | t0051 | g0211 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01934 | hp1 | a0001 | c0005 | t0026 | g0062 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01934 | hp2 | a0001 | c0001 | t0081 | g0257 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01943 | hp1 | a0001 | c0001 | t0017 | g0283 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01943 | hp2 | a0001 | c0002 | t0004 | g0178 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01952 | hp1 | a0001 | c0002 | t0032 | g0168 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0091 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01978 | hp1 | a0001 | c0001 | t0016 | g0279 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0086 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0255 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01981 | hp2 | a0001 | c0001 | t0130 | g0256 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02004 | hp1 | a0001 | c0002 | t0012 | g0194 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02004 | hp2 | a0001 | c0001 | t0014 | g0158 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02027 | hp1 | a0001 | c0001 | t0054 | g0259 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02027 | hp2 | a0001 | c0001 | t0104 | g0023 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02056 | hp1 | a0001 | c0001 | t0030 | g0253 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02056 | hp2 | a0001 | c0001 | t0066 | g0015 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02071 | hp1 | a0007 | c0013 | t0115 | g0217 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02071 | hp2 | a0001 | c0001 | t0108 | g0025 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02080 | hp2 | a0001 | c0002 | t0072 | g0176 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02083 | hp1 | a0001 | c0002 | t0007 | g0169 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02083 | hp2 | a0001 | c0001 | t0110 | g0227 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0285 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02129 | hp2 | a0001 | c0001 | t0014 | g0226 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02132 | hp1 | a0001 | c0001 | t0015 | g0243 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0298 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02135 | hp1 | a0001 | c0001 | t0016 | g0293 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02135 | hp2 | a0003 | c0006 | t0010 | g0230 | EAS | KHV | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02145 | hp1 | a0001 | c0005 | t0055 | g0069 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02145 | hp2 | a0001 | c0002 | t0089 | g0078 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02148 | hp1 | a0001 | c0002 | t0070 | g0087 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02148 | hp2 | a0001 | c0002 | t0036 | g0179 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02155 | hp1 | a0001 | c0002 | t0074 | g0120 | EAS | CDX | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02155 | hp2 | a0001 | c0001 | t0017 | g0286 | EAS | CDX | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CDX | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02165 | hp2 | a0001 | c0002 | t0031 | g0181 | EAS | CDX | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02257 | hp1 | a0006 | c0012 | t0097 | g0054 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02257 | hp2 | a0001 | c0002 | t0092 | g0081 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02258 | hp1 | a0001 | c0001 | t0101 | g0250 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02258 | hp2 | a0001 | c0001 | t0117 | g0231 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02273 | hp1 | a0001 | c0001 | t0014 | g0161 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02273 | hp2 | a0001 | c0001 | t0016 | g0269 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02293 | hp2 | a0001 | c0002 | t0009 | g0186 | AMR | PEL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02451 | hp1 | a0001 | c0002 | t0096 | g0083 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02451 | hp2 | a0001 | c0002 | t0091 | g0057 | AFR | ACB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02615 | hp1 | a0001 | c0002 | t0019 | g0010 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02615 | hp2 | a0001 | c0009 | t0048 | g0173 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02622 | hp1 | a0001 | c0002 | t0035 | g0077 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02622 | hp2 | a0001 | c0001 | t0120 | g0234 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02647 | hp1 | a0001 | c0001 | t0024 | g0199 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02647 | hp2 | a0001 | c0002 | t0053 | g0155 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02723 | hp1 | a0001 | c0005 | t0058 | g0053 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02723 | hp2 | a0001 | c0002 | t0085 | g0058 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02818 | hp1 | a0001 | c0002 | t0033 | g0074 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02818 | hp2 | a0001 | c0001 | t0121 | g0300 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02922 | hp1 | a0001 | c0001 | t0100 | g0063 | AFR | ESN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02922 | hp2 | a0001 | c0001 | t0114 | g0073 | AFR | ESN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02970 | hp1 | a0001 | c0001 | t0099 | g0237 | AFR | ESN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG02970 | hp2 | a0001 | c0002 | t0088 | g0079 | AFR | ESN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03041 | hp1 | a0001 | c0001 | t0103 | g0066 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03041 | hp2 | a0001 | c0001 | t0024 | g0205 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03139 | hp1 | a0001 | c0002 | t0086 | g0055 | AFR | ESN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03139 | hp2 | a0001 | c0002 | t0033 | g0076 | AFR | ESN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0239 | AFR | ESN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03195 | hp2 | a0001 | c0002 | t0045 | g0014 | AFR | ESN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03209 | hp1 | a0001 | c0001 | t0024 | g0206 | AFR | MSL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03209 | hp2 | a0001 | c0005 | t0050 | g0218 | AFR | MSL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03225 | hp1 | a0001 | c0002 | t0023 | g0140 | AFR | MSL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03225 | hp2 | a0001 | c0002 | t0047 | g0248 | AFR | MSL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0177 | SAS | PJL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03239 | hp2 | a0001 | c0001 | t0118 | g0214 | SAS | PJL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03492 | hp1 | a0001 | c0002 | t0046 | g0119 | SAS | PJL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0124 | SAS | PJL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0068 | AFR | ESN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03516 | hp2 | a0001 | c0005 | t0026 | g0061 | AFR | ESN | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03540 | hp1 | a0001 | c0001 | t0105 | g0240 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03540 | hp2 | a0001 | c0002 | t0078 | g0304 | AFR | GWD | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03579 | hp1 | a0001 | c0001 | t0111 | g0036 | AFR | MSL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03579 | hp2 | a0001 | c0002 | t0023 | g0056 | AFR | MSL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03654 | hp1 | a0001 | c0002 | t0011 | g0112 | SAS | PJL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0303 | SAS | PJL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03669 | hp1 | a0001 | c0002 | t0052 | g0113 | SAS | PJL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03669 | hp2 | a0001 | c0001 | t0044 | g0301 | SAS | PJL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03710 | hp1 | a0001 | c0001 | t0021 | g0302 | SAS | PJL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03831 | hp1 | a0002 | c0003 | t0044 | g0049 | SAS | BEB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03927 | hp1 | a0001 | c0001 | t0109 | g0167 | SAS | BEB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG03927 | hp2 | a0001 | c0001 | t0015 | g0249 | SAS | BEB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG04115 | hp1 | a0001 | c0002 | t0031 | g0165 | SAS | STU | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG04115 | hp2 | a0001 | c0001 | t0106 | g0229 | SAS | STU | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0102 | SAS | BEB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG04184 | hp2 | a0001 | c0001 | t0112 | g0212 | SAS | BEB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0097 | SAS | STU | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG04199 | hp2 | a0001 | c0001 | t0124 | g0141 | SAS | STU | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG04204 | hp1 | a0001 | c0001 | t0080 | g0295 | SAS | STU | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG04204 | hp2 | a0002 | c0003 | t0006 | g0041 | SAS | STU | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG04228 | hp1 | a0001 | c0008 | t0013 | g0174 | SAS | STU | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG04228 | hp2 | a0001 | c0001 | t0014 | g0223 | SAS | STU | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18612 | hp1 | a0001 | c0002 | t0028 | g0139 | EAS | CHB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | CHB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | CHB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18747 | hp2 | a0002 | c0003 | t0043 | g0046 | EAS | CHB | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18906 | hp1 | a0001 | c0002 | t0087 | g0200 | AFR | YRI | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0064 | AFR | YRI | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18943 | hp1 | a0001 | c0001 | t0022 | g0272 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18943 | hp2 | a0002 | c0007 | t0009 | g0005 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18944 | hp1 | a0001 | c0002 | t0004 | g0101 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18944 | hp2 | a0002 | c0007 | t0009 | g0045 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18945 | hp1 | a0001 | c0001 | t0119 | g0202 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18947 | hp1 | a0004 | c0010 | t0042 | g0052 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18947 | hp2 | a0001 | c0002 | t0011 | g0151 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18949 | hp1 | a0001 | c0004 | t0008 | g0104 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18949 | hp2 | a0001 | c0001 | t0039 | g0297 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18950 | hp2 | a0001 | c0002 | t0019 | g0089 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18951 | hp2 | a0001 | c0004 | t0034 | g0095 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18957 | hp1 | a0001 | c0002 | t0056 | g0191 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18957 | hp2 | a0001 | c0001 | t0021 | g0232 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18959 | hp1 | a0001 | c0004 | t0034 | g0103 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18959 | hp2 | a0001 | c0002 | t0011 | g0098 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18960 | hp1 | a0001 | c0001 | t0122 | g0017 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18961 | hp2 | a0001 | c0001 | t0022 | g0275 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18962 | hp1 | a0001 | c0001 | t0029 | g0260 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18962 | hp2 | a0001 | c0001 | t0010 | g0209 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18963 | hp1 | a0002 | c0007 | t0009 | g0005 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18963 | hp2 | a0001 | c0004 | t0008 | g0107 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18966 | hp1 | a0001 | c0002 | t0004 | g0009 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18966 | hp2 | a0001 | c0001 | t0025 | g0022 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18973 | hp2 | a0001 | c0002 | t0064 | g0090 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18977 | hp1 | a0001 | c0002 | t0019 | g0154 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18977 | hp2 | a0001 | c0002 | t0004 | g0007 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18978 | hp2 | a0001 | c0002 | t0008 | g0149 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18979 | hp1 | a0001 | c0002 | t0004 | g0135 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18981 | hp1 | a0001 | c0002 | t0011 | g0150 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18981 | hp2 | a0001 | c0001 | t0017 | g0289 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18983 | hp1 | a0001 | c0002 | t0004 | g0009 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18986 | hp1 | a0001 | c0002 | t0007 | g0099 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18991 | hp1 | a0001 | c0001 | t0098 | g0287 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18991 | hp2 | a0005 | c0011 | t0123 | g0266 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18992 | hp1 | a0001 | c0002 | t0069 | g0060 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18992 | hp2 | a0001 | c0002 | t0007 | g0006 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18993 | hp1 | a0001 | c0002 | t0011 | g0147 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18994 | hp1 | a0001 | c0001 | t0062 | g0254 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0221 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18995 | hp2 | a0001 | c0002 | t0076 | g0193 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18997 | hp1 | a0001 | c0001 | t0016 | g0163 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18997 | hp2 | a0001 | c0002 | t0004 | g0007 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18998 | hp1 | a0001 | c0002 | t0073 | g0288 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA18998 | hp2 | a0002 | c0003 | t0042 | g0051 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19004 | hp2 | a0001 | c0002 | t0007 | g0006 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19005 | hp1 | a0001 | c0001 | t0022 | g0267 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19005 | hp2 | a0001 | c0002 | t0028 | g0131 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19007 | hp1 | a0001 | c0001 | t0015 | g0013 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0241 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19010 | hp2 | a0001 | c0001 | t0113 | g0245 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19011 | hp1 | a0001 | c0001 | t0015 | g0013 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19011 | hp2 | a0001 | c0001 | t0016 | g0270 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19012 | hp2 | a0001 | c0002 | t0071 | g0192 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19056 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19057 | hp1 | a0001 | c0001 | t0041 | g0021 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19060 | hp1 | a0002 | c0003 | t0021 | g0047 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19060 | hp2 | a0001 | c0002 | t0012 | g0035 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19062 | hp1 | a0001 | c0001 | t0116 | g0028 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19062 | hp2 | a0001 | c0002 | t0067 | g0190 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19064 | hp2 | a0001 | c0002 | t0008 | g0271 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19065 | hp1 | a0003 | c0006 | t0014 | g0213 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19066 | hp1 | a0002 | c0003 | t0021 | g0048 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19067 | hp2 | a0001 | c0002 | t0009 | g0118 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19068 | hp2 | a0002 | c0003 | t0043 | g0050 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19074 | hp1 | a0001 | c0004 | t0008 | g0094 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19077 | hp1 | a0001 | c0001 | t0018 | g0291 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19077 | hp2 | a0001 | c0001 | t0010 | g0233 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19078 | hp1 | a0001 | c0002 | t0007 | g0142 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19078 | hp2 | a0001 | c0001 | t0005 | g0242 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19079 | hp2 | a0001 | c0001 | t0039 | g0247 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19080 | hp2 | a0001 | c0001 | t0041 | g0020 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19081 | hp2 | a0001 | c0001 | t0107 | g0027 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19082 | hp1 | a0001 | c0002 | t0057 | g0145 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19082 | hp2 | a0001 | c0001 | t0040 | g0244 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19084 | hp1 | a0001 | c0001 | t0040 | g0246 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19084 | hp2 | a0001 | c0001 | t0030 | g0280 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19085 | hp2 | a0001 | c0004 | t0008 | g0100 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19086 | hp2 | a0001 | c0004 | t0008 | g0105 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19088 | hp2 | a0001 | c0002 | t0004 | g0128 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19091 | hp1 | a0001 | c0001 | t0029 | g0274 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA19091 | hp2 | a0001 | c0004 | t0095 | g0134 | EAS | JPT | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA20129 | hp1 | a0001 | c0002 | t0023 | g0075 | AFR | ASW | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA20129 | hp2 | a0001 | c0001 | t0125 | g0294 | AFR | ASW | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA20752 | hp1 | a0002 | c0003 | t0006 | g0037 | EUR | TSI | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA20752 | hp2 | a0001 | c0002 | t0036 | g0187 | EUR | TSI | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA20905 | hp1 | a0001 | c0002 | t0004 | g0195 | SAS | GIH | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA20905 | hp2 | a0001 | c0014 | t0090 | g0121 | SAS | GIH | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01123 | hp1 | a0001 | c0002 | t0019 | g0010 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| HG01123 | hp2 | a0002 | c0003 | t0006 | g0001 | AMR | CLM | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0071 | AFR | USA | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA20300 | hp2 | a0001 | c0001 | t0010 | g0160 | AFR | USA | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA21309 | hp1 | a0001 | c0005 | t0084 | g0059 | AFR | LWK | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| NA21309 | hp2 | a0001 | c0002 | t0035 | g0084 | AFR | LWK | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0013 | g0171 | REF | REF | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0102 | g0065 | REF | REF | MANSC1_chr12_12321056_12355242 | MANSC1 | chr12 | 12321056 | 12355242 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:12330086
|
G | A | 1 | a0007 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.1237C>T | p.Arg413Cys | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1502/5532 | 1237/1296 | 413/431 | chr12 | 12330086 | ||
| chr12:12330200
|
T | A | 1 | a0003 | 4 | HG00597.hp2 HG00673.hp2 HG02135.hp2 others(1): Show |
missense_variant | MODERATE | c.1123A>T | p.Asn375Tyr | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1388/5532 | 1123/1296 | 375/431 | chr12 | 12330200 | ||
| chr12:12330299
|
A | G | 1 | a0006 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.1024T>C | p.Ser342Pro | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1289/5532 | 1024/1296 | 342/431 | chr12 | 12330299 | ||
| chr12:12330917
|
G | GTCTATGG others(9): Show |
1 | a0005 | 1 | NA18991.hp2 | frameshift_variant&stop_gained | HIGH | c.405_406insATTGAAAG others(8): Show |
p.Pro136fs | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 670/5532 | 405/1296 | 135/431 | chr12 | 12330917 | ||
| chr12:12330937
|
T | A | 1 | a0004 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.386A>T | p.Asn129Ile | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 651/5532 | 386/1296 | 129/431 | chr12 | 12330937 | ||
| chr12:12343152
|
C | T | 2 | a0002a0004 | 22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
missense_variant | MODERATE | c.163G>A | p.Val55Ile | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/4 | 428/5532 | 163/1296 | 55/431 | chr12 | 12343152 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:12330096
|
C | T | 1 | a0001c0008 | 2 | HG01433.hp2 HG04228.hp1 |
synonymous_variant | LOW | c.1227G>A | p.Ser409Ser | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1492/5532 | 1227/1296 | 409/431 | chr12 | 12330096 | ||
| chr12:12330341
|
G | A | 8 | a0001c0002a0001c0004a0001c0005others(5): Show | 153 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
synonymous_variant | LOW | c.982C>T | p.Leu328Leu | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1247/5532 | 982/1296 | 328/431 | chr12 | 12330341 | ||
| chr12:12330384
|
C | T | 1 | a0001c0005 | 7 | HG01891.hp2 HG01934.hp1 HG02145.hp1 others(4): Show |
synonymous_variant | LOW | c.939G>A | p.Ser313Ser | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1204/5532 | 939/1296 | 313/431 | chr12 | 12330384 | ||
| chr12:12330779
|
A | G | 7 | a0001c0002a0001c0004a0001c0005others(4): Show | 151 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(148): Show |
synonymous_variant | LOW | c.544T>C | p.Leu182Leu | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 809/5532 | 544/1296 | 182/431 | chr12 | 12330779 | ||
| chr12:12338421
|
T | C | 1 | a0001c0014 | 1 | NA20905.hp2 | splice_region_variant&synonymous_variant | LOW | c.363A>G | p.Thr121Thr | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/4 | 628/5532 | 363/1296 | 121/431 | chr12 | 12338421 | ||
| chr12:12343219
|
C | T | 1 | a0001c0004 | 8 | NA18949.hp1 NA18951.hp2 NA18959.hp1 others(5): Show |
synonymous_variant | LOW | c.96G>A | p.Lys32Lys | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/4 | 361/5532 | 96/1296 | 32/431 | chr12 | 12343219 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:12326183
|
C | T | 1 | a0001c0001t0022 | 3 | NA18943.hp1 NA18961.hp2 NA19005.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3844G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3844 | chr12 | 12326183 | |||||
| chr12:12326201
|
T | C | 1 | a0001c0002t0061 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3826A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3826 | chr12 | 12326201 | |||||
| chr12:12326206
|
C | T | 1 | a0001c0001t0117 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3821G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3821 | chr12 | 12326206 | |||||
| chr12:12326234
|
C | T | 1 | a0001c0002t0028 | 2 | NA18612.hp1 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3793G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3793 | chr12 | 12326234 | |||||
| chr12:12326316
|
C | T | 75 | a0001c0001t0005a0001c0001t0015a0001c0001t0016others(72): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*3711G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3711 | chr12 | 12326316 | |||||
| chr12:12326550
|
A | T | 1 | a0001c0005t0084 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3477T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3477 | chr12 | 12326550 | |||||
| chr12:12326603
|
G | GT | 6 | a0001c0001t0106a0001c0001t0108a0001c0001t0113others(3): Show | 6 | HG01168.hp1 HG02071.hp2 HG02615.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3423dupA | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3423 | chr12 | 12326603 | |||||
| chr12:12326603
|
G | GTT | 20 | a0001c0001t0003a0001c0001t0017a0001c0001t0022others(17): Show | 52 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*3422_*3423dupAA | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3423 | chr12 | 12326603 | |||||
| chr12:12326611
|
T | G | 8 | a0001c0001t0111a0001c0001t0112a0001c0002t0089others(5): Show | 15 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3416A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3416 | chr12 | 12326611 | |||||
| chr12:12326614
|
G | T | 1 | a0001c0001t0029 | 2 | NA18962.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3413C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3413 | chr12 | 12326614 | |||||
| chr12:12326628
|
G | GT | 76 | a0001c0001t0003a0001c0001t0005a0001c0001t0015others(73): Show | 205 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*3398dupA | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3398 | chr12 | 12326628 | |||||
| chr12:12326628
|
G | GTT | 7 | a0001c0001t0108a0001c0001t0129a0001c0002t0064others(4): Show | 7 | HG00140.hp1 HG01168.hp1 HG01243.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3397_*3398dupAA | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3398 | chr12 | 12326628 | |||||
| chr12:12326661
|
G | A | 1 | a0001c0005t0058 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3366C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3366 | chr12 | 12326661 | |||||
| chr12:12326903
|
C | T | 22 | a0001c0001t0003a0001c0001t0017a0001c0001t0022others(19): Show | 54 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*3124G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3124 | chr12 | 12326903 | |||||
| chr12:12327015
|
G | A | 1 | a0001c0005t0084 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3012C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 3012 | chr12 | 12327015 | |||||
| chr12:12327071
|
A | T | 1 | a0001c0002t0063 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2956T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 2956 | chr12 | 12327071 | |||||
| chr12:12327100
|
A | G | 1 | a0001c0005t0084 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2927T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 2927 | chr12 | 12327100 | |||||
| chr12:12327108
|
C | T | 32 | a0001c0001t0002a0001c0001t0010a0001c0001t0014others(29): Show | 71 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2919G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 2919 | chr12 | 12327108 | |||||
| chr12:12327115
|
T | C | 23 | a0001c0001t0003a0001c0001t0017a0001c0001t0022others(20): Show | 55 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2912A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 2912 | chr12 | 12327115 | |||||
| chr12:12327154
|
C | T | 24 | a0001c0001t0003a0001c0001t0017a0001c0001t0022others(21): Show | 56 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2873G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 2873 | chr12 | 12327154 | |||||
| chr12:12327359
|
G | A | 1 | a0001c0005t0058 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2668C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 2668 | chr12 | 12327359 | |||||
| chr12:12327371
|
G | T | 1 | a0001c0005t0058 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2656C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 2656 | chr12 | 12327371 | |||||
| chr12:12327426
|
T | C | 23 | a0001c0001t0003a0001c0001t0017a0001c0001t0022others(20): Show | 55 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2601A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 2601 | chr12 | 12327426 | |||||
| chr12:12327959
|
TGTCTTAA others(4): Show |
T | 1 | a0001c0001t0098 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2057_*2067delGCAA others(7): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 2057 | chr12 | 12327959 | |||||
| chr12:12327971
|
T | C | 1 | a0001c0001t0105 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2056A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 2056 | chr12 | 12327971 | |||||
| chr12:12328152
|
CT | C | 9 | a0001c0002t0035a0001c0002t0078a0001c0002t0093others(6): Show | 17 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1874delA | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1874 | chr12 | 12328152 | |||||
| chr12:12328203
|
T | A | 1 | a0001c0002t0069 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1824A>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1824 | chr12 | 12328203 | |||||
| chr12:12328204
|
C | G | 1 | a0001c0002t0069 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1823G>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1823 | chr12 | 12328204 | |||||
| chr12:12328216
|
T | C | 8 | a0001c0001t0125a0001c0005t0026a0001c0005t0050others(5): Show | 9 | HG01891.hp1 HG01891.hp2 HG01934.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1811A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1811 | chr12 | 12328216 | |||||
| chr12:12328282
|
G | A | 2 | a0001c0002t0060a0001c0002t0061 | 2 | HG00280.hp2 HG00639.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1745C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1745 | chr12 | 12328282 | |||||
| chr12:12328310
|
C | T | 26 | a0001c0001t0062a0001c0001t0103a0001c0002t0008others(23): Show | 47 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1717G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1717 | chr12 | 12328310 | |||||
| chr12:12328342
|
C | T | 1 | a0001c0002t0073 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1685G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1685 | chr12 | 12328342 | |||||
| chr12:12328343
|
G | A | 13 | a0001c0001t0003a0001c0001t0017a0001c0001t0018others(10): Show | 42 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1684C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1684 | chr12 | 12328343 | |||||
| chr12:12328362
|
C | T | 59 | a0001c0001t0003a0001c0001t0017a0001c0001t0018others(56): Show | 155 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*1665G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1665 | chr12 | 12328362 | |||||
| chr12:12328402
|
G | A | 8 | a0001c0001t0131a0001c0002t0011a0001c0002t0012others(5): Show | 20 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1625C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1625 | chr12 | 12328402 | |||||
| chr12:12328406
|
G | A | 2 | a0001c0005t0050a0001c0005t0051 | 2 | HG01891.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1621C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1621 | chr12 | 12328406 | |||||
| chr12:12328417
|
C | T | 1 | a0001c0002t0053 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1610G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1610 | chr12 | 12328417 | |||||
| chr12:12328526
|
G | A | 13 | a0001c0001t0003a0001c0001t0017a0001c0001t0018others(10): Show | 42 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1501C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1501 | chr12 | 12328526 | |||||
| chr12:12328547
|
C | T | 39 | a0001c0001t0099a0001c0001t0109a0001c0001t0121others(36): Show | 106 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*1480G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1480 | chr12 | 12328547 | |||||
| chr12:12328594
|
C | T | 7 | a0001c0005t0026a0001c0005t0050a0001c0005t0051others(4): Show | 8 | HG01891.hp1 HG01891.hp2 HG01934.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1433G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1433 | chr12 | 12328594 | |||||
| chr12:12328619
|
A | G | 90 | a0001c0001t0003a0001c0001t0017a0001c0001t0018others(87): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*1408T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1408 | chr12 | 12328619 | |||||
| chr12:12328662
|
A | C | 1 | a0001c0001t0111 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1365T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1365 | chr12 | 12328662 | |||||
| chr12:12328680
|
T | C | 42 | a0001c0001t0107a0001c0001t0109a0001c0001t0116others(39): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*1347A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1347 | chr12 | 12328680 | |||||
| chr12:12328712
|
G | A | 13 | a0001c0001t0003a0001c0001t0017a0001c0001t0018others(10): Show | 42 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1315C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1315 | chr12 | 12328712 | |||||
| chr12:12328852
|
T | G | 4 | a0001c0002t0027a0001c0002t0059a0001c0002t0060others(1): Show | 5 | HG00280.hp2 HG00639.hp1 HG01069.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1175A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1175 | chr12 | 12328852 | |||||
| chr12:12328856
|
C | G | 5 | a0001c0001t0122a0001c0002t0027a0001c0002t0059others(2): Show | 6 | HG00280.hp2 HG00639.hp1 HG01069.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1171G>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1171 | chr12 | 12328856 | |||||
| chr12:12328857
|
G | A | 12 | a0001c0001t0003a0001c0001t0017a0001c0001t0018others(9): Show | 40 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1170C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1170 | chr12 | 12328857 | |||||
| chr12:12328857
|
G | C | 1 | a0001c0001t0122 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1170C>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1170 | chr12 | 12328857 | |||||
| chr12:12328861
|
G | A | 3 | a0001c0002t0057a0001c0002t0073a0001c0002t0074 | 3 | HG02155.hp1 NA18998.hp1 NA19082.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1166C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1166 | chr12 | 12328861 | |||||
| chr12:12328875
|
C | T | 1 | a0001c0001t0125 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1152G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1152 | chr12 | 12328875 | |||||
| chr12:12328880
|
T | C | 104 | a0001c0001t0003a0001c0001t0016a0001c0001t0017others(101): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*1147A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1147 | chr12 | 12328880 | |||||
| chr12:12328880
|
T | G | 1 | a0001c0002t0067 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1147A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1147 | chr12 | 12328880 | |||||
| chr12:12328890
|
A | G | 1 | a0001c0002t0067 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1137T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1137 | chr12 | 12328890 | |||||
| chr12:12328936
|
C | T | 7 | a0001c0005t0026a0001c0005t0050a0001c0005t0051others(4): Show | 8 | HG01891.hp1 HG01891.hp2 HG01934.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1091G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1091 | chr12 | 12328936 | |||||
| chr12:12328981
|
C | T | 1 | a0001c0001t0110 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1046G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1046 | chr12 | 12328981 | |||||
| chr12:12328984
|
T | TCA | 24 | a0001c0001t0016a0001c0001t0017a0001c0001t0022others(21): Show | 44 | HG00140.hp1 HG00408.hp2 HG00673.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1041_*1042dupTG | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1042 | chr12 | 12328984 | |||||
| chr12:12328984
|
T | TCACA | 26 | a0001c0001t0003a0001c0001t0014a0001c0001t0018others(23): Show | 70 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1039_*1042dupTGTG | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1042 | chr12 | 12328984 | |||||
| chr12:12328984
|
T | TCACACA | 29 | a0001c0001t0002a0001c0001t0015a0001c0001t0030others(26): Show | 98 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1037_*1042dupTGTG others(2): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1042 | chr12 | 12328984 | |||||
| chr12:12328984
|
T | TCACACAC others(1): Show |
21 | a0001c0001t0005a0001c0001t0010a0001c0001t0021others(18): Show | 47 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1035_*1042dupTGTG others(4): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1042 | chr12 | 12328984 | |||||
| chr12:12328984
|
T | TCACACAC others(3): Show |
17 | a0001c0001t0025a0001c0001t0040a0001c0001t0044others(14): Show | 24 | HG00438.hp2 HG00673.hp2 HG01081.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1033_*1042dupTGTG others(6): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1042 | chr12 | 12328984 | |||||
| chr12:12328984
|
T | TCACACAC others(5): Show |
5 | a0001c0001t0118a0001c0001t0119a0001c0002t0082others(2): Show | 5 | HG00423.hp1 HG00609.hp2 HG02257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1031_*1042dupTGTG others(8): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1042 | chr12 | 12328984 | |||||
| chr12:12328984
|
T | TCACACAC others(7): Show |
1 | a0001c0001t0120 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1029_*1042dupTGTG others(10): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1042 | chr12 | 12328984 | |||||
| chr12:12328984
|
TCA | T | 5 | a0001c0002t0047a0001c0002t0087a0001c0005t0050others(2): Show | 5 | HG01891.hp1 HG02615.hp2 HG03209.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1041_*1042delTG | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1041 | chr12 | 12328984 | |||||
| chr12:12328984
|
TCACACAC others(3): Show |
T | 3 | a0001c0001t0024a0001c0001t0038a0001c0001t0099 | 6 | HG01167.hp2 HG01169.hp2 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1033_*1042delTGTG others(6): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1033 | chr12 | 12328984 | |||||
| chr12:12328988
|
A | T | 2 | a0001c0009t0048a0001c0009t0049 | 2 | HG01891.hp1 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1039T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1039 | chr12 | 12328988 | |||||
| chr12:12329027
|
A | C | 2 | a0001c0002t0085a0001c0002t0086 | 2 | HG02723.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1000T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 1000 | chr12 | 12329027 | |||||
| chr12:12329257
|
A | G | 1 | a0001c0002t0047 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*770T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 770 | chr12 | 12329257 | |||||
| chr12:12329329
|
G | A | 1 | a0001c0005t0084 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*698C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 698 | chr12 | 12329329 | |||||
| chr12:12329514
|
T | C | 43 | a0001c0001t0016a0001c0001t0021a0001c0001t0044others(40): Show | 73 | HG00140.hp1 HG00621.hp1 HG00642.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*513A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 513 | chr12 | 12329514 | |||||
| chr12:12329607
|
C | A | 1 | a0001c0001t0098 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*420G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 420 | chr12 | 12329607 | |||||
| chr12:12329765
|
T | G | 1 | a0001c0001t0121 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*262A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 262 | chr12 | 12329765 | |||||
| chr12:12329824
|
C | T | 1 | a0001c0001t0038 | 2 | HG01167.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*203G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 203 | chr12 | 12329824 | |||||
| chr12:12329849
|
G | A | 2 | a0001c0001t0041a0001c0001t0122 | 3 | NA18960.hp1 NA19057.hp1 NA19080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*178C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 178 | chr12 | 12329849 | |||||
| chr12:12329869
|
A | G | 104 | a0001c0001t0003a0001c0001t0016a0001c0001t0017others(101): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*158T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 158 | chr12 | 12329869 | |||||
| chr12:12329886
|
C | A | 18 | a0001c0001t0016a0001c0001t0021a0001c0001t0044others(15): Show | 32 | HG00140.hp1 HG00621.hp1 HG00673.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*141G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 141 | chr12 | 12329886 | |||||
| chr12:12329922
|
C | T | 1 | a0001c0002t0046 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*105G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 105 | chr12 | 12329922 | |||||
| chr12:12329942
|
CCTG | C | 20 | a0001c0001t0016a0001c0001t0021a0001c0001t0044others(17): Show | 34 | HG00140.hp1 HG00621.hp1 HG00673.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*82_*84delCAG | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 4/4 | 82 | chr12 | 12329942 | |||||
| chr12:12350123
|
A | C | 1 | a0001c0002t0045 | 1 | HG03195.hp2 | 5_prime_UTR_variant | MODIFIER | c.-146T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/4 | 6809 | chr12 | 12350123 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:12330993
|
G | A | 218 | a0001c0001t0002g0303a0001c0001t0003g0004a0001c0001t0003g0016others(215): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.365-35C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12330993 | ||||||
| chr12:12331007
|
C | T | 4 | a0001c0005t0026g0061a0001c0005t0026g0062a0001c0005t0055g0069others(1): Show | 4 | HG01934.hp1 HG02145.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.365-49G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331007 | ||||||
| chr12:12331202
|
G | A | 23 | a0001c0001t0002g0303a0001c0001t0021g0232a0001c0001t0021g0302others(20): Show | 27 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.365-244C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331202 | ||||||
| chr12:12331392
|
C | T | 100 | a0001c0001t0112g0212a0001c0001t0133g0070a0001c0002t0001g0002others(97): Show | 107 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.365-434G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331392 | ||||||
| chr12:12331483
|
C | T | 1 | a0001c0002t0019g0089 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.365-525G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331483 | ||||||
| chr12:12331484
|
G | A | 1 | a0001c0002t0053g0155 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.365-526C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331484 | ||||||
| chr12:12331486
|
A | T | 165 | a0001c0001t0002g0303a0001c0001t0021g0232a0001c0001t0021g0302others(162): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.365-528T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331486 | ||||||
| chr12:12331535
|
T | G | 1 | a0001c0002t0047g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.365-577A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331535 | ||||||
| chr12:12331635
|
G | A | 1 | a0001c0002t0053g0155 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.365-677C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331635 | ||||||
| chr12:12331656
|
T | A | 69 | a0001c0001t0002g0303a0001c0001t0021g0232a0001c0001t0021g0302others(66): Show | 73 | HG00140.hp1 HG00621.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.365-698A>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331656 | ||||||
| chr12:12331670
|
A | C | 96 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0085others(93): Show | 103 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.365-712T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331670 | ||||||
| chr12:12331715
|
G | A | 95 | a0001c0002t0001g0002a0001c0002t0001g0008a0001c0002t0001g0085others(92): Show | 102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.365-757C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331715 | ||||||
| chr12:12331717
|
G | A | 1 | a0001c0001t0103g0066 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.365-759C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331717 | ||||||
| chr12:12331728
|
C | T | 50 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(47): Show | 52 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.365-770G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331728 | ||||||
| chr12:12331744
|
T | C | 1 | a0001c0002t0067g0190 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.365-786A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331744 | ||||||
| chr12:12331836
|
G | T | 1 | a0001c0002t0001g0116 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.365-878C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331836 | ||||||
| chr12:12331882
|
A | C | 1 | a0001c0002t0067g0190 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.365-924T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331882 | ||||||
| chr12:12331957
|
C | T | 193 | a0001c0001t0002g0034a0001c0001t0003g0004a0001c0001t0003g0016others(190): Show | 202 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.365-999G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12331957 | ||||||
| chr12:12332139
|
A | G | 1 | a0001c0001t0100g0063 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.365-1181T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332139 | ||||||
| chr12:12332178
|
G | A | 2 | a0001c0009t0048g0173a0001c0009t0049g0201 | 2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.365-1220C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332178 | ||||||
| chr12:12332237
|
C | T | 1 | a0001c0002t0001g0102 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.365-1279G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332237 | ||||||
| chr12:12332358
|
T | C | 20 | a0001c0001t0021g0232a0001c0001t0124g0141a0002c0003t0006g0001others(17): Show | 24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-1400A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332358 | ||||||
| chr12:12332417
|
G | A | 20 | a0001c0001t0021g0232a0001c0001t0124g0141a0002c0003t0006g0001others(17): Show | 24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-1459C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332417 | ||||||
| chr12:12332514
|
G | A | 20 | a0001c0001t0021g0232a0001c0001t0124g0141a0002c0003t0006g0001others(17): Show | 24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-1556C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332514 | ||||||
| chr12:12332589
|
C | T | 1 | a0001c0001t0121g0300 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.365-1631G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332589 | ||||||
| chr12:12332621
|
G | A | 20 | a0001c0001t0021g0232a0001c0001t0124g0141a0002c0003t0006g0001others(17): Show | 24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-1663C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332621 | ||||||
| chr12:12332623
|
C | T | 1 | a0001c0002t0047g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.365-1665G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332623 | ||||||
| chr12:12332664
|
G | A | 1 | a0001c0002t0052g0113 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.365-1706C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332664 | ||||||
| chr12:12332665
|
C | T | 78 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(75): Show | 83 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.365-1707G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332665 | ||||||
| chr12:12332768
|
C | G | 1 | a0001c0002t0019g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.365-1810G>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332768 | ||||||
| chr12:12332873
|
A | G | 1 | a0001c0002t0001g0097 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.365-1915T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332873 | ||||||
| chr12:12332947
|
C | A | 20 | a0001c0001t0021g0232a0001c0001t0124g0141a0002c0003t0006g0001others(17): Show | 24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-1989G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12332947 | ||||||
| chr12:12333044
|
A | AATATATA others(5): Show |
18 | a0001c0001t0021g0232a0002c0003t0006g0001a0002c0003t0006g0037others(15): Show | 22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.365-2098_365-2087d others(14): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333044 | ||||||
| chr12:12333044
|
A | AATATATA others(9): Show |
2 | a0001c0001t0124g0141a0002c0003t0043g0050 | 2 | HG04199.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.365-2102_365-2087d others(18): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333044 | ||||||
| chr12:12333142
|
G | A | 1 | a0001c0001t0005g0221 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.365-2184C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333142 | ||||||
| chr12:12333150
|
A | G | 20 | a0001c0001t0021g0232a0001c0001t0124g0141a0002c0003t0006g0001others(17): Show | 24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-2192T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333150 | ||||||
| chr12:12333299
|
A | G | 153 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(150): Show | 164 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.365-2341T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333299 | ||||||
| chr12:12333329
|
G | A | 20 | a0001c0001t0021g0232a0001c0001t0124g0141a0002c0003t0006g0001others(17): Show | 24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-2371C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333329 | ||||||
| chr12:12333494
|
C | G | 20 | a0001c0001t0021g0232a0001c0001t0124g0141a0002c0003t0006g0001others(17): Show | 24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-2536G>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333494 | ||||||
| chr12:12333505
|
C | T | 1 | a0001c0002t0045g0014 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.365-2547G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333505 | ||||||
| chr12:12333510
|
C | T | 20 | a0001c0001t0021g0232a0001c0001t0124g0141a0002c0003t0006g0001others(17): Show | 24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-2552G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333510 | ||||||
| chr12:12333598
|
A | C | 3 | a0001c0005t0026g0061a0001c0005t0026g0062a0001c0005t0055g0069 | 3 | HG01934.hp1 HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.365-2640T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333598 | ||||||
| chr12:12333991
|
G | C | 1 | a0001c0002t0007g0006 | 2 | NA18992.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.365-3033C>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12333991 | ||||||
| chr12:12334014
|
C | T | 50 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(47): Show | 52 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.365-3056G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334014 | ||||||
| chr12:12334055
|
C | A | 1 | a0001c0002t0011g0098 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.365-3097G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334055 | ||||||
| chr12:12334073
|
A | AC | 9 | a0001c0001t0133g0070a0001c0002t0008g0149a0001c0005t0026g0061others(6): Show | 9 | HG00621.hp1 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.365-3116dupG | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334073 | ||||||
| chr12:12334073
|
AC | A | 18 | a0001c0001t0021g0232a0001c0001t0124g0141a0002c0003t0006g0001others(15): Show | 22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.365-3116delG | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334073 | ||||||
| chr12:12334078
|
C | A | 7 | a0001c0001t0005g0003a0001c0001t0005g0241a0001c0001t0005g0242others(4): Show | 10 | NA18986.hp2 NA18994.hp2 NA19007.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-3120G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334078 | ||||||
| chr12:12334079
|
C | T | 7 | a0001c0001t0005g0003a0001c0001t0005g0241a0001c0001t0005g0242others(4): Show | 10 | NA18986.hp2 NA18994.hp2 NA19007.hp1 others(7): Show |
intron_variant | MODIFIER | c.365-3121G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334079 | ||||||
| chr12:12334114
|
C | G | 1 | a0001c0002t0001g0091 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.365-3156G>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334114 | ||||||
| chr12:12334131
|
T | C | 2 | a0002c0003t0006g0040a0002c0003t0126g0044 | 2 | HG00735.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.365-3173A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334131 | ||||||
| chr12:12334162
|
A | C | 20 | a0001c0001t0021g0232a0001c0001t0124g0141a0002c0003t0006g0001others(17): Show | 24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-3204T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334162 | ||||||
| chr12:12334211
|
C | T | 1 | a0001c0004t0008g0104 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.365-3253G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334211 | ||||||
| chr12:12334215
|
G | A | 1 | a0002c0003t0021g0048 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.365-3257C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334215 | ||||||
| chr12:12334227
|
C | A | 4 | a0001c0001t0018g0196a0001c0001t0018g0197a0001c0001t0018g0198others(1): Show | 4 | HG00280.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.365-3269G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334227 | ||||||
| chr12:12334288
|
GA | G | 67 | a0001c0001t0002g0034a0001c0001t0002g0251a0001c0001t0029g0274others(64): Show | 73 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.365-3331delT | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334288 | ||||||
| chr12:12334315
|
A | C | 2 | a0001c0009t0048g0173a0001c0009t0049g0201 | 2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.365-3357T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334315 | ||||||
| chr12:12334365
|
T | C | 2 | a0001c0001t0015g0243a0001c0001t0015g0249 | 2 | HG02132.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.365-3407A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334365 | ||||||
| chr12:12334511
|
A | T | 1 | a0001c0001t0125g0294 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.365-3553T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334511 | ||||||
| chr12:12334513
|
G | A | 20 | a0001c0001t0021g0232a0001c0001t0124g0141a0002c0003t0006g0001others(17): Show | 24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-3555C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334513 | ||||||
| chr12:12334517
|
G | A | 1 | a0001c0002t0045g0014 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.365-3559C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334517 | ||||||
| chr12:12334619
|
C | T | 1 | a0001c0002t0009g0186 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.365-3661G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334619 | ||||||
| chr12:12334634
|
C | T | 1 | a0001c0002t0094g0082 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.365-3676G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334634 | ||||||
| chr12:12334736
|
T | C | 1 | a0001c0001t0121g0300 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.364+3684A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334736 | ||||||
| chr12:12334746
|
C | T | 72 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(69): Show | 78 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.364+3674G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334746 | ||||||
| chr12:12334764
|
A | G | 50 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(47): Show | 52 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.364+3656T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334764 | ||||||
| chr12:12334948
|
C | A | 1 | a0001c0005t0084g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.364+3472G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334948 | ||||||
| chr12:12334956
|
G | A | 1 | a0001c0002t0027g0030 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.364+3464C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12334956 | ||||||
| chr12:12335085
|
C | T | 1 | a0001c0002t0063g0111 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.364+3335G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335085 | ||||||
| chr12:12335133
|
T | C | 57 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(54): Show | 59 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.364+3287A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335133 | ||||||
| chr12:12335211
|
G | A | 2 | a0001c0001t0010g0160a0001c0001t0039g0297 | 2 | NA18949.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.364+3209C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335211 | ||||||
| chr12:12335262
|
G | T | 1 | a0001c0002t0001g0177 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.364+3158C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335262 | ||||||
| chr12:12335319
|
G | A | 1 | a0001c0002t0045g0014 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.364+3101C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335319 | ||||||
| chr12:12335339
|
C | CTTT | 97 | a0001c0001t0002g0034a0001c0001t0109g0167a0001c0002t0001g0002others(94): Show | 104 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.364+3078_364+3080d others(5): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335339 | ||||||
| chr12:12335339
|
CT | C | 8 | a0001c0001t0024g0199a0001c0001t0024g0205a0001c0001t0024g0206others(5): Show | 8 | HG01167.hp2 HG01169.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.364+3080delA | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335339 | ||||||
| chr12:12335343
|
T | C | 1 | a0001c0005t0084g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.364+3077A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335343 | ||||||
| chr12:12335358
|
C | T | 107 | a0001c0001t0002g0034a0001c0001t0109g0167a0001c0002t0001g0002others(104): Show | 114 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.364+3062G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335358 | ||||||
| chr12:12335380
|
G | A | 1 | a0001c0009t0049g0201 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.364+3040C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335380 | ||||||
| chr12:12335389
|
A | G | 5 | a0001c0002t0032g0096a0001c0002t0032g0168a0001c0002t0036g0179others(2): Show | 5 | HG01099.hp2 HG01952.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.364+3031T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335389 | ||||||
| chr12:12335416
|
C | T | 99 | a0001c0001t0002g0034a0001c0001t0109g0167a0001c0002t0001g0002others(96): Show | 106 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.364+3004G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335416 | ||||||
| chr12:12335525
|
G | C | 200 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(197): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.364+2895C>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335525 | ||||||
| chr12:12335586
|
G | A | 1 | a0001c0001t0030g0253 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.364+2834C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335586 | ||||||
| chr12:12335735
|
A | G | 254 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(251): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.364+2685T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335735 | ||||||
| chr12:12335853
|
T | A | 178 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(175): Show | 190 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.364+2567A>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335853 | ||||||
| chr12:12335855
|
A | T | 26 | a0001c0001t0002g0011a0001c0001t0002g0018a0001c0001t0002g0024others(23): Show | 27 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.364+2565T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335855 | ||||||
| chr12:12335888
|
C | A | 69 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(66): Show | 75 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.364+2532G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335888 | ||||||
| chr12:12335911
|
G | A | 2 | a0001c0001t0002g0210a0001c0001t0002g0296 | 2 | NA19056.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.364+2509C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335911 | ||||||
| chr12:12335958
|
G | A | 1 | a0001c0002t0007g0169 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.364+2462C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335958 | ||||||
| chr12:12335967
|
G | A | 6 | a0001c0001t0002g0024a0001c0001t0002g0026a0001c0001t0104g0023others(3): Show | 6 | HG00621.hp2 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.364+2453C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12335967 | ||||||
| chr12:12336012
|
A | G | 70 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(67): Show | 76 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.364+2408T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12336012 | ||||||
| chr12:12336059
|
C | T | 2 | a0001c0002t0004g0007a0001c0002t0004g0101 | 3 | NA18944.hp1 NA18977.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.364+2361G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12336059 | ||||||
| chr12:12336184
|
G | A | 69 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(66): Show | 75 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.364+2236C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12336184 | ||||||
| chr12:12336252
|
C | T | 1 | a0001c0009t0049g0201 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.364+2168G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12336252 | ||||||
| chr12:12336593
|
C | G | 178 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(175): Show | 190 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.364+1827G>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12336593 | ||||||
| chr12:12336614
|
C | T | 1 | a0002c0003t0021g0047 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.364+1806G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12336614 | ||||||
| chr12:12336671
|
C | T | 97 | a0001c0001t0002g0034a0001c0002t0001g0002a0001c0002t0001g0008others(94): Show | 104 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.364+1749G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12336671 | ||||||
| chr12:12336743
|
G | T | 2 | a0001c0001t0015g0243a0001c0001t0015g0249 | 2 | HG02132.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.364+1677C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12336743 | ||||||
| chr12:12337115
|
CA | C | 75 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(72): Show | 81 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.364+1304delT | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337115 | ||||||
| chr12:12337115
|
CAAA | C | 178 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(175): Show | 190 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.364+1302_364+1304d others(5): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337115 | ||||||
| chr12:12337141
|
G | A | 1 | a0001c0002t0012g0035 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.364+1279C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337141 | ||||||
| chr12:12337231
|
C | G | 3 | a0001c0001t0024g0199a0001c0002t0087g0200a0001c0009t0049g0201 | 3 | HG01891.hp1 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.364+1189G>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337231 | ||||||
| chr12:12337255
|
C | T | 1 | a0001c0001t0099g0237 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.364+1165G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337255 | ||||||
| chr12:12337256
|
G | A | 1 | a0001c0002t0009g0118 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.364+1164C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337256 | ||||||
| chr12:12337374
|
G | A | 77 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(74): Show | 82 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.364+1046C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337374 | ||||||
| chr12:12337421
|
C | T | 1 | a0001c0002t0011g0151 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.364+999G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337421 | ||||||
| chr12:12337422
|
G | A | 2 | a0001c0002t0001g0114a0001c0002t0001g0123 | 2 | HG00140.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.364+998C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337422 | ||||||
| chr12:12337466
|
C | T | 78 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(75): Show | 83 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.364+954G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337466 | ||||||
| chr12:12337469
|
G | T | 1 | a0001c0001t0133g0070 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.364+951C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337469 | ||||||
| chr12:12337512
|
G | C | 1 | a0001c0005t0084g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.364+908C>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337512 | ||||||
| chr12:12337516
|
G | A | 52 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(49): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.364+904C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337516 | ||||||
| chr12:12337532
|
T | G | 2 | a0001c0001t0125g0294a0001c0002t0035g0084 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.364+888A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337532 | ||||||
| chr12:12337539
|
C | T | 1 | a0001c0002t0069g0060 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.364+881G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337539 | ||||||
| chr12:12337619
|
G | T | 6 | a0001c0001t0024g0205a0001c0001t0024g0206a0001c0001t0038g0203others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.364+801C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337619 | ||||||
| chr12:12337953
|
A | G | 1 | a0001c0002t0083g0185 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.364+467T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337953 | ||||||
| chr12:12337980
|
G | A | 18 | a0002c0003t0006g0001a0002c0003t0006g0037a0002c0003t0006g0039others(15): Show | 22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.364+440C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12337980 | ||||||
| chr12:12338047
|
T | C | 1 | a0002c0003t0128g0038 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.364+373A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12338047 | ||||||
| chr12:12338117
|
T | C | 1 | a0001c0002t0004g0135 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.364+303A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12338117 | ||||||
| chr12:12338334
|
T | C | 25 | a0001c0001t0003g0004a0001c0001t0003g0261a0001c0001t0003g0265others(22): Show | 27 | HG00408.hp2 HG00609.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.364+86A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3/3 | chr12 | 12338334 | ||||||
| chr12:12338890
|
A | AAC | 74 | a0001c0001t0133g0070a0001c0002t0001g0002a0001c0002t0001g0008others(71): Show | 79 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.224-332_224-331dup others(2): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | ||||||
| chr12:12338890
|
A | AACAC | 86 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0024others(83): Show | 93 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.224-334_224-331dup others(4): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | ||||||
| chr12:12338890
|
A | AACACAC | 6 | a0001c0001t0002g0018a0001c0001t0014g0223a0001c0001t0015g0243others(3): Show | 6 | HG00438.hp2 HG02132.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.224-336_224-331dup others(6): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | ||||||
| chr12:12338890
|
A | AACACACA others(3): Show |
44 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(41): Show | 46 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.224-340_224-331dup others(10): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | ||||||
| chr12:12338890
|
A | AACACACA others(5): Show |
3 | a0001c0001t0130g0256a0001c0002t0073g0288a0001c0005t0084g0059 | 3 | HG01981.hp2 NA18998.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.224-342_224-331dup others(12): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | ||||||
| chr12:12338890
|
A | AACACACA others(7): Show |
1 | a0001c0001t0121g0300 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.224-344_224-331dup others(14): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | ||||||
| chr12:12338890
|
A | AACACACA others(9): Show |
11 | a0001c0001t0125g0294a0001c0002t0047g0248a0001c0009t0049g0201others(8): Show | 15 | HG00735.hp1 HG00735.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.224-346_224-331dup others(16): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | ||||||
| chr12:12338890
|
A | AACACACA others(11): Show |
10 | a0001c0001t0018g0196a0001c0001t0018g0197a0001c0001t0018g0198others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.224-348_224-331dup others(18): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | ||||||
| chr12:12338890
|
A | AACACACA others(13): Show |
2 | a0001c0002t0087g0200a0002c0003t0006g0041 | 2 | HG04204.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.224-350_224-331dup others(20): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | ||||||
| chr12:12338890
|
A | AACACACA others(15): Show |
2 | a0001c0001t0080g0295a0002c0003t0042g0051 | 2 | HG04204.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.224-352_224-331dup others(22): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | ||||||
| chr12:12338890
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0017g0286 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.224-331_224-330ins others(11): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | ||||||
| chr12:12338890
|
AACACAC | A | 4 | a0001c0001t0024g0205a0001c0001t0024g0206a0001c0001t0038g0203others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-336_224-331del others(6): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338890 | ||||||
| chr12:12338903
|
A | T | 4 | a0001c0001t0024g0205a0001c0001t0024g0206a0001c0001t0038g0203others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-343T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338903 | ||||||
| chr12:12338917
|
A | ACACACAC others(17): Show |
1 | a0002c0003t0043g0050 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.224-358_224-357ins others(24): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338917 | ||||||
| chr12:12338949
|
C | T | 1 | a0001c0001t0014g0226 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.224-389G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338949 | ||||||
| chr12:12338956
|
A | T | 3 | a0001c0001t0024g0199a0001c0002t0087g0200a0001c0009t0049g0201 | 3 | HG01891.hp1 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.224-396T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12338956 | ||||||
| chr12:12339080
|
G | C | 4 | a0001c0001t0018g0196a0001c0001t0018g0197a0001c0001t0018g0198others(1): Show | 4 | HG00280.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-520C>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12339080 | ||||||
| chr12:12339351
|
C | T | 3 | a0001c0002t0001g0108a0001c0002t0001g0146a0001c0002t0001g0148 | 3 | HG00558.hp2 NA18978.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.224-791G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12339351 | ||||||
| chr12:12339450
|
T | C | 1 | a0001c0005t0084g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.224-890A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12339450 | ||||||
| chr12:12339473
|
G | C | 1 | a0001c0001t0099g0237 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.224-913C>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12339473 | ||||||
| chr12:12339531
|
G | C | 1 | a0001c0001t0099g0237 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.224-971C>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12339531 | ||||||
| chr12:12339531
|
G | T | 1 | a0001c0002t0045g0014 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.224-971C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12339531 | ||||||
| chr12:12339547
|
T | G | 1 | a0001c0002t0023g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.224-987A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12339547 | ||||||
| chr12:12339719
|
T | C | 1 | a0001c0002t0087g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.224-1159A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12339719 | ||||||
| chr12:12339891
|
C | T | 52 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(49): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.224-1331G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12339891 | ||||||
| chr12:12340156
|
C | T | 1 | a0001c0001t0125g0294 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.224-1596G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12340156 | ||||||
| chr12:12340401
|
T | A | 1 | a0001c0002t0094g0082 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.224-1841A>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12340401 | ||||||
| chr12:12340969
|
C | T | 6 | a0001c0002t0035g0077a0001c0002t0035g0084a0001c0002t0088g0079others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+2123G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12340969 | ||||||
| chr12:12341150
|
C | T | 71 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(68): Show | 77 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.223+1942G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341150 | ||||||
| chr12:12341157
|
C | T | 1 | a0001c0002t0082g0137 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.223+1935G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341157 | ||||||
| chr12:12341309
|
C | A | 1 | a0001c0002t0087g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.223+1783G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341309 | ||||||
| chr12:12341357
|
C | A | 1 | a0001c0002t0082g0137 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.223+1735G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341357 | ||||||
| chr12:12341460
|
A | C | 19 | a0001c0005t0084g0059a0002c0003t0006g0001a0002c0003t0006g0037others(16): Show | 23 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.223+1632T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341460 | ||||||
| chr12:12341476
|
A | G | 1 | a0001c0002t0013g0172 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.223+1616T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341476 | ||||||
| chr12:12341497
|
G | A | 6 | a0001c0001t0002g0018a0001c0001t0025g0019a0001c0001t0025g0022others(3): Show | 6 | HG00438.hp2 NA18960.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+1595C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341497 | ||||||
| chr12:12341502
|
G | A | 80 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(77): Show | 85 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.223+1590C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341502 | ||||||
| chr12:12341538
|
G | T | 1 | a0001c0002t0011g0098 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.223+1554C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341538 | ||||||
| chr12:12341670
|
G | A | 1 | a0001c0005t0026g0061 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.223+1422C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341670 | ||||||
| chr12:12341682
|
G | C | 3 | a0001c0002t0037g0072a0001c0002t0037g0133a0001c0014t0090g0121 | 3 | HG01081.hp2 HG01516.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.223+1410C>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341682 | ||||||
| chr12:12341689
|
G | A | 7 | a0001c0001t0002g0012a0001c0001t0002g0222a0001c0001t0002g0225others(4): Show | 8 | HG02074.hp1 HG02074.hp2 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.223+1403C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341689 | ||||||
| chr12:12341711
|
G | C | 1 | a0001c0002t0011g0098 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.223+1381C>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341711 | ||||||
| chr12:12341777
|
A | G | 19 | a0001c0005t0084g0059a0002c0003t0006g0001a0002c0003t0006g0037others(16): Show | 23 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.223+1315T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341777 | ||||||
| chr12:12341816
|
C | T | 1 | a0001c0001t0003g0281 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.223+1276G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341816 | ||||||
| chr12:12341827
|
T | C | 19 | a0001c0005t0084g0059a0002c0003t0006g0001a0002c0003t0006g0037others(16): Show | 23 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.223+1265A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341827 | ||||||
| chr12:12341884
|
C | T | 19 | a0001c0005t0084g0059a0002c0003t0006g0001a0002c0003t0006g0037others(16): Show | 23 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.223+1208G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341884 | ||||||
| chr12:12341939
|
C | G | 4 | a0001c0001t0133g0070a0001c0005t0026g0061a0001c0005t0026g0062others(1): Show | 4 | HG00621.hp1 HG01934.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+1153G>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341939 | ||||||
| chr12:12341958
|
CTCCG | C | 19 | a0001c0005t0084g0059a0002c0003t0006g0001a0002c0003t0006g0037others(16): Show | 23 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.223+1130_223+1133d others(6): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12341958 | ||||||
| chr12:12342016
|
C | T | 1 | a0001c0001t0121g0300 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.223+1076G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342016 | ||||||
| chr12:12342063
|
C | A | 52 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(49): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.223+1029G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342063 | ||||||
| chr12:12342109
|
A | G | 1 | a0001c0002t0047g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.223+983T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342109 | ||||||
| chr12:12342156
|
T | C | 82 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(79): Show | 87 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.223+936A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342156 | ||||||
| chr12:12342239
|
G | C | 1 | a0001c0002t0001g0124 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.223+853C>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342239 | ||||||
| chr12:12342333
|
T | C | 2 | a0001c0002t0035g0084a0001c0002t0096g0083 | 2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.223+759A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342333 | ||||||
| chr12:12342366
|
C | T | 1 | a0003c0006t0002g0220 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.223+726G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342366 | ||||||
| chr12:12342574
|
GTGTTTTT others(1): Show |
G | 34 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0258others(31): Show | 36 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.223+510_223+517del others(8): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342574 | ||||||
| chr12:12342576
|
GTTTTTTT others(3): Show |
G | 1 | a0002c0003t0043g0046 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.223+506_223+515del others(10): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342576 | ||||||
| chr12:12342576
|
GTTTTTTT others(4): Show |
G | 17 | a0002c0003t0006g0001a0002c0003t0006g0037a0002c0003t0006g0039others(14): Show | 21 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.223+505_223+515del others(11): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342576 | ||||||
| chr12:12342577
|
T | G | 2 | a0001c0002t0085g0058a0001c0002t0086g0055 | 2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.223+515A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342577 | ||||||
| chr12:12342577
|
TTTTTTTG | T | 16 | a0001c0001t0003g0255a0001c0001t0003g0273a0001c0001t0003g0276others(13): Show | 16 | HG00280.hp1 HG00323.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.223+508_223+514del others(7): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342577 | ||||||
| chr12:12342579
|
TTTTTG | T | 18 | a0001c0001t0002g0034a0001c0001t0014g0223a0001c0001t0038g0204others(15): Show | 19 | HG00408.hp1 HG00544.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.223+508_223+512del others(5): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342579 | ||||||
| chr12:12342580
|
TTTTG | T | 142 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(139): Show | 153 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.223+508_223+511del others(4): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342580 | ||||||
| chr12:12342581
|
TTTG | T | 27 | a0001c0001t0002g0225a0001c0001t0024g0199a0001c0001t0099g0237others(24): Show | 27 | HG00597.hp1 HG00673.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.223+508_223+510del others(3): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342581 | ||||||
| chr12:12342582
|
TTG | T | 34 | a0001c0001t0005g0067a0001c0001t0005g0242a0001c0001t0100g0063others(31): Show | 34 | HG00621.hp1 HG00642.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.223+508_223+509del others(2): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342582 | ||||||
| chr12:12342583
|
TG | T | 5 | a0001c0001t0005g0068a0001c0001t0005g0071a0001c0002t0023g0056others(2): Show | 5 | HG02451.hp1 HG03516.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.223+508delC | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342583 | ||||||
| chr12:12342584
|
G | T | 6 | a0001c0001t0005g0064a0001c0001t0103g0066a0001c0001t0111g0036others(3): Show | 6 | HG02145.hp2 HG02622.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+508C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342584 | ||||||
| chr12:12342591
|
T | G | 1 | a0002c0003t0043g0046 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.223+501A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342591 | ||||||
| chr12:12342592
|
T | G | 18 | a0001c0001t0002g0236a0002c0003t0006g0001a0002c0003t0006g0037others(15): Show | 22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.223+500A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342592 | ||||||
| chr12:12342593
|
T | G | 1 | a0001c0001t0106g0229 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.223+499A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342593 | ||||||
| chr12:12342594
|
T | G | 1 | a0003c0006t0025g0228 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.223+498A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342594 | ||||||
| chr12:12342596
|
T | G | 2 | a0001c0001t0005g0242a0003c0006t0010g0230 | 2 | HG02135.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.223+496A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342596 | ||||||
| chr12:12342597
|
T | G | 71 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(68): Show | 76 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.223+495A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342597 | ||||||
| chr12:12342601
|
T | G | 2 | a0001c0001t0106g0229a0001c0001t0116g0028 | 2 | HG04115.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.223+491A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342601 | ||||||
| chr12:12342602
|
T | G | 4 | a0001c0001t0002g0210a0001c0001t0002g0224a0001c0001t0002g0296others(1): Show | 4 | HG02071.hp1 NA19056.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+490A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342602 | ||||||
| chr12:12342704
|
G | A | 1 | a0001c0002t0031g0181 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.223+388C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342704 | ||||||
| chr12:12342741
|
A | T | 18 | a0002c0003t0006g0001a0002c0003t0006g0037a0002c0003t0006g0039others(15): Show | 22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.223+351T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342741 | ||||||
| chr12:12342837
|
A | G | 256 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(253): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.223+255T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342837 | ||||||
| chr12:12342839
|
T | C | 1 | a0001c0001t0002g0215 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.223+253A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342839 | ||||||
| chr12:12342841
|
G | A | 2 | a0001c0001t0125g0294a0001c0002t0045g0014 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.223+251C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342841 | ||||||
| chr12:12342991
|
C | T | 3 | a0001c0002t0037g0072a0001c0002t0037g0133a0001c0014t0090g0121 | 3 | HG01081.hp2 HG01516.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.223+101G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12342991 | ||||||
| chr12:12343025
|
C | T | 97 | a0001c0001t0002g0034a0001c0002t0001g0002a0001c0002t0001g0008others(94): Show | 104 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.223+67G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12343025 | ||||||
| chr12:12343077
|
G | T | 4 | a0001c0001t0133g0070a0001c0005t0026g0061a0001c0005t0026g0062others(1): Show | 4 | HG00621.hp1 HG01934.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+15C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 2/3 | chr12 | 12343077 | ||||||
| chr12:12343475
|
C | T | 1 | a0001c0001t0121g0300 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-100-61G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12343475 | ||||||
| chr12:12343537
|
C | A | 19 | a0001c0005t0084g0059a0002c0003t0006g0001a0002c0003t0006g0037others(16): Show | 23 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.-100-123G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12343537 | ||||||
| chr12:12343564
|
T | C | 1 | a0001c0001t0101g0250 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-100-150A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12343564 | ||||||
| chr12:12343625
|
C | A | 1 | a0001c0002t0045g0014 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-100-211G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12343625 | ||||||
| chr12:12343690
|
G | A | 1 | a0001c0005t0084g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-100-276C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12343690 | ||||||
| chr12:12343701
|
A | G | 19 | a0001c0001t0121g0300a0002c0003t0006g0001a0002c0003t0006g0037others(16): Show | 23 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.-100-287T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12343701 | ||||||
| chr12:12343706
|
T | A | 1 | a0001c0001t0121g0300 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-100-292A>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12343706 | ||||||
| chr12:12343738
|
C | T | 1 | a0001c0002t0011g0147 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-100-324G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12343738 | ||||||
| chr12:12343824
|
A | G | 82 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(79): Show | 87 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.-100-410T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12343824 | ||||||
| chr12:12343964
|
T | A | 8 | a0001c0004t0008g0094a0001c0004t0008g0100a0001c0004t0008g0104others(5): Show | 8 | NA18949.hp1 NA18951.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.-100-550A>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12343964 | ||||||
| chr12:12344001
|
G | A | 18 | a0002c0003t0006g0001a0002c0003t0006g0037a0002c0003t0006g0039others(15): Show | 22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-100-587C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344001 | ||||||
| chr12:12344043
|
G | A | 1 | a0001c0002t0007g0138 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-100-629C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344043 | ||||||
| chr12:12344229
|
T | C | 4 | a0001c0001t0133g0070a0001c0005t0026g0061a0001c0005t0026g0062others(1): Show | 4 | HG00621.hp1 HG01934.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-100-815A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344229 | ||||||
| chr12:12344232
|
A | G | 1 | a0001c0001t0010g0209 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-100-818T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344232 | ||||||
| chr12:12344289
|
G | T | 1 | a0001c0005t0084g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-100-875C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344289 | ||||||
| chr12:12344366
|
C | T | 1 | a0001c0005t0084g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-100-952G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344366 | ||||||
| chr12:12344399
|
T | C | 19 | a0001c0005t0084g0059a0002c0003t0006g0001a0002c0003t0006g0037others(16): Show | 23 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.-100-985A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344399 | ||||||
| chr12:12344419
|
T | C | 1 | a0001c0005t0084g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-100-1005A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344419 | ||||||
| chr12:12344461
|
C | T | 19 | a0001c0005t0084g0059a0002c0003t0006g0001a0002c0003t0006g0037others(16): Show | 23 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.-100-1047G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344461 | ||||||
| chr12:12344471
|
A | G | 18 | a0002c0003t0006g0001a0002c0003t0006g0037a0002c0003t0006g0039others(15): Show | 22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-100-1057T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344471 | ||||||
| chr12:12344475
|
C | CT | 7 | a0001c0001t0005g0241a0001c0001t0018g0196a0001c0001t0018g0197others(4): Show | 7 | HG00280.hp1 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-100-1062dupA | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344475 | ||||||
| chr12:12344475
|
CT | C | 49 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(46): Show | 51 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-100-1062delA | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344475 | ||||||
| chr12:12344545
|
C | T | 5 | a0001c0002t0020g0106a0001c0002t0020g0109a0001c0002t0020g0125others(2): Show | 5 | HG00642.hp2 HG01099.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.-100-1131G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344545 | ||||||
| chr12:12344568
|
C | T | 2 | a0001c0001t0038g0203a0001c0001t0038g0204 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-100-1154G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344568 | ||||||
| chr12:12344599
|
A | C | 1 | a0001c0002t0001g0116 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-100-1185T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344599 | ||||||
| chr12:12344686
|
A | G | 19 | a0001c0005t0084g0059a0002c0003t0006g0001a0002c0003t0006g0037others(16): Show | 23 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.-100-1272T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344686 | ||||||
| chr12:12344703
|
A | G | 1 | a0001c0005t0084g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-100-1289T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344703 | ||||||
| chr12:12344712
|
C | T | 3 | a0001c0002t0001g0108a0001c0002t0001g0146a0001c0002t0001g0148 | 3 | HG00558.hp2 NA18978.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-100-1298G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344712 | ||||||
| chr12:12344913
|
T | G | 18 | a0002c0003t0006g0001a0002c0003t0006g0037a0002c0003t0006g0039others(15): Show | 22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-100-1499A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344913 | ||||||
| chr12:12344915
|
CCATATAT others(3): Show |
C | 1 | a0001c0002t0053g0155 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-100-1511_-100-150 others(14): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344915 | ||||||
| chr12:12344916
|
C | CAT | 49 | a0001c0001t0002g0153a0001c0001t0002g0159a0001c0001t0002g0222others(46): Show | 51 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.-100-1504_-100-150 others(6): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
C | CATAT | 25 | a0001c0001t0003g0276a0001c0001t0003g0277a0001c0001t0003g0299others(22): Show | 26 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.-100-1506_-100-150 others(8): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
C | CATATAT | 23 | a0001c0001t0002g0024a0001c0001t0002g0216a0001c0001t0003g0004others(20): Show | 27 | HG01168.hp1 HG01346.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.-100-1508_-100-150 others(10): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
C | CATATATA others(1): Show |
25 | a0001c0001t0002g0011a0001c0001t0002g0034a0001c0001t0002g0156others(22): Show | 27 | HG00544.hp1 HG00597.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-100-1510_-100-150 others(12): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
C | CATATATA others(3): Show |
19 | a0001c0001t0002g0018a0001c0001t0003g0262a0001c0001t0003g0265others(16): Show | 19 | HG00408.hp2 HG01081.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.-100-1512_-100-150 others(14): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
C | CATATATA others(5): Show |
10 | a0001c0001t0002g0210a0001c0001t0003g0258a0001c0001t0003g0261others(7): Show | 10 | HG01358.hp2 HG01952.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.-100-1514_-100-150 others(16): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
C | CATATATA others(7): Show |
1 | a0001c0002t0069g0060 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-100-1516_-100-150 others(18): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
C | CATATATA others(9): Show |
2 | a0001c0001t0066g0015a0001c0004t0008g0094 | 2 | HG02056.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-100-1518_-100-150 others(20): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
C | CATATATA others(11): Show |
1 | a0001c0001t0081g0257 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-100-1520_-100-150 others(22): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
C | CATATATA others(17): Show |
1 | a0001c0002t0012g0035 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-100-1526_-100-150 others(28): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
CAT | C | 21 | a0001c0001t0005g0067a0001c0001t0010g0233a0001c0001t0014g0161others(18): Show | 21 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.-100-1504_-100-150 others(6): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
CATAT | C | 20 | a0001c0001t0002g0162a0001c0001t0002g0235a0001c0001t0002g0236others(17): Show | 20 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.-100-1506_-100-150 others(8): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
CATATAT | C | 10 | a0001c0001t0002g0238a0001c0001t0010g0239a0001c0001t0018g0197others(7): Show | 10 | HG00621.hp1 HG01069.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-100-1508_-100-150 others(10): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
CATATATA others(1): Show |
C | 7 | a0001c0001t0003g0292a0001c0001t0005g0071a0001c0001t0024g0206others(4): Show | 7 | HG02257.hp2 HG03139.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-100-1510_-100-150 others(12): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
CATATATA others(3): Show |
C | 6 | a0001c0001t0125g0294a0001c0002t0007g0152a0001c0002t0012g0188others(3): Show | 6 | HG00408.hp1 HG00741.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.-100-1512_-100-150 others(14): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
CATATATA others(5): Show |
C | 6 | a0001c0002t0056g0191a0001c0002t0067g0190a0001c0002t0071g0192others(3): Show | 7 | HG01255.hp2 NA18943.hp2 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.-100-1514_-100-150 others(16): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
CATATATA others(7): Show |
C | 4 | a0002c0003t0006g0001a0002c0003t0006g0039a0002c0003t0006g0040others(1): Show | 7 | HG00735.hp1 HG00735.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-100-1516_-100-150 others(18): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
CATATATA others(9): Show |
C | 5 | a0002c0003t0006g0041a0002c0003t0126g0044a0002c0003t0127g0042others(2): Show | 5 | HG00140.hp1 HG01261.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-100-1518_-100-150 others(20): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
CATATATA others(11): Show |
C | 8 | a0001c0001t0015g0249a0001c0001t0016g0293a0002c0003t0021g0047others(5): Show | 8 | HG02135.hp1 HG03927.hp2 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.-100-1520_-100-150 others(22): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
CATATATA others(13): Show |
C | 1 | a0001c0002t0035g0077 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-100-1522_-100-150 others(24): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
CATATATA others(15): Show |
C | 13 | a0001c0001t0002g0026a0001c0001t0005g0003a0001c0001t0005g0241others(10): Show | 16 | HG00621.hp2 HG01243.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.-100-1524_-100-150 others(26): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
CATATATA others(17): Show |
C | 7 | a0001c0001t0003g0255a0001c0002t0035g0084a0001c0002t0088g0079others(4): Show | 7 | HG01884.hp1 HG01981.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-100-1526_-100-150 others(28): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
CATATATA others(23): Show |
C | 1 | a0001c0002t0061g0033 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-100-1532_-100-150 others(34): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344916
|
CATATATA others(25): Show |
C | 1 | a0001c0005t0058g0053 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-100-1534_-100-150 others(36): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344916 | ||||||
| chr12:12344938
|
T | TATATATA others(3): Show |
2 | a0001c0002t0037g0072a0001c0002t0037g0133 | 2 | HG01081.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-100-1525_-100-152 others(14): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12344938 | ||||||
| chr12:12345023
|
A | G | 1 | a0001c0005t0084g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-100-1609T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345023 | ||||||
| chr12:12345044
|
G | A | 1 | a0001c0005t0058g0053 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-100-1630C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345044 | ||||||
| chr12:12345117
|
C | G | 81 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(78): Show | 86 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-100-1703G>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345117 | ||||||
| chr12:12345117
|
C | T | 1 | a0001c0001t0111g0036 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-100-1703G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345117 | ||||||
| chr12:12345215
|
G | A | 48 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(45): Show | 50 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-100-1801C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345215 | ||||||
| chr12:12345291
|
G | A | 4 | a0001c0001t0018g0196a0001c0001t0018g0197a0001c0001t0018g0198others(1): Show | 4 | HG00280.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-100-1877C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345291 | ||||||
| chr12:12345320
|
C | CA | 145 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(142): Show | 156 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.-100-1907dupT | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345320 | ||||||
| chr12:12345320
|
C | CAA | 6 | a0001c0001t0015g0249a0001c0001t0018g0198a0001c0001t0107g0027others(3): Show | 6 | HG01168.hp2 HG01981.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-100-1908_-100-190 others(6): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345320 | ||||||
| chr12:12345462
|
A | T | 6 | a0001c0002t0023g0056a0001c0002t0023g0140a0001c0002t0085g0058others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-100-2048T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345462 | ||||||
| chr12:12345470
|
G | A | 1 | a0001c0001t0016g0293 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-100-2056C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345470 | ||||||
| chr12:12345760
|
T | C | 1 | a0001c0001t0101g0250 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-100-2346A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345760 | ||||||
| chr12:12345820
|
T | C | 1 | a0001c0001t0114g0073 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-100-2406A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345820 | ||||||
| chr12:12345949
|
A | C | 4 | a0001c0001t0024g0205a0001c0001t0024g0206a0001c0001t0038g0203others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-100-2535T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12345949 | ||||||
| chr12:12346062
|
A | G | 1 | a0001c0005t0058g0053 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-100-2648T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346062 | ||||||
| chr12:12346089
|
C | T | 18 | a0002c0003t0006g0001a0002c0003t0006g0037a0002c0003t0006g0039others(15): Show | 22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-100-2675G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346089 | ||||||
| chr12:12346100
|
C | T | 1 | a0001c0001t0030g0253 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-100-2686G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346100 | ||||||
| chr12:12346146
|
G | A | 48 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(45): Show | 50 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-100-2732C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346146 | ||||||
| chr12:12346160
|
C | A | 2 | a0001c0001t0002g0251a0001c0001t0002g0252 | 2 | HG00558.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.-100-2746G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346160 | ||||||
| chr12:12346183
|
GAATGGCA others(12): Show |
G | 48 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(45): Show | 50 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-100-2788_-100-277 others(23): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346183 | ||||||
| chr12:12346197
|
C | CTG | 144 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(141): Show | 154 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.-100-2784_-100-278 others(6): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346197 | ||||||
| chr12:12346245
|
T | C | 4 | a0001c0001t0018g0196a0001c0001t0018g0197a0001c0001t0018g0198others(1): Show | 4 | HG00280.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-100-2831A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346245 | ||||||
| chr12:12346258
|
G | A | 1 | a0001c0002t0045g0014 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-100-2844C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346258 | ||||||
| chr12:12346265
|
C | T | 3 | a0001c0001t0119g0202a0001c0002t0011g0150a0001c0002t0011g0151 | 3 | NA18945.hp1 NA18947.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.-100-2851G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346265 | ||||||
| chr12:12346266
|
G | A | 52 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(49): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.-100-2852C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346266 | ||||||
| chr12:12346270
|
C | CA | 34 | a0001c0001t0025g0022a0001c0002t0001g0143a0001c0002t0001g0144others(31): Show | 38 | HG00140.hp1 HG00597.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-100-2857dupT | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346270 | ||||||
| chr12:12346298
|
A | G | 2 | a0001c0001t0109g0167a0001c0001t0124g0141 | 2 | HG03927.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-100-2884T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346298 | ||||||
| chr12:12346490
|
A | T | 48 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(45): Show | 50 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-100-3076T>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346490 | ||||||
| chr12:12346538
|
A | G | 18 | a0002c0003t0006g0001a0002c0003t0006g0037a0002c0003t0006g0039others(15): Show | 22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-100-3124T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346538 | ||||||
| chr12:12346650
|
T | G | 1 | a0001c0002t0023g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-100-3236A>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346650 | ||||||
| chr12:12346659
|
AT | A | 3 | a0002c0003t0042g0051a0002c0003t0043g0050a0004c0010t0042g0052 | 3 | NA18947.hp1 NA18998.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-100-3246delA | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346659 | ||||||
| chr12:12346914
|
G | A | 2 | a0001c0002t0094g0082a0001c0009t0049g0201 | 2 | HG01109.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-101+3164C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346914 | ||||||
| chr12:12346966
|
G | GT | 8 | a0001c0001t0003g0255a0001c0001t0030g0253a0001c0001t0062g0254others(5): Show | 8 | HG01517.hp1 HG01981.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.-101+3111dupA | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346966 | ||||||
| chr12:12346975
|
T | A | 18 | a0002c0003t0006g0001a0002c0003t0006g0037a0002c0003t0006g0039others(15): Show | 22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-101+3103A>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346975 | ||||||
| chr12:12346999
|
C | T | 1 | a0001c0001t0121g0300 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-101+3079G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12346999 | ||||||
| chr12:12347066
|
T | C | 35 | a0001c0001t0109g0167a0001c0001t0121g0300a0001c0002t0001g0177others(32): Show | 36 | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-101+3012A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347066 | ||||||
| chr12:12347080
|
C | T | 48 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0255others(45): Show | 50 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-101+2998G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347080 | ||||||
| chr12:12347177
|
C | A | 1 | a0001c0002t0004g0195 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-101+2901G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347177 | ||||||
| chr12:12347266
|
C | T | 1 | a0001c0001t0121g0300 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-101+2812G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347266 | ||||||
| chr12:12347290
|
A | C | 1 | a0001c0001t0016g0163 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-101+2788T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347290 | ||||||
| chr12:12347323
|
G | A | 18 | a0002c0003t0006g0001a0002c0003t0006g0037a0002c0003t0006g0039others(15): Show | 22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-101+2755C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347323 | ||||||
| chr12:12347348
|
C | T | 13 | a0001c0001t0002g0034a0001c0002t0001g0085a0001c0002t0001g0086others(10): Show | 14 | HG00741.hp2 HG01346.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-101+2730G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347348 | ||||||
| chr12:12347422
|
G | T | 191 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(188): Show | 203 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.-101+2656C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347422 | ||||||
| chr12:12347663
|
T | C | 81 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(78): Show | 86 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-101+2415A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347663 | ||||||
| chr12:12347896
|
T | TA | 35 | a0001c0001t0109g0167a0001c0001t0121g0300a0001c0002t0001g0177others(32): Show | 36 | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-101+2181dupT | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347896 | ||||||
| chr12:12347950
|
C | T | 86 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(83): Show | 91 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.-101+2128G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347950 | ||||||
| chr12:12347978
|
G | A | 2 | a0001c0002t0035g0084a0001c0002t0096g0083 | 2 | HG02451.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-101+2100C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12347978 | ||||||
| chr12:12348185
|
A | G | 4 | a0001c0001t0018g0196a0001c0001t0018g0197a0001c0001t0018g0198others(1): Show | 4 | HG00280.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-101+1893T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12348185 | ||||||
| chr12:12348265
|
G | A | 174 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(171): Show | 182 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.-101+1813C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12348265 | ||||||
| chr12:12348267
|
A | G | 1 | a0001c0001t0111g0036 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-101+1811T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12348267 | ||||||
| chr12:12348370
|
T | C | 2 | a0001c0002t0011g0150a0001c0002t0011g0151 | 2 | NA18947.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.-101+1708A>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12348370 | ||||||
| chr12:12348477
|
G | A | 1 | a0001c0002t0053g0155 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-101+1601C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12348477 | ||||||
| chr12:12348717
|
C | CA | 111 | a0001c0001t0002g0034a0001c0001t0002g0156a0001c0001t0002g0159others(108): Show | 118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.-101+1360dupT | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12348717 | ||||||
| chr12:12348717
|
C | CAA | 131 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(128): Show | 138 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.-101+1359_-101+136 others(6): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12348717 | ||||||
| chr12:12348717
|
C | CAAA | 7 | a0001c0001t0002g0296a0001c0001t0003g0298a0001c0001t0003g0299others(4): Show | 7 | HG02132.hp2 HG02818.hp2 HG04204.hp1 others(4): Show |
intron_variant | MODIFIER | c.-101+1358_-101+136 others(7): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12348717 | ||||||
| chr12:12348736
|
A | G | 6 | a0001c0001t0002g0018a0001c0001t0025g0019a0001c0001t0025g0022others(3): Show | 6 | HG00438.hp2 NA18960.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.-101+1342T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12348736 | ||||||
| chr12:12348957
|
C | T | 1 | a0001c0002t0012g0035 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-101+1121G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12348957 | ||||||
| chr12:12349067
|
G | A | 174 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(171): Show | 182 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.-101+1011C>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12349067 | ||||||
| chr12:12349083
|
A | C | 1 | a0001c0001t0002g0034 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-101+995T>G | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12349083 | ||||||
| chr12:12349216
|
C | T | 5 | a0001c0002t0027g0030a0001c0002t0027g0031a0001c0002t0059g0029others(2): Show | 5 | HG00280.hp2 HG00639.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.-101+862G>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12349216 | ||||||
| chr12:12349220
|
G | T | 12 | a0001c0001t0002g0018a0001c0001t0002g0024a0001c0001t0002g0026others(9): Show | 12 | HG00438.hp2 HG00621.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.-101+858C>A | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12349220 | ||||||
| chr12:12349566
|
A | G | 2 | a0001c0001t0003g0016a0001c0001t0066g0015 | 2 | HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.-101+512T>C | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12349566 | ||||||
| chr12:12349984
|
C | A | 3 | a0001c0001t0002g0303a0001c0001t0021g0302a0001c0001t0044g0301 | 3 | HG03654.hp2 HG03669.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-101+94G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12349984 | ||||||
| chr12:12350070
|
C | A | 1 | a0001c0002t0078g0304 | 1 | HG03540.hp2 | splice_region_variant&intron_variant | LOW | c.-101+8G>T | MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 1/3 | chr12 | 12350070 |