Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6777 |
|---|---|
| ensemblid | ENSG00000173757.11 |
| hgncid | 11367 |
| symbol | STAT5B |
| name | signal transducer and activator of transcription 5B |
| refseq_nuc | NM_012448.4 |
| refseq_prot | NP_036580.2 |
| ensembl_nuc | ENST00000293328.8 |
| ensembl_prot | ENSP00000293328.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 42199177 |
| end | 42276391 |
| strand | - |
| ver | v1.2 |
| region | chr17:42199177-42276391 |
| region5000 | chr17:42194177-42281391 |
| regionname0 | STAT5B_chr17_42199177_42276391 |
| regionname5000 | STAT5B_chr17_42194177_42281391 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 787 | 255 | 82 | 35 | 94 | 8 | 34 | 63 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0002 | 0/0 | 787 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0003 | 0/0 | 787 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0004 | 0/0 | 787 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0005 | 0/0 | 787 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0006 | 0/0 | 787 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2364 | 246 | 78 | 35 | 93 | 8 | 30 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| c0002 | 0/0 | 2364 | 4 | 0 | 0 | 0 | 0 | 4 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| c0003 | 0/0 | 2364 | 2 | 2 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| c0004 | 0/0 | 2364 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| c0005 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| c0006 | 0/0 | 2364 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| c0007 | 0/0 | 2364 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| c0008 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| c0009 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| c0010 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| c0011 | 0/0 | 2364 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 2716 | 150 | 27 | 19 | 76 | 5 | 22 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0002 | 0/0 | 2714 | 17 | 14 | 2 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0003 | 0/0 | 2718 | 15 | 2 | 6 | 3 | 2 | 2 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0004 | 0/0 | 2712 | 10 | 1 | 3 | 4 | 1 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0005 | 0/1 | 2714 | 8 | 3 | 2 | 0 | 0 | 2 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0006 | 0/0 | 2712 | 7 | 1 | 1 | 5 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0007 | 0/0 | 2710 | 6 | 6 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0008 | 0/0 | 2714 | 6 | 4 | 2 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0009 | 0/0 | 2712 | 5 | 0 | 0 | 5 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0010 | 0/0 | 2716 | 5 | 5 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0011 | 0/0 | 2716 | 4 | 4 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0012 | 0/0 | 2716 | 4 | 1 | 0 | 1 | 0 | 2 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0013 | 0/0 | 2696 | 3 | 3 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0014 | 0/0 | 2716 | 3 | 3 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0015 | 0/0 | 2718 | 2 | 2 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0016 | 0/0 | 2716 | 2 | 0 | 0 | 0 | 0 | 2 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0017 | 0/0 | 2716 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0018 | 0/0 | 2714 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0019 | 0/0 | 2714 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0020 | 0/0 | 2714 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0021 | 0/0 | 2714 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0022 | 0/0 | 2714 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0023 | 0/0 | 2716 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0024 | 0/0 | 2664 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0025 | 0/0 | 2716 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0026 | 0/0 | 2716 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0027 | 0/0 | 2718 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0028 | 0/0 | 2714 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| t0029 | 0/0 | 2716 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0081 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0133 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2364 | 246 | 78 | 35 | 93 | 8 | 30 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0002 | 0/0 | 2364 | 4 | 0 | 0 | 0 | 0 | 4 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0003 | 0/0 | 2364 | 2 | 2 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0005 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0007 | 0/0 | 2364 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0009 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0002c0004 | 0/0 | 2364 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0003c0010 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0004c0006 | 0/0 | 2364 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0005c0008 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0006c0011 | 0/0 | 2364 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5079 | 143 | 27 | 18 | 74 | 5 | 18 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0002 | 0/0 | 5077 | 16 | 13 | 2 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0003 | 0/0 | 5081 | 14 | 2 | 6 | 2 | 2 | 2 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0004 | 0/0 | 5075 | 10 | 1 | 3 | 4 | 1 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0005 | 0/1 | 5077 | 8 | 3 | 2 | 0 | 0 | 2 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0006 | 0/0 | 5075 | 7 | 1 | 1 | 5 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0007 | 0/0 | 5073 | 6 | 6 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0008 | 0/0 | 5077 | 3 | 1 | 2 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0009 | 0/0 | 5075 | 5 | 0 | 0 | 5 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0010 | 0/0 | 5079 | 5 | 5 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0011 | 0/0 | 5079 | 4 | 4 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0012 | 0/0 | 5079 | 4 | 1 | 0 | 1 | 0 | 2 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0013 | 0/0 | 5059 | 3 | 3 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0014 | 0/0 | 5079 | 2 | 2 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0015 | 0/0 | 5081 | 2 | 2 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0016 | 0/0 | 5079 | 2 | 0 | 0 | 0 | 0 | 2 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0017 | 0/0 | 5079 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0018 | 0/0 | 5077 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0019 | 0/0 | 5077 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0020 | 0/0 | 5077 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0021 | 0/0 | 5077 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0022 | 0/0 | 5077 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0023 | 0/0 | 5079 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0025 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0026 | 0/0 | 5079 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0027 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0028 | 0/0 | 5077 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0001t0029 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0002t0001 | 0/0 | 5079 | 4 | 0 | 0 | 0 | 0 | 4 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0003t0008 | 0/0 | 5077 | 2 | 2 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0005t0024 | 0/0 | 5027 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0007t0001 | 0/0 | 5079 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0001c0009t0008 | 0/0 | 5077 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0002c0004t0003 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0003c0010t0002 | 0/0 | 5077 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0004c0006t0001 | 0/0 | 5079 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0005c0008t0014 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| a0006c0011t0001 | 0/0 | 5079 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | copy fasta | chr17 | 42194177 | 42281391 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0081 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0005g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0005g0133 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0006g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0006g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0006g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0006g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0007g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0007g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0007g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0007g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0008g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0008g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0009g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0009g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0009g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0009g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0009g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0010g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0010g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0010g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0010g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0010g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0011g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0011g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0011g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0011g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0012g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0012g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0012g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0012g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0013g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0013g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0013g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0014g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0014g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0015g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0015g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0016g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0016g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0017g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0018g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0019g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0020g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0021g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0022g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0023g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0025g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0026g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0027g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0028g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0029g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0003t0008g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0003t0008g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0005t0024g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0007t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0009t0008g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0002c0004t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0003c0010t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0004c0006t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0005c0008t0014g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0006c0011t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0049 | EUR | GBR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | GBR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00408 | hp1 | a0001 | c0001 | t0009 | g0144 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00423 | hp1 | a0002 | c0004 | t0003 | g0119 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00639 | hp1 | a0004 | c0006 | t0001 | g0078 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0099 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0057 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0096 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01109 | hp2 | a0001 | c0001 | t0023 | g0208 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0118 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0087 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0124 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01243 | hp2 | a0001 | c0001 | t0008 | g0155 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0095 | AMR | CLM | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | IBS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | IBS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | IBS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0094 | EUR | IBS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01884 | hp2 | a0001 | c0001 | t0013 | g0105 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | PEL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0257 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0138 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0242 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0129 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0136 | AMR | PEL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0117 | AMR | PEL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CDX | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02257 | hp1 | a0001 | c0001 | t0022 | g0143 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02257 | hp2 | a0001 | c0001 | t0012 | g0024 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02258 | hp2 | a0001 | c0001 | t0013 | g0104 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02572 | hp2 | a0001 | c0001 | t0015 | g0140 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02602 | hp1 | a0001 | c0001 | t0018 | g0017 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0113 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02630 | hp1 | a0001 | c0001 | t0028 | g0207 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02630 | hp2 | a0003 | c0010 | t0002 | g0240 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0146 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0111 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02698 | hp2 | a0001 | c0001 | t0012 | g0008 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0069 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02717 | hp2 | a0001 | c0001 | t0015 | g0106 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02723 | hp2 | a0001 | c0001 | t0020 | g0248 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0013 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0089 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0244 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02809 | hp2 | a0001 | c0003 | t0008 | g0159 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02818 | hp1 | a0001 | c0001 | t0025 | g0231 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02886 | hp1 | a0001 | c0001 | t0010 | g0020 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0245 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0246 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0243 | AFR | ESN | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02965 | hp1 | a0001 | c0001 | t0029 | g0206 | AFR | ESN | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02965 | hp2 | a0001 | c0001 | t0010 | g0021 | AFR | ESN | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02976 | hp1 | a0005 | c0008 | t0014 | g0198 | AFR | ESN | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03041 | hp2 | a0001 | c0001 | t0011 | g0224 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03098 | hp1 | a0001 | c0001 | t0014 | g0191 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03098 | hp2 | a0001 | c0001 | t0013 | g0139 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | ESN | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | ESN | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03209 | hp2 | a0001 | c0009 | t0008 | g0258 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0067 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03225 | hp2 | a0001 | c0001 | t0011 | g0210 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03490 | hp1 | a0001 | c0001 | t0012 | g0029 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0027 | SAS | STU | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0053 | SAS | STU | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0103 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03710 | hp2 | a0001 | c0001 | t0016 | g0212 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03831 | hp1 | a0001 | c0001 | t0017 | g0072 | SAS | BEB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0249 | SAS | BEB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03927 | hp1 | a0001 | c0001 | t0016 | g0225 | SAS | BEB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0228 | SAS | BEB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | STU | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | STU | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0137 | SAS | STU | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | STU | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0014 | SAS | STU | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | STU | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0066 | AFR | YRI | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18612 | hp2 | a0001 | c0007 | t0001 | g0166 | EAS | CHB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18906 | hp1 | a0001 | c0001 | t0014 | g0195 | AFR | YRI | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18939 | hp2 | a0001 | c0001 | t0027 | g0034 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18957 | hp1 | a0001 | c0001 | t0006 | g0256 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18964 | hp1 | a0001 | c0001 | t0009 | g0083 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18968 | hp2 | a0001 | c0001 | t0026 | g0180 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18975 | hp2 | a0006 | c0011 | t0001 | g0132 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18977 | hp1 | a0001 | c0001 | t0012 | g0178 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18977 | hp2 | a0001 | c0001 | t0006 | g0252 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18979 | hp2 | a0001 | c0001 | t0009 | g0084 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18999 | hp2 | a0001 | c0001 | t0009 | g0086 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19030 | hp1 | a0001 | c0005 | t0024 | g0107 | AFR | LWK | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19043 | hp1 | a0001 | c0001 | t0011 | g0211 | AFR | LWK | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | LWK | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19066 | hp1 | a0001 | c0001 | t0006 | g0254 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19067 | hp2 | a0001 | c0001 | t0009 | g0085 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19077 | hp1 | a0001 | c0001 | t0006 | g0253 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0172 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19091 | hp1 | a0001 | c0001 | t0006 | g0255 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ASW | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | ASW | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | TSI | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0151 | EUR | TSI | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | GIH | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | GIH | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0250 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02559 | hp1 | a0001 | c0001 | t0010 | g0023 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03471 | hp2 | a0001 | c0001 | t0021 | g0247 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG06807 | hp1 | a0001 | c0003 | t0008 | g0158 | AFR | USA | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | USA | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA20300 | hp1 | a0001 | c0001 | t0019 | g0234 | AFR | USA | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | USA | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA21309 | hp1 | a0001 | c0001 | t0008 | g0074 | AFR | LWK | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0229 | AFR | LWK | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0133 | REF | REF | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0081 | REF | REF | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:42207674
|
C | T | 1 | a0004 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.1961G>A | p.Arg654Gln | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/19 | 2115/5079 | 1961/2364 | 654/787 | chr17 | 42207674 | ||
| chr17:42210488
|
G | A | 1 | a0005 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1690C>T | p.Pro564Ser | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 14/19 | 1844/5079 | 1690/2364 | 564/787 | chr17 | 42210488 | ||
| chr17:42218745
|
T | A | 1 | a0003 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.967A>T | p.Ile323Phe | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 8/19 | 1121/5079 | 967/2364 | 323/787 | chr17 | 42218745 | ||
| chr17:42219830
|
G | T | 1 | a0002 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.563C>A | p.Pro188Gln | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 6/19 | 717/5079 | 563/2364 | 188/787 | chr17 | 42219830 | ||
| chr17:42219833
|
C | G | 1 | a0002 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.560G>C | p.Gly187Ala | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 6/19 | 714/5079 | 560/2364 | 187/787 | chr17 | 42219833 | ||
| chr17:42223543
|
G | A | 1 | a0006 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.389C>T | p.Ala130Val | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/19 | 543/5079 | 389/2364 | 130/787 | chr17 | 42223543 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:42210453
|
G | A | 1 | a0001c0007 | 1 | NA18612.hp2 | synonymous_variant | LOW | c.1725C>T | p.Asp575Asp | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 14/19 | 1879/5079 | 1725/2364 | 575/787 | chr17 | 42210453 | ||
| chr17:42217205
|
T | C | 1 | a0001c0009 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1335A>G | p.Glu445Glu | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 11/19 | 1489/5079 | 1335/2364 | 445/787 | chr17 | 42217205 | ||
| chr17:42218219
|
G | T | 1 | a0001c0002 | 4 | HG02698.hp1 HG02738.hp1 HG03710.hp1 others(1): Show |
synonymous_variant | LOW | c.1101C>A | p.Pro367Pro | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 9/19 | 1255/5079 | 1101/2364 | 367/787 | chr17 | 42218219 | ||
| chr17:42218327
|
C | T | 1 | a0001c0003 | 2 | HG02809.hp2 HG06807.hp1 |
synonymous_variant | LOW | c.993G>A | p.Thr331Thr | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 9/19 | 1147/5079 | 993/2364 | 331/787 | chr17 | 42218327 | ||
| chr17:42218794
|
G | T | 1 | a0001c0005 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.918C>A | p.Pro306Pro | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 8/19 | 1072/5079 | 918/2364 | 306/787 | chr17 | 42218794 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:42199227
|
TGTAACTC others(45): Show |
T | 1 | a0001c0005t0024 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2459_*2510delCTCA others(48): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 2459 | chr17 | 42199227 | |||||
| chr17:42199351
|
C | G | 1 | a0001c0001t0020 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2387G>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 2387 | chr17 | 42199351 | |||||
| chr17:42199419
|
C | T | 1 | a0001c0005t0024 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2319G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 2319 | chr17 | 42199419 | |||||
| chr17:42199493
|
G | A | 1 | a0001c0001t0021 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2245C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 2245 | chr17 | 42199493 | |||||
| chr17:42199570
|
A | G | 4 | a0001c0001t0013a0001c0001t0015a0001c0001t0022others(1): Show | 7 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2168T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 2168 | chr17 | 42199570 | |||||
| chr17:42200124
|
C | T | 2 | a0001c0001t0012a0001c0001t0023 | 5 | HG01109.hp2 HG02257.hp2 HG02698.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1614G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 1614 | chr17 | 42200124 | |||||
| chr17:42200563
|
G | A | 5 | a0001c0001t0002a0001c0001t0009a0001c0001t0019others(2): Show | 24 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1175C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 1175 | chr17 | 42200563 | |||||
| chr17:42200843
|
C | T | 1 | a0001c0001t0027 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*895G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 895 | chr17 | 42200843 | |||||
| chr17:42200844
|
G | A | 5 | a0001c0001t0013a0001c0001t0014a0001c0001t0015others(2): Show | 9 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*894C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 894 | chr17 | 42200844 | |||||
| chr17:42201168
|
C | T | 1 | a0001c0001t0019 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*570G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 570 | chr17 | 42201168 | |||||
| chr17:42201187
|
G | A | 2 | a0001c0001t0013a0001c0001t0015 | 5 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*551C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 551 | chr17 | 42201187 | |||||
| chr17:42201497
|
G | A | 1 | a0001c0001t0026 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*241C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 241 | chr17 | 42201497 | |||||
| chr17:42201513
|
C | T | 1 | a0001c0001t0018 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*225G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 225 | chr17 | 42201513 | |||||
| chr17:42201514
|
G | A | 1 | a0001c0001t0016 | 2 | HG03710.hp2 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*224C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 224 | chr17 | 42201514 | |||||
| chr17:42201524
|
G | GCA | 4 | a0001c0001t0003a0001c0001t0015a0001c0001t0027others(1): Show | 18 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*212_*213dupTG | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 213 | chr17 | 42201524 | |||||
| chr17:42201524
|
GCA | G | 12 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(9): Show | 37 | HG01167.hp1 HG01169.hp1 HG01192.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*212_*213delTG | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 212 | chr17 | 42201524 | |||||
| chr17:42201524
|
GCACA | G | 3 | a0001c0001t0004a0001c0001t0006a0001c0001t0009 | 22 | HG00140.hp1 HG00408.hp1 HG00733.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*210_*213delTGTG | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 210 | chr17 | 42201524 | |||||
| chr17:42201524
|
GCACACA | G | 1 | a0001c0001t0007 | 6 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*208_*213delTGTGTG | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 208 | chr17 | 42201524 | |||||
| chr17:42201524
|
GCACACAC others(13): Show |
G | 1 | a0001c0001t0013 | 3 | HG01884.hp2 HG02258.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*194_*213delTGTGTG others(14): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 194 | chr17 | 42201524 | |||||
| chr17:42201551
|
C | A | 1 | a0001c0001t0010 | 5 | HG02559.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*187G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 187 | chr17 | 42201551 | |||||
| chr17:42201704
|
A | G | 21 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(18): Show | 60 | HG00408.hp1 HG01109.hp2 HG01167.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*34T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 34 | chr17 | 42201704 | |||||
| chr17:42201726
|
G | A | 2 | a0001c0001t0028a0001c0001t0029 | 2 | HG02630.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 12 | chr17 | 42201726 | |||||
| chr17:42201727
|
A | C | 1 | a0001c0001t0017 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 19/19 | 11 | chr17 | 42201727 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:42202040
|
C | T | 6 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0013g0139others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2238-176G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 18/18 | chr17 | 42202040 | ||||||
| chr17:42202195
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2237+145G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 18/18 | chr17 | 42202195 | ||||||
| chr17:42202208
|
G | A | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2237+132C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 18/18 | chr17 | 42202208 | ||||||
| chr17:42202325
|
A | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2237+15T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 18/18 | chr17 | 42202325 | ||||||
| chr17:42202476
|
C | T | 1 | a0001c0001t0004g0089 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2130-29G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 17/18 | chr17 | 42202476 | ||||||
| chr17:42202540
|
G | T | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2130-93C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 17/18 | chr17 | 42202540 | ||||||
| chr17:42203389
|
G | A | 3 | a0001c0001t0008g0074a0001c0001t0008g0124a0001c0001t0018g0017 | 3 | HG01243.hp1 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2078-581C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42203389 | ||||||
| chr17:42203753
|
A | G | 1 | a0001c0007t0001g0166 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2078-945T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42203753 | ||||||
| chr17:42203840
|
T | A | 1 | a0001c0001t0003g0098 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2078-1032A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42203840 | ||||||
| chr17:42203959
|
C | A | 5 | a0001c0001t0011g0146a0001c0001t0011g0210a0001c0001t0011g0211others(2): Show | 5 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2078-1151G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42203959 | ||||||
| chr17:42203975
|
T | C | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2078-1167A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42203975 | ||||||
| chr17:42204001
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2078-1193C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42204001 | ||||||
| chr17:42204204
|
C | T | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2078-1396G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42204204 | ||||||
| chr17:42204294
|
A | G | 1 | a0001c0005t0024g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2078-1486T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42204294 | ||||||
| chr17:42204342
|
T | G | 11 | a0001c0001t0001g0097a0001c0001t0003g0091a0001c0001t0003g0092others(8): Show | 11 | HG00639.hp2 HG00642.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.2078-1534A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42204342 | ||||||
| chr17:42204435
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2078-1627A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42204435 | ||||||
| chr17:42204521
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2078-1713C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42204521 | ||||||
| chr17:42204845
|
C | A | 5 | a0001c0001t0011g0146a0001c0001t0011g0210a0001c0001t0011g0211others(2): Show | 5 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2078-2037G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42204845 | ||||||
| chr17:42205059
|
G | A | 1 | a0001c0001t0009g0144 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2078-2251C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42205059 | ||||||
| chr17:42205215
|
G | A | 9 | a0001c0001t0001g0114a0001c0001t0001g0174a0001c0001t0001g0175others(6): Show | 9 | HG00438.hp1 HG02074.hp1 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.2077+2343C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42205215 | ||||||
| chr17:42205316
|
C | A | 25 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0125others(22): Show | 25 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.2077+2242G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42205316 | ||||||
| chr17:42205351
|
T | TA | 38 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0022others(35): Show | 38 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.2077+2206dupT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42205351 | ||||||
| chr17:42205711
|
A | T | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2077+1847T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42205711 | ||||||
| chr17:42206066
|
G | T | 1 | a0001c0001t0008g0155 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2077+1492C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42206066 | ||||||
| chr17:42206209
|
T | C | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2077+1349A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42206209 | ||||||
| chr17:42206234
|
C | T | 3 | a0001c0001t0001g0112a0001c0001t0001g0156a0001c0001t0001g0157 | 3 | HG01891.hp1 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2077+1324G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42206234 | ||||||
| chr17:42206274
|
G | C | 1 | a0001c0001t0001g0028 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2077+1284C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42206274 | ||||||
| chr17:42206448
|
A | C | 24 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0125others(21): Show | 24 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.2077+1110T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42206448 | ||||||
| chr17:42206556
|
G | A | 3 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0215 | 3 | NA18970.hp2 NA19076.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.2077+1002C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42206556 | ||||||
| chr17:42206562
|
T | C | 4 | a0001c0001t0001g0112a0001c0001t0001g0154a0001c0001t0001g0156others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2077+996A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42206562 | ||||||
| chr17:42206581
|
C | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2077+977G>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42206581 | ||||||
| chr17:42206700
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2077+858G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42206700 | ||||||
| chr17:42206711
|
G | A | 1 | a0001c0001t0010g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2077+847C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42206711 | ||||||
| chr17:42206878
|
C | CT | 12 | a0001c0001t0001g0090a0001c0001t0001g0097a0001c0001t0002g0249others(9): Show | 12 | HG00642.hp1 HG01257.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.2077+679dupA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42206878 | ||||||
| chr17:42206878
|
CT | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(81): Show | 85 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.2077+679delA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42206878 | ||||||
| chr17:42207011
|
C | T | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2077+547G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42207011 | ||||||
| chr17:42207079
|
G | A | 5 | a0001c0001t0011g0146a0001c0001t0011g0210a0001c0001t0011g0211others(2): Show | 5 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2077+479C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42207079 | ||||||
| chr17:42207190
|
C | T | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2077+368G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42207190 | ||||||
| chr17:42207349
|
G | A | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2077+209C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42207349 | ||||||
| chr17:42207432
|
C | T | 2 | a0001c0001t0003g0149a0001c0001t0003g0151 | 2 | HG01993.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2077+126G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42207432 | ||||||
| chr17:42207461
|
A | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2077+97T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42207461 | ||||||
| chr17:42207487
|
G | GCA | 9 | a0001c0001t0003g0027a0001c0001t0011g0146a0001c0001t0011g0211others(6): Show | 9 | HG02647.hp1 HG02698.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.2077+69_2077+70dup others(2): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42207487 | ||||||
| chr17:42207487
|
GCA | G | 158 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(155): Show | 158 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.2077+69_2077+70del others(2): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42207487 | ||||||
| chr17:42207487
|
GCACA | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0108others(8): Show | 12 | HG01433.hp2 HG01884.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.2077+67_2077+70del others(4): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42207487 | ||||||
| chr17:42207487
|
GCACACA | G | 8 | a0001c0001t0001g0200a0001c0001t0003g0091a0001c0001t0003g0093others(5): Show | 8 | HG01192.hp1 HG01192.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2077+65_2077+70del others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42207487 | ||||||
| chr17:42207487
|
GCACACAC others(1): Show |
G | 7 | a0001c0001t0001g0097a0001c0001t0003g0094a0001c0001t0003g0096others(4): Show | 7 | HG00639.hp2 HG00642.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.2077+63_2077+70del others(8): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42207487 | ||||||
| chr17:42207493
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2077+65T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42207493 | ||||||
| chr17:42207495
|
A | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2077+63T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42207495 | ||||||
| chr17:42207497
|
A | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2077+61T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42207497 | ||||||
| chr17:42207521
|
ACAC | A | 38 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0125others(35): Show | 38 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.2077+34_2077+36del others(3): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42207521 | ||||||
| chr17:42207522
|
CACAA | C | 4 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0015g0106others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2077+32_2077+35del others(4): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42207522 | ||||||
| chr17:42207523
|
AC | A | 6 | a0001c0001t0004g0018a0001c0001t0006g0252a0001c0001t0006g0253others(3): Show | 6 | NA18957.hp1 NA18977.hp2 NA19066.hp1 others(3): Show |
intron_variant | MODIFIER | c.2077+34delG | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42207523 | ||||||
| chr17:42207526
|
A | C | 1 | a0001c0001t0022g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2077+32T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42207526 | ||||||
| chr17:42207546
|
G | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2077+12C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 16/18 | chr17 | 42207546 | ||||||
| chr17:42207894
|
C | T | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1907-166G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42207894 | ||||||
| chr17:42207919
|
G | A | 6 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0013g0139others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1907-191C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42207919 | ||||||
| chr17:42208043
|
C | T | 6 | a0001c0001t0007g0242a0001c0001t0007g0243a0001c0001t0007g0244others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1907-315G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42208043 | ||||||
| chr17:42208182
|
G | A | 1 | a0001c0001t0026g0180 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1907-454C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42208182 | ||||||
| chr17:42208184
|
G | C | 1 | a0001c0001t0001g0197 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1907-456C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42208184 | ||||||
| chr17:42208185
|
C | G | 1 | a0001c0001t0001g0197 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1907-457G>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42208185 | ||||||
| chr17:42208313
|
T | C | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1907-585A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42208313 | ||||||
| chr17:42208334
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1907-606A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42208334 | ||||||
| chr17:42208543
|
G | C | 1 | a0001c0001t0001g0148 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1907-815C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42208543 | ||||||
| chr17:42208546
|
G | C | 5 | a0001c0001t0011g0146a0001c0001t0011g0210a0001c0001t0011g0211others(2): Show | 5 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1907-818C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42208546 | ||||||
| chr17:42208683
|
C | T | 1 | a0001c0001t0004g0041 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1907-955G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42208683 | ||||||
| chr17:42208709
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1907-981T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42208709 | ||||||
| chr17:42208714
|
T | A | 1 | a0001c0001t0001g0197 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1907-986A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42208714 | ||||||
| chr17:42208717
|
G | T | 1 | a0001c0001t0001g0197 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1907-989C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42208717 | ||||||
| chr17:42208783
|
G | A | 1 | a0001c0001t0003g0053 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1907-1055C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42208783 | ||||||
| chr17:42208802
|
G | C | 1 | a0001c0001t0001g0197 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1907-1074C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42208802 | ||||||
| chr17:42208803
|
C | G | 1 | a0001c0001t0001g0197 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1907-1075G>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42208803 | ||||||
| chr17:42208873
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1907-1145T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42208873 | ||||||
| chr17:42209032
|
CT | C | 7 | a0001c0001t0008g0155a0001c0001t0013g0104a0001c0001t0013g0105others(4): Show | 7 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1906+1138delA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42209032 | ||||||
| chr17:42209090
|
A | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1906+1081T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42209090 | ||||||
| chr17:42209147
|
A | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1906+1024T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42209147 | ||||||
| chr17:42209344
|
C | T | 1 | a0001c0005t0024g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1906+827G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42209344 | ||||||
| chr17:42209618
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0033others(2): Show | 5 | HG00609.hp2 HG00673.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1906+553C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42209618 | ||||||
| chr17:42209667
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1906+504G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42209667 | ||||||
| chr17:42209897
|
G | A | 1 | a0001c0009t0008g0258 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1906+274C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42209897 | ||||||
| chr17:42209995
|
C | G | 1 | a0001c0001t0001g0153 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1906+176G>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42209995 | ||||||
| chr17:42210069
|
GTA | G | 6 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0013g0139others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1906+100_1906+101d others(4): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 15/18 | chr17 | 42210069 | ||||||
| chr17:42210676
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1681-179T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 13/18 | chr17 | 42210676 | ||||||
| chr17:42210690
|
A | T | 8 | a0001c0001t0006g0118a0001c0001t0006g0129a0001c0001t0006g0252others(5): Show | 8 | HG01175.hp1 HG02145.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.1681-193T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 13/18 | chr17 | 42210690 | ||||||
| chr17:42210725
|
C | G | 2 | a0001c0001t0012g0024a0001c0001t0012g0029 | 2 | HG02257.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1681-228G>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 13/18 | chr17 | 42210725 | ||||||
| chr17:42210772
|
G | A | 5 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0013g0139others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1681-275C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 13/18 | chr17 | 42210772 | ||||||
| chr17:42210913
|
G | A | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1681-416C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 13/18 | chr17 | 42210913 | ||||||
| chr17:42210922
|
C | A | 1 | a0001c0001t0001g0068 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1681-425G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 13/18 | chr17 | 42210922 | ||||||
| chr17:42210990
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0199 | 2 | HG02074.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1681-493G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 13/18 | chr17 | 42210990 | ||||||
| chr17:42211012
|
C | A | 5 | a0001c0001t0006g0118a0001c0001t0006g0129a0001c0001t0008g0074others(2): Show | 5 | HG01175.hp1 HG01243.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1681-515G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 13/18 | chr17 | 42211012 | ||||||
| chr17:42211086
|
G | A | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1681-589C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 13/18 | chr17 | 42211086 | ||||||
| chr17:42211094
|
A | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1681-597T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 13/18 | chr17 | 42211094 | ||||||
| chr17:42211105
|
A | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1681-608T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 13/18 | chr17 | 42211105 | ||||||
| chr17:42211183
|
G | A | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1681-686C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 13/18 | chr17 | 42211183 | ||||||
| chr17:42211278
|
C | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(235): Show | 239 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1680+706G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 13/18 | chr17 | 42211278 | ||||||
| chr17:42211362
|
G | C | 10 | a0001c0001t0006g0118a0001c0001t0006g0129a0001c0001t0006g0252others(7): Show | 10 | HG01175.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1680+622C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 13/18 | chr17 | 42211362 | ||||||
| chr17:42211398
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1680+586G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 13/18 | chr17 | 42211398 | ||||||
| chr17:42211449
|
T | C | 1 | a0001c0001t0007g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1680+535A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 13/18 | chr17 | 42211449 | ||||||
| chr17:42211545
|
T | C | 5 | a0001c0001t0011g0146a0001c0001t0011g0210a0001c0001t0011g0211others(2): Show | 5 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1680+439A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 13/18 | chr17 | 42211545 | ||||||
| chr17:42211778
|
G | A | 1 | a0001c0001t0022g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1680+206C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 13/18 | chr17 | 42211778 | ||||||
| chr17:42211873
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1680+111G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 13/18 | chr17 | 42211873 | ||||||
| chr17:42212448
|
A | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1474-258T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42212448 | ||||||
| chr17:42212580
|
C | T | 8 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0013g0139others(5): Show | 8 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1474-390G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42212580 | ||||||
| chr17:42212673
|
A | G | 1 | a0001c0001t0003g0047 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1474-483T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42212673 | ||||||
| chr17:42212698
|
G | A | 5 | a0001c0001t0006g0252a0001c0001t0006g0253a0001c0001t0006g0254others(2): Show | 5 | NA18957.hp1 NA18977.hp2 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.1474-508C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42212698 | ||||||
| chr17:42212847
|
C | T | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1474-657G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42212847 | ||||||
| chr17:42213155
|
T | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1474-965A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42213155 | ||||||
| chr17:42213185
|
A | T | 1 | a0001c0001t0001g0134 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1474-995T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42213185 | ||||||
| chr17:42213196
|
G | A | 1 | a0001c0001t0008g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1474-1006C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42213196 | ||||||
| chr17:42213530
|
T | C | 3 | a0001c0001t0008g0074a0001c0001t0008g0124a0001c0001t0018g0017 | 3 | HG01243.hp1 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1474-1340A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42213530 | ||||||
| chr17:42213582
|
C | A | 72 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0012others(69): Show | 72 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.1474-1392G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42213582 | ||||||
| chr17:42213666
|
C | T | 1 | a0001c0001t0010g0020 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1474-1476G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42213666 | ||||||
| chr17:42213668
|
T | C | 1 | a0001c0001t0010g0020 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1474-1478A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42213668 | ||||||
| chr17:42213776
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(255): Show | 259 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.1474-1586T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42213776 | ||||||
| chr17:42213856
|
G | A | 5 | a0001c0001t0010g0020a0001c0001t0010g0021a0001c0001t0010g0023others(2): Show | 5 | HG02559.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1474-1666C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42213856 | ||||||
| chr17:42214003
|
C | T | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1474-1813G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42214003 | ||||||
| chr17:42214096
|
T | C | 1 | a0001c0001t0007g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1474-1906A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42214096 | ||||||
| chr17:42214151
|
TA | T | 10 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0075others(7): Show | 10 | HG01167.hp1 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1473+1862delT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42214151 | ||||||
| chr17:42214171
|
A | G | 4 | a0001c0001t0001g0112a0001c0001t0001g0154a0001c0001t0001g0156others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1473+1843T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42214171 | ||||||
| chr17:42214413
|
A | AG | 11 | a0001c0001t0008g0074a0001c0001t0008g0124a0001c0001t0013g0104others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1473+1600_1473+160 others(5): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42214413 | ||||||
| chr17:42214633
|
GT | G | 6 | a0001c0001t0001g0205a0001c0001t0007g0229a0001c0001t0008g0155others(3): Show | 6 | HG01243.hp2 HG02630.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1473+1380delA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42214633 | ||||||
| chr17:42214635
|
T | C | 35 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0001g0148others(32): Show | 35 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1473+1379A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42214635 | ||||||
| chr17:42214662
|
G | A | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1473+1352C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42214662 | ||||||
| chr17:42214716
|
A | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1473+1298T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42214716 | ||||||
| chr17:42214874
|
C | A | 1 | a0001c0001t0001g0259 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1473+1140G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42214874 | ||||||
| chr17:42214875
|
C | G | 3 | a0001c0001t0014g0191a0001c0001t0014g0195a0005c0008t0014g0198 | 3 | HG02976.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1473+1139G>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42214875 | ||||||
| chr17:42214876
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1473+1138G>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42214876 | ||||||
| chr17:42214897
|
T | C | 6 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0013g0139others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1473+1117A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42214897 | ||||||
| chr17:42215012
|
T | C | 2 | a0001c0001t0002g0232a0001c0001t0002g0233 | 2 | HG02451.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1473+1002A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42215012 | ||||||
| chr17:42215077
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0153 | 3 | HG02559.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1473+937A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42215077 | ||||||
| chr17:42215163
|
C | G | 1 | a0001c0005t0024g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1473+851G>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42215163 | ||||||
| chr17:42215291
|
T | C | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1473+723A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42215291 | ||||||
| chr17:42215745
|
A | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0016others(63): Show | 67 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1473+269T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42215745 | ||||||
| chr17:42215832
|
G | C | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1473+182C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42215832 | ||||||
| chr17:42215852
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1473+162G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42215852 | ||||||
| chr17:42215899
|
A | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1473+115T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42215899 | ||||||
| chr17:42215972
|
G | A | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1473+42C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42215972 | ||||||
| chr17:42216123
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1381-17C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 11/18 | chr17 | 42216123 | ||||||
| chr17:42216165
|
CTT | C | 5 | a0001c0001t0011g0146a0001c0001t0011g0210a0001c0001t0011g0211others(2): Show | 5 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1381-61_1381-60del others(2): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 11/18 | chr17 | 42216165 | ||||||
| chr17:42216253
|
GAAT | G | 4 | a0001c0001t0001g0205a0001c0001t0008g0155a0001c0001t0028g0207others(1): Show | 4 | HG01243.hp2 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381-150_1381-148d others(5): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 11/18 | chr17 | 42216253 | ||||||
| chr17:42216421
|
T | A | 1 | a0001c0001t0008g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1381-315A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 11/18 | chr17 | 42216421 | ||||||
| chr17:42216647
|
G | A | 1 | a0001c0001t0011g0211 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1380+513C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 11/18 | chr17 | 42216647 | ||||||
| chr17:42216692
|
C | CT | 8 | a0001c0001t0001g0128a0001c0001t0006g0252a0001c0001t0013g0104others(5): Show | 8 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1380+467dupA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 11/18 | chr17 | 42216692 | ||||||
| chr17:42216718
|
T | A | 3 | a0001c0001t0004g0049a0001c0001t0004g0057a0001c0001t0004g0117 | 3 | HG00140.hp1 HG00741.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1380+442A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 11/18 | chr17 | 42216718 | ||||||
| chr17:42216932
|
A | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1380+228T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 11/18 | chr17 | 42216932 | ||||||
| chr17:42217130
|
C | T | 1 | a0001c0001t0012g0008 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1380+30G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 11/18 | chr17 | 42217130 | ||||||
| chr17:42217131
|
G | A | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1380+29C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 11/18 | chr17 | 42217131 | ||||||
| chr17:42217689
|
C | CT | 17 | a0001c0001t0001g0028a0001c0001t0001g0196a0001c0001t0002g0003others(14): Show | 17 | HG01169.hp1 HG01433.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1170-226dupA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 9/18 | chr17 | 42217689 | ||||||
| chr17:42217705
|
T | G | 1 | a0001c0001t0001g0227 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1170-241A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 9/18 | chr17 | 42217705 | ||||||
| chr17:42217708
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1170-244C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 9/18 | chr17 | 42217708 | ||||||
| chr17:42218524
|
C | T | 1 | a0001c0009t0008g0258 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.990-194G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 8/18 | chr17 | 42218524 | ||||||
| chr17:42218586
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.989+137G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 8/18 | chr17 | 42218586 | ||||||
| chr17:42218615
|
G | C | 3 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0003g0221 | 3 | NA18939.hp1 NA19003.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.989+108C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 8/18 | chr17 | 42218615 | ||||||
| chr17:42219013
|
C | A | 1 | a0001c0001t0001g0126 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.834-135G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 7/18 | chr17 | 42219013 | ||||||
| chr17:42219262
|
A | G | 1 | a0001c0001t0022g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.833+50T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 7/18 | chr17 | 42219262 | ||||||
| chr17:42219523
|
C | A | 1 | a0001c0001t0001g0114 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.682-60G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 6/18 | chr17 | 42219523 | ||||||
| chr17:42219566
|
A | G | 9 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0051others(6): Show | 9 | HG02258.hp1 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-103T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 6/18 | chr17 | 42219566 | ||||||
| chr17:42219847
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG01169.hp2 | splice_region_variant&intron_variant | LOW | c.551-5T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42219847 | ||||||
| chr17:42219852
|
G | A | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-10C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42219852 | ||||||
| chr17:42219854
|
G | A | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-12C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42219854 | ||||||
| chr17:42219880
|
C | T | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-38G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42219880 | ||||||
| chr17:42219890
|
C | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0033a0001c0001t0001g0070 | 3 | HG00609.hp2 HG00673.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.551-48G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42219890 | ||||||
| chr17:42219899
|
C | T | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-57G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42219899 | ||||||
| chr17:42219917
|
C | T | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-75G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42219917 | ||||||
| chr17:42219938
|
T | C | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-96A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42219938 | ||||||
| chr17:42219939
|
G | A | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-97C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42219939 | ||||||
| chr17:42219948
|
T | C | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-106A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42219948 | ||||||
| chr17:42219956
|
T | C | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-114A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42219956 | ||||||
| chr17:42219960
|
G | A | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-118C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42219960 | ||||||
| chr17:42219981
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.551-139C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42219981 | ||||||
| chr17:42220005
|
T | C | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-163A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220005 | ||||||
| chr17:42220009
|
C | T | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-167G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220009 | ||||||
| chr17:42220035
|
G | A | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-193C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220035 | ||||||
| chr17:42220155
|
G | T | 2 | a0001c0001t0001g0130a0002c0004t0003g0119 | 2 | HG00423.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.551-313C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220155 | ||||||
| chr17:42220184
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.551-342C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220184 | ||||||
| chr17:42220248
|
T | C | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-406A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220248 | ||||||
| chr17:42220249
|
G | A | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-407C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220249 | ||||||
| chr17:42220269
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.551-427C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220269 | ||||||
| chr17:42220280
|
G | A | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-438C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220280 | ||||||
| chr17:42220302
|
A | T | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-460T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220302 | ||||||
| chr17:42220304
|
T | G | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-462A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220304 | ||||||
| chr17:42220364
|
T | C | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.551-522A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220364 | ||||||
| chr17:42220378
|
G | C | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.551-536C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220378 | ||||||
| chr17:42220397
|
A | G | 3 | a0001c0001t0008g0074a0001c0001t0008g0124a0001c0001t0018g0017 | 3 | HG01243.hp1 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.551-555T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220397 | ||||||
| chr17:42220398
|
C | A | 1 | a0001c0001t0001g0222 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.551-556G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220398 | ||||||
| chr17:42220475
|
A | C | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-633T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220475 | ||||||
| chr17:42220498
|
A | C | 59 | a0001c0001t0001g0016a0001c0001t0001g0147a0001c0001t0001g0205others(56): Show | 59 | HG00408.hp1 HG00423.hp1 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.551-656T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220498 | ||||||
| chr17:42220515
|
A | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(81): Show | 85 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.551-673T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220515 | ||||||
| chr17:42220547
|
A | G | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-705T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220547 | ||||||
| chr17:42220581
|
A | G | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-739T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220581 | ||||||
| chr17:42220593
|
A | G | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-751T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220593 | ||||||
| chr17:42220601
|
A | G | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-759T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220601 | ||||||
| chr17:42220613
|
A | G | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-771T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220613 | ||||||
| chr17:42220615
|
C | G | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-773G>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220615 | ||||||
| chr17:42220618
|
G | A | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-776C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220618 | ||||||
| chr17:42220625
|
C | T | 1 | a0002c0004t0003g0119 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551-783G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220625 | ||||||
| chr17:42220648
|
A | G | 2 | a0001c0007t0001g0166a0002c0004t0003g0119 | 2 | HG00423.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.551-806T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220648 | ||||||
| chr17:42220721
|
C | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0161a0001c0001t0001g0203others(1): Show | 4 | HG01981.hp1 HG02735.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.551-879G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220721 | ||||||
| chr17:42220735
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.551-893C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220735 | ||||||
| chr17:42220758
|
G | T | 1 | a0001c0001t0004g0138 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.551-916C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220758 | ||||||
| chr17:42220822
|
A | G | 6 | a0001c0001t0001g0071a0001c0001t0011g0146a0001c0001t0011g0210others(3): Show | 6 | HG00558.hp2 HG01109.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.551-980T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220822 | ||||||
| chr17:42220824
|
C | T | 6 | a0001c0001t0001g0071a0001c0001t0011g0146a0001c0001t0011g0210others(3): Show | 6 | HG00558.hp2 HG01109.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.551-982G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220824 | ||||||
| chr17:42220835
|
G | A | 4 | a0001c0001t0011g0146a0001c0001t0011g0211a0001c0001t0011g0224others(1): Show | 4 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-993C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220835 | ||||||
| chr17:42220837
|
A | G | 4 | a0001c0001t0011g0146a0001c0001t0011g0211a0001c0001t0011g0224others(1): Show | 4 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-995T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220837 | ||||||
| chr17:42220840
|
A | G | 4 | a0001c0001t0011g0146a0001c0001t0011g0211a0001c0001t0011g0224others(1): Show | 4 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.551-998T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220840 | ||||||
| chr17:42220910
|
C | G | 1 | a0001c0001t0025g0231 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.551-1068G>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220910 | ||||||
| chr17:42220966
|
A | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(80): Show | 84 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.551-1124T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220966 | ||||||
| chr17:42220987
|
A | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(7): Show | 10 | HG00558.hp2 HG02027.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.551-1145T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42220987 | ||||||
| chr17:42221046
|
G | A | 1 | a0001c0003t0008g0158 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.551-1204C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42221046 | ||||||
| chr17:42221065
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(187): Show | 191 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.551-1223G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42221065 | ||||||
| chr17:42221240
|
C | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0070 | 2 | HG00609.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.551-1398G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42221240 | ||||||
| chr17:42221494
|
G | A | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.551-1652C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42221494 | ||||||
| chr17:42221567
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.551-1725C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42221567 | ||||||
| chr17:42221920
|
GTGTC | G | 6 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0013g0139others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.550+1458_550+1461d others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42221920 | ||||||
| chr17:42221966
|
TGTGTGGT others(18): Show |
T | 3 | a0001c0001t0008g0074a0001c0001t0008g0124a0001c0001t0018g0017 | 3 | HG01243.hp1 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.550+1391_550+1415d others(27): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42221966 | ||||||
| chr17:42221983
|
CTGTGTGT others(32): Show |
C | 2 | a0001c0001t0001g0031a0001c0001t0001g0116 | 2 | NA18962.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.550+1360_550+1398d others(41): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42221983 | ||||||
| chr17:42222075
|
G | A | 7 | a0001c0001t0006g0118a0001c0001t0006g0129a0001c0001t0006g0252others(4): Show | 7 | HG01175.hp1 HG02145.hp2 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.550+1307C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42222075 | ||||||
| chr17:42222459
|
T | C | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.550+923A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42222459 | ||||||
| chr17:42222680
|
A | AT | 11 | a0001c0001t0001g0182a0001c0001t0001g0184a0001c0001t0001g0209others(8): Show | 11 | HG01109.hp2 HG02056.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.550+701dupA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42222680 | ||||||
| chr17:42222680
|
AT | A | 11 | a0001c0001t0001g0060a0001c0001t0001g0121a0001c0001t0001g0135others(8): Show | 11 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.550+701delA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42222680 | ||||||
| chr17:42222721
|
G | A | 37 | a0001c0001t0001g0205a0001c0001t0002g0003a0001c0001t0002g0004others(34): Show | 37 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.550+661C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42222721 | ||||||
| chr17:42222872
|
C | T | 12 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0043others(9): Show | 12 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(9): Show |
intron_variant | MODIFIER | c.550+510G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42222872 | ||||||
| chr17:42222926
|
C | T | 3 | a0001c0001t0009g0084a0001c0001t0009g0085a0001c0001t0009g0086 | 3 | NA18979.hp2 NA18999.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.550+456G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42222926 | ||||||
| chr17:42223187
|
C | G | 60 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0002g0003others(57): Show | 60 | HG00408.hp1 HG01109.hp2 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.550+195G>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42223187 | ||||||
| chr17:42223188
|
G | C | 2 | a0001c0001t0002g0245a0001c0001t0002g0246 | 2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.550+194C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42223188 | ||||||
| chr17:42223263
|
T | G | 4 | a0001c0001t0001g0209a0001c0001t0011g0146a0001c0001t0011g0211others(1): Show | 4 | HG02647.hp1 HG03041.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.550+119A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42223263 | ||||||
| chr17:42223317
|
A | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.550+65T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 5/18 | chr17 | 42223317 | ||||||
| chr17:42223640
|
C | T | 7 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0236others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.376-84G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 4/18 | chr17 | 42223640 | ||||||
| chr17:42223698
|
C | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.376-142G>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 4/18 | chr17 | 42223698 | ||||||
| chr17:42223828
|
T | C | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.376-272A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 4/18 | chr17 | 42223828 | ||||||
| chr17:42223863
|
G | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0016others(123): Show | 127 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.376-307C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 4/18 | chr17 | 42223863 | ||||||
| chr17:42223978
|
A | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.376-422T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 4/18 | chr17 | 42223978 | ||||||
| chr17:42224133
|
C | T | 5 | a0001c0001t0009g0083a0001c0001t0009g0084a0001c0001t0009g0085others(2): Show | 5 | HG00408.hp1 NA18964.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.376-577G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 4/18 | chr17 | 42224133 | ||||||
| chr17:42224298
|
C | T | 1 | a0001c0001t0021g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.375+481G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 4/18 | chr17 | 42224298 | ||||||
| chr17:42224318
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.375+461C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 4/18 | chr17 | 42224318 | ||||||
| chr17:42224348
|
A | AT | 7 | a0001c0001t0001g0030a0001c0001t0013g0104a0001c0001t0013g0105others(4): Show | 7 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.375+430dupA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 4/18 | chr17 | 42224348 | ||||||
| chr17:42224417
|
G | T | 1 | a0001c0001t0001g0259 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.375+362C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 4/18 | chr17 | 42224417 | ||||||
| chr17:42225150
|
G | A | 10 | a0001c0001t0001g0090a0001c0001t0001g0097a0001c0001t0003g0091others(7): Show | 10 | HG00639.hp2 HG00642.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.286-282C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42225150 | ||||||
| chr17:42225362
|
G | A | 9 | a0001c0001t0001g0209a0001c0001t0008g0074a0001c0001t0008g0124others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.286-494C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42225362 | ||||||
| chr17:42225659
|
C | T | 6 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0013g0139others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-791G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42225659 | ||||||
| chr17:42226078
|
T | A | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.286-1210A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42226078 | ||||||
| chr17:42226155
|
G | A | 22 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0125others(19): Show | 22 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.286-1287C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42226155 | ||||||
| chr17:42226188
|
G | C | 6 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0013g0139others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-1320C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42226188 | ||||||
| chr17:42226260
|
T | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.285+1269A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42226260 | ||||||
| chr17:42226486
|
C | T | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.285+1043G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42226486 | ||||||
| chr17:42226499
|
G | C | 18 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0167others(15): Show | 18 | HG00423.hp2 HG02027.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.285+1030C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42226499 | ||||||
| chr17:42226692
|
C | T | 1 | a0001c0001t0008g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.285+837G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42226692 | ||||||
| chr17:42226808
|
CA | C | 10 | a0001c0001t0001g0042a0001c0001t0001g0193a0001c0001t0002g0236others(7): Show | 10 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.285+720delT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42226808 | ||||||
| chr17:42226971
|
C | CA | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0142others(4): Show | 7 | HG01243.hp2 HG02080.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+557dupT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42226971 | ||||||
| chr17:42227010
|
C | T | 3 | a0001c0001t0001g0097a0001c0001t0003g0094a0001c0001t0003g0098 | 3 | HG00642.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.285+519G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42227010 | ||||||
| chr17:42227026
|
T | C | 2 | a0001c0001t0002g0238a0001c0001t0002g0239 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.285+503A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42227026 | ||||||
| chr17:42227136
|
A | AAAAT | 8 | a0001c0001t0004g0018a0001c0001t0013g0104a0001c0001t0013g0105others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.285+389_285+392dup others(4): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42227136 | ||||||
| chr17:42227136
|
A | AAAATAAA others(1): Show |
15 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0065others(12): Show | 15 | HG01243.hp1 HG01993.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.285+385_285+392dup others(8): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42227136 | ||||||
| chr17:42227136
|
A | AAAATAAA others(5): Show |
139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(136): Show | 140 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.285+381_285+392dup others(12): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42227136 | ||||||
| chr17:42227136
|
A | AAAATAAA others(9): Show |
88 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(85): Show | 88 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.285+377_285+392dup others(16): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42227136 | ||||||
| chr17:42227136
|
A | AAAATAAA others(13): Show |
5 | a0001c0001t0001g0030a0001c0001t0001g0112a0001c0001t0001g0122others(2): Show | 5 | HG01891.hp1 HG02080.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+373_285+392dup others(20): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42227136 | ||||||
| chr17:42227378
|
TA | T | 10 | a0001c0001t0002g0230a0001c0001t0002g0245a0001c0001t0002g0246others(7): Show | 10 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.285+150delT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42227378 | ||||||
| chr17:42227453
|
G | T | 1 | a0001c0002t0001g0111 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.285+76C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42227453 | ||||||
| chr17:42227455
|
GAGAA | G | 6 | a0001c0001t0001g0209a0001c0001t0011g0146a0001c0001t0011g0210others(3): Show | 6 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+70_285+73delTT others(2): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 3/18 | chr17 | 42227455 | ||||||
| chr17:42227751
|
A | C | 1 | a0001c0001t0010g0020 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.129-66T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42227751 | ||||||
| chr17:42227901
|
TA | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0062a0001c0001t0001g0102others(3): Show | 6 | HG01515.hp1 HG02896.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-217delT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42227901 | ||||||
| chr17:42227936
|
T | C | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.129-251A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42227936 | ||||||
| chr17:42228083
|
CA | C | 6 | a0001c0001t0001g0209a0001c0001t0011g0146a0001c0001t0011g0210others(3): Show | 6 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.129-399delT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42228083 | ||||||
| chr17:42228252
|
G | A | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.129-567C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42228252 | ||||||
| chr17:42228358
|
C | T | 37 | a0001c0001t0001g0205a0001c0001t0002g0003a0001c0001t0002g0004others(34): Show | 37 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.129-673G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42228358 | ||||||
| chr17:42228552
|
A | G | 5 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0033others(2): Show | 5 | HG00609.hp2 HG00673.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.129-867T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42228552 | ||||||
| chr17:42228697
|
C | T | 37 | a0001c0001t0001g0205a0001c0001t0002g0003a0001c0001t0002g0004others(34): Show | 37 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.129-1012G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42228697 | ||||||
| chr17:42228707
|
G | A | 6 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0013g0139others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.129-1022C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42228707 | ||||||
| chr17:42228799
|
C | T | 6 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0013g0139others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.129-1114G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42228799 | ||||||
| chr17:42229090
|
G | A | 1 | a0001c0001t0003g0053 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.129-1405C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42229090 | ||||||
| chr17:42229113
|
CCT | C | 6 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0013g0139others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.129-1430_129-1429d others(4): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42229113 | ||||||
| chr17:42229213
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.129-1528C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42229213 | ||||||
| chr17:42229643
|
T | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0058others(3): Show | 6 | HG02280.hp2 HG02486.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-1958A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42229643 | ||||||
| chr17:42229862
|
C | T | 1 | a0001c0001t0009g0144 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.128+2138G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42229862 | ||||||
| chr17:42229973
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.128+2027G>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42229973 | ||||||
| chr17:42230256
|
G | A | 5 | a0001c0001t0006g0252a0001c0001t0006g0253a0001c0001t0006g0254others(2): Show | 5 | NA18957.hp1 NA18977.hp2 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.128+1744C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42230256 | ||||||
| chr17:42230521
|
A | G | 2 | a0001c0001t0008g0124a0001c0001t0018g0017 | 2 | HG01243.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.128+1479T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42230521 | ||||||
| chr17:42231020
|
T | C | 1 | a0001c0001t0002g0235 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.128+980A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42231020 | ||||||
| chr17:42231300
|
C | T | 3 | a0001c0001t0001g0205a0001c0001t0028g0207a0001c0001t0029g0206 | 3 | HG02630.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.128+700G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42231300 | ||||||
| chr17:42231453
|
C | T | 1 | a0001c0001t0028g0207 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.128+547G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42231453 | ||||||
| chr17:42231505
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0194 | 2 | NA18991.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.128+495G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42231505 | ||||||
| chr17:42231860
|
T | A | 1 | a0001c0001t0023g0208 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.128+140A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42231860 | ||||||
| chr17:42231868
|
A | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.128+132T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 2/18 | chr17 | 42231868 | ||||||
| chr17:42232167
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-10-30C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42232167 | ||||||
| chr17:42232190
|
C | T | 22 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0125others(19): Show | 22 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.-10-53G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42232190 | ||||||
| chr17:42232201
|
G | A | 1 | a0001c0001t0018g0017 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-10-64C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42232201 | ||||||
| chr17:42232261
|
A | G | 8 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(5): Show | 8 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10-124T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42232261 | ||||||
| chr17:42232341
|
C | A | 45 | a0001c0001t0001g0205a0001c0001t0002g0003a0001c0001t0002g0004others(42): Show | 45 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.-10-204G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42232341 | ||||||
| chr17:42232448
|
C | T | 62 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0002g0003others(59): Show | 62 | HG00408.hp1 HG01109.hp2 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.-10-311G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42232448 | ||||||
| chr17:42232840
|
G | GT | 29 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0051others(26): Show | 29 | HG00408.hp1 HG01109.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.-10-704dupA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42232840 | ||||||
| chr17:42232840
|
GT | G | 7 | a0001c0001t0001g0002a0001c0001t0001g0120a0001c0001t0001g0203others(4): Show | 7 | HG00140.hp1 HG01981.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-704delA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42232840 | ||||||
| chr17:42232910
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-10-773G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42232910 | ||||||
| chr17:42233091
|
G | GC | 8 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0013g0139others(5): Show | 8 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-955dupG | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42233091 | ||||||
| chr17:42233150
|
T | A | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-10-1013A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42233150 | ||||||
| chr17:42233341
|
G | A | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-10-1204C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42233341 | ||||||
| chr17:42233488
|
C | CT | 6 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0013g0139others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-1352dupA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42233488 | ||||||
| chr17:42233680
|
T | G | 1 | a0001c0001t0020g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-10-1543A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42233680 | ||||||
| chr17:42233715
|
A | C | 9 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0013g0139others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-1578T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42233715 | ||||||
| chr17:42234255
|
T | G | 5 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0013g0139others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-2118A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42234255 | ||||||
| chr17:42234790
|
T | A | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-10-2653A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42234790 | ||||||
| chr17:42234871
|
A | T | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-10-2734T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42234871 | ||||||
| chr17:42235108
|
A | C | 20 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0232others(17): Show | 20 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10-2971T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42235108 | ||||||
| chr17:42235154
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-10-3017C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42235154 | ||||||
| chr17:42235403
|
CA | C | 7 | a0001c0001t0006g0118a0001c0001t0006g0129a0001c0001t0006g0252others(4): Show | 7 | HG01175.hp1 HG02145.hp2 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-3267delT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42235403 | ||||||
| chr17:42235948
|
G | A | 1 | a0001c0001t0002g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-10-3811C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42235948 | ||||||
| chr17:42236140
|
G | T | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-10-4003C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42236140 | ||||||
| chr17:42236412
|
G | A | 4 | a0001c0001t0004g0041a0001c0001t0004g0049a0001c0001t0004g0057others(1): Show | 4 | HG00140.hp1 HG00733.hp1 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-4275C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42236412 | ||||||
| chr17:42236766
|
A | C | 4 | a0001c0001t0009g0083a0001c0001t0009g0084a0001c0001t0009g0085others(1): Show | 4 | NA18964.hp1 NA18979.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-4629T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42236766 | ||||||
| chr17:42236918
|
A | C | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-10-4781T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42236918 | ||||||
| chr17:42236988
|
T | C | 3 | a0001c0001t0008g0074a0001c0001t0008g0124a0001c0001t0018g0017 | 3 | HG01243.hp1 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-10-4851A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42236988 | ||||||
| chr17:42237022
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-10-4885C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42237022 | ||||||
| chr17:42237079
|
C | G | 1 | a0001c0001t0002g0237 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-10-4942G>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42237079 | ||||||
| chr17:42237228
|
C | T | 2 | a0001c0001t0001g0217a0001c0001t0001g0218 | 2 | HG02083.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.-10-5091G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42237228 | ||||||
| chr17:42237350
|
T | G | 1 | a0001c0001t0001g0162 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-10-5213A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42237350 | ||||||
| chr17:42237394
|
T | C | 1 | a0001c0009t0008g0258 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-10-5257A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42237394 | ||||||
| chr17:42237482
|
T | C | 1 | a0001c0001t0005g0137 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-10-5345A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42237482 | ||||||
| chr17:42237744
|
G | C | 3 | a0001c0001t0008g0074a0001c0001t0008g0124a0001c0001t0018g0017 | 3 | HG01243.hp1 HG02602.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-10-5607C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42237744 | ||||||
| chr17:42238092
|
TTCTATCC others(1): Show |
T | 7 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0006g0118others(4): Show | 7 | HG01175.hp1 HG02145.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-5963_-10-5956d others(10): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42238092 | ||||||
| chr17:42238092
|
TTCTATCC others(5): Show |
T | 22 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0001t0002g0235others(19): Show | 22 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.-10-5967_-10-5956d others(14): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42238092 | ||||||
| chr17:42238092
|
TTCTATCC others(9): Show |
T | 10 | a0001c0001t0001g0205a0001c0001t0007g0229a0001c0001t0007g0242others(7): Show | 10 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10-5971_-10-5956d others(18): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42238092 | ||||||
| chr17:42238092
|
TTCTATCC others(13): Show |
T | 3 | a0001c0001t0002g0230a0001c0001t0002g0245a0001c0001t0002g0246 | 3 | HG02895.hp2 HG02896.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-10-5975_-10-5956d others(22): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42238092 | ||||||
| chr17:42238095
|
TATCC | T | 54 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0028others(51): Show | 54 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.-10-5962_-10-5959d others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42238095 | ||||||
| chr17:42238095
|
TATCCATC others(1): Show |
T | 58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(55): Show | 58 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.-10-5966_-10-5959d others(10): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42238095 | ||||||
| chr17:42238095
|
TATCCATC others(5): Show |
T | 40 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(37): Show | 40 | HG00558.hp1 HG00621.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.-10-5970_-10-5959d others(14): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42238095 | ||||||
| chr17:42238095
|
TATCCATC others(9): Show |
T | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0025others(46): Show | 50 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-10-5974_-10-5959d others(18): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42238095 | ||||||
| chr17:42238095
|
TATCCATC others(13): Show |
T | 4 | a0001c0001t0004g0041a0001c0001t0004g0049a0001c0001t0004g0057others(1): Show | 4 | HG00140.hp1 HG00733.hp1 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-5978_-10-5959d others(22): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42238095 | ||||||
| chr17:42238266
|
T | C | 3 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0215 | 3 | NA18970.hp2 NA19076.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-10-6129A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42238266 | ||||||
| chr17:42238314
|
C | CT | 48 | a0001c0001t0001g0112a0001c0001t0001g0142a0001c0001t0001g0179others(45): Show | 48 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.-10-6178dupA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42238314 | ||||||
| chr17:42238314
|
C | CTT | 5 | a0001c0001t0001g0205a0001c0001t0002g0241a0001c0001t0008g0155others(2): Show | 5 | HG01243.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-6179_-10-6178d others(4): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42238314 | ||||||
| chr17:42238451
|
C | CT | 27 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0109others(24): Show | 27 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.-10-6315dupA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42238451 | ||||||
| chr17:42238451
|
C | CTT | 8 | a0001c0001t0002g0232a0001c0001t0002g0241a0001c0001t0006g0118others(5): Show | 8 | HG01175.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-6316_-10-6315d others(4): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42238451 | ||||||
| chr17:42238451
|
CT | C | 7 | a0001c0001t0001g0046a0001c0001t0001g0061a0001c0001t0001g0157others(4): Show | 7 | HG00642.hp1 HG01517.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-6315delA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42238451 | ||||||
| chr17:42238611
|
G | A | 24 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0048others(21): Show | 24 | HG01433.hp2 HG02258.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.-10-6474C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42238611 | ||||||
| chr17:42238688
|
T | G | 1 | a0001c0001t0008g0155 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-10-6551A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42238688 | ||||||
| chr17:42238756
|
C | T | 60 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0002g0003others(57): Show | 60 | HG00408.hp1 HG01109.hp2 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.-10-6619G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42238756 | ||||||
| chr17:42238872
|
T | TC | 6 | a0001c0001t0001g0209a0001c0001t0011g0146a0001c0001t0011g0210others(3): Show | 6 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-6736_-10-6735i others(3): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42238872 | ||||||
| chr17:42239016
|
G | C | 1 | a0001c0001t0021g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-10-6879C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42239016 | ||||||
| chr17:42239226
|
G | A | 9 | a0001c0001t0002g0230a0001c0001t0002g0245a0001c0001t0002g0246others(6): Show | 9 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-7089C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42239226 | ||||||
| chr17:42239246
|
C | CA | 28 | a0001c0001t0001g0022a0001c0001t0001g0071a0001c0001t0001g0075others(25): Show | 28 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.-10-7110dupT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42239246 | ||||||
| chr17:42239246
|
C | CAA | 34 | a0001c0001t0001g0012a0001c0001t0002g0004a0001c0001t0002g0230others(31): Show | 34 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.-10-7111_-10-7110d others(4): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42239246 | ||||||
| chr17:42239246
|
C | CAAA | 7 | a0001c0001t0001g0205a0001c0001t0002g0003a0001c0001t0002g0249others(4): Show | 7 | HG02145.hp1 HG02630.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-7112_-10-7110d others(5): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42239246 | ||||||
| chr17:42239246
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0002g0241a0003c0010t0002g0240 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-10-7121_-10-7110d others(14): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42239246 | ||||||
| chr17:42239777
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-10-7640C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42239777 | ||||||
| chr17:42239864
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-10-7727C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42239864 | ||||||
| chr17:42239996
|
C | T | 1 | a0001c0001t0005g0095 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-10-7859G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42239996 | ||||||
| chr17:42240005
|
G | A | 1 | a0001c0001t0023g0208 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-10-7868C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42240005 | ||||||
| chr17:42240189
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-10-8052C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42240189 | ||||||
| chr17:42240340
|
G | A | 29 | a0001c0001t0001g0025a0001c0001t0001g0165a0001c0001t0001g0168others(26): Show | 29 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.-10-8203C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42240340 | ||||||
| chr17:42241065
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-10-8928G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42241065 | ||||||
| chr17:42241255
|
T | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(255): Show | 259 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.-10-9118A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42241255 | ||||||
| chr17:42241420
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-10-9283T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42241420 | ||||||
| chr17:42241445
|
A | AT | 7 | a0001c0001t0001g0165a0001c0001t0001g0251a0001c0001t0002g0230others(4): Show | 7 | HG00621.hp2 HG02809.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-9309dupA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42241445 | ||||||
| chr17:42241718
|
C | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0016others(66): Show | 70 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.-10-9581G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42241718 | ||||||
| chr17:42241929
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0153 | 3 | HG02559.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-10-9792G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42241929 | ||||||
| chr17:42241991
|
G | C | 1 | a0001c0001t0001g0148 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-10-9854C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42241991 | ||||||
| chr17:42242072
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0016others(112): Show | 116 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.-10-9935G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42242072 | ||||||
| chr17:42242152
|
G | A | 6 | a0001c0001t0001g0209a0001c0001t0011g0146a0001c0001t0011g0210others(3): Show | 6 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-10015C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42242152 | ||||||
| chr17:42242349
|
C | T | 2 | a0001c0001t0005g0087a0001c0001t0005g0133 | 2 | HG01192.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-10-10212G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42242349 | ||||||
| chr17:42242562
|
G | C | 1 | a0001c0001t0001g0002 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-10-10425C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42242562 | ||||||
| chr17:42242942
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-10-10805A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42242942 | ||||||
| chr17:42242988
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-10-10851C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42242988 | ||||||
| chr17:42243002
|
TC | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-10-10866delG | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243002 | ||||||
| chr17:42243123
|
TA | T | 31 | a0001c0001t0001g0042a0001c0001t0001g0148a0001c0001t0001g0205others(28): Show | 31 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.-10-10987delT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243123 | ||||||
| chr17:42243157
|
AAT | A | 5 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0013g0139others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-11022_-10-1102 others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243157 | ||||||
| chr17:42243173
|
C | CT | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-10-11037dupA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243173 | ||||||
| chr17:42243188
|
TA | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(175): Show | 179 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.-10-11052delT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243188 | ||||||
| chr17:42243192
|
A | T | 1 | a0001c0001t0001g0045 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-10-11055T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243192 | ||||||
| chr17:42243193
|
A | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(120): Show | 124 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.-10-11056T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243193 | ||||||
| chr17:42243214
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-10-11077C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243214 | ||||||
| chr17:42243249
|
T | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-10-11112A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243249 | ||||||
| chr17:42243313
|
G | A | 1 | a0001c0001t0003g0136 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-10-11176C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243313 | ||||||
| chr17:42243317
|
C | T | 3 | a0001c0001t0005g0005a0001c0001t0005g0067a0001c0001t0005g0069 | 3 | HG01884.hp1 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-10-11180G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243317 | ||||||
| chr17:42243466
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-10-11329A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243466 | ||||||
| chr17:42243527
|
T | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-10-11390A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243527 | ||||||
| chr17:42243579
|
G | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0042 | 2 | NA18957.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-10-11442C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243579 | ||||||
| chr17:42243841
|
T | C | 6 | a0001c0001t0001g0209a0001c0001t0011g0146a0001c0001t0011g0210others(3): Show | 6 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-11704A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243841 | ||||||
| chr17:42243877
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-10-11740T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243877 | ||||||
| chr17:42243879
|
G | A | 1 | a0001c0001t0029g0206 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-10-11742C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243879 | ||||||
| chr17:42243909
|
T | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-10-11772A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243909 | ||||||
| chr17:42243910
|
G | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-10-11773C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243910 | ||||||
| chr17:42243911
|
G | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-10-11774C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243911 | ||||||
| chr17:42243914
|
A | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-10-11777T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243914 | ||||||
| chr17:42243915
|
T | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-10-11778A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243915 | ||||||
| chr17:42243917
|
A | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-10-11780T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243917 | ||||||
| chr17:42243918
|
TGGA | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-10-11784_-10-1178 others(7): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243918 | ||||||
| chr17:42243923
|
T | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-10-11786A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243923 | ||||||
| chr17:42243924
|
T | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-10-11787A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42243924 | ||||||
| chr17:42244092
|
CT | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(105): Show | 109 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.-10-11956delA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42244092 | ||||||
| chr17:42244137
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(112): Show | 116 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-10-12000T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42244137 | ||||||
| chr17:42244190
|
T | C | 32 | a0001c0001t0001g0251a0001c0001t0002g0003a0001c0001t0002g0004others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10-12053A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42244190 | ||||||
| chr17:42244254
|
A | AT | 9 | a0001c0001t0001g0162a0001c0001t0001g0174a0001c0001t0001g0259others(6): Show | 9 | HG00140.hp2 HG01993.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-12118dupA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42244254 | ||||||
| chr17:42244254
|
A | ATT | 9 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0011g0146others(6): Show | 9 | HG01109.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-12119_-10-1211 others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42244254 | ||||||
| chr17:42244254
|
AT | A | 7 | a0001c0001t0001g0042a0001c0001t0001g0157a0001c0001t0001g0160others(4): Show | 7 | HG01167.hp2 HG02280.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-12118delA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42244254 | ||||||
| chr17:42244368
|
A | G | 3 | a0001c0001t0001g0205a0001c0001t0028g0207a0001c0001t0029g0206 | 3 | HG02630.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-10-12231T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42244368 | ||||||
| chr17:42244532
|
G | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(120): Show | 124 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.-10-12395C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42244532 | ||||||
| chr17:42244647
|
C | T | 1 | a0001c0009t0008g0258 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-10-12510G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42244647 | ||||||
| chr17:42244786
|
G | A | 1 | a0001c0001t0021g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-10-12649C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42244786 | ||||||
| chr17:42244817
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0110 | 2 | HG02027.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.-10-12680A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42244817 | ||||||
| chr17:42244992
|
C | T | 1 | a0001c0001t0002g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-10-12855G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42244992 | ||||||
| chr17:42245073
|
A | AT | 13 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0130others(10): Show | 13 | HG02027.hp2 HG02559.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10-12937dupA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42245073 | ||||||
| chr17:42245073
|
A | ATT | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(90): Show | 94 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-10-12938_-10-1293 others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42245073 | ||||||
| chr17:42245073
|
A | ATTT | 9 | a0001c0001t0001g0168a0001c0001t0001g0201a0001c0001t0001g0204others(6): Show | 9 | HG02055.hp1 HG02895.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-12939_-10-1293 others(7): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42245073 | ||||||
| chr17:42245073
|
A | ATTTT | 6 | a0001c0001t0001g0209a0001c0001t0011g0146a0001c0001t0011g0210others(3): Show | 6 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-12940_-10-1293 others(8): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42245073 | ||||||
| chr17:42245147
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-10-13010C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42245147 | ||||||
| chr17:42245226
|
C | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0123 | 2 | HG01175.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-10-13089G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42245226 | ||||||
| chr17:42245581
|
G | C | 1 | a0001c0001t0001g0134 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-10-13444C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42245581 | ||||||
| chr17:42245683
|
C | T | 9 | a0001c0001t0001g0251a0001c0001t0006g0252a0001c0001t0006g0253others(6): Show | 9 | HG02809.hp2 HG03209.hp2 HG04199.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-13546G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42245683 | ||||||
| chr17:42245758
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-10-13621C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42245758 | ||||||
| chr17:42245794
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-10-13657T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42245794 | ||||||
| chr17:42246203
|
C | T | 1 | a0001c0001t0007g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-10-14066G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42246203 | ||||||
| chr17:42246243
|
C | T | 1 | a0001c0001t0021g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-10-14106G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42246243 | ||||||
| chr17:42246351
|
A | AT | 3 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0013g0139 | 3 | HG01884.hp2 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-10-14215dupA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42246351 | ||||||
| chr17:42246404
|
A | T | 2 | a0001c0001t0004g0089a0001c0001t0005g0069 | 2 | HG02717.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-10-14267T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42246404 | ||||||
| chr17:42246512
|
T | C | 7 | a0001c0001t0001g0251a0001c0001t0006g0252a0001c0001t0006g0253others(4): Show | 7 | HG03209.hp2 HG04199.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-14375A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42246512 | ||||||
| chr17:42246613
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0033others(2): Show | 5 | HG00609.hp2 HG00673.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-14476C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42246613 | ||||||
| chr17:42246807
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(112): Show | 116 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-10-14670G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42246807 | ||||||
| chr17:42246854
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0220 | 2 | NA19000.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-10-14717G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42246854 | ||||||
| chr17:42246955
|
C | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(112): Show | 116 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-10-14818G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42246955 | ||||||
| chr17:42247426
|
A | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0190 | 2 | HG01167.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.-10-15289T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42247426 | ||||||
| chr17:42247450
|
A | C | 1 | a0001c0001t0001g0170 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-10-15313T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42247450 | ||||||
| chr17:42247458
|
C | T | 2 | a0001c0001t0022g0143a0001c0005t0024g0107 | 2 | HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-10-15321G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42247458 | ||||||
| chr17:42247930
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(119): Show | 123 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.-10-15793A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42247930 | ||||||
| chr17:42247952
|
TA | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(70): Show | 74 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.-10-15816delT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42247952 | ||||||
| chr17:42247988
|
T | A | 1 | a0001c0001t0001g0077 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-10-15851A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42247988 | ||||||
| chr17:42248087
|
G | A | 1 | a0001c0001t0003g0091 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-10-15950C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42248087 | ||||||
| chr17:42248273
|
C | CA | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(78): Show | 82 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.-10-16137dupT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42248273 | ||||||
| chr17:42248273
|
C | CAA | 9 | a0001c0001t0001g0152a0001c0001t0001g0184a0001c0001t0001g0192others(6): Show | 9 | HG00642.hp2 HG01243.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-16138_-10-1613 others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42248273 | ||||||
| chr17:42248273
|
CA | C | 8 | a0001c0001t0001g0209a0001c0001t0002g0238a0001c0001t0011g0146others(5): Show | 8 | HG01109.hp2 HG01169.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10-16137delT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42248273 | ||||||
| chr17:42248375
|
G | GA | 5 | a0001c0001t0001g0039a0001c0001t0001g0123a0001c0001t0004g0100others(2): Show | 5 | HG01109.hp2 HG01175.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-16239dupT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42248375 | ||||||
| chr17:42248375
|
GA | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(102): Show | 106 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-10-16239delT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42248375 | ||||||
| chr17:42248394
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(112): Show | 116 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-10-16257G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42248394 | ||||||
| chr17:42248825
|
G | A | 6 | a0001c0001t0001g0209a0001c0001t0011g0146a0001c0001t0011g0210others(3): Show | 6 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-16688C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42248825 | ||||||
| chr17:42248914
|
T | C | 9 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0011g0146others(6): Show | 9 | HG01109.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-16777A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42248914 | ||||||
| chr17:42249111
|
G | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0203 | 2 | HG02735.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-10-16974C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42249111 | ||||||
| chr17:42249165
|
G | C | 1 | a0001c0001t0008g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-10-17028C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42249165 | ||||||
| chr17:42249229
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-10-17092G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42249229 | ||||||
| chr17:42249392
|
C | CA | 9 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0011g0146others(6): Show | 9 | HG01109.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-17256dupT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42249392 | ||||||
| chr17:42249549
|
A | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(121): Show | 125 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.-10-17412T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42249549 | ||||||
| chr17:42249592
|
A | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0220 | 2 | NA19000.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-10-17455T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42249592 | ||||||
| chr17:42249721
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-10-17584G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42249721 | ||||||
| chr17:42249920
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-10-17783G>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42249920 | ||||||
| chr17:42250110
|
C | T | 9 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0031others(6): Show | 9 | HG02074.hp2 HG02083.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-17973G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42250110 | ||||||
| chr17:42250144
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-10-18007C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42250144 | ||||||
| chr17:42250495
|
A | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG00733.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-10-18358T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42250495 | ||||||
| chr17:42250546
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-10-18409A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42250546 | ||||||
| chr17:42250564
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-10-18427A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42250564 | ||||||
| chr17:42250593
|
G | A | 1 | a0001c0001t0021g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-10-18456C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42250593 | ||||||
| chr17:42250923
|
C | CA | 9 | a0001c0001t0001g0039a0001c0001t0001g0135a0001c0001t0001g0199others(6): Show | 9 | HG01981.hp2 HG02055.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-18787dupT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42250923 | ||||||
| chr17:42250962
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-10-18825C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42250962 | ||||||
| chr17:42251191
|
T | C | 1 | a0001c0001t0002g0237 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-10-19054A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42251191 | ||||||
| chr17:42251744
|
A | C | 1 | a0001c0005t0024g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-10-19607T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42251744 | ||||||
| chr17:42251917
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(112): Show | 116 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-10-19780G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42251917 | ||||||
| chr17:42251998
|
C | CA | 32 | a0001c0001t0001g0002a0001c0001t0001g0131a0001c0001t0001g0157others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10-19862dupT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42251998 | ||||||
| chr17:42251998
|
C | CAA | 7 | a0001c0001t0006g0256a0001c0001t0007g0229a0001c0001t0007g0242others(4): Show | 7 | HG02109.hp1 HG02145.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-19863_-10-1986 others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42251998 | ||||||
| chr17:42252131
|
T | A | 1 | a0001c0001t0016g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-10-19994A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42252131 | ||||||
| chr17:42252269
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-10-20132C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42252269 | ||||||
| chr17:42252516
|
T | C | 1 | a0001c0007t0001g0166 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-10-20379A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42252516 | ||||||
| chr17:42252710
|
T | C | 1 | a0001c0001t0012g0029 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-10-20573A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42252710 | ||||||
| chr17:42253107
|
C | CCTTT | 16 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0050others(13): Show | 16 | HG01109.hp2 HG01891.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-10-20974_-10-2097 others(8): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42253107 | ||||||
| chr17:42253107
|
CCTTT | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(86): Show | 90 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.-10-20974_-10-2097 others(8): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42253107 | ||||||
| chr17:42253127
|
T | C | 1 | a0001c0001t0012g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-10-20990A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42253127 | ||||||
| chr17:42253140
|
T | C | 6 | a0001c0001t0001g0209a0001c0001t0011g0146a0001c0001t0011g0210others(3): Show | 6 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-21003A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42253140 | ||||||
| chr17:42253553
|
A | C | 14 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0232others(11): Show | 14 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-10-21416T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42253553 | ||||||
| chr17:42253686
|
T | G | 1 | a0001c0001t0001g0154 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-10-21549A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42253686 | ||||||
| chr17:42253863
|
G | A | 1 | a0001c0001t0001g0010 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-10-21726C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42253863 | ||||||
| chr17:42254251
|
G | A | 9 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0011g0146others(6): Show | 9 | HG01109.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+21997C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42254251 | ||||||
| chr17:42254273
|
A | T | 1 | a0001c0001t0005g0069 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-11+21975T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42254273 | ||||||
| chr17:42254286
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-11+21962C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42254286 | ||||||
| chr17:42254360
|
A | G | 1 | a0001c0001t0005g0137 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-11+21888T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42254360 | ||||||
| chr17:42254522
|
TA | T | 7 | a0001c0001t0001g0061a0001c0001t0001g0181a0001c0001t0005g0005others(4): Show | 7 | HG01517.hp1 HG01884.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+21725delT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42254522 | ||||||
| chr17:42255045
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-11+21203G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42255045 | ||||||
| chr17:42255179
|
C | T | 3 | a0001c0001t0002g0230a0001c0001t0002g0245a0001c0001t0002g0246 | 3 | HG02895.hp2 HG02896.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-11+21069G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42255179 | ||||||
| chr17:42255338
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-11+20910G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42255338 | ||||||
| chr17:42255417
|
C | G | 1 | a0001c0001t0001g0101 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-11+20831G>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42255417 | ||||||
| chr17:42255828
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-11+20420G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42255828 | ||||||
| chr17:42255833
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-11+20415C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42255833 | ||||||
| chr17:42256039
|
C | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(112): Show | 116 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-11+20209G>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42256039 | ||||||
| chr17:42256115
|
C | T | 1 | a0001c0001t0001g0196 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-11+20133G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42256115 | ||||||
| chr17:42256171
|
C | T | 5 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0001t0002g0235others(2): Show | 5 | HG01891.hp2 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+20077G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42256171 | ||||||
| chr17:42256379
|
C | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(112): Show | 116 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-11+19869G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42256379 | ||||||
| chr17:42256723
|
G | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(69): Show | 73 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.-11+19525C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42256723 | ||||||
| chr17:42256861
|
C | CA | 25 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0040others(22): Show | 25 | HG00621.hp1 HG00673.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.-11+19386dupT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42256861 | ||||||
| chr17:42256861
|
C | CAAAAA | 13 | a0001c0001t0001g0209a0001c0001t0002g0003a0001c0001t0002g0233others(10): Show | 13 | HG02451.hp2 HG02630.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11+19382_-11+1938 others(9): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42256861 | ||||||
| chr17:42256861
|
C | CAAAAAA | 15 | a0001c0001t0001g0251a0001c0001t0002g0004a0001c0001t0002g0230others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-11+19381_-11+1938 others(10): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42256861 | ||||||
| chr17:42256861
|
C | CAAAAAAA | 6 | a0001c0001t0002g0232a0001c0001t0006g0252a0001c0001t0006g0255others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+19380_-11+1938 others(11): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42256861 | ||||||
| chr17:42256861
|
CAA | C | 6 | a0001c0001t0001g0150a0001c0001t0001g0168a0001c0001t0001g0171others(3): Show | 6 | HG03669.hp2 HG04115.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+19385_-11+1938 others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42256861 | ||||||
| chr17:42256861
|
CAAA | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(60): Show | 64 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.-11+19384_-11+1938 others(7): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42256861 | ||||||
| chr17:42256861
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0003g0136 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-11+19377_-11+1938 others(14): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42256861 | ||||||
| chr17:42256861
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0071 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-11+19376_-11+1938 others(15): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42256861 | ||||||
| chr17:42256916
|
C | T | 1 | a0001c0001t0003g0091 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-11+19332G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42256916 | ||||||
| chr17:42256995
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-11+19253A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42256995 | ||||||
| chr17:42257379
|
CAG | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(112): Show | 116 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-11+18867_-11+1886 others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42257379 | ||||||
| chr17:42257457
|
T | A | 3 | a0001c0001t0001g0205a0001c0001t0028g0207a0001c0001t0029g0206 | 3 | HG02630.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-11+18791A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42257457 | ||||||
| chr17:42257501
|
C | T | 13 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0232others(10): Show | 13 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+18747G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42257501 | ||||||
| chr17:42257674
|
T | C | 1 | a0001c0001t0002g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-11+18574A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42257674 | ||||||
| chr17:42257682
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-11+18566A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42257682 | ||||||
| chr17:42257724
|
T | C | 3 | a0001c0001t0001g0050a0001c0001t0001g0056a0001c0001t0001g0127 | 3 | NA18964.hp2 NA18970.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-11+18524A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42257724 | ||||||
| chr17:42258027
|
G | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(112): Show | 116 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-11+18221C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42258027 | ||||||
| chr17:42258040
|
C | A | 6 | a0001c0001t0001g0209a0001c0001t0011g0146a0001c0001t0011g0210others(3): Show | 6 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+18208G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42258040 | ||||||
| chr17:42258085
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-11+18163C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42258085 | ||||||
| chr17:42258462
|
T | C | 1 | a0001c0001t0008g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11+17786A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42258462 | ||||||
| chr17:42258518
|
A | G | 1 | a0001c0001t0008g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11+17730T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42258518 | ||||||
| chr17:42258635
|
C | T | 6 | a0001c0001t0001g0209a0001c0001t0011g0146a0001c0001t0011g0210others(3): Show | 6 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+17613G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42258635 | ||||||
| chr17:42258814
|
T | C | 3 | a0001c0001t0001g0205a0001c0001t0028g0207a0001c0001t0029g0206 | 3 | HG02630.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-11+17434A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42258814 | ||||||
| chr17:42259190
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-11+17058A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42259190 | ||||||
| chr17:42259373
|
C | T | 1 | a0001c0003t0008g0159 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-11+16875G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42259373 | ||||||
| chr17:42259608
|
G | A | 1 | a0001c0001t0003g0149 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-11+16640C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42259608 | ||||||
| chr17:42259851
|
G | C | 1 | a0001c0001t0001g0022 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-11+16397C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42259851 | ||||||
| chr17:42259902
|
T | C | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11+16346A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42259902 | ||||||
| chr17:42259902
|
T | G | 1 | a0001c0001t0001g0147 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-11+16346A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42259902 | ||||||
| chr17:42259935
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-11+16313C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42259935 | ||||||
| chr17:42260043
|
A | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11+16205T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42260043 | ||||||
| chr17:42260147
|
G | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(167): Show | 171 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.-11+16101C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42260147 | ||||||
| chr17:42260300
|
T | C | 1 | a0001c0002t0001g0103 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-11+15948A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42260300 | ||||||
| chr17:42260342
|
C | A | 1 | a0001c0002t0001g0014 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-11+15906G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42260342 | ||||||
| chr17:42260803
|
A | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(112): Show | 116 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-11+15445T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42260803 | ||||||
| chr17:42260917
|
C | CT | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(120): Show | 124 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.-11+15330dupA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42260917 | ||||||
| chr17:42261169
|
A | G | 1 | a0001c0002t0001g0111 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-11+15079T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42261169 | ||||||
| chr17:42261674
|
C | A | 5 | a0001c0001t0009g0083a0001c0001t0009g0084a0001c0001t0009g0085others(2): Show | 5 | HG00408.hp1 NA18964.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+14574G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42261674 | ||||||
| chr17:42261797
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-11+14451A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42261797 | ||||||
| chr17:42261905
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-11+14343C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42261905 | ||||||
| chr17:42262061
|
T | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-11+14187A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262061 | ||||||
| chr17:42262314
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-11+13934G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262314 | ||||||
| chr17:42262319
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-11+13929G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262319 | ||||||
| chr17:42262320
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-11+13928C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262320 | ||||||
| chr17:42262369
|
A | G | 1 | a0001c0001t0029g0206 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-11+13879T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262369 | ||||||
| chr17:42262468
|
CT | C | 34 | a0001c0001t0001g0251a0001c0001t0002g0003a0001c0001t0002g0004others(31): Show | 34 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.-11+13779delA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262468 | ||||||
| chr17:42262675
|
G | C | 1 | a0001c0001t0006g0252 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-11+13573C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262675 | ||||||
| chr17:42262744
|
G | GTATA | 43 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0001g0251others(40): Show | 43 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.-11+13500_-11+1350 others(8): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262744 | ||||||
| chr17:42262752
|
A | ATATATG | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(68): Show | 72 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.-11+13495_-11+1349 others(10): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262752 | ||||||
| chr17:42262765
|
T | C | 6 | a0001c0001t0006g0252a0001c0001t0006g0253a0001c0001t0006g0254others(3): Show | 6 | HG03471.hp2 NA18957.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+13483A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262765 | ||||||
| chr17:42262769
|
CATATATG others(51): Show |
C | 1 | a0001c0001t0001g0007 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-11+13421_-11+1347 others(62): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262769 | ||||||
| chr17:42262774
|
A | ATGTATAT others(19): Show |
1 | a0001c0001t0001g0121 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-11+13448_-11+1347 others(30): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262774 | ||||||
| chr17:42262778
|
A | ATATATAT others(41): Show |
2 | a0001c0001t0001g0128a0001c0001t0003g0027 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-11+13422_-11+1346 others(52): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262778 | ||||||
| chr17:42262785
|
T | C | 1 | a0001c0001t0022g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-11+13463A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262785 | ||||||
| chr17:42262794
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-11+13454T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262794 | ||||||
| chr17:42262809
|
T | TAC | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-11+13437_-11+1343 others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262809 | ||||||
| chr17:42262815
|
CATATATA others(75): Show |
C | 1 | a0001c0001t0002g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-11+13351_-11+1343 others(86): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262815 | ||||||
| chr17:42262839
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-11+13409G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262839 | ||||||
| chr17:42262840
|
A | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11+13408T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262840 | ||||||
| chr17:42262844
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-11+13404T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262844 | ||||||
| chr17:42262848
|
G | A | 3 | a0001c0001t0001g0101a0001c0003t0008g0158a0001c0003t0008g0159 | 3 | HG00673.hp2 HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11+13400C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262848 | ||||||
| chr17:42262851
|
T | C | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11+13397A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262851 | ||||||
| chr17:42262853
|
T | C | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11+13395A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262853 | ||||||
| chr17:42262859
|
C | CACAT | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(110): Show | 114 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.-11+13388_-11+1338 others(8): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262859 | ||||||
| chr17:42262859
|
C | T | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11+13389G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262859 | ||||||
| chr17:42262866
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-11+13382C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262866 | ||||||
| chr17:42262883
|
CAT | C | 9 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0011g0146others(6): Show | 9 | HG01109.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+13363_-11+1336 others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262883 | ||||||
| chr17:42262892
|
G | A | 3 | a0001c0001t0002g0230a0001c0001t0002g0245a0001c0001t0002g0246 | 3 | HG02895.hp2 HG02896.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-11+13356C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262892 | ||||||
| chr17:42262892
|
GTGTGTAT others(5): Show |
G | 4 | a0001c0001t0002g0241a0001c0001t0007g0229a0001c0001t0021g0247others(1): Show | 4 | HG02622.hp2 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+13344_-11+1335 others(16): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262892 | ||||||
| chr17:42262910
|
A | G | 1 | a0001c0001t0020g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-11+13338T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262910 | ||||||
| chr17:42262918
|
G | A | 1 | a0001c0001t0020g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-11+13330C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262918 | ||||||
| chr17:42262920
|
G | A | 1 | a0001c0001t0020g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-11+13328C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262920 | ||||||
| chr17:42262922
|
GTA | G | 5 | a0001c0001t0001g0142a0001c0001t0001g0165a0001c0001t0001g0182others(2): Show | 5 | HG00621.hp2 HG02080.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+13324_-11+1332 others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262922 | ||||||
| chr17:42262924
|
A | G | 6 | a0001c0001t0001g0209a0001c0001t0011g0146a0001c0001t0011g0210others(3): Show | 6 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+13324T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262924 | ||||||
| chr17:42262932
|
A | G | 60 | a0001c0001t0001g0002a0001c0001t0001g0114a0001c0001t0001g0121others(57): Show | 60 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.-11+13316T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262932 | ||||||
| chr17:42262934
|
G | A | 59 | a0001c0001t0001g0002a0001c0001t0001g0121a0001c0001t0001g0148others(56): Show | 59 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.-11+13314C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262934 | ||||||
| chr17:42262934
|
G | GTA | 7 | a0001c0001t0001g0051a0001c0001t0001g0108a0001c0001t0003g0098others(4): Show | 7 | HG00408.hp1 HG00639.hp2 HG00642.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+13312_-11+1331 others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262934 | ||||||
| chr17:42262942
|
A | ATATG | 6 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0077others(3): Show | 6 | HG00741.hp2 HG01433.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+13305_-11+1330 others(8): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262942 | ||||||
| chr17:42262942
|
A | ATG | 3 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0110 | 3 | HG01081.hp2 HG02056.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-11+13304_-11+1330 others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262942 | ||||||
| chr17:42262942
|
A | ATGTG | 3 | a0001c0001t0001g0033a0001c0001t0001g0070a0002c0004t0003g0119 | 3 | HG00423.hp1 HG00609.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.-11+13302_-11+1330 others(8): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262942 | ||||||
| chr17:42262942
|
A | G | 9 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0052others(6): Show | 9 | HG01175.hp2 HG01255.hp2 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11+13306T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262942 | ||||||
| chr17:42262942
|
ATG | A | 5 | a0001c0001t0001g0101a0001c0001t0001g0142a0001c0001t0004g0041others(2): Show | 5 | HG00673.hp2 HG00733.hp1 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+13304_-11+1330 others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262942 | ||||||
| chr17:42262944
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(85): Show | 89 | HG00642.hp2 HG01109.hp2 HG01167.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+13304C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262944 | ||||||
| chr17:42262946
|
G | A | 5 | a0001c0001t0001g0209a0001c0001t0011g0146a0001c0001t0011g0211others(2): Show | 5 | HG02258.hp2 HG02647.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+13302C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262946 | ||||||
| chr17:42262958
|
GTGTGTGT others(17): Show |
G | 2 | a0001c0001t0014g0191a0001c0001t0014g0195 | 2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-11+13266_-11+1328 others(28): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262958 | ||||||
| chr17:42262958
|
GTGTGTGT others(21): Show |
G | 1 | a0001c0001t0001g0156 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-11+13262_-11+1328 others(32): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262958 | ||||||
| chr17:42262962
|
GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0001g0216 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-11+13272_-11+1328 others(18): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262962 | ||||||
| chr17:42262962
|
GTGTGTGT others(11): Show |
G | 1 | a0001c0001t0029g0206 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-11+13268_-11+1328 others(22): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262962 | ||||||
| chr17:42262964
|
GTGTGTGT others(3): Show |
G | 3 | a0001c0001t0001g0173a0001c0001t0001g0177a0001c0001t0001g0186 | 3 | NA18995.hp1 NA19005.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-11+13274_-11+1328 others(14): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262964 | ||||||
| chr17:42262964
|
GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0022g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-11+13270_-11+1328 others(18): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262964 | ||||||
| chr17:42262964
|
GTGTGTGT others(9): Show |
G | 1 | a0001c0001t0001g0259 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-11+13268_-11+1328 others(20): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262964 | ||||||
| chr17:42262964
|
GTGTGTGT others(11): Show |
G | 3 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0215 | 3 | NA18970.hp2 NA19076.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-11+13266_-11+1328 others(22): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262964 | ||||||
| chr17:42262964
|
GTGTGTGT others(13): Show |
G | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-11+13264_-11+1328 others(24): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262964 | ||||||
| chr17:42262964
|
GTGTGTGT others(15): Show |
G | 5 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0200others(2): Show | 5 | HG01167.hp2 HG01981.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+13262_-11+1328 others(26): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262964 | ||||||
| chr17:42262964
|
GTGTGTGT others(17): Show |
G | 3 | a0001c0001t0001g0148a0001c0001t0001g0183a0001c0001t0001g0190 | 3 | HG02004.hp1 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-11+13260_-11+1328 others(28): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262964 | ||||||
| chr17:42262964
|
GTGTGTGT others(19): Show |
G | 2 | a0001c0001t0001g0167a0001c0001t0003g0221 | 2 | NA19011.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-11+13258_-11+1328 others(30): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262964 | ||||||
| chr17:42262964
|
GTGTGTGT others(21): Show |
G | 27 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0168others(24): Show | 27 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.-11+13256_-11+1328 others(32): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262964 | ||||||
| chr17:42262966
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0063 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-11+13281_-11+1328 others(14): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262966 | ||||||
| chr17:42262966
|
GTGTGTAT others(3): Show |
G | 1 | a0001c0001t0006g0129 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-11+13272_-11+1328 others(14): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262966 | ||||||
| chr17:42262966
|
GTGTGTAT others(5): Show |
G | 1 | a0001c0001t0001g0165 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-11+13270_-11+1328 others(16): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262966 | ||||||
| chr17:42262966
|
GTGTGTAT others(13): Show |
G | 1 | a0001c0001t0001g0170 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-11+13262_-11+1328 others(24): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262966 | ||||||
| chr17:42262966
|
GTGTGTAT others(15): Show |
G | 2 | a0001c0001t0001g0162a0001c0001t0002g0189 | 2 | HG00140.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-11+13260_-11+1328 others(26): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262966 | ||||||
| chr17:42262966
|
GTGTGTAT others(17): Show |
G | 2 | a0001c0001t0001g0161a0001c0001t0001g0203 | 2 | HG02735.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-11+13258_-11+1328 others(28): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262966 | ||||||
| chr17:42262966
|
GTGTGTAT others(19): Show |
G | 2 | a0001c0001t0016g0212a0001c0001t0016g0225 | 2 | HG03710.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-11+13256_-11+1328 others(30): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262966 | ||||||
| chr17:42262966
|
GTGTGTAT others(21): Show |
G | 1 | a0001c0001t0001g0217 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-11+13254_-11+1328 others(32): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262966 | ||||||
| chr17:42262968
|
G | A | 5 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 5 | HG01515.hp1 HG01517.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+13280C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262968 | ||||||
| chr17:42262968
|
G | GTA | 3 | a0001c0001t0003g0053a0001c0001t0004g0057a0001c0001t0008g0124 | 3 | HG00741.hp1 HG01243.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-11+13279_-11+1328 others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262968 | ||||||
| chr17:42262968
|
GTGTA | G | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0004g0117 | 3 | HG02148.hp2 NA18612.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.-11+13276_-11+1327 others(8): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262968 | ||||||
| chr17:42262968
|
GTGTATA | G | 3 | a0001c0001t0001g0068a0001c0001t0005g0069a0001c0001t0015g0140 | 3 | HG01257.hp2 HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-11+13274_-11+1327 others(10): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262968 | ||||||
| chr17:42262968
|
GTGTATAT others(7): Show |
G | 4 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0011g0210others(1): Show | 4 | HG01109.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+13266_-11+1327 others(18): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262968 | ||||||
| chr17:42262968
|
GTGTATAT others(11): Show |
G | 7 | a0001c0001t0001g0147a0001c0001t0001g0157a0001c0001t0007g0242others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+13262_-11+1327 others(22): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262968 | ||||||
| chr17:42262968
|
GTGTATAT others(13): Show |
G | 1 | a0001c0001t0001g0154 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-11+13260_-11+1327 others(24): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262968 | ||||||
| chr17:42262968
|
GTGTATAT others(15): Show |
G | 2 | a0001c0001t0001g0001a0001c0001t0001g0153 | 3 | HG02559.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-11+13258_-11+1327 others(26): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262968 | ||||||
| chr17:42262968
|
GTGTATAT others(19): Show |
G | 1 | a0001c0001t0002g0249 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-11+13254_-11+1327 others(30): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262968 | ||||||
| chr17:42262970
|
G | A | 22 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0051others(19): Show | 22 | HG00140.hp1 HG00408.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.-11+13278C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262970 | ||||||
| chr17:42262970
|
G | GTA | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0109others(1): Show | 4 | HG00621.hp1 HG01169.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+13276_-11+1327 others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262970 | ||||||
| chr17:42262970
|
G | GTATA | 12 | a0001c0001t0001g0015a0001c0001t0001g0052a0001c0001t0001g0054others(9): Show | 12 | HG00408.hp2 HG01109.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11+13274_-11+1327 others(8): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262970 | ||||||
| chr17:42262970
|
G | GTATATA | 4 | a0001c0001t0001g0226a0001c0001t0005g0228a0001c0002t0001g0103others(1): Show | 4 | HG00639.hp1 HG03710.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+13272_-11+1327 others(10): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262970 | ||||||
| chr17:42262970
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0126 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-11+13268_-11+1327 others(14): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262970 | ||||||
| chr17:42262970
|
G | GTATATAT others(5): Show |
1 | a0001c0001t0001g0134 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-11+13266_-11+1327 others(16): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262970 | ||||||
| chr17:42262970
|
G | GTATATAT others(11): Show |
1 | a0001c0001t0001g0127 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-11+13260_-11+1327 others(22): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262970 | ||||||
| chr17:42262970
|
G | GTATATAT others(17): Show |
1 | a0001c0001t0001g0128 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-11+13254_-11+1327 others(28): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262970 | ||||||
| chr17:42262970
|
G | GTGTA | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG01192.hp1 HG02083.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+13277_-11+1327 others(8): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262970 | ||||||
| chr17:42262970
|
G | GTGTATAT others(1): Show |
3 | a0001c0001t0001g0090a0001c0001t0009g0084a0001c0001t0009g0085 | 3 | HG01257.hp1 NA18979.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-11+13277_-11+1327 others(12): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262970 | ||||||
| chr17:42262970
|
G | GTGTATAT others(3): Show |
2 | a0001c0001t0001g0009a0001c0001t0009g0086 | 2 | HG00673.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.-11+13277_-11+1327 others(14): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262970 | ||||||
| chr17:42262970
|
G | GTGTATAT others(13): Show |
1 | a0001c0001t0001g0064 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-11+13277_-11+1327 others(24): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262970 | ||||||
| chr17:42262970
|
G | GTGTGTAT others(3): Show |
1 | a0001c0001t0009g0083 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-11+13277_-11+1327 others(14): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262970 | ||||||
| chr17:42262970
|
GTA | G | 16 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0075others(13): Show | 16 | HG00438.hp2 HG01175.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11+13276_-11+1327 others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262970 | ||||||
| chr17:42262970
|
GTATA | G | 3 | a0001c0001t0001g0012a0001c0001t0001g0130a0001c0001t0005g0067 | 3 | HG03225.hp1 NA18991.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-11+13274_-11+1327 others(8): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262970 | ||||||
| chr17:42262970
|
GTATATA | G | 6 | a0001c0001t0001g0022a0001c0001t0001g0131a0001c0001t0010g0021others(3): Show | 6 | HG02074.hp2 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+13272_-11+1327 others(10): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262970 | ||||||
| chr17:42262970
|
GTATATAT others(5): Show |
G | 2 | a0001c0001t0001g0010a0001c0001t0010g0020 | 2 | HG02886.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-11+13266_-11+1327 others(16): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262970 | ||||||
| chr17:42262970
|
GTATATAT others(9): Show |
G | 3 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0100 | 3 | NA19000.hp2 NA19009.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-11+13262_-11+1327 others(20): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262970 | ||||||
| chr17:42262970
|
GTATATAT others(11): Show |
G | 1 | a0001c0001t0003g0136 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-11+13260_-11+1327 others(22): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262970 | ||||||
| chr17:42262970
|
GTATATAT others(25): Show |
G | 1 | a0001c0001t0001g0112 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-11+13246_-11+1327 others(36): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262970 | ||||||
| chr17:42262972
|
A | G | 15 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0030others(12): Show | 15 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.-11+13276T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262972 | ||||||
| chr17:42262974
|
A | G | 9 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0097others(6): Show | 9 | HG00438.hp2 HG01515.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11+13274T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262974 | ||||||
| chr17:42262976
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0130 | 2 | NA18968.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-11+13272T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262976 | ||||||
| chr17:42262978
|
A | G | 2 | a0001c0001t0010g0021a0001c0001t0010g0113 | 2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-11+13270T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262978 | ||||||
| chr17:42262984
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0010g0020 | 2 | HG02886.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-11+13264T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262984 | ||||||
| chr17:42262988
|
A | G | 3 | a0001c0001t0004g0018a0001c0001t0004g0019a0001c0001t0004g0100 | 3 | NA19000.hp2 NA19009.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-11+13260T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262988 | ||||||
| chr17:42262989
|
TATATATA others(21): Show |
T | 7 | a0001c0001t0001g0251a0001c0001t0006g0252a0001c0001t0006g0253others(4): Show | 7 | HG02723.hp2 HG04199.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+13231_-11+1325 others(32): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262989 | ||||||
| chr17:42262990
|
A | G | 1 | a0001c0001t0003g0136 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-11+13258T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262990 | ||||||
| chr17:42262991
|
TATATATA others(19): Show |
T | 1 | a0001c0009t0008g0258 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-11+13231_-11+1325 others(30): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262991 | ||||||
| chr17:42262993
|
TATATATA others(17): Show |
T | 13 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0232others(10): Show | 13 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+13231_-11+1325 others(28): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262993 | ||||||
| chr17:42262995
|
TATATATA others(15): Show |
T | 5 | a0001c0001t0001g0182a0001c0001t0002g0237a0001c0001t0025g0231others(2): Show | 5 | HG02809.hp2 HG02818.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+13231_-11+1325 others(26): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262995 | ||||||
| chr17:42262999
|
TATATATA others(11): Show |
T | 4 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0201others(1): Show | 4 | HG00642.hp2 HG03669.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+13231_-11+1324 others(22): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42262999 | ||||||
| chr17:42263001
|
TATATATA others(9): Show |
T | 4 | a0001c0001t0003g0149a0001c0001t0003g0151a0001c0001t0007g0257others(1): Show | 4 | HG01993.hp1 HG02055.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+13231_-11+1324 others(20): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263001 | ||||||
| chr17:42263003
|
TATATATA others(7): Show |
T | 2 | a0001c0001t0001g0209a0001c0001t0002g0230 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-11+13231_-11+1324 others(18): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263003 | ||||||
| chr17:42263009
|
TATATATA others(1): Show |
T | 3 | a0001c0001t0011g0146a0001c0001t0011g0211a0001c0001t0011g0224 | 3 | HG02647.hp1 HG03041.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-11+13231_-11+1323 others(12): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263009 | ||||||
| chr17:42263017
|
A | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(73): Show | 77 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-11+13231T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263017 | ||||||
| chr17:42263019
|
A | T | 1 | a0001c0001t0001g0016 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-11+13229T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263019 | ||||||
| chr17:42263022
|
A | C | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(253): Show | 257 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.-11+13226T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263022 | ||||||
| chr17:42263031
|
AT | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0065others(81): Show | 85 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-11+13216delA | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263031 | ||||||
| chr17:42263031
|
ATT | A | 35 | a0001c0001t0001g0164a0001c0001t0001g0251a0001c0001t0002g0003others(32): Show | 35 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.-11+13215_-11+1321 others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263031 | ||||||
| chr17:42263712
|
A | C | 1 | a0001c0001t0001g0176 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-11+12536T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263712 | ||||||
| chr17:42263869
|
G | A | 1 | a0001c0001t0008g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11+12379C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263869 | ||||||
| chr17:42263871
|
G | GCA | 28 | a0001c0001t0001g0097a0001c0001t0001g0108a0001c0001t0001g0168others(25): Show | 28 | HG00639.hp2 HG00642.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-11+12375_-11+1237 others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263871 | ||||||
| chr17:42263871
|
G | GCACA | 18 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(15): Show | 18 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.-11+12373_-11+1237 others(8): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263871 | ||||||
| chr17:42263871
|
G | GCACACA | 22 | a0001c0001t0001g0002a0001c0001t0001g0130a0001c0001t0001g0142others(19): Show | 22 | HG01981.hp1 HG02004.hp1 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.-11+12371_-11+1237 others(10): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263871 | ||||||
| chr17:42263871
|
G | GCACACAC others(1): Show |
7 | a0001c0001t0001g0163a0001c0001t0001g0204a0001c0001t0001g0222others(4): Show | 7 | HG02735.hp2 HG03490.hp2 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+12369_-11+1237 others(12): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263871 | ||||||
| chr17:42263871
|
G | GCACACAC others(3): Show |
2 | a0001c0001t0001g0167a0001c0001t0001g0185 | 2 | HG00609.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-11+12367_-11+1237 others(14): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263871 | ||||||
| chr17:42263871
|
G | GCGCA | 3 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0201 | 4 | HG02559.hp2 HG03669.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+12376_-11+1237 others(8): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263871 | ||||||
| chr17:42263871
|
G | GCGCACA | 7 | a0001c0001t0001g0147a0001c0001t0001g0152a0001c0001t0001g0154others(4): Show | 7 | HG00642.hp2 HG01243.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+12376_-11+1237 others(10): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263871 | ||||||
| chr17:42263871
|
G | GCGCACAC others(3): Show |
1 | a0001c0001t0001g0157 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-11+12376_-11+1237 others(14): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263871 | ||||||
| chr17:42263871
|
GCA | G | 27 | a0001c0001t0001g0009a0001c0001t0001g0068a0001c0001t0001g0070others(24): Show | 27 | HG00558.hp2 HG00673.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.-11+12375_-11+1237 others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263871 | ||||||
| chr17:42263871
|
GCACA | G | 94 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0016others(91): Show | 94 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.-11+12373_-11+1237 others(8): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263871 | ||||||
| chr17:42263871
|
GCACACA | G | 9 | a0001c0001t0001g0015a0001c0001t0001g0177a0001c0001t0001g0186others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11+12371_-11+1237 others(10): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263871 | ||||||
| chr17:42263871
|
GCACACAC others(1): Show |
G | 4 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0103others(1): Show | 4 | HG02698.hp1 HG02738.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+12369_-11+1237 others(12): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263871 | ||||||
| chr17:42263875
|
A | G | 1 | a0001c0001t0004g0089 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-11+12373T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263875 | ||||||
| chr17:42263877
|
A | G | 1 | a0001c0005t0024g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-11+12371T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263877 | ||||||
| chr17:42263879
|
A | G | 5 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0013g0139others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+12369T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263879 | ||||||
| chr17:42263881
|
A | G | 5 | a0001c0001t0013g0104a0001c0001t0013g0105a0001c0001t0013g0139others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+12367T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263881 | ||||||
| chr17:42263911
|
A | G | 1 | a0001c0005t0024g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-11+12337T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263911 | ||||||
| chr17:42263932
|
G | T | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11+12316C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263932 | ||||||
| chr17:42263947
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-11+12301G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42263947 | ||||||
| chr17:42264031
|
A | G | 9 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0011g0146others(6): Show | 9 | HG01109.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+12217T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42264031 | ||||||
| chr17:42264208
|
A | T | 1 | a0001c0001t0001g0162 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-11+12040T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42264208 | ||||||
| chr17:42264273
|
C | T | 1 | a0001c0001t0009g0144 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-11+11975G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42264273 | ||||||
| chr17:42264367
|
C | T | 1 | a0001c0001t0007g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-11+11881G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42264367 | ||||||
| chr17:42264563
|
T | G | 32 | a0001c0001t0001g0251a0001c0001t0002g0003a0001c0001t0002g0004others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.-11+11685A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42264563 | ||||||
| chr17:42264661
|
T | G | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11+11587A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42264661 | ||||||
| chr17:42265084
|
G | A | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11+11164C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265084 | ||||||
| chr17:42265176
|
G | A | 9 | a0001c0001t0001g0205a0001c0001t0001g0209a0001c0001t0011g0146others(6): Show | 9 | HG01109.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+11072C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265176 | ||||||
| chr17:42265364
|
G | A | 1 | a0001c0001t0005g0137 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-11+10884C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265364 | ||||||
| chr17:42265377
|
C | CTTTTTTT others(4): Show |
6 | a0001c0001t0001g0001a0001c0001t0001g0153a0001c0001t0001g0154others(3): Show | 7 | HG01243.hp2 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+10860_-11+1087 others(15): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265377 | ||||||
| chr17:42265377
|
C | CTTTTTTT others(6): Show |
4 | a0001c0001t0001g0199a0001c0001t0001g0205a0001c0001t0028g0207others(1): Show | 4 | HG02074.hp1 HG02630.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+10870_-11+1087 others(17): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265377 | ||||||
| chr17:42265377
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0011g0224 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-11+10870_-11+1087 others(19): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265377 | ||||||
| chr17:42265377
|
C | CTTTTTTT others(9): Show |
11 | a0001c0001t0001g0209a0001c0001t0001g0219a0001c0001t0001g0251others(8): Show | 11 | HG00423.hp2 HG01109.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+10870_-11+1087 others(20): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265377 | ||||||
| chr17:42265377
|
C | CTTTTTTT others(10): Show |
10 | a0001c0001t0002g0230a0001c0001t0006g0252a0001c0001t0007g0229others(7): Show | 10 | HG02055.hp1 HG02109.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11+10870_-11+1087 others(21): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265377 | ||||||
| chr17:42265377
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0007g0242 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-11+10870_-11+1087 others(22): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265377 | ||||||
| chr17:42265377
|
C | CTTTTTTT others(12): Show |
11 | a0001c0001t0002g0004a0001c0001t0002g0233a0001c0001t0002g0235others(8): Show | 11 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11+10870_-11+1087 others(23): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265377 | ||||||
| chr17:42265377
|
C | CTTTTTTT others(13): Show |
3 | a0001c0001t0002g0003a0001c0001t0002g0232a0001c0001t0025g0231 | 3 | HG02486.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-11+10870_-11+1087 others(24): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265377 | ||||||
| chr17:42265377
|
C | CTTTTTTT others(17): Show |
3 | a0001c0001t0001g0160a0001c0001t0022g0143a0005c0008t0014g0198 | 3 | HG01167.hp2 HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-11+10870_-11+1087 others(28): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265377 | ||||||
| chr17:42265377
|
C | CTTTTTTT others(18): Show |
6 | a0001c0001t0001g0002a0001c0001t0001g0152a0001c0001t0001g0196others(3): Show | 6 | HG00642.hp2 HG01981.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+10870_-11+1087 others(29): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265377 | ||||||
| chr17:42265377
|
C | CTTTTTTT others(19): Show |
15 | a0001c0001t0001g0150a0001c0001t0001g0162a0001c0001t0001g0192others(12): Show | 15 | HG00140.hp2 HG02083.hp2 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.-11+10870_-11+1087 others(30): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265377 | ||||||
| chr17:42265377
|
C | CTTTTTTT others(20): Show |
12 | a0001c0001t0001g0148a0001c0001t0001g0161a0001c0001t0001g0163others(9): Show | 12 | HG00558.hp1 HG02004.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11+10870_-11+1087 others(31): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265377 | ||||||
| chr17:42265377
|
C | CTTTTTTT others(21): Show |
11 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0001g0181others(8): Show | 11 | HG00609.hp1 HG02027.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+10870_-11+1087 others(32): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265377 | ||||||
| chr17:42265377
|
C | CTTTTTTT others(22): Show |
10 | a0001c0001t0001g0147a0001c0001t0001g0173a0001c0001t0001g0174others(7): Show | 10 | HG00438.hp1 HG01993.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11+10870_-11+1087 others(33): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265377 | ||||||
| chr17:42265377
|
C | CTTTTTTT others(23): Show |
3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | NA19002.hp1 NA19009.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-11+10870_-11+1087 others(34): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265377 | ||||||
| chr17:42265377
|
C | CTTTTTTT others(24): Show |
1 | a0001c0001t0001g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-11+10870_-11+1087 others(35): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265377 | ||||||
| chr17:42265377
|
C | CTTTTTTT others(25): Show |
1 | a0001c0001t0001g0167 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-11+10870_-11+1087 others(36): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265377 | ||||||
| chr17:42265377
|
C | CTTTTTTT others(26): Show |
2 | a0001c0001t0001g0165a0001c0007t0001g0166 | 2 | HG00621.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-11+10870_-11+1087 others(37): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265377 | ||||||
| chr17:42265377
|
C | CTTTTTTT others(27): Show |
1 | a0001c0001t0001g0164 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-11+10870_-11+1087 others(38): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265377 | ||||||
| chr17:42265377
|
C | T | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11+10871G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265377 | ||||||
| chr17:42265390
|
G | T | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11+10858C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265390 | ||||||
| chr17:42265391
|
A | T | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11+10857T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265391 | ||||||
| chr17:42265392
|
G | T | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11+10856C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265392 | ||||||
| chr17:42265393
|
A | T | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11+10855T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265393 | ||||||
| chr17:42265394
|
C | T | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11+10854G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265394 | ||||||
| chr17:42265395
|
G | T | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11+10853C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265395 | ||||||
| chr17:42265402
|
C | T | 32 | a0001c0001t0001g0251a0001c0001t0002g0003a0001c0001t0002g0004others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.-11+10846G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265402 | ||||||
| chr17:42265410
|
C | A | 3 | a0001c0001t0001g0205a0001c0001t0028g0207a0001c0001t0029g0206 | 3 | HG02630.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-11+10838G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265410 | ||||||
| chr17:42265433
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-11+10815A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265433 | ||||||
| chr17:42265500
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-11+10748C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265500 | ||||||
| chr17:42265560
|
C | T | 3 | a0001c0001t0001g0163a0001c0001t0016g0212a0001c0001t0016g0225 | 3 | HG03710.hp2 HG03927.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-11+10688G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265560 | ||||||
| chr17:42265667
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-11+10581A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265667 | ||||||
| chr17:42265824
|
T | C | 2 | a0001c0001t0015g0106a0001c0001t0015g0140 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-11+10424A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265824 | ||||||
| chr17:42265971
|
C | T | 5 | a0001c0001t0009g0083a0001c0001t0009g0084a0001c0001t0009g0085others(2): Show | 5 | HG00408.hp1 NA18964.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+10277G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42265971 | ||||||
| chr17:42266065
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-11+10183T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42266065 | ||||||
| chr17:42266197
|
T | G | 6 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0201others(3): Show | 6 | HG00642.hp2 HG01993.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+10051A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42266197 | ||||||
| chr17:42266198
|
C | T | 3 | a0001c0001t0001g0205a0001c0001t0028g0207a0001c0001t0029g0206 | 3 | HG02630.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-11+10050G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42266198 | ||||||
| chr17:42266288
|
G | C | 2 | a0001c0003t0008g0158a0001c0003t0008g0159 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-11+9960C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42266288 | ||||||
| chr17:42266327
|
A | C | 32 | a0001c0001t0001g0251a0001c0001t0002g0003a0001c0001t0002g0004others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.-11+9921T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42266327 | ||||||
| chr17:42266546
|
T | A | 5 | a0001c0001t0009g0083a0001c0001t0009g0084a0001c0001t0009g0085others(2): Show | 5 | HG00408.hp1 NA18964.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+9702A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42266546 | ||||||
| chr17:42266546
|
T | TA | 9 | a0001c0001t0001g0097a0001c0001t0003g0094a0001c0001t0003g0096others(6): Show | 9 | HG00639.hp2 HG00642.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11+9701dupT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42266546 | ||||||
| chr17:42266553
|
A | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-11+9695T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42266553 | ||||||
| chr17:42266554
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0110 | 3 | HG02027.hp2 HG02056.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.-11+9694T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42266554 | ||||||
| chr17:42266556
|
A | T | 1 | a0001c0001t0001g0109 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-11+9692T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42266556 | ||||||
| chr17:42266560
|
A | T | 1 | a0001c0001t0022g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-11+9688T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42266560 | ||||||
| chr17:42266583
|
T | C | 3 | a0001c0001t0011g0146a0001c0001t0011g0211a0001c0001t0011g0224 | 3 | HG02647.hp1 HG03041.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-11+9665A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42266583 | ||||||
| chr17:42266706
|
T | C | 3 | a0001c0001t0007g0229a0001c0001t0020g0248a0001c0001t0021g0247 | 3 | HG02723.hp2 HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-11+9542A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42266706 | ||||||
| chr17:42266868
|
T | A | 1 | a0001c0001t0022g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-11+9380A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42266868 | ||||||
| chr17:42266882
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0203 | 2 | HG02735.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-11+9366T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42266882 | ||||||
| chr17:42266938
|
A | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(70): Show | 74 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.-11+9310T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42266938 | ||||||
| chr17:42267277
|
CCTT | C | 7 | a0001c0001t0001g0088a0001c0001t0001g0109a0001c0001t0001g0131others(4): Show | 7 | HG01192.hp1 NA18975.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+8968_-11+8970d others(5): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42267277 | ||||||
| chr17:42267284
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-11+8964G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42267284 | ||||||
| chr17:42267285
|
T | A | 1 | a0001c0001t0001g0135 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-11+8963A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42267285 | ||||||
| chr17:42267286
|
T | A | 1 | a0001c0001t0001g0135 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-11+8962A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42267286 | ||||||
| chr17:42267350
|
G | C | 12 | a0001c0001t0001g0090a0001c0001t0001g0097a0001c0001t0003g0091others(9): Show | 12 | HG00639.hp2 HG00642.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11+8898C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42267350 | ||||||
| chr17:42267649
|
G | A | 6 | a0001c0001t0001g0209a0001c0001t0011g0146a0001c0001t0011g0210others(3): Show | 6 | HG01109.hp2 HG02647.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+8599C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42267649 | ||||||
| chr17:42267681
|
G | A | 1 | a0001c0001t0005g0137 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-11+8567C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42267681 | ||||||
| chr17:42267687
|
G | A | 2 | a0001c0001t0022g0143a0001c0005t0024g0107 | 2 | HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-11+8561C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42267687 | ||||||
| chr17:42267958
|
C | CA | 5 | a0001c0001t0001g0002a0001c0001t0001g0101a0001c0001t0001g0203others(2): Show | 5 | HG00673.hp2 HG01981.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+8289dupT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42267958 | ||||||
| chr17:42268141
|
A | C | 1 | a0001c0001t0002g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-11+8107T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42268141 | ||||||
| chr17:42268423
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-11+7825A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42268423 | ||||||
| chr17:42268982
|
T | G | 1 | a0001c0001t0004g0138 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-11+7266A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42268982 | ||||||
| chr17:42269061
|
C | A | 32 | a0001c0001t0001g0251a0001c0001t0002g0003a0001c0001t0002g0004others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.-11+7187G>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42269061 | ||||||
| chr17:42269451
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-11+6797G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42269451 | ||||||
| chr17:42269495
|
G | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(112): Show | 116 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-11+6753C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42269495 | ||||||
| chr17:42269507
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0153a0001c0001t0001g0154others(3): Show | 7 | HG01243.hp2 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+6741C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42269507 | ||||||
| chr17:42269745
|
C | T | 1 | a0001c0001t0007g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-11+6503G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42269745 | ||||||
| chr17:42269791
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-11+6457G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42269791 | ||||||
| chr17:42269834
|
G | GA | 11 | a0001c0001t0001g0102a0001c0001t0001g0220a0001c0001t0001g0222others(8): Show | 11 | HG04199.hp1 NA18939.hp1 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+6413dupT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42269834 | ||||||
| chr17:42270096
|
G | A | 32 | a0001c0001t0001g0251a0001c0001t0002g0003a0001c0001t0002g0004others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.-11+6152C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42270096 | ||||||
| chr17:42270314
|
G | C | 7 | a0001c0001t0001g0251a0001c0001t0006g0252a0001c0001t0006g0253others(4): Show | 7 | HG03209.hp2 HG04199.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+5934C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42270314 | ||||||
| chr17:42270323
|
G | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(112): Show | 116 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-11+5925C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42270323 | ||||||
| chr17:42270434
|
G | C | 1 | a0001c0002t0001g0103 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-11+5814C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42270434 | ||||||
| chr17:42271478
|
T | C | 34 | a0001c0001t0001g0251a0001c0001t0002g0003a0001c0001t0002g0004others(31): Show | 34 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.-11+4770A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42271478 | ||||||
| chr17:42271582
|
T | TA | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(120): Show | 124 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.-11+4665dupT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42271582 | ||||||
| chr17:42271591
|
A | G | 34 | a0001c0001t0001g0251a0001c0001t0002g0003a0001c0001t0002g0004others(31): Show | 34 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.-11+4657T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42271591 | ||||||
| chr17:42271671
|
G | A | 1 | a0001c0001t0022g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-11+4577C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42271671 | ||||||
| chr17:42272167
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-11+4081A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42272167 | ||||||
| chr17:42272229
|
C | T | 32 | a0001c0001t0001g0251a0001c0001t0002g0003a0001c0001t0002g0004others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.-11+4019G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42272229 | ||||||
| chr17:42272237
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-11+4011C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42272237 | ||||||
| chr17:42272294
|
T | A | 1 | a0001c0001t0001g0227 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-11+3954A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42272294 | ||||||
| chr17:42272490
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-11+3758G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42272490 | ||||||
| chr17:42272646
|
A | C | 1 | a0001c0001t0012g0008 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-11+3602T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42272646 | ||||||
| chr17:42273302
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-11+2946T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42273302 | ||||||
| chr17:42273476
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-11+2772A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42273476 | ||||||
| chr17:42273501
|
G | T | 1 | a0001c0001t0007g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-11+2747C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42273501 | ||||||
| chr17:42273858
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(70): Show | 74 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.-11+2390C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42273858 | ||||||
| chr17:42274049
|
A | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-11+2199T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274049 | ||||||
| chr17:42274150
|
G | C | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2098C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274150 | ||||||
| chr17:42274152
|
G | GTTCTCAC others(5): Show |
1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2095_-11+2096i others(14): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274152 | ||||||
| chr17:42274154
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2094T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274154 | ||||||
| chr17:42274160
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2088C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274160 | ||||||
| chr17:42274164
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2084C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274164 | ||||||
| chr17:42274168
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2080T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274168 | ||||||
| chr17:42274171
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2077A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274171 | ||||||
| chr17:42274173
|
G | C | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2075C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274173 | ||||||
| chr17:42274174
|
T | G | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2074A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274174 | ||||||
| chr17:42274175
|
T | G | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2073A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274175 | ||||||
| chr17:42274178
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2070C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274178 | ||||||
| chr17:42274182
|
A | T | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2066T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274182 | ||||||
| chr17:42274183
|
T | A | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2065A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274183 | ||||||
| chr17:42274185
|
G | C | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2063C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274185 | ||||||
| chr17:42274187
|
A | T | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2061T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274187 | ||||||
| chr17:42274189
|
A | T | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2059T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274189 | ||||||
| chr17:42274193
|
T | G | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2055A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274193 | ||||||
| chr17:42274197
|
T | G | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2051A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274197 | ||||||
| chr17:42274201
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2047C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274201 | ||||||
| chr17:42274206
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2042C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274206 | ||||||
| chr17:42274207
|
T | A | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2041A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274207 | ||||||
| chr17:42274210
|
A | T | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2038T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274210 | ||||||
| chr17:42274211
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2037C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274211 | ||||||
| chr17:42274215
|
C | G | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2033G>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274215 | ||||||
| chr17:42274217
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2031T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274217 | ||||||
| chr17:42274218
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-11+2030C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274218 | ||||||
| chr17:42274220
|
T | A | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2028A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274220 | ||||||
| chr17:42274221
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2027T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274221 | ||||||
| chr17:42274223
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2025C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274223 | ||||||
| chr17:42274229
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2019T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274229 | ||||||
| chr17:42274231
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2017G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274231 | ||||||
| chr17:42274233
|
A | T | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2015T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274233 | ||||||
| chr17:42274234
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2014T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274234 | ||||||
| chr17:42274241
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2007C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274241 | ||||||
| chr17:42274248
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+2000T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274248 | ||||||
| chr17:42274257
|
T | G | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+1991A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274257 | ||||||
| chr17:42274259
|
T | G | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+1989A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274259 | ||||||
| chr17:42274260
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+1988A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274260 | ||||||
| chr17:42274267
|
G | C | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+1981C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274267 | ||||||
| chr17:42274270
|
G | C | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+1978C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274270 | ||||||
| chr17:42274276
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+1972G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274276 | ||||||
| chr17:42274277
|
T | G | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+1971A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274277 | ||||||
| chr17:42274281
|
C | CA | 33 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0112others(30): Show | 33 | HG00423.hp1 HG00438.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.-11+1966dupT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274281 | ||||||
| chr17:42274281
|
CAAA | C | 25 | a0001c0001t0001g0142a0001c0001t0001g0205a0001c0001t0001g0209others(22): Show | 25 | HG00423.hp2 HG00558.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-11+1964_-11+1966d others(5): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274281 | ||||||
| chr17:42274281
|
CAAAA | C | 53 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0161others(50): Show | 53 | HG00140.hp2 HG00438.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.-11+1963_-11+1966d others(6): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274281 | ||||||
| chr17:42274281
|
CAAAAA | C | 35 | a0001c0001t0001g0001a0001c0001t0001g0147a0001c0001t0001g0148others(32): Show | 36 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.-11+1962_-11+1966d others(7): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274281 | ||||||
| chr17:42274281
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0011g0146 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-11+1957_-11+1966d others(12): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274281 | ||||||
| chr17:42274284
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+1964T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274284 | ||||||
| chr17:42274286
|
A | T | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+1962T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274286 | ||||||
| chr17:42274291
|
AAAAAAAA others(20): Show |
A | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+1930_-11+1956d others(29): Show |
STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274291 | ||||||
| chr17:42274304
|
A | C | 1 | a0001c0001t0001g0007 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-11+1944T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274304 | ||||||
| chr17:42274324
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+1924G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274324 | ||||||
| chr17:42274328
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+1920C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274328 | ||||||
| chr17:42274337
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+1911A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274337 | ||||||
| chr17:42274338
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+1910C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274338 | ||||||
| chr17:42274339
|
G | C | 1 | a0001c0001t0001g0141 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-11+1909C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274339 | ||||||
| chr17:42274340
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+1908T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274340 | ||||||
| chr17:42274341
|
G | T | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+1907C>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274341 | ||||||
| chr17:42274347
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+1901T>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274347 | ||||||
| chr17:42274348
|
A | T | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11+1900T>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274348 | ||||||
| chr17:42274421
|
G | A | 1 | a0001c0001t0007g0257 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-11+1827C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274421 | ||||||
| chr17:42274471
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0142others(113): Show | 117 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-11+1777A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274471 | ||||||
| chr17:42274478
|
T | G | 1 | a0001c0001t0022g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-11+1770A>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274478 | ||||||
| chr17:42274806
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-11+1442A>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274806 | ||||||
| chr17:42274806
|
T | C | 1 | a0001c0001t0009g0144 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-11+1442A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274806 | ||||||
| chr17:42275129
|
G | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0147others(112): Show | 116 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-11+1119C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42275129 | ||||||
| chr17:42275131
|
G | A | 3 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0005g0228 | 3 | HG03654.hp1 HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-11+1117C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42275131 | ||||||
| chr17:42275308
|
T | C | 1 | a0001c0009t0008g0258 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-11+940A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42275308 | ||||||
| chr17:42275640
|
C | G | 1 | a0001c0001t0005g0005 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-11+608G>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42275640 | ||||||
| chr17:42275797
|
G | C | 1 | a0001c0001t0005g0228 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-11+451C>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42275797 | ||||||
| chr17:42275938
|
G | A | 32 | a0001c0001t0001g0251a0001c0001t0002g0003a0001c0001t0002g0004others(29): Show | 32 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.-11+310C>T | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42275938 | ||||||
| chr17:42275966
|
A | G | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-11+282T>C | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42275966 | ||||||
| chr17:42276148
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-11+100A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42276148 | ||||||
| chr17:42276216
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-11+32G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42276216 |