Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23112 |
| ensemblid | ENSG00000100354.21 |
| hgncid | 29190 |
| symbol | TNRC6B |
| name | trinucleotide repeat containing adaptor 6B |
| refseq_nuc | NM_001162501.2 |
| refseq_prot | NP_001155973.1 |
| ensembl_nuc | ENST00000454349.7 |
| ensembl_prot | ENSP00000401946.2 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 40177925 |
| end | 40335808 |
| strand | + |
| ver | v1.2 |
| region | chr22:40177925-40335808 |
| region5000 | chr22:40172925-40340808 |
| regionname0 | TNRC6B_chr22_40177925_40335808 |
| regionname5000 | TNRC6B_chr22_40172925_40340808 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1833 | 246 | 37 | 38 | 130 | 11 | 28 | 98 | TNRC6B_chr22_40172925_40340808 | TNRC6B | MREKE others(1828): Show |
chr22 | 40172925 | 40340808 |
| a0002 | 0/0 | 1832 | 45 | 22 | 13 | 2 | 1 | 7 | 2 | TNRC6B_chr22_40172925_40340808 | TNRC6B | MREKE others(1827): Show |
chr22 | 40172925 | 40340808 |
| a0003 | 0/0 | 1833 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | MREKE others(1828): Show |
chr22 | 40172925 | 40340808 |
| a0004 | 0/0 | 1833 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TNRC6B_chr22_40172925_40340808 | TNRC6B | MREKE others(1828): Show |
chr22 | 40172925 | 40340808 |
| a0005 | 0/0 | 1833 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | MREKE others(1828): Show |
chr22 | 40172925 | 40340808 |
| a0006 | 0/0 | 1833 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | MREKE others(1828): Show |
chr22 | 40172925 | 40340808 |
| a0007 | 0/0 | 1832 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | MREKE others(1827): Show |
chr22 | 40172925 | 40340808 |
| a0008 | 0/0 | 1832 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | MREKE others(1827): Show |
chr22 | 40172925 | 40340808 |
| a0009 | 0/0 | 1832 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | MREKE others(1827): Show |
chr22 | 40172925 | 40340808 |
| a0010 | 0/0 | 1833 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | MREKE others(1828): Show |
chr22 | 40172925 | 40340808 |
| a0011 | 0/0 | 1833 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | MREKE others(1828): Show |
chr22 | 40172925 | 40340808 |
| a0012 | 0/0 | 1833 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | MREKE others(1828): Show |
chr22 | 40172925 | 40340808 |
| a0013 | 0/0 | 1833 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | MREKE others(1828): Show |
chr22 | 40172925 | 40340808 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 5499 | 238 | 36 | 37 | 126 | 9 | 28 | TNRC6B_chr22_40172925_40340808 | TNRC6B | ATGAG others(5494): Show |
chr22 | 40172925 | 40340808 | ||
| a0001c0005 | 0/0 | 5499 | 2 | 0 | 0 | 0 | 2 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | ATGAG others(5494): Show |
chr22 | 40172925 | 40340808 | ||
| a0001c0008 | 0/0 | 5499 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | ATGAG others(5494): Show |
chr22 | 40172925 | 40340808 | ||
| a0001c0013 | 0/0 | 5499 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | ATGAG others(5494): Show |
chr22 | 40172925 | 40340808 | ||
| a0001c0015 | 0/0 | 5499 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | ATGAG others(5494): Show |
chr22 | 40172925 | 40340808 | ||
| a0001c0017 | 0/0 | 5499 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | ATGAG others(5494): Show |
chr22 | 40172925 | 40340808 | ||
| a0001c0020 | 0/0 | 5499 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | ATGAG others(5494): Show |
chr22 | 40172925 | 40340808 | ||
| a0002c0002 | 0/0 | 5496 | 44 | 21 | 13 | 2 | 1 | 7 | TNRC6B_chr22_40172925_40340808 | TNRC6B | ATGAG others(5491): Show |
chr22 | 40172925 | 40340808 | ||
| a0002c0012 | 0/0 | 5496 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | ATGAG others(5491): Show |
chr22 | 40172925 | 40340808 | ||
| a0003c0004 | 0/0 | 5499 | 3 | 2 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | ATGAG others(5494): Show |
chr22 | 40172925 | 40340808 | ||
| a0004c0003 | 0/0 | 5499 | 3 | 0 | 0 | 3 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | ATGAG others(5494): Show |
chr22 | 40172925 | 40340808 | ||
| a0005c0007 | 0/0 | 5499 | 2 | 0 | 2 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | ATGAG others(5494): Show |
chr22 | 40172925 | 40340808 | ||
| a0006c0006 | 0/0 | 5499 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | ATGAG others(5494): Show |
chr22 | 40172925 | 40340808 | ||
| a0007c0019 | 0/0 | 5496 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | ATGAG others(5491): Show |
chr22 | 40172925 | 40340808 | ||
| a0008c0011 | 0/0 | 5496 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | ATGAG others(5491): Show |
chr22 | 40172925 | 40340808 | ||
| a0009c0010 | 0/0 | 5496 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | ATGAG others(5491): Show |
chr22 | 40172925 | 40340808 | ||
| a0010c0014 | 0/0 | 5499 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | ATGAG others(5494): Show |
chr22 | 40172925 | 40340808 | ||
| a0011c0009 | 0/0 | 5499 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | ATGAG others(5494): Show |
chr22 | 40172925 | 40340808 | ||
| a0012c0018 | 0/0 | 5499 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | ATGAG others(5494): Show |
chr22 | 40172925 | 40340808 | ||
| a0013c0016 | 0/0 | 5499 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | ATGAG others(5494): Show |
chr22 | 40172925 | 40340808 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 18285 | 29 | 0 | 4 | 24 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0002 | 0/0 | 18286 | 24 | 0 | 4 | 14 | 2 | 4 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0003 | 0/0 | 18286 | 9 | 0 | 2 | 5 | 1 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0004 | 0/0 | 18286 | 7 | 0 | 1 | 5 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0005 | 0/0 | 18287 | 6 | 0 | 0 | 6 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0006 | 0/0 | 18285 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0007 | 0/0 | 18285 | 6 | 0 | 3 | 3 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0008 | 0/0 | 18287 | 6 | 0 | 3 | 2 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0010 | 0/0 | 18286 | 5 | 0 | 1 | 4 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0011 | 0/0 | 18286 | 5 | 0 | 0 | 5 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0012 | 0/0 | 18287 | 5 | 2 | 0 | 1 | 0 | 2 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0013 | 0/0 | 18287 | 4 | 0 | 1 | 2 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0014 | 0/0 | 18284 | 3 | 0 | 3 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18279): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0015 | 0/0 | 18284 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18279): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0016 | 0/0 | 18287 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0017 | 0/0 | 18286 | 3 | 0 | 1 | 2 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0018 | 0/0 | 18287 | 3 | 0 | 0 | 3 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0019 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0020 | 0/0 | 18286 | 3 | 0 | 0 | 2 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0021 | 0/0 | 18285 | 3 | 1 | 0 | 2 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0022 | 0/0 | 18286 | 3 | 0 | 0 | 0 | 0 | 3 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0023 | 0/1 | 18285 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0024 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0025 | 0/0 | 18286 | 2 | 0 | 2 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0026 | 1/0 | 18280 | 2 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18275): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0027 | 0/0 | 18287 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0028 | 0/0 | 18285 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0029 | 0/0 | 18286 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0030 | 0/0 | 18286 | 2 | 0 | 1 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0031 | 0/0 | 18286 | 2 | 0 | 1 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0033 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0034 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0035 | 0/0 | 18283 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18278): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0037 | 0/0 | 18284 | 2 | 0 | 0 | 0 | 0 | 2 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18279): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0038 | 0/0 | 18287 | 2 | 0 | 1 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0039 | 0/0 | 18283 | 2 | 0 | 1 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18278): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0040 | 0/0 | 18286 | 2 | 0 | 2 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0042 | 0/0 | 18283 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18278): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0043 | 0/0 | 18284 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18279): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0044 | 0/0 | 18284 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18279): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0045 | 0/0 | 18286 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0046 | 0/0 | 18282 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18277): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0047 | 0/0 | 18282 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18277): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0048 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0049 | 0/0 | 18282 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18277): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0050 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0051 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0052 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0053 | 0/0 | 18283 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18278): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0054 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0055 | 0/0 | 18286 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0056 | 0/0 | 18286 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0057 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0058 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0061 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0062 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0063 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0064 | 0/0 | 18284 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18279): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0065 | 0/0 | 18284 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18279): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0066 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0067 | 0/0 | 18284 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18279): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0068 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0069 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0071 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0072 | 0/0 | 18287 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0073 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0074 | 0/0 | 18286 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0075 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0076 | 0/0 | 18282 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18277): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0077 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0078 | 0/0 | 18287 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0080 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0081 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0082 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0086 | 0/0 | 18287 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0088 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0089 | 0/0 | 18286 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0093 | 0/0 | 18286 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0108 | 0/0 | 18286 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0109 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0113 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0114 | 0/0 | 18286 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0115 | 0/0 | 18287 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0116 | 0/0 | 18283 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18278): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0117 | 0/0 | 18285 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0118 | 0/0 | 18284 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18279): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0119 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0120 | 0/0 | 18288 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18283): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0121 | 0/0 | 18287 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0122 | 0/0 | 18286 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0123 | 0/0 | 18287 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0124 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0125 | 0/0 | 18288 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18283): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0126 | 0/0 | 18281 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18276): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0127 | 0/0 | 18287 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0128 | 0/0 | 18285 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0129 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0130 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0131 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0132 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0133 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0134 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0135 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0137 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0138 | 0/0 | 18284 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18279): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0139 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0140 | 0/0 | 18288 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18283): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0142 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0143 | 0/0 | 18288 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18283): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0144 | 0/0 | 18284 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18279): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0145 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0146 | 0/0 | 18283 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18278): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0148 | 0/0 | 18285 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0001t0149 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0005t0004 | 0/0 | 18286 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0005t0141 | 0/0 | 18287 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0008t0002 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0008t0070 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0013t0005 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0001c0015t0024 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0001c0017t0079 | 0/0 | 18286 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0001c0020t0023 | 0/0 | 18285 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0006 | 0/0 | 18282 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18277): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0009 | 0/0 | 18279 | 6 | 1 | 3 | 0 | 1 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18274): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0032 | 0/0 | 18279 | 2 | 0 | 0 | 0 | 0 | 2 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18274): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0033 | 0/0 | 18282 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18277): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0034 | 0/0 | 18282 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18277): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0036 | 0/0 | 18283 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18278): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0041 | 0/0 | 18280 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18275): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0083 | 0/0 | 18279 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18274): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0084 | 0/0 | 18282 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18277): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0085 | 0/0 | 18285 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0087 | 0/0 | 18273 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18268): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0090 | 0/0 | 18282 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18277): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0091 | 0/0 | 18283 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18278): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0092 | 0/0 | 18283 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18278): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0094 | 0/0 | 18284 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18279): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0096 | 0/0 | 18281 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18276): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0097 | 0/0 | 18282 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18277): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0098 | 0/0 | 18278 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18273): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0099 | 0/0 | 18279 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18274): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0100 | 0/0 | 18278 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18273): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0101 | 0/0 | 18280 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18275): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0102 | 0/0 | 18284 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18279): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0103 | 0/0 | 18284 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18279): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0104 | 0/0 | 18279 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18274): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0105 | 0/0 | 18280 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18275): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0106 | 0/0 | 18279 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18274): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0107 | 0/0 | 18281 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18276): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0110 | 0/0 | 18279 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18274): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0151 | 0/0 | 18280 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18275): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0152 | 0/0 | 18283 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18278): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0153 | 0/0 | 18282 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18277): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0154 | 0/0 | 18280 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18275): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0155 | 0/0 | 18284 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18279): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0156 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0002c0002t0157 | 0/0 | 18281 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18276): Show |
chr22 | 40172925 | 40340808 |
| a0002c0012t0006 | 0/0 | 18282 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18277): Show |
chr22 | 40172925 | 40340808 |
| a0003c0004t0019 | 0/0 | 18287 | 2 | 1 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0003c0004t0136 | 0/0 | 18284 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18279): Show |
chr22 | 40172925 | 40340808 |
| a0004c0003t0001 | 0/0 | 18285 | 3 | 0 | 0 | 3 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0005c0007t0059 | 0/0 | 18278 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18273): Show |
chr22 | 40172925 | 40340808 |
| a0005c0007t0060 | 0/0 | 18279 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18274): Show |
chr22 | 40172925 | 40340808 |
| a0006c0006t0111 | 0/0 | 18285 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18280): Show |
chr22 | 40172925 | 40340808 |
| a0006c0006t0112 | 0/0 | 18286 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0007c0019t0095 | 0/0 | 18279 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18274): Show |
chr22 | 40172925 | 40340808 |
| a0008c0011t0006 | 0/0 | 18282 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18277): Show |
chr22 | 40172925 | 40340808 |
| a0009c0010t0150 | 0/0 | 18284 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18279): Show |
chr22 | 40172925 | 40340808 |
| a0010c0014t0004 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0011c0009t0002 | 0/0 | 18286 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18281): Show |
chr22 | 40172925 | 40340808 |
| a0012c0018t0005 | 0/0 | 18287 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18282): Show |
chr22 | 40172925 | 40340808 |
| a0013c0016t0147 | 0/0 | 18283 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | AGAGA others(18278): Show |
chr22 | 40172925 | 40340808 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0007g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0007g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0007g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0007g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0007g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0007g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0008g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0008g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0008g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0008g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0008g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0008g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0010g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0010g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0010g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0010g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0010g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0011g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0011g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0011g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0011g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0011g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0012g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0012g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0012g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0012g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0012g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0013g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0013g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0013g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0013g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0014g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0014g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0014g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0015g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0015g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0015g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0016g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0016g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0016g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0017g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0017g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0017g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0018g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0018g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0018g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0019g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0020g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0020g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0020g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0021g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0021g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0021g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0022g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0022g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0022g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0023g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0024g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0025g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0025g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0026g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0026g0303 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0027g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0027g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0028g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0028g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0029g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0029g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0030g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0030g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0031g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0031g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0033g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0034g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0035g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0035g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0037g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0037g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0038g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0038g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0039g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0039g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0040g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0040g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0042g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0043g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0044g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0045g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0046g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0047g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0048g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0049g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0050g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0051g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0052g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0053g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0054g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0055g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0056g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0057g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0058g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0061g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0062g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0063g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0064g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0065g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0066g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0067g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0068g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0069g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0071g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0072g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0073g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0074g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0075g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0076g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0077g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0078g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0080g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0081g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0082g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0086g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0088g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0089g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0093g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0108g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0109g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0113g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0114g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0115g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0116g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0117g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0118g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0119g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0120g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0121g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0122g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0123g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0124g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0125g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0126g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0127g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0128g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0129g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0130g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0131g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0132g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0133g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0134g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0135g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0137g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0138g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0139g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0140g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0142g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0143g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0144g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0145g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0146g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0148g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0001t0149g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0005t0004g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0005t0141g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0008t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0008t0070g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0013t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0015t0024g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0017t0079g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0001c0020t0023g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0009g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0009g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0009g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0009g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0009g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0009g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0032g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0032g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0033g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0034g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0036g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0036g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0041g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0083g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0084g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0085g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0087g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0090g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0091g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0092g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0094g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0096g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0097g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0098g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0099g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0100g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0101g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0102g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0103g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0104g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0105g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0106g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0107g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0110g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0151g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0152g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0153g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0154g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0155g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0156g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0002t0157g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0002c0012t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0003c0004t0019g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0003c0004t0019g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0003c0004t0136g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0004c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0004c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0004c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0005c0007t0059g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0005c0007t0060g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0006c0006t0111g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0006c0006t0112g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0007c0019t0095g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0008c0011t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0009c0010t0150g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0010c0014t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0011c0009t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0012c0018t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| a0013c0016t0147g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0026 | g0283 | EUR | GBR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00140 | hp2 | a0002 | c0002 | t0009 | g0121 | EUR | GBR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00280 | hp1 | a0001 | c0001 | t0045 | g0062 | EUR | FIN | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00280 | hp2 | a0001 | c0001 | t0020 | g0267 | EUR | FIN | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00408 | hp1 | a0001 | c0001 | t0131 | g0027 | EAS | CHS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00408 | hp2 | a0001 | c0001 | t0013 | g0237 | EAS | CHS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00423 | hp1 | a0001 | c0001 | t0137 | g0199 | EAS | CHS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00423 | hp2 | a0001 | c0020 | t0023 | g0063 | EAS | CHS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0190 | EAS | CHS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00438 | hp2 | a0001 | c0001 | t0068 | g0285 | EAS | CHS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00544 | hp1 | a0001 | c0001 | t0029 | g0238 | EAS | CHS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0179 | EAS | CHS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00639 | hp2 | a0002 | c0002 | t0083 | g0093 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00642 | hp1 | a0002 | c0002 | t0009 | g0117 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00733 | hp1 | a0001 | c0001 | t0040 | g0048 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00733 | hp2 | a0001 | c0001 | t0031 | g0299 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00735 | hp1 | a0001 | c0001 | t0008 | g0223 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00741 | hp1 | a0001 | c0001 | t0008 | g0289 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG00741 | hp2 | a0001 | c0001 | t0014 | g0059 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01069 | hp1 | a0001 | c0001 | t0030 | g0220 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01069 | hp2 | a0001 | c0001 | t0038 | g0073 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01070 | hp1 | a0002 | c0002 | t0009 | g0120 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01070 | hp2 | a0001 | c0001 | t0008 | g0250 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01071 | hp1 | a0002 | c0002 | t0009 | g0123 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0072 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01106 | hp2 | a0001 | c0001 | t0143 | g0180 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01109 | hp1 | a0001 | c0001 | t0093 | g0147 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01109 | hp2 | a0002 | c0002 | t0099 | g0125 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01167 | hp1 | a0005 | c0007 | t0060 | g0255 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01167 | hp2 | a0002 | c0002 | t0085 | g0116 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01169 | hp1 | a0005 | c0007 | t0059 | g0231 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01175 | hp1 | a0003 | c0004 | t0019 | g0208 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01175 | hp2 | a0001 | c0017 | t0079 | g0252 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01243 | hp1 | a0002 | c0002 | t0090 | g0092 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01243 | hp2 | a0002 | c0002 | t0152 | g0096 | AMR | PUR | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01255 | hp2 | a0001 | c0001 | t0007 | g0280 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01257 | hp1 | a0001 | c0001 | t0025 | g0259 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01257 | hp2 | a0002 | c0002 | t0104 | g0118 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01258 | hp1 | a0001 | c0001 | t0025 | g0258 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01258 | hp2 | a0001 | c0001 | t0121 | g0306 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01261 | hp1 | a0001 | c0001 | t0040 | g0040 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01261 | hp2 | a0002 | c0002 | t0087 | g0100 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0181 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01346 | hp2 | a0001 | c0001 | t0114 | g0081 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01361 | hp1 | a0001 | c0001 | t0010 | g0295 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01361 | hp2 | a0002 | c0002 | t0098 | g0122 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01496 | hp1 | a0001 | c0001 | t0039 | g0078 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01496 | hp2 | a0002 | c0002 | t0153 | g0109 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0215 | EUR | IBS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0282 | EUR | IBS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01516 | hp1 | a0001 | c0001 | t0013 | g0247 | EUR | IBS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01516 | hp2 | a0001 | c0005 | t0004 | g0171 | EUR | IBS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01517 | hp1 | a0001 | c0001 | t0072 | g0277 | EUR | IBS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01517 | hp2 | a0001 | c0005 | t0141 | g0172 | EUR | IBS | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01884 | hp1 | a0006 | c0006 | t0112 | g0001 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01884 | hp2 | a0007 | c0019 | t0095 | g0166 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01891 | hp1 | a0001 | c0001 | t0065 | g0224 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01891 | hp2 | a0001 | c0001 | t0035 | g0143 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01928 | hp1 | a0001 | c0001 | t0014 | g0058 | AMR | PEL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01928 | hp2 | a0001 | c0001 | t0007 | g0300 | AMR | PEL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01934 | hp1 | a0002 | c0002 | t0107 | g0099 | AMR | PEL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01934 | hp2 | a0001 | c0001 | t0017 | g0034 | AMR | PEL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01943 | hp1 | a0001 | c0001 | t0013 | g0287 | AMR | PEL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02015 | hp1 | a0001 | c0001 | t0005 | g0189 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02015 | hp2 | a0001 | c0001 | t0028 | g0266 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02027 | hp1 | a0001 | c0001 | t0140 | g0196 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02027 | hp2 | a0001 | c0001 | t0125 | g0025 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02040 | hp1 | a0001 | c0001 | t0021 | g0183 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02040 | hp2 | a0001 | c0001 | t0029 | g0275 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02055 | hp1 | a0001 | c0001 | t0120 | g0089 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02055 | hp2 | a0002 | c0002 | t0100 | g0098 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02071 | hp2 | a0001 | c0001 | t0144 | g0066 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0192 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02074 | hp2 | a0001 | c0001 | t0010 | g0308 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02129 | hp1 | a0001 | c0001 | t0130 | g0162 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0195 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0197 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02135 | hp2 | a0001 | c0001 | t0073 | g0225 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02145 | hp1 | a0002 | c0002 | t0094 | g0009 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02145 | hp2 | a0001 | c0001 | t0115 | g0090 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02165 | hp1 | a0001 | c0001 | t0017 | g0006 | EAS | CDX | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | CDX | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02257 | hp1 | a0001 | c0001 | t0012 | g0206 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02257 | hp2 | a0006 | c0006 | t0111 | g0214 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02258 | hp1 | a0002 | c0002 | t0110 | g0112 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02258 | hp2 | a0001 | c0001 | t0035 | g0148 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02280 | hp1 | a0003 | c0004 | t0019 | g0207 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02280 | hp2 | a0002 | c0002 | t0102 | g0105 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02293 | hp1 | a0001 | c0001 | t0014 | g0057 | AMR | PEL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02293 | hp2 | a0001 | c0001 | t0126 | g0305 | AMR | PEL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02523 | hp1 | a0001 | c0001 | t0008 | g0269 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02523 | hp2 | a0001 | c0001 | t0020 | g0211 | EAS | KHV | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02602 | hp1 | a0001 | c0001 | t0022 | g0201 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0281 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02615 | hp1 | a0002 | c0002 | t0034 | g0010 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02615 | hp2 | a0008 | c0011 | t0006 | g0094 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02622 | hp1 | a0002 | c0002 | t0154 | g0155 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02622 | hp2 | a0001 | c0001 | t0049 | g0142 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02630 | hp1 | a0001 | c0001 | t0042 | g0003 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02630 | hp2 | a0001 | c0001 | t0012 | g0169 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02647 | hp1 | a0001 | c0001 | t0078 | g0278 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02647 | hp2 | a0001 | c0001 | t0034 | g0091 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02698 | hp1 | a0001 | c0001 | t0146 | g0173 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02698 | hp2 | a0001 | c0001 | t0043 | g0157 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02717 | hp1 | a0002 | c0002 | t0009 | g0104 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02717 | hp2 | a0001 | c0001 | t0052 | g0002 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02723 | hp1 | a0001 | c0001 | t0054 | g0132 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0151 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02809 | hp1 | a0002 | c0002 | t0084 | g0008 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02809 | hp2 | a0001 | c0001 | t0015 | g0174 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02818 | hp1 | a0001 | c0001 | t0089 | g0150 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02818 | hp2 | a0001 | c0001 | t0015 | g0141 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02895 | hp1 | a0002 | c0002 | t0006 | g0097 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02895 | hp2 | a0001 | c0015 | t0024 | g0131 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02896 | hp1 | a0002 | c0002 | t0006 | g0095 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02896 | hp2 | a0001 | c0001 | t0127 | g0084 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0135 | AFR | ESN | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02976 | hp2 | a0001 | c0001 | t0108 | g0145 | AFR | ESN | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03017 | hp1 | a0001 | c0001 | t0122 | g0067 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03017 | hp2 | a0002 | c0002 | t0009 | g0115 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03041 | hp1 | a0001 | c0001 | t0024 | g0137 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03041 | hp2 | a0002 | c0002 | t0006 | g0144 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03139 | hp1 | a0001 | c0001 | t0016 | g0087 | AFR | ESN | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03139 | hp2 | a0002 | c0002 | t0156 | g0110 | AFR | ESN | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03195 | hp1 | a0002 | c0002 | t0155 | g0156 | AFR | ESN | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03195 | hp2 | a0001 | c0001 | t0086 | g0213 | AFR | ESN | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03225 | hp1 | a0001 | c0001 | t0015 | g0140 | AFR | MSL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03225 | hp2 | a0002 | c0002 | t0096 | g0005 | AFR | MSL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03239 | hp2 | a0002 | c0002 | t0032 | g0128 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03491 | hp1 | a0001 | c0001 | t0128 | g0085 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03491 | hp2 | a0001 | c0001 | t0037 | g0076 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03492 | hp1 | a0001 | c0001 | t0037 | g0077 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03492 | hp2 | a0001 | c0001 | t0039 | g0165 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03516 | hp1 | a0001 | c0001 | t0016 | g0086 | AFR | ESN | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03516 | hp2 | a0002 | c0002 | t0103 | g0108 | AFR | ESN | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03540 | hp1 | a0002 | c0002 | t0097 | g0113 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03540 | hp2 | a0001 | c0001 | t0033 | g0146 | AFR | GWD | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03579 | hp1 | a0009 | c0010 | t0150 | g0101 | AFR | MSL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03579 | hp2 | a0001 | c0001 | t0046 | g0153 | AFR | MSL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03669 | hp1 | a0002 | c0002 | t0105 | g0119 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03669 | hp2 | a0001 | c0001 | t0030 | g0221 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03704 | hp1 | a0001 | c0001 | t0117 | g0055 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03704 | hp2 | a0001 | c0001 | t0008 | g0244 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03710 | hp1 | a0001 | c0001 | t0148 | g0068 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03710 | hp2 | a0001 | c0001 | t0074 | g0222 | SAS | PJL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0185 | SAS | BEB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03831 | hp2 | a0002 | c0002 | t0041 | g0127 | SAS | BEB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03834 | hp1 | a0001 | c0001 | t0031 | g0216 | SAS | BEB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03834 | hp2 | a0001 | c0001 | t0022 | g0126 | SAS | BEB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03927 | hp1 | a0001 | c0001 | t0123 | g0070 | SAS | BEB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | BEB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03942 | hp1 | a0001 | c0001 | t0012 | g0178 | SAS | BEB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03942 | hp2 | a0001 | c0001 | t0038 | g0075 | SAS | BEB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG04115 | hp1 | a0002 | c0002 | t0032 | g0129 | SAS | STU | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG04115 | hp2 | a0001 | c0001 | t0022 | g0202 | SAS | STU | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | BEB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG04184 | hp2 | a0001 | c0001 | t0012 | g0188 | SAS | BEB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG04199 | hp1 | a0002 | c0002 | t0106 | g0154 | SAS | STU | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0228 | SAS | STU | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG04204 | hp1 | a0001 | c0001 | t0076 | g0243 | SAS | STU | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG04204 | hp2 | a0002 | c0002 | t0033 | g0159 | SAS | STU | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18522 | hp1 | a0001 | c0001 | t0016 | g0088 | AFR | YRI | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18522 | hp2 | a0002 | c0002 | t0036 | g0012 | AFR | YRI | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0187 | EAS | CHB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18906 | hp1 | a0002 | c0002 | t0151 | g0111 | AFR | YRI | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18906 | hp2 | a0001 | c0001 | t0047 | g0152 | AFR | YRI | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18939 | hp1 | a0001 | c0001 | t0028 | g0284 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18941 | hp2 | a0010 | c0014 | t0004 | g0186 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18942 | hp2 | a0001 | c0013 | t0005 | g0194 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18943 | hp2 | a0011 | c0009 | t0002 | g0229 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18944 | hp1 | a0002 | c0002 | t0092 | g0103 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18945 | hp1 | a0001 | c0001 | t0061 | g0301 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18945 | hp2 | a0001 | c0001 | t0149 | g0022 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18946 | hp1 | a0001 | c0001 | t0124 | g0030 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18946 | hp2 | a0001 | c0001 | t0066 | g0292 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18947 | hp1 | a0001 | c0001 | t0082 | g0240 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18947 | hp2 | a0001 | c0001 | t0018 | g0050 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18949 | hp1 | a0001 | c0001 | t0057 | g0245 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18951 | hp2 | a0001 | c0001 | t0119 | g0074 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18954 | hp1 | a0001 | c0001 | t0010 | g0271 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18954 | hp2 | a0001 | c0001 | t0020 | g0193 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18959 | hp1 | a0001 | c0001 | t0062 | g0248 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18959 | hp2 | a0001 | c0001 | t0142 | g0204 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18960 | hp1 | a0001 | c0001 | t0109 | g0130 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18960 | hp2 | a0001 | c0001 | t0010 | g0253 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18961 | hp1 | a0001 | c0001 | t0064 | g0298 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18962 | hp1 | a0001 | c0001 | t0134 | g0176 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18962 | hp2 | a0004 | c0003 | t0001 | g0020 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18963 | hp1 | a0001 | c0001 | t0019 | g0210 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18963 | hp2 | a0004 | c0003 | t0001 | g0021 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18973 | hp1 | a0001 | c0001 | t0011 | g0011 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18973 | hp2 | a0001 | c0001 | t0063 | g0276 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18974 | hp2 | a0002 | c0002 | t0091 | g0102 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18975 | hp1 | a0001 | c0001 | t0011 | g0042 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18979 | hp2 | a0001 | c0001 | t0077 | g0254 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18981 | hp1 | a0001 | c0001 | t0129 | g0045 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18981 | hp2 | a0001 | c0001 | t0071 | g0241 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18984 | hp1 | a0001 | c0001 | t0011 | g0065 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18984 | hp2 | a0001 | c0001 | t0069 | g0297 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18986 | hp1 | a0001 | c0001 | t0058 | g0264 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18991 | hp2 | a0001 | c0001 | t0007 | g0293 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18993 | hp1 | a0001 | c0001 | t0138 | g0167 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18994 | hp1 | a0001 | c0001 | t0013 | g0290 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18994 | hp2 | a0001 | c0001 | t0011 | g0047 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18995 | hp1 | a0012 | c0018 | t0005 | g0198 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18995 | hp2 | a0001 | c0001 | t0027 | g0232 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19004 | hp2 | a0001 | c0001 | t0012 | g0182 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19005 | hp1 | a0001 | c0001 | t0132 | g0004 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19005 | hp2 | a0001 | c0001 | t0113 | g0268 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19007 | hp1 | a0001 | c0001 | t0145 | g0168 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19007 | hp2 | a0001 | c0001 | t0081 | g0260 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19010 | hp2 | a0001 | c0001 | t0027 | g0256 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19012 | hp1 | a0001 | c0001 | t0080 | g0261 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19043 | hp1 | a0001 | c0001 | t0088 | g0138 | AFR | LWK | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19043 | hp2 | a0001 | c0001 | t0055 | g0134 | AFR | LWK | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19058 | hp2 | a0001 | c0001 | t0135 | g0177 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19062 | hp1 | a0001 | c0001 | t0018 | g0044 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19062 | hp2 | a0001 | c0001 | t0139 | g0175 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19064 | hp1 | a0001 | c0001 | t0005 | g0191 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19065 | hp1 | a0001 | c0001 | t0007 | g0273 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19068 | hp2 | a0001 | c0001 | t0067 | g0236 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19070 | hp1 | a0001 | c0001 | t0118 | g0083 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19077 | hp1 | a0001 | c0001 | t0011 | g0052 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19077 | hp2 | a0001 | c0001 | t0050 | g0233 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19080 | hp1 | a0001 | c0001 | t0021 | g0203 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19080 | hp2 | a0001 | c0001 | t0007 | g0291 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19081 | hp1 | a0001 | c0001 | t0075 | g0164 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19082 | hp1 | a0001 | c0001 | t0017 | g0016 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19082 | hp2 | a0001 | c0008 | t0002 | g0257 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19085 | hp1 | a0001 | c0001 | t0018 | g0079 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19085 | hp2 | a0001 | c0001 | t0010 | g0265 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19086 | hp2 | a0001 | c0001 | t0008 | g0288 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19088 | hp2 | a0001 | c0001 | t0133 | g0031 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19091 | hp1 | a0001 | c0008 | t0070 | g0234 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19091 | hp2 | a0004 | c0003 | t0001 | g0019 | EAS | JPT | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19240 | hp1 | a0001 | c0001 | t0056 | g0133 | AFR | YRI | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA19240 | hp2 | a0001 | c0001 | t0021 | g0170 | AFR | YRI | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA20805 | hp1 | a0001 | c0001 | t0116 | g0161 | EUR | TSI | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0251 | EUR | TSI | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA20905 | hp1 | a0013 | c0016 | t0147 | g0200 | SAS | GIH | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0160 | SAS | GIH | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01123 | hp1 | a0001 | c0001 | t0044 | g0060 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG01123 | hp2 | a0001 | c0001 | t0007 | g0279 | AMR | CLM | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02559 | hp1 | a0002 | c0012 | t0006 | g0114 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG02559 | hp2 | a0001 | c0001 | t0048 | g0139 | AFR | ACB | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03471 | hp1 | a0002 | c0002 | t0036 | g0106 | AFR | MSL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| HG03471 | hp2 | a0003 | c0004 | t0136 | g0209 | AFR | MSL | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA20300 | hp1 | a0002 | c0002 | t0157 | g0107 | AFR | USA | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA20300 | hp2 | a0002 | c0002 | t0101 | g0124 | AFR | USA | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA21309 | hp1 | a0001 | c0001 | t0051 | g0149 | AFR | LWK | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| NA21309 | hp2 | a0001 | c0001 | t0053 | g0136 | AFR | LWK | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0023 | g0158 | REF | REF | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0026 | g0303 | REF | REF | TNRC6B_chr22_40172925_40340808 | TNRC6B | chr22 | 40172925 | 40340808 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:40262125 | G | A | 1 | a0011 | 1 | NA18943.hp2 | missense_variant | MODERATE | c.409G>A | p.Ala137Thr | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/23 | 620/18280 | 409/5502 | 137/1833 | chr22 | 40262125 | |||
| chr22:40262141 | C | T | 1 | a0007 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.425C>T | p.Ala142Val | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/23 | 636/18280 | 425/5502 | 142/1833 | chr22 | 40262141 | |||
| chr22:40264769 | C | G | 1 | a0012 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.539C>G | p.Ser180Cys | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/23 | 750/18280 | 539/5502 | 180/1833 | chr22 | 40264769 | |||
| chr22:40266436 | C | T | 1 | a0013 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.2206C>T | p.Arg736Cys | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/23 | 2417/18280 | 2206/5502 | 736/1833 | chr22 | 40266436 | |||
| chr22:40266599 | G | A | 1 | a0004 | 3 | NA18962.hp2 NA18963.hp2 NA19091.hp2 |
missense_variant | MODERATE | c.2369G>A | p.Ser790Asn | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/23 | 2580/18280 | 2369/5502 | 790/1833 | chr22 | 40266599 | |||
| chr22:40266839 | A | C | 1 | a0005 | 2 | HG01167.hp1 HG01169.hp1 |
missense_variant | MODERATE | c.2609A>C | p.Glu870Ala | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/23 | 2820/18280 | 2609/5502 | 870/1833 | chr22 | 40266839 | |||
| chr22:40270226 | T | C | 1 | a0003 | 3 | HG01175.hp1 HG02280.hp1 HG03471.hp2 |
missense_variant | MODERATE | c.2911T>C | p.Ser971Pro | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/23 | 3122/18280 | 2911/5502 | 971/1833 | chr22 | 40270226 | |||
| chr22:40273478 | G | A | 2 | a0006 a0009 |
3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
missense_variant | MODERATE | c.3019G>A | p.Ala1007Thr | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/23 | 3230/18280 | 3019/5502 | 1007/1833 | chr22 | 40273478 | |||
| chr22:40281188 | T | A | 1 | a0008 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.3481T>A | p.Ser1161Thr | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/23 | 3692/18280 | 3481/5502 | 1161/1833 | chr22 | 40281188 | |||
| chr22:40301172 | TGCA | T | 4 | a0002 a0007 a0008 others(1): Show |
48 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(45): Show |
conservative_inframe_deletion | MODERATE | c.3982_3984delCAG | p.Gln1328del | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/23 | 4193/18280 | 3982/5502 | 1328/1833 | INFO_REALIGN_3_PRIME | chr22 | 40301172 | ||
| chr22:40301315 | A | G | 1 | a0010 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.4102A>G | p.Ile1368Val | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/23 | 4313/18280 | 4102/5502 | 1368/1833 | chr22 | 40301315 | |||
| chr22:40323074 | G | A | 1 | a0002 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.5335G>A | p.Ala1779Thr | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5546/18280 | 5335/5502 | 1779/1833 | chr22 | 40323074 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:40261962 | C | T | 1 | a0001c0020 | 1 | HG00423.hp2 | synonymous_variant | LOW | c.246C>T | p.Ser82Ser | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/23 | 457/18280 | 246/5502 | 82/1833 | chr22 | 40261962 | |||
| chr22:40264809 | C | T | 1 | a0001c0008 | 2 | NA19082.hp2 NA19091.hp1 |
synonymous_variant | LOW | c.579C>T | p.Asp193Asp | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/23 | 790/18280 | 579/5502 | 193/1833 | chr22 | 40264809 | |||
| chr22:40265145 | T | C | 1 | a0001c0005 | 2 | HG01516.hp2 HG01517.hp2 |
synonymous_variant | LOW | c.915T>C | p.Asn305Asn | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/23 | 1126/18280 | 915/5502 | 305/1833 | chr22 | 40265145 | |||
| chr22:40266009 | C | T | 1 | a0001c0017 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.1779C>T | p.Tyr593Tyr | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/23 | 1990/18280 | 1779/5502 | 593/1833 | chr22 | 40266009 | |||
| chr22:40266936 | T | C | 2 | a0006c0006 a0009c0010 |
3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.2706T>C | p.Tyr902Tyr | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/23 | 2917/18280 | 2706/5502 | 902/1833 | chr22 | 40266936 | |||
| chr22:40300463 | C | T | 1 | a0001c0015 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.3717C>T | p.Ala1239Ala | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 13/23 | 3928/18280 | 3717/5502 | 1239/1833 | chr22 | 40300463 | |||
| chr22:40315308 | A | G | 1 | a0001c0013 | 1 | NA18942.hp2 | synonymous_variant | LOW | c.4704A>G | p.Thr1568Thr | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 20/23 | 4915/18280 | 4704/5502 | 1568/1833 | chr22 | 40315308 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:40177976 | T | G | 1 | a0002c0002t0041 | 1 | HG03831.hp2 | 5_prime_UTR_variant | MODIFIER | c.-160T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/23 | 160 | chr22 | 40177976 | ||||||
| chr22:40178093 | C | T | 1 | a0001c0001t0040 | 2 | HG00733.hp1 HG01261.hp1 |
5_prime_UTR_variant | MODIFIER | c.-43C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/23 | 43 | chr22 | 40178093 | ||||||
| chr22:40323732 | G | C | 6 | a0001c0001t0014 a0001c0001t0042 a0001c0001t0043 others(3): Show |
8 | HG00280.hp1 HG00423.hp2 HG00741.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*491G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 491 | chr22 | 40323732 | ||||||
| chr22:40324023 | G | A | 5 | a0001c0001t0015 a0001c0001t0046 a0001c0001t0047 others(2): Show |
7 | HG02559.hp2 HG02622.hp2 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*782G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 782 | chr22 | 40324023 | ||||||
| chr22:40324290 | G | GT | 8 | a0002c0002t0151 a0002c0002t0152 a0002c0002t0153 others(5): Show |
8 | HG01243.hp2 HG01496.hp2 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1064dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 1065 | INFO_REALIGN_3_PRIME | chr22 | 40324290 | |||||
| chr22:40324598 | C | T | 1 | a0001c0001t0149 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1357C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 1357 | chr22 | 40324598 | ||||||
| chr22:40324606 | G | A | 1 | a0001c0001t0050 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1365G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 1365 | chr22 | 40324606 | ||||||
| chr22:40324630 | G | A | 1 | a0001c0001t0051 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1389G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 1389 | chr22 | 40324630 | ||||||
| chr22:40324671 | C | T | 1 | a0001c0001t0148 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1430C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 1430 | chr22 | 40324671 | ||||||
| chr22:40324700 | A | G | 65 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(62): Show |
141 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*1459A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 1459 | chr22 | 40324700 | ||||||
| chr22:40324949 | G | C | 7 | a0001c0001t0024 a0001c0001t0052 a0001c0001t0053 others(4): Show |
7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1708G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 1708 | chr22 | 40324949 | ||||||
| chr22:40324959 | C | T | 128 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(125): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*1718C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 1718 | chr22 | 40324959 | ||||||
| chr22:40325058 | G | A | 63 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0024 others(60): Show |
76 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1817G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 1817 | chr22 | 40325058 | ||||||
| chr22:40325350 | T | C | 1 | a0002c0002t0083 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2109T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 2109 | chr22 | 40325350 | ||||||
| chr22:40325523 | C | T | 1 | a0002c0002t0110 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2282C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 2282 | chr22 | 40325523 | ||||||
| chr22:40325575 | A | G | 2 | a0006c0006t0111 a0006c0006t0112 |
2 | HG01884.hp1 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2334A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 2334 | chr22 | 40325575 | ||||||
| chr22:40326741 | A | G | 66 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(63): Show |
142 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*3500A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 3500 | chr22 | 40326741 | ||||||
| chr22:40326807 | G | A | 7 | a0001c0001t0024 a0001c0001t0052 a0001c0001t0053 others(4): Show |
7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3566G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 3566 | chr22 | 40326807 | ||||||
| chr22:40326844 | G | A | 1 | a0001c0001t0115 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3603G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 3603 | chr22 | 40326844 | ||||||
| chr22:40326930 | T | C | 1 | a0002c0002t0084 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3689T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 3689 | chr22 | 40326930 | ||||||
| chr22:40327350 | G | A | 3 | a0001c0001t0010 a0001c0001t0057 a0001c0001t0058 |
7 | HG01361.hp1 HG02074.hp2 NA18949.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4109G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 4109 | chr22 | 40327350 | ||||||
| chr22:40327705 | A | G | 167 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(164): Show |
301 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(298): Show |
3_prime_UTR_variant | MODIFIER | c.*4464A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 4464 | chr22 | 40327705 | ||||||
| chr22:40327775 | C | G | 26 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0012 others(23): Show |
48 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*4534C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 4534 | chr22 | 40327775 | ||||||
| chr22:40327916 | A | G | 1 | a0001c0001t0133 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4675A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 4675 | chr22 | 40327916 | ||||||
| chr22:40328153 | A | G | 2 | a0001c0001t0022 a0013c0016t0147 |
4 | HG02602.hp1 HG03834.hp2 HG04115.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4912A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 4912 | chr22 | 40328153 | ||||||
| chr22:40328417 | A | G | 3 | a0001c0001t0080 a0001c0001t0081 a0001c0001t0082 |
3 | NA18947.hp1 NA19007.hp2 NA19012.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5176A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5176 | chr22 | 40328417 | ||||||
| chr22:40328579 | A | T | 1 | a0001c0001t0132 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5338A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5338 | chr22 | 40328579 | ||||||
| chr22:40328693 | C | T | 1 | a0001c0001t0108 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5452C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5452 | chr22 | 40328693 | ||||||
| chr22:40329019 | CA | C | 59 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0024 others(56): Show |
72 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*5790delA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5790 | INFO_REALIGN_3_PRIME | chr22 | 40329019 | |||||
| chr22:40329032 | C | A | 1 | a0001c0001t0061 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5791C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5791 | chr22 | 40329032 | ||||||
| chr22:40329043 | C | A | 3 | a0001c0001t0027 a0001c0001t0062 a0001c0001t0063 |
4 | NA18959.hp1 NA18973.hp2 NA18995.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5802C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5802 | chr22 | 40329043 | ||||||
| chr22:40329113 | C | T | 1 | a0001c0001t0049 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5872C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5872 | chr22 | 40329113 | ||||||
| chr22:40329137 | T | A | 2 | a0002c0002t0032 a0002c0002t0041 |
3 | HG03239.hp2 HG03831.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5896T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5896 | chr22 | 40329137 | ||||||
| chr22:40329145 | A | G | 1 | a0001c0017t0079 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5904A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5904 | chr22 | 40329145 | ||||||
| chr22:40329196 | C | G | 2 | a0002c0002t0107 a0002c0002t0157 |
2 | HG01934.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5955C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 5955 | chr22 | 40329196 | ||||||
| chr22:40329561 | C | T | 1 | a0002c0002t0106 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6320C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 6320 | chr22 | 40329561 | ||||||
| chr22:40329590 | T | G | 1 | a0001c0001t0042 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6349T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 6349 | chr22 | 40329590 | ||||||
| chr22:40329688 | G | A | 2 | a0001c0001t0134 a0001c0001t0135 |
2 | NA18962.hp1 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6447G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 6447 | chr22 | 40329688 | ||||||
| chr22:40329849 | A | G | 2 | a0001c0001t0146 a0002c0002t0105 |
2 | HG02698.hp1 HG03669.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6608A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 6608 | chr22 | 40329849 | ||||||
| chr22:40329899 | A | C | 1 | a0002c0002t0104 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6658A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 6658 | chr22 | 40329899 | ||||||
| chr22:40330179 | T | C | 45 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0011 others(42): Show |
94 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*6938T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 6938 | chr22 | 40330179 | ||||||
| chr22:40330485 | C | T | 1 | a0001c0001t0145 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7244C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 7244 | chr22 | 40330485 | ||||||
| chr22:40330745 | C | T | 121 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(118): Show |
199 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*7504C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 7504 | chr22 | 40330745 | ||||||
| chr22:40330758 | A | G | 121 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(118): Show |
199 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*7517A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 7517 | chr22 | 40330758 | ||||||
| chr22:40331319 | T | G | 7 | a0001c0001t0034 a0001c0001t0093 a0001c0001t0127 others(4): Show |
7 | HG01109.hp1 HG02145.hp1 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*8078T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8078 | chr22 | 40331319 | ||||||
| chr22:40331385 | T | A | 1 | a0007c0019t0095 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8144T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8144 | chr22 | 40331385 | ||||||
| chr22:40331639 | T | G | 1 | a0001c0001t0122 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8398T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8398 | chr22 | 40331639 | ||||||
| chr22:40331645 | AT | A | 77 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(74): Show |
146 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*8429delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8429 | INFO_REALIGN_3_PRIME | chr22 | 40331645 | |||||
| chr22:40331645 | ATT | A | 39 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0011 others(36): Show |
86 | HG00423.hp1 HG00423.hp2 HG00735.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*8428_*8429delTT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8428 | INFO_REALIGN_3_PRIME | chr22 | 40331645 | |||||
| chr22:40331645 | ATTT | A | 10 | a0001c0001t0042 a0001c0001t0043 a0001c0001t0046 others(7): Show |
10 | HG01261.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*8427_*8429delTTT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8427 | INFO_REALIGN_3_PRIME | chr22 | 40331645 | |||||
| chr22:40331668 | T | C | 2 | a0001c0001t0093 a0009c0010t0150 |
2 | HG01109.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8427T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8427 | chr22 | 40331668 | ||||||
| chr22:40331669 | T | A | 2 | a0001c0001t0093 a0009c0010t0150 |
2 | HG01109.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8428T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8428 | chr22 | 40331669 | ||||||
| chr22:40331670 | T | A | 2 | a0001c0001t0093 a0009c0010t0150 |
2 | HG01109.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8429T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8429 | chr22 | 40331670 | ||||||
| chr22:40331670 | T | C | 1 | a0002c0002t0087 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8429T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8429 | chr22 | 40331670 | ||||||
| chr22:40331671 | C | A | 3 | a0001c0001t0093 a0002c0002t0087 a0009c0010t0150 |
3 | HG01109.hp1 HG01261.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8430C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8430 | chr22 | 40331671 | ||||||
| chr22:40331788 | G | T | 4 | a0001c0001t0042 a0001c0001t0051 a0001c0001t0093 others(1): Show |
4 | HG01109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8547G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8547 | chr22 | 40331788 | ||||||
| chr22:40331895 | T | A | 1 | a0001c0001t0142 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8654T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 8654 | chr22 | 40331895 | ||||||
| chr22:40332541 | ATTC | A | 19 | a0001c0001t0039 a0001c0001t0076 a0001c0001t0144 others(16): Show |
26 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*9306_*9308delCTT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 9306 | INFO_REALIGN_3_PRIME | chr22 | 40332541 | |||||
| chr22:40332578 | A | G | 1 | a0001c0001t0139 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9337A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 9337 | chr22 | 40332578 | ||||||
| chr22:40332831 | C | T | 2 | a0001c0001t0029 a0001c0001t0050 |
3 | HG00544.hp1 HG02040.hp2 NA19077.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9590C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 9590 | chr22 | 40332831 | ||||||
| chr22:40333071 | C | T | 5 | a0001c0001t0034 a0001c0001t0127 a0002c0002t0034 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9830C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 9830 | chr22 | 40333071 | ||||||
| chr22:40333150 | C | T | 1 | a0001c0001t0117 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9909C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 9909 | chr22 | 40333150 | ||||||
| chr22:40333194 | G | A | 5 | a0001c0001t0034 a0001c0001t0127 a0002c0002t0034 others(2): Show |
5 | HG02145.hp1 HG02615.hp1 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9953G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 9953 | chr22 | 40333194 | ||||||
| chr22:40333209 | C | T | 2 | a0001c0001t0044 a0001c0001t0075 |
2 | HG01123.hp1 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9968C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 9968 | chr22 | 40333209 | ||||||
| chr22:40333210 | G | A | 4 | a0001c0001t0034 a0002c0002t0034 a0002c0002t0084 others(1): Show |
4 | HG02145.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9969G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 9969 | chr22 | 40333210 | ||||||
| chr22:40333331 | C | T | 2 | a0001c0001t0093 a0009c0010t0150 |
2 | HG01109.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10090C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 10090 | chr22 | 40333331 | ||||||
| chr22:40333559 | G | C | 1 | a0001c0001t0149 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10318G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 10318 | chr22 | 40333559 | ||||||
| chr22:40333610 | A | G | 39 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0011 others(36): Show |
85 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*10369A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 10369 | chr22 | 40333610 | ||||||
| chr22:40333705 | C | T | 2 | a0005c0007t0059 a0005c0007t0060 |
2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10464C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 10464 | chr22 | 40333705 | ||||||
| chr22:40333895 | C | G | 1 | a0001c0001t0073 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10654C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 10654 | chr22 | 40333895 | ||||||
| chr22:40334079 | A | T | 1 | a0001c0001t0131 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10838A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 10838 | chr22 | 40334079 | ||||||
| chr22:40334137 | A | G | 2 | a0001c0001t0093 a0009c0010t0150 |
2 | HG01109.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10896A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 10896 | chr22 | 40334137 | ||||||
| chr22:40334942 | A | C | 1 | a0002c0002t0092 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11701A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 11701 | chr22 | 40334942 | ||||||
| chr22:40335130 | C | A | 1 | a0002c0002t0099 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11889C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 11889 | chr22 | 40335130 | ||||||
| chr22:40335162 | C | CT | 26 | a0001c0001t0011 a0001c0001t0013 a0001c0001t0016 others(23): Show |
37 | HG00408.hp2 HG01106.hp2 HG01516.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*11948dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 11949 | INFO_REALIGN_3_PRIME | chr22 | 40335162 | |||||
| chr22:40335162 | CT | C | 18 | a0001c0001t0028 a0001c0001t0030 a0001c0001t0035 others(15): Show |
22 | HG01069.hp1 HG01243.hp1 HG01257.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*11948delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 11948 | INFO_REALIGN_3_PRIME | chr22 | 40335162 | |||||
| chr22:40335189 | T | A | 1 | a0001c0001t0071 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11948T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 11948 | chr22 | 40335189 | ||||||
| chr22:40335307 | T | C | 1 | a0001c0001t0066 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12066T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 12066 | chr22 | 40335307 | ||||||
| chr22:40335477 | C | CA | 13 | a0001c0001t0034 a0001c0001t0051 a0001c0001t0068 others(10): Show |
13 | HG00438.hp2 HG01109.hp1 HG01167.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*12252dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 12253 | INFO_REALIGN_3_PRIME | chr22 | 40335477 | |||||
| chr22:40335477 | CA | C | 7 | a0001c0001t0067 a0001c0001t0118 a0001c0001t0119 others(4): Show |
7 | NA18945.hp2 NA18946.hp1 NA18951.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*12252delA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 12252 | INFO_REALIGN_3_PRIME | chr22 | 40335477 | |||||
| chr22:40335540 | G | A | 1 | a0001c0001t0123 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12299G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 12299 | chr22 | 40335540 | ||||||
| chr22:40335557 | G | C | 1 | a0006c0006t0112 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12316G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 12316 | chr22 | 40335557 | ||||||
| chr22:40335570 | C | T | 1 | a0002c0002t0091 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12329C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 12329 | chr22 | 40335570 | ||||||
| chr22:40335764 | G | GAAAAAA | 9 | a0001c0001t0014 a0001c0001t0044 a0001c0001t0047 others(6): Show |
11 | HG00741.hp2 HG01123.hp1 HG01496.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*12526_*12531dupAA others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 12532 | INFO_REALIGN_3_PRIME | chr22 | 40335764 | |||||
| chr22:40335764 | G | GAAAAAAA | 157 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(154): Show |
290 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*12525_*12531dupAA others(5): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 23/23 | 12532 | INFO_REALIGN_3_PRIME | chr22 | 40335764 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:40178166 | T | A | 214 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(211): Show |
214 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.5+26T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40178166 | |||||||
| chr22:40178764 | C | T | 1 | a0001c0001t0010g0308 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.5+624C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40178764 | |||||||
| chr22:40179168 | C | T | 1 | a0001c0001t0003g0215 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.5+1028C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40179168 | |||||||
| chr22:40179180 | T | A | 1 | a0006c0006t0112g0001 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5+1040T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40179180 | |||||||
| chr22:40179943 | A | T | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+1803A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40179943 | |||||||
| chr22:40179976 | A | C | 1 | a0001c0001t0086g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5+1836A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40179976 | |||||||
| chr22:40180059 | T | G | 1 | a0001c0001t0031g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5+1919T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40180059 | |||||||
| chr22:40180298 | T | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+2158T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40180298 | |||||||
| chr22:40180392 | A | T | 1 | a0001c0001t0002g0307 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.5+2252A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40180392 | |||||||
| chr22:40180449 | T | A | 2 | a0001c0001t0002g0217 a0001c0001t0002g0218 |
2 | HG00639.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.5+2309T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40180449 | |||||||
| chr22:40180600 | C | T | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+2460C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40180600 | |||||||
| chr22:40180791 | C | T | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+2651C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40180791 | |||||||
| chr22:40180868 | G | T | 47 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(44): Show |
47 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.5+2728G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40180868 | |||||||
| chr22:40180928 | A | T | 1 | a0007c0019t0095g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5+2788A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40180928 | |||||||
| chr22:40181188 | C | T | 1 | a0001c0001t0039g0165 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.5+3048C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40181188 | |||||||
| chr22:40181340 | G | GTCCTCAC others(13): Show |
1 | a0001c0001t0075g0164 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.5+3224_5+3243dupTC others(18): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40181340 | ||||||
| chr22:40181444 | A | G | 1 | a0001c0001t0126g0305 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.5+3304A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40181444 | |||||||
| chr22:40181555 | A | T | 1 | a0001c0001t0004g0212 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.5+3415A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40181555 | |||||||
| chr22:40181948 | G | GA | 211 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(208): Show |
211 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.5+3820dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40181948 | ||||||
| chr22:40181967 | C | T | 1 | a0001c0001t0130g0162 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.5+3827C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40181967 | |||||||
| chr22:40182137 | C | G | 1 | a0001c0001t0116g0161 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.5+3997C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182137 | |||||||
| chr22:40182339 | T | G | 2 | a0001c0001t0030g0220 a0001c0001t0030g0221 |
2 | HG01069.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.5+4199T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182339 | |||||||
| chr22:40182404 | C | T | 1 | a0001c0001t0003g0160 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.5+4264C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182404 | |||||||
| chr22:40182405 | G | A | 1 | a0001c0001t0052g0002 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5+4265G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182405 | |||||||
| chr22:40182471 | G | A | 1 | a0001c0001t0042g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5+4331G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182471 | |||||||
| chr22:40182494 | A | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+4354A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182494 | |||||||
| chr22:40182626 | G | A | 1 | a0001c0001t0039g0165 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.5+4486G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182626 | |||||||
| chr22:40182653 | T | C | 1 | a0001c0001t0138g0167 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.5+4513T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182653 | |||||||
| chr22:40182760 | A | G | 214 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(211): Show |
214 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.5+4620A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182760 | |||||||
| chr22:40182794 | G | A | 1 | a0001c0001t0132g0004 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.5+4654G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182794 | |||||||
| chr22:40182798 | G | A | 1 | a0002c0002t0096g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5+4658G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182798 | |||||||
| chr22:40182830 | T | G | 1 | a0001c0001t0017g0006 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.5+4690T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182830 | |||||||
| chr22:40182896 | G | A | 2 | a0001c0001t0008g0223 a0001c0001t0074g0222 |
2 | HG00735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.5+4756G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182896 | |||||||
| chr22:40182954 | A | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+4814A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40182954 | |||||||
| chr22:40183071 | C | CAG | 216 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(213): Show |
216 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.5+4931_5+4932insAG | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183071 | |||||||
| chr22:40183081 | G | T | 1 | a0001c0001t0002g0304 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.5+4941G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183081 | |||||||
| chr22:40183086 | G | A | 305 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(302): Show |
305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.5+4946G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183086 | |||||||
| chr22:40183217 | G | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+5077G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183217 | |||||||
| chr22:40183419 | C | T | 216 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(213): Show |
216 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.5+5279C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183419 | |||||||
| chr22:40183422 | T | C | 1 | a0001c0001t0001g0007 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5+5282T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183422 | |||||||
| chr22:40183431 | C | T | 1 | a0001c0001t0061g0301 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.5+5291C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183431 | |||||||
| chr22:40183510 | G | A | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5+5370G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183510 | |||||||
| chr22:40183649 | G | A | 1 | a0001c0001t0145g0168 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.5+5509G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183649 | |||||||
| chr22:40183668 | G | C | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+5528G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183668 | |||||||
| chr22:40183696 | G | T | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+5556G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183696 | |||||||
| chr22:40183801 | G | T | 224 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(221): Show |
224 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.5+5661G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183801 | |||||||
| chr22:40183893 | C | T | 1 | a0002c0002t0033g0159 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5+5753C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40183893 | |||||||
| chr22:40184157 | G | A | 3 | a0002c0002t0034g0010 a0002c0002t0084g0008 a0002c0002t0094g0009 |
3 | HG02145.hp1 HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.5+6017G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40184157 | |||||||
| chr22:40184730 | T | C | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+6590T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40184730 | |||||||
| chr22:40184797 | G | A | 1 | a0001c0001t0075g0164 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.5+6657G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40184797 | |||||||
| chr22:40184804 | T | G | 1 | a0001c0001t0011g0011 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.5+6664T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40184804 | |||||||
| chr22:40184918 | G | T | 1 | a0001c0001t0002g0218 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5+6778G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40184918 | |||||||
| chr22:40185005 | G | T | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+6865G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40185005 | |||||||
| chr22:40185017 | A | G | 3 | a0003c0004t0019g0207 a0003c0004t0019g0208 a0003c0004t0136g0209 |
3 | HG01175.hp1 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.5+6877A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40185017 | |||||||
| chr22:40185147 | C | T | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5+7007C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40185147 | |||||||
| chr22:40185210 | T | C | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+7070T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40185210 | |||||||
| chr22:40185221 | C | G | 1 | a0001c0001t0043g0157 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.5+7081C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40185221 | |||||||
| chr22:40185579 | C | G | 2 | a0002c0002t0154g0155 a0002c0002t0155g0156 |
2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.5+7439C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40185579 | |||||||
| chr22:40185594 | T | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+7454T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40185594 | |||||||
| chr22:40185663 | G | A | 1 | a0002c0002t0036g0012 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5+7523G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40185663 | |||||||
| chr22:40185724 | G | A | 1 | a0001c0001t0003g0013 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.5+7584G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40185724 | |||||||
| chr22:40185818 | A | G | 217 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(214): Show |
217 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.5+7678A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40185818 | |||||||
| chr22:40186231 | C | T | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+8091C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186231 | |||||||
| chr22:40186369 | C | T | 1 | a0002c0002t0106g0154 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5+8229C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186369 | |||||||
| chr22:40186394 | G | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+8254G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186394 | |||||||
| chr22:40186471 | G | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+8331G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186471 | |||||||
| chr22:40186480 | C | T | 131 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(128): Show |
131 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.5+8340C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186480 | |||||||
| chr22:40186505 | C | T | 1 | a0001c0001t0118g0083 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.5+8365C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186505 | |||||||
| chr22:40186506 | G | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+8366G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186506 | |||||||
| chr22:40186517 | A | T | 1 | a0001c0001t0001g0082 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.5+8377A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186517 | |||||||
| chr22:40186525 | G | A | 8 | a0001c0001t0016g0086 a0001c0001t0016g0087 a0001c0001t0016g0088 others(5): Show |
8 | HG02055.hp1 HG02145.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.5+8385G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186525 | |||||||
| chr22:40186607 | G | A | 1 | a0001c0001t0034g0091 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5+8467G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186607 | |||||||
| chr22:40186737 | C | CA | 50 | a0001c0001t0022g0126 a0001c0001t0073g0225 a0001c0001t0109g0130 others(47): Show |
50 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.5+8611dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40186737 | ||||||
| chr22:40186762 | A | G | 1 | a0001c0001t0031g0299 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.5+8622A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186762 | |||||||
| chr22:40186866 | G | GT | 7 | a0001c0001t0002g0296 a0001c0001t0064g0298 a0001c0001t0069g0297 others(4): Show |
7 | HG01346.hp2 HG02293.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.5+8734dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40186866 | ||||||
| chr22:40186964 | C | T | 17 | a0001c0001t0022g0126 a0002c0002t0009g0115 a0002c0002t0009g0117 others(14): Show |
17 | HG00140.hp2 HG00642.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.5+8824C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40186964 | |||||||
| chr22:40187533 | C | T | 2 | a0001c0001t0046g0153 a0001c0001t0047g0152 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.5+9393C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40187533 | |||||||
| chr22:40187640 | G | C | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+9500G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40187640 | |||||||
| chr22:40187657 | G | A | 1 | a0001c0001t0138g0167 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.5+9517G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40187657 | |||||||
| chr22:40187676 | G | A | 2 | a0001c0001t0012g0169 a0001c0001t0021g0170 |
2 | HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.5+9536G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40187676 | |||||||
| chr22:40187783 | A | G | 1 | a0001c0001t0115g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5+9643A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40187783 | |||||||
| chr22:40187881 | G | T | 1 | a0001c0001t0010g0295 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5+9741G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40187881 | |||||||
| chr22:40187991 | G | A | 1 | a0001c0001t0001g0014 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.5+9851G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40187991 | |||||||
| chr22:40188124 | G | A | 4 | a0001c0001t0054g0132 a0001c0001t0055g0134 a0001c0001t0056g0133 others(1): Show |
4 | HG02723.hp1 HG02895.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.5+9984G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40188124 | |||||||
| chr22:40188147 | T | C | 14 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(11): Show |
14 | HG00408.hp1 HG02027.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.5+10007T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40188147 | |||||||
| chr22:40188358 | C | T | 1 | a0001c0001t0145g0168 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.5+10218C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40188358 | |||||||
| chr22:40188387 | G | A | 217 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(214): Show |
217 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.5+10247G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40188387 | |||||||
| chr22:40188619 | C | T | 1 | a0001c0001t0002g0294 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.5+10479C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40188619 | |||||||
| chr22:40188958 | T | C | 77 | a0001c0001t0006g0135 a0001c0001t0015g0140 a0001c0001t0015g0141 others(74): Show |
77 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.5+10818T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40188958 | |||||||
| chr22:40189191 | G | A | 1 | a0001c0001t0002g0226 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.5+11051G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40189191 | |||||||
| chr22:40189498 | C | CA | 14 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0002g0226 others(11): Show |
14 | HG00735.hp2 HG01106.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.5+11375dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40189498 | ||||||
| chr22:40189498 | CA | C | 91 | a0001c0001t0006g0151 a0001c0001t0007g0291 a0001c0001t0007g0293 others(88): Show |
91 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.5+11375delA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40189498 | ||||||
| chr22:40189518 | G | T | 4 | a0001c0001t0022g0126 a0002c0002t0032g0128 a0002c0002t0032g0129 others(1): Show |
4 | HG03239.hp2 HG03831.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.5+11378G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40189518 | |||||||
| chr22:40189740 | A | G | 216 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(213): Show |
216 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.5+11600A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40189740 | |||||||
| chr22:40189834 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.5+11694A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40189834 | |||||||
| chr22:40189978 | A | T | 1 | a0001c0001t0108g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5+11838A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40189978 | |||||||
| chr22:40190052 | T | G | 1 | a0001c0001t0109g0130 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.5+11912T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40190052 | |||||||
| chr22:40190065 | C | G | 42 | a0001c0001t0001g0219 a0001c0001t0004g0179 a0001c0001t0004g0181 others(39): Show |
42 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.5+11925C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40190065 | |||||||
| chr22:40190100 | G | T | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+11960G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40190100 | |||||||
| chr22:40190230 | C | A | 7 | a0001c0001t0024g0137 a0001c0001t0052g0002 a0001c0001t0053g0136 others(4): Show |
7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.5+12090C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40190230 | |||||||
| chr22:40190250 | C | T | 1 | a0001c0001t0012g0206 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5+12110C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40190250 | |||||||
| chr22:40190735 | C | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+12595C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40190735 | |||||||
| chr22:40190747 | C | T | 4 | a0001c0001t0006g0151 a0001c0001t0034g0091 a0001c0001t0051g0149 others(1): Show |
4 | HG02647.hp2 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.5+12607C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40190747 | |||||||
| chr22:40190823 | T | C | 1 | a0002c0002t0090g0092 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.5+12683T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40190823 | |||||||
| chr22:40191079 | G | A | 1 | a0001c0001t0124g0030 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.5+12939G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40191079 | |||||||
| chr22:40191096 | G | T | 49 | a0001c0001t0109g0130 a0002c0002t0006g0095 a0002c0002t0006g0097 others(46): Show |
49 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.5+12956G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40191096 | |||||||
| chr22:40191114 | G | A | 1 | a0005c0007t0059g0231 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.5+12974G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40191114 | |||||||
| chr22:40191240 | A | G | 217 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(214): Show |
217 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.5+13100A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40191240 | |||||||
| chr22:40191280 | T | C | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+13140T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40191280 | |||||||
| chr22:40191292 | G | A | 2 | a0001c0005t0004g0171 a0001c0005t0141g0172 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.5+13152G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40191292 | |||||||
| chr22:40191713 | C | G | 2 | a0001c0001t0008g0289 a0001c0001t0126g0305 |
2 | HG00741.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.5+13573C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40191713 | |||||||
| chr22:40191843 | T | C | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5+13703T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40191843 | |||||||
| chr22:40192197 | G | A | 1 | a0001c0001t0133g0031 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.5+14057G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40192197 | |||||||
| chr22:40192349 | G | A | 1 | a0002c0002t0083g0093 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5+14209G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40192349 | |||||||
| chr22:40192446 | G | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+14306G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40192446 | |||||||
| chr22:40192478 | A | G | 3 | a0003c0004t0019g0207 a0003c0004t0019g0208 a0003c0004t0136g0209 |
3 | HG01175.hp1 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.5+14338A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40192478 | |||||||
| chr22:40192531 | T | C | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+14391T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40192531 | |||||||
| chr22:40192616 | CA | C | 46 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(43): Show |
46 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.5+14487delA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40192616 | ||||||
| chr22:40192645 | G | C | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+14505G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40192645 | |||||||
| chr22:40192800 | G | A | 1 | a0001c0001t0027g0232 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.5+14660G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40192800 | |||||||
| chr22:40192864 | C | T | 1 | a0005c0007t0059g0231 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.5+14724C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40192864 | |||||||
| chr22:40192881 | A | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+14741A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40192881 | |||||||
| chr22:40192936 | G | T | 4 | a0001c0001t0002g0226 a0001c0001t0002g0230 a0001c0001t0002g0307 others(1): Show |
4 | NA18943.hp2 NA18965.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.5+14796G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40192936 | |||||||
| chr22:40193049 | C | G | 1 | a0001c0001t0118g0083 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.5+14909C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40193049 | |||||||
| chr22:40193123 | A | G | 2 | a0001c0001t0008g0288 a0001c0001t0069g0297 |
2 | NA18984.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.5+14983A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40193123 | |||||||
| chr22:40193246 | G | C | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+15106G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40193246 | |||||||
| chr22:40193342 | A | G | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5+15202A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40193342 | |||||||
| chr22:40193865 | AAAAG | A | 43 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(40): Show |
43 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.5+15731_5+15734del others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40193865 | ||||||
| chr22:40193927 | C | T | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+15787C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40193927 | |||||||
| chr22:40194090 | A | G | 1 | a0001c0001t0035g0148 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.5+15950A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40194090 | |||||||
| chr22:40194115 | C | T | 4 | a0001c0001t0016g0086 a0001c0001t0016g0087 a0001c0001t0016g0088 others(1): Show |
4 | HG02055.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.5+15975C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40194115 | |||||||
| chr22:40194122 | G | T | 1 | a0002c0002t0033g0159 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5+15982G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40194122 | |||||||
| chr22:40194225 | T | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+16085T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40194225 | |||||||
| chr22:40195254 | T | G | 215 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(212): Show |
215 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.5+17114T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40195254 | |||||||
| chr22:40195308 | T | A | 131 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(128): Show |
131 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.5+17168T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40195308 | |||||||
| chr22:40195376 | G | A | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5+17236G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40195376 | |||||||
| chr22:40195521 | G | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0032 others(2): Show |
5 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.5+17381G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40195521 | |||||||
| chr22:40195620 | T | G | 2 | a0001c0001t0046g0153 a0001c0001t0047g0152 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.5+17480T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40195620 | |||||||
| chr22:40195751 | G | T | 215 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(212): Show |
215 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.5+17611G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40195751 | |||||||
| chr22:40195919 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0003g0163 |
2 | NA18998.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.5+17779G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40195919 | |||||||
| chr22:40195979 | G | A | 1 | a0001c0001t0073g0225 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.5+17839G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40195979 | |||||||
| chr22:40196020 | G | C | 1 | a0008c0011t0006g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5+17880G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40196020 | |||||||
| chr22:40196076 | CT | C | 213 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(210): Show |
213 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.5+17948delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40196076 | ||||||
| chr22:40196210 | A | G | 131 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(128): Show |
131 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.5+18070A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40196210 | |||||||
| chr22:40196237 | C | G | 1 | a0001c0001t0013g0287 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.5+18097C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40196237 | |||||||
| chr22:40196244 | GGCTCAAG others(7460): Show |
G | 1 | a0001c0001t0003g0215 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.5+18107_5+25573del | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40196244 | ||||||
| chr22:40196321 | T | C | 1 | a0001c0001t0086g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.5+18181T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40196321 | |||||||
| chr22:40196454 | G | A | 1 | a0001c0001t0146g0173 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.5+18314G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40196454 | |||||||
| chr22:40196533 | G | A | 1 | a0002c0002t0105g0119 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5+18393G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40196533 | |||||||
| chr22:40196621 | A | G | 1 | a0001c0001t0046g0153 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5+18481A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40196621 | |||||||
| chr22:40196624 | ATGGAACT others(18): Show |
A | 215 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(212): Show |
215 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.5+18513_5+18537del others(25): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40196624 | ||||||
| chr22:40196705 | A | T | 1 | a0002c0002t0087g0100 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5+18565A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40196705 | |||||||
| chr22:40196990 | T | C | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+18850T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40196990 | |||||||
| chr22:40197226 | C | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+19086C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40197226 | |||||||
| chr22:40197257 | C | T | 1 | a0001c0001t0088g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5+19117C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40197257 | |||||||
| chr22:40197288 | G | GT | 54 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(51): Show |
54 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.5+19157dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40197288 | ||||||
| chr22:40197288 | GT | G | 7 | a0001c0001t0016g0086 a0001c0001t0016g0087 a0001c0001t0016g0088 others(4): Show |
7 | HG02055.hp1 HG02896.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.5+19157delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40197288 | ||||||
| chr22:40197310 | C | T | 1 | a0001c0001t0077g0254 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.5+19170C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40197310 | |||||||
| chr22:40197316 | G | A | 45 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(42): Show |
45 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.5+19176G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40197316 | |||||||
| chr22:40197334 | G | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+19194G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40197334 | |||||||
| chr22:40197344 | G | A | 1 | a0001c0001t0022g0201 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5+19204G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40197344 | |||||||
| chr22:40197531 | C | T | 1 | a0001c0001t0002g0235 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.5+19391C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40197531 | |||||||
| chr22:40197541 | C | T | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+19401C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40197541 | |||||||
| chr22:40197606 | C | CT | 6 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(3): Show |
6 | HG00280.hp1 NA18612.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.5+19481dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40197606 | ||||||
| chr22:40197606 | CT | C | 60 | a0001c0001t0006g0135 a0001c0001t0006g0151 a0001c0001t0008g0250 others(57): Show |
60 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.5+19481delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40197606 | ||||||
| chr22:40197721 | C | T | 1 | a0001c0001t0017g0006 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.5+19581C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40197721 | |||||||
| chr22:40198417 | C | T | 1 | a0001c0001t0008g0250 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.5+20277C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40198417 | |||||||
| chr22:40198558 | C | T | 1 | a0002c0002t0096g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5+20418C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40198558 | |||||||
| chr22:40198629 | A | G | 1 | a0001c0001t0027g0256 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.5+20489A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40198629 | |||||||
| chr22:40198698 | A | G | 84 | a0001c0001t0006g0135 a0001c0001t0006g0151 a0001c0001t0015g0140 others(81): Show |
84 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.5+20558A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40198698 | |||||||
| chr22:40198777 | G | A | 1 | a0001c0001t0013g0247 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5+20637G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40198777 | |||||||
| chr22:40198816 | C | T | 7 | a0001c0001t0024g0137 a0001c0001t0052g0002 a0001c0001t0053g0136 others(4): Show |
7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.5+20676C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40198816 | |||||||
| chr22:40199267 | C | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+21127C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40199267 | |||||||
| chr22:40199371 | A | G | 4 | a0001c0001t0001g0053 a0001c0001t0001g0064 a0001c0001t0001g0071 others(1): Show |
4 | NA18939.hp2 NA18979.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.5+21231A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40199371 | |||||||
| chr22:40199549 | T | G | 1 | a0002c0002t0036g0012 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5+21409T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40199549 | |||||||
| chr22:40199558 | A | G | 7 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(4): Show |
7 | NA18612.hp2 NA18943.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.5+21418A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40199558 | |||||||
| chr22:40199654 | T | G | 1 | a0001c0001t0042g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5+21514T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40199654 | |||||||
| chr22:40199870 | C | T | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+21730C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40199870 | |||||||
| chr22:40199879 | C | G | 2 | a0002c0002t0154g0155 a0002c0002t0155g0156 |
2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.5+21739C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40199879 | |||||||
| chr22:40199887 | T | A | 1 | a0001c0001t0071g0241 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.5+21747T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40199887 | |||||||
| chr22:40200027 | G | A | 2 | a0002c0002t0034g0010 a0002c0002t0084g0008 |
2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.5+21887G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40200027 | |||||||
| chr22:40200046 | G | A | 1 | a0002c0002t0033g0159 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5+21906G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40200046 | |||||||
| chr22:40200278 | C | CT | 181 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0017 others(178): Show |
181 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.5+22162dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40200278 | ||||||
| chr22:40200278 | C | CTT | 33 | a0001c0001t0001g0032 a0001c0001t0001g0071 a0001c0001t0002g0217 others(30): Show |
33 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.5+22161_5+22162dup others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40200278 | ||||||
| chr22:40200278 | C | CTTT | 49 | a0001c0001t0001g0028 a0001c0001t0014g0059 a0001c0001t0015g0140 others(46): Show |
49 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.5+22160_5+22162dup others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40200278 | ||||||
| chr22:40200278 | C | CTTTT | 15 | a0001c0001t0035g0143 a0001c0001t0046g0153 a0002c0002t0006g0097 others(12): Show |
15 | HG01167.hp2 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.5+22159_5+22162dup others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40200278 | ||||||
| chr22:40200278 | CTTTTT | C | 6 | a0001c0001t0024g0137 a0001c0001t0052g0002 a0001c0001t0054g0132 others(3): Show |
6 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.5+22158_5+22162del others(5): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40200278 | ||||||
| chr22:40200380 | G | A | 3 | a0001c0001t0002g0246 a0001c0001t0008g0289 a0001c0001t0013g0247 |
3 | HG00741.hp1 HG01516.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.5+22240G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40200380 | |||||||
| chr22:40200381 | G | A | 1 | a0001c0001t0013g0290 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.5+22241G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40200381 | |||||||
| chr22:40200508 | T | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+22368T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40200508 | |||||||
| chr22:40200535 | G | A | 1 | a0002c0002t0006g0095 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5+22395G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40200535 | |||||||
| chr22:40200583 | C | T | 3 | a0002c0002t0032g0128 a0002c0002t0032g0129 a0002c0002t0041g0127 |
3 | HG03239.hp2 HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.5+22443C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40200583 | |||||||
| chr22:40200620 | A | T | 48 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(45): Show |
48 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.5+22480A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40200620 | |||||||
| chr22:40200884 | T | A | 83 | a0001c0001t0006g0135 a0001c0001t0006g0151 a0001c0001t0015g0140 others(80): Show |
83 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.5+22744T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40200884 | |||||||
| chr22:40201663 | G | A | 85 | a0001c0001t0006g0135 a0001c0001t0006g0151 a0001c0001t0015g0140 others(82): Show |
85 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.5+23523G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40201663 | |||||||
| chr22:40201869 | G | C | 1 | a0001c0001t0068g0285 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5+23729G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40201869 | |||||||
| chr22:40201964 | C | G | 1 | a0002c0002t0151g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5+23824C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40201964 | |||||||
| chr22:40202249 | G | GTTGTTTT others(7): Show |
81 | a0001c0001t0006g0135 a0001c0001t0006g0151 a0001c0001t0015g0140 others(78): Show |
81 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.5+24112_5+24125dup others(14): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40202249 | ||||||
| chr22:40202260 | G | GTTTTTGT others(8): Show |
4 | a0002c0002t0041g0127 a0002c0002t0107g0099 a0006c0006t0111g0214 others(1): Show |
4 | HG01884.hp1 HG01934.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.5+24125_5+24126ins others(15): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40202260 | ||||||
| chr22:40202260 | G | T | 2 | a0001c0001t0007g0273 a0001c0001t0067g0236 |
2 | NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.5+24120G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40202260 | |||||||
| chr22:40202260 | GT | G | 49 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(46): Show |
49 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.5+24134delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40202260 | ||||||
| chr22:40203328 | A | G | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5+25188A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40203328 | |||||||
| chr22:40203379 | G | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+25239G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40203379 | |||||||
| chr22:40203414 | G | A | 1 | a0002c0002t0105g0119 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5+25274G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40203414 | |||||||
| chr22:40203532 | A | C | 26 | a0001c0001t0015g0140 a0001c0001t0015g0141 a0001c0001t0016g0086 others(23): Show |
26 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.5+25392A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40203532 | |||||||
| chr22:40203627 | G | A | 216 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(213): Show |
216 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.5+25487G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40203627 | |||||||
| chr22:40203700 | C | A | 1 | a0001c0001t0042g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5+25560C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40203700 | |||||||
| chr22:40203873 | T | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+25733T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40203873 | |||||||
| chr22:40203875 | C | T | 214 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(211): Show |
214 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.5+25735C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40203875 | |||||||
| chr22:40204114 | C | T | 1 | a0001c0001t0018g0079 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.5+25974C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40204114 | |||||||
| chr22:40204326 | A | C | 1 | a0001c0001t0004g0212 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.5+26186A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40204326 | |||||||
| chr22:40204483 | G | A | 216 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(213): Show |
216 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.5+26343G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40204483 | |||||||
| chr22:40204542 | G | A | 1 | a0002c0002t0096g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5+26402G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40204542 | |||||||
| chr22:40204774 | TCTGCTG | T | 3 | a0001c0001t0007g0291 a0001c0001t0007g0293 a0001c0001t0066g0292 |
3 | NA18946.hp2 NA18991.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.5+26646_5+26651del others(6): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40204774 | ||||||
| chr22:40205437 | A | C | 1 | a0001c0001t0039g0078 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.5+27297A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40205437 | |||||||
| chr22:40205438 | T | C | 1 | a0001c0001t0050g0233 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.5+27298T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40205438 | |||||||
| chr22:40205445 | A | G | 1 | a0002c0002t0096g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5+27305A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40205445 | |||||||
| chr22:40205635 | A | T | 216 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(213): Show |
216 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.5+27495A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40205635 | |||||||
| chr22:40206068 | T | A | 216 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(213): Show |
216 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.5+27928T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40206068 | |||||||
| chr22:40206181 | T | C | 1 | a0001c0001t0132g0004 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.5+28041T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40206181 | |||||||
| chr22:40206466 | ATG | A | 81 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(78): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.5+28328_5+28329del others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40206466 | ||||||
| chr22:40206616 | G | A | 83 | a0001c0001t0006g0135 a0001c0001t0006g0151 a0001c0001t0015g0140 others(80): Show |
83 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.5+28476G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40206616 | |||||||
| chr22:40206811 | G | T | 217 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(214): Show |
217 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.5+28671G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40206811 | |||||||
| chr22:40206944 | G | A | 86 | a0001c0001t0006g0135 a0001c0001t0006g0151 a0001c0001t0015g0140 others(83): Show |
86 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.5+28804G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40206944 | |||||||
| chr22:40207285 | A | G | 86 | a0001c0001t0006g0135 a0001c0001t0006g0151 a0001c0001t0015g0140 others(83): Show |
86 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.5+29145A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207285 | |||||||
| chr22:40207359 | G | C | 86 | a0001c0001t0006g0135 a0001c0001t0006g0151 a0001c0001t0015g0140 others(83): Show |
86 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.5+29219G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207359 | |||||||
| chr22:40207399 | C | T | 85 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(82): Show |
85 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.5+29259C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207399 | |||||||
| chr22:40207406 | C | CA | 46 | a0001c0001t0001g0026 a0001c0001t0001g0219 a0001c0001t0002g0235 others(43): Show |
46 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.5+29279dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40207406 | ||||||
| chr22:40207406 | C | CAA | 58 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0017 others(55): Show |
58 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.5+29278_5+29279dup others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40207406 | ||||||
| chr22:40207406 | C | CAAA | 22 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0046 others(19): Show |
22 | HG00733.hp1 HG01346.hp2 NA18941.hp1 others(19): Show |
intron_variant | MODIFIER | c.5+29277_5+29279dup others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40207406 | ||||||
| chr22:40207406 | C | CAAAA | 8 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(5): Show |
8 | HG01261.hp1 HG02129.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.5+29276_5+29279dup others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40207406 | ||||||
| chr22:40207413 | AAAAAAAT others(4): Show |
A | 1 | a0006c0006t0112g0001 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5+29275_5+29285del others(11): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40207413 | ||||||
| chr22:40207415 | AAAAATAT others(4): Show |
A | 1 | a0006c0006t0111g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.5+29277_5+29287del others(11): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40207415 | ||||||
| chr22:40207416 | AAAATATA others(5): Show |
A | 3 | a0002c0002t0036g0012 a0002c0002t0156g0110 a0008c0011t0006g0094 |
3 | HG02615.hp2 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5+29278_5+29289del others(12): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40207416 | ||||||
| chr22:40207417 | AAATATAT others(4): Show |
A | 4 | a0001c0001t0006g0135 a0001c0001t0022g0126 a0002c0002t0096g0005 others(1): Show |
4 | HG01934.hp1 HG02976.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.5+29279_5+29289del others(11): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40207417 | ||||||
| chr22:40207417 | AAATATAT others(6): Show |
A | 1 | a0001c0001t0042g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5+29279_5+29291del others(13): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40207417 | ||||||
| chr22:40207418 | A | T | 1 | a0001c0001t0026g0283 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5+29278A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207418 | |||||||
| chr22:40207418 | AATATATA others(5): Show |
A | 67 | a0001c0001t0006g0151 a0001c0001t0015g0140 a0001c0001t0015g0141 others(64): Show |
67 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.5+29293_5+29304del others(12): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40207418 | ||||||
| chr22:40207419 | ATATATAT others(4): Show |
A | 8 | a0001c0001t0016g0086 a0001c0001t0016g0087 a0001c0001t0016g0088 others(5): Show |
8 | HG02055.hp1 HG02145.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.5+29280_5+29290del others(11): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207419 | |||||||
| chr22:40207419 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0108g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5+29280_5+29292del others(13): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207419 | |||||||
| chr22:40207420 | T | A | 171 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(168): Show |
171 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.5+29280T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207420 | |||||||
| chr22:40207422 | T | A | 125 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(122): Show |
125 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.5+29282T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207422 | |||||||
| chr22:40207424 | T | A | 41 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0017 others(38): Show |
41 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.5+29284T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207424 | |||||||
| chr22:40207426 | T | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0003g0018 others(2): Show |
5 | HG00544.hp2 HG02083.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.5+29286T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207426 | |||||||
| chr22:40207432 | T | A | 5 | a0001c0001t0086g0213 a0001c0001t0088g0138 a0002c0002t0006g0095 others(2): Show |
5 | HG01243.hp2 HG02896.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.5+29292T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207432 | |||||||
| chr22:40207533 | T | C | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+29393T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207533 | |||||||
| chr22:40207576 | C | A | 219 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(216): Show |
219 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.5+29436C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207576 | |||||||
| chr22:40207728 | A | G | 133 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(130): Show |
133 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.5+29588A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207728 | |||||||
| chr22:40207939 | C | T | 1 | a0001c0001t0128g0085 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.5+29799C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207939 | |||||||
| chr22:40207975 | A | G | 219 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(216): Show |
219 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.5+29835A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40207975 | |||||||
| chr22:40208006 | C | T | 1 | a0007c0019t0095g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5+29866C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208006 | |||||||
| chr22:40208031 | G | A | 1 | a0001c0001t0114g0081 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.5+29891G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208031 | |||||||
| chr22:40208070 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.5+29930G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208070 | |||||||
| chr22:40208110 | T | A | 6 | a0001c0001t0015g0140 a0001c0001t0015g0141 a0001c0001t0046g0153 others(3): Show |
6 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.5+29970T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208110 | |||||||
| chr22:40208111 | C | CA | 20 | a0001c0001t0002g0239 a0001c0001t0002g0242 a0001c0001t0002g0246 others(17): Show |
20 | HG00544.hp1 HG00642.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.5+29992dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40208111 | ||||||
| chr22:40208115 | AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0130g0162 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.5+29983_5+30000del others(18): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40208115 | ||||||
| chr22:40208119 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0012g0178 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5+29987_5+30000del others(14): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40208119 | ||||||
| chr22:40208120 | A | C | 85 | a0001c0001t0006g0135 a0001c0001t0006g0151 a0001c0001t0015g0140 others(82): Show |
85 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.5+29980A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208120 | |||||||
| chr22:40208126 | AAAAAAAC | A | 74 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(71): Show |
74 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.5+29993_5+29999del others(7): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40208126 | ||||||
| chr22:40208127 | A | C | 130 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(127): Show |
130 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.5+29987A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208127 | |||||||
| chr22:40208127 | AAAAAAC | A | 10 | a0001c0001t0001g0023 a0001c0001t0001g0043 a0001c0001t0001g0064 others(7): Show |
10 | HG01346.hp2 HG01928.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.5+29993_5+29998del others(6): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40208127 | ||||||
| chr22:40208128 | A | C | 1 | a0001c0001t0002g0281 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5+29988A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208128 | |||||||
| chr22:40208133 | C | A | 48 | a0001c0001t0002g0217 a0001c0001t0004g0179 a0001c0001t0004g0181 others(45): Show |
48 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.5+29993C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208133 | |||||||
| chr22:40208435 | G | A | 1 | a0001c0001t0013g0247 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5+30295G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208435 | |||||||
| chr22:40208542 | C | T | 1 | a0001c0001t0132g0004 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.5+30402C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208542 | |||||||
| chr22:40208712 | T | C | 219 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(216): Show |
219 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.5+30572T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208712 | |||||||
| chr22:40208878 | C | T | 2 | a0001c0001t0037g0076 a0001c0001t0037g0077 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.5+30738C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208878 | |||||||
| chr22:40208941 | T | G | 217 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(214): Show |
217 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.5+30801T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40208941 | |||||||
| chr22:40209159 | G | A | 218 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(215): Show |
218 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.5+31019G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40209159 | |||||||
| chr22:40209263 | GC | G | 218 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(215): Show |
218 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.5+31128delC | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40209263 | ||||||
| chr22:40209360 | A | T | 1 | a0006c0006t0112g0001 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5+31220A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40209360 | |||||||
| chr22:40209500 | G | C | 1 | a0001c0001t0117g0055 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.5+31360G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40209500 | |||||||
| chr22:40209569 | G | A | 1 | a0001c0001t0029g0238 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.5+31429G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40209569 | |||||||
| chr22:40209677 | C | T | 218 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(215): Show |
218 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.5+31537C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40209677 | |||||||
| chr22:40209696 | G | A | 6 | a0001c0001t0002g0239 a0001c0001t0002g0249 a0001c0001t0002g0251 others(3): Show |
6 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.5+31556G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40209696 | |||||||
| chr22:40209821 | C | G | 4 | a0001c0001t0022g0126 a0001c0001t0022g0201 a0001c0001t0022g0202 others(1): Show |
4 | HG02602.hp1 HG03834.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.5+31681C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40209821 | |||||||
| chr22:40209875 | C | T | 1 | a0007c0019t0095g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5+31735C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40209875 | |||||||
| chr22:40209997 | A | G | 218 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(215): Show |
218 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.5+31857A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40209997 | |||||||
| chr22:40210017 | C | CA | 209 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(206): Show |
209 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.5+31892dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40210017 | ||||||
| chr22:40210017 | C | CAA | 7 | a0001c0001t0001g0056 a0001c0001t0004g0179 a0001c0001t0039g0165 others(4): Show |
7 | HG00544.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.5+31891_5+31892dup others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40210017 | ||||||
| chr22:40210127 | G | C | 1 | a0002c0012t0006g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5+31987G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40210127 | |||||||
| chr22:40210150 | C | G | 1 | a0001c0001t0068g0285 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5+32010C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40210150 | |||||||
| chr22:40210289 | A | T | 218 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(215): Show |
218 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.5+32149A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40210289 | |||||||
| chr22:40210473 | G | T | 3 | a0001c0001t0022g0126 a0001c0001t0022g0201 a0001c0001t0022g0202 |
3 | HG02602.hp1 HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.5+32333G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40210473 | |||||||
| chr22:40210526 | C | A | 3 | a0002c0002t0006g0097 a0002c0002t0100g0098 a0002c0012t0006g0114 |
3 | HG02055.hp2 HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.5+32386C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40210526 | |||||||
| chr22:40210693 | T | C | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+32553T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40210693 | |||||||
| chr22:40211041 | C | G | 1 | a0001c0001t0038g0075 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5+32901C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40211041 | |||||||
| chr22:40211113 | ATCT | A | 218 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(215): Show |
218 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.5+32984_5+32986del others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40211113 | ||||||
| chr22:40211138 | G | T | 1 | a0001c0001t0031g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5+32998G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40211138 | |||||||
| chr22:40211208 | G | T | 1 | a0001c0001t0017g0034 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.5+33068G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40211208 | |||||||
| chr22:40211375 | G | A | 1 | a0001c0001t0003g0041 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.5+33235G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40211375 | |||||||
| chr22:40211383 | C | CT | 218 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(215): Show |
218 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.5+33251dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40211383 | ||||||
| chr22:40211620 | G | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5+33480G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40211620 | |||||||
| chr22:40211625 | G | A | 47 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(44): Show |
47 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.5+33485G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40211625 | |||||||
| chr22:40211829 | G | A | 3 | a0001c0001t0012g0206 a0001c0001t0121g0306 a0001c0001t0143g0180 |
3 | HG01106.hp2 HG01258.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.5+33689G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40211829 | |||||||
| chr22:40212118 | T | C | 1 | a0002c0002t0107g0099 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.6-33897T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40212118 | |||||||
| chr22:40212296 | G | T | 2 | a0001c0001t0086g0213 a0001c0001t0108g0145 |
2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.6-33719G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40212296 | |||||||
| chr22:40212482 | A | G | 1 | a0005c0007t0059g0231 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.6-33533A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40212482 | |||||||
| chr22:40212669 | A | G | 1 | a0002c0002t0097g0113 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.6-33346A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40212669 | |||||||
| chr22:40212773 | C | T | 2 | a0001c0001t0137g0199 a0012c0018t0005g0198 |
2 | HG00423.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.6-33242C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40212773 | |||||||
| chr22:40212892 | T | C | 209 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(206): Show |
209 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.6-33123T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40212892 | |||||||
| chr22:40212942 | C | T | 1 | a0002c0002t0110g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6-33073C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40212942 | |||||||
| chr22:40213074 | G | A | 1 | a0002c0002t0110g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6-32941G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40213074 | |||||||
| chr22:40213123 | T | A | 1 | a0001c0001t0021g0203 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.6-32892T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40213123 | |||||||
| chr22:40213147 | A | G | 209 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(206): Show |
209 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.6-32868A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40213147 | |||||||
| chr22:40213300 | G | T | 1 | a0001c0001t0002g0246 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.6-32715G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40213300 | |||||||
| chr22:40213338 | C | T | 1 | a0001c0001t0001g0014 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.6-32677C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40213338 | |||||||
| chr22:40213557 | C | G | 1 | a0001c0001t0049g0142 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6-32458C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40213557 | |||||||
| chr22:40213645 | A | G | 8 | a0001c0001t0006g0135 a0001c0001t0006g0151 a0001c0001t0033g0146 others(5): Show |
8 | HG01109.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.6-32370A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40213645 | |||||||
| chr22:40213705 | A | T | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-32310A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40213705 | |||||||
| chr22:40214282 | A | T | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6-31733A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40214282 | |||||||
| chr22:40214322 | C | T | 7 | a0001c0001t0006g0151 a0001c0001t0033g0146 a0001c0001t0034g0091 others(4): Show |
7 | HG01109.hp1 HG02258.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.6-31693C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40214322 | |||||||
| chr22:40214394 | C | A | 100 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(97): Show |
100 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.6-31621C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40214394 | |||||||
| chr22:40214439 | A | C | 1 | a0001c0001t0119g0074 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.6-31576A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40214439 | |||||||
| chr22:40214549 | G | GTT | 167 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(164): Show |
167 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.6-31456_6-31455dup others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40214549 | ||||||
| chr22:40214549 | G | GTTT | 40 | a0001c0001t0001g0219 a0001c0001t0004g0179 a0001c0001t0004g0181 others(37): Show |
40 | HG00544.hp2 HG01106.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.6-31457_6-31455dup others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40214549 | ||||||
| chr22:40214596 | G | C | 210 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(207): Show |
210 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.6-31419G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40214596 | |||||||
| chr22:40214862 | T | C | 1 | a0002c0002t0085g0116 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.6-31153T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40214862 | |||||||
| chr22:40214892 | T | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-31123T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40214892 | |||||||
| chr22:40215008 | G | A | 110 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(107): Show |
110 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.6-31007G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40215008 | |||||||
| chr22:40215010 | AAT | A | 96 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(93): Show |
96 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.6-31004_6-31003del others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40215010 | |||||||
| chr22:40215077 | T | C | 4 | a0001c0001t0014g0057 a0001c0001t0014g0058 a0001c0001t0014g0059 others(1): Show |
4 | HG00741.hp2 HG01123.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.6-30938T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40215077 | |||||||
| chr22:40215106 | TAAC | T | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0032 others(3): Show |
6 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.6-30906_6-30904del others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40215106 | ||||||
| chr22:40215188 | T | C | 1 | a0001c0001t0089g0150 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.6-30827T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40215188 | |||||||
| chr22:40215284 | A | AT | 207 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(204): Show |
207 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.6-30726dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40215284 | ||||||
| chr22:40215484 | A | G | 1 | a0001c0001t0003g0041 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.6-30531A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40215484 | |||||||
| chr22:40215624 | A | G | 207 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(204): Show |
207 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.6-30391A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40215624 | |||||||
| chr22:40216127 | A | G | 222 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(219): Show |
222 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.6-29888A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40216127 | |||||||
| chr22:40216152 | C | T | 7 | a0002c0002t0009g0120 a0002c0002t0009g0121 a0002c0002t0009g0123 others(4): Show |
7 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.6-29863C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40216152 | |||||||
| chr22:40216166 | C | T | 1 | a0001c0001t0088g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6-29849C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40216166 | |||||||
| chr22:40216167 | G | A | 1 | a0001c0001t0002g0226 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.6-29848G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40216167 | |||||||
| chr22:40216319 | G | A | 1 | a0001c0017t0079g0252 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.6-29696G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40216319 | |||||||
| chr22:40216765 | G | C | 1 | a0012c0018t0005g0198 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.6-29250G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40216765 | |||||||
| chr22:40216820 | T | C | 1 | a0001c0001t0001g0014 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.6-29195T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40216820 | |||||||
| chr22:40216937 | C | T | 1 | a0001c0001t0002g0251 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.6-29078C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40216937 | |||||||
| chr22:40216970 | G | A | 222 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(219): Show |
222 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.6-29045G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40216970 | |||||||
| chr22:40217032 | A | G | 224 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(221): Show |
224 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.6-28983A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40217032 | |||||||
| chr22:40217069 | A | G | 222 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(219): Show |
222 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.6-28946A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40217069 | |||||||
| chr22:40217145 | A | G | 1 | a0001c0001t0002g0246 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.6-28870A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40217145 | |||||||
| chr22:40217278 | A | C | 89 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(86): Show |
89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-28737A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40217278 | |||||||
| chr22:40217407 | G | A | 4 | a0001c0001t0016g0086 a0001c0001t0016g0087 a0001c0001t0016g0088 others(1): Show |
4 | HG02055.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.6-28608G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40217407 | |||||||
| chr22:40217458 | G | A | 3 | a0002c0002t0034g0010 a0002c0002t0084g0008 a0002c0002t0094g0009 |
3 | HG02145.hp1 HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.6-28557G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40217458 | |||||||
| chr22:40217843 | C | T | 1 | a0002c0002t0152g0096 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6-28172C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40217843 | |||||||
| chr22:40217929 | C | T | 3 | a0002c0002t0034g0010 a0002c0002t0084g0008 a0002c0002t0094g0009 |
3 | HG02145.hp1 HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.6-28086C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40217929 | |||||||
| chr22:40217972 | C | CA | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0003g0054 others(5): Show |
8 | HG02698.hp2 HG03491.hp2 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.6-28025dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40217972 | ||||||
| chr22:40217972 | C | CAA | 127 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(124): Show |
127 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.6-28026_6-28025dup others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40217972 | ||||||
| chr22:40217972 | C | CAAA | 83 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(80): Show |
83 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.6-28027_6-28025dup others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40217972 | ||||||
| chr22:40218129 | A | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-27886A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40218129 | |||||||
| chr22:40218186 | G | T | 3 | a0001c0001t0007g0279 a0001c0001t0007g0280 a0001c0001t0007g0300 |
3 | HG01123.hp2 HG01255.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.6-27829G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40218186 | |||||||
| chr22:40218226 | A | G | 1 | a0001c0001t0030g0221 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.6-27789A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40218226 | |||||||
| chr22:40218314 | TTTTTCTT others(3): Show |
T | 3 | a0001c0001t0002g0282 a0001c0001t0072g0277 a0001c0001t0078g0278 |
3 | HG01515.hp2 HG01517.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.6-27696_6-27687del others(10): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40218314 | ||||||
| chr22:40218324 | C | CT | 134 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(131): Show |
134 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.6-27671dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40218324 | ||||||
| chr22:40218324 | C | CTT | 87 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(84): Show |
87 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.6-27672_6-27671dup others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40218324 | ||||||
| chr22:40218324 | C | CTTT | 7 | a0001c0001t0002g0281 a0001c0001t0002g0302 a0001c0001t0007g0279 others(4): Show |
7 | HG01123.hp2 HG01255.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.6-27673_6-27671dup others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40218324 | ||||||
| chr22:40218445 | G | A | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6-27570G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40218445 | |||||||
| chr22:40218508 | T | G | 132 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(129): Show |
132 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.6-27507T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40218508 | |||||||
| chr22:40218623 | G | T | 222 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(219): Show |
222 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.6-27392G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40218623 | |||||||
| chr22:40218671 | A | T | 3 | a0001c0001t0002g0246 a0001c0001t0008g0289 a0001c0001t0013g0247 |
3 | HG00741.hp1 HG01516.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.6-27344A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40218671 | |||||||
| chr22:40219272 | G | T | 132 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(129): Show |
132 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.6-26743G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40219272 | |||||||
| chr22:40219757 | C | T | 1 | a0001c0001t0134g0176 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.6-26258C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40219757 | |||||||
| chr22:40220064 | T | G | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6-25951T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40220064 | |||||||
| chr22:40220069 | T | C | 1 | a0001c0001t0127g0084 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.6-25946T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40220069 | |||||||
| chr22:40220108 | G | A | 220 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(217): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.6-25907G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40220108 | |||||||
| chr22:40220120 | C | T | 1 | a0001c0001t0005g0197 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.6-25895C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40220120 | |||||||
| chr22:40220241 | C | A | 1 | a0001c0001t0007g0300 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.6-25774C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40220241 | |||||||
| chr22:40220699 | C | T | 43 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(40): Show |
43 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.6-25316C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40220699 | |||||||
| chr22:40220703 | A | G | 223 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(220): Show |
223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.6-25312A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40220703 | |||||||
| chr22:40220707 | A | G | 1 | a0001c0001t0117g0055 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.6-25308A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40220707 | |||||||
| chr22:40220844 | T | G | 1 | a0001c0001t0001g0014 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.6-25171T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40220844 | |||||||
| chr22:40221090 | A | G | 1 | a0001c0001t0116g0161 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.6-24925A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40221090 | |||||||
| chr22:40221096 | G | A | 223 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(220): Show |
223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.6-24919G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40221096 | |||||||
| chr22:40221715 | A | T | 1 | a0001c0001t0057g0245 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.6-24300A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40221715 | |||||||
| chr22:40221751 | G | GC | 15 | a0001c0001t0016g0086 a0001c0001t0016g0087 a0001c0001t0016g0088 others(12): Show |
15 | HG01243.hp2 HG01261.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.6-24254dupC | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40221751 | ||||||
| chr22:40221751 | G | GCCCCC | 15 | a0001c0001t0001g0219 a0001c0001t0004g0184 a0001c0001t0004g0205 others(12): Show |
15 | HG00423.hp1 HG00438.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.6-24258_6-24254dup others(5): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40221751 | ||||||
| chr22:40221761 | C | CCT | 13 | a0001c0001t0001g0015 a0001c0001t0001g0032 a0001c0001t0001g0043 others(10): Show |
13 | HG00738.hp2 HG01934.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.6-24254_6-24253ins others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40221761 | |||||||
| chr22:40221761 | C | CT | 81 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0017 others(78): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.6-24242dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40221761 | ||||||
| chr22:40221761 | CT | C | 73 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0228 others(70): Show |
73 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.6-24242delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40221761 | ||||||
| chr22:40221762 | T | C | 16 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0239 others(13): Show |
16 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.6-24253T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40221762 | |||||||
| chr22:40222059 | A | G | 48 | a0001c0001t0001g0219 a0001c0001t0004g0179 a0001c0001t0004g0181 others(45): Show |
48 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.6-23956A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222059 | |||||||
| chr22:40222089 | A | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-23926A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222089 | |||||||
| chr22:40222094 | T | C | 1 | a0001c0001t0002g0246 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.6-23921T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222094 | |||||||
| chr22:40222210 | T | C | 6 | a0001c0001t0015g0140 a0001c0001t0015g0141 a0001c0001t0046g0153 others(3): Show |
6 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.6-23805T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222210 | |||||||
| chr22:40222411 | G | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0032 others(2): Show |
5 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.6-23604G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222411 | |||||||
| chr22:40222567 | G | A | 26 | a0001c0001t0015g0140 a0001c0001t0015g0141 a0001c0001t0016g0086 others(23): Show |
26 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.6-23448G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222567 | |||||||
| chr22:40222625 | C | T | 1 | a0001c0001t0021g0203 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.6-23390C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222625 | |||||||
| chr22:40222728 | C | CT | 13 | a0001c0001t0093g0147 a0002c0002t0036g0012 a0002c0002t0036g0106 others(10): Show |
13 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.6-23254dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | ||||||
| chr22:40222728 | C | CTT | 9 | a0001c0001t0042g0003 a0001c0001t0052g0002 a0002c0002t0032g0128 others(6): Show |
9 | HG01257.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.6-23255_6-23254dup others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | ||||||
| chr22:40222728 | C | CTTT | 13 | a0001c0001t0024g0137 a0001c0001t0053g0136 a0001c0001t0054g0132 others(10): Show |
13 | HG01243.hp2 HG01496.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.6-23256_6-23254dup others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | ||||||
| chr22:40222728 | C | CTTTTTTT | 29 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0033 others(26): Show |
29 | HG00733.hp1 HG00738.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.6-23260_6-23254dup others(7): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | ||||||
| chr22:40222728 | C | CTTTTTTT others(1): Show |
29 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0053 others(26): Show |
29 | HG00280.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.6-23261_6-23254dup others(8): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | ||||||
| chr22:40222728 | C | CTTTTTTT others(2): Show |
22 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(19): Show |
22 | HG00423.hp2 HG00544.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.6-23262_6-23254dup others(9): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | ||||||
| chr22:40222728 | C | CTTTTTTT others(3): Show |
14 | a0001c0001t0001g0024 a0001c0001t0004g0181 a0001c0001t0004g0205 others(11): Show |
14 | HG00438.hp1 HG01346.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.6-23263_6-23254dup others(10): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | ||||||
| chr22:40222728 | C | CTTTTTTT others(4): Show |
4 | a0001c0001t0005g0191 a0001c0001t0037g0077 a0001c0001t0140g0196 others(1): Show |
4 | HG02027.hp1 HG03492.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.6-23264_6-23254dup others(11): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | ||||||
| chr22:40222728 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0005g0192 a0001c0001t0139g0175 a0001c0001t0149g0022 |
3 | HG02074.hp1 NA18945.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.6-23265_6-23254dup others(12): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | ||||||
| chr22:40222728 | C | CTTTTTTT others(7): Show |
6 | a0001c0001t0003g0018 a0001c0001t0003g0072 a0001c0001t0004g0184 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.6-23267_6-23254dup others(14): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | ||||||
| chr22:40222728 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0012g0188 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.6-23268_6-23254dup others(15): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | ||||||
| chr22:40222728 | C | T | 2 | a0001c0001t0012g0169 a0001c0001t0015g0174 |
2 | HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.6-23287C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222728 | |||||||
| chr22:40222728 | CT | C | 12 | a0001c0001t0006g0151 a0001c0001t0015g0140 a0001c0001t0015g0141 others(9): Show |
12 | HG00639.hp2 HG01070.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.6-23254delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | ||||||
| chr22:40222728 | CTT | C | 8 | a0001c0001t0011g0011 a0001c0001t0016g0086 a0001c0001t0016g0087 others(5): Show |
8 | HG02145.hp2 HG02896.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.6-23255_6-23254del others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | ||||||
| chr22:40222728 | CTTTTTT | C | 8 | a0001c0001t0001g0080 a0001c0001t0008g0244 a0001c0001t0057g0245 others(5): Show |
8 | HG00423.hp1 HG03704.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.6-23259_6-23254del others(6): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | ||||||
| chr22:40222728 | CTTTTTTT | C | 77 | a0001c0001t0001g0219 a0001c0001t0002g0217 a0001c0001t0002g0218 others(74): Show |
77 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.6-23260_6-23254del others(7): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | ||||||
| chr22:40222728 | CTTTTTTT others(1): Show |
C | 7 | a0001c0001t0002g0235 a0001c0001t0010g0253 a0001c0001t0062g0248 others(4): Show |
7 | HG02129.hp2 HG02896.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.6-23261_6-23254del others(8): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | ||||||
| chr22:40222728 | CTTTTTTT others(2): Show |
C | 7 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(4): Show |
7 | NA18612.hp2 NA18943.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.6-23262_6-23254del others(9): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | ||||||
| chr22:40222728 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0131g0027 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.6-23263_6-23254del others(10): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | ||||||
| chr22:40222728 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0047g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.6-23264_6-23254del others(11): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | ||||||
| chr22:40222728 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0011g0065 a0001c0001t0018g0044 |
2 | NA18984.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.6-23267_6-23254del others(14): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40222728 | ||||||
| chr22:40222737 | T | C | 4 | a0001c0001t0002g0226 a0001c0001t0002g0230 a0001c0001t0002g0307 others(1): Show |
4 | NA18943.hp2 NA18965.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.6-23278T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222737 | |||||||
| chr22:40222807 | A | G | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-23208A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222807 | |||||||
| chr22:40222871 | G | C | 4 | a0001c0001t0016g0086 a0001c0001t0016g0087 a0001c0001t0016g0088 others(1): Show |
4 | HG02055.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.6-23144G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222871 | |||||||
| chr22:40222888 | G | A | 1 | a0001c0001t0077g0254 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.6-23127G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40222888 | |||||||
| chr22:40223005 | C | T | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-23010C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223005 | |||||||
| chr22:40223023 | A | G | 1 | a0001c0001t0064g0298 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.6-22992A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223023 | |||||||
| chr22:40223074 | C | A | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-22941C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223074 | |||||||
| chr22:40223210 | G | A | 3 | a0003c0004t0019g0207 a0003c0004t0019g0208 a0003c0004t0136g0209 |
3 | HG01175.hp1 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.6-22805G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223210 | |||||||
| chr22:40223381 | C | T | 1 | a0001c0001t0063g0276 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.6-22634C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223381 | |||||||
| chr22:40223407 | G | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-22608G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223407 | |||||||
| chr22:40223451 | TGTTTC | T | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-22563_6-22559del others(5): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223451 | |||||||
| chr22:40223651 | A | G | 1 | a0001c0001t0015g0141 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.6-22364A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223651 | |||||||
| chr22:40223704 | A | G | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-22311A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223704 | |||||||
| chr22:40223775 | C | A | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-22240C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223775 | |||||||
| chr22:40223923 | A | G | 1 | a0001c0001t0130g0162 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.6-22092A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40223923 | |||||||
| chr22:40224171 | A | C | 1 | a0001c0001t0138g0167 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.6-21844A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40224171 | |||||||
| chr22:40224194 | G | A | 2 | a0001c0001t0008g0288 a0001c0001t0069g0297 |
2 | NA18984.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.6-21821G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40224194 | |||||||
| chr22:40224463 | C | A | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-21552C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40224463 | |||||||
| chr22:40224526 | A | G | 1 | a0001c0001t0013g0247 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.6-21489A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40224526 | |||||||
| chr22:40224561 | G | A | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-21454G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40224561 | |||||||
| chr22:40224664 | C | T | 1 | a0002c0002t0087g0100 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6-21351C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40224664 | |||||||
| chr22:40224897 | C | T | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-21118C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40224897 | |||||||
| chr22:40224928 | G | A | 2 | a0001c0001t0008g0288 a0001c0001t0069g0297 |
2 | NA18984.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.6-21087G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40224928 | |||||||
| chr22:40225284 | G | A | 89 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(86): Show |
89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-20731G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40225284 | |||||||
| chr22:40225400 | C | G | 89 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(86): Show |
89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-20615C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40225400 | |||||||
| chr22:40225641 | G | A | 89 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(86): Show |
89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-20374G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40225641 | |||||||
| chr22:40225738 | G | A | 1 | a0001c0001t0146g0173 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.6-20277G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40225738 | |||||||
| chr22:40225742 | C | CA | 18 | a0001c0001t0015g0140 a0001c0001t0015g0141 a0001c0001t0016g0086 others(15): Show |
18 | HG01109.hp1 HG01109.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.6-20248dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40225742 | ||||||
| chr22:40225742 | C | CAAA | 6 | a0001c0001t0002g0249 a0001c0001t0002g0251 a0001c0001t0008g0250 others(3): Show |
6 | HG00733.hp2 HG00738.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.6-20250_6-20248dup others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40225742 | ||||||
| chr22:40225742 | C | CAAAA | 57 | a0001c0001t0002g0217 a0001c0001t0002g0235 a0001c0001t0002g0239 others(54): Show |
57 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.6-20251_6-20248dup others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40225742 | ||||||
| chr22:40225742 | C | CAAAAA | 23 | a0001c0001t0002g0218 a0001c0001t0002g0227 a0001c0001t0002g0228 others(20): Show |
23 | HG00140.hp1 HG00438.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.6-20252_6-20248dup others(5): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40225742 | ||||||
| chr22:40225742 | CA | C | 116 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(113): Show |
116 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.6-20248delA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40225742 | ||||||
| chr22:40225873 | T | G | 44 | a0001c0001t0001g0219 a0001c0001t0004g0179 a0001c0001t0004g0181 others(41): Show |
44 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.6-20142T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40225873 | |||||||
| chr22:40226221 | T | C | 3 | a0001c0001t0012g0169 a0001c0001t0015g0174 a0001c0001t0021g0170 |
3 | HG02630.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.6-19794T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40226221 | |||||||
| chr22:40226476 | C | T | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-19539C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40226476 | |||||||
| chr22:40226940 | T | TA | 12 | a0001c0001t0003g0069 a0001c0001t0003g0160 a0001c0001t0003g0215 others(9): Show |
12 | HG00733.hp1 HG01255.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.6-19074dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40226940 | ||||||
| chr22:40226973 | A | C | 2 | a0001c0001t0013g0237 a0001c0001t0073g0225 |
2 | HG00408.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.6-19042A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40226973 | |||||||
| chr22:40227075 | A | AATT | 36 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0046 others(33): Show |
36 | HG01243.hp1 HG01346.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.6-18900_6-18898dup others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40227075 | ||||||
| chr22:40227075 | AATT | A | 168 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0017 others(165): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.6-18900_6-18898del others(3): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40227075 | ||||||
| chr22:40227075 | AATTATT | A | 19 | a0001c0001t0006g0135 a0001c0001t0015g0140 a0001c0001t0015g0141 others(16): Show |
19 | HG01891.hp2 HG02145.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.6-18903_6-18898del others(6): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40227075 | ||||||
| chr22:40227075 | AATTATTA others(2): Show |
A | 10 | a0001c0001t0001g0053 a0001c0001t0001g0064 a0001c0001t0001g0071 others(7): Show |
10 | HG02055.hp1 HG02896.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.6-18906_6-18898del others(9): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40227075 | ||||||
| chr22:40227188 | C | T | 1 | a0001c0001t0014g0058 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.6-18827C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40227188 | |||||||
| chr22:40227245 | T | C | 89 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(86): Show |
89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-18770T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40227245 | |||||||
| chr22:40227277 | G | A | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6-18738G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40227277 | |||||||
| chr22:40227323 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.6-18692A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40227323 | |||||||
| chr22:40227358 | C | CT | 92 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0046 others(89): Show |
92 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.6-18632dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40227358 | ||||||
| chr22:40227358 | C | CTT | 33 | a0001c0001t0002g0218 a0001c0001t0002g0228 a0001c0001t0002g0230 others(30): Show |
33 | HG00438.hp2 HG00735.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.6-18633_6-18632dup others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40227358 | ||||||
| chr22:40227358 | CT | C | 42 | a0001c0001t0001g0023 a0001c0001t0004g0179 a0001c0001t0004g0181 others(39): Show |
42 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.6-18632delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40227358 | ||||||
| chr22:40227392 | G | T | 1 | a0001c0017t0079g0252 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.6-18623G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40227392 | |||||||
| chr22:40227426 | T | C | 91 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(88): Show |
91 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.6-18589T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40227426 | |||||||
| chr22:40227427 | G | A | 89 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(86): Show |
89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-18588G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40227427 | |||||||
| chr22:40227520 | T | G | 1 | a0002c0002t0036g0012 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6-18495T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40227520 | |||||||
| chr22:40227678 | A | G | 2 | a0001c0001t0137g0199 a0012c0018t0005g0198 |
2 | HG00423.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.6-18337A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40227678 | |||||||
| chr22:40228035 | G | A | 1 | a0002c0002t0154g0155 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6-17980G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40228035 | |||||||
| chr22:40228212 | G | A | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6-17803G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40228212 | |||||||
| chr22:40228543 | A | G | 249 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(246): Show |
249 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.6-17472A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40228543 | |||||||
| chr22:40228585 | T | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-17430T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40228585 | |||||||
| chr22:40228804 | A | G | 302 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(299): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.6-17211A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40228804 | |||||||
| chr22:40228992 | GACCTAAG others(11): Show |
G | 1 | a0001c0001t0123g0070 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.6-17003_6-16986del others(18): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40228992 | ||||||
| chr22:40229042 | C | T | 1 | a0001c0001t0002g0227 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.6-16973C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40229042 | |||||||
| chr22:40229046 | A | G | 1 | a0001c0001t0002g0294 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.6-16969A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40229046 | |||||||
| chr22:40229445 | CT | C | 7 | a0001c0001t0024g0137 a0001c0001t0052g0002 a0001c0001t0053g0136 others(4): Show |
7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.6-16558delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40229445 | ||||||
| chr22:40229456 | T | C | 1 | a0001c0001t0145g0168 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.6-16559T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40229456 | |||||||
| chr22:40229520 | G | T | 1 | a0001c0001t0001g0219 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.6-16495G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40229520 | |||||||
| chr22:40229573 | C | CT | 89 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(86): Show |
89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-16441dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40229573 | ||||||
| chr22:40229905 | A | G | 89 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(86): Show |
89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-16110A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40229905 | |||||||
| chr22:40229947 | C | T | 89 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(86): Show |
89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-16068C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40229947 | |||||||
| chr22:40230282 | CT | C | 99 | a0001c0001t0001g0024 a0001c0001t0002g0217 a0001c0001t0002g0218 others(96): Show |
99 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.6-15709delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40230282 | ||||||
| chr22:40230282 | CTT | C | 8 | a0001c0001t0008g0250 a0001c0001t0010g0253 a0001c0001t0028g0266 others(5): Show |
8 | HG01070.hp2 HG01167.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.6-15710_6-15709del others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40230282 | ||||||
| chr22:40230329 | G | A | 1 | a0001c0001t0088g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6-15686G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40230329 | |||||||
| chr22:40230479 | A | G | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6-15536A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40230479 | |||||||
| chr22:40230511 | C | G | 1 | a0001c0001t0088g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6-15504C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40230511 | |||||||
| chr22:40230588 | G | A | 6 | a0002c0002t0151g0111 a0002c0002t0152g0096 a0002c0002t0153g0109 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.6-15427G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40230588 | |||||||
| chr22:40230647 | G | C | 1 | a0002c0002t0096g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6-15368G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40230647 | |||||||
| chr22:40230684 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.6-15331T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40230684 | |||||||
| chr22:40231001 | C | T | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6-15014C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40231001 | |||||||
| chr22:40231053 | C | A | 89 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(86): Show |
89 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-14962C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40231053 | |||||||
| chr22:40231053 | C | CTA | 5 | a0001c0001t0006g0151 a0001c0001t0033g0146 a0001c0001t0034g0091 others(2): Show |
5 | HG01109.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.6-14948_6-14947dup others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40231053 | ||||||
| chr22:40231055 | A | C | 137 | a0001c0001t0001g0219 a0001c0001t0002g0217 a0001c0001t0002g0218 others(134): Show |
137 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.6-14960A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40231055 | |||||||
| chr22:40231057 | A | C | 76 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0230 others(73): Show |
76 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.6-14958A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40231057 | |||||||
| chr22:40231083 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.6-14932A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40231083 | |||||||
| chr22:40231265 | C | T | 3 | a0001c0001t0012g0169 a0001c0001t0015g0174 a0001c0001t0021g0170 |
3 | HG02630.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.6-14750C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40231265 | |||||||
| chr22:40231315 | C | T | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-14700C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40231315 | |||||||
| chr22:40231525 | CT | C | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-14483delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40231525 | ||||||
| chr22:40231767 | T | C | 1 | a0001c0001t0002g0304 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.6-14248T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40231767 | |||||||
| chr22:40231872 | C | T | 7 | a0001c0001t0002g0262 a0001c0001t0002g0263 a0001c0001t0002g0274 others(4): Show |
7 | HG00408.hp2 HG02083.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.6-14143C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40231872 | |||||||
| chr22:40231998 | T | C | 1 | a0013c0016t0147g0200 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.6-14017T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40231998 | |||||||
| chr22:40232046 | G | C | 25 | a0001c0001t0015g0140 a0001c0001t0015g0141 a0001c0001t0016g0086 others(22): Show |
25 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.6-13969G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232046 | |||||||
| chr22:40232062 | A | T | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.6-13953A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232062 | |||||||
| chr22:40232224 | T | C | 2 | a0001c0001t0039g0165 a0001c0001t0128g0085 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.6-13791T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232224 | |||||||
| chr22:40232229 | C | T | 1 | a0001c0001t0047g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.6-13786C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232229 | |||||||
| chr22:40232230 | G | A | 1 | a0001c0001t0031g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.6-13785G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232230 | |||||||
| chr22:40232330 | G | A | 1 | a0001c0001t0003g0160 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.6-13685G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232330 | |||||||
| chr22:40232383 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.6-13632T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232383 | |||||||
| chr22:40232562 | C | T | 2 | a0001c0001t0046g0153 a0001c0001t0047g0152 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.6-13453C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232562 | |||||||
| chr22:40232591 | T | C | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-13424T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232591 | |||||||
| chr22:40232750 | C | T | 91 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(88): Show |
91 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.6-13265C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232750 | |||||||
| chr22:40232922 | C | T | 3 | a0001c0001t0025g0258 a0001c0001t0025g0259 a0001c0001t0026g0283 |
3 | HG00140.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.6-13093C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40232922 | |||||||
| chr22:40233134 | T | C | 91 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(88): Show |
91 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.6-12881T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40233134 | |||||||
| chr22:40233295 | C | G | 1 | a0001c0001t0035g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6-12720C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40233295 | |||||||
| chr22:40233316 | G | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-12699G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40233316 | |||||||
| chr22:40233441 | G | T | 47 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(44): Show |
47 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.6-12574G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40233441 | |||||||
| chr22:40233537 | G | A | 1 | a0002c0002t0085g0116 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.6-12478G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40233537 | |||||||
| chr22:40233620 | C | CA | 8 | a0001c0001t0002g0235 a0001c0001t0014g0057 a0001c0001t0028g0266 others(5): Show |
8 | HG00544.hp1 HG02015.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.6-12381dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40233620 | ||||||
| chr22:40233719 | G | A | 1 | a0001c0001t0035g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6-12296G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40233719 | |||||||
| chr22:40233801 | A | G | 89 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(86): Show |
89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-12214A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40233801 | |||||||
| chr22:40233965 | G | C | 2 | a0001c0001t0137g0199 a0012c0018t0005g0198 |
2 | HG00423.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.6-12050G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40233965 | |||||||
| chr22:40233976 | C | T | 7 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0032 others(4): Show |
7 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.6-12039C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40233976 | |||||||
| chr22:40234009 | G | A | 1 | a0002c0012t0006g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.6-12006G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40234009 | |||||||
| chr22:40234268 | C | T | 1 | a0002c0002t0101g0124 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.6-11747C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40234268 | |||||||
| chr22:40234404 | A | G | 1 | a0002c0002t0087g0100 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6-11611A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40234404 | |||||||
| chr22:40234670 | A | T | 1 | a0001c0001t0001g0029 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.6-11345A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40234670 | |||||||
| chr22:40234945 | A | T | 27 | a0001c0001t0004g0179 a0001c0001t0004g0184 a0001c0001t0004g0187 others(24): Show |
27 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.6-11070A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40234945 | |||||||
| chr22:40235029 | C | T | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-10986C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235029 | |||||||
| chr22:40235106 | G | C | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-10909G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235106 | |||||||
| chr22:40235335 | G | A | 87 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(84): Show |
87 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.6-10680G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235335 | |||||||
| chr22:40235433 | C | A | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-10582C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235433 | |||||||
| chr22:40235448 | G | A | 1 | a0001c0001t0004g0187 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.6-10567G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235448 | |||||||
| chr22:40235491 | C | T | 1 | a0002c0002t0100g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6-10524C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235491 | |||||||
| chr22:40235613 | G | A | 90 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(87): Show |
90 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.6-10402G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235613 | |||||||
| chr22:40235735 | A | G | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-10280A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235735 | |||||||
| chr22:40235755 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0026 others(2): Show |
5 | HG02083.hp1 NA18944.hp2 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.6-10260C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235755 | |||||||
| chr22:40235791 | T | C | 6 | a0001c0001t0015g0140 a0001c0001t0015g0141 a0001c0001t0046g0153 others(3): Show |
6 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.6-10224T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235791 | |||||||
| chr22:40235917 | A | G | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
5 | NA18612.hp2 NA18943.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.6-10098A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40235917 | |||||||
| chr22:40236043 | A | C | 253 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(250): Show |
253 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.6-9972A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40236043 | |||||||
| chr22:40236079 | C | T | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-9936C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40236079 | |||||||
| chr22:40236506 | C | G | 84 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(81): Show |
84 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.6-9509C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40236506 | |||||||
| chr22:40236768 | A | G | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-9247A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40236768 | |||||||
| chr22:40237057 | C | T | 1 | a0001c0001t0088g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6-8958C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40237057 | |||||||
| chr22:40237214 | A | G | 14 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(11): Show |
14 | HG00408.hp1 HG02027.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.6-8801A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40237214 | |||||||
| chr22:40237305 | A | G | 1 | a0001c0001t0002g0227 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.6-8710A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40237305 | |||||||
| chr22:40237459 | A | C | 1 | a0001c0001t0088g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6-8556A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40237459 | |||||||
| chr22:40237487 | G | A | 2 | a0001c0001t0013g0237 a0002c0002t0009g0121 |
2 | HG00140.hp2 HG00408.hp2 |
intron_variant | MODIFIER | c.6-8528G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40237487 | |||||||
| chr22:40237508 | G | A | 1 | a0001c0001t0019g0210 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.6-8507G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40237508 | |||||||
| chr22:40237687 | T | A | 3 | a0002c0002t0083g0093 a0002c0002t0097g0113 a0007c0019t0095g0166 |
3 | HG00639.hp2 HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.6-8328T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40237687 | |||||||
| chr22:40237778 | C | T | 1 | a0002c0002t0036g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.6-8237C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40237778 | |||||||
| chr22:40237829 | T | TG | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-8184dupG | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40237829 | ||||||
| chr22:40238049 | C | T | 1 | a0001c0001t0055g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.6-7966C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40238049 | |||||||
| chr22:40238409 | A | G | 1 | a0002c0002t0032g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6-7606A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40238409 | |||||||
| chr22:40238503 | A | G | 89 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(86): Show |
89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-7512A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40238503 | |||||||
| chr22:40239063 | C | T | 1 | a0002c0002t0099g0125 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.6-6952C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40239063 | |||||||
| chr22:40239109 | G | A | 1 | a0002c0002t0094g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.6-6906G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40239109 | |||||||
| chr22:40239122 | G | A | 7 | a0002c0002t0151g0111 a0002c0002t0152g0096 a0002c0002t0153g0109 others(4): Show |
7 | HG01243.hp2 HG01496.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.6-6893G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40239122 | |||||||
| chr22:40239167 | C | T | 1 | a0001c0001t0119g0074 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.6-6848C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40239167 | |||||||
| chr22:40239194 | C | A | 1 | a0001c0001t0122g0067 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.6-6821C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40239194 | |||||||
| chr22:40239272 | G | A | 26 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(23): Show |
26 | HG00280.hp1 HG00423.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.6-6743G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40239272 | |||||||
| chr22:40239479 | A | G | 1 | a0001c0001t0117g0055 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.6-6536A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40239479 | |||||||
| chr22:40239717 | T | C | 91 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(88): Show |
91 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.6-6298T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40239717 | |||||||
| chr22:40240072 | T | C | 241 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(238): Show |
241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.6-5943T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40240072 | |||||||
| chr22:40240254 | T | C | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6-5761T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40240254 | |||||||
| chr22:40240329 | A | T | 1 | a0002c0002t0110g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6-5686A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40240329 | |||||||
| chr22:40240590 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.6-5425C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40240590 | |||||||
| chr22:40240611 | C | T | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-5404C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40240611 | |||||||
| chr22:40240795 | A | G | 141 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(138): Show |
141 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.6-5220A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40240795 | |||||||
| chr22:40240888 | T | C | 1 | a0001c0001t0026g0283 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.6-5127T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40240888 | |||||||
| chr22:40241031 | C | T | 2 | a0001c0001t0015g0140 a0001c0001t0049g0142 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.6-4984C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40241031 | |||||||
| chr22:40241096 | G | A | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6-4919G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40241096 | |||||||
| chr22:40241308 | A | G | 1 | a0002c0002t0083g0093 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.6-4707A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40241308 | |||||||
| chr22:40241333 | C | T | 1 | a0001c0001t0002g0263 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.6-4682C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40241333 | |||||||
| chr22:40241346 | G | A | 1 | a0001c0001t0088g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6-4669G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40241346 | |||||||
| chr22:40241723 | T | C | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6-4292T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40241723 | |||||||
| chr22:40241800 | T | G | 89 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(86): Show |
89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-4215T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40241800 | |||||||
| chr22:40242094 | A | G | 1 | a0002c0002t0105g0119 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.6-3921A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40242094 | |||||||
| chr22:40242112 | T | C | 1 | a0001c0001t0008g0289 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6-3903T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40242112 | |||||||
| chr22:40242179 | A | AGT | 113 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(110): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.6-3806_6-3805dupTG | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40242179 | ||||||
| chr22:40242179 | A | AGTGT | 13 | a0001c0001t0001g0035 a0001c0001t0003g0163 a0001c0001t0037g0076 others(10): Show |
13 | HG00423.hp1 HG02293.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.6-3808_6-3805dupTG others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40242179 | ||||||
| chr22:40242179 | AGT | A | 27 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(24): Show |
27 | HG00438.hp1 HG01884.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.6-3806_6-3805delTG | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40242179 | ||||||
| chr22:40242179 | AGTGT | A | 5 | a0001c0001t0001g0061 a0001c0001t0006g0151 a0001c0001t0065g0224 others(2): Show |
5 | HG01891.hp1 HG02723.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.6-3808_6-3805delTG others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40242179 | ||||||
| chr22:40242179 | AGTGTGTG others(1): Show |
A | 86 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(83): Show |
86 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.6-3812_6-3805delTG others(6): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40242179 | ||||||
| chr22:40242219 | C | T | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-3796C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40242219 | |||||||
| chr22:40242329 | A | G | 1 | a0001c0001t0005g0190 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.6-3686A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40242329 | |||||||
| chr22:40242394 | A | G | 1 | a0002c0002t0152g0096 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6-3621A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40242394 | |||||||
| chr22:40242517 | G | A | 6 | a0001c0001t0016g0087 a0001c0001t0016g0088 a0001c0001t0039g0165 others(3): Show |
6 | HG02145.hp2 HG02896.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.6-3498G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40242517 | |||||||
| chr22:40242520 | TC | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(1): Show |
4 | NA18612.hp2 NA18943.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.6-3492delC | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40242520 | ||||||
| chr22:40242675 | C | T | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-3340C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40242675 | |||||||
| chr22:40242710 | G | A | 1 | a0002c0002t0033g0159 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.6-3305G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40242710 | |||||||
| chr22:40242930 | C | T | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-3085C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40242930 | |||||||
| chr22:40243120 | C | T | 7 | a0001c0001t0006g0151 a0001c0001t0033g0146 a0001c0001t0034g0091 others(4): Show |
7 | HG01109.hp1 HG02258.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.6-2895C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40243120 | |||||||
| chr22:40243291 | G | A | 222 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(219): Show |
222 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.6-2724G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40243291 | |||||||
| chr22:40243419 | C | G | 90 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(87): Show |
90 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.6-2596C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40243419 | |||||||
| chr22:40243513 | A | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-2502A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40243513 | |||||||
| chr22:40243702 | C | T | 83 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.6-2313C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40243702 | |||||||
| chr22:40243726 | A | G | 1 | a0001c0001t0001g0043 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.6-2289A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40243726 | |||||||
| chr22:40244276 | A | G | 10 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(7): Show |
10 | HG02083.hp1 NA18944.hp2 NA18962.hp2 others(7): Show |
intron_variant | MODIFIER | c.6-1739A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40244276 | |||||||
| chr22:40244281 | G | A | 248 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(245): Show |
248 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.6-1734G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40244281 | |||||||
| chr22:40244481 | A | G | 1 | a0002c0002t0099g0125 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.6-1534A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40244481 | |||||||
| chr22:40244512 | C | T | 81 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(78): Show |
81 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.6-1503C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40244512 | |||||||
| chr22:40244716 | G | T | 4 | a0001c0001t0022g0126 a0001c0001t0022g0201 a0001c0001t0022g0202 others(1): Show |
4 | HG02602.hp1 HG03834.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.6-1299G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40244716 | |||||||
| chr22:40244765 | C | T | 1 | a0002c0002t0006g0095 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.6-1250C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40244765 | |||||||
| chr22:40245074 | C | CATTT | 48 | a0001c0001t0004g0179 a0001c0001t0004g0184 a0001c0001t0004g0187 others(45): Show |
48 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.6-912_6-909dupATTT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40245074 | ||||||
| chr22:40245074 | C | CATTTATT others(1): Show |
12 | a0001c0001t0004g0181 a0001c0001t0004g0185 a0001c0001t0012g0178 others(9): Show |
12 | HG01258.hp2 HG01346.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.6-916_6-909dupATTT others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40245074 | ||||||
| chr22:40245074 | C | CATTTATT others(5): Show |
1 | a0001c0001t0143g0180 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.6-920_6-909dupATTT others(8): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40245074 | ||||||
| chr22:40245074 | CATTT | C | 91 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(88): Show |
91 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.6-912_6-909delATTT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40245074 | ||||||
| chr22:40245074 | CATTTATT others(5): Show |
C | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6-920_6-909delATTT others(8): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40245074 | ||||||
| chr22:40245160 | G | T | 89 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(86): Show |
89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-855G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40245160 | |||||||
| chr22:40245375 | G | A | 1 | a0001c0001t0119g0074 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.6-640G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40245375 | |||||||
| chr22:40245378 | A | C | 2 | a0001c0001t0016g0087 a0001c0001t0016g0088 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.6-637A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40245378 | |||||||
| chr22:40245438 | AAAATAG | A | 3 | a0001c0001t0039g0165 a0001c0001t0115g0090 a0001c0001t0128g0085 |
3 | HG02145.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.6-561_6-556delTAGA others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40245438 | ||||||
| chr22:40245711 | CGT | C | 136 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(133): Show |
136 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.6-285_6-284delGT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40245711 | ||||||
| chr22:40245711 | CGTGT | C | 87 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(84): Show |
87 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.6-287_6-284delGTGT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | 40245711 | ||||||
| chr22:40245793 | C | T | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.6-222C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40245793 | |||||||
| chr22:40245888 | T | C | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0032 others(3): Show |
6 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.6-127T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40245888 | |||||||
| chr22:40245976 | G | A | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-39G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | 40245976 | |||||||
| chr22:40246121 | G | A | 1 | a0011c0009t0002g0229 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.93+19G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40246121 | |||||||
| chr22:40246364 | G | A | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.93+262G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40246364 | |||||||
| chr22:40246448 | G | A | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.93+346G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40246448 | |||||||
| chr22:40246457 | G | C | 1 | a0001c0001t0002g0217 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.93+355G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40246457 | |||||||
| chr22:40246648 | C | G | 91 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(88): Show |
91 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.93+546C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40246648 | |||||||
| chr22:40246739 | G | A | 3 | a0002c0002t0034g0010 a0002c0002t0084g0008 a0002c0002t0094g0009 |
3 | HG02145.hp1 HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.93+637G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40246739 | |||||||
| chr22:40246795 | C | T | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.93+693C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40246795 | |||||||
| chr22:40247003 | G | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.93+901G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40247003 | |||||||
| chr22:40247203 | A | G | 1 | a0001c0001t0018g0079 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.93+1101A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40247203 | |||||||
| chr22:40247462 | A | G | 51 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(48): Show |
51 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.93+1360A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40247462 | |||||||
| chr22:40247543 | A | G | 1 | a0001c0001t0001g0007 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.93+1441A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40247543 | |||||||
| chr22:40247791 | CTGGTG | C | 49 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(46): Show |
49 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.93+1695_93+1699del others(5): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr22 | 40247791 | ||||||
| chr22:40247835 | C | T | 89 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(86): Show |
89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.93+1733C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40247835 | |||||||
| chr22:40247868 | C | T | 80 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0228 others(77): Show |
80 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.93+1766C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40247868 | |||||||
| chr22:40248076 | A | G | 7 | a0001c0001t0006g0151 a0001c0001t0033g0146 a0001c0001t0034g0091 others(4): Show |
7 | HG01109.hp1 HG02258.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+1974A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40248076 | |||||||
| chr22:40248077 | G | GA | 10 | a0001c0001t0002g0218 a0001c0001t0002g0227 a0001c0001t0002g0239 others(7): Show |
10 | HG00642.hp2 HG02258.hp1 HG04184.hp1 others(7): Show |
intron_variant | MODIFIER | c.93+1990dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr22 | 40248077 | ||||||
| chr22:40248142 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0003g0163 |
2 | NA18998.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.93+2040C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40248142 | |||||||
| chr22:40248151 | A | G | 1 | a0001c0001t0008g0289 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.93+2049A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40248151 | |||||||
| chr22:40248242 | C | G | 1 | a0001c0001t0146g0173 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.93+2140C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40248242 | |||||||
| chr22:40248471 | T | G | 1 | a0010c0014t0004g0186 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.93+2369T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40248471 | |||||||
| chr22:40248707 | G | T | 1 | a0001c0001t0002g0218 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.94-2472G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40248707 | |||||||
| chr22:40248713 | G | A | 6 | a0001c0001t0002g0239 a0001c0001t0002g0249 a0001c0001t0002g0251 others(3): Show |
6 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.94-2466G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40248713 | |||||||
| chr22:40249568 | G | A | 1 | a0001c0001t0008g0269 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.94-1611G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40249568 | |||||||
| chr22:40249591 | A | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.94-1588A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40249591 | |||||||
| chr22:40250046 | C | T | 2 | a0001c0001t0015g0140 a0001c0001t0049g0142 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.94-1133C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40250046 | |||||||
| chr22:40250066 | T | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.94-1113T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40250066 | |||||||
| chr22:40250068 | C | T | 6 | a0001c0001t0002g0239 a0001c0001t0002g0249 a0001c0001t0002g0251 others(3): Show |
6 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.94-1111C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40250068 | |||||||
| chr22:40250433 | C | T | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.94-746C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40250433 | |||||||
| chr22:40250458 | ACTTT | A | 6 | a0001c0001t0016g0087 a0001c0001t0016g0088 a0001c0001t0039g0165 others(3): Show |
6 | HG02145.hp2 HG02896.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.94-716_94-713delCT others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr22 | 40250458 | ||||||
| chr22:40250797 | A | G | 1 | a0001c0001t0088g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.94-382A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40250797 | |||||||
| chr22:40250933 | CT | C | 251 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0017 others(248): Show |
251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.94-228delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr22 | 40250933 | ||||||
| chr22:40251163 | T | C | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.94-16T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 2/22 | chr22 | 40251163 | |||||||
| chr22:40251214 | T | C | 1 | a0001c0001t0015g0141 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.115+14T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40251214 | |||||||
| chr22:40251218 | T | C | 1 | a0001c0001t0002g0217 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.115+18T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40251218 | |||||||
| chr22:40251400 | G | A | 1 | a0001c0001t0002g0263 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.115+200G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40251400 | |||||||
| chr22:40251419 | C | A | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.115+219C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40251419 | |||||||
| chr22:40251435 | A | G | 1 | a0001c0001t0024g0137 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.115+235A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40251435 | |||||||
| chr22:40251456 | G | A | 1 | a0001c0001t0002g0242 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.115+256G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40251456 | |||||||
| chr22:40251495 | G | T | 6 | a0001c0001t0016g0087 a0001c0001t0016g0088 a0001c0001t0039g0165 others(3): Show |
6 | HG02145.hp2 HG02896.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.115+295G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40251495 | |||||||
| chr22:40251735 | A | G | 1 | a0001c0001t0115g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.115+535A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40251735 | |||||||
| chr22:40251893 | C | T | 1 | a0001c0001t0088g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.115+693C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40251893 | |||||||
| chr22:40252036 | A | G | 4 | a0001c0001t0001g0053 a0001c0001t0001g0064 a0001c0001t0001g0071 others(1): Show |
4 | HG02280.hp1 NA18979.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+836A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40252036 | |||||||
| chr22:40252194 | A | G | 46 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(43): Show |
46 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.115+994A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40252194 | |||||||
| chr22:40252418 | G | A | 1 | a0001c0001t0013g0290 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.115+1218G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40252418 | |||||||
| chr22:40252968 | C | T | 4 | a0002c0002t0009g0120 a0002c0002t0009g0121 a0002c0002t0009g0123 others(1): Show |
4 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+1768C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40252968 | |||||||
| chr22:40253005 | A | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.115+1805A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40253005 | |||||||
| chr22:40253102 | CT | C | 33 | a0001c0001t0006g0135 a0001c0001t0006g0151 a0001c0001t0015g0140 others(30): Show |
33 | HG01109.hp1 HG01891.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.115+1915delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40253102 | ||||||
| chr22:40253245 | C | A | 3 | a0003c0004t0019g0207 a0003c0004t0019g0208 a0003c0004t0136g0209 |
3 | HG01175.hp1 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.115+2045C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40253245 | |||||||
| chr22:40253248 | A | AT | 6 | a0001c0001t0001g0071 a0001c0001t0002g0302 a0001c0001t0022g0202 others(3): Show |
6 | HG01261.hp2 HG03017.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+2063dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40253248 | ||||||
| chr22:40253333 | G | A | 2 | a0001c0001t0030g0220 a0001c0001t0030g0221 |
2 | HG01069.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.115+2133G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40253333 | |||||||
| chr22:40253336 | T | C | 233 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(230): Show |
233 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.115+2136T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40253336 | |||||||
| chr22:40253516 | T | C | 3 | a0001c0001t0033g0146 a0001c0001t0035g0148 a0001c0001t0093g0147 |
3 | HG01109.hp1 HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.115+2316T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40253516 | |||||||
| chr22:40253668 | T | C | 1 | a0001c0001t0005g0191 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.115+2468T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40253668 | |||||||
| chr22:40253691 | C | T | 7 | a0001c0001t0024g0137 a0001c0001t0052g0002 a0001c0001t0053g0136 others(4): Show |
7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+2491C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40253691 | |||||||
| chr22:40253699 | C | T | 1 | a0006c0006t0112g0001 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115+2499C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40253699 | |||||||
| chr22:40253811 | G | A | 1 | a0001c0001t0119g0074 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.115+2611G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40253811 | |||||||
| chr22:40253819 | CCTT | C | 90 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(87): Show |
90 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.115+2628_115+2630d others(5): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40253819 | ||||||
| chr22:40254200 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0071 |
2 | NA18979.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.115+3000C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40254200 | |||||||
| chr22:40254280 | G | A | 5 | a0002c0002t0009g0120 a0002c0002t0009g0121 a0002c0002t0009g0123 others(2): Show |
5 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+3080G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40254280 | |||||||
| chr22:40254613 | C | T | 3 | a0001c0001t0002g0282 a0001c0001t0072g0277 a0001c0001t0078g0278 |
3 | HG01515.hp2 HG01517.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.115+3413C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40254613 | |||||||
| chr22:40254748 | G | A | 3 | a0002c0002t0032g0128 a0002c0002t0032g0129 a0002c0002t0041g0127 |
3 | HG03239.hp2 HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.115+3548G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40254748 | |||||||
| chr22:40254931 | A | G | 1 | a0002c0002t0083g0093 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.115+3731A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40254931 | |||||||
| chr22:40255004 | G | T | 1 | a0001c0001t0055g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.115+3804G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40255004 | |||||||
| chr22:40255037 | A | G | 7 | a0001c0001t0024g0137 a0001c0001t0052g0002 a0001c0001t0053g0136 others(4): Show |
7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.115+3837A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40255037 | |||||||
| chr22:40255141 | T | A | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.115+3941T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40255141 | |||||||
| chr22:40255358 | G | A | 1 | a0001c0001t0011g0011 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.115+4158G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40255358 | |||||||
| chr22:40255414 | A | C | 1 | a0001c0001t0035g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.115+4214A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40255414 | |||||||
| chr22:40255460 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.115+4260C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40255460 | |||||||
| chr22:40255604 | A | T | 1 | a0001c0001t0002g0242 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.115+4404A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40255604 | |||||||
| chr22:40255716 | T | G | 1 | a0001c0001t0047g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.115+4516T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40255716 | |||||||
| chr22:40255723 | A | G | 1 | a0001c0001t0088g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.115+4523A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40255723 | |||||||
| chr22:40255794 | T | C | 5 | a0001c0001t0016g0086 a0001c0001t0016g0087 a0001c0001t0016g0088 others(2): Show |
5 | HG02055.hp1 HG02896.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+4594T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40255794 | |||||||
| chr22:40255843 | CTTGTTTG others(5): Show |
C | 146 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(143): Show |
146 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.115+4658_115+4669d others(14): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40255843 | ||||||
| chr22:40256470 | C | A | 6 | a0001c0001t0015g0140 a0001c0001t0015g0141 a0001c0001t0046g0153 others(3): Show |
6 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+5270C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40256470 | |||||||
| chr22:40256573 | G | A | 1 | a0001c0001t0067g0236 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.116-5259G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40256573 | |||||||
| chr22:40256797 | A | G | 234 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(231): Show |
234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.116-5035A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40256797 | |||||||
| chr22:40256869 | A | G | 94 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(91): Show |
94 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.116-4963A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40256869 | |||||||
| chr22:40256920 | A | G | 2 | a0002c0002t0085g0116 a0002c0002t0099g0125 |
2 | HG01109.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.116-4912A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40256920 | |||||||
| chr22:40257783 | G | A | 2 | a0002c0002t0107g0099 a0002c0002t0157g0107 |
2 | HG01934.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.116-4049G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40257783 | |||||||
| chr22:40257878 | T | C | 234 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(231): Show |
234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.116-3954T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40257878 | |||||||
| chr22:40257943 | G | A | 1 | a0002c0002t0009g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.116-3889G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40257943 | |||||||
| chr22:40258064 | A | G | 1 | a0001c0001t0031g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.116-3768A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40258064 | |||||||
| chr22:40258071 | C | CT | 54 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0033 others(51): Show |
54 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.116-3731dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | ||||||
| chr22:40258071 | C | CTT | 12 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0003g0163 others(9): Show |
12 | HG00735.hp2 HG01261.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.116-3732_116-3731d others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | ||||||
| chr22:40258071 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.116-3741_116-3731d others(13): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | ||||||
| chr22:40258071 | C | CTTTTTTT others(5): Show |
17 | a0001c0001t0002g0230 a0001c0001t0002g0281 a0001c0001t0002g0296 others(14): Show |
17 | HG00140.hp1 HG00280.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.116-3742_116-3731d others(14): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | ||||||
| chr22:40258071 | C | CTTTTTTT others(6): Show |
26 | a0001c0001t0002g0226 a0001c0001t0002g0228 a0001c0001t0002g0239 others(23): Show |
26 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.116-3743_116-3731d others(15): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | ||||||
| chr22:40258071 | C | CTTTTTTT others(7): Show |
14 | a0001c0001t0002g0246 a0001c0001t0002g0262 a0001c0001t0002g0282 others(11): Show |
14 | HG00408.hp2 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.116-3744_116-3731d others(16): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | ||||||
| chr22:40258071 | C | CTTTTTTT others(8): Show |
11 | a0001c0001t0002g0217 a0001c0001t0002g0272 a0001c0001t0008g0223 others(8): Show |
11 | HG00438.hp2 HG00544.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.116-3745_116-3731d others(17): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | ||||||
| chr22:40258071 | C | CTTTTTTT others(9): Show |
4 | a0001c0001t0002g0218 a0001c0001t0010g0295 a0001c0001t0013g0290 others(1): Show |
4 | HG01361.hp1 HG01517.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-3746_116-3731d others(18): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | ||||||
| chr22:40258071 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0027g0232 a0001c0001t0057g0245 |
2 | NA18949.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.116-3747_116-3731d others(19): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | ||||||
| chr22:40258071 | C | CTTTTTTT others(11): Show |
3 | a0001c0001t0002g0294 a0001c0001t0002g0302 a0001c0001t0028g0284 |
3 | HG02165.hp2 NA18939.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.116-3748_116-3731d others(20): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | ||||||
| chr22:40258071 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0010g0253 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.116-3750_116-3731d others(22): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | ||||||
| chr22:40258071 | C | CTTTTTTT others(14): Show |
2 | a0001c0001t0010g0308 a0001c0001t0063g0276 |
2 | HG02074.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.116-3751_116-3731d others(23): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | ||||||
| chr22:40258071 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0002g0227 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.116-3754_116-3731d others(26): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | ||||||
| chr22:40258071 | CT | C | 14 | a0001c0001t0002g0235 a0001c0001t0034g0091 a0001c0001t0035g0148 others(11): Show |
14 | HG01175.hp1 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.116-3731delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | ||||||
| chr22:40258071 | CTT | C | 53 | a0001c0001t0006g0135 a0001c0001t0006g0151 a0001c0001t0015g0140 others(50): Show |
53 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.116-3732_116-3731d others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | ||||||
| chr22:40258071 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0007g0279 a0001c0001t0007g0280 a0001c0001t0007g0300 |
3 | HG01123.hp2 HG01255.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.116-3741_116-3731d others(13): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40258071 | ||||||
| chr22:40258101 | T | TTTTTTTT others(3): Show |
1 | a0006c0006t0112g0001 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.116-3731_116-3730i others(12): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40258101 | |||||||
| chr22:40258272 | T | C | 143 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
143 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.116-3560T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40258272 | |||||||
| chr22:40258306 | T | G | 1 | a0006c0006t0112g0001 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.116-3526T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40258306 | |||||||
| chr22:40258601 | C | A | 1 | a0002c0002t0009g0115 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.116-3231C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40258601 | |||||||
| chr22:40259025 | C | T | 1 | a0001c0001t0002g0263 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.116-2807C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40259025 | |||||||
| chr22:40259304 | A | G | 3 | a0001c0001t0012g0206 a0001c0001t0121g0306 a0001c0001t0143g0180 |
3 | HG01106.hp2 HG01258.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.116-2528A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40259304 | |||||||
| chr22:40259444 | G | A | 1 | a0001c0001t0051g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.116-2388G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40259444 | |||||||
| chr22:40259500 | G | A | 1 | a0002c0002t0006g0095 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.116-2332G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40259500 | |||||||
| chr22:40259736 | G | A | 2 | a0001c0001t0086g0213 a0001c0001t0108g0145 |
2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.116-2096G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40259736 | |||||||
| chr22:40259830 | C | T | 1 | a0001c0001t0017g0006 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.116-2002C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40259830 | |||||||
| chr22:40260087 | A | G | 1 | a0001c0001t0011g0052 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.116-1745A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40260087 | |||||||
| chr22:40260094 | G | C | 1 | a0001c0001t0086g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.116-1738G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40260094 | |||||||
| chr22:40260201 | C | CT | 141 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(138): Show |
141 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.116-1617dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | 40260201 | ||||||
| chr22:40260308 | A | T | 1 | a0001c0001t0028g0284 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.116-1524A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40260308 | |||||||
| chr22:40260473 | A | G | 1 | a0001c0001t0086g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.116-1359A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40260473 | |||||||
| chr22:40260540 | G | A | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.116-1292G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40260540 | |||||||
| chr22:40260736 | C | G | 1 | a0001c0001t0029g0275 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.116-1096C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40260736 | |||||||
| chr22:40260884 | G | A | 286 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(283): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.116-948G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40260884 | |||||||
| chr22:40260892 | G | A | 1 | a0001c0001t0086g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.116-940G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40260892 | |||||||
| chr22:40260923 | G | A | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.116-909G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40260923 | |||||||
| chr22:40261414 | T | G | 2 | a0002c0002t0036g0012 a0008c0011t0006g0094 |
2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.116-418T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | chr22 | 40261414 | |||||||
| chr22:40262521 | GA | G | 21 | a0002c0002t0006g0097 a0002c0002t0009g0104 a0002c0002t0009g0115 others(18): Show |
21 | HG00140.hp2 HG00642.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.457+350delA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr22 | 40262521 | ||||||
| chr22:40262665 | T | C | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.457+492T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40262665 | |||||||
| chr22:40262687 | T | C | 2 | a0002c0002t0036g0012 a0008c0011t0006g0094 |
2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.457+514T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40262687 | |||||||
| chr22:40262762 | G | C | 1 | a0001c0001t0034g0091 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.457+589G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40262762 | |||||||
| chr22:40262824 | G | A | 1 | a0001c0001t0002g0294 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.457+651G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40262824 | |||||||
| chr22:40262907 | G | A | 3 | a0001c0001t0012g0169 a0001c0001t0015g0174 a0001c0001t0021g0170 |
3 | HG02630.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.457+734G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40262907 | |||||||
| chr22:40263016 | G | A | 1 | a0001c0001t0005g0195 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.457+843G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263016 | |||||||
| chr22:40263034 | C | T | 2 | a0001c0001t0015g0174 a0001c0001t0139g0175 |
2 | HG02809.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.457+861C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263034 | |||||||
| chr22:40263039 | T | TA | 7 | a0001c0001t0006g0151 a0001c0001t0033g0146 a0001c0001t0034g0091 others(4): Show |
7 | HG01109.hp1 HG02258.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.457+884dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr22 | 40263039 | ||||||
| chr22:40263039 | TA | T | 78 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(75): Show |
78 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.457+884delA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr22 | 40263039 | ||||||
| chr22:40263039 | TAA | T | 7 | a0001c0001t0002g0239 a0001c0001t0002g0249 a0001c0001t0002g0251 others(4): Show |
7 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.457+883_457+884del others(2): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr22 | 40263039 | ||||||
| chr22:40263169 | A | G | 1 | a0001c0001t0004g0184 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.457+996A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263169 | |||||||
| chr22:40263222 | T | C | 1 | a0001c0001t0123g0070 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.457+1049T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263222 | |||||||
| chr22:40263247 | T | A | 93 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(90): Show |
93 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.457+1074T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263247 | |||||||
| chr22:40263279 | A | T | 1 | a0001c0001t0013g0290 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.457+1106A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263279 | |||||||
| chr22:40263457 | G | A | 1 | a0001c0001t0046g0153 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.458-1231G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263457 | |||||||
| chr22:40263569 | T | C | 163 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(160): Show |
163 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.458-1119T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263569 | |||||||
| chr22:40263579 | C | T | 1 | a0001c0001t0007g0280 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.458-1109C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263579 | |||||||
| chr22:40263580 | G | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.458-1108G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263580 | |||||||
| chr22:40263753 | G | A | 1 | a0010c0014t0004g0186 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.458-935G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263753 | |||||||
| chr22:40263777 | A | G | 90 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(87): Show |
90 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.458-911A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40263777 | |||||||
| chr22:40264005 | T | C | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.458-683T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40264005 | |||||||
| chr22:40264110 | C | T | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.458-578C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40264110 | |||||||
| chr22:40264185 | A | G | 1 | a0001c0001t0029g0275 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.458-503A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40264185 | |||||||
| chr22:40264257 | A | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.458-431A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4/22 | chr22 | 40264257 | |||||||
| chr22:40267399 | G | A | 85 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(82): Show |
85 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.2806+363G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40267399 | |||||||
| chr22:40267749 | G | A | 3 | a0006c0006t0111g0214 a0006c0006t0112g0001 a0009c0010t0150g0101 |
3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2806+713G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40267749 | |||||||
| chr22:40267857 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2806+821G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40267857 | |||||||
| chr22:40267870 | C | CA | 95 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(92): Show |
95 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.2806+844dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | 40267870 | ||||||
| chr22:40267884 | C | T | 8 | a0001c0001t0006g0135 a0001c0001t0006g0151 a0001c0001t0033g0146 others(5): Show |
8 | HG01109.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2806+848C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40267884 | |||||||
| chr22:40268008 | A | G | 1 | a0001c0001t0109g0130 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2806+972A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268008 | |||||||
| chr22:40268046 | G | A | 3 | a0006c0006t0111g0214 a0006c0006t0112g0001 a0009c0010t0150g0101 |
3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2806+1010G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268046 | |||||||
| chr22:40268079 | A | G | 6 | a0001c0001t0002g0239 a0001c0001t0002g0249 a0001c0001t0002g0251 others(3): Show |
6 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.2806+1043A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268079 | |||||||
| chr22:40268156 | C | T | 1 | a0002c0002t0094g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2806+1120C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268156 | |||||||
| chr22:40268161 | C | T | 86 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(83): Show |
86 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.2806+1125C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268161 | |||||||
| chr22:40268186 | A | C | 1 | a0001c0001t0017g0034 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2806+1150A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268186 | |||||||
| chr22:40268236 | C | T | 1 | a0002c0002t0009g0115 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2806+1200C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268236 | |||||||
| chr22:40268379 | C | T | 1 | a0001c0001t0117g0055 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2806+1343C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268379 | |||||||
| chr22:40268640 | G | A | 3 | a0006c0006t0111g0214 a0006c0006t0112g0001 a0009c0010t0150g0101 |
3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2807-1482G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268640 | |||||||
| chr22:40268674 | G | T | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.2807-1448G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268674 | |||||||
| chr22:40268756 | G | A | 1 | a0001c0001t0086g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2807-1366G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268756 | |||||||
| chr22:40268785 | A | G | 3 | a0006c0006t0111g0214 a0006c0006t0112g0001 a0009c0010t0150g0101 |
3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2807-1337A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268785 | |||||||
| chr22:40268907 | C | T | 5 | a0001c0001t0015g0140 a0001c0001t0049g0142 a0006c0006t0111g0214 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2807-1215C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268907 | |||||||
| chr22:40268912 | C | CAAAAAAA others(4): Show |
1 | a0009c0010t0150g0101 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2807-1204_2807-120 others(15): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | 40268912 | ||||||
| chr22:40268916 | A | AAAAAAAA others(4): Show |
2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2807-1204_2807-120 others(15): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | 40268916 | ||||||
| chr22:40268916 | A | AAAT | 12 | a0001c0001t0002g0218 a0001c0001t0012g0182 a0001c0001t0012g0188 others(9): Show |
12 | HG00639.hp2 HG01891.hp1 HG03471.hp2 others(9): Show |
intron_variant | MODIFIER | c.2807-1178_2807-117 others(7): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | 40268916 | ||||||
| chr22:40268916 | AAATAATA others(2): Show |
A | 4 | a0001c0001t0001g0053 a0001c0001t0001g0064 a0001c0001t0001g0071 others(1): Show |
4 | NA18939.hp2 NA18979.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.2807-1184_2807-117 others(13): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | 40268916 | ||||||
| chr22:40268919 | T | A | 8 | a0001c0001t0016g0086 a0001c0001t0016g0087 a0001c0001t0016g0088 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.2807-1203T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268919 | |||||||
| chr22:40268922 | T | A | 4 | a0001c0001t0016g0086 a0001c0001t0016g0087 a0001c0001t0016g0088 others(1): Show |
4 | HG02055.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2807-1200T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40268922 | |||||||
| chr22:40269053 | C | A | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2807-1069C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40269053 | |||||||
| chr22:40269063 | T | C | 88 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.2807-1059T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40269063 | |||||||
| chr22:40269126 | C | CT | 7 | a0002c0002t0009g0123 a0002c0002t0091g0102 a0002c0002t0092g0103 others(4): Show |
7 | HG01071.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2807-969dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | 40269126 | ||||||
| chr22:40269126 | CT | C | 104 | a0001c0001t0001g0051 a0001c0001t0001g0064 a0001c0001t0002g0217 others(101): Show |
104 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.2807-969delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | 40269126 | ||||||
| chr22:40269126 | CTT | C | 125 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(122): Show |
125 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.2807-970_2807-969d others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | 40269126 | ||||||
| chr22:40269221 | C | T | 93 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(90): Show |
93 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.2807-901C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40269221 | |||||||
| chr22:40269706 | C | A | 2 | a0001c0001t0037g0076 a0001c0001t0037g0077 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2807-416C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40269706 | |||||||
| chr22:40269786 | G | T | 3 | a0006c0006t0111g0214 a0006c0006t0112g0001 a0009c0010t0150g0101 |
3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2807-336G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | chr22 | 40269786 | |||||||
| chr22:40269887 | C | CA | 167 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(164): Show |
167 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.2807-213dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | 40269887 | ||||||
| chr22:40269887 | C | CAA | 15 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(12): Show |
15 | HG01123.hp1 HG02027.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.2807-214_2807-213d others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | 40269887 | ||||||
| chr22:40270313 | CT | C | 19 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(16): Show |
19 | HG01884.hp1 HG02027.hp2 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.2965+51delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr22 | 40270313 | ||||||
| chr22:40270393 | C | T | 2 | a0002c0002t0090g0092 a0002c0002t0152g0096 |
2 | HG01243.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.2965+113C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40270393 | |||||||
| chr22:40270469 | G | A | 1 | a0001c0015t0024g0131 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2965+189G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40270469 | |||||||
| chr22:40270481 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0045g0062 |
2 | HG00280.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.2965+201G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40270481 | |||||||
| chr22:40270693 | G | A | 3 | a0006c0006t0111g0214 a0006c0006t0112g0001 a0009c0010t0150g0101 |
3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2965+413G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40270693 | |||||||
| chr22:40270852 | G | C | 2 | a0001c0005t0004g0171 a0001c0005t0141g0172 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2965+572G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40270852 | |||||||
| chr22:40270918 | G | C | 48 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(45): Show |
48 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.2965+638G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40270918 | |||||||
| chr22:40270940 | C | T | 1 | a0002c0002t0085g0116 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2965+660C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40270940 | |||||||
| chr22:40270966 | G | A | 3 | a0006c0006t0111g0214 a0006c0006t0112g0001 a0009c0010t0150g0101 |
3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2965+686G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40270966 | |||||||
| chr22:40271087 | G | A | 3 | a0006c0006t0111g0214 a0006c0006t0112g0001 a0009c0010t0150g0101 |
3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2965+807G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40271087 | |||||||
| chr22:40271436 | C | G | 1 | a0007c0019t0095g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2965+1156C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40271436 | |||||||
| chr22:40271573 | G | A | 2 | a0001c0001t0010g0265 a0001c0001t0058g0264 |
2 | NA18986.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2965+1293G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40271573 | |||||||
| chr22:40271767 | C | G | 3 | a0006c0006t0111g0214 a0006c0006t0112g0001 a0009c0010t0150g0101 |
3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2965+1487C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40271767 | |||||||
| chr22:40271988 | CT | C | 258 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(255): Show |
258 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.2966-1434delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr22 | 40271988 | ||||||
| chr22:40271992 | A | G | 258 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(255): Show |
258 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.2966-1433A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40271992 | |||||||
| chr22:40272070 | G | A | 232 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(229): Show |
232 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.2966-1355G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40272070 | |||||||
| chr22:40272087 | G | T | 3 | a0003c0004t0019g0207 a0003c0004t0019g0208 a0003c0004t0136g0209 |
3 | HG01175.hp1 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2966-1338G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40272087 | |||||||
| chr22:40272227 | C | T | 7 | a0001c0001t0024g0137 a0001c0001t0052g0002 a0001c0001t0053g0136 others(4): Show |
7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2966-1198C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40272227 | |||||||
| chr22:40272237 | A | G | 1 | a0001c0001t0035g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2966-1188A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40272237 | |||||||
| chr22:40272384 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2966-1041T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40272384 | |||||||
| chr22:40272631 | G | A | 46 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(43): Show |
46 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.2966-794G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40272631 | |||||||
| chr22:40272789 | C | T | 1 | a0001c0001t0022g0202 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2966-636C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40272789 | |||||||
| chr22:40272984 | C | G | 91 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(88): Show |
91 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.2966-441C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 6/22 | chr22 | 40272984 | |||||||
| chr22:40273644 | A | G | 94 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(91): Show |
94 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.3141+44A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40273644 | |||||||
| chr22:40273794 | G | A | 1 | a0001c0001t0034g0091 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3141+194G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40273794 | |||||||
| chr22:40273826 | T | C | 1 | a0001c0001t0002g0294 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3141+226T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40273826 | |||||||
| chr22:40274354 | C | T | 3 | a0006c0006t0111g0214 a0006c0006t0112g0001 a0009c0010t0150g0101 |
3 | HG01884.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3141+754C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40274354 | |||||||
| chr22:40274422 | C | CT | 42 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(39): Show |
42 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.3141+838dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr22 | 40274422 | ||||||
| chr22:40274422 | C | CTTTTTTT others(15): Show |
2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3141+838_3141+839i others(24): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr22 | 40274422 | ||||||
| chr22:40274554 | G | T | 5 | a0002c0002t0151g0111 a0002c0002t0153g0109 a0002c0002t0154g0155 others(2): Show |
5 | HG01496.hp2 HG02622.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3141+954G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40274554 | |||||||
| chr22:40274810 | A | T | 7 | a0001c0001t0024g0137 a0001c0001t0052g0002 a0001c0001t0053g0136 others(4): Show |
7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3141+1210A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40274810 | |||||||
| chr22:40274890 | A | G | 3 | a0001c0001t0002g0282 a0001c0001t0072g0277 a0001c0001t0078g0278 |
3 | HG01515.hp2 HG01517.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.3141+1290A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40274890 | |||||||
| chr22:40274971 | C | G | 1 | a0001c0001t0002g0270 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3141+1371C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40274971 | |||||||
| chr22:40275106 | T | C | 1 | a0002c0002t0105g0119 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3141+1506T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40275106 | |||||||
| chr22:40275126 | A | G | 1 | a0001c0001t0126g0305 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3141+1526A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40275126 | |||||||
| chr22:40275494 | G | A | 49 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(46): Show |
49 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.3142-1583G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40275494 | |||||||
| chr22:40275584 | A | G | 1 | a0001c0001t0002g0270 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3142-1493A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40275584 | |||||||
| chr22:40275680 | T | C | 1 | a0001c0001t0014g0057 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3142-1397T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40275680 | |||||||
| chr22:40275704 | A | C | 1 | a0001c0001t0122g0067 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3142-1373A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40275704 | |||||||
| chr22:40275716 | T | C | 2 | a0001c0001t0015g0140 a0001c0001t0049g0142 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3142-1361T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40275716 | |||||||
| chr22:40275915 | C | T | 2 | a0002c0002t0107g0099 a0002c0002t0157g0107 |
2 | HG01934.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3142-1162C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40275915 | |||||||
| chr22:40275959 | C | CA | 9 | a0001c0001t0001g0037 a0001c0001t0002g0217 a0001c0001t0003g0041 others(6): Show |
9 | HG00639.hp1 HG02145.hp2 HG03831.hp2 others(6): Show |
intron_variant | MODIFIER | c.3142-1107dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr22 | 40275959 | ||||||
| chr22:40276057 | A | G | 2 | a0002c0002t0091g0102 a0002c0002t0092g0103 |
2 | NA18944.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.3142-1020A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40276057 | |||||||
| chr22:40276074 | A | G | 231 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(228): Show |
231 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.3142-1003A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40276074 | |||||||
| chr22:40276076 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3142-1001G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40276076 | |||||||
| chr22:40276122 | C | T | 1 | a0001c0001t0145g0168 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3142-955C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40276122 | |||||||
| chr22:40276203 | C | G | 1 | a0001c0001t0001g0036 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3142-874C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40276203 | |||||||
| chr22:40276204 | G | A | 4 | a0001c0001t0016g0086 a0001c0001t0016g0087 a0001c0001t0016g0088 others(1): Show |
4 | HG02055.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3142-873G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40276204 | |||||||
| chr22:40276826 | A | C | 1 | a0001c0001t0115g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3142-251A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 7/22 | chr22 | 40276826 | |||||||
| chr22:40277521 | A | G | 2 | a0001c0001t0004g0181 a0001c0001t0004g0185 |
2 | HG01346.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.3216+370A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 8/22 | chr22 | 40277521 | |||||||
| chr22:40277577 | C | T | 1 | a0001c0001t0067g0236 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3217-422C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 8/22 | chr22 | 40277577 | |||||||
| chr22:40277681 | T | C | 232 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(229): Show |
232 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.3217-318T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 8/22 | chr22 | 40277681 | |||||||
| chr22:40277728 | G | T | 1 | a0001c0001t0001g0061 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3217-271G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 8/22 | chr22 | 40277728 | |||||||
| chr22:40277823 | A | T | 1 | a0001c0001t0026g0283 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3217-176A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 8/22 | chr22 | 40277823 | |||||||
| chr22:40277995 | C | T | 224 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(221): Show |
224 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
splice_region_variant&intron_variant | LOW | c.3217-4C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 8/22 | chr22 | 40277995 | |||||||
| chr22:40278281 | C | T | 1 | a0001c0001t0088g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3262+237C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40278281 | |||||||
| chr22:40278341 | C | T | 1 | a0001c0001t0005g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3262+297C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40278341 | |||||||
| chr22:40278555 | T | C | 1 | a0001c0001t0002g0270 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3262+511T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40278555 | |||||||
| chr22:40278556 | C | CA | 20 | a0001c0001t0001g0015 a0001c0001t0001g0028 a0001c0001t0001g0035 others(17): Show |
20 | HG00642.hp2 HG01106.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3262+530dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr22 | 40278556 | ||||||
| chr22:40278583 | G | A | 7 | a0001c0001t0004g0179 a0001c0001t0004g0184 a0001c0001t0004g0187 others(4): Show |
7 | HG00544.hp2 HG02523.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.3262+539G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40278583 | |||||||
| chr22:40278589 | G | A | 86 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(83): Show |
86 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.3262+545G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40278589 | |||||||
| chr22:40278776 | G | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3262+732G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40278776 | |||||||
| chr22:40278811 | C | T | 2 | a0001c0001t0030g0220 a0001c0001t0030g0221 |
2 | HG01069.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.3262+767C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40278811 | |||||||
| chr22:40279087 | A | G | 144 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(141): Show |
144 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.3263-908A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40279087 | |||||||
| chr22:40279195 | C | T | 1 | a0001c0001t0020g0211 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3263-800C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40279195 | |||||||
| chr22:40279528 | C | G | 1 | a0001c0001t0027g0256 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3263-467C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40279528 | |||||||
| chr22:40279557 | A | G | 143 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
143 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.3263-438A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40279557 | |||||||
| chr22:40279947 | G | A | 2 | a0001c0001t0012g0169 a0001c0001t0021g0170 |
2 | HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3263-48G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40279947 | |||||||
| chr22:40279953 | A | G | 2 | a0002c0002t0107g0099 a0002c0002t0157g0107 |
2 | HG01934.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3263-42A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 9/22 | chr22 | 40279953 | |||||||
| chr22:40280433 | G | A | 2 | a0001c0001t0019g0210 a0001c0001t0038g0075 |
2 | HG03942.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.3411+290G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 10/22 | chr22 | 40280433 | |||||||
| chr22:40280658 | A | G | 1 | a0001c0001t0002g0230 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3412-461A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 10/22 | chr22 | 40280658 | |||||||
| chr22:40280668 | T | G | 6 | a0001c0001t0002g0239 a0001c0001t0002g0249 a0001c0001t0002g0251 others(3): Show |
6 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.3412-451T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 10/22 | chr22 | 40280668 | |||||||
| chr22:40280742 | G | A | 2 | a0001c0001t0012g0182 a0001c0001t0142g0204 |
2 | NA18959.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.3412-377G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 10/22 | chr22 | 40280742 | |||||||
| chr22:40280844 | G | A | 3 | a0002c0002t0151g0111 a0002c0002t0153g0109 a0002c0002t0156g0110 |
3 | HG01496.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3412-275G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 10/22 | chr22 | 40280844 | |||||||
| chr22:40280857 | G | A | 1 | a0001c0001t0031g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3412-262G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 10/22 | chr22 | 40280857 | |||||||
| chr22:40280947 | T | C | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3412-172T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 10/22 | chr22 | 40280947 | |||||||
| chr22:40280982 | T | A | 85 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(82): Show |
85 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.3412-137T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 10/22 | chr22 | 40280982 | |||||||
| chr22:40280992 | A | G | 5 | a0001c0001t0003g0072 a0001c0001t0037g0076 a0001c0001t0037g0077 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.3412-127A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 10/22 | chr22 | 40280992 | |||||||
| chr22:40280997 | T | C | 224 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(221): Show |
224 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.3412-122T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 10/22 | chr22 | 40280997 | |||||||
| chr22:40281491 | C | T | 7 | a0001c0001t0024g0137 a0001c0001t0052g0002 a0001c0001t0053g0136 others(4): Show |
7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3582+202C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40281491 | |||||||
| chr22:40281495 | A | AT | 134 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(131): Show |
134 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.3582+217dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr22 | 40281495 | ||||||
| chr22:40281495 | AT | A | 6 | a0001c0001t0002g0296 a0001c0001t0002g0304 a0001c0001t0086g0213 others(3): Show |
6 | HG02615.hp2 HG02717.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.3582+217delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr22 | 40281495 | ||||||
| chr22:40281511 | C | T | 224 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(221): Show |
224 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.3582+222C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40281511 | |||||||
| chr22:40281679 | A | G | 8 | a0001c0001t0024g0137 a0001c0001t0035g0143 a0001c0001t0052g0002 others(5): Show |
8 | HG01891.hp2 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.3582+390A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40281679 | |||||||
| chr22:40281717 | TGG | T | 4 | a0001c0001t0001g0053 a0001c0001t0001g0064 a0001c0001t0001g0071 others(1): Show |
4 | NA18939.hp2 NA18979.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.3582+430_3582+431d others(4): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr22 | 40281717 | ||||||
| chr22:40282017 | AC | A | 7 | a0001c0001t0024g0137 a0001c0001t0052g0002 a0001c0001t0053g0136 others(4): Show |
7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3582+730delC | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr22 | 40282017 | ||||||
| chr22:40282147 | T | G | 1 | a0001c0001t0020g0267 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3582+858T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40282147 | |||||||
| chr22:40282693 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3582+1404A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40282693 | |||||||
| chr22:40282736 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3582+1447A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40282736 | |||||||
| chr22:40282783 | T | C | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3582+1494T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40282783 | |||||||
| chr22:40282945 | A | G | 3 | a0003c0004t0019g0207 a0003c0004t0019g0208 a0003c0004t0136g0209 |
3 | HG01175.hp1 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3582+1656A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40282945 | |||||||
| chr22:40283195 | C | T | 83 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(80): Show |
83 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.3582+1906C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283195 | |||||||
| chr22:40283200 | G | A | 1 | a0001c0001t0038g0075 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3582+1911G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283200 | |||||||
| chr22:40283229 | G | A | 83 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(80): Show |
83 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.3582+1940G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283229 | |||||||
| chr22:40283261 | A | T | 1 | a0002c0002t0105g0119 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3582+1972A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283261 | |||||||
| chr22:40283302 | T | C | 1 | a0001c0001t0019g0210 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3582+2013T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283302 | |||||||
| chr22:40283327 | C | T | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3582+2038C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283327 | |||||||
| chr22:40283329 | T | C | 1 | a0001c0001t0066g0292 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3582+2040T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283329 | |||||||
| chr22:40283330 | G | A | 1 | a0001c0001t0062g0248 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3582+2041G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283330 | |||||||
| chr22:40283358 | C | G | 144 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(141): Show |
144 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.3582+2069C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283358 | |||||||
| chr22:40283365 | G | A | 1 | a0001c0001t0144g0066 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3582+2076G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283365 | |||||||
| chr22:40283931 | A | G | 1 | a0001c0001t0050g0233 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3583-1714A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40283931 | |||||||
| chr22:40284186 | T | C | 2 | a0001c0001t0012g0169 a0001c0001t0021g0170 |
2 | HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3583-1459T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40284186 | |||||||
| chr22:40284541 | A | G | 6 | a0001c0001t0002g0262 a0001c0001t0002g0263 a0001c0001t0002g0274 others(3): Show |
6 | HG02083.hp2 NA18947.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.3583-1104A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40284541 | |||||||
| chr22:40284646 | A | G | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0026 others(5): Show |
8 | HG02083.hp1 NA18944.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.3583-999A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40284646 | |||||||
| chr22:40284696 | C | T | 257 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(254): Show |
257 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.3583-949C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40284696 | |||||||
| chr22:40284697 | C | T | 8 | a0001c0001t0006g0135 a0001c0001t0006g0151 a0001c0001t0033g0146 others(5): Show |
8 | HG01109.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.3583-948C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40284697 | |||||||
| chr22:40284809 | C | T | 2 | a0001c0001t0086g0213 a0001c0001t0108g0145 |
2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3583-836C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40284809 | |||||||
| chr22:40284858 | C | T | 1 | a0001c0001t0122g0067 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3583-787C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40284858 | |||||||
| chr22:40285015 | T | G | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3583-630T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40285015 | |||||||
| chr22:40285265 | A | G | 1 | a0001c0001t0130g0162 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3583-380A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40285265 | |||||||
| chr22:40285330 | A | G | 2 | a0001c0001t0002g0228 a0001c0001t0008g0244 |
2 | HG03704.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.3583-315A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40285330 | |||||||
| chr22:40285415 | C | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3583-230C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40285415 | |||||||
| chr22:40285481 | T | C | 1 | a0001c0001t0015g0141 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3583-164T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 11/22 | chr22 | 40285481 | |||||||
| chr22:40285784 | C | T | 135 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(132): Show |
135 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.3708+14C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40285784 | |||||||
| chr22:40286052 | A | G | 1 | a0002c0002t0036g0012 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3708+282A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40286052 | |||||||
| chr22:40286114 | C | A | 1 | a0001c0001t0122g0067 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3708+344C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40286114 | |||||||
| chr22:40286394 | C | T | 1 | a0001c0001t0108g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3708+624C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40286394 | |||||||
| chr22:40286459 | A | G | 1 | a0002c0002t0097g0113 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3708+689A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40286459 | |||||||
| chr22:40286624 | A | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3708+854A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40286624 | |||||||
| chr22:40286651 | T | C | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3708+881T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40286651 | |||||||
| chr22:40286847 | A | G | 1 | a0001c0001t0122g0067 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3708+1077A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40286847 | |||||||
| chr22:40286915 | T | C | 1 | a0001c0001t0040g0048 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3708+1145T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40286915 | |||||||
| chr22:40286923 | G | C | 1 | a0001c0001t0122g0067 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3708+1153G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40286923 | |||||||
| chr22:40287117 | C | T | 1 | a0001c0001t0122g0067 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3708+1347C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40287117 | |||||||
| chr22:40287184 | T | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3708+1414T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40287184 | |||||||
| chr22:40287209 | A | G | 2 | a0001c0001t0012g0182 a0001c0001t0142g0204 |
2 | NA18959.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.3708+1439A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40287209 | |||||||
| chr22:40287334 | A | AAGACCAG others(30): Show |
1 | a0001c0001t0072g0277 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3708+1565_3708+160 others(41): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40287334 | ||||||
| chr22:40287464 | G | A | 1 | a0001c0001t0013g0290 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3708+1694G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40287464 | |||||||
| chr22:40287497 | C | A | 50 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(47): Show |
50 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.3708+1727C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40287497 | |||||||
| chr22:40287710 | A | G | 1 | a0001c0017t0079g0252 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3708+1940A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40287710 | |||||||
| chr22:40287836 | G | A | 50 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(47): Show |
50 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.3708+2066G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40287836 | |||||||
| chr22:40287881 | A | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3708+2111A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40287881 | |||||||
| chr22:40288056 | C | G | 143 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
143 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.3708+2286C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40288056 | |||||||
| chr22:40288203 | A | G | 8 | a0001c0001t0006g0135 a0001c0001t0006g0151 a0001c0001t0033g0146 others(5): Show |
8 | HG01109.hp1 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.3708+2433A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40288203 | |||||||
| chr22:40288275 | T | TCCA | 147 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(144): Show |
147 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.3708+2506_3708+250 others(7): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40288275 | ||||||
| chr22:40288279 | G | A | 258 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(255): Show |
258 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.3708+2509G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40288279 | |||||||
| chr22:40288561 | G | T | 6 | a0001c0001t0014g0057 a0001c0001t0014g0058 a0001c0001t0014g0059 others(3): Show |
6 | HG00423.hp2 HG00741.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.3708+2791G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40288561 | |||||||
| chr22:40288732 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3708+2962G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40288732 | |||||||
| chr22:40288762 | C | A | 4 | a0001c0001t0006g0151 a0001c0001t0034g0091 a0001c0001t0051g0149 others(1): Show |
4 | HG02647.hp2 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.3708+2992C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40288762 | |||||||
| chr22:40288839 | C | CT | 88 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0035 others(85): Show |
88 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.3708+3089dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40288839 | ||||||
| chr22:40288839 | C | CTT | 16 | a0001c0001t0001g0219 a0001c0001t0004g0185 a0001c0001t0004g0187 others(13): Show |
16 | HG00438.hp1 HG01106.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.3708+3088_3708+308 others(6): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40288839 | ||||||
| chr22:40288846 | T | TC | 4 | a0001c0001t0015g0140 a0001c0001t0015g0141 a0001c0001t0048g0139 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3708+3076_3708+307 others(5): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40288846 | |||||||
| chr22:40288941 | G | A | 1 | a0002c0002t0009g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3708+3171G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40288941 | |||||||
| chr22:40288963 | G | A | 49 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(46): Show |
49 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.3708+3193G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40288963 | |||||||
| chr22:40289015 | T | C | 2 | a0005c0007t0059g0231 a0005c0007t0060g0255 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.3708+3245T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40289015 | |||||||
| chr22:40289414 | G | T | 1 | a0001c0001t0004g0205 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3708+3644G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40289414 | |||||||
| chr22:40289899 | G | T | 1 | a0008c0011t0006g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3708+4129G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40289899 | |||||||
| chr22:40290141 | C | A | 1 | a0001c0001t0001g0080 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3708+4371C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40290141 | |||||||
| chr22:40290378 | C | T | 1 | a0001c0013t0005g0194 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.3708+4608C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40290378 | |||||||
| chr22:40290382 | G | A | 140 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(137): Show |
140 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.3708+4612G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40290382 | |||||||
| chr22:40291114 | G | C | 3 | a0001c0001t0012g0169 a0001c0001t0015g0174 a0001c0001t0021g0170 |
3 | HG02630.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3708+5344G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40291114 | |||||||
| chr22:40291614 | C | T | 6 | a0002c0002t0151g0111 a0002c0002t0153g0109 a0002c0002t0154g0155 others(3): Show |
6 | HG01496.hp2 HG02622.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.3708+5844C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40291614 | |||||||
| chr22:40291753 | C | T | 258 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(255): Show |
258 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.3708+5983C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40291753 | |||||||
| chr22:40292167 | T | C | 136 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(133): Show |
136 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.3708+6397T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40292167 | |||||||
| chr22:40292193 | C | CA | 136 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(133): Show |
136 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.3708+6432dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40292193 | ||||||
| chr22:40292271 | T | C | 1 | a0001c0001t0088g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3708+6501T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40292271 | |||||||
| chr22:40292352 | CA | C | 6 | a0001c0001t0001g0053 a0001c0001t0001g0064 a0001c0001t0001g0071 others(3): Show |
6 | HG02976.hp1 NA18939.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.3708+6599delA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40292352 | ||||||
| chr22:40292352 | CAA | C | 128 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(125): Show |
128 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.3708+6598_3708+659 others(6): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40292352 | ||||||
| chr22:40292405 | A | G | 134 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(131): Show |
134 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.3708+6635A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40292405 | |||||||
| chr22:40292633 | A | C | 2 | a0001c0001t0039g0165 a0001c0001t0128g0085 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3708+6863A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40292633 | |||||||
| chr22:40292686 | G | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3708+6916G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40292686 | |||||||
| chr22:40292713 | G | A | 5 | a0001c0001t0016g0086 a0001c0001t0016g0087 a0001c0001t0016g0088 others(2): Show |
5 | HG02055.hp1 HG02896.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3708+6943G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40292713 | |||||||
| chr22:40292913 | A | G | 87 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(84): Show |
87 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.3708+7143A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40292913 | |||||||
| chr22:40292946 | T | C | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3708+7176T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40292946 | |||||||
| chr22:40293190 | C | CT | 22 | a0001c0001t0004g0187 a0001c0001t0006g0135 a0001c0001t0033g0146 others(19): Show |
22 | HG01071.hp1 HG01109.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.3709-7242dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40293190 | ||||||
| chr22:40293190 | C | CTT | 116 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(113): Show |
116 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.3709-7243_3709-724 others(6): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40293190 | ||||||
| chr22:40293190 | C | CTTT | 90 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0033 others(87): Show |
90 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.3709-7244_3709-724 others(7): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40293190 | ||||||
| chr22:40293190 | C | CTTTT | 16 | a0001c0001t0001g0051 a0001c0001t0001g0286 a0001c0001t0002g0262 others(13): Show |
16 | HG01123.hp2 HG01255.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.3709-7245_3709-724 others(8): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40293190 | ||||||
| chr22:40293256 | C | T | 49 | a0001c0001t0001g0219 a0001c0001t0004g0179 a0001c0001t0004g0181 others(46): Show |
49 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.3709-7199C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40293256 | |||||||
| chr22:40293375 | G | A | 86 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(83): Show |
86 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.3709-7080G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40293375 | |||||||
| chr22:40293816 | A | G | 2 | a0001c0001t0001g0219 a0001c0001t0130g0162 |
2 | HG02129.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.3709-6639A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40293816 | |||||||
| chr22:40293930 | G | A | 1 | a0001c0001t0115g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3709-6525G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40293930 | |||||||
| chr22:40294070 | C | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3709-6385C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40294070 | |||||||
| chr22:40294073 | C | CA | 15 | a0001c0001t0002g0246 a0002c0002t0009g0104 a0002c0002t0032g0129 others(12): Show |
15 | HG01167.hp2 HG01175.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.3709-6360dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40294073 | ||||||
| chr22:40294073 | CA | C | 227 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(224): Show |
227 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.3709-6360delA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40294073 | ||||||
| chr22:40294073 | CAAAAAAA others(3): Show |
C | 1 | a0006c0006t0111g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3709-6369_3709-636 others(14): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40294073 | ||||||
| chr22:40294074 | A | C | 1 | a0002c0002t0087g0100 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3709-6381A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40294074 | |||||||
| chr22:40294108 | C | T | 1 | a0006c0006t0111g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3709-6347C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40294108 | |||||||
| chr22:40294286 | A | G | 1 | a0001c0001t0035g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3709-6169A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40294286 | |||||||
| chr22:40294381 | A | G | 142 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(139): Show |
142 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.3709-6074A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40294381 | |||||||
| chr22:40294582 | A | T | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3709-5873A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40294582 | |||||||
| chr22:40294620 | A | G | 4 | a0001c0001t0027g0232 a0001c0001t0027g0256 a0001c0001t0062g0248 others(1): Show |
4 | NA18959.hp1 NA18973.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.3709-5835A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40294620 | |||||||
| chr22:40294830 | G | A | 49 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(46): Show |
49 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.3709-5625G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40294830 | |||||||
| chr22:40294937 | G | A | 2 | a0001c0001t0033g0146 a0001c0001t0093g0147 |
2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3709-5518G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40294937 | |||||||
| chr22:40295146 | G | T | 7 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0008g0223 others(4): Show |
7 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.3709-5309G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295146 | |||||||
| chr22:40295201 | C | A | 1 | a0001c0001t0057g0245 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3709-5254C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295201 | |||||||
| chr22:40295213 | C | T | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3709-5242C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295213 | |||||||
| chr22:40295287 | C | T | 3 | a0002c0002t0032g0128 a0002c0002t0032g0129 a0002c0002t0041g0127 |
3 | HG03239.hp2 HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.3709-5168C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295287 | |||||||
| chr22:40295335 | G | A | 2 | a0001c0001t0006g0151 a0001c0001t0089g0150 |
2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.3709-5120G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295335 | |||||||
| chr22:40295351 | G | A | 4 | a0002c0002t0006g0097 a0002c0002t0009g0104 a0002c0002t0100g0098 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3709-5104G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295351 | |||||||
| chr22:40295398 | C | T | 4 | a0001c0001t0046g0153 a0001c0001t0047g0152 a0001c0001t0086g0213 others(1): Show |
4 | HG02976.hp2 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3709-5057C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295398 | |||||||
| chr22:40295474 | CA | C | 132 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(129): Show |
132 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.3709-4964delA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40295474 | ||||||
| chr22:40295487 | A | G | 2 | a0002c0002t0091g0102 a0002c0002t0092g0103 |
2 | NA18944.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.3709-4968A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295487 | |||||||
| chr22:40295583 | G | A | 1 | a0002c0002t0033g0159 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3709-4872G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295583 | |||||||
| chr22:40295683 | A | C | 1 | a0001c0001t0031g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3709-4772A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295683 | |||||||
| chr22:40295702 | A | G | 50 | a0001c0001t0001g0219 a0001c0001t0004g0179 a0001c0001t0004g0181 others(47): Show |
50 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.3709-4753A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295702 | |||||||
| chr22:40295729 | C | CA | 49 | a0001c0001t0001g0219 a0001c0001t0004g0179 a0001c0001t0004g0181 others(46): Show |
49 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.3709-4717dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40295729 | ||||||
| chr22:40295999 | G | C | 1 | a0001c0001t0108g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3709-4456G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40295999 | |||||||
| chr22:40296326 | A | AT | 40 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(37): Show |
40 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.3709-4106dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40296326 | ||||||
| chr22:40296326 | A | ATT | 6 | a0001c0001t0016g0086 a0001c0001t0030g0220 a0001c0001t0030g0221 others(3): Show |
6 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.3709-4107_3709-410 others(6): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40296326 | ||||||
| chr22:40296602 | G | A | 2 | a0001c0001t0020g0267 a0001c0017t0079g0252 |
2 | HG00280.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.3709-3853G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40296602 | |||||||
| chr22:40296631 | C | CT | 33 | a0001c0001t0001g0046 a0001c0001t0004g0185 a0001c0001t0143g0180 others(30): Show |
33 | HG00140.hp2 HG00642.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.3709-3811dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40296631 | ||||||
| chr22:40297072 | T | C | 1 | a0001c0001t0051g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3709-3383T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40297072 | |||||||
| chr22:40297088 | A | G | 1 | a0001c0001t0005g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3709-3367A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40297088 | |||||||
| chr22:40297172 | G | A | 1 | a0001c0001t0040g0048 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3709-3283G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40297172 | |||||||
| chr22:40297267 | C | T | 1 | a0001c0001t0117g0055 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3709-3188C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40297267 | |||||||
| chr22:40297358 | G | A | 1 | a0001c0001t0115g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3709-3097G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40297358 | |||||||
| chr22:40297660 | A | G | 1 | a0001c0001t0038g0075 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3709-2795A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40297660 | |||||||
| chr22:40297770 | C | T | 1 | a0001c0001t0123g0070 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3709-2685C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40297770 | |||||||
| chr22:40297905 | A | G | 1 | a0001c0001t0002g0281 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3709-2550A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40297905 | |||||||
| chr22:40297986 | A | T | 7 | a0001c0001t0024g0137 a0001c0001t0052g0002 a0001c0001t0053g0136 others(4): Show |
7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3709-2469A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40297986 | |||||||
| chr22:40298009 | C | T | 1 | a0001c0001t0013g0247 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3709-2446C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298009 | |||||||
| chr22:40298018 | G | T | 4 | a0001c0001t0016g0086 a0001c0001t0016g0087 a0001c0001t0016g0088 others(1): Show |
4 | HG02055.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3709-2437G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298018 | |||||||
| chr22:40298125 | AAAAAAT | A | 10 | a0001c0001t0015g0140 a0001c0001t0015g0141 a0001c0001t0046g0153 others(7): Show |
10 | HG02280.hp2 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.3709-2308_3709-230 others(10): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40298125 | ||||||
| chr22:40298164 | AT | A | 3 | a0001c0001t0012g0169 a0001c0001t0015g0174 a0001c0001t0021g0170 |
3 | HG02630.hp2 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3709-2289delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40298164 | ||||||
| chr22:40298166 | T | A | 215 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(212): Show |
215 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.3709-2289T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298166 | |||||||
| chr22:40298174 | A | C | 3 | a0002c0002t0032g0128 a0002c0002t0032g0129 a0002c0002t0041g0127 |
3 | HG03239.hp2 HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.3709-2281A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298174 | |||||||
| chr22:40298311 | C | A | 301 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(298): Show |
301 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.3709-2144C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298311 | |||||||
| chr22:40298456 | A | T | 1 | a0001c0001t0133g0031 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3709-1999A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298456 | |||||||
| chr22:40298458 | G | A | 2 | a0001c0001t0003g0072 a0001c0001t0038g0073 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3709-1997G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298458 | |||||||
| chr22:40298590 | T | C | 1 | a0001c0001t0035g0148 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3709-1865T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298590 | |||||||
| chr22:40298594 | G | A | 6 | a0001c0001t0015g0140 a0001c0001t0015g0141 a0001c0001t0046g0153 others(3): Show |
6 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.3709-1861G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298594 | |||||||
| chr22:40298715 | T | C | 230 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(227): Show |
230 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.3709-1740T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298715 | |||||||
| chr22:40298723 | T | C | 144 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(141): Show |
144 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.3709-1732T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298723 | |||||||
| chr22:40298794 | G | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3709-1661G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298794 | |||||||
| chr22:40298822 | C | T | 1 | a0001c0001t0042g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3709-1633C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298822 | |||||||
| chr22:40298839 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3709-1616G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40298839 | |||||||
| chr22:40299144 | C | CA | 12 | a0001c0001t0002g0281 a0001c0001t0005g0190 a0001c0001t0015g0141 others(9): Show |
12 | HG00140.hp2 HG00438.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.3709-1298dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40299144 | ||||||
| chr22:40299152 | A | C | 1 | a0001c0001t0047g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3709-1303A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299152 | |||||||
| chr22:40299153 | A | C | 9 | a0001c0001t0002g0262 a0001c0001t0002g0263 a0001c0001t0002g0274 others(6): Show |
9 | HG01884.hp1 HG02083.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.3709-1302A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299153 | |||||||
| chr22:40299154 | A | C | 2 | a0001c0001t0089g0150 a0002c0002t0151g0111 |
2 | HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3709-1301A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299154 | |||||||
| chr22:40299158 | C | A | 2 | a0001c0001t0002g0281 a0001c0001t0143g0180 |
2 | HG01106.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3709-1297C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299158 | |||||||
| chr22:40299158 | C | CA | 9 | a0001c0001t0002g0302 a0001c0001t0010g0308 a0001c0001t0042g0003 others(6): Show |
9 | HG00438.hp2 HG02074.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.3709-1281dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40299158 | ||||||
| chr22:40299162 | A | C | 4 | a0001c0001t0002g0242 a0001c0001t0002g0307 a0001c0001t0033g0146 others(1): Show |
4 | HG01109.hp1 HG03540.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3709-1293A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299162 | |||||||
| chr22:40299163 | A | C | 151 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(148): Show |
151 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.3709-1292A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299163 | |||||||
| chr22:40299165 | A | C | 2 | a0001c0001t0015g0140 a0001c0001t0049g0142 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3709-1290A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299165 | |||||||
| chr22:40299168 | A | C | 142 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(139): Show |
142 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.3709-1287A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299168 | |||||||
| chr22:40299170 | A | C | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3709-1285A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299170 | |||||||
| chr22:40299175 | C | A | 1 | a0001c0001t0078g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3709-1280C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299175 | |||||||
| chr22:40299240 | C | CT | 8 | a0001c0001t0014g0059 a0001c0001t0030g0221 a0001c0001t0035g0143 others(5): Show |
8 | HG00741.hp2 HG01175.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.3709-1199dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | 40299240 | ||||||
| chr22:40299360 | C | G | 142 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(139): Show |
142 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.3709-1095C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299360 | |||||||
| chr22:40299375 | G | T | 1 | a0002c0002t0009g0117 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3709-1080G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299375 | |||||||
| chr22:40299436 | T | G | 4 | a0001c0001t0002g0242 a0001c0001t0002g0296 a0001c0001t0002g0304 others(1): Show |
4 | NA18977.hp2 NA19005.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.3709-1019T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299436 | |||||||
| chr22:40299510 | A | T | 1 | a0002c0002t0096g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3709-945A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299510 | |||||||
| chr22:40299555 | A | G | 1 | a0001c0001t0045g0062 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3709-900A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299555 | |||||||
| chr22:40299625 | G | A | 1 | a0001c0001t0011g0011 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3709-830G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299625 | |||||||
| chr22:40299657 | T | G | 2 | a0002c0002t0107g0099 a0002c0002t0157g0107 |
2 | HG01934.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3709-798T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299657 | |||||||
| chr22:40299751 | G | A | 44 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(41): Show |
44 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.3709-704G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40299751 | |||||||
| chr22:40300019 | T | G | 2 | a0001c0001t0086g0213 a0001c0001t0108g0145 |
2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3709-436T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | chr22 | 40300019 | |||||||
| chr22:40300877 | T | A | 3 | a0001c0001t0039g0165 a0001c0001t0115g0090 a0001c0001t0128g0085 |
3 | HG02145.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3841-33T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 13/22 | chr22 | 40300877 | |||||||
| chr22:40301077 | A | G | 1 | a0001c0001t0008g0289 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3936+72A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 14/22 | chr22 | 40301077 | |||||||
| chr22:40301086 | C | T | 1 | a0001c0001t0004g0205 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3937-64C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 14/22 | chr22 | 40301086 | |||||||
| chr22:40301109 | G | A | 4 | a0001c0001t0015g0140 a0001c0001t0015g0141 a0001c0001t0048g0139 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3937-41G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 14/22 | chr22 | 40301109 | |||||||
| chr22:40301373 | A | G | 142 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(139): Show |
142 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.4120+40A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40301373 | |||||||
| chr22:40301401 | A | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4120+68A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40301401 | |||||||
| chr22:40301529 | T | C | 1 | a0001c0001t0076g0243 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4120+196T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40301529 | |||||||
| chr22:40301577 | C | T | 226 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(223): Show |
226 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.4120+244C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40301577 | |||||||
| chr22:40301585 | T | G | 144 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(141): Show |
144 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.4120+252T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40301585 | |||||||
| chr22:40301587 | G | T | 9 | a0001c0001t0006g0151 a0001c0001t0010g0295 a0001c0001t0033g0146 others(6): Show |
9 | HG01109.hp1 HG01361.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.4120+254G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40301587 | |||||||
| chr22:40301603 | C | G | 2 | a0001c0001t0086g0213 a0001c0001t0108g0145 |
2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.4120+270C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40301603 | |||||||
| chr22:40301691 | A | G | 4 | a0001c0001t0015g0140 a0001c0001t0015g0141 a0001c0001t0048g0139 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4120+358A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40301691 | |||||||
| chr22:40302089 | C | A | 1 | a0001c0001t0018g0079 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.4120+756C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302089 | |||||||
| chr22:40302260 | C | A | 1 | a0001c0001t0035g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4120+927C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302260 | |||||||
| chr22:40302277 | T | A | 1 | a0001c0001t0114g0081 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4120+944T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302277 | |||||||
| chr22:40302278 | C | A | 1 | a0001c0001t0088g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4120+945C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302278 | |||||||
| chr22:40302309 | T | TAAATGTA others(30): Show |
1 | a0002c0002t0032g0128 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4120+976_4120+977i others(39): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302309 | |||||||
| chr22:40302358 | C | T | 1 | a0001c0001t0002g0270 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4120+1025C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302358 | |||||||
| chr22:40302361 | G | A | 1 | a0001c0001t0026g0283 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4120+1028G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302361 | |||||||
| chr22:40302389 | C | G | 4 | a0001c0001t0016g0086 a0001c0001t0016g0087 a0001c0001t0016g0088 others(1): Show |
4 | HG02055.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.4120+1056C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302389 | |||||||
| chr22:40302431 | G | A | 1 | a0001c0001t0002g0270 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4120+1098G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302431 | |||||||
| chr22:40302564 | C | T | 1 | a0002c0002t0099g0125 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4120+1231C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302564 | |||||||
| chr22:40302632 | CAAAAAAA others(2): Show |
C | 43 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(40): Show |
43 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.4120+1310_4120+131 others(13): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr22 | 40302632 | ||||||
| chr22:40302714 | G | A | 2 | a0001c0001t0015g0141 a0001c0001t0048g0139 |
2 | HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.4120+1381G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40302714 | |||||||
| chr22:40303021 | C | CCTT | 14 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(11): Show |
14 | HG01069.hp2 HG01071.hp2 HG03195.hp2 others(11): Show |
intron_variant | MODIFIER | c.4120+1713_4120+171 others(7): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr22 | 40303021 | ||||||
| chr22:40303021 | CCTTCTT | C | 39 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(36): Show |
39 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.4120+1710_4120+171 others(10): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr22 | 40303021 | ||||||
| chr22:40303041 | TTCTTC | T | 11 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(8): Show |
11 | HG02071.hp2 HG02083.hp1 HG03834.hp2 others(8): Show |
intron_variant | MODIFIER | c.4120+1710_4120+171 others(9): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr22 | 40303041 | ||||||
| chr22:40303046 | C | CT | 8 | a0001c0001t0001g0051 a0001c0001t0002g0235 a0001c0001t0003g0054 others(5): Show |
8 | HG02027.hp2 HG02129.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.4120+1734dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr22 | 40303046 | ||||||
| chr22:40303046 | CT | C | 65 | a0001c0001t0001g0286 a0001c0001t0006g0135 a0001c0001t0006g0151 others(62): Show |
65 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.4120+1734delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr22 | 40303046 | ||||||
| chr22:40303089 | G | A | 49 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(46): Show |
49 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.4120+1756G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40303089 | |||||||
| chr22:40303133 | G | T | 1 | a0002c0002t0032g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4120+1800G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40303133 | |||||||
| chr22:40303261 | G | A | 2 | a0002c0002t0036g0012 a0008c0011t0006g0094 |
2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4120+1928G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40303261 | |||||||
| chr22:40303273 | A | T | 2 | a0002c0002t0036g0012 a0008c0011t0006g0094 |
2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4120+1940A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40303273 | |||||||
| chr22:40303276 | G | T | 4 | a0001c0001t0086g0213 a0001c0001t0108g0145 a0002c0002t0036g0012 others(1): Show |
4 | HG02615.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4120+1943G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40303276 | |||||||
| chr22:40303277 | T | C | 2 | a0002c0002t0036g0012 a0008c0011t0006g0094 |
2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4120+1944T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40303277 | |||||||
| chr22:40303278 | G | C | 2 | a0002c0002t0036g0012 a0008c0011t0006g0094 |
2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4120+1945G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40303278 | |||||||
| chr22:40303586 | T | C | 1 | a0001c0001t0122g0067 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4120+2253T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40303586 | |||||||
| chr22:40304349 | G | A | 1 | a0001c0001t0018g0079 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.4120+3016G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40304349 | |||||||
| chr22:40304433 | A | G | 1 | a0001c0001t0131g0027 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.4120+3100A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40304433 | |||||||
| chr22:40304530 | G | A | 7 | a0001c0001t0024g0137 a0001c0001t0052g0002 a0001c0001t0053g0136 others(4): Show |
7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.4120+3197G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40304530 | |||||||
| chr22:40304610 | C | T | 3 | a0002c0002t0034g0010 a0002c0002t0084g0008 a0002c0002t0094g0009 |
3 | HG02145.hp1 HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4120+3277C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40304610 | |||||||
| chr22:40304894 | A | G | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4120+3561A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40304894 | |||||||
| chr22:40304932 | C | T | 1 | a0012c0018t0005g0198 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.4121-3580C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40304932 | |||||||
| chr22:40305225 | G | A | 1 | a0001c0001t0108g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4121-3287G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40305225 | |||||||
| chr22:40305431 | G | A | 1 | a0001c0001t0051g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4121-3081G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40305431 | |||||||
| chr22:40305512 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.4121-3000A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40305512 | |||||||
| chr22:40305833 | A | G | 47 | a0001c0001t0001g0219 a0001c0001t0004g0179 a0001c0001t0004g0181 others(44): Show |
47 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.4121-2679A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40305833 | |||||||
| chr22:40306044 | G | A | 1 | a0002c0002t0103g0108 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4121-2468G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40306044 | |||||||
| chr22:40306059 | G | A | 1 | a0001c0001t0074g0222 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4121-2453G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40306059 | |||||||
| chr22:40306070 | C | T | 1 | a0001c0001t0013g0247 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.4121-2442C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40306070 | |||||||
| chr22:40306119 | C | T | 2 | a0001c0001t0035g0143 a0001c0001t0075g0164 |
2 | HG01891.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.4121-2393C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40306119 | |||||||
| chr22:40306252 | G | A | 1 | a0001c0001t0131g0027 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.4121-2260G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40306252 | |||||||
| chr22:40306291 | CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0047g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4121-2209_4121-219 others(21): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr22 | 40306291 | ||||||
| chr22:40306815 | G | T | 1 | a0002c0002t0096g0005 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4121-1697G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40306815 | |||||||
| chr22:40307071 | T | G | 95 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(92): Show |
95 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.4121-1441T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40307071 | |||||||
| chr22:40307089 | T | C | 1 | a0001c0001t0006g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4121-1423T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40307089 | |||||||
| chr22:40307241 | A | G | 148 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
148 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.4121-1271A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40307241 | |||||||
| chr22:40307279 | C | G | 6 | a0001c0001t0006g0151 a0001c0001t0033g0146 a0001c0001t0035g0148 others(3): Show |
6 | HG01109.hp1 HG02258.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.4121-1233C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40307279 | |||||||
| chr22:40307566 | G | A | 3 | a0001c0001t0033g0146 a0001c0001t0035g0148 a0001c0001t0093g0147 |
3 | HG01109.hp1 HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4121-946G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40307566 | |||||||
| chr22:40307884 | C | G | 55 | a0001c0001t0024g0137 a0001c0001t0034g0091 a0001c0001t0052g0002 others(52): Show |
55 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.4121-628C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40307884 | |||||||
| chr22:40307885 | G | A | 1 | a0001c0001t0007g0293 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.4121-627G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40307885 | |||||||
| chr22:40307954 | T | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4121-558T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40307954 | |||||||
| chr22:40307971 | C | G | 1 | a0001c0001t0005g0191 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.4121-541C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40307971 | |||||||
| chr22:40308048 | C | T | 217 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(214): Show |
217 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.4121-464C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40308048 | |||||||
| chr22:40308167 | G | T | 3 | a0002c0002t0032g0128 a0002c0002t0032g0129 a0002c0002t0041g0127 |
3 | HG03239.hp2 HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.4121-345G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40308167 | |||||||
| chr22:40308265 | G | C | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4121-247G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40308265 | |||||||
| chr22:40308467 | A | G | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4121-45A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 15/22 | chr22 | 40308467 | |||||||
| chr22:40308895 | C | T | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4258+246C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 16/22 | chr22 | 40308895 | |||||||
| chr22:40309086 | T | G | 1 | a0001c0001t0086g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4258+437T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 16/22 | chr22 | 40309086 | |||||||
| chr22:40310035 | C | T | 1 | a0001c0001t0114g0081 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4259-782C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 16/22 | chr22 | 40310035 | |||||||
| chr22:40310071 | C | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0003g0163 |
3 | NA18986.hp2 NA18998.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.4259-746C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 16/22 | chr22 | 40310071 | |||||||
| chr22:40310101 | C | T | 1 | a0001c0001t0002g0270 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4259-716C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 16/22 | chr22 | 40310101 | |||||||
| chr22:40310261 | G | A | 1 | a0001c0001t0014g0057 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.4259-556G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 16/22 | chr22 | 40310261 | |||||||
| chr22:40310632 | G | A | 7 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(4): Show |
7 | NA18612.hp2 NA18943.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.4259-185G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 16/22 | chr22 | 40310632 | |||||||
| chr22:40310677 | G | A | 2 | a0002c0002t0104g0118 a0002c0002t0105g0119 |
2 | HG01257.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.4259-140G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 16/22 | chr22 | 40310677 | |||||||
| chr22:40311227 | T | C | 1 | a0001c0001t0088g0138 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4435+234T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 17/22 | chr22 | 40311227 | |||||||
| chr22:40311654 | G | A | 1 | a0001c0001t0002g0270 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4435+661G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 17/22 | chr22 | 40311654 | |||||||
| chr22:40311687 | G | A | 1 | a0001c0001t0044g0060 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.4435+694G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 17/22 | chr22 | 40311687 | |||||||
| chr22:40311824 | T | C | 48 | a0001c0001t0001g0219 a0001c0001t0004g0179 a0001c0001t0004g0181 others(45): Show |
48 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.4436-681T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 17/22 | chr22 | 40311824 | |||||||
| chr22:40311835 | G | T | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4436-670G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 17/22 | chr22 | 40311835 | |||||||
| chr22:40311839 | G | A | 15 | a0001c0001t0015g0140 a0001c0001t0015g0141 a0001c0001t0015g0174 others(12): Show |
15 | HG02559.hp2 HG02622.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.4436-666G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 17/22 | chr22 | 40311839 | |||||||
| chr22:40311909 | G | T | 1 | a0001c0001t0001g0036 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4436-596G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 17/22 | chr22 | 40311909 | |||||||
| chr22:40312309 | T | C | 2 | a0002c0002t0083g0093 a0002c0002t0097g0113 |
2 | HG00639.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4436-196T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 17/22 | chr22 | 40312309 | |||||||
| chr22:40312403 | G | A | 1 | a0001c0001t0135g0177 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4436-102G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 17/22 | chr22 | 40312403 | |||||||
| chr22:40312675 | T | C | 142 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(139): Show |
142 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.4582+24T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 18/22 | chr22 | 40312675 | |||||||
| chr22:40312784 | T | G | 7 | a0001c0001t0015g0140 a0001c0001t0015g0141 a0001c0001t0015g0174 others(4): Show |
7 | HG02559.hp2 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.4583-118T>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 18/22 | chr22 | 40312784 | |||||||
| chr22:40313107 | G | A | 1 | a0002c0002t0034g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4678+110G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40313107 | |||||||
| chr22:40313196 | C | T | 1 | a0001c0001t0012g0182 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.4678+199C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40313196 | |||||||
| chr22:40313339 | C | A | 1 | a0001c0001t0020g0211 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4678+342C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40313339 | |||||||
| chr22:40313655 | T | C | 1 | a0001c0001t0068g0285 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4678+658T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40313655 | |||||||
| chr22:40313905 | C | T | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4678+908C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40313905 | |||||||
| chr22:40314191 | C | T | 6 | a0001c0001t0014g0057 a0001c0001t0014g0058 a0001c0001t0014g0059 others(3): Show |
6 | HG00280.hp1 HG00423.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.4679-1092C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40314191 | |||||||
| chr22:40314309 | C | T | 1 | a0001c0001t0004g0205 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.4679-974C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40314309 | |||||||
| chr22:40314651 | T | C | 2 | a0001c0001t0086g0213 a0001c0001t0108g0145 |
2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.4679-632T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40314651 | |||||||
| chr22:40314715 | A | T | 1 | a0001c0001t0013g0290 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.4679-568A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40314715 | |||||||
| chr22:40314948 | C | T | 1 | a0001c0001t0148g0068 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4679-335C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40314948 | |||||||
| chr22:40315113 | A | G | 7 | a0001c0001t0024g0137 a0001c0001t0052g0002 a0001c0001t0053g0136 others(4): Show |
7 | HG02717.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.4679-170A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40315113 | |||||||
| chr22:40315223 | A | AT | 102 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(99): Show |
102 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.4679-57dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr22 | 40315223 | ||||||
| chr22:40315244 | G | A | 7 | a0001c0001t0004g0179 a0001c0001t0004g0184 a0001c0001t0004g0187 others(4): Show |
7 | HG00544.hp2 HG02523.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.4679-39G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 19/22 | chr22 | 40315244 | |||||||
| chr22:40315602 | A | C | 2 | a0001c0001t0001g0219 a0001c0001t0130g0162 |
2 | HG02129.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.4903+95A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 20/22 | chr22 | 40315602 | |||||||
| chr22:40315616 | G | T | 85 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(82): Show |
85 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.4903+109G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 20/22 | chr22 | 40315616 | |||||||
| chr22:40315862 | A | G | 1 | a0001c0001t0002g0294 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4904-80A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 20/22 | chr22 | 40315862 | |||||||
| chr22:40316126 | G | A | 1 | a0001c0001t0043g0157 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4974+114G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40316126 | |||||||
| chr22:40316196 | T | TA | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
5 | NA18612.hp2 NA18943.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.4974+185dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr22 | 40316196 | ||||||
| chr22:40316227 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.4974+215G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40316227 | |||||||
| chr22:40316278 | C | T | 1 | a0001c0001t0143g0180 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4974+266C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40316278 | |||||||
| chr22:40316353 | C | CA | 12 | a0001c0001t0005g0191 a0001c0001t0015g0140 a0001c0001t0015g0141 others(9): Show |
12 | HG01884.hp1 HG02015.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.4974+352dupA | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr22 | 40316353 | ||||||
| chr22:40316435 | G | A | 5 | a0001c0001t0003g0072 a0001c0001t0037g0076 a0001c0001t0037g0077 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.4974+423G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40316435 | |||||||
| chr22:40316455 | C | T | 1 | a0001c0001t0123g0070 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4974+443C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40316455 | |||||||
| chr22:40316470 | A | C | 3 | a0003c0004t0019g0207 a0003c0004t0019g0208 a0003c0004t0136g0209 |
3 | HG01175.hp1 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.4974+458A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40316470 | |||||||
| chr22:40316488 | C | A | 1 | a0001c0001t0114g0081 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4974+476C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40316488 | |||||||
| chr22:40316633 | G | A | 136 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(133): Show |
136 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.4974+621G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40316633 | |||||||
| chr22:40316649 | A | G | 2 | a0001c0001t0027g0256 a0001c0001t0028g0284 |
2 | NA18939.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.4974+637A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40316649 | |||||||
| chr22:40316764 | G | T | 1 | a0001c0001t0003g0013 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4974+752G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40316764 | |||||||
| chr22:40317041 | C | T | 1 | a0001c0001t0002g0228 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4974+1029C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40317041 | |||||||
| chr22:40317077 | A | G | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4974+1065A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40317077 | |||||||
| chr22:40317555 | C | A | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4974+1543C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40317555 | |||||||
| chr22:40317612 | T | C | 4 | a0002c0002t0006g0097 a0002c0002t0009g0104 a0002c0002t0100g0098 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.4974+1600T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40317612 | |||||||
| chr22:40317616 | C | T | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4974+1604C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40317616 | |||||||
| chr22:40317801 | G | A | 41 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(38): Show |
41 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.4974+1789G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40317801 | |||||||
| chr22:40317857 | T | A | 220 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(217): Show |
220 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.4974+1845T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40317857 | |||||||
| chr22:40317879 | A | G | 1 | a0001c0001t0010g0295 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.4974+1867A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40317879 | |||||||
| chr22:40317911 | A | G | 1 | a0001c0001t0003g0054 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.4974+1899A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40317911 | |||||||
| chr22:40318105 | C | T | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4974+2093C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318105 | |||||||
| chr22:40318130 | G | T | 1 | a0001c0001t0003g0215 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4974+2118G>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318130 | |||||||
| chr22:40318148 | C | T | 1 | a0001c0001t0003g0013 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4974+2136C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318148 | |||||||
| chr22:40318177 | A | G | 1 | a0001c0001t0042g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4974+2165A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318177 | |||||||
| chr22:40318274 | A | G | 1 | a0001c0001t0029g0238 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.4974+2262A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318274 | |||||||
| chr22:40318352 | C | G | 2 | a0001c0001t0003g0072 a0001c0001t0038g0073 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.4974+2340C>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318352 | |||||||
| chr22:40318363 | T | C | 6 | a0001c0001t0022g0126 a0001c0001t0022g0201 a0001c0001t0022g0202 others(3): Show |
6 | HG02602.hp1 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.4974+2351T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318363 | |||||||
| chr22:40318560 | T | A | 1 | a0007c0019t0095g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4975-2530T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318560 | |||||||
| chr22:40318771 | A | G | 1 | a0001c0001t0011g0052 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.4975-2319A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318771 | |||||||
| chr22:40318869 | C | T | 1 | a0001c0001t0042g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4975-2221C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318869 | |||||||
| chr22:40318964 | C | T | 7 | a0002c0002t0151g0111 a0002c0002t0152g0096 a0002c0002t0153g0109 others(4): Show |
7 | HG01243.hp2 HG01496.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.4975-2126C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40318964 | |||||||
| chr22:40319024 | T | C | 46 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(43): Show |
46 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.4975-2066T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319024 | |||||||
| chr22:40319026 | G | A | 1 | a0001c0001t0042g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4975-2064G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319026 | |||||||
| chr22:40319226 | C | A | 1 | a0002c0002t0087g0100 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4975-1864C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319226 | |||||||
| chr22:40319257 | C | T | 2 | a0001c0001t0002g0246 a0001c0001t0013g0247 |
2 | HG01516.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.4975-1833C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319257 | |||||||
| chr22:40319276 | A | C | 1 | a0001c0001t0029g0238 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.4975-1814A>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319276 | |||||||
| chr22:40319299 | A | G | 219 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(216): Show |
219 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.4975-1791A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319299 | |||||||
| chr22:40319411 | ACTTTT | A | 45 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0184 others(42): Show |
45 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.4975-1668_4975-166 others(9): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr22 | 40319411 | ||||||
| chr22:40319422 | C | CT | 15 | a0001c0001t0002g0228 a0001c0001t0002g0281 a0001c0001t0014g0057 others(12): Show |
15 | HG01261.hp2 HG01361.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.4975-1649dupT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr22 | 40319422 | ||||||
| chr22:40319422 | CT | C | 7 | a0001c0001t0003g0013 a0001c0001t0017g0006 a0001c0001t0028g0284 others(4): Show |
7 | HG01167.hp2 HG02165.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.4975-1649delT | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr22 | 40319422 | ||||||
| chr22:40319624 | C | T | 1 | a0001c0001t0012g0178 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4975-1466C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319624 | |||||||
| chr22:40319643 | C | T | 1 | a0001c0001t0035g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4975-1447C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319643 | |||||||
| chr22:40319661 | T | C | 15 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(12): Show |
15 | HG00408.hp1 HG02027.hp2 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.4975-1429T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319661 | |||||||
| chr22:40319845 | A | G | 1 | a0001c0001t0065g0224 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4975-1245A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319845 | |||||||
| chr22:40319873 | C | T | 1 | a0001c0001t0054g0132 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4975-1217C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319873 | |||||||
| chr22:40319899 | G | A | 6 | a0001c0001t0002g0239 a0001c0001t0002g0249 a0001c0001t0002g0251 others(3): Show |
6 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.4975-1191G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319899 | |||||||
| chr22:40319918 | C | T | 2 | a0001c0001t0010g0265 a0001c0001t0058g0264 |
2 | NA18986.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.4975-1172C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319918 | |||||||
| chr22:40319937 | G | A | 1 | a0001c0001t0007g0279 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4975-1153G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40319937 | |||||||
| chr22:40320053 | G | A | 4 | a0002c0002t0006g0144 a0002c0002t0036g0106 a0002c0002t0102g0105 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.4975-1037G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40320053 | |||||||
| chr22:40320251 | G | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4975-839G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40320251 | |||||||
| chr22:40320304 | A | G | 1 | a0001c0001t0042g0003 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4975-786A>G | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40320304 | |||||||
| chr22:40320352 | C | T | 2 | a0001c0001t0033g0146 a0001c0001t0093g0147 |
2 | HG01109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.4975-738C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40320352 | |||||||
| chr22:40320429 | G | A | 1 | a0001c0001t0011g0011 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.4975-661G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40320429 | |||||||
| chr22:40320484 | C | A | 131 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(128): Show |
131 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.4975-606C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40320484 | |||||||
| chr22:40320618 | G | A | 130 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(127): Show |
130 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.4975-472G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40320618 | |||||||
| chr22:40320618 | G | C | 59 | a0001c0001t0006g0135 a0001c0001t0006g0151 a0001c0001t0033g0146 others(56): Show |
59 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.4975-472G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40320618 | |||||||
| chr22:40320680 | G | C | 1 | a0001c0001t0086g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4975-410G>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40320680 | |||||||
| chr22:40320952 | C | A | 1 | a0001c0001t0054g0132 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4975-138C>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 21/22 | chr22 | 40320952 | |||||||
| chr22:40321239 | C | T | 2 | a0002c0002t0107g0099 a0002c0002t0157g0107 |
2 | HG01934.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5114+10C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40321239 | |||||||
| chr22:40321347 | C | T | 1 | a0001c0001t0008g0288 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.5114+118C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40321347 | |||||||
| chr22:40321380 | G | A | 1 | a0001c0001t0067g0236 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.5114+151G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40321380 | |||||||
| chr22:40321573 | G | A | 4 | a0001c0001t0015g0140 a0001c0001t0015g0141 a0001c0001t0048g0139 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.5114+344G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40321573 | |||||||
| chr22:40321655 | G | A | 2 | a0001c0001t0086g0213 a0001c0001t0108g0145 |
2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.5114+426G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40321655 | |||||||
| chr22:40321819 | C | T | 1 | a0002c0002t0006g0095 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5114+590C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40321819 | |||||||
| chr22:40321890 | G | A | 1 | a0001c0001t0007g0279 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.5114+661G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40321890 | |||||||
| chr22:40321976 | C | T | 1 | a0001c0001t0007g0300 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.5114+747C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40321976 | |||||||
| chr22:40321979 | A | T | 16 | a0001c0001t0015g0140 a0001c0001t0015g0141 a0001c0001t0015g0174 others(13): Show |
16 | HG01891.hp2 HG02559.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.5114+750A>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40321979 | |||||||
| chr22:40322096 | G | A | 83 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(80): Show |
83 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.5115-758G>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40322096 | |||||||
| chr22:40322349 | T | A | 2 | a0006c0006t0111g0214 a0006c0006t0112g0001 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.5115-505T>A | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40322349 | |||||||
| chr22:40322495 | C | T | 4 | a0001c0001t0022g0126 a0001c0001t0022g0201 a0001c0001t0022g0202 others(1): Show |
4 | HG02602.hp1 HG03834.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.5115-359C>T | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40322495 | |||||||
| chr22:40322768 | T | C | 1 | a0001c0001t0004g0184 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.5115-86T>C | TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 22/22 | chr22 | 40322768 |