Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9655 |
| ensemblid | ENSG00000171150.9 |
| hgncid | 16852 |
| symbol | SOCS5 |
| name | suppressor of cytokine signaling 5 |
| refseq_nuc | NM_144949.3 |
| refseq_prot | NP_659198.1 |
| ensembl_nuc | ENST00000394861.3 |
| ensembl_prot | ENSP00000378330.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 46699295 |
| end | 46763129 |
| strand | + |
| ver | v1.2 |
| region | chr2:46699295-46763129 |
| region5000 | chr2:46694295-46768129 |
| regionname0 | SOCS5_chr2_46699295_46763129 |
| regionname5000 | SOCS5_chr2_46694295_46768129 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 536 | 379 | 88 | 70 | 165 | 16 | 38 | 133 | SOCS5_chr2_46694295_46768129 | SOCS5 | MDKVG others(531): Show |
chr2 | 46694295 | 46768129 |
| a0002 | 0/0 | 536 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | MDKVG others(531): Show |
chr2 | 46694295 | 46768129 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1608 | 277 | 70 | 36 | 141 | 6 | 23 | SOCS5_chr2_46694295_46768129 | SOCS5 | ATGGA others(1603): Show |
chr2 | 46694295 | 46768129 | ||
| a0001c0002 | 0/1 | 1608 | 70 | 14 | 22 | 15 | 7 | 11 | SOCS5_chr2_46694295_46768129 | SOCS5 | ATGGA others(1603): Show |
chr2 | 46694295 | 46768129 | ||
| a0001c0003 | 0/0 | 1608 | 21 | 2 | 8 | 7 | 2 | 2 | SOCS5_chr2_46694295_46768129 | SOCS5 | ATGGA others(1603): Show |
chr2 | 46694295 | 46768129 | ||
| a0001c0004 | 0/0 | 1608 | 7 | 0 | 3 | 1 | 1 | 2 | SOCS5_chr2_46694295_46768129 | SOCS5 | ATGGA others(1603): Show |
chr2 | 46694295 | 46768129 | ||
| a0001c0005 | 0/0 | 1608 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | ATGGA others(1603): Show |
chr2 | 46694295 | 46768129 | ||
| a0001c0006 | 0/0 | 1608 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | ATGGA others(1603): Show |
chr2 | 46694295 | 46768129 | ||
| a0001c0008 | 0/0 | 1608 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | ATGGA others(1603): Show |
chr2 | 46694295 | 46768129 | ||
| a0001c0009 | 0/0 | 1608 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | ATGGA others(1603): Show |
chr2 | 46694295 | 46768129 | ||
| a0002c0007 | 0/0 | 1608 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | ATGGA others(1603): Show |
chr2 | 46694295 | 46768129 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4766 | 102 | 12 | 12 | 70 | 1 | 7 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0001t0002 | 1/0 | 4766 | 93 | 8 | 8 | 60 | 4 | 12 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0001t0004 | 0/0 | 4766 | 26 | 23 | 2 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0001t0005 | 0/0 | 4766 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0001t0006 | 0/0 | 4764 | 20 | 5 | 8 | 5 | 0 | 2 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4759): Show |
chr2 | 46694295 | 46768129 |
| a0001c0001t0007 | 0/0 | 4766 | 15 | 11 | 4 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0001t0008 | 0/0 | 4754 | 5 | 4 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4749): Show |
chr2 | 46694295 | 46768129 |
| a0001c0001t0009 | 0/0 | 4766 | 4 | 0 | 0 | 4 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0001t0012 | 0/0 | 4766 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0001t0014 | 0/0 | 4766 | 2 | 2 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0001t0017 | 0/0 | 4766 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0001t0018 | 0/0 | 4766 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0001t0019 | 0/0 | 4766 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0001t0020 | 0/0 | 4766 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0001t0021 | 0/0 | 4766 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0001t0022 | 0/0 | 4766 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0001t0023 | 0/0 | 4766 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0001t0024 | 0/0 | 4766 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0002t0003 | 0/1 | 4766 | 63 | 12 | 21 | 14 | 5 | 10 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0002t0010 | 0/0 | 4766 | 4 | 0 | 1 | 0 | 2 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0002t0012 | 0/0 | 4766 | 2 | 1 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0002t0015 | 0/0 | 4766 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0003t0005 | 0/0 | 4766 | 21 | 2 | 8 | 7 | 2 | 2 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0004t0011 | 0/0 | 4766 | 4 | 0 | 1 | 1 | 1 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0004t0013 | 0/0 | 4766 | 3 | 0 | 2 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0005t0008 | 0/0 | 4754 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4749): Show |
chr2 | 46694295 | 46768129 |
| a0001c0006t0002 | 0/0 | 4766 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0008t0016 | 0/0 | 4766 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0001c0009t0005 | 0/0 | 4766 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| a0002c0007t0001 | 0/0 | 4766 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | GTCCG others(4761): Show |
chr2 | 46694295 | 46768129 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0003 | 0/0 | 7 | 0 | 1 | 5 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0037 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0006g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0006g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0006g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0006g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0006g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0006g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0006g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0006g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0007g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0007g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0007g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0007g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0007g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0008g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0008g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0008g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0009g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0012g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0014g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0014g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0017g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0018g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0019g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0020g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0021g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0022g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0023g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0001t0024g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0001 | 0/0 | 9 | 0 | 3 | 3 | 1 | 2 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0122 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0010g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0010g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0010g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0012g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0012g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0002t0015g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0003t0005g0011 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0003t0005g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0003t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0003t0005g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0003t0005g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0003t0005g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0003t0005g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0003t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0003t0005g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0003t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0003t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0003t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0003t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0003t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0003t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0003t0005g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0003t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0003t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0004t0011g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0004t0011g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0004t0011g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0004t0011g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0004t0013g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0004t0013g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0005t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0006t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0008t0016g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0001c0009t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| a0002c0007t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0137 | EUR | GBR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | GBR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00280 | hp1 | a0001 | c0002 | t0003 | g0114 | EUR | FIN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00280 | hp2 | a0001 | c0001 | t0012 | g0123 | EUR | FIN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0251 | EUR | FIN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00323 | hp2 | a0001 | c0002 | t0003 | g0150 | EUR | FIN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | CHS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00438 | hp2 | a0001 | c0002 | t0003 | g0130 | EAS | CHS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | CHS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00639 | hp1 | a0001 | c0002 | t0003 | g0100 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00733 | hp1 | a0001 | c0003 | t0005 | g0238 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00733 | hp2 | a0001 | c0001 | t0006 | g0012 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0182 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0131 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00741 | hp1 | a0001 | c0001 | t0007 | g0014 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0120 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01069 | hp2 | a0001 | c0003 | t0005 | g0044 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01070 | hp1 | a0001 | c0002 | t0003 | g0239 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01070 | hp2 | a0001 | c0004 | t0011 | g0301 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0240 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0019 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01074 | hp2 | a0001 | c0003 | t0005 | g0086 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01081 | hp2 | a0001 | c0001 | t0007 | g0066 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0019 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0128 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0308 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01109 | hp2 | a0001 | c0001 | t0008 | g0152 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01167 | hp1 | a0001 | c0002 | t0003 | g0149 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01167 | hp2 | a0001 | c0001 | t0006 | g0047 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0046 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01175 | hp2 | a0001 | c0002 | t0003 | g0132 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01192 | hp1 | a0001 | c0002 | t0003 | g0134 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0073 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0074 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0102 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01257 | hp1 | a0001 | c0003 | t0005 | g0237 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01257 | hp2 | a0001 | c0004 | t0013 | g0025 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01258 | hp2 | a0001 | c0004 | t0013 | g0025 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01346 | hp1 | a0001 | c0001 | t0006 | g0051 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01346 | hp2 | a0001 | c0003 | t0005 | g0011 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01358 | hp1 | a0001 | c0002 | t0003 | g0111 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01358 | hp2 | a0001 | c0001 | t0006 | g0013 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0048 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01361 | hp2 | a0001 | c0003 | t0005 | g0031 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01433 | hp1 | a0001 | c0009 | t0005 | g0031 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01433 | hp2 | a0001 | c0002 | t0010 | g0091 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0162 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01515 | hp1 | a0001 | c0004 | t0011 | g0303 | EUR | IBS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01515 | hp2 | a0001 | c0003 | t0005 | g0011 | EUR | IBS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01516 | hp1 | a0001 | c0002 | t0010 | g0016 | EUR | IBS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0247 | EUR | IBS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01517 | hp1 | a0001 | c0003 | t0005 | g0011 | EUR | IBS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01517 | hp2 | a0001 | c0002 | t0010 | g0016 | EUR | IBS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01952 | hp2 | a0001 | c0002 | t0003 | g0021 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0012 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01978 | hp2 | a0001 | c0002 | t0003 | g0116 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01981 | hp1 | a0001 | c0002 | t0003 | g0020 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02004 | hp1 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02015 | hp2 | a0001 | c0002 | t0003 | g0109 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0075 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02055 | hp2 | a0001 | c0001 | t0019 | g0245 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02056 | hp1 | a0001 | c0003 | t0005 | g0094 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02080 | hp1 | a0001 | c0001 | t0006 | g0062 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02132 | hp1 | a0001 | c0004 | t0011 | g0302 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02135 | hp2 | a0001 | c0001 | t0006 | g0054 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0133 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CDX | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | CDX | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0136 | EAS | CDX | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0065 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0296 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0235 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02273 | hp1 | a0001 | c0002 | t0003 | g0126 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0071 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02280 | hp2 | a0001 | c0002 | t0003 | g0020 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02293 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02300 | hp1 | a0001 | c0003 | t0005 | g0087 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02300 | hp2 | a0001 | c0003 | t0005 | g0236 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02451 | hp1 | a0001 | c0005 | t0008 | g0083 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0080 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0140 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0060 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0069 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02630 | hp1 | a0001 | c0003 | t0005 | g0098 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02630 | hp2 | a0001 | c0002 | t0003 | g0124 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02647 | hp1 | a0001 | c0002 | t0012 | g0153 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02647 | hp2 | a0001 | c0003 | t0005 | g0146 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0265 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02683 | hp2 | a0001 | c0004 | t0013 | g0181 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02698 | hp1 | a0001 | c0003 | t0005 | g0043 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02698 | hp2 | a0001 | c0002 | t0003 | g0021 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0052 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02735 | hp1 | a0001 | c0002 | t0010 | g0088 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02738 | hp2 | a0001 | c0002 | t0003 | g0119 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0084 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0078 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02886 | hp2 | a0001 | c0002 | t0003 | g0018 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0214 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02895 | hp2 | a0001 | c0002 | t0003 | g0106 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0079 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0077 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02897 | hp2 | a0001 | c0002 | t0003 | g0105 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02922 | hp1 | a0001 | c0002 | t0003 | g0113 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0068 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02965 | hp1 | a0001 | c0001 | t0017 | g0171 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0151 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02976 | hp2 | a0001 | c0001 | t0018 | g0138 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03041 | hp1 | a0001 | c0002 | t0003 | g0018 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0190 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03098 | hp2 | a0001 | c0001 | t0014 | g0147 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03130 | hp1 | a0001 | c0001 | t0008 | g0022 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0072 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0067 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03209 | hp2 | a0001 | c0001 | t0020 | g0053 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0082 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03239 | hp1 | a0001 | c0002 | t0003 | g0108 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03239 | hp2 | a0001 | c0001 | t0006 | g0049 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0085 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03486 | hp2 | a0001 | c0008 | t0016 | g0142 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0298 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0076 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0121 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03540 | hp2 | a0001 | c0002 | t0003 | g0017 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0141 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0184 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03654 | hp1 | a0001 | c0001 | t0006 | g0013 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0261 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0210 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0299 | SAS | STU | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03688 | hp2 | a0001 | c0002 | t0003 | g0127 | SAS | STU | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03704 | hp2 | a0001 | c0002 | t0003 | g0115 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03710 | hp1 | a0001 | c0002 | t0003 | g0001 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03831 | hp1 | a0001 | c0003 | t0005 | g0090 | SAS | BEB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03831 | hp2 | a0001 | c0004 | t0011 | g0304 | SAS | BEB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0253 | SAS | BEB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03834 | hp2 | a0001 | c0002 | t0003 | g0001 | SAS | BEB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0112 | SAS | BEB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | BEB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | STU | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0300 | SAS | STU | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | BEB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG04184 | hp2 | a0001 | c0002 | t0003 | g0154 | SAS | BEB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG04199 | hp1 | a0001 | c0002 | t0003 | g0129 | SAS | STU | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | STU | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | STU | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG04204 | hp2 | a0001 | c0001 | t0024 | g0297 | SAS | STU | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | YRI | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0057 | AFR | YRI | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18747 | hp1 | a0001 | c0003 | t0005 | g0089 | EAS | CHB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0058 | AFR | YRI | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | YRI | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18939 | hp2 | a0001 | c0002 | t0012 | g0103 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18943 | hp1 | a0001 | c0003 | t0005 | g0015 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18944 | hp1 | a0001 | c0001 | t0006 | g0056 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18945 | hp2 | a0001 | c0001 | t0022 | g0169 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18946 | hp2 | a0001 | c0003 | t0005 | g0093 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18952 | hp1 | a0001 | c0001 | t0006 | g0055 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18952 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18953 | hp2 | a0001 | c0001 | t0009 | g0006 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18956 | hp2 | a0001 | c0001 | t0009 | g0006 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18965 | hp2 | a0001 | c0001 | t0021 | g0029 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18971 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18977 | hp1 | a0001 | c0002 | t0003 | g0045 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18978 | hp1 | a0001 | c0003 | t0005 | g0092 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18993 | hp1 | a0002 | c0007 | t0001 | g0188 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18993 | hp2 | a0001 | c0002 | t0003 | g0117 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18994 | hp1 | a0001 | c0001 | t0006 | g0061 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18998 | hp2 | a0001 | c0003 | t0005 | g0015 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19002 | hp1 | a0001 | c0003 | t0005 | g0099 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19006 | hp2 | a0001 | c0001 | t0009 | g0006 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19011 | hp1 | a0001 | c0002 | t0003 | g0081 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0070 | AFR | LWK | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | LWK | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19043 | hp1 | a0001 | c0002 | t0015 | g0104 | AFR | LWK | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | LWK | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19056 | hp1 | a0001 | c0002 | t0003 | g0107 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19057 | hp1 | a0001 | c0002 | t0003 | g0096 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19064 | hp1 | a0001 | c0002 | t0003 | g0118 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19068 | hp1 | a0001 | c0001 | t0009 | g0006 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19083 | hp2 | a0001 | c0002 | t0003 | g0135 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19087 | hp1 | a0001 | c0006 | t0002 | g0272 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19091 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | YRI | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA19240 | hp2 | a0001 | c0001 | t0014 | g0148 | AFR | YRI | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0042 | AFR | ASW | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0059 | AFR | ASW | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA20752 | hp1 | a0001 | c0002 | t0003 | g0101 | EUR | TSI | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA20805 | hp1 | a0001 | c0002 | t0003 | g0001 | EUR | TSI | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0260 | EUR | TSI | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0256 | SAS | GIH | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | GIH | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01123 | hp1 | a0001 | c0002 | t0003 | g0095 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0050 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02109 | hp1 | a0001 | c0002 | t0003 | g0125 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0017 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02486 | hp2 | a0001 | c0001 | t0023 | g0222 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA18955 | hp2 | a0001 | c0002 | t0003 | g0097 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA21309 | hp1 | a0001 | c0002 | t0003 | g0110 | AFR | LWK | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0003 | g0122 | REF | REF | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0037 | REF | REF | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:46759662 | G | A | 1 | a0002 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.1132G>A | p.Gly378Arg | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 1299/4766 | 1132/1611 | 378/536 | chr2 | 46759662 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:46758866 | T | C | 1 | a0001c0005 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.336T>C | p.Asp112Asp | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 503/4766 | 336/1611 | 112/536 | chr2 | 46758866 | |||
| chr2:46759043 | T | G | 1 | a0001c0006 | 1 | NA19087.hp1 | synonymous_variant | LOW | c.513T>G | p.Thr171Thr | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 680/4766 | 513/1611 | 171/536 | chr2 | 46759043 | |||
| chr2:46759277 | A | G | 1 | a0001c0002 | 69 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(66): Show |
synonymous_variant | LOW | c.747A>G | p.Thr249Thr | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 914/4766 | 747/1611 | 249/536 | chr2 | 46759277 | |||
| chr2:46759577 | C | G | 1 | a0001c0004 | 7 | HG01070.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
synonymous_variant | LOW | c.1047C>G | p.Thr349Thr | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 1214/4766 | 1047/1611 | 349/536 | chr2 | 46759577 | |||
| chr2:46759670 | C | A | 1 | a0001c0008 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.1140C>A | p.Pro380Pro | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 1307/4766 | 1140/1611 | 380/536 | chr2 | 46759670 | |||
| chr2:46760000 | G | A | 2 | a0001c0003 a0001c0009 |
22 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(19): Show |
synonymous_variant | LOW | c.1470G>A | p.Ala490Ala | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 1637/4766 | 1470/1611 | 490/536 | chr2 | 46760000 | |||
| chr2:46760027 | T | C | 1 | a0001c0009 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.1497T>C | p.Asp499Asp | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 1664/4766 | 1497/1611 | 499/536 | chr2 | 46760027 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:46699392 | G | A | 1 | a0001c0001t0009 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-70G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/2 | 59139 | chr2 | 46699392 | ||||||
| chr2:46760161 | T | G | 25 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(22): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*20T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 20 | chr2 | 46760161 | ||||||
| chr2:46760199 | C | T | 1 | a0001c0001t0006 | 20 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*58C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 58 | chr2 | 46760199 | ||||||
| chr2:46760202 | C | T | 1 | a0001c0001t0006 | 20 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*61C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 61 | chr2 | 46760202 | ||||||
| chr2:46760316 | G | A | 1 | a0001c0002t0015 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*175G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 175 | chr2 | 46760316 | ||||||
| chr2:46760405 | G | A | 1 | a0001c0001t0006 | 20 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*264G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 264 | chr2 | 46760405 | ||||||
| chr2:46760628 | A | G | 4 | a0001c0001t0005 a0001c0002t0010 a0001c0003t0005 others(1): Show |
27 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*487A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 487 | chr2 | 46760628 | ||||||
| chr2:46760796 | T | G | 18 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(15): Show |
147 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*655T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 655 | chr2 | 46760796 | ||||||
| chr2:46760840 | C | T | 1 | a0001c0001t0024 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*699C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 699 | chr2 | 46760840 | ||||||
| chr2:46760933 | G | T | 1 | a0001c0001t0023 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*792G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 792 | chr2 | 46760933 | ||||||
| chr2:46760934 | T | C | 3 | a0001c0001t0009 a0001c0004t0011 a0001c0004t0013 |
11 | HG01070.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*793T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 793 | chr2 | 46760934 | ||||||
| chr2:46760946 | C | T | 1 | a0001c0001t0020 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*805C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 805 | chr2 | 46760946 | ||||||
| chr2:46761136 | G | A | 2 | a0001c0002t0003 a0001c0002t0015 |
63 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*995G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 995 | chr2 | 46761136 | ||||||
| chr2:46761370 | G | A | 1 | a0001c0008t0016 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1229G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 1229 | chr2 | 46761370 | ||||||
| chr2:46761490 | A | G | 1 | a0001c0001t0019 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1349A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 1349 | chr2 | 46761490 | ||||||
| chr2:46761651 | G | T | 1 | a0001c0001t0022 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1510G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 1510 | chr2 | 46761651 | ||||||
| chr2:46762123 | A | T | 2 | a0001c0001t0009 a0001c0004t0011 |
8 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1982A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 1982 | chr2 | 46762123 | ||||||
| chr2:46762219 | A | C | 1 | a0001c0001t0018 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2078A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 2078 | chr2 | 46762219 | ||||||
| chr2:46762262 | T | G | 1 | a0001c0001t0014 | 2 | HG03098.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2121T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 2121 | chr2 | 46762262 | ||||||
| chr2:46762291 | T | C | 1 | a0001c0001t0009 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2150T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 2150 | chr2 | 46762291 | ||||||
| chr2:46762730 | T | G | 5 | a0001c0001t0012 a0001c0002t0003 a0001c0002t0010 others(2): Show |
70 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*2589T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 2589 | chr2 | 46762730 | ||||||
| chr2:46762731 | GTTAACGG others(5): Show |
G | 2 | a0001c0001t0008 a0001c0005t0008 |
6 | HG01109.hp2 HG02451.hp1 HG02970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2595_*2606delCGGT others(8): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 2595 | INFO_REALIGN_3_PRIME | chr2 | 46762731 | |||||
| chr2:46762873 | TAC | T | 1 | a0001c0001t0006 | 20 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2747_*2748delAC | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 2747 | INFO_REALIGN_3_PRIME | chr2 | 46762873 | |||||
| chr2:46763052 | G | T | 1 | a0001c0001t0017 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2911G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 2911 | chr2 | 46763052 | ||||||
| chr2:46763071 | A | G | 1 | a0001c0001t0007 | 15 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2930A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 2930 | chr2 | 46763071 | ||||||
| chr2:46763099 | G | C | 1 | a0001c0001t0021 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2958G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 2958 | chr2 | 46763099 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:46699508 | G | T | 1 | a0001c0001t0002g0309 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-13+59G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46699508 | |||||||
| chr2:46699512 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-13+63G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46699512 | |||||||
| chr2:46699545 | C | T | 1 | a0001c0001t0004g0308 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-13+96C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46699545 | |||||||
| chr2:46699574 | C | A | 3 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 |
3 | HG03195.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-13+125C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46699574 | |||||||
| chr2:46699580 | G | C | 230 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(227): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.-13+131G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46699580 | |||||||
| chr2:46699608 | G | A | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+159G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46699608 | |||||||
| chr2:46699823 | G | A | 1 | a0001c0001t0007g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-13+374G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46699823 | |||||||
| chr2:46699887 | G | A | 1 | a0001c0001t0002g0241 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-13+438G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46699887 | |||||||
| chr2:46699919 | G | T | 2 | a0001c0002t0003g0239 a0001c0002t0003g0240 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-13+470G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46699919 | |||||||
| chr2:46700228 | A | T | 5 | a0001c0003t0005g0031 a0001c0003t0005g0236 a0001c0003t0005g0237 others(2): Show |
5 | HG00733.hp1 HG01257.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+779A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46700228 | |||||||
| chr2:46700229 | C | T | 5 | a0001c0003t0005g0031 a0001c0003t0005g0236 a0001c0003t0005g0237 others(2): Show |
5 | HG00733.hp1 HG01257.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+780C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46700229 | |||||||
| chr2:46700253 | T | C | 1 | a0001c0001t0002g0242 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-13+804T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46700253 | |||||||
| chr2:46700463 | T | C | 2 | a0001c0003t0005g0043 a0001c0003t0005g0044 |
2 | HG01069.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-13+1014T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46700463 | |||||||
| chr2:46700539 | A | C | 1 | a0001c0001t0004g0235 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-13+1090A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46700539 | |||||||
| chr2:46700724 | A | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
118 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.-13+1275A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46700724 | |||||||
| chr2:46700769 | G | A | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+1320G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46700769 | |||||||
| chr2:46700974 | C | T | 3 | a0001c0001t0008g0022 a0001c0001t0008g0151 a0001c0001t0008g0152 |
4 | HG01109.hp2 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+1525C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46700974 | |||||||
| chr2:46701027 | C | G | 95 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
116 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-13+1578C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46701027 | |||||||
| chr2:46701149 | C | T | 1 | a0001c0002t0003g0150 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-13+1700C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46701149 | |||||||
| chr2:46701187 | C | A | 1 | a0001c0002t0003g0045 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-13+1738C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46701187 | |||||||
| chr2:46701339 | T | A | 1 | a0001c0001t0001g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-13+1890T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46701339 | |||||||
| chr2:46701443 | A | G | 1 | a0001c0002t0003g0149 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-13+1994A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46701443 | |||||||
| chr2:46701811 | T | TTTTTTTT others(289): Show |
13 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(10): Show |
14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(298): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(289): Show |
4 | a0001c0001t0004g0077 a0001c0001t0004g0078 a0001c0001t0004g0079 others(1): Show |
4 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(298): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(280): Show |
1 | a0001c0002t0003g0081 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(289): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(294): Show |
2 | a0001c0001t0008g0022 a0001c0001t0008g0151 |
3 | HG02970.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(303): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(295): Show |
5 | a0001c0001t0001g0023 a0001c0001t0004g0084 a0001c0001t0008g0082 others(2): Show |
6 | HG01109.hp2 HG02451.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(304): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(296): Show |
2 | a0001c0001t0001g0156 a0001c0001t0004g0085 |
2 | HG03486.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(305): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(297): Show |
6 | a0001c0003t0005g0043 a0001c0003t0005g0086 a0001c0003t0005g0087 others(3): Show |
6 | HG00733.hp1 HG01074.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(306): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(298): Show |
11 | a0001c0002t0010g0016 a0001c0002t0010g0088 a0001c0002t0010g0091 others(8): Show |
15 | HG01069.hp2 HG01346.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(307): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(286): Show |
1 | a0001c0002t0003g0095 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(295): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(299): Show |
2 | a0001c0003t0005g0093 a0001c0003t0005g0094 |
2 | HG02056.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(308): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(285): Show |
2 | a0001c0002t0003g0096 a0001c0002t0003g0097 |
2 | NA18955.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(294): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(287): Show |
29 | a0001c0001t0012g0123 a0001c0002t0003g0001 a0001c0002t0003g0017 others(26): Show |
40 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(296): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(300): Show |
2 | a0001c0003t0005g0098 a0001c0003t0005g0099 |
2 | HG02630.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(309): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(288): Show |
14 | a0001c0002t0003g0020 a0001c0002t0003g0021 a0001c0002t0003g0124 others(11): Show |
16 | HG00323.hp2 HG00438.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(297): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(289): Show |
3 | a0001c0002t0003g0134 a0001c0002t0003g0135 a0001c0002t0003g0136 |
3 | HG01192.hp1 HG02165.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(298): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(302): Show |
2 | a0001c0001t0001g0157 a0001c0001t0004g0133 |
2 | HG02145.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(311): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(290): Show |
1 | a0001c0002t0003g0137 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(299): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(303): Show |
6 | a0001c0001t0001g0024 a0001c0001t0001g0158 a0001c0001t0001g0159 others(3): Show |
7 | HG02451.hp2 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(312): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(304): Show |
46 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0038 others(43): Show |
54 | HG00408.hp1 HG00558.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(313): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(304): Show |
1 | a0001c0001t0001g0200 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(313): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(305): Show |
21 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0027 others(18): Show |
30 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(314): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(305): Show |
3 | a0001c0001t0001g0028 a0001c0001t0001g0219 a0001c0001t0001g0220 |
4 | NA18948.hp1 NA18998.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(314): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(306): Show |
11 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0221 others(8): Show |
12 | HG02293.hp1 HG02486.hp2 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(315): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(306): Show |
1 | a0001c0001t0001g0229 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(315): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(294): Show |
1 | a0001c0002t0003g0154 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(303): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(307): Show |
5 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(2): Show |
5 | HG02976.hp2 NA18906.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(316): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(307): Show |
1 | a0001c0001t0001g0233 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(316): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(308): Show |
3 | a0001c0001t0004g0040 a0001c0001t0004g0041 a0001c0001t0004g0139 |
3 | HG03195.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(317): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(309): Show |
3 | a0001c0001t0004g0140 a0001c0001t0004g0141 a0001c0008t0016g0142 |
3 | HG02615.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(318): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(310): Show |
4 | a0001c0001t0001g0234 a0001c0001t0004g0143 a0001c0001t0004g0144 others(1): Show |
4 | HG01109.hp1 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(319): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(312): Show |
1 | a0001c0001t0004g0145 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(321): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(314): Show |
1 | a0001c0003t0005g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(323): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(316): Show |
1 | a0001c0001t0014g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(325): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701811 | T | TTTTTTTT others(321): Show |
1 | a0001c0001t0014g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(330): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | ||||||
| chr2:46701863 | A | G | 231 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.-13+2414A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46701863 | |||||||
| chr2:46702068 | A | G | 2 | a0001c0001t0002g0305 a0001c0001t0002g0306 |
2 | NA18960.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-13+2619A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46702068 | |||||||
| chr2:46702096 | G | A | 1 | a0001c0001t0002g0243 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-13+2647G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46702096 | |||||||
| chr2:46702427 | A | G | 21 | a0001c0002t0010g0016 a0001c0002t0010g0088 a0001c0002t0010g0091 others(18): Show |
25 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.-13+2978A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46702427 | |||||||
| chr2:46702504 | G | C | 1 | a0001c0003t0005g0015 | 2 | NA18943.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-13+3055G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46702504 | |||||||
| chr2:46702569 | T | C | 10 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 others(7): Show |
10 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+3120T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46702569 | |||||||
| chr2:46702678 | T | G | 7 | a0001c0001t0004g0077 a0001c0001t0004g0078 a0001c0001t0004g0079 others(4): Show |
7 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+3229T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46702678 | |||||||
| chr2:46702722 | CAT | C | 10 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 others(7): Show |
10 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+3276_-13+3277d others(4): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46702722 | ||||||
| chr2:46702734 | T | C | 50 | a0001c0002t0003g0001 a0001c0002t0003g0017 a0001c0002t0003g0018 others(47): Show |
63 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.-13+3285T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46702734 | |||||||
| chr2:46702812 | G | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
142 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-13+3363G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46702812 | |||||||
| chr2:46702831 | T | G | 1 | a0001c0001t0006g0046 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-13+3382T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46702831 | |||||||
| chr2:46702963 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
142 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-13+3514A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46702963 | |||||||
| chr2:46703030 | A | G | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+3581A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46703030 | |||||||
| chr2:46703206 | A | G | 3 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 |
3 | HG03491.hp1 HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-13+3757A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46703206 | |||||||
| chr2:46703276 | T | A | 7 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(4): Show |
8 | HG00741.hp1 HG01081.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+3827T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46703276 | |||||||
| chr2:46703354 | G | GTT | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
141 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.-13+3916_-13+3917d others(4): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46703354 | ||||||
| chr2:46703374 | G | A | 239 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.-13+3925G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46703374 | |||||||
| chr2:46703637 | T | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
120 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.-13+4188T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46703637 | |||||||
| chr2:46703774 | A | G | 1 | a0001c0002t0003g0081 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-13+4325A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46703774 | |||||||
| chr2:46703829 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-13+4380A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46703829 | |||||||
| chr2:46703886 | T | G | 1 | a0001c0001t0001g0161 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-13+4437T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46703886 | |||||||
| chr2:46704004 | A | G | 1 | a0001c0001t0004g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-13+4555A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46704004 | |||||||
| chr2:46704032 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+4583A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46704032 | |||||||
| chr2:46704102 | C | G | 11 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 others(8): Show |
11 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+4653C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46704102 | |||||||
| chr2:46704255 | C | T | 1 | a0001c0001t0024g0297 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-13+4806C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46704255 | |||||||
| chr2:46704293 | C | T | 1 | a0001c0001t0007g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-13+4844C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46704293 | |||||||
| chr2:46704357 | A | G | 1 | a0001c0001t0004g0039 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-13+4908A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46704357 | |||||||
| chr2:46704534 | T | A | 9 | a0001c0001t0004g0133 a0001c0001t0004g0139 a0001c0001t0004g0140 others(6): Show |
9 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+5085T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46704534 | |||||||
| chr2:46704588 | T | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+5139T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46704588 | |||||||
| chr2:46704713 | A | G | 2 | a0001c0001t0004g0040 a0001c0001t0004g0041 |
2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-13+5264A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46704713 | |||||||
| chr2:46704829 | A | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0232 |
2 | NA19076.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-13+5380A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46704829 | |||||||
| chr2:46705062 | G | C | 9 | a0001c0001t0004g0133 a0001c0001t0004g0139 a0001c0001t0004g0140 others(6): Show |
9 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+5613G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705062 | |||||||
| chr2:46705321 | A | C | 1 | a0001c0001t0007g0014 | 2 | HG00741.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-13+5872A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705321 | |||||||
| chr2:46705378 | T | A | 1 | a0001c0002t0010g0016 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-13+5929T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705378 | |||||||
| chr2:46705384 | G | A | 234 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(231): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.-13+5935G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705384 | |||||||
| chr2:46705405 | T | G | 53 | a0001c0001t0012g0123 a0001c0002t0003g0001 a0001c0002t0003g0017 others(50): Show |
66 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.-13+5956T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705405 | |||||||
| chr2:46705409 | A | T | 1 | a0001c0002t0010g0016 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-13+5960A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705409 | |||||||
| chr2:46705416 | G | A | 307 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(304): Show |
374 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.-13+5967G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705416 | |||||||
| chr2:46705526 | GATTACCA | G | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0008g0022 others(4): Show |
8 | HG01109.hp2 HG02451.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+6078_-13+6084d others(9): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705526 | |||||||
| chr2:46705527 | A | G | 111 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0004g0032 others(108): Show |
130 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.-13+6078A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705527 | |||||||
| chr2:46705658 | T | A | 234 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(231): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.-13+6209T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705658 | |||||||
| chr2:46705773 | A | G | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0008g0022 others(4): Show |
8 | HG01109.hp2 HG02451.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+6324A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705773 | |||||||
| chr2:46705810 | C | A | 8 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(5): Show |
10 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+6361C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705810 | |||||||
| chr2:46705882 | A | G | 1 | a0001c0001t0004g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-13+6433A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705882 | |||||||
| chr2:46705926 | A | T | 20 | a0001c0002t0010g0016 a0001c0002t0010g0088 a0001c0002t0010g0091 others(17): Show |
24 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.-13+6477A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705926 | |||||||
| chr2:46705990 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-13+6541A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705990 | |||||||
| chr2:46705994 | G | C | 1 | a0001c0002t0003g0100 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-13+6545G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705994 | |||||||
| chr2:46706076 | G | A | 11 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 others(8): Show |
11 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+6627G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46706076 | |||||||
| chr2:46706116 | T | C | 1 | a0001c0001t0006g0052 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-13+6667T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46706116 | |||||||
| chr2:46706314 | G | A | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+6865G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46706314 | |||||||
| chr2:46706405 | T | C | 1 | a0001c0002t0003g0100 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-13+6956T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46706405 | |||||||
| chr2:46706468 | C | G | 2 | a0001c0001t0002g0294 a0001c0001t0002g0295 |
2 | HG00408.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-13+7019C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46706468 | |||||||
| chr2:46706684 | A | T | 1 | a0001c0001t0002g0293 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-13+7235A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46706684 | |||||||
| chr2:46706823 | G | T | 13 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(10): Show |
14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+7374G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46706823 | |||||||
| chr2:46706859 | C | G | 1 | a0001c0001t0004g0084 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-13+7410C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46706859 | |||||||
| chr2:46706873 | A | G | 1 | a0001c0003t0005g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-13+7424A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46706873 | |||||||
| chr2:46706918 | C | T | 3 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 |
3 | HG03195.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-13+7469C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46706918 | |||||||
| chr2:46707005 | TGCTG | T | 4 | a0001c0003t0005g0092 a0001c0003t0005g0093 a0001c0003t0005g0094 others(1): Show |
4 | HG02056.hp1 NA18946.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+7557_-13+7560d others(6): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707005 | |||||||
| chr2:46707011 | A | T | 4 | a0001c0003t0005g0092 a0001c0003t0005g0093 a0001c0003t0005g0094 others(1): Show |
4 | HG02056.hp1 NA18946.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+7562A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707011 | |||||||
| chr2:46707012 | C | T | 4 | a0001c0003t0005g0092 a0001c0003t0005g0093 a0001c0003t0005g0094 others(1): Show |
4 | HG02056.hp1 NA18946.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+7563C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707012 | |||||||
| chr2:46707176 | G | T | 1 | a0001c0001t0002g0292 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-13+7727G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707176 | |||||||
| chr2:46707209 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+7760T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707209 | |||||||
| chr2:46707311 | C | A | 1 | a0001c0003t0005g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-13+7862C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707311 | |||||||
| chr2:46707366 | T | C | 52 | a0001c0001t0012g0123 a0001c0002t0003g0001 a0001c0002t0003g0017 others(49): Show |
65 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.-13+7917T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707366 | |||||||
| chr2:46707436 | T | C | 1 | a0001c0001t0002g0294 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-13+7987T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707436 | |||||||
| chr2:46707481 | A | G | 2 | a0001c0001t0002g0290 a0001c0001t0002g0291 |
2 | HG00558.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-13+8032A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707481 | |||||||
| chr2:46707570 | G | A | 1 | a0001c0008t0016g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-13+8121G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707570 | |||||||
| chr2:46707693 | G | A | 11 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(8): Show |
11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+8244G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707693 | |||||||
| chr2:46707769 | C | T | 122 | a0001c0001t0004g0032 a0001c0001t0004g0039 a0001c0001t0004g0040 others(119): Show |
144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.-13+8320C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707769 | |||||||
| chr2:46707797 | G | T | 99 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
120 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.-13+8348G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707797 | |||||||
| chr2:46707934 | T | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+8485T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707934 | |||||||
| chr2:46708001 | C | A | 11 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(8): Show |
11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+8552C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46708001 | |||||||
| chr2:46708054 | CTGTT | C | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+8609_-13+8612d others(6): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46708054 | ||||||
| chr2:46708115 | T | C | 8 | a0001c0001t0004g0077 a0001c0001t0004g0078 a0001c0001t0004g0079 others(5): Show |
8 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13+8666T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46708115 | |||||||
| chr2:46708176 | A | G | 1 | a0001c0001t0007g0076 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-13+8727A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46708176 | |||||||
| chr2:46708343 | G | C | 1 | a0001c0001t0019g0245 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-13+8894G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46708343 | |||||||
| chr2:46708433 | C | T | 11 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(8): Show |
11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+8984C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46708433 | |||||||
| chr2:46708434 | G | A | 1 | a0001c0001t0007g0014 | 2 | HG00741.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-13+8985G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46708434 | |||||||
| chr2:46708569 | G | A | 11 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(8): Show |
11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+9120G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46708569 | |||||||
| chr2:46708652 | G | C | 63 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 others(60): Show |
76 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-13+9203G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46708652 | |||||||
| chr2:46708782 | G | C | 4 | a0001c0001t0001g0163 a0001c0001t0001g0201 a0001c0001t0001g0202 others(1): Show |
4 | HG00140.hp2 HG01099.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+9333G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46708782 | |||||||
| chr2:46708880 | C | CT | 21 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(18): Show |
30 | HG01496.hp1 HG02027.hp1 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.-13+9456dupT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46708880 | ||||||
| chr2:46708880 | CT | C | 26 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0217 others(23): Show |
27 | HG01175.hp2 HG01346.hp1 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.-13+9456delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46708880 | ||||||
| chr2:46708880 | CTT | C | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.-13+9455_-13+9456d others(4): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46708880 | ||||||
| chr2:46708880 | CTTT | C | 17 | a0001c0001t0001g0158 a0001c0001t0001g0164 a0001c0001t0001g0165 others(14): Show |
18 | HG00741.hp1 HG01070.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.-13+9454_-13+9456d others(5): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46708880 | ||||||
| chr2:46709037 | C | T | 3 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 |
3 | HG03195.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-13+9588C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709037 | |||||||
| chr2:46709044 | G | A | 1 | a0001c0001t0005g0162 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-13+9595G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709044 | |||||||
| chr2:46709126 | C | T | 13 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(10): Show |
14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+9677C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709126 | |||||||
| chr2:46709151 | T | G | 1 | a0001c0002t0003g0154 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-13+9702T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709151 | |||||||
| chr2:46709178 | C | G | 234 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(231): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.-13+9729C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709178 | |||||||
| chr2:46709311 | C | G | 1 | a0001c0003t0005g0098 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-13+9862C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709311 | |||||||
| chr2:46709610 | G | A | 1 | a0001c0002t0012g0103 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-13+10161G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709610 | |||||||
| chr2:46709645 | T | G | 1 | a0001c0002t0015g0104 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-13+10196T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709645 | |||||||
| chr2:46709698 | A | T | 20 | a0001c0002t0010g0016 a0001c0002t0010g0088 a0001c0002t0010g0091 others(17): Show |
24 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.-13+10249A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709698 | |||||||
| chr2:46709755 | A | G | 18 | a0001c0001t0004g0133 a0001c0001t0004g0139 a0001c0001t0004g0140 others(15): Show |
20 | HG00280.hp2 HG00733.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-13+10306A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709755 | |||||||
| chr2:46709836 | C | T | 1 | a0001c0001t0002g0276 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-13+10387C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709836 | |||||||
| chr2:46709948 | G | T | 1 | a0001c0008t0016g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-13+10499G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709948 | |||||||
| chr2:46709989 | C | G | 1 | a0001c0002t0003g0120 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-13+10540C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709989 | |||||||
| chr2:46710131 | T | G | 1 | a0001c0001t0001g0166 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-13+10682T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710131 | |||||||
| chr2:46710202 | A | G | 242 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(239): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.-13+10753A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710202 | |||||||
| chr2:46710277 | A | G | 11 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(8): Show |
11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+10828A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710277 | |||||||
| chr2:46710348 | C | T | 1 | a0001c0002t0012g0103 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-13+10899C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710348 | |||||||
| chr2:46710349 | G | A | 1 | a0001c0001t0020g0053 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-13+10900G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710349 | |||||||
| chr2:46710425 | G | T | 11 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(8): Show |
11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+10976G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710425 | |||||||
| chr2:46710431 | C | T | 1 | a0001c0001t0006g0061 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-13+10982C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710431 | |||||||
| chr2:46710547 | T | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+11098T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710547 | |||||||
| chr2:46710600 | A | G | 21 | a0001c0002t0010g0016 a0001c0002t0010g0088 a0001c0002t0010g0091 others(18): Show |
25 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.-13+11151A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710600 | |||||||
| chr2:46710638 | A | T | 1 | a0001c0001t0002g0247 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-13+11189A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710638 | |||||||
| chr2:46710726 | A | G | 1 | a0001c0002t0003g0136 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-13+11277A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710726 | |||||||
| chr2:46710879 | C | A | 11 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(8): Show |
11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+11430C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710879 | |||||||
| chr2:46711120 | T | G | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+11671T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711120 | |||||||
| chr2:46711165 | A | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+11716A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711165 | |||||||
| chr2:46711246 | A | G | 49 | a0001c0001t0012g0123 a0001c0002t0003g0001 a0001c0002t0003g0018 others(46): Show |
61 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.-13+11797A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711246 | |||||||
| chr2:46711254 | A | C | 49 | a0001c0001t0012g0123 a0001c0002t0003g0001 a0001c0002t0003g0018 others(46): Show |
61 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.-13+11805A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711254 | |||||||
| chr2:46711365 | C | A | 3 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 |
3 | HG03195.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-13+11916C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711365 | |||||||
| chr2:46711597 | C | T | 50 | a0001c0002t0003g0001 a0001c0002t0003g0017 a0001c0002t0003g0018 others(47): Show |
63 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.-13+12148C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711597 | |||||||
| chr2:46711643 | C | A | 1 | a0001c0001t0023g0222 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-13+12194C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711643 | |||||||
| chr2:46711650 | T | C | 51 | a0001c0001t0012g0123 a0001c0002t0003g0001 a0001c0002t0003g0017 others(48): Show |
64 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.-13+12201T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711650 | |||||||
| chr2:46711853 | G | A | 1 | a0001c0003t0005g0015 | 2 | NA18943.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-13+12404G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711853 | |||||||
| chr2:46711898 | A | G | 2 | a0001c0001t0004g0032 a0001c0001t0019g0245 |
3 | HG02055.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-13+12449A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711898 | |||||||
| chr2:46711953 | A | G | 1 | a0001c0001t0004g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-13+12504A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711953 | |||||||
| chr2:46712003 | G | T | 1 | a0001c0001t0006g0060 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-13+12554G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712003 | |||||||
| chr2:46712010 | T | C | 11 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 others(8): Show |
11 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+12561T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712010 | |||||||
| chr2:46712139 | T | C | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+12690T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712139 | |||||||
| chr2:46712306 | C | CT | 163 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
191 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.-13+12867dupT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46712306 | ||||||
| chr2:46712316 | T | TC | 20 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(17): Show |
22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-13+12870dupC | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46712316 | ||||||
| chr2:46712336 | C | CT | 48 | a0001c0001t0002g0241 a0001c0001t0002g0273 a0001c0001t0002g0274 others(45): Show |
59 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.-13+12912dupT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46712336 | ||||||
| chr2:46712336 | C | CTT | 6 | a0001c0002t0003g0021 a0001c0002t0003g0097 a0001c0002t0003g0119 others(3): Show |
7 | HG00438.hp2 HG00738.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+12911_-13+1291 others(6): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46712336 | ||||||
| chr2:46712336 | CT | C | 48 | a0001c0001t0002g0277 a0001c0001t0004g0085 a0001c0001t0004g0139 others(45): Show |
57 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.-13+12912delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46712336 | ||||||
| chr2:46712336 | CTT | C | 49 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0192 others(46): Show |
53 | HG00741.hp1 HG01081.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.-13+12911_-13+1291 others(6): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46712336 | ||||||
| chr2:46712336 | CTTT | C | 86 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
107 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.-13+12910_-13+1291 others(7): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46712336 | ||||||
| chr2:46712449 | T | G | 5 | a0001c0001t0001g0163 a0001c0001t0001g0167 a0001c0001t0001g0201 others(2): Show |
5 | HG00140.hp2 HG01099.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+13000T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712449 | |||||||
| chr2:46712490 | C | T | 2 | a0001c0001t0007g0074 a0001c0001t0007g0075 |
2 | HG01243.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-13+13041C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712490 | |||||||
| chr2:46712491 | G | A | 1 | a0001c0001t0002g0298 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-13+13042G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712491 | |||||||
| chr2:46712492 | T | A | 20 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(17): Show |
22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-13+13043T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712492 | |||||||
| chr2:46712500 | C | T | 1 | a0001c0001t0004g0084 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-13+13051C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712500 | |||||||
| chr2:46712518 | A | G | 2 | a0001c0002t0003g0117 a0001c0002t0003g0118 |
2 | NA18993.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-13+13069A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712518 | |||||||
| chr2:46712544 | A | G | 11 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(8): Show |
11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+13095A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712544 | |||||||
| chr2:46712585 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-13+13136G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712585 | |||||||
| chr2:46712621 | C | T | 1 | a0001c0002t0003g0129 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-13+13172C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712621 | |||||||
| chr2:46712633 | T | C | 234 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(231): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.-13+13184T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712633 | |||||||
| chr2:46712756 | C | T | 1 | a0001c0001t0007g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-13+13307C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712756 | |||||||
| chr2:46712794 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-13+13345C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712794 | |||||||
| chr2:46712971 | G | A | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+13522G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712971 | |||||||
| chr2:46713138 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+13689T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713138 | |||||||
| chr2:46713224 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+13775C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713224 | |||||||
| chr2:46713225 | G | A | 1 | a0001c0003t0005g0089 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-13+13776G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713225 | |||||||
| chr2:46713366 | G | T | 20 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(17): Show |
22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-13+13917G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713366 | |||||||
| chr2:46713427 | G | T | 1 | a0001c0001t0001g0244 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-13+13978G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713427 | |||||||
| chr2:46713521 | C | T | 1 | a0001c0001t0023g0222 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-13+14072C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713521 | |||||||
| chr2:46713547 | T | C | 13 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(10): Show |
14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+14098T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713547 | |||||||
| chr2:46713564 | T | C | 13 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(10): Show |
14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+14115T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713564 | |||||||
| chr2:46713581 | A | G | 20 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(17): Show |
22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-13+14132A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713581 | |||||||
| chr2:46713612 | C | T | 1 | a0001c0001t0004g0190 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-13+14163C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713612 | |||||||
| chr2:46713659 | G | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0189 a0001c0001t0001g0191 others(1): Show |
5 | NA18977.hp2 NA18980.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+14210G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713659 | |||||||
| chr2:46713730 | G | A | 1 | a0001c0001t0002g0248 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-13+14281G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713730 | |||||||
| chr2:46713733 | A | C | 1 | a0001c0001t0023g0222 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-13+14284A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713733 | |||||||
| chr2:46713747 | T | C | 13 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(10): Show |
14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+14298T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713747 | |||||||
| chr2:46713992 | C | T | 1 | a0001c0008t0016g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-13+14543C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713992 | |||||||
| chr2:46714088 | G | A | 10 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 others(7): Show |
10 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+14639G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46714088 | |||||||
| chr2:46714108 | G | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0307 |
2 | NA18951.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-13+14659G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46714108 | |||||||
| chr2:46714162 | A | G | 9 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0274 others(6): Show |
9 | HG00408.hp2 HG00558.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13+14713A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46714162 | |||||||
| chr2:46714218 | A | G | 3 | a0001c0001t0001g0038 a0001c0001t0004g0032 a0001c0001t0019g0245 |
4 | HG02055.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+14769A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46714218 | |||||||
| chr2:46714419 | G | A | 2 | a0001c0001t0001g0203 a0001c0002t0003g0132 |
2 | HG01175.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-13+14970G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46714419 | |||||||
| chr2:46714496 | C | G | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | NA18946.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.-13+15047C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46714496 | |||||||
| chr2:46714526 | A | G | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0008g0022 others(4): Show |
8 | HG01109.hp2 HG02451.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+15077A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46714526 | |||||||
| chr2:46714650 | C | T | 1 | a0001c0002t0015g0104 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-13+15201C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46714650 | |||||||
| chr2:46714693 | A | G | 20 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(17): Show |
22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-13+15244A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46714693 | |||||||
| chr2:46714798 | T | G | 5 | a0001c0001t0002g0249 a0001c0004t0011g0301 a0001c0004t0011g0302 others(2): Show |
5 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+15349T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46714798 | |||||||
| chr2:46715149 | G | C | 1 | a0001c0001t0002g0270 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-13+15700G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46715149 | |||||||
| chr2:46715150 | C | A | 1 | a0001c0002t0012g0153 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-13+15701C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46715150 | |||||||
| chr2:46715371 | C | CA | 25 | a0001c0001t0001g0158 a0001c0001t0001g0195 a0001c0001t0001g0204 others(22): Show |
27 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.-13+15936dupA | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46715371 | ||||||
| chr2:46715371 | CA | C | 54 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0002g0306 others(51): Show |
67 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.-13+15936delA | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46715371 | ||||||
| chr2:46715409 | T | C | 1 | a0001c0002t0003g0120 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-13+15960T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46715409 | |||||||
| chr2:46715494 | T | G | 1 | a0001c0001t0018g0138 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-13+16045T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46715494 | |||||||
| chr2:46715652 | T | A | 6 | a0001c0001t0002g0007 a0001c0001t0002g0250 a0001c0001t0002g0275 others(3): Show |
9 | NA18948.hp2 NA18950.hp1 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+16203T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46715652 | |||||||
| chr2:46715830 | T | A | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+16381T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46715830 | |||||||
| chr2:46715915 | A | G | 1 | a0001c0002t0003g0081 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-13+16466A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46715915 | |||||||
| chr2:46715984 | C | T | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+16535C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46715984 | |||||||
| chr2:46716052 | T | C | 212 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(209): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.-13+16603T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716052 | |||||||
| chr2:46716110 | C | G | 11 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0241 others(8): Show |
17 | HG01496.hp1 HG02027.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.-13+16661C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716110 | |||||||
| chr2:46716111 | CT | C | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(208): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.-13+16676delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46716111 | ||||||
| chr2:46716147 | C | T | 232 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.-13+16698C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716147 | |||||||
| chr2:46716194 | T | C | 1 | a0001c0001t0002g0243 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-13+16745T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716194 | |||||||
| chr2:46716303 | G | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG03491.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-13+16854G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716303 | |||||||
| chr2:46716367 | A | AT | 10 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0004g0144 others(7): Show |
11 | HG00733.hp1 HG01109.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.-13+16947dupT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46716367 | ||||||
| chr2:46716367 | AT | A | 118 | a0001c0001t0001g0004 a0001c0001t0001g0179 a0001c0001t0001g0180 others(115): Show |
154 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.-13+16947delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46716367 | ||||||
| chr2:46716367 | ATT | A | 110 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0023 others(107): Show |
129 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.-13+16946_-13+1694 others(6): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46716367 | ||||||
| chr2:46716367 | ATTTTTTT others(7): Show |
A | 3 | a0001c0001t0001g0038 a0001c0001t0004g0032 a0001c0001t0019g0245 |
4 | HG02055.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+16934_-13+1694 others(18): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46716367 | ||||||
| chr2:46716388 | T | C | 11 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(8): Show |
11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+16939T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716388 | |||||||
| chr2:46716457 | C | G | 1 | a0001c0002t0003g0095 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-13+17008C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716457 | |||||||
| chr2:46716549 | C | T | 7 | a0001c0001t0004g0077 a0001c0001t0004g0078 a0001c0001t0004g0079 others(4): Show |
7 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+17100C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716549 | |||||||
| chr2:46716637 | C | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+17188C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716637 | |||||||
| chr2:46716662 | G | A | 2 | a0001c0003t0005g0011 a0001c0003t0005g0087 |
4 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+17213G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716662 | |||||||
| chr2:46716673 | C | T | 19 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(16): Show |
21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-13+17224C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716673 | |||||||
| chr2:46716733 | C | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | NA19010.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.-13+17284C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716733 | |||||||
| chr2:46716815 | A | G | 6 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0161 others(3): Show |
8 | HG00438.hp1 HG00642.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13+17366A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716815 | |||||||
| chr2:46716928 | A | G | 19 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(16): Show |
21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-13+17479A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716928 | |||||||
| chr2:46717003 | G | A | 1 | a0001c0001t0006g0060 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-13+17554G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717003 | |||||||
| chr2:46717041 | T | G | 216 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(213): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.-13+17592T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717041 | |||||||
| chr2:46717126 | A | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(232): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.-13+17677A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717126 | |||||||
| chr2:46717252 | A | C | 2 | a0001c0001t0001g0197 a0001c0001t0001g0225 |
2 | NA18964.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-13+17803A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717252 | |||||||
| chr2:46717368 | G | A | 1 | a0001c0001t0005g0162 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-13+17919G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717368 | |||||||
| chr2:46717414 | G | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(210): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.-13+17965G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717414 | |||||||
| chr2:46717525 | G | A | 1 | a0001c0001t0002g0249 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-13+18076G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717525 | |||||||
| chr2:46717558 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-13+18109A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717558 | |||||||
| chr2:46717692 | T | C | 1 | a0001c0004t0011g0303 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-13+18243T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717692 | |||||||
| chr2:46717760 | G | A | 1 | a0001c0003t0005g0089 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-13+18311G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717760 | |||||||
| chr2:46717778 | A | G | 1 | a0001c0003t0005g0044 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-13+18329A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717778 | |||||||
| chr2:46717797 | G | C | 4 | a0001c0001t0001g0166 a0001c0001t0001g0193 a0001c0001t0001g0196 others(1): Show |
4 | NA18944.hp2 NA18949.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+18348G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717797 | |||||||
| chr2:46717888 | A | T | 1 | a0001c0004t0011g0301 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-13+18439A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717888 | |||||||
| chr2:46717903 | A | C | 1 | a0001c0001t0001g0175 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-13+18454A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717903 | |||||||
| chr2:46717970 | T | C | 3 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 |
3 | HG03195.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-13+18521T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717970 | |||||||
| chr2:46718022 | G | C | 11 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(8): Show |
11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+18573G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718022 | |||||||
| chr2:46718095 | TTG | T | 305 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(302): Show |
369 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.-13+18668_-13+1866 others(6): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46718095 | ||||||
| chr2:46718214 | A | G | 1 | a0001c0006t0002g0272 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-13+18765A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718214 | |||||||
| chr2:46718256 | G | A | 2 | a0001c0001t0002g0294 a0001c0001t0002g0295 |
2 | HG00408.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-13+18807G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718256 | |||||||
| chr2:46718349 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-13+18900T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718349 | |||||||
| chr2:46718460 | T | A | 1 | a0001c0004t0011g0302 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-13+19011T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718460 | |||||||
| chr2:46718511 | A | G | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+19062A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718511 | |||||||
| chr2:46718754 | G | A | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+19305G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718754 | |||||||
| chr2:46718815 | G | T | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+19366G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718815 | |||||||
| chr2:46718884 | G | A | 6 | a0001c0001t0002g0007 a0001c0001t0002g0250 a0001c0001t0002g0275 others(3): Show |
9 | NA18948.hp2 NA18950.hp1 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+19435G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718884 | |||||||
| chr2:46718887 | A | G | 1 | a0001c0001t0004g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-13+19438A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718887 | |||||||
| chr2:46718992 | A | G | 4 | a0001c0001t0004g0080 a0001c0001t0004g0145 a0001c0001t0014g0147 others(1): Show |
4 | HG02572.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+19543A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718992 | |||||||
| chr2:46719050 | A | G | 1 | a0001c0002t0012g0153 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-13+19601A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719050 | |||||||
| chr2:46719140 | A | G | 2 | a0001c0002t0003g0100 a0001c0002t0003g0128 |
2 | HG00639.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-13+19691A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719140 | |||||||
| chr2:46719204 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-13+19755A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719204 | |||||||
| chr2:46719246 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-13+19797T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719246 | |||||||
| chr2:46719385 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-13+19936A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719385 | |||||||
| chr2:46719416 | G | A | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+19967G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719416 | |||||||
| chr2:46719535 | T | G | 1 | a0001c0001t0002g0253 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-13+20086T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719535 | |||||||
| chr2:46719652 | C | G | 2 | a0001c0001t0008g0022 a0001c0001t0008g0152 |
3 | HG01109.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-13+20203C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719652 | |||||||
| chr2:46719694 | G | A | 2 | a0001c0001t0008g0082 a0001c0005t0008g0083 |
2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-13+20245G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719694 | |||||||
| chr2:46719802 | T | A | 5 | a0001c0001t0008g0022 a0001c0001t0008g0082 a0001c0001t0008g0151 others(2): Show |
6 | HG01109.hp2 HG02451.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+20353T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719802 | |||||||
| chr2:46719870 | C | T | 2 | a0001c0001t0007g0074 a0001c0001t0007g0075 |
2 | HG01243.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-13+20421C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719870 | |||||||
| chr2:46719980 | A | G | 1 | a0001c0001t0004g0144 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-13+20531A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719980 | |||||||
| chr2:46720065 | T | G | 4 | a0001c0002t0003g0017 a0001c0002t0003g0105 a0001c0002t0003g0106 others(1): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+20616T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46720065 | |||||||
| chr2:46720277 | G | T | 6 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0002t0003g0017 others(3): Show |
7 | HG01256.hp1 HG01258.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+20828G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46720277 | |||||||
| chr2:46720291 | G | A | 1 | a0001c0003t0005g0086 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-13+20842G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46720291 | |||||||
| chr2:46720301 | G | A | 18 | a0001c0003t0005g0011 a0001c0003t0005g0015 a0001c0003t0005g0031 others(15): Show |
21 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.-13+20852G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46720301 | |||||||
| chr2:46720537 | T | C | 20 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(17): Show |
22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-13+21088T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46720537 | |||||||
| chr2:46720607 | A | C | 1 | a0001c0008t0016g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-13+21158A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46720607 | |||||||
| chr2:46720662 | T | C | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+21213T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46720662 | |||||||
| chr2:46720896 | C | T | 13 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(10): Show |
14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+21447C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46720896 | |||||||
| chr2:46720936 | C | T | 19 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(16): Show |
21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-13+21487C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46720936 | |||||||
| chr2:46721011 | C | G | 54 | a0001c0002t0003g0001 a0001c0002t0003g0017 a0001c0002t0003g0018 others(51): Show |
68 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.-13+21562C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721011 | |||||||
| chr2:46721036 | T | C | 179 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.-13+21587T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721036 | |||||||
| chr2:46721067 | C | T | 1 | a0001c0001t0004g0139 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-13+21618C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721067 | |||||||
| chr2:46721175 | A | G | 3 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0266 |
3 | HG00639.hp2 HG00642.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.-13+21726A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721175 | |||||||
| chr2:46721306 | C | CT | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+21858dupT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46721306 | ||||||
| chr2:46721461 | A | C | 1 | a0001c0001t0002g0282 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-13+22012A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721461 | |||||||
| chr2:46721520 | A | G | 1 | a0001c0003t0005g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-13+22071A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721520 | |||||||
| chr2:46721563 | C | G | 9 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(6): Show |
11 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+22114C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721563 | |||||||
| chr2:46721595 | C | A | 1 | a0001c0001t0006g0048 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-13+22146C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721595 | |||||||
| chr2:46721627 | G | C | 1 | a0001c0001t0006g0048 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-13+22178G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721627 | |||||||
| chr2:46721698 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+22249T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721698 | |||||||
| chr2:46721714 | G | C | 1 | a0001c0003t0005g0015 | 2 | NA18943.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-13+22265G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721714 | |||||||
| chr2:46721722 | G | C | 1 | a0001c0003t0005g0043 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-13+22273G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721722 | |||||||
| chr2:46721877 | A | G | 1 | a0001c0002t0003g0137 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-13+22428A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721877 | |||||||
| chr2:46721882 | G | A | 1 | a0001c0003t0005g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-13+22433G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721882 | |||||||
| chr2:46721883 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-13+22434C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721883 | |||||||
| chr2:46722198 | A | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(232): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.-13+22749A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46722198 | |||||||
| chr2:46722263 | C | A | 1 | a0001c0008t0016g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-13+22814C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46722263 | |||||||
| chr2:46722301 | A | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+22852A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46722301 | |||||||
| chr2:46722310 | G | C | 1 | a0001c0001t0001g0205 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-13+22861G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46722310 | |||||||
| chr2:46722333 | GA | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(205): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.-13+22891delA | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46722333 | ||||||
| chr2:46722545 | A | G | 99 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
120 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.-13+23096A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46722545 | |||||||
| chr2:46722605 | A | C | 1 | a0001c0002t0003g0127 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-13+23156A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46722605 | |||||||
| chr2:46722877 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-13+23428T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46722877 | |||||||
| chr2:46722980 | T | G | 1 | a0001c0003t0005g0094 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-13+23531T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46722980 | |||||||
| chr2:46723087 | T | A | 1 | a0001c0008t0016g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-13+23638T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46723087 | |||||||
| chr2:46723282 | G | T | 239 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.-13+23833G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46723282 | |||||||
| chr2:46723444 | T | C | 20 | a0001c0002t0010g0016 a0001c0002t0010g0088 a0001c0002t0010g0091 others(17): Show |
24 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.-13+23995T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46723444 | |||||||
| chr2:46723530 | T | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+24081T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46723530 | |||||||
| chr2:46723573 | T | C | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0008g0022 others(4): Show |
8 | HG01109.hp2 HG02451.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+24124T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46723573 | |||||||
| chr2:46723630 | C | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(207): Show |
251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.-13+24181C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46723630 | |||||||
| chr2:46723819 | G | T | 1 | a0001c0001t0001g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-13+24370G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46723819 | |||||||
| chr2:46723973 | T | C | 4 | a0001c0002t0003g0017 a0001c0002t0003g0105 a0001c0002t0003g0106 others(1): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+24524T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46723973 | |||||||
| chr2:46724050 | A | C | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+24601A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724050 | |||||||
| chr2:46724105 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-13+24656C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724105 | |||||||
| chr2:46724335 | C | G | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+24886C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724335 | |||||||
| chr2:46724388 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+24939C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724388 | |||||||
| chr2:46724467 | T | G | 1 | a0001c0001t0007g0076 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-13+25018T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724467 | |||||||
| chr2:46724627 | C | T | 7 | a0001c0001t0004g0133 a0001c0001t0004g0139 a0001c0001t0004g0140 others(4): Show |
7 | HG01109.hp1 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+25178C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724627 | |||||||
| chr2:46724664 | G | A | 16 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(13): Show |
19 | HG01070.hp2 HG01515.hp1 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.-13+25215G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724664 | |||||||
| chr2:46724724 | A | G | 1 | a0001c0008t0016g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-13+25275A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724724 | |||||||
| chr2:46724774 | G | A | 1 | a0001c0001t0002g0254 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-13+25325G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724774 | |||||||
| chr2:46724960 | T | C | 2 | a0001c0001t0004g0032 a0001c0001t0019g0245 |
3 | HG02055.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-13+25511T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724960 | |||||||
| chr2:46724977 | G | A | 18 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0006g0052 others(15): Show |
21 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-13+25528G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724977 | |||||||
| chr2:46724999 | C | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+25550C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724999 | |||||||
| chr2:46725039 | A | T | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0009g0006 others(4): Show |
10 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13+25590A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46725039 | |||||||
| chr2:46725295 | C | G | 1 | a0001c0001t0007g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-13+25846C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46725295 | |||||||
| chr2:46725307 | A | G | 20 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(17): Show |
22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-13+25858A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46725307 | |||||||
| chr2:46725330 | T | C | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+25881T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46725330 | |||||||
| chr2:46725619 | T | C | 16 | a0001c0001t0001g0159 a0001c0001t0001g0168 a0001c0001t0007g0014 others(13): Show |
17 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.-13+26170T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46725619 | |||||||
| chr2:46725648 | C | A | 1 | a0001c0001t0008g0152 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-13+26199C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46725648 | |||||||
| chr2:46725715 | T | G | 1 | a0001c0001t0001g0158 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-13+26266T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46725715 | |||||||
| chr2:46726095 | T | G | 1 | a0001c0001t0001g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-13+26646T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726095 | |||||||
| chr2:46726128 | G | A | 1 | a0001c0003t0005g0098 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-13+26679G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726128 | |||||||
| chr2:46726266 | T | G | 1 | a0001c0001t0002g0290 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-13+26817T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726266 | |||||||
| chr2:46726313 | A | C | 20 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(17): Show |
22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-13+26864A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726313 | |||||||
| chr2:46726326 | A | G | 231 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.-13+26877A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726326 | |||||||
| chr2:46726343 | G | C | 26 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0006g0012 others(23): Show |
31 | HG00733.hp2 HG01070.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.-13+26894G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726343 | |||||||
| chr2:46726366 | A | G | 30 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0064 others(27): Show |
36 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-13+26917A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726366 | |||||||
| chr2:46726452 | G | C | 1 | a0001c0001t0004g0078 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-13+27003G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726452 | |||||||
| chr2:46726502 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+27053T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726502 | |||||||
| chr2:46726544 | G | A | 3 | a0001c0002t0003g0117 a0001c0002t0003g0118 a0001c0002t0012g0103 |
3 | NA18939.hp2 NA18993.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-13+27095G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726544 | |||||||
| chr2:46726551 | G | A | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+27102G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726551 | |||||||
| chr2:46726574 | C | G | 2 | a0001c0001t0004g0032 a0001c0001t0019g0245 |
3 | HG02055.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-13+27125C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726574 | |||||||
| chr2:46726624 | C | T | 50 | a0001c0002t0003g0001 a0001c0002t0003g0017 a0001c0002t0003g0018 others(47): Show |
63 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.-13+27175C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726624 | |||||||
| chr2:46726628 | A | T | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0004g0032 others(6): Show |
13 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-13+27179A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726628 | |||||||
| chr2:46726645 | A | G | 2 | a0001c0001t0006g0052 a0001c0001t0006g0059 |
2 | HG02717.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-13+27196A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726645 | |||||||
| chr2:46726720 | CAGTATTT others(15): Show |
C | 1 | a0001c0002t0003g0136 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-13+27272_-13+2729 others(26): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726720 | |||||||
| chr2:46726734 | T | G | 19 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(16): Show |
26 | HG00621.hp2 HG02015.hp1 HG02273.hp2 others(23): Show |
intron_variant | MODIFIER | c.-13+27285T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726734 | |||||||
| chr2:46726738 | A | AATT | 5 | a0001c0001t0002g0008 a0001c0001t0002g0246 a0001c0001t0002g0247 others(2): Show |
5 | HG01516.hp2 HG02129.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+27320_-13+2732 others(7): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46726738 | ||||||
| chr2:46726738 | A | AATTATTA others(5): Show |
1 | a0001c0001t0014g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-13+27311_-13+2732 others(16): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46726738 | ||||||
| chr2:46726738 | A | AATTATTA others(8): Show |
3 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0080 |
3 | HG02572.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-13+27308_-13+2732 others(19): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46726738 | ||||||
| chr2:46726738 | AATT | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-13+27320_-13+2732 others(7): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46726738 | ||||||
| chr2:46726738 | AATTATT | A | 23 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0006g0012 others(20): Show |
28 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.-13+27317_-13+2732 others(10): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46726738 | ||||||
| chr2:46726811 | C | A | 1 | a0001c0001t0001g0203 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-13+27362C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726811 | |||||||
| chr2:46726917 | C | T | 5 | a0001c0001t0001g0205 a0001c0001t0004g0182 a0001c0001t0004g0190 others(2): Show |
5 | HG00738.hp1 HG02071.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+27468C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726917 | |||||||
| chr2:46726948 | G | T | 2 | a0001c0003t0005g0011 a0001c0003t0005g0087 |
4 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+27499G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726948 | |||||||
| chr2:46727144 | C | CT | 9 | a0001c0001t0001g0064 a0001c0001t0001g0191 a0001c0001t0004g0143 others(6): Show |
9 | HG00738.hp1 HG01258.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+27717dupT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46727144 | ||||||
| chr2:46727144 | C | CTTTT | 8 | a0001c0001t0006g0013 a0001c0001t0006g0046 a0001c0001t0006g0047 others(5): Show |
9 | HG00280.hp2 HG01123.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+27714_-13+2771 others(8): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46727144 | ||||||
| chr2:46727144 | C | CTTTTTT | 9 | a0001c0001t0006g0055 a0001c0001t0006g0056 a0001c0001t0006g0057 others(6): Show |
9 | HG02080.hp1 HG02615.hp2 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+27712_-13+2771 others(10): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46727144 | ||||||
| chr2:46727144 | CT | C | 150 | a0001c0001t0001g0167 a0001c0001t0001g0195 a0001c0001t0001g0219 others(147): Show |
189 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.-13+27717delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46727144 | ||||||
| chr2:46727144 | CTT | C | 23 | a0001c0001t0002g0247 a0001c0001t0002g0255 a0001c0001t0002g0256 others(20): Show |
24 | HG00323.hp2 HG01109.hp2 HG01516.hp2 others(21): Show |
intron_variant | MODIFIER | c.-13+27716_-13+2771 others(6): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46727144 | ||||||
| chr2:46727218 | A | G | 27 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0006g0012 others(24): Show |
32 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-13+27769A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727218 | |||||||
| chr2:46727235 | G | A | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+27786G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727235 | |||||||
| chr2:46727250 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-13+27801G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727250 | |||||||
| chr2:46727263 | C | T | 1 | a0001c0003t0005g0090 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-13+27814C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727263 | |||||||
| chr2:46727270 | T | A | 4 | a0001c0002t0003g0017 a0001c0002t0003g0105 a0001c0002t0003g0106 others(1): Show |
5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+27821T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727270 | |||||||
| chr2:46727273 | C | T | 2 | a0001c0001t0002g0273 a0001c0001t0002g0280 |
2 | NA18980.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-13+27824C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727273 | |||||||
| chr2:46727690 | C | G | 1 | a0001c0004t0013g0181 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-13+28241C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727690 | |||||||
| chr2:46727743 | G | A | 6 | a0001c0001t0002g0033 a0001c0001t0002g0255 a0001c0001t0002g0257 others(3): Show |
7 | HG02027.hp2 HG02155.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+28294G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727743 | |||||||
| chr2:46727823 | C | G | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+28374C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727823 | |||||||
| chr2:46727894 | G | A | 1 | a0001c0001t0005g0162 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-13+28445G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727894 | |||||||
| chr2:46727924 | T | C | 1 | a0001c0002t0003g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-13+28475T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727924 | |||||||
| chr2:46727949 | TTGA | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
117 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-13+28503_-13+2850 others(7): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46727949 | ||||||
| chr2:46728035 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0180 |
2 | NA18962.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-13+28586C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728035 | |||||||
| chr2:46728041 | G | T | 11 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(8): Show |
11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+28592G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728041 | |||||||
| chr2:46728046 | T | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.-13+28597T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728046 | |||||||
| chr2:46728218 | A | T | 5 | a0001c0001t0001g0163 a0001c0001t0001g0167 a0001c0001t0001g0201 others(2): Show |
5 | HG00140.hp2 HG01099.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+28769A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728218 | |||||||
| chr2:46728240 | C | T | 91 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
112 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.-13+28791C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728240 | |||||||
| chr2:46728311 | G | A | 1 | a0001c0002t0003g0154 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-13+28862G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728311 | |||||||
| chr2:46728404 | C | T | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+28955C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728404 | |||||||
| chr2:46728460 | G | T | 18 | a0001c0003t0005g0011 a0001c0003t0005g0015 a0001c0003t0005g0031 others(15): Show |
21 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.-13+29011G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728460 | |||||||
| chr2:46728495 | T | G | 1 | a0001c0001t0020g0053 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-13+29046T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728495 | |||||||
| chr2:46728716 | C | T | 8 | a0001c0001t0004g0133 a0001c0001t0004g0139 a0001c0001t0004g0140 others(5): Show |
8 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13+29267C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728716 | |||||||
| chr2:46728752 | C | T | 3 | a0001c0001t0004g0133 a0001c0001t0004g0141 a0001c0001t0004g0144 |
3 | HG02145.hp1 HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-13+29303C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728752 | |||||||
| chr2:46728800 | G | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
120 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.-13+29351G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728800 | |||||||
| chr2:46728808 | T | C | 230 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(227): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.-13+29359T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728808 | |||||||
| chr2:46728818 | A | C | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+29369A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728818 | |||||||
| chr2:46728896 | C | G | 1 | a0001c0001t0002g0290 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-13+29447C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728896 | |||||||
| chr2:46728901 | A | T | 27 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0006g0012 others(24): Show |
32 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-13+29452A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728901 | |||||||
| chr2:46728962 | G | C | 1 | a0001c0001t0004g0084 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-13+29513G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728962 | |||||||
| chr2:46729154 | G | A | 7 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0080 others(4): Show |
7 | HG02572.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12-29365G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729154 | |||||||
| chr2:46729230 | T | C | 9 | a0001c0001t0004g0133 a0001c0001t0004g0139 a0001c0001t0004g0140 others(6): Show |
9 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12-29289T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729230 | |||||||
| chr2:46729301 | T | G | 1 | a0001c0002t0003g0130 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-12-29218T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729301 | |||||||
| chr2:46729340 | A | AT | 27 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0006g0012 others(24): Show |
32 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-12-29179_-12-2917 others(5): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729340 | |||||||
| chr2:46729370 | A | C | 1 | a0001c0008t0016g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-29149A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729370 | |||||||
| chr2:46729438 | A | G | 1 | a0001c0001t0007g0067 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-12-29081A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729438 | |||||||
| chr2:46729479 | C | T | 2 | a0001c0001t0004g0032 a0001c0001t0019g0245 |
3 | HG02055.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-12-29040C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729479 | |||||||
| chr2:46729480 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-12-29039G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729480 | |||||||
| chr2:46729621 | C | T | 1 | a0001c0001t0007g0073 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-12-28898C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729621 | |||||||
| chr2:46729650 | C | T | 8 | a0001c0001t0004g0133 a0001c0001t0004g0139 a0001c0001t0004g0140 others(5): Show |
8 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-28869C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729650 | |||||||
| chr2:46729655 | A | G | 2 | a0001c0001t0002g0035 a0001c0001t0002g0262 |
3 | HG02572.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-12-28864A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729655 | |||||||
| chr2:46729671 | G | C | 229 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(226): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.-12-28848G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729671 | |||||||
| chr2:46729874 | A | T | 1 | a0001c0008t0016g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-28645A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729874 | |||||||
| chr2:46729881 | C | G | 1 | a0001c0008t0016g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-28638C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729881 | |||||||
| chr2:46730070 | C | G | 8 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(5): Show |
10 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12-28449C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730070 | |||||||
| chr2:46730077 | A | G | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-28442A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730077 | |||||||
| chr2:46730116 | T | C | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-28403T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730116 | |||||||
| chr2:46730339 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-28180G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730339 | |||||||
| chr2:46730376 | G | A | 18 | a0001c0003t0005g0011 a0001c0003t0005g0015 a0001c0003t0005g0031 others(15): Show |
21 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-28143G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730376 | |||||||
| chr2:46730509 | C | T | 1 | a0001c0003t0005g0098 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-12-28010C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730509 | |||||||
| chr2:46730512 | A | G | 2 | a0001c0001t0004g0140 a0001c0001t0018g0138 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-12-28007A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730512 | |||||||
| chr2:46730567 | T | C | 1 | a0001c0001t0002g0258 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-12-27952T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730567 | |||||||
| chr2:46730580 | A | G | 13 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(10): Show |
14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-27939A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730580 | |||||||
| chr2:46730609 | G | A | 18 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0006g0052 others(15): Show |
21 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-12-27910G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730609 | |||||||
| chr2:46730642 | C | G | 1 | a0001c0003t0005g0044 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-12-27877C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730642 | |||||||
| chr2:46730648 | A | G | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-27871A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730648 | |||||||
| chr2:46730706 | A | G | 52 | a0001c0001t0012g0123 a0001c0002t0003g0001 a0001c0002t0003g0018 others(49): Show |
65 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.-12-27813A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730706 | |||||||
| chr2:46730762 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-12-27757A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730762 | |||||||
| chr2:46730915 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-12-27604A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730915 | |||||||
| chr2:46730960 | C | T | 1 | a0001c0001t0004g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-12-27559C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730960 | |||||||
| chr2:46730974 | C | G | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-27545C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730974 | |||||||
| chr2:46731019 | A | G | 1 | a0001c0001t0002g0279 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-12-27500A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46731019 | |||||||
| chr2:46731046 | G | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-27473G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46731046 | |||||||
| chr2:46731055 | T | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-27464T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46731055 | |||||||
| chr2:46731143 | T | G | 1 | a0001c0001t0001g0038 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-12-27376T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46731143 | |||||||
| chr2:46731212 | G | T | 2 | a0001c0002t0003g0115 a0001c0002t0003g0121 |
2 | HG03540.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-12-27307G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46731212 | |||||||
| chr2:46731229 | G | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0199 a0001c0001t0001g0208 others(2): Show |
6 | NA18939.hp1 NA18953.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-27290G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46731229 | |||||||
| chr2:46731253 | C | T | 1 | a0001c0008t0016g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-27266C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46731253 | |||||||
| chr2:46731271 | T | A | 1 | a0001c0001t0007g0071 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-12-27248T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46731271 | |||||||
| chr2:46731356 | A | G | 1 | a0001c0002t0003g0126 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-12-27163A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46731356 | |||||||
| chr2:46731523 | A | G | 1 | a0001c0001t0019g0245 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-12-26996A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46731523 | |||||||
| chr2:46731776 | T | TA | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-26741dupA | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46731776 | ||||||
| chr2:46732070 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-26449G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732070 | |||||||
| chr2:46732114 | T | G | 1 | a0001c0001t0002g0259 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-12-26405T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732114 | |||||||
| chr2:46732151 | G | T | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0009g0006 others(4): Show |
10 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-26368G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732151 | |||||||
| chr2:46732201 | T | C | 1 | a0001c0001t0002g0287 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-12-26318T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732201 | |||||||
| chr2:46732212 | A | G | 1 | a0001c0001t0004g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-12-26307A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732212 | |||||||
| chr2:46732221 | A | G | 1 | a0001c0001t0002g0262 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-12-26298A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732221 | |||||||
| chr2:46732268 | C | T | 1 | a0001c0001t0002g0264 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-12-26251C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732268 | |||||||
| chr2:46732274 | A | T | 1 | a0001c0001t0001g0173 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-12-26245A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732274 | |||||||
| chr2:46732492 | G | A | 19 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(16): Show |
21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-26027G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732492 | |||||||
| chr2:46732531 | G | A | 1 | a0001c0001t0018g0138 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-12-25988G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732531 | |||||||
| chr2:46732588 | C | G | 5 | a0001c0001t0008g0022 a0001c0001t0008g0082 a0001c0001t0008g0151 others(2): Show |
6 | HG01109.hp2 HG02451.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-25931C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732588 | |||||||
| chr2:46732623 | C | G | 2 | a0001c0001t0002g0305 a0001c0001t0002g0306 |
2 | NA18960.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-12-25896C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732623 | |||||||
| chr2:46732865 | G | A | 51 | a0001c0002t0003g0001 a0001c0002t0003g0017 a0001c0002t0003g0018 others(48): Show |
64 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.-12-25654G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732865 | |||||||
| chr2:46732920 | C | T | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0009g0006 others(4): Show |
10 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-25599C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732920 | |||||||
| chr2:46732940 | A | C | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-25579A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732940 | |||||||
| chr2:46732962 | T | A | 16 | a0001c0002t0010g0016 a0001c0002t0010g0088 a0001c0002t0010g0091 others(13): Show |
20 | HG01069.hp2 HG01074.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12-25557T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732962 | |||||||
| chr2:46732973 | C | G | 1 | a0001c0001t0001g0221 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-12-25546C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732973 | |||||||
| chr2:46732978 | G | T | 1 | a0001c0001t0006g0058 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-12-25541G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732978 | |||||||
| chr2:46733037 | C | T | 1 | a0001c0001t0007g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-12-25482C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733037 | |||||||
| chr2:46733158 | G | A | 18 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0006g0052 others(15): Show |
21 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-12-25361G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733158 | |||||||
| chr2:46733180 | C | T | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-25339C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733180 | |||||||
| chr2:46733190 | G | T | 65 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(62): Show |
79 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.-12-25329G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733190 | |||||||
| chr2:46733199 | A | T | 11 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(8): Show |
11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-25320A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733199 | |||||||
| chr2:46733276 | G | A | 1 | a0001c0001t0002g0036 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-12-25243G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733276 | |||||||
| chr2:46733419 | G | T | 1 | a0001c0008t0016g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-25100G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733419 | |||||||
| chr2:46733483 | G | A | 1 | a0001c0001t0006g0058 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-12-25036G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733483 | |||||||
| chr2:46733568 | C | CA | 15 | a0001c0001t0004g0078 a0001c0002t0010g0016 a0001c0002t0010g0091 others(12): Show |
19 | HG01069.hp2 HG01074.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.-12-24939dupA | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46733568 | ||||||
| chr2:46733568 | CA | C | 16 | a0001c0001t0004g0133 a0001c0001t0004g0139 a0001c0001t0004g0140 others(13): Show |
18 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.-12-24939delA | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46733568 | ||||||
| chr2:46733577 | AAAAG | A | 10 | a0001c0001t0006g0054 a0001c0001t0006g0055 a0001c0001t0006g0056 others(7): Show |
13 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12-24938_-12-2493 others(8): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46733577 | ||||||
| chr2:46733581 | G | A | 5 | a0001c0002t0010g0088 a0001c0003t0005g0043 a0001c0004t0011g0302 others(2): Show |
5 | HG01515.hp1 HG02132.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12-24938G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733581 | |||||||
| chr2:46733581 | G | GA | 6 | a0001c0001t0001g0221 a0001c0001t0002g0254 a0001c0002t0003g0001 others(3): Show |
6 | HG01975.hp1 HG02738.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-24923dupA | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46733581 | ||||||
| chr2:46733581 | GA | G | 12 | a0001c0001t0002g0290 a0001c0001t0004g0077 a0001c0001t0004g0079 others(9): Show |
13 | HG01074.hp1 HG01099.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12-24923delA | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46733581 | ||||||
| chr2:46733582 | A | G | 2 | a0001c0002t0010g0088 a0001c0003t0005g0043 |
2 | HG02698.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-12-24937A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733582 | |||||||
| chr2:46733647 | G | A | 1 | a0001c0001t0008g0082 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-12-24872G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733647 | |||||||
| chr2:46733650 | A | T | 1 | a0001c0002t0003g0114 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-12-24869A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733650 | |||||||
| chr2:46733688 | A | T | 18 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0006g0052 others(15): Show |
21 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-12-24831A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733688 | |||||||
| chr2:46733857 | G | A | 18 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0006g0052 others(15): Show |
21 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-12-24662G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733857 | |||||||
| chr2:46733887 | AAC | A | 3 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 |
3 | HG03195.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-12-24630_-12-2462 others(6): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46733887 | ||||||
| chr2:46733891 | T | G | 1 | a0001c0002t0015g0104 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-12-24628T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733891 | |||||||
| chr2:46733898 | C | T | 8 | a0001c0001t0004g0133 a0001c0001t0004g0139 a0001c0001t0004g0140 others(5): Show |
8 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-24621C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733898 | |||||||
| chr2:46733921 | A | C | 19 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(16): Show |
21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-24598A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733921 | |||||||
| chr2:46733958 | A | G | 1 | a0001c0002t0015g0104 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-12-24561A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733958 | |||||||
| chr2:46734176 | A | G | 4 | a0001c0001t0006g0052 a0001c0001t0006g0057 a0001c0001t0006g0058 others(1): Show |
4 | HG02717.hp1 NA18522.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-24343A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734176 | |||||||
| chr2:46734217 | T | A | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-24302T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734217 | |||||||
| chr2:46734228 | T | A | 26 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0006g0012 others(23): Show |
31 | HG00733.hp2 HG01070.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.-12-24291T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734228 | |||||||
| chr2:46734243 | A | G | 1 | a0001c0001t0002g0284 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-12-24276A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734243 | |||||||
| chr2:46734501 | T | G | 3 | a0001c0001t0002g0267 a0001c0001t0002g0278 a0001c0001t0002g0282 |
3 | HG01496.hp1 HG02486.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-12-24018T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734501 | |||||||
| chr2:46734559 | A | G | 2 | a0001c0001t0007g0066 a0001c0001t0007g0067 |
2 | HG01081.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-12-23960A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734559 | |||||||
| chr2:46734649 | G | C | 6 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0080 others(3): Show |
6 | HG02572.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-23870G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734649 | |||||||
| chr2:46734652 | C | G | 1 | a0001c0001t0001g0166 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-12-23867C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734652 | |||||||
| chr2:46734653 | C | G | 1 | a0001c0001t0004g0078 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-12-23866C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734653 | |||||||
| chr2:46734869 | T | C | 1 | a0001c0002t0003g0136 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-12-23650T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734869 | |||||||
| chr2:46734871 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-23648T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734871 | |||||||
| chr2:46734998 | A | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-23521A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734998 | |||||||
| chr2:46735024 | A | G | 1 | a0001c0003t0005g0043 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-12-23495A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46735024 | |||||||
| chr2:46735184 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-12-23335G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46735184 | |||||||
| chr2:46735240 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-12-23279G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46735240 | |||||||
| chr2:46735600 | A | T | 229 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(226): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.-12-22919A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46735600 | |||||||
| chr2:46735727 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0172 |
3 | HG02257.hp2 HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-12-22792A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46735727 | |||||||
| chr2:46735738 | G | T | 1 | a0001c0001t0004g0210 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-12-22781G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46735738 | |||||||
| chr2:46735817 | C | T | 1 | a0001c0001t0002g0243 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-12-22702C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46735817 | |||||||
| chr2:46735867 | A | G | 13 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(10): Show |
14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-22652A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46735867 | |||||||
| chr2:46736018 | C | G | 2 | a0001c0003t0005g0093 a0001c0003t0005g0099 |
2 | NA18946.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-12-22501C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46736018 | |||||||
| chr2:46736096 | G | A | 11 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(8): Show |
11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-22423G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46736096 | |||||||
| chr2:46736131 | T | G | 21 | a0001c0002t0010g0016 a0001c0002t0010g0088 a0001c0002t0010g0091 others(18): Show |
25 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.-12-22388T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46736131 | |||||||
| chr2:46736243 | A | G | 6 | a0001c0002t0003g0019 a0001c0002t0003g0102 a0001c0002t0003g0108 others(3): Show |
7 | HG01074.hp1 HG01099.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12-22276A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46736243 | |||||||
| chr2:46736395 | T | A | 1 | a0001c0001t0002g0260 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-12-22124T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46736395 | |||||||
| chr2:46736396 | C | G | 8 | a0001c0001t0004g0077 a0001c0001t0004g0078 a0001c0001t0004g0079 others(5): Show |
8 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-22123C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46736396 | |||||||
| chr2:46736471 | A | G | 21 | a0001c0002t0010g0016 a0001c0002t0010g0088 a0001c0002t0010g0091 others(18): Show |
25 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.-12-22048A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46736471 | |||||||
| chr2:46736688 | C | T | 1 | a0001c0002t0003g0136 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-12-21831C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46736688 | |||||||
| chr2:46736714 | T | C | 1 | a0001c0001t0004g0145 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-12-21805T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46736714 | |||||||
| chr2:46736842 | A | AT | 26 | a0001c0001t0004g0077 a0001c0001t0004g0078 a0001c0001t0004g0079 others(23): Show |
28 | HG00280.hp2 HG00733.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-12-21664dupT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46736842 | ||||||
| chr2:46736842 | AT | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
125 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.-12-21664delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46736842 | ||||||
| chr2:46736921 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-12-21598A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46736921 | |||||||
| chr2:46737114 | C | G | 13 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(10): Show |
14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-21405C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46737114 | |||||||
| chr2:46737149 | A | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
144 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-12-21370A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46737149 | |||||||
| chr2:46737240 | T | G | 1 | a0001c0001t0001g0195 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-12-21279T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46737240 | |||||||
| chr2:46737643 | G | A | 11 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(8): Show |
11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-20876G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46737643 | |||||||
| chr2:46737661 | A | G | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-20858A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46737661 | |||||||
| chr2:46737856 | T | TA | 14 | a0001c0001t0001g0038 a0001c0001t0004g0032 a0001c0001t0006g0052 others(11): Show |
15 | HG02055.hp2 HG02080.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12-20649dupA | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46737856 | ||||||
| chr2:46737871 | T | C | 45 | a0001c0001t0012g0123 a0001c0002t0003g0001 a0001c0002t0003g0019 others(42): Show |
56 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.-12-20648T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46737871 | |||||||
| chr2:46737975 | A | G | 20 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(17): Show |
22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12-20544A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46737975 | |||||||
| chr2:46738223 | A | T | 11 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(8): Show |
11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-20296A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46738223 | |||||||
| chr2:46738252 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-20267C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46738252 | |||||||
| chr2:46738363 | C | G | 1 | a0001c0001t0004g0210 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-12-20156C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46738363 | |||||||
| chr2:46738488 | C | G | 19 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(16): Show |
21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-20031C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46738488 | |||||||
| chr2:46738504 | T | G | 13 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(10): Show |
14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-20015T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46738504 | |||||||
| chr2:46738566 | C | G | 1 | a0001c0001t0002g0257 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-12-19953C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46738566 | |||||||
| chr2:46738867 | G | A | 11 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(8): Show |
11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-19652G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46738867 | |||||||
| chr2:46738869 | G | A | 18 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0006g0052 others(15): Show |
21 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-12-19650G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46738869 | |||||||
| chr2:46738926 | G | A | 5 | a0001c0002t0003g0017 a0001c0002t0003g0105 a0001c0002t0003g0106 others(2): Show |
6 | HG02109.hp2 HG02451.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-19593G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46738926 | |||||||
| chr2:46739030 | C | T | 2 | a0001c0001t0004g0032 a0001c0001t0019g0245 |
3 | HG02055.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-12-19489C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739030 | |||||||
| chr2:46739228 | A | G | 1 | a0001c0001t0017g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-19291A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739228 | |||||||
| chr2:46739301 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0172 |
3 | HG02257.hp2 HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-12-19218A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739301 | |||||||
| chr2:46739365 | C | G | 11 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(8): Show |
11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-19154C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739365 | |||||||
| chr2:46739392 | G | A | 117 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
141 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.-12-19127G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739392 | |||||||
| chr2:46739393 | A | T | 16 | a0001c0002t0010g0016 a0001c0002t0010g0088 a0001c0002t0010g0091 others(13): Show |
20 | HG01069.hp2 HG01074.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12-19126A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739393 | |||||||
| chr2:46739414 | A | G | 1 | a0001c0003t0005g0086 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-12-19105A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739414 | |||||||
| chr2:46739665 | G | A | 1 | a0001c0008t0016g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-18854G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739665 | |||||||
| chr2:46739691 | G | A | 144 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0163 others(141): Show |
172 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.-12-18828G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739691 | |||||||
| chr2:46739897 | A | G | 3 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0262 |
5 | HG02572.hp2 HG02622.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12-18622A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739897 | |||||||
| chr2:46739958 | C | G | 1 | a0001c0001t0001g0230 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-12-18561C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739958 | |||||||
| chr2:46739979 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-18540C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739979 | |||||||
| chr2:46740267 | G | A | 1 | a0001c0003t0005g0236 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-12-18252G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46740267 | |||||||
| chr2:46740335 | T | A | 1 | a0001c0003t0005g0092 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-12-18184T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46740335 | |||||||
| chr2:46740555 | A | G | 3 | a0001c0003t0005g0043 a0001c0003t0005g0044 a0001c0003t0005g0086 |
3 | HG01069.hp2 HG01074.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-12-17964A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46740555 | |||||||
| chr2:46740672 | CTGATACC others(11126): Show |
C | 1 | a0001c0001t0008g0022 | 2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-12-17846_-12-6714 others(3): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46740672 | |||||||
| chr2:46740734 | C | A | 7 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0080 others(4): Show |
7 | HG02572.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12-17785C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46740734 | |||||||
| chr2:46740912 | C | T | 224 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(221): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-12-17607C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46740912 | |||||||
| chr2:46740982 | T | C | 1 | a0001c0003t0005g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-12-17537T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46740982 | |||||||
| chr2:46741042 | T | C | 1 | a0001c0002t0010g0016 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-12-17477T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741042 | |||||||
| chr2:46741058 | C | T | 1 | a0001c0001t0021g0029 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-12-17461C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741058 | |||||||
| chr2:46741111 | C | T | 3 | a0001c0002t0003g0001 a0001c0002t0003g0112 a0001c0002t0003g0129 |
3 | HG03710.hp1 HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-12-17408C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741111 | |||||||
| chr2:46741122 | C | G | 1 | a0001c0001t0001g0197 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-12-17397C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741122 | |||||||
| chr2:46741122 | C | T | 8 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(5): Show |
10 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12-17397C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741122 | |||||||
| chr2:46741147 | T | A | 13 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(10): Show |
14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-17372T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741147 | |||||||
| chr2:46741154 | T | A | 1 | a0001c0001t0007g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-12-17365T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741154 | |||||||
| chr2:46741274 | C | G | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-17245C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741274 | |||||||
| chr2:46741314 | G | A | 1 | a0001c0002t0003g0001 | 2 | NA18971.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-12-17205G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741314 | |||||||
| chr2:46741322 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-12-17197C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741322 | |||||||
| chr2:46741326 | A | G | 242 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(239): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.-12-17193A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741326 | |||||||
| chr2:46741384 | G | A | 19 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(16): Show |
21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-17135G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741384 | |||||||
| chr2:46741388 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-12-17131G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741388 | |||||||
| chr2:46741422 | A | C | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-17097A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741422 | |||||||
| chr2:46741555 | C | T | 19 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(16): Show |
21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-16964C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741555 | |||||||
| chr2:46741577 | A | G | 273 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
333 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.-12-16942A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741577 | |||||||
| chr2:46741611 | T | G | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-16908T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741611 | |||||||
| chr2:46741643 | G | A | 1 | a0001c0002t0003g0128 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-12-16876G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741643 | |||||||
| chr2:46741841 | A | G | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-16678A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741841 | |||||||
| chr2:46742058 | A | G | 5 | a0001c0001t0009g0006 a0001c0004t0011g0301 a0001c0004t0011g0302 others(2): Show |
8 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-16461A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742058 | |||||||
| chr2:46742215 | T | C | 3 | a0001c0001t0001g0038 a0001c0001t0004g0032 a0001c0001t0019g0245 |
4 | HG02055.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-16304T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742215 | |||||||
| chr2:46742252 | C | G | 25 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0006g0012 others(22): Show |
30 | HG00733.hp2 HG01070.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.-12-16267C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742252 | |||||||
| chr2:46742281 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-12-16238G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742281 | |||||||
| chr2:46742304 | T | G | 1 | a0001c0001t0002g0260 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-12-16215T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742304 | |||||||
| chr2:46742379 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0159 a0001c0001t0001g0160 others(5): Show |
8 | HG01255.hp2 HG02145.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-16140G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742379 | |||||||
| chr2:46742402 | T | A | 10 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0241 others(7): Show |
16 | HG00558.hp2 HG02027.hp1 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.-12-16117T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742402 | |||||||
| chr2:46742468 | G | A | 5 | a0001c0001t0009g0006 a0001c0004t0011g0301 a0001c0004t0011g0302 others(2): Show |
8 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-16051G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742468 | |||||||
| chr2:46742496 | T | C | 3 | a0001c0001t0001g0164 a0001c0001t0001g0174 a0001c0001t0001g0180 |
3 | NA18957.hp2 NA18962.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-12-16023T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742496 | |||||||
| chr2:46742727 | G | A | 3 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 |
3 | HG03195.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-12-15792G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742727 | |||||||
| chr2:46742783 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-12-15736A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742783 | |||||||
| chr2:46742820 | T | C | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-15699T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742820 | |||||||
| chr2:46743113 | T | A | 1 | a0001c0008t0016g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-15406T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743113 | |||||||
| chr2:46743261 | G | A | 2 | a0001c0001t0004g0184 a0001c0001t0004g0235 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-12-15258G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743261 | |||||||
| chr2:46743327 | G | A | 224 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(221): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-12-15192G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743327 | |||||||
| chr2:46743409 | C | T | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0009g0006 others(4): Show |
10 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-15110C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743409 | |||||||
| chr2:46743448 | A | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.-12-15071A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743448 | |||||||
| chr2:46743601 | A | G | 4 | a0001c0001t0008g0082 a0001c0001t0008g0151 a0001c0001t0008g0152 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-14918A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743601 | |||||||
| chr2:46743687 | T | G | 27 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0006g0012 others(24): Show |
32 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-12-14832T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743687 | |||||||
| chr2:46743748 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(91): Show |
115 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.-12-14771A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743748 | |||||||
| chr2:46743769 | T | C | 1 | a0001c0001t0006g0046 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-12-14750T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743769 | |||||||
| chr2:46743778 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-14741T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743778 | |||||||
| chr2:46743878 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-12-14641T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743878 | |||||||
| chr2:46743951 | G | A | 1 | a0001c0001t0006g0048 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-12-14568G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743951 | |||||||
| chr2:46743987 | A | G | 1 | a0001c0001t0002g0293 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-12-14532A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743987 | |||||||
| chr2:46743987 | A | T | 26 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0006g0012 others(23): Show |
31 | HG00733.hp2 HG01070.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.-12-14532A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743987 | |||||||
| chr2:46743996 | CT | C | 240 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(237): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.-12-14512delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46743996 | ||||||
| chr2:46744050 | C | T | 15 | a0001c0001t0002g0007 a0001c0001t0002g0250 a0001c0001t0002g0275 others(12): Show |
18 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.-12-14469C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744050 | |||||||
| chr2:46744056 | C | T | 13 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(10): Show |
14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-14463C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744056 | |||||||
| chr2:46744080 | C | T | 19 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(16): Show |
21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-14439C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744080 | |||||||
| chr2:46744084 | G | A | 1 | a0001c0002t0003g0081 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-12-14435G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744084 | |||||||
| chr2:46744208 | G | T | 5 | a0001c0001t0009g0006 a0001c0004t0011g0301 a0001c0004t0011g0302 others(2): Show |
8 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-14311G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744208 | |||||||
| chr2:46744242 | GGCCTCCC others(531): Show |
G | 1 | a0001c0005t0008g0083 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12-14264_-12-1372 others(4): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46744242 | ||||||
| chr2:46744249 | C | T | 8 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(5): Show |
10 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12-14270C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744249 | |||||||
| chr2:46744276 | C | T | 1 | a0001c0003t0005g0090 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-12-14243C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744276 | |||||||
| chr2:46744283 | C | G | 1 | a0001c0001t0008g0082 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-12-14236C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744283 | |||||||
| chr2:46744299 | C | A | 15 | a0001c0001t0004g0032 a0001c0001t0007g0014 a0001c0001t0007g0065 others(12): Show |
17 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.-12-14220C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744299 | |||||||
| chr2:46744327 | G | A | 11 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(8): Show |
11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-14192G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744327 | |||||||
| chr2:46744516 | A | C | 2 | a0001c0002t0003g0096 a0001c0002t0003g0097 |
2 | NA18955.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-12-14003A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744516 | |||||||
| chr2:46744528 | C | CT | 6 | a0001c0001t0004g0182 a0001c0001t0004g0184 a0001c0001t0004g0190 others(3): Show |
6 | HG00738.hp1 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-13978dupT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46744528 | ||||||
| chr2:46744661 | G | T | 8 | a0001c0001t0004g0133 a0001c0001t0004g0139 a0001c0001t0004g0140 others(5): Show |
8 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-13858G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744661 | |||||||
| chr2:46744688 | C | T | 13 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(10): Show |
14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-13831C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744688 | |||||||
| chr2:46744771 | G | A | 1 | a0001c0001t0006g0048 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-12-13748G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744771 | |||||||
| chr2:46744792 | T | A | 4 | a0001c0001t0008g0082 a0001c0001t0008g0151 a0001c0001t0008g0152 others(1): Show |
4 | HG01109.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-13727T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744792 | |||||||
| chr2:46744817 | C | T | 1 | a0001c0002t0003g0132 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-12-13702C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744817 | |||||||
| chr2:46744827 | T | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.-12-13692T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744827 | |||||||
| chr2:46744883 | G | A | 1 | a0001c0002t0003g0149 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-12-13636G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744883 | |||||||
| chr2:46745001 | C | G | 13 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(10): Show |
14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-13518C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745001 | |||||||
| chr2:46745045 | G | A | 13 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(10): Show |
14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-13474G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745045 | |||||||
| chr2:46745060 | A | G | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-13459A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745060 | |||||||
| chr2:46745070 | C | T | 1 | a0001c0002t0003g0127 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-12-13449C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745070 | |||||||
| chr2:46745122 | G | C | 1 | a0001c0008t0016g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-13397G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745122 | |||||||
| chr2:46745291 | T | C | 1 | a0001c0001t0017g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-13228T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745291 | |||||||
| chr2:46745524 | T | G | 7 | a0001c0001t0009g0006 a0001c0004t0011g0301 a0001c0004t0011g0302 others(4): Show |
11 | HG01070.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-12995T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745524 | |||||||
| chr2:46745571 | A | C | 8 | a0001c0001t0004g0077 a0001c0001t0004g0078 a0001c0001t0004g0079 others(5): Show |
8 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-12948A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745571 | |||||||
| chr2:46745585 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-12-12934T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745585 | |||||||
| chr2:46745629 | A | C | 60 | a0001c0001t0004g0077 a0001c0001t0004g0078 a0001c0001t0004g0079 others(57): Show |
73 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.-12-12890A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745629 | |||||||
| chr2:46745702 | AG | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0155 |
3 | HG00558.hp1 HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-12-12814delG | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46745702 | ||||||
| chr2:46745738 | A | G | 3 | a0001c0001t0004g0133 a0001c0001t0004g0141 a0001c0001t0004g0144 |
3 | HG02145.hp1 HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-12-12781A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745738 | |||||||
| chr2:46745767 | T | G | 22 | a0001c0002t0010g0016 a0001c0002t0010g0088 a0001c0002t0010g0091 others(19): Show |
26 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.-12-12752T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745767 | |||||||
| chr2:46746050 | GT | G | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0009g0006 others(6): Show |
13 | HG01070.hp2 HG01256.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12-12457delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46746050 | ||||||
| chr2:46746165 | A | C | 1 | a0001c0001t0006g0049 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-12-12354A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746165 | |||||||
| chr2:46746256 | C | G | 1 | a0001c0001t0004g0032 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-12-12263C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746256 | |||||||
| chr2:46746261 | T | A | 78 | a0001c0001t0004g0032 a0001c0001t0004g0039 a0001c0001t0004g0040 others(75): Show |
94 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-12-12258T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746261 | |||||||
| chr2:46746316 | C | T | 1 | a0001c0001t0002g0248 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-12-12203C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746316 | |||||||
| chr2:46746438 | T | G | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-12081T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746438 | |||||||
| chr2:46746543 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-11976C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746543 | |||||||
| chr2:46746563 | A | G | 1 | a0001c0002t0003g0127 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-12-11956A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746563 | |||||||
| chr2:46746630 | G | C | 1 | a0001c0001t0001g0229 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-12-11889G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746630 | |||||||
| chr2:46746646 | C | CA | 21 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(18): Show |
23 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-12-11860dupA | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46746646 | ||||||
| chr2:46746691 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-11828A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746691 | |||||||
| chr2:46746767 | C | T | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0009g0006 others(4): Show |
10 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-11752C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746767 | |||||||
| chr2:46746779 | A | G | 19 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(16): Show |
21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-11740A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746779 | |||||||
| chr2:46746781 | C | G | 19 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(16): Show |
21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-11738C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746781 | |||||||
| chr2:46746813 | G | T | 20 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(17): Show |
22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12-11706G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746813 | |||||||
| chr2:46746922 | C | CT | 71 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0175 others(68): Show |
85 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.-12-11576dupT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46746922 | ||||||
| chr2:46746922 | CT | C | 10 | a0001c0001t0002g0273 a0001c0001t0002g0280 a0001c0001t0004g0084 others(7): Show |
10 | HG01109.hp1 HG01515.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12-11576delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46746922 | ||||||
| chr2:46746922 | CTTT | C | 19 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(16): Show |
21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-11578_-12-1157 others(7): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46746922 | ||||||
| chr2:46746922 | CTTTTTTT | C | 13 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(10): Show |
14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-11582_-12-1157 others(11): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46746922 | ||||||
| chr2:46746926 | T | C | 5 | a0001c0003t0005g0015 a0001c0003t0005g0092 a0001c0003t0005g0093 others(2): Show |
6 | HG02056.hp1 NA18943.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-11593T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746926 | |||||||
| chr2:46747011 | G | A | 1 | a0001c0002t0003g0129 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-12-11508G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46747011 | |||||||
| chr2:46747296 | C | T | 1 | a0001c0002t0010g0016 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-12-11223C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46747296 | |||||||
| chr2:46747399 | A | T | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0009g0006 others(6): Show |
13 | HG01070.hp2 HG01256.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12-11120A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46747399 | |||||||
| chr2:46747470 | C | T | 20 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(17): Show |
22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12-11049C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46747470 | |||||||
| chr2:46747482 | C | T | 8 | a0001c0001t0004g0133 a0001c0001t0004g0139 a0001c0001t0004g0140 others(5): Show |
8 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-11037C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46747482 | |||||||
| chr2:46747510 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-12-11009C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46747510 | |||||||
| chr2:46747527 | A | T | 20 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(17): Show |
22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12-10992A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46747527 | |||||||
| chr2:46747529 | T | A | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0009g0006 others(6): Show |
13 | HG01070.hp2 HG01256.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12-10990T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46747529 | |||||||
| chr2:46747913 | G | T | 5 | a0001c0003t0005g0011 a0001c0003t0005g0043 a0001c0003t0005g0044 others(2): Show |
7 | HG01069.hp2 HG01074.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12-10606G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46747913 | |||||||
| chr2:46748122 | C | T | 3 | a0001c0003t0005g0043 a0001c0003t0005g0044 a0001c0003t0005g0086 |
3 | HG01069.hp2 HG01074.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-12-10397C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748122 | |||||||
| chr2:46748189 | C | CT | 59 | a0001c0001t0001g0197 a0001c0001t0002g0273 a0001c0001t0002g0281 others(56): Show |
73 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.-12-10314dupT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46748189 | ||||||
| chr2:46748189 | CT | C | 22 | a0001c0001t0001g0175 a0001c0001t0006g0012 a0001c0001t0006g0013 others(19): Show |
24 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.-12-10314delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46748189 | ||||||
| chr2:46748197 | T | C | 14 | a0001c0003t0005g0011 a0001c0003t0005g0015 a0001c0003t0005g0043 others(11): Show |
17 | HG01069.hp2 HG01074.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12-10322T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748197 | |||||||
| chr2:46748205 | T | G | 1 | a0001c0001t0002g0249 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-12-10314T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748205 | |||||||
| chr2:46748230 | G | A | 1 | a0001c0001t0004g0210 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-12-10289G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748230 | |||||||
| chr2:46748249 | G | A | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-10270G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748249 | |||||||
| chr2:46748303 | A | G | 1 | a0001c0001t0004g0210 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-12-10216A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748303 | |||||||
| chr2:46748377 | C | T | 1 | a0001c0001t0002g0008 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-12-10142C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748377 | |||||||
| chr2:46748450 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0159 a0001c0001t0001g0160 others(3): Show |
6 | HG01255.hp2 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-10069G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748450 | |||||||
| chr2:46748468 | T | A | 1 | a0001c0001t0017g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-10051T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748468 | |||||||
| chr2:46748500 | T | C | 1 | a0001c0003t0005g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-12-10019T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748500 | |||||||
| chr2:46748689 | A | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
110 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.-12-9830A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748689 | |||||||
| chr2:46748710 | A | G | 1 | a0001c0001t0006g0059 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-12-9809A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748710 | |||||||
| chr2:46748808 | G | A | 20 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(17): Show |
22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12-9711G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748808 | |||||||
| chr2:46748814 | A | T | 2 | a0001c0002t0003g0115 a0001c0002t0003g0121 |
2 | HG03540.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-12-9705A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748814 | |||||||
| chr2:46748829 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-9690G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748829 | |||||||
| chr2:46749078 | G | C | 54 | a0001c0002t0003g0001 a0001c0002t0003g0017 a0001c0002t0003g0018 others(51): Show |
68 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.-12-9441G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749078 | |||||||
| chr2:46749173 | G | A | 20 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(17): Show |
22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12-9346G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749173 | |||||||
| chr2:46749229 | C | T | 1 | a0001c0001t0004g0139 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-12-9290C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749229 | |||||||
| chr2:46749233 | C | G | 1 | a0001c0002t0010g0016 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-12-9286C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749233 | |||||||
| chr2:46749237 | T | A | 20 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(17): Show |
22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12-9282T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749237 | |||||||
| chr2:46749402 | G | A | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-9117G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749402 | |||||||
| chr2:46749516 | C | G | 231 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.-12-9003C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749516 | |||||||
| chr2:46749589 | G | A | 6 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0080 others(3): Show |
6 | HG02572.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-8930G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749589 | |||||||
| chr2:46749604 | A | G | 20 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(17): Show |
22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12-8915A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749604 | |||||||
| chr2:46749670 | T | C | 1 | a0001c0001t0002g0251 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-12-8849T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749670 | |||||||
| chr2:46749695 | C | T | 27 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0006g0012 others(24): Show |
32 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-12-8824C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749695 | |||||||
| chr2:46749728 | C | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
117 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-12-8791C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749728 | |||||||
| chr2:46749958 | T | C | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-8561T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749958 | |||||||
| chr2:46750050 | G | A | 9 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 others(6): Show |
9 | HG01109.hp2 HG02451.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12-8469G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750050 | |||||||
| chr2:46750112 | G | C | 231 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.-12-8407G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750112 | |||||||
| chr2:46750124 | G | C | 7 | a0001c0001t0004g0077 a0001c0001t0004g0078 a0001c0001t0004g0079 others(4): Show |
7 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12-8395G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750124 | |||||||
| chr2:46750173 | G | A | 19 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(16): Show |
21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-8346G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750173 | |||||||
| chr2:46750273 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0179 a0001c0001t0001g0183 others(1): Show |
5 | HG00408.hp1 NA18968.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12-8246C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750273 | |||||||
| chr2:46750280 | C | G | 1 | a0001c0001t0021g0029 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-12-8239C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750280 | |||||||
| chr2:46750326 | G | C | 1 | a0001c0008t0016g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-8193G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750326 | |||||||
| chr2:46750470 | C | G | 1 | a0001c0001t0024g0297 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-12-8049C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750470 | |||||||
| chr2:46750523 | T | C | 1 | a0001c0001t0017g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-7996T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750523 | |||||||
| chr2:46750530 | C | T | 19 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(16): Show |
21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-7989C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750530 | |||||||
| chr2:46750610 | G | A | 4 | a0001c0001t0002g0010 a0001c0001t0002g0241 a0001c0001t0002g0283 others(1): Show |
6 | HG02027.hp1 HG02080.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-7909G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750610 | |||||||
| chr2:46750612 | A | G | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-7907A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750612 | |||||||
| chr2:46750625 | A | G | 1 | a0001c0001t0001g0002 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-12-7894A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750625 | |||||||
| chr2:46750627 | A | G | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-7892A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750627 | |||||||
| chr2:46750631 | C | T | 2 | a0001c0002t0003g0018 a0001c0002t0003g0132 |
3 | HG01175.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-12-7888C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750631 | |||||||
| chr2:46750730 | G | A | 5 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0080 others(2): Show |
5 | HG02572.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12-7789G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750730 | |||||||
| chr2:46750754 | A | G | 56 | a0001c0001t0004g0210 a0001c0002t0003g0001 a0001c0002t0003g0017 others(53): Show |
70 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.-12-7765A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750754 | |||||||
| chr2:46750917 | T | C | 226 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-12-7602T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750917 | |||||||
| chr2:46750951 | C | T | 226 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-12-7568C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750951 | |||||||
| chr2:46750974 | A | G | 15 | a0001c0001t0005g0162 a0001c0003t0005g0011 a0001c0003t0005g0015 others(12): Show |
18 | HG01069.hp2 HG01074.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.-12-7545A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750974 | |||||||
| chr2:46751039 | T | C | 1 | a0001c0003t0005g0238 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-12-7480T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751039 | |||||||
| chr2:46751065 | A | C | 2 | a0001c0001t0001g0244 a0001c0001t0004g0078 |
2 | HG02818.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.-12-7454A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751065 | |||||||
| chr2:46751094 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-12-7425T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751094 | |||||||
| chr2:46751150 | G | A | 8 | a0001c0001t0001g0166 a0001c0001t0001g0193 a0001c0001t0001g0196 others(5): Show |
8 | HG03195.hp2 NA18522.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-7369G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751150 | |||||||
| chr2:46751150 | G | T | 8 | a0001c0001t0004g0133 a0001c0001t0004g0139 a0001c0001t0004g0140 others(5): Show |
8 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-7369G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751150 | |||||||
| chr2:46751210 | A | G | 57 | a0001c0001t0004g0210 a0001c0001t0012g0123 a0001c0002t0003g0001 others(54): Show |
71 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.-12-7309A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751210 | |||||||
| chr2:46751219 | A | G | 1 | a0001c0002t0003g0125 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-12-7300A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751219 | |||||||
| chr2:46751498 | A | G | 2 | a0001c0001t0007g0072 a0001c0001t0007g0073 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-12-7021A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751498 | |||||||
| chr2:46751504 | A | G | 306 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(303): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.-12-7015A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751504 | |||||||
| chr2:46751585 | T | A | 8 | a0001c0001t0004g0133 a0001c0001t0004g0139 a0001c0001t0004g0140 others(5): Show |
8 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-6934T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751585 | |||||||
| chr2:46751690 | G | T | 19 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(16): Show |
21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-6829G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751690 | |||||||
| chr2:46751691 | C | T | 19 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(16): Show |
21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-6828C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751691 | |||||||
| chr2:46751806 | A | G | 1 | a0001c0001t0008g0022 | 2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-12-6713A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751806 | |||||||
| chr2:46751811 | G | A | 8 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(5): Show |
10 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12-6708G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751811 | |||||||
| chr2:46751841 | G | T | 19 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(16): Show |
21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-6678G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751841 | |||||||
| chr2:46751914 | T | C | 1 | a0001c0001t0006g0055 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-12-6605T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751914 | |||||||
| chr2:46752090 | A | T | 6 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(3): Show |
7 | HG01070.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12-6429A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752090 | |||||||
| chr2:46752091 | C | T | 6 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(3): Show |
7 | HG01070.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12-6428C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752091 | |||||||
| chr2:46752105 | G | A | 19 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(16): Show |
21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-6414G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752105 | |||||||
| chr2:46752108 | G | A | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-6411G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752108 | |||||||
| chr2:46752134 | C | T | 2 | a0001c0001t0007g0068 a0001c0001t0007g0069 |
2 | HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-12-6385C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752134 | |||||||
| chr2:46752168 | CT | C | 24 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0080 others(21): Show |
26 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.-12-6337delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46752168 | ||||||
| chr2:46752269 | C | T | 2 | a0001c0001t0002g0276 a0001c0001t0004g0145 |
2 | HG02970.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.-12-6250C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752269 | |||||||
| chr2:46752358 | C | G | 13 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(10): Show |
14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-6161C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752358 | |||||||
| chr2:46752517 | T | C | 86 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
107 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-12-6002T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752517 | |||||||
| chr2:46752534 | TG | T | 4 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(1): Show |
4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-5980delG | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46752534 | ||||||
| chr2:46752547 | G | T | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0008g0022 others(4): Show |
8 | HG01109.hp2 HG02451.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-5972G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752547 | |||||||
| chr2:46752574 | G | C | 1 | a0001c0001t0001g0180 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-12-5945G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752574 | |||||||
| chr2:46752691 | A | G | 1 | a0001c0002t0003g0112 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-12-5828A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752691 | |||||||
| chr2:46752711 | T | G | 1 | a0001c0001t0002g0261 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-12-5808T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752711 | |||||||
| chr2:46752758 | A | T | 1 | a0001c0002t0003g0101 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-12-5761A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752758 | |||||||
| chr2:46752809 | T | C | 1 | a0001c0002t0003g0130 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-12-5710T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752809 | |||||||
| chr2:46752966 | C | A | 19 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(16): Show |
21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-5553C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752966 | |||||||
| chr2:46752997 | G | C | 1 | a0001c0001t0008g0151 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12-5522G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752997 | |||||||
| chr2:46753200 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-5319C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46753200 | |||||||
| chr2:46753349 | A | G | 1 | a0001c0003t0005g0043 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-12-5170A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46753349 | |||||||
| chr2:46753402 | G | T | 1 | a0001c0001t0001g0178 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-12-5117G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46753402 | |||||||
| chr2:46753562 | T | C | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0008g0022 others(4): Show |
8 | HG01109.hp2 HG02451.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-4957T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46753562 | |||||||
| chr2:46753752 | C | T | 1 | a0001c0001t0002g0288 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-12-4767C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46753752 | |||||||
| chr2:46753900 | T | C | 23 | a0001c0001t0005g0162 a0001c0002t0010g0016 a0001c0002t0010g0088 others(20): Show |
27 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.-12-4619T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46753900 | |||||||
| chr2:46753981 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-4538A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46753981 | |||||||
| chr2:46754068 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-4451G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46754068 | |||||||
| chr2:46754482 | A | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
117 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-12-4037A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46754482 | |||||||
| chr2:46754559 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-12-3960G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46754559 | |||||||
| chr2:46754768 | A | G | 3 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 |
3 | HG03195.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-12-3751A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46754768 | |||||||
| chr2:46754789 | C | T | 1 | a0001c0001t0002g0270 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-12-3730C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46754789 | |||||||
| chr2:46754920 | C | A | 1 | a0001c0001t0004g0194 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-12-3599C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46754920 | |||||||
| chr2:46755138 | G | A | 1 | a0001c0008t0016g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-3381G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755138 | |||||||
| chr2:46755418 | T | G | 2 | a0001c0001t0006g0050 a0001c0001t0006g0051 |
2 | HG01123.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-12-3101T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755418 | |||||||
| chr2:46755454 | T | G | 1 | a0001c0001t0001g0223 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-12-3065T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755454 | |||||||
| chr2:46755472 | G | A | 1 | a0001c0002t0015g0104 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-12-3047G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755472 | |||||||
| chr2:46755500 | T | G | 13 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(10): Show |
14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-3019T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755500 | |||||||
| chr2:46755530 | T | A | 1 | a0001c0002t0003g0113 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12-2989T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755530 | |||||||
| chr2:46755550 | A | C | 20 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(17): Show |
22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12-2969A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755550 | |||||||
| chr2:46755756 | C | G | 2 | a0001c0001t0008g0082 a0001c0005t0008g0083 |
2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-12-2763C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755756 | |||||||
| chr2:46755806 | G | A | 2 | a0001c0001t0004g0032 a0001c0001t0019g0245 |
3 | HG02055.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-12-2713G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755806 | |||||||
| chr2:46755857 | T | C | 7 | a0001c0001t0004g0077 a0001c0001t0004g0078 a0001c0001t0004g0079 others(4): Show |
7 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12-2662T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755857 | |||||||
| chr2:46755883 | C | T | 2 | a0001c0002t0003g0096 a0001c0002t0003g0097 |
2 | NA18955.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-12-2636C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755883 | |||||||
| chr2:46755959 | A | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
118 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.-12-2560A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755959 | |||||||
| chr2:46756046 | G | A | 7 | a0001c0001t0004g0077 a0001c0001t0004g0078 a0001c0001t0004g0079 others(4): Show |
7 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12-2473G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756046 | |||||||
| chr2:46756139 | G | A | 8 | a0001c0001t0004g0133 a0001c0001t0004g0139 a0001c0001t0004g0140 others(5): Show |
8 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-2380G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756139 | |||||||
| chr2:46756147 | G | A | 1 | a0001c0001t0017g0171 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-2372G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756147 | |||||||
| chr2:46756437 | A | T | 1 | a0001c0001t0004g0085 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-12-2082A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756437 | |||||||
| chr2:46756482 | AGATTTGG others(12): Show |
A | 1 | a0001c0002t0003g0125 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-12-2035_-12-2017d others(21): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46756482 | ||||||
| chr2:46756547 | T | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-1972T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756547 | |||||||
| chr2:46756583 | G | A | 1 | a0001c0001t0002g0283 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-12-1936G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756583 | |||||||
| chr2:46756591 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-1928A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756591 | |||||||
| chr2:46756611 | T | A | 1 | a0001c0001t0001g0176 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-12-1908T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756611 | |||||||
| chr2:46756637 | G | C | 1 | a0001c0002t0003g0111 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-12-1882G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756637 | |||||||
| chr2:46756707 | A | G | 5 | a0001c0001t0001g0026 a0001c0001t0001g0199 a0001c0001t0001g0208 others(2): Show |
6 | NA18953.hp1 NA18959.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-1812A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756707 | |||||||
| chr2:46756772 | C | T | 1 | a0001c0002t0003g0136 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-12-1747C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756772 | |||||||
| chr2:46756773 | G | A | 18 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0046 others(15): Show |
20 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12-1746G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756773 | |||||||
| chr2:46756927 | C | T | 4 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0004g0041 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-1592C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756927 | |||||||
| chr2:46757053 | A | G | 2 | a0001c0002t0003g0117 a0001c0002t0003g0118 |
2 | NA18993.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-12-1466A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757053 | |||||||
| chr2:46757121 | C | T | 1 | a0001c0002t0012g0103 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-12-1398C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757121 | |||||||
| chr2:46757142 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-12-1377G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757142 | |||||||
| chr2:46757343 | T | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(202): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.-12-1176T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757343 | |||||||
| chr2:46757459 | A | T | 6 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(3): Show |
7 | HG01070.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12-1060A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757459 | |||||||
| chr2:46757488 | C | T | 223 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(220): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-12-1031C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757488 | |||||||
| chr2:46757547 | A | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0213 |
2 | NA19009.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-12-972A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757547 | |||||||
| chr2:46757577 | C | T | 1 | a0001c0002t0003g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-12-942C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757577 | |||||||
| chr2:46757595 | G | GGT | 6 | a0001c0004t0011g0301 a0001c0004t0011g0302 a0001c0004t0011g0303 others(3): Show |
7 | HG01070.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12-922_-12-921dup others(2): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46757595 | ||||||
| chr2:46757633 | G | A | 1 | a0001c0001t0021g0029 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-12-886G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757633 | |||||||
| chr2:46757691 | A | G | 95 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
115 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-12-828A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757691 | |||||||
| chr2:46757700 | C | T | 1 | a0001c0001t0012g0123 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-12-819C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757700 | |||||||
| chr2:46757764 | G | A | 1 | a0001c0002t0003g0045 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-12-755G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757764 | |||||||
| chr2:46757993 | T | C | 2 | a0001c0001t0004g0032 a0001c0001t0019g0245 |
3 | HG02055.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-12-526T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757993 | |||||||
| chr2:46758018 | A | C | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-501A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46758018 | |||||||
| chr2:46758044 | C | A | 1 | a0001c0001t0002g0292 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-12-475C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46758044 | |||||||
| chr2:46758098 | T | C | 1 | a0001c0001t0009g0006 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-421T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46758098 | |||||||
| chr2:46758106 | T | A | 1 | a0001c0003t0005g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-12-413T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46758106 | |||||||
| chr2:46758353 | T | C | 2 | a0001c0001t0004g0184 a0001c0001t0004g0235 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-12-166T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46758353 | |||||||
| chr2:46758405 | G | A | 13 | a0001c0001t0007g0014 a0001c0001t0007g0065 a0001c0001t0007g0066 others(10): Show |
14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-114G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46758405 |