Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | MAVWI others(782): Show |
chr17 | 42194177 | 42281391 |
| a0002 | 0/0 | 787 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | MAVWI others(782): Show |
chr17 | 42194177 | 42281391 |
| a0003 | 0/0 | 787 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | MAVWI others(782): Show |
chr17 | 42194177 | 42281391 |
| a0004 | 0/0 | 787 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | MAVWI others(782): Show |
chr17 | 42194177 | 42281391 |
| a0005 | 0/0 | 787 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | MAVWI others(782): Show |
chr17 | 42194177 | 42281391 |
| a0006 | 0/0 | 787 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | MAVWI others(782): Show |
chr17 | 42194177 | 42281391 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2361 | 246 | 78 | 35 | 93 | 8 | 30 | STAT5B_chr17_42194177_42281391 | STAT5B | ATGGC others(2356): Show |
chr17 | 42194177 | 42281391 | ||
| a0001c0002 | 0/0 | 2361 | 4 | 0 | 0 | 0 | 0 | 4 | STAT5B_chr17_42194177_42281391 | STAT5B | ATGGC others(2356): Show |
chr17 | 42194177 | 42281391 | ||
| a0001c0003 | 0/0 | 2361 | 2 | 2 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | ATGGC others(2356): Show |
chr17 | 42194177 | 42281391 | ||
| a0001c0005 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | ATGGC others(2356): Show |
chr17 | 42194177 | 42281391 | ||
| a0001c0007 | 0/0 | 2361 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | ATGGC others(2356): Show |
chr17 | 42194177 | 42281391 | ||
| a0001c0009 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | ATGGC others(2356): Show |
chr17 | 42194177 | 42281391 | ||
| a0002c0004 | 0/0 | 2361 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | ATGGC others(2356): Show |
chr17 | 42194177 | 42281391 | ||
| a0003c0006 | 0/0 | 2361 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | ATGGC others(2356): Show |
chr17 | 42194177 | 42281391 | ||
| a0004c0010 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | ATGGC others(2356): Show |
chr17 | 42194177 | 42281391 | ||
| a0005c0008 | 0/0 | 2361 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | ATGGC others(2356): Show |
chr17 | 42194177 | 42281391 | ||
| a0006c0011 | 0/0 | 2361 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | ATGGC others(2356): Show |
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 | GGCGG others(5074): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0002 | 0/0 | 5077 | 16 | 13 | 2 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5072): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0003 | 0/0 | 5081 | 14 | 2 | 6 | 2 | 2 | 2 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5076): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0004 | 0/0 | 5075 | 10 | 1 | 3 | 4 | 1 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5070): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0005 | 0/1 | 5077 | 8 | 3 | 2 | 0 | 0 | 2 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5072): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0006 | 0/0 | 5075 | 7 | 1 | 1 | 5 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5070): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0007 | 0/0 | 5073 | 6 | 6 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5068): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0008 | 0/0 | 5077 | 3 | 1 | 2 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5072): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0009 | 0/0 | 5075 | 5 | 0 | 0 | 5 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5070): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0010 | 0/0 | 5079 | 5 | 5 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5074): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0011 | 0/0 | 5079 | 4 | 4 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5074): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0012 | 0/0 | 5079 | 4 | 1 | 0 | 1 | 0 | 2 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5074): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0013 | 0/0 | 5059 | 3 | 3 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5054): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0014 | 0/0 | 5079 | 2 | 2 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5074): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0015 | 0/0 | 5081 | 2 | 2 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5076): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0016 | 0/0 | 5079 | 2 | 0 | 0 | 0 | 0 | 2 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5074): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0017 | 0/0 | 5079 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5074): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0018 | 0/0 | 5077 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5072): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0019 | 0/0 | 5077 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5072): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0020 | 0/0 | 5077 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5072): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0021 | 0/0 | 5077 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5072): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0022 | 0/0 | 5077 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5072): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0023 | 0/0 | 5079 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5074): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0025 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5074): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0026 | 0/0 | 5079 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5074): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0027 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5076): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0028 | 0/0 | 5077 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5072): Show |
chr17 | 42194177 | 42281391 |
| a0001c0001t0029 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5074): Show |
chr17 | 42194177 | 42281391 |
| a0001c0002t0001 | 0/0 | 5079 | 4 | 0 | 0 | 0 | 0 | 4 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5074): Show |
chr17 | 42194177 | 42281391 |
| a0001c0003t0008 | 0/0 | 5077 | 2 | 2 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5072): Show |
chr17 | 42194177 | 42281391 |
| a0001c0005t0024 | 0/0 | 5027 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5022): Show |
chr17 | 42194177 | 42281391 |
| a0001c0007t0001 | 0/0 | 5079 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5074): Show |
chr17 | 42194177 | 42281391 |
| a0001c0009t0008 | 0/0 | 5077 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5072): Show |
chr17 | 42194177 | 42281391 |
| a0002c0004t0003 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5076): Show |
chr17 | 42194177 | 42281391 |
| a0003c0006t0001 | 0/0 | 5079 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5074): Show |
chr17 | 42194177 | 42281391 |
| a0004c0010t0002 | 0/0 | 5077 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5072): Show |
chr17 | 42194177 | 42281391 |
| a0005c0008t0014 | 0/0 | 5079 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5074): Show |
chr17 | 42194177 | 42281391 |
| a0006c0011t0001 | 0/0 | 5079 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | GGCGG others(5074): Show |
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 | 2 | 0 | 1 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0034 | 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 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0078 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0085 | 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 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0112 | 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 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0133 | 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 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0152 | 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 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0163 | 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 |
| a0001c0001t0001g0166 | 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 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0172 | 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 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0178 | 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 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0195 | 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 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0228 | 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 |
| a0001c0001t0002g0234 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0003g0148 | 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 |
| a0001c0001t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0005g0086 | 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 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0005g0130 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0005g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0006g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0007g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0007g0241 | 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 |
| a0001c0001t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0008g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0008g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0009g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0009g0082 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0009g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0010g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0010g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0010g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0010g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0011g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0011g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0011g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0011g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0012g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0012g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0012g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0012g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0013g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0013g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0013g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0014g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0014g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0015g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0015g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0016g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0016g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0017g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0018g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0019g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0020g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0021g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0022g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0023g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0025g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0026g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0027g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0028g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0001t0029g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0003t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0003t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0005t0024g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0007t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0001c0009t0008g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0002c0004t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0003c0006t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0004c0010t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0005c0008t0014g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| a0006c0011t0001g0131 | 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 | g0043 | EUR | GBR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | GBR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00408 | hp1 | a0001 | c0001 | t0009 | g0142 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00423 | hp1 | a0002 | c0004 | t0003 | g0109 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00639 | hp1 | a0003 | c0006 | t0001 | g0044 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0069 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0042 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0045 | 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 | g0207 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0128 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0086 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0114 | AMR | PUR | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01243 | hp2 | a0001 | c0001 | t0008 | g0153 | 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 | g0024 | 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 | g0031 | AMR | CLM | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | IBS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0097 | EUR | IBS | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01884 | hp2 | a0001 | c0001 | t0013 | g0102 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | PEL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0255 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0240 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0120 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | PEL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0121 | AMR | PEL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CDX | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CDX | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02257 | hp1 | a0001 | c0001 | t0022 | g0141 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02257 | hp2 | a0001 | c0001 | t0012 | g0062 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02258 | hp2 | a0001 | c0001 | t0013 | g0103 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0151 | 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 | g0215 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02572 | hp2 | a0001 | c0001 | t0015 | g0138 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02602 | hp1 | a0001 | c0001 | t0018 | g0075 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0126 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02630 | hp1 | a0001 | c0001 | t0028 | g0204 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02630 | hp2 | a0004 | c0010 | t0002 | g0231 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0144 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0113 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02698 | hp2 | a0001 | c0001 | t0012 | g0009 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02717 | hp2 | a0001 | c0001 | t0015 | g0104 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02723 | hp2 | a0001 | c0001 | t0020 | g0245 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0051 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0087 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0242 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02809 | hp2 | a0001 | c0003 | t0008 | g0156 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02818 | hp1 | a0001 | c0001 | t0025 | g0229 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02886 | hp1 | a0001 | c0001 | t0010 | g0018 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0241 | AFR | ESN | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02965 | hp1 | a0001 | c0001 | t0029 | g0203 | AFR | ESN | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02965 | hp2 | a0001 | c0001 | t0010 | g0074 | AFR | ESN | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02976 | hp1 | a0005 | c0008 | t0014 | g0196 | AFR | ESN | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03041 | hp2 | a0001 | c0001 | t0011 | g0222 | AFR | GWD | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03098 | hp1 | a0001 | c0001 | t0014 | g0184 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03098 | hp2 | a0001 | c0001 | t0013 | g0137 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | ESN | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | ESN | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03209 | hp2 | a0001 | c0009 | t0008 | g0256 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03225 | hp2 | a0001 | c0001 | t0011 | g0206 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0127 | 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 | g0058 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0060 | SAS | STU | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0022 | SAS | STU | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0101 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03710 | hp2 | a0001 | c0001 | t0016 | g0210 | SAS | PJL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03831 | hp1 | a0001 | c0001 | t0017 | g0048 | SAS | BEB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | BEB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03927 | hp1 | a0001 | c0001 | t0016 | g0223 | SAS | BEB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0226 | SAS | BEB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | STU | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | STU | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0129 | SAS | STU | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | STU | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0066 | SAS | STU | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0077 | AFR | YRI | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18612 | hp2 | a0001 | c0007 | t0001 | g0164 | EAS | CHB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18906 | hp1 | a0001 | c0001 | t0014 | g0190 | AFR | YRI | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18939 | hp2 | a0001 | c0001 | t0027 | g0021 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18957 | hp1 | a0001 | c0001 | t0006 | g0254 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18964 | hp1 | a0001 | c0001 | t0009 | g0081 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18968 | hp2 | a0001 | c0001 | t0026 | g0177 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18975 | hp2 | a0006 | c0011 | t0001 | g0131 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18977 | hp1 | a0001 | c0001 | t0012 | g0181 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18977 | hp2 | a0001 | c0001 | t0006 | g0250 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18979 | hp2 | a0001 | c0001 | t0009 | g0082 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA18999 | hp2 | a0001 | c0001 | t0009 | g0083 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0098 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0167 | 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 | g0219 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0025 | 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 | g0105 | AFR | LWK | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19043 | hp1 | a0001 | c0001 | t0011 | g0209 | AFR | LWK | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | LWK | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19066 | hp1 | a0001 | c0001 | t0006 | g0252 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19067 | hp2 | a0001 | c0001 | t0009 | g0084 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19077 | hp1 | a0001 | c0001 | t0006 | g0251 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0173 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19091 | hp1 | a0001 | c0001 | t0006 | g0253 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ASW | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | ASW | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0148 | EUR | TSI | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | GIH | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | GIH | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0248 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02559 | hp1 | a0001 | c0001 | t0010 | g0070 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG03471 | hp2 | a0001 | c0001 | t0021 | g0246 | AFR | MSL | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| HG06807 | hp1 | a0001 | c0003 | t0008 | g0157 | 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 | g0235 | AFR | USA | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | USA | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA21309 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | LWK | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0227 | AFR | LWK | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0130 | REF | REF | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0078 | REF | REF | STAT5B_chr17_42194177_42281391 | STAT5B | chr17 | 42194177 | 42281391 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:42207674 | C | T | 1 | a0003 | 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 | a0004 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0013 a0001c0001t0015 a0001c0001t0022 others(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 | a0001c0001t0012 a0001c0001t0023 |
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 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0019 others(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 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0015 others(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 | a0001c0001t0013 a0001c0001t0015 |
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 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0027 others(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 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(9): Show |
36 | HG01167.hp1 HG01169.hp1 HG01192.hp1 others(33): 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 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0009 |
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 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(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 | a0001c0001t0028 a0001c0001t0029 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:42202040 | C | T | 6 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0013g0137 others(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 | a0001c0001t0001g0140 | 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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0004g0087 | 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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0008g0014 a0001c0001t0008g0114 a0001c0001t0018g0075 |
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 | a0001c0007t0001g0164 | 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 | a0001c0001t0003g0093 | 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 | a0001c0001t0011g0144 a0001c0001t0011g0206 a0001c0001t0011g0209 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0047 | 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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0005t0024g0105 | 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 | a0001c0001t0001g0096 a0001c0001t0003g0088 a0001c0001t0003g0089 others(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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0011g0144 a0001c0001t0011g0206 a0001c0001t0011g0209 others(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 | a0001c0001t0009g0142 | 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 | a0001c0001t0001g0112 a0001c0001t0001g0170 a0001c0001t0001g0171 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0127 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0038 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0008g0153 | 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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0125 a0001c0001t0001g0151 a0001c0001t0001g0155 |
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 | a0001c0001t0001g0046 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0127 others(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 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0213 |
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 | a0001c0001t0001g0125 a0001c0001t0001g0151 a0001c0001t0001g0154 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0054 | 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 | a0001c0001t0010g0074 | 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 | a0001c0001t0001g0090 a0001c0001t0001g0096 a0001c0001t0002g0247 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0011g0144 a0001c0001t0011g0206 a0001c0001t0011g0209 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0003g0147 a0001c0001t0003g0148 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0003g0060 a0001c0001t0011g0144 a0001c0001t0011g0209 others(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 | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(152): Show |
157 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(154): 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 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0106 others(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 | a0001c0001t0001g0198 a0001c0001t0003g0088 a0001c0001t0003g0091 others(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 | a0001c0001t0001g0096 a0001c0001t0003g0092 a0001c0001t0003g0093 others(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 | a0001c0001t0001g0106 | 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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0127 others(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 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0015g0104 others(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 | a0001c0001t0004g0016 a0001c0001t0006g0250 a0001c0001t0006g0251 others(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 | a0001c0001t0022g0141 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0013g0137 others(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 | a0001c0001t0007g0240 a0001c0001t0007g0241 a0001c0001t0007g0242 others(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 | a0001c0001t0026g0177 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0195 | 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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0125 | 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 | a0001c0001t0001g0146 | 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 | a0001c0001t0011g0144 a0001c0001t0011g0206 a0001c0001t0011g0209 others(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 | a0001c0001t0004g0069 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0003g0022 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0008g0153 a0001c0001t0013g0102 a0001c0001t0013g0103 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0005t0024g0105 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0096 | 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 | a0001c0009t0008g0256 | 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0013g0137 others(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 | a0001c0001t0001g0106 | 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 | a0001c0001t0006g0120 a0001c0001t0006g0128 a0001c0001t0006g0250 others(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 | a0001c0001t0012g0058 a0001c0001t0012g0062 |
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 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0013g0137 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0176 a0001c0001t0001g0197 |
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 | a0001c0001t0006g0120 a0001c0001t0006g0128 a0001c0001t0008g0014 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | 236 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(233): Show |
238 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(235): 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 | a0001c0001t0006g0120 a0001c0001t0006g0128 a0001c0001t0006g0250 others(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 | a0001c0001t0001g0192 | 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 | a0001c0001t0007g0255 | 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 | a0001c0001t0011g0144 a0001c0001t0011g0206 a0001c0001t0011g0209 others(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 | a0001c0001t0022g0141 | 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 | a0001c0001t0001g0071 | 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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0013g0137 others(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 | a0001c0001t0003g0061 | 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 | a0001c0001t0006g0250 a0001c0001t0006g0251 a0001c0001t0006g0252 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0132 | 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 | a0001c0001t0008g0014 | 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 | a0001c0001t0008g0014 a0001c0001t0008g0114 a0001c0001t0018g0075 |
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 | 71 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0019 others(68): Show |
71 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(68): 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 | a0001c0001t0010g0018 | 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 | a0001c0001t0010g0018 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1474-1478A>G | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 12/18 | chr17 | 42213668 | |||||||
| chr17:42213856 | G | A | 5 | a0001c0001t0010g0018 a0001c0001t0010g0070 a0001c0001t0010g0074 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0007g0255 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0151 a0001c0001t0001g0154 others(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 | a0001c0001t0008g0014 a0001c0001t0008g0114 a0001c0001t0013g0102 others(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 | a0001c0001t0001g0205 a0001c0001t0007g0227 a0001c0001t0008g0153 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0112 a0001c0001t0001g0146 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0257 | 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 | a0001c0001t0014g0184 a0001c0001t0014g0190 a0005c0008t0014g0196 |
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 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0013g0137 others(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 | a0001c0001t0002g0230 a0001c0001t0002g0233 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0152 |
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 | a0001c0005t0024g0105 | 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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0030 | 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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0031 | 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 | a0001c0001t0011g0144 a0001c0001t0011g0206 a0001c0001t0011g0209 others(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 | a0001c0001t0001g0205 a0001c0001t0008g0153 a0001c0001t0028g0204 others(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 | a0001c0001t0008g0014 | 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 | a0001c0001t0011g0209 | 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 | a0001c0001t0001g0122 a0001c0001t0006g0250 a0001c0001t0013g0102 others(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 | a0001c0001t0004g0042 a0001c0001t0004g0043 a0001c0001t0004g0121 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0012g0009 | 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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0194 a0001c0001t0002g0005 others(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 | a0001c0001t0001g0225 | 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 | a0001c0009t0008g0256 | 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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0003g0221 |
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 | a0001c0001t0001g0118 | 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 | a0001c0001t0022g0141 | 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 | a0001c0001t0001g0112 | 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 | 8 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0029 others(5): 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 | a0001c0001t0001g0041 | 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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 |
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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0001c0001t0001g0188 | 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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0001c0001t0001g0115 a0002c0004t0003g0109 |
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 | a0001c0001t0001g0146 | 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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0008g0014 a0001c0001t0008g0114 a0001c0001t0018g0075 |
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 | a0001c0001t0001g0219 | 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 | a0002c0004t0003g0109 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0145 a0001c0001t0001g0205 others(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 | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(80): Show |
84 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(81): 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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0002c0004t0003g0109 | 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 | a0001c0007t0001g0164 a0002c0004t0003g0109 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0159 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0064 | 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 | a0001c0001t0004g0136 | 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 | a0001c0001t0001g0034 a0001c0001t0011g0144 a0001c0001t0011g0206 others(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 | a0001c0001t0001g0034 a0001c0001t0011g0144 a0001c0001t0011g0206 others(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 | a0001c0001t0011g0144 a0001c0001t0011g0209 a0001c0001t0011g0222 others(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 | a0001c0001t0011g0144 a0001c0001t0011g0209 a0001c0001t0011g0222 others(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 | a0001c0001t0011g0144 a0001c0001t0011g0209 a0001c0001t0011g0222 others(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 | a0001c0001t0025g0229 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(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 | a0001c0003t0008g0157 | 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 | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(186): Show |
190 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(187): 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 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0217 | 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 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0013g0137 others(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 | a0001c0001t0008g0014 a0001c0001t0008g0114 a0001c0001t0018g0075 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0116 |
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 | a0001c0001t0006g0120 a0001c0001t0006g0128 a0001c0001t0006g0250 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0180 a0001c0001t0001g0183 a0001c0001t0001g0208 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0124 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0205 a0001c0001t0002g0005 a0001c0001t0002g0006 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(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 | a0001c0001t0009g0082 a0001c0001t0009g0083 a0001c0001t0009g0084 |
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 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0002g0005 others(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 | a0001c0001t0002g0243 a0001c0001t0002g0244 |
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 | a0001c0001t0001g0208 a0001c0001t0011g0144 a0001c0001t0011g0209 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0232 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0009g0081 a0001c0001t0009g0082 a0001c0001t0009g0083 others(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 | a0001c0001t0021g0246 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0073 a0001c0001t0013g0102 a0001c0001t0013g0103 others(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 | a0001c0001t0001g0257 | 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 | a0001c0001t0001g0090 a0001c0001t0001g0096 a0001c0001t0003g0088 others(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 | a0001c0001t0001g0208 a0001c0001t0008g0014 a0001c0001t0008g0114 others(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 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0013g0137 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0127 others(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 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0013g0137 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(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 | a0001c0001t0008g0014 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0191 a0001c0001t0002g0234 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0096 a0001c0001t0003g0093 a0001c0001t0003g0097 |
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 | a0001c0001t0002g0237 a0001c0001t0002g0238 |
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 | a0001c0001t0004g0016 a0001c0001t0013g0102 a0001c0001t0013g0103 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0079 others(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 |
137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
139 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(136): 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 |
87 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(84): 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 | a0001c0001t0001g0073 a0001c0001t0001g0117 a0001c0001t0001g0125 others(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 | a0001c0001t0002g0228 a0001c0001t0002g0243 a0001c0001t0002g0244 others(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 | a0001c0002t0001g0113 | 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 | a0001c0001t0001g0208 a0001c0001t0011g0144 a0001c0001t0011g0206 others(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 | a0001c0001t0010g0018 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0057 a0001c0001t0001g0100 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0208 a0001c0001t0011g0144 a0001c0001t0011g0206 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0205 a0001c0001t0002g0005 a0001c0001t0002g0006 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0205 a0001c0001t0002g0005 a0001c0001t0002g0006 others(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 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0013g0137 others(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 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0013g0137 others(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 | a0001c0001t0003g0022 | 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 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0013g0137 others(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 | a0001c0001t0001g0056 | 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 | 5 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0068 others(2): 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 | a0001c0001t0009g0142 | 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0006g0250 a0001c0001t0006g0251 a0001c0001t0006g0252 others(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 | a0001c0001t0008g0114 a0001c0001t0018g0075 |
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 | a0001c0001t0002g0236 | 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 | a0001c0001t0001g0205 a0001c0001t0028g0204 a0001c0001t0029g0203 |
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 | a0001c0001t0028g0204 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0192 |
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 | a0001c0001t0023g0207 | 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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0178 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0127 others(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 | a0001c0001t0018g0075 | 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 | a0001c0001t0001g0036 a0001c0001t0001g0045 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0205 a0001c0001t0002g0005 a0001c0001t0002g0006 others(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 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0002g0005 others(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 | 28 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0029 others(25): 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 | a0001c0001t0001g0004 a0001c0001t0001g0111 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0117 | 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 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0013g0137 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0013g0137 others(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 | a0001c0001t0020g0245 | 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 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0013g0137 others(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 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0013g0137 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0230 others(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 | a0001c0001t0001g0079 | 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 | a0001c0001t0006g0120 a0001c0001t0006g0128 a0001c0001t0006g0250 others(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 | a0001c0001t0002g0185 | 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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0004g0042 a0001c0001t0004g0043 a0001c0001t0004g0069 others(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 | a0001c0001t0009g0081 a0001c0001t0009g0082 a0001c0001t0009g0083 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0008g0014 a0001c0001t0008g0114 a0001c0001t0018g0075 |
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 | a0001c0001t0001g0132 | 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 | a0001c0001t0002g0239 | 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 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
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 | a0001c0001t0001g0160 | 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 | a0001c0009t0008g0256 | 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 | a0001c0001t0005g0129 | 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 | a0001c0001t0008g0014 a0001c0001t0008g0114 a0001c0001t0018g0075 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0006g0120 others(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 | a0001c0001t0002g0230 a0001c0001t0002g0232 a0001c0001t0002g0233 others(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 | a0001c0001t0001g0205 a0001c0001t0007g0227 a0001c0001t0007g0240 others(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 | a0001c0001t0002g0228 a0001c0001t0002g0243 a0001c0001t0002g0244 |
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 | 53 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0027 others(50): Show |
53 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(50): 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 | 57 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(54): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0023 others(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 | a0001c0001t0004g0042 a0001c0001t0004g0043 a0001c0001t0004g0069 others(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 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0213 |
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 | a0001c0001t0001g0125 a0001c0001t0001g0140 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0205 a0001c0001t0002g0232 a0001c0001t0008g0153 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0065 a0001c0001t0001g0107 others(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 | a0001c0001t0002g0230 a0001c0001t0002g0232 a0001c0001t0006g0128 others(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 | a0001c0001t0001g0036 a0001c0001t0001g0050 a0001c0001t0001g0155 others(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 | 23 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0029 others(20): 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 | a0001c0001t0008g0153 | 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 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0002g0005 others(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 | a0001c0001t0001g0208 a0001c0001t0011g0144 a0001c0001t0011g0206 others(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 | a0001c0001t0021g0246 | 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 | a0001c0001t0002g0228 a0001c0001t0002g0243 a0001c0001t0002g0244 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0052 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0013 a0001c0001t0002g0006 a0001c0001t0002g0228 others(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 | a0001c0001t0001g0205 a0001c0001t0002g0005 a0001c0001t0002g0247 others(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 | a0001c0001t0002g0232 a0004c0010t0002g0231 |
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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0053 | 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 | a0001c0001t0023g0207 | 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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0163 a0001c0001t0001g0166 others(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 | a0001c0001t0001g0186 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-10-8928G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42241065 | |||||||
| chr17:42241420 | A | G | 1 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0249 a0001c0001t0002g0228 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0152 |
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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0208 a0001c0001t0011g0144 a0001c0001t0011g0206 others(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 | 1 | a0001c0001t0005g0086 | 1 | HG01192.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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0146 a0001c0001t0001g0205 others(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 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0013g0137 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0003g0135 | 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 | a0001c0001t0005g0007 a0001c0001t0005g0032 a0001c0001t0005g0033 |
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 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0037 |
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 | a0001c0001t0001g0208 a0001c0001t0011g0144 a0001c0001t0011g0206 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0029g0203 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0249 a0001c0001t0002g0005 a0001c0001t0002g0006 others(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 | a0001c0001t0001g0160 a0001c0001t0001g0171 a0001c0001t0001g0257 others(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 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0011g0144 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0155 a0001c0001t0001g0158 others(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 | a0001c0001t0001g0205 a0001c0001t0028g0204 a0001c0001t0029g0203 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0009t0008g0256 | 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 | a0001c0001t0021g0246 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0108 |
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 | a0001c0001t0002g0228 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0166 a0001c0001t0001g0199 a0001c0001t0001g0202 others(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 | a0001c0001t0001g0208 a0001c0001t0011g0144 a0001c0001t0011g0206 others(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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0110 |
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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0249 a0001c0001t0006g0250 a0001c0001t0006g0251 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0007g0227 | 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 | a0001c0001t0021g0246 | 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 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0013g0137 |
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 | a0001c0001t0004g0087 a0001c0001t0005g0032 |
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 | a0001c0001t0001g0249 a0001c0001t0006g0250 a0001c0001t0006g0251 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0166 a0001c0001t0001g0218 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0158 a0001c0001t0001g0187 |
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 | a0001c0001t0001g0169 | 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 | a0001c0001t0022g0141 a0001c0005t0024g0105 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0030 | 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 | a0001c0001t0003g0088 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(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 | a0001c0001t0001g0150 a0001c0001t0001g0180 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0208 a0001c0001t0002g0237 a0001c0001t0011g0144 others(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 | a0001c0001t0001g0056 a0001c0001t0001g0110 a0001c0001t0004g0098 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0208 a0001c0001t0011g0144 a0001c0001t0011g0206 others(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 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0011g0144 others(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 | a0001c0001t0001g0159 a0001c0001t0001g0201 |
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 | a0001c0001t0008g0114 | 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0011g0144 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0166 a0001c0001t0001g0218 |
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 | a0001c0001t0001g0036 a0001c0001t0001g0057 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | a0001c0001t0001g0214 | 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 | 1 | a0001c0001t0001g0002 | 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 | a0001c0001t0001g0257 | 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 | a0001c0001t0021g0246 | 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 | a0001c0001t0001g0056 a0001c0001t0001g0134 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0194 | 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 | a0001c0001t0002g0239 | 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 | a0001c0005t0024g0105 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0133 a0001c0001t0001g0155 others(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 | a0001c0001t0006g0254 a0001c0001t0007g0227 a0001c0001t0007g0240 others(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 | a0001c0001t0016g0210 | 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 | a0001c0001t0001g0036 a0001c0001t0001g0057 |
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 | a0001c0007t0001g0164 | 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 | a0001c0001t0012g0058 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0012g0062 | 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 | a0001c0001t0001g0208 a0001c0001t0011g0144 a0001c0001t0011g0206 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0230 others(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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0011g0144 others(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 | a0001c0001t0005g0032 | 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0005g0129 | 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 | a0001c0001t0001g0036 a0001c0001t0001g0182 a0001c0001t0005g0007 others(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 | a0001c0001t0001g0182 | 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 | a0001c0001t0002g0228 a0001c0001t0002g0243 a0001c0001t0002g0244 |
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 | a0001c0001t0001g0168 | 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0194 | 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 | a0001c0001t0002g0230 a0001c0001t0002g0233 a0001c0001t0002g0236 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0059 others(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 | a0001c0001t0001g0208 a0001c0001t0002g0005 a0001c0001t0002g0233 others(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 | a0001c0001t0001g0249 a0001c0001t0002g0006 a0001c0001t0002g0228 others(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 | a0001c0001t0002g0230 a0001c0001t0006g0250 a0001c0001t0006g0253 others(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 | a0001c0001t0001g0149 a0001c0001t0001g0166 a0001c0001t0001g0168 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0003g0135 | 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0003g0088 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0205 a0001c0001t0028g0204 a0001c0001t0029g0203 |
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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0230 others(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 | a0001c0001t0002g0185 | 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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0123 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0208 a0001c0001t0011g0144 a0001c0001t0011g0206 others(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 | a0001c0001t0001g0025 | 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 | a0001c0001t0008g0014 | 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 | a0001c0001t0008g0014 | 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 | a0001c0001t0001g0208 a0001c0001t0011g0144 a0001c0001t0011g0206 others(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 | a0001c0001t0001g0205 a0001c0001t0028g0204 a0001c0001t0029g0203 |
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 | a0001c0001t0001g0004 | 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 | a0001c0003t0008g0156 | 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 | a0001c0001t0003g0147 | 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 | a0001c0001t0001g0065 | 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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): 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 | a0001c0002t0001g0101 | 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 | a0001c0002t0001g0066 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0002t0001g0113 | 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 | a0001c0001t0009g0081 a0001c0001t0009g0082 a0001c0001t0009g0083 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0029g0203 | 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 | a0001c0001t0001g0249 a0001c0001t0002g0005 a0001c0001t0002g0006 others(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 | a0001c0001t0006g0250 | 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 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0001g0249 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0006g0250 a0001c0001t0006g0251 a0001c0001t0006g0252 others(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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0122 a0001c0001t0003g0060 |
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 | a0001c0001t0022g0141 | 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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0002g0127 | 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 | a0001c0001t0001g0257 | 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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0099 a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0011g0144 others(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 | a0001c0001t0002g0228 a0001c0001t0002g0243 a0001c0001t0002g0244 |
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 | a0001c0001t0002g0232 a0001c0001t0007g0227 a0001c0001t0021g0246 others(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 | a0001c0001t0020g0245 | 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 | a0001c0001t0020g0245 | 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 | a0001c0001t0020g0245 | 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 | a0001c0001t0001g0140 a0001c0001t0001g0163 a0001c0001t0001g0183 others(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 | a0001c0001t0001g0208 a0001c0001t0011g0144 a0001c0001t0011g0206 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0112 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0146 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0106 a0001c0001t0003g0093 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0108 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0002c0004t0003g0109 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0099 a0001c0001t0001g0140 a0001c0001t0004g0069 others(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 | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(84): 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 | a0001c0001t0001g0208 a0001c0001t0011g0144 a0001c0001t0011g0209 others(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 | a0001c0001t0014g0184 a0001c0001t0014g0190 |
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 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0029g0203 | 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 | a0001c0001t0001g0172 a0001c0001t0001g0178 a0001c0001t0001g0188 |
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 | a0001c0001t0022g0141 | 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 | a0001c0001t0001g0257 | 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 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0213 |
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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0198 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0175 a0001c0001t0001g0187 |
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 | a0001c0001t0001g0165 a0001c0001t0003g0221 |
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 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0166 others(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 | a0001c0001t0001g0047 | 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 | a0001c0001t0006g0120 | 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0169 | 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 | a0001c0001t0001g0160 a0001c0001t0002g0185 |
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 | a0001c0001t0001g0159 a0001c0001t0001g0201 |
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 | a0001c0001t0016g0210 a0001c0001t0016g0223 |
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 | a0001c0001t0001g0215 | 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 | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0057 others(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 | a0001c0001t0003g0022 a0001c0001t0004g0042 a0001c0001t0008g0114 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0004g0121 |
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 | a0001c0001t0001g0031 a0001c0001t0005g0032 a0001c0001t0015g0138 |
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 | a0001c0001t0002g0243 a0001c0001t0002g0244 a0001c0001t0011g0206 others(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 | a0001c0001t0001g0145 a0001c0001t0001g0155 a0001c0001t0007g0240 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0152 |
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 | a0001c0001t0002g0247 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0041 a0001c0001t0001g0050 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0037 others(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 | a0001c0001t0001g0224 a0001c0001t0005g0226 a0001c0002t0001g0101 others(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 | a0001c0001t0001g0118 | 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 | a0001c0001t0001g0132 | 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0054 others(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 | a0001c0001t0001g0090 a0001c0001t0009g0082 a0001c0001t0009g0084 |
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 | a0001c0001t0001g0010 a0001c0001t0009g0083 |
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 | a0001c0001t0001g0076 | 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 | a0001c0001t0009g0081 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0005g0033 |
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 | a0001c0001t0001g0065 a0001c0001t0001g0133 a0001c0001t0010g0070 others(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 | a0001c0001t0001g0011 a0001c0001t0010g0018 |
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 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0098 |
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 | a0001c0001t0003g0135 | 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 | a0001c0001t0001g0125 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0096 others(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 | a0001c0001t0001g0100 a0001c0001t0001g0115 |
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 | a0001c0001t0010g0074 a0001c0001t0010g0126 |
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 | a0001c0001t0001g0011 a0001c0001t0010g0018 |
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 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0098 |
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 | a0001c0001t0001g0249 a0001c0001t0006g0250 a0001c0001t0006g0251 others(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 | a0001c0001t0003g0135 | 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 | a0001c0009t0008g0256 | 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 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0230 others(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 | a0001c0001t0001g0183 a0001c0001t0002g0239 a0001c0001t0025g0229 others(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 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0199 others(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 | a0001c0001t0003g0147 a0001c0001t0003g0148 a0001c0001t0007g0255 others(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 | a0001c0001t0001g0208 a0001c0001t0002g0228 |
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 | a0001c0001t0011g0144 a0001c0001t0011g0209 a0001c0001t0011g0222 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0015 | 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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(251): Show |
256 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(253): 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0249 a0001c0001t0002g0005 others(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 | a0001c0001t0001g0170 | 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 | a0001c0001t0008g0014 | 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 | a0001c0001t0001g0096 a0001c0001t0001g0106 a0001c0001t0001g0166 others(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 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0115 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0161 a0001c0001t0001g0202 a0001c0001t0001g0219 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0179 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0149 a0001c0001t0001g0199 |
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 | a0001c0001t0001g0145 a0001c0001t0001g0150 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0019 others(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 | 93 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(90): Show |
93 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(90): 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 | a0001c0001t0001g0037 a0001c0001t0001g0178 a0001c0001t0001g0188 others(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 | a0001c0002t0001g0051 a0001c0002t0001g0066 a0001c0002t0001g0101 others(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 | a0001c0001t0004g0087 | 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 | a0001c0005t0024g0105 | 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 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0013g0137 others(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 | a0001c0001t0013g0102 a0001c0001t0013g0103 a0001c0001t0013g0137 others(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 | a0001c0005t0024g0105 | 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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0013 | 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 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0011g0144 others(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 | a0001c0001t0001g0160 | 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 | a0001c0001t0009g0142 | 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 | a0001c0001t0007g0227 | 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 | a0001c0001t0001g0249 a0001c0001t0002g0005 a0001c0001t0002g0006 others(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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0011g0144 others(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 | a0001c0001t0005g0129 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0197 a0001c0001t0001g0205 a0001c0001t0028g0204 others(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 | a0001c0001t0011g0222 | 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 | a0001c0001t0001g0208 a0001c0001t0001g0217 a0001c0001t0001g0249 others(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 | a0001c0001t0002g0228 a0001c0001t0006g0250 a0001c0001t0007g0227 others(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 | a0001c0001t0007g0240 | 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 | a0001c0001t0002g0006 a0001c0001t0002g0232 a0001c0001t0002g0233 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0230 a0001c0001t0025g0229 |
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 | a0001c0001t0001g0158 a0001c0001t0022g0141 a0005c0008t0014g0196 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0150 a0001c0001t0001g0194 others(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 | a0001c0001t0001g0149 a0001c0001t0001g0160 a0001c0001t0001g0191 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0159 a0001c0001t0001g0161 others(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 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0145 a0001c0001t0001g0170 a0001c0001t0001g0171 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 |
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 | a0001c0001t0001g0166 | 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0163 a0001c0007t0001g0164 |
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 | a0001c0001t0001g0162 | 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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0249 a0001c0001t0002g0005 a0001c0001t0002g0006 others(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 | a0001c0001t0001g0205 a0001c0001t0028g0204 a0001c0001t0029g0203 |
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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0198 | 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 | a0001c0001t0001g0161 a0001c0001t0016g0210 a0001c0001t0016g0223 |
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 | a0001c0001t0001g0107 | 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 | a0001c0001t0015g0104 a0001c0001t0015g0138 |
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 | a0001c0001t0009g0081 a0001c0001t0009g0082 a0001c0001t0009g0083 others(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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0199 others(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 | a0001c0001t0001g0205 a0001c0001t0028g0204 a0001c0001t0029g0203 |
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 | a0001c0003t0008g0156 a0001c0003t0008g0157 |
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 | a0001c0001t0001g0249 a0001c0001t0002g0005 a0001c0001t0002g0006 others(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 | a0001c0001t0009g0081 a0001c0001t0009g0082 a0001c0001t0009g0083 others(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 | a0001c0001t0001g0096 a0001c0001t0003g0092 a0001c0001t0003g0093 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0108 |
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 | a0001c0001t0001g0107 | 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 | a0001c0001t0022g0141 | 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 | a0001c0001t0011g0144 a0001c0001t0011g0209 a0001c0001t0011g0222 |
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 | a0001c0001t0007g0227 a0001c0001t0020g0245 a0001c0001t0021g0246 |
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 | a0001c0001t0022g0141 | 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 | a0001c0001t0001g0159 a0001c0001t0001g0201 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | 6 | a0001c0001t0001g0085 a0001c0001t0001g0107 a0001c0001t0001g0132 others(3): Show |
6 | HG01192.hp1 NA18975.hp2 NA18982.hp2 others(3): 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0090 a0001c0001t0001g0096 a0001c0001t0003g0088 others(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 | a0001c0001t0001g0208 a0001c0001t0011g0144 a0001c0001t0011g0206 others(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 | a0001c0001t0005g0129 | 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 | a0001c0001t0022g0141 a0001c0005t0024g0105 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0099 a0001c0001t0001g0201 others(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 | a0001c0001t0002g0228 | 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 | a0001c0001t0001g0202 | 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 | a0001c0001t0004g0136 | 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 | a0001c0001t0001g0249 a0001c0001t0002g0005 a0001c0001t0002g0006 others(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 | a0001c0001t0001g0010 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0152 others(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 | a0001c0001t0007g0255 | 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 | a0001c0001t0001g0107 | 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 | a0001c0001t0001g0100 a0001c0001t0001g0218 a0001c0001t0001g0219 others(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 | a0001c0001t0001g0249 a0001c0001t0002g0005 a0001c0001t0002g0006 others(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 | a0001c0001t0001g0249 a0001c0001t0006g0250 a0001c0001t0006g0251 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0002t0001g0101 | 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 | a0001c0001t0001g0249 a0001c0001t0002g0005 a0001c0001t0002g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0249 a0001c0001t0002g0005 a0001c0001t0002g0006 others(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 | a0001c0001t0022g0141 | 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0249 a0001c0001t0002g0005 a0001c0001t0002g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0012g0009 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0007g0227 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | 32 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0110 others(29): Show |
32 | HG00423.hp1 HG00438.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.-11+1966dupT | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42274281 | |||||||
| chr17:42274281 | CAAA | C | 25 | a0001c0001t0001g0140 a0001c0001t0001g0205 a0001c0001t0001g0208 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0159 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0145 a0001c0001t0001g0146 others(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 | a0001c0001t0011g0144 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0007g0255 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0022g0141 | 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0009g0142 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0005g0226 |
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 | a0001c0009t0008g0256 | 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 | a0001c0001t0005g0007 | 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 | a0001c0001t0005g0226 | 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 | a0001c0001t0001g0249 a0001c0001t0002g0005 a0001c0001t0002g0006 others(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 | a0001c0001t0002g0005 a0001c0001t0002g0006 |
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 | a0001c0001t0001g0257 | 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 | a0001c0001t0001g0004 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-11+32G>A | STAT5B | ENSG00000173757.11 | transcript | ENST00000293328.8 | protein_coding | 1/18 | chr17 | 42276216 |