Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6688 |
| ensemblid | ENSG00000066336.13 |
| hgncid | 11241 |
| symbol | SPI1 |
| name | Spi-1 proto-oncogene |
| refseq_nuc | NM_003120.3 |
| refseq_prot | NP_003111.2 |
| ensembl_nuc | ENST00000378538.8 |
| ensembl_prot | ENSP00000367799.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 47354860 |
| end | 47378547 |
| strand | - |
| ver | v1.2 |
| region | chr11:47354860-47378547 |
| region5000 | chr11:47349860-47383547 |
| regionname0 | SPI1_chr11_47354860_47378547 |
| regionname5000 | SPI1_chr11_47349860_47383547 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 270 | 387 | 90 | 74 | 163 | 14 | 44 | 118 | SPI1_chr11_47349860_47383547 | SPI1 | MLQAC others(265): Show |
chr11 | 47349860 | 47383547 |
| a0002 | 0/0 | 270 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | MLQAC others(265): Show |
chr11 | 47349860 | 47383547 |
| a0003 | 0/0 | 270 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | MLQAC others(265): Show |
chr11 | 47349860 | 47383547 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 810 | 386 | 90 | 74 | 162 | 14 | 44 | SPI1_chr11_47349860_47383547 | SPI1 | ATGTT others(805): Show |
chr11 | 47349860 | 47383547 | ||
| a0001c0003 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | ATGTT others(805): Show |
chr11 | 47349860 | 47383547 | ||
| a0002c0002 | 0/0 | 810 | 2 | 0 | 0 | 2 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | ATGTT others(805): Show |
chr11 | 47349860 | 47383547 | ||
| a0003c0004 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | ATGTT others(805): Show |
chr11 | 47349860 | 47383547 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1374 | 259 | 64 | 47 | 107 | 11 | 29 | SPI1_chr11_47349860_47383547 | SPI1 | AAAAT others(1369): Show |
chr11 | 47349860 | 47383547 |
| a0001c0001t0002 | 1/0 | 1374 | 117 | 26 | 23 | 53 | 1 | 13 | SPI1_chr11_47349860_47383547 | SPI1 | AAAAT others(1369): Show |
chr11 | 47349860 | 47383547 |
| a0001c0001t0003 | 0/0 | 1374 | 5 | 0 | 2 | 0 | 2 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | AAAAT others(1369): Show |
chr11 | 47349860 | 47383547 |
| a0001c0001t0004 | 0/0 | 1374 | 3 | 0 | 2 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | AAAAT others(1369): Show |
chr11 | 47349860 | 47383547 |
| a0001c0001t0005 | 0/0 | 1374 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | AAAAT others(1369): Show |
chr11 | 47349860 | 47383547 |
| a0001c0001t0006 | 0/0 | 1374 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | AAAAT others(1369): Show |
chr11 | 47349860 | 47383547 |
| a0001c0003t0001 | 0/0 | 1374 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | AAAAT others(1369): Show |
chr11 | 47349860 | 47383547 |
| a0002c0002t0001 | 0/0 | 1374 | 2 | 0 | 0 | 2 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | AAAAT others(1369): Show |
chr11 | 47349860 | 47383547 |
| a0003c0004t0002 | 0/0 | 1374 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | AAAAT others(1369): Show |
chr11 | 47349860 | 47383547 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 22 | 9 | 5 | 6 | 2 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0002 | 0/0 | 19 | 1 | 3 | 14 | 1 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0016 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0077 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0003 | 0/0 | 7 | 1 | 0 | 5 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0008 | 0/0 | 5 | 1 | 2 | 2 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0219 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0004g0022 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0001t0006g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0001c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0002c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| a0003c0004t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | GBR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | FIN | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0023 | EUR | FIN | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0125 | EUR | FIN | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | CHS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | CLM | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | CLM | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | IBS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | IBS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | PEL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0129 | AMR | PEL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | ACB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02165 | hp2 | a0001 | c0001 | t0005 | g0142 | EAS | CDX | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | ESN | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | MSL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | MSL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | MSL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | MSL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | MSL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | STU | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0022 | SAS | STU | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0128 | SAS | PJL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0163 | SAS | BEB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | BEB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | BEB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | STU | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | STU | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | BEB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | STU | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | STU | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | STU | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | STU | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | YRI | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19006 | hp1 | a0003 | c0004 | t0002 | g0183 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | LWK | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19058 | hp1 | a0001 | c0001 | t0006 | g0081 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19085 | hp2 | a0001 | c0003 | t0001 | g0244 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | YRI | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | YRI | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ASW | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ASW | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | TSI | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | TSI | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0127 | EUR | TSI | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | GIH | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | GIH | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | ACB | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | MSL | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | USA | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | USA | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | LWK | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | LWK | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0077 | REF | REF | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0219 | REF | REF | SPI1_chr11_47349860_47383547 | SPI1 | chr11 | 47349860 | 47383547 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47355241 | G | T | 1 | a0003 | 1 | NA19006.hp1 | missense_variant | MODERATE | c.799C>A | p.His267Asn | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 5/5 | 993/1374 | 799/813 | 267/270 | chr11 | 47355241 | |||
| chr11:47358871 | C | T | 1 | a0002 | 2 | HG00597.hp1 NA18962.hp2 |
missense_variant | MODERATE | c.466G>A | p.Gly156Arg | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/5 | 660/1374 | 466/813 | 156/270 | chr11 | 47358871 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47355323 | G | T | 1 | a0001c0003 | 1 | NA19085.hp2 | synonymous_variant | LOW | c.717C>A | p.Gly239Gly | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 5/5 | 911/1374 | 717/813 | 239/270 | chr11 | 47355323 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47354895 | A | C | 1 | a0001c0001t0003 | 5 | HG00323.hp2 HG01496.hp2 HG02004.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*332T>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 5/5 | 332 | chr11 | 47354895 | ||||||
| chr11:47354897 | G | A | 6 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(3): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*330C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 5/5 | 330 | chr11 | 47354897 | ||||||
| chr11:47354944 | C | T | 1 | a0001c0001t0005 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*283G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 5/5 | 283 | chr11 | 47354944 | ||||||
| chr11:47354993 | C | G | 1 | a0001c0001t0004 | 3 | HG01074.hp2 HG01981.hp2 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*234G>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 5/5 | 234 | chr11 | 47354993 | ||||||
| chr11:47355138 | G | C | 1 | a0001c0001t0006 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*89C>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 5/5 | 89 | chr11 | 47355138 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47355715 | C | G | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.494-169G>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47355715 | |||||||
| chr11:47355720 | A | C | 2 | a0001c0001t0002g0069 a0001c0001t0002g0070 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.494-174T>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47355720 | |||||||
| chr11:47355732 | A | G | 45 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(42): Show |
74 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.494-186T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47355732 | |||||||
| chr11:47355774 | A | AC | 77 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(74): Show |
107 | HG00323.hp1 HG00558.hp1 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.494-229dupG | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47355774 | |||||||
| chr11:47355774 | A | ACC | 51 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0028 others(48): Show |
66 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.494-230_494-229dup others(2): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47355774 | |||||||
| chr11:47355786 | C | T | 1 | a0001c0001t0002g0180 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.494-240G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47355786 | |||||||
| chr11:47355828 | T | G | 1 | a0001c0001t0002g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.494-282A>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47355828 | |||||||
| chr11:47355864 | A | ACT | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(171): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.494-319_494-318ins others(2): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47355864 | |||||||
| chr11:47355959 | CCACT | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(67): Show |
116 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.494-417_494-414del others(4): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47355959 | |||||||
| chr11:47355975 | AC | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(171): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.494-430delG | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47355975 | |||||||
| chr11:47356103 | A | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.494-557T>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356103 | |||||||
| chr11:47356137 | C | G | 1 | a0001c0001t0003g0127 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.494-591G>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356137 | |||||||
| chr11:47356261 | A | G | 2 | a0001c0001t0002g0069 a0001c0001t0002g0070 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.494-715T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356261 | |||||||
| chr11:47356305 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0067 a0001c0001t0001g0068 |
5 | HG01243.hp2 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-759T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356305 | |||||||
| chr11:47356329 | A | ATTCACAA others(18): Show |
1 | a0001c0001t0002g0203 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.494-808_494-784dup others(25): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356329 | |||||||
| chr11:47356342 | TCA | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(168): Show |
265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.494-798_494-797del others(2): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356342 | |||||||
| chr11:47356389 | C | A | 1 | a0001c0001t0001g0018 | 3 | HG02258.hp1 HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.494-843G>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356389 | |||||||
| chr11:47356467 | CCA | C | 4 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0103 others(1): Show |
4 | HG00558.hp2 NA18964.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-923_494-922del others(2): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356467 | |||||||
| chr11:47356507 | T | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.494-961A>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356507 | |||||||
| chr11:47356521 | TGCTCA | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(172): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.494-980_494-976del others(5): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356521 | |||||||
| chr11:47356543 | G | C | 1 | a0001c0001t0003g0127 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.494-997C>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356543 | |||||||
| chr11:47356694 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(211): Show |
310 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.494-1148A>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356694 | |||||||
| chr11:47356752 | T | C | 1 | a0001c0001t0001g0241 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.494-1206A>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356752 | |||||||
| chr11:47356762 | C | T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0243 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.494-1216G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356762 | |||||||
| chr11:47356799 | C | T | 5 | a0001c0001t0002g0020 a0001c0001t0002g0037 a0001c0001t0002g0157 others(2): Show |
8 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.494-1253G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356799 | |||||||
| chr11:47356845 | C | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(77): Show |
117 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.494-1299G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356845 | |||||||
| chr11:47356848 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(74): Show |
124 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.494-1302T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356848 | |||||||
| chr11:47356883 | TAC | T | 84 | a0001c0001t0001g0071 a0001c0001t0001g0124 a0001c0001t0002g0003 others(81): Show |
115 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.494-1339_494-1338d others(4): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356883 | |||||||
| chr11:47356925 | TCA | T | 67 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(64): Show |
95 | HG00323.hp1 HG00558.hp1 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.494-1381_494-1380d others(4): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356925 | |||||||
| chr11:47356936 | A | G | 10 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0025 others(7): Show |
16 | HG02451.hp2 HG02486.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.494-1390T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356936 | |||||||
| chr11:47356937 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.494-1391G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356937 | |||||||
| chr11:47356967 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0053 |
3 | HG02723.hp1 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.494-1421G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356967 | |||||||
| chr11:47356974 | TCA | T | 77 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0025 others(74): Show |
111 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.494-1430_494-1429d others(4): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356974 | |||||||
| chr11:47356998 | ACACACAC others(5): Show |
A | 1 | a0001c0001t0001g0105 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.494-1464_494-1453d others(14): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47356998 | |||||||
| chr11:47357068 | C | T | 2 | a0001c0001t0002g0069 a0001c0001t0002g0070 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.494-1522G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357068 | |||||||
| chr11:47357130 | TCA | T | 3 | a0001c0001t0001g0124 a0001c0001t0001g0155 a0001c0001t0001g0156 |
3 | HG02451.hp2 HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.494-1586_494-1585d others(4): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357130 | |||||||
| chr11:47357130 | TCACACAT others(19): Show |
T | 1 | a0001c0001t0001g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.494-1610_494-1585d others(28): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357130 | |||||||
| chr11:47357161 | CAT | C | 3 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 |
3 | HG02257.hp2 HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.494-1617_494-1616d others(4): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357161 | |||||||
| chr11:47357181 | ACT | A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0002g0172 |
3 | HG02109.hp1 HG02572.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.494-1637_494-1636d others(4): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357181 | |||||||
| chr11:47357202 | CAT | C | 5 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0056 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+1640_493+1641d others(4): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357202 | |||||||
| chr11:47357292 | TC | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(172): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.493+1551delG | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357292 | |||||||
| chr11:47357300 | A | G | 1 | a0001c0001t0002g0021 | 3 | NA18980.hp1 NA18983.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.493+1544T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357300 | |||||||
| chr11:47357350 | TCA | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(79): Show |
113 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.493+1492_493+1493d others(4): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357350 | |||||||
| chr11:47357360 | T | TACAC | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(170): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.493+1480_493+1483d others(6): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357360 | |||||||
| chr11:47357432 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0071 |
3 | HG02572.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.493+1412G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357432 | |||||||
| chr11:47357444 | C | T | 5 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0056 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.493+1400G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357444 | |||||||
| chr11:47357457 | A | G | 1 | a0001c0001t0002g0189 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.493+1387T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357457 | |||||||
| chr11:47357508 | TCA | T | 25 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0060 others(22): Show |
27 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.493+1334_493+1335d others(4): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357508 | |||||||
| chr11:47357574 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.493+1270G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357574 | |||||||
| chr11:47357576 | CTT | C | 82 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(79): Show |
113 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.493+1266_493+1267d others(4): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357576 | |||||||
| chr11:47357601 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.493+1243A>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357601 | |||||||
| chr11:47357661 | G | C | 67 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(64): Show |
94 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.493+1183C>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357661 | |||||||
| chr11:47357762 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.493+1082G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357762 | |||||||
| chr11:47357785 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.493+1059G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357785 | |||||||
| chr11:47357856 | C | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(159): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.493+988G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357856 | |||||||
| chr11:47357859 | C | T | 5 | a0001c0001t0002g0020 a0001c0001t0002g0037 a0001c0001t0002g0157 others(2): Show |
8 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.493+985G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357859 | |||||||
| chr11:47357891 | CTCAT | C | 3 | a0001c0001t0001g0083 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG01175.hp1 HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.493+949_493+952del others(4): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357891 | |||||||
| chr11:47357969 | A | G | 1 | a0001c0001t0002g0163 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.493+875T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47357969 | |||||||
| chr11:47358064 | G | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(171): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.493+780C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47358064 | |||||||
| chr11:47358095 | A | C | 72 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(69): Show |
100 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.493+749T>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47358095 | |||||||
| chr11:47358289 | CAT | C | 72 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(69): Show |
100 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.493+553_493+554del others(2): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47358289 | |||||||
| chr11:47358459 | C | A | 2 | a0001c0001t0002g0191 a0001c0001t0002g0214 |
2 | NA18980.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.493+385G>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47358459 | |||||||
| chr11:47358510 | A | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(171): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.493+334T>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47358510 | |||||||
| chr11:47358536 | G | T | 17 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0019 others(14): Show |
27 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.493+308C>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47358536 | |||||||
| chr11:47358540 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.493+304C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47358540 | |||||||
| chr11:47358566 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.493+278G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47358566 | |||||||
| chr11:47358591 | A | G | 1 | a0001c0001t0001g0033 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.493+253T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47358591 | |||||||
| chr11:47358636 | A | C | 1 | a0001c0001t0002g0172 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.493+208T>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47358636 | |||||||
| chr11:47358667 | TACAC | T | 5 | a0001c0001t0002g0020 a0001c0001t0002g0037 a0001c0001t0002g0157 others(2): Show |
8 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.493+173_493+176del others(4): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47358667 | |||||||
| chr11:47358725 | G | GCA | 71 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(68): Show |
116 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.493+117_493+118dup others(2): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47358725 | |||||||
| chr11:47358785 | G | C | 1 | a0001c0001t0002g0178 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.493+59C>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47358785 | |||||||
| chr11:47358789 | G | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(155): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.493+55C>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47358789 | |||||||
| chr11:47358813 | C | T | 1 | a0001c0001t0002g0216 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.493+31G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 4/4 | chr11 | 47358813 | |||||||
| chr11:47359042 | G | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0034 others(105): Show |
153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.331-36C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 3/4 | chr11 | 47359042 | |||||||
| chr11:47359137 | GGAA | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(257): Show |
385 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.331-134_331-132del others(3): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 3/4 | chr11 | 47359137 | |||||||
| chr11:47359143 | A | G | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0002g0069 others(2): Show |
5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.331-137T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 3/4 | chr11 | 47359143 | |||||||
| chr11:47359355 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.331-349G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 3/4 | chr11 | 47359355 | |||||||
| chr11:47359444 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(70): Show |
121 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.330+409G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 3/4 | chr11 | 47359444 | |||||||
| chr11:47359592 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.330+261C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 3/4 | chr11 | 47359592 | |||||||
| chr11:47359612 | T | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.330+241A>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 3/4 | chr11 | 47359612 | |||||||
| chr11:47359635 | G | A | 8 | a0001c0001t0002g0020 a0001c0001t0002g0037 a0001c0001t0002g0157 others(5): Show |
11 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.330+218C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 3/4 | chr11 | 47359635 | |||||||
| chr11:47359803 | A | C | 1 | a0001c0001t0002g0052 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.330+50T>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 3/4 | chr11 | 47359803 | |||||||
| chr11:47359804 | C | A | 1 | a0001c0001t0002g0052 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.330+49G>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 3/4 | chr11 | 47359804 | |||||||
| chr11:47359806 | A | C | 1 | a0001c0001t0002g0052 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.330+47T>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 3/4 | chr11 | 47359806 | |||||||
| chr11:47359822 | C | G | 1 | a0001c0001t0001g0034 | 2 | HG01517.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.330+31G>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 3/4 | chr11 | 47359822 | |||||||
| chr11:47360091 | A | G | 17 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0019 others(14): Show |
27 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.143-51T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47360091 | |||||||
| chr11:47360290 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.143-250G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47360290 | |||||||
| chr11:47360336 | C | T | 16 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0019 others(13): Show |
26 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.143-296G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47360336 | |||||||
| chr11:47360483 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.143-443G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47360483 | |||||||
| chr11:47360566 | G | T | 8 | a0001c0001t0002g0020 a0001c0001t0002g0037 a0001c0001t0002g0157 others(5): Show |
11 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.143-526C>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47360566 | |||||||
| chr11:47360823 | C | CA | 18 | a0001c0001t0001g0080 a0001c0001t0001g0085 a0001c0001t0001g0092 others(15): Show |
21 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.143-784dupT | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47360823 | |||||||
| chr11:47360875 | A | T | 88 | a0001c0001t0001g0201 a0001c0001t0001g0207 a0001c0001t0001g0236 others(85): Show |
120 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.143-835T>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47360875 | |||||||
| chr11:47361052 | C | T | 5 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0056 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-1012G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47361052 | |||||||
| chr11:47361067 | G | A | 1 | a0001c0001t0001g0018 | 3 | HG02258.hp1 HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.143-1027C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47361067 | |||||||
| chr11:47361354 | G | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0133 a0001c0001t0001g0140 |
4 | NA18956.hp1 NA18967.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-1314C>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47361354 | |||||||
| chr11:47361501 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.143-1461T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47361501 | |||||||
| chr11:47361509 | T | G | 1 | a0001c0001t0001g0097 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.143-1469A>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47361509 | |||||||
| chr11:47361552 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.143-1512C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47361552 | |||||||
| chr11:47361569 | A | G | 1 | a0001c0001t0002g0177 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.143-1529T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47361569 | |||||||
| chr11:47361724 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(171): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.143-1684A>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47361724 | |||||||
| chr11:47361822 | C | A | 6 | a0001c0001t0001g0019 a0001c0001t0003g0125 a0001c0001t0003g0126 others(3): Show |
8 | HG00323.hp2 HG01070.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-1782G>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47361822 | |||||||
| chr11:47361834 | T | C | 6 | a0001c0001t0002g0176 a0001c0001t0002g0192 a0001c0001t0002g0203 others(3): Show |
6 | NA18971.hp1 NA19002.hp2 NA19006.hp1 others(3): Show |
intron_variant | MODIFIER | c.143-1794A>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47361834 | |||||||
| chr11:47361906 | CTTTTAG | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(166): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.143-1872_143-1867d others(8): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47361906 | |||||||
| chr11:47362100 | G | C | 1 | a0001c0001t0002g0040 | 2 | HG02080.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.143-2060C>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47362100 | |||||||
| chr11:47362358 | C | G | 1 | a0001c0001t0002g0203 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.143-2318G>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47362358 | |||||||
| chr11:47362447 | T | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.143-2407A>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47362447 | |||||||
| chr11:47362570 | C | CT | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(142): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.143-2531dupA | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47362570 | |||||||
| chr11:47362570 | C | CTT | 9 | a0001c0001t0001g0059 a0001c0001t0001g0074 a0001c0001t0001g0099 others(6): Show |
9 | HG00423.hp2 NA18956.hp1 NA18967.hp1 others(6): Show |
intron_variant | MODIFIER | c.143-2532_143-2531d others(4): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47362570 | |||||||
| chr11:47362570 | CTTTTTT | C | 16 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0019 others(13): Show |
26 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.143-2536_143-2531d others(8): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47362570 | |||||||
| chr11:47362570 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0130 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.143-2540_143-2531d others(12): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47362570 | |||||||
| chr11:47362570 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0107 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.143-2541_143-2531d others(13): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47362570 | |||||||
| chr11:47362638 | C | T | 24 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0035 others(21): Show |
28 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.143-2598G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47362638 | |||||||
| chr11:47362684 | T | C | 2 | a0001c0001t0002g0170 a0001c0001t0002g0193 |
2 | NA19056.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.143-2644A>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47362684 | |||||||
| chr11:47362854 | T | A | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.143-2814A>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47362854 | |||||||
| chr11:47362914 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.143-2874C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47362914 | |||||||
| chr11:47362926 | C | CA | 27 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(24): Show |
43 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.143-2887dupT | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47362926 | |||||||
| chr11:47362932 | A | AT | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(142): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.143-2893dupA | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47362932 | |||||||
| chr11:47362932 | A | T | 1 | a0001c0001t0001g0089 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.143-2892T>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47362932 | |||||||
| chr11:47362933 | T | A | 85 | a0001c0001t0001g0201 a0001c0001t0001g0207 a0001c0001t0002g0003 others(82): Show |
117 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.143-2893A>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47362933 | |||||||
| chr11:47363046 | A | G | 85 | a0001c0001t0001g0201 a0001c0001t0001g0207 a0001c0001t0002g0003 others(82): Show |
117 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.143-3006T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47363046 | |||||||
| chr11:47363258 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.143-3218G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47363258 | |||||||
| chr11:47363360 | A | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0152 a0001c0001t0001g0153 |
4 | HG02109.hp1 HG02572.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-3320T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47363360 | |||||||
| chr11:47363436 | G | A | 2 | a0001c0001t0002g0165 a0001c0001t0002g0175 |
2 | HG01928.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.143-3396C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47363436 | |||||||
| chr11:47363453 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.143-3413C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47363453 | |||||||
| chr11:47363520 | C | CA | 5 | a0001c0001t0001g0043 a0001c0001t0001g0108 a0001c0001t0001g0111 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.143-3481dupT | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47363520 | |||||||
| chr11:47363643 | G | A | 85 | a0001c0001t0001g0201 a0001c0001t0001g0207 a0001c0001t0002g0003 others(82): Show |
117 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.143-3603C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47363643 | |||||||
| chr11:47363799 | C | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0228 a0001c0001t0001g0229 others(3): Show |
7 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.143-3759G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47363799 | |||||||
| chr11:47363817 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.143-3777G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47363817 | |||||||
| chr11:47363849 | C | G | 15 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0028 others(12): Show |
23 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.143-3809G>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47363849 | |||||||
| chr11:47363957 | G | A | 8 | a0001c0001t0002g0020 a0001c0001t0002g0037 a0001c0001t0002g0157 others(5): Show |
11 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.143-3917C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47363957 | |||||||
| chr11:47363963 | C | CA | 13 | a0001c0001t0002g0052 a0001c0001t0002g0057 a0001c0001t0002g0163 others(10): Show |
13 | HG00639.hp1 HG00642.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-3924dupT | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47363963 | |||||||
| chr11:47363963 | C | CAA | 18 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0019 others(15): Show |
28 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.143-3925_143-3924d others(4): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47363963 | |||||||
| chr11:47363963 | CA | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.143-3924delT | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47363963 | |||||||
| chr11:47364058 | C | CT | 5 | a0001c0001t0001g0036 a0001c0001t0001g0101 a0001c0001t0001g0124 others(2): Show |
6 | HG02109.hp1 HG02155.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-4019dupA | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47364058 | |||||||
| chr11:47364094 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.143-4054T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47364094 | |||||||
| chr11:47364372 | G | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(166): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.143-4332C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47364372 | |||||||
| chr11:47364424 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.143-4384C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47364424 | |||||||
| chr11:47364473 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.143-4433T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47364473 | |||||||
| chr11:47364522 | T | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(169): Show |
265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.143-4482A>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47364522 | |||||||
| chr11:47364678 | C | T | 2 | a0001c0001t0002g0069 a0001c0001t0002g0070 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.143-4638G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47364678 | |||||||
| chr11:47365156 | C | T | 22 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0060 others(19): Show |
24 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.143-5116G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47365156 | |||||||
| chr11:47365662 | AACTTTCA others(15): Show |
A | 90 | a0001c0001t0001g0014 a0001c0001t0001g0061 a0001c0001t0001g0062 others(87): Show |
124 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.143-5644_143-5623d others(24): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47365662 | |||||||
| chr11:47365900 | T | C | 3 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0001c0001t0002g0162 |
3 | HG02818.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.143-5860A>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47365900 | |||||||
| chr11:47366048 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.143-6008G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47366048 | |||||||
| chr11:47366268 | C | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.143-6228G>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47366268 | |||||||
| chr11:47366294 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0053 |
3 | HG02723.hp1 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.143-6254G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47366294 | |||||||
| chr11:47366562 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.143-6522G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47366562 | |||||||
| chr11:47366602 | G | C | 1 | a0001c0001t0002g0167 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.143-6562C>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47366602 | |||||||
| chr11:47366629 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.143-6589G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47366629 | |||||||
| chr11:47366663 | G | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(41): Show |
73 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.143-6623C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47366663 | |||||||
| chr11:47366799 | C | T | 5 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0056 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-6759G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47366799 | |||||||
| chr11:47366822 | A | AAAAAG | 43 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(40): Show |
68 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.143-6787_143-6783d others(7): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47366822 | |||||||
| chr11:47366822 | A | AAAAAGAA others(3): Show |
53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(50): Show |
80 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.143-6792_143-6783d others(12): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47366822 | |||||||
| chr11:47366822 | A | AAAAAGAA others(8): Show |
12 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0035 others(9): Show |
15 | HG01433.hp1 HG01517.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.143-6797_143-6783d others(17): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47366822 | |||||||
| chr11:47366822 | A | AAAAAGAA others(13): Show |
15 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0030 others(12): Show |
16 | HG00621.hp1 HG02056.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.143-6802_143-6783d others(22): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47366822 | |||||||
| chr11:47366822 | A | AAAAAGAA others(18): Show |
1 | a0001c0001t0001g0060 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.143-6807_143-6783d others(27): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47366822 | |||||||
| chr11:47366822 | A | AAAAAGAA others(23): Show |
3 | a0001c0001t0001g0131 a0001c0001t0001g0137 a0001c0001t0001g0141 |
3 | HG03017.hp2 NA18949.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.143-6812_143-6783d others(32): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47366822 | |||||||
| chr11:47366822 | AAAAAG | A | 68 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0207 others(65): Show |
96 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.143-6787_143-6783d others(7): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47366822 | |||||||
| chr11:47366822 | AAAAAGAA others(3): Show |
A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(43): Show |
75 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.143-6792_143-6783d others(12): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47366822 | |||||||
| chr11:47367012 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.143-6972G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47367012 | |||||||
| chr11:47367024 | A | G | 1 | a0001c0001t0002g0216 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.143-6984T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47367024 | |||||||
| chr11:47367509 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.143-7469T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47367509 | |||||||
| chr11:47367512 | C | T | 3 | a0001c0001t0001g0230 a0001c0001t0001g0263 a0001c0001t0001g0264 |
3 | HG01069.hp2 HG01099.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.143-7472G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47367512 | |||||||
| chr11:47367532 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0049 a0001c0001t0001g0051 others(1): Show |
6 | HG01496.hp1 HG02145.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.143-7492G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47367532 | |||||||
| chr11:47367553 | C | CA | 6 | a0001c0001t0002g0171 a0001c0001t0002g0177 a0001c0001t0002g0179 others(3): Show |
6 | HG00735.hp1 HG00741.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.143-7514dupT | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47367553 | |||||||
| chr11:47367553 | C | CAA | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(148): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.143-7515_143-7514d others(4): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47367553 | |||||||
| chr11:47367553 | C | CAAA | 21 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0029 others(18): Show |
27 | HG00438.hp2 HG00544.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.143-7516_143-7514d others(5): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47367553 | |||||||
| chr11:47367672 | A | G | 86 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0207 others(83): Show |
118 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.143-7632T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47367672 | |||||||
| chr11:47367726 | A | G | 2 | a0001c0001t0002g0187 a0001c0001t0002g0198 |
2 | HG03942.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.143-7686T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47367726 | |||||||
| chr11:47367748 | A | AT | 12 | a0001c0001t0001g0004 a0001c0001t0001g0046 a0001c0001t0001g0079 others(9): Show |
19 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(16): Show |
intron_variant | MODIFIER | c.143-7709dupA | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47367748 | |||||||
| chr11:47367748 | A | ATT | 14 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0062 others(11): Show |
16 | HG01433.hp1 HG01517.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.143-7710_143-7709d others(4): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47367748 | |||||||
| chr11:47367748 | A | ATTT | 11 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0130 others(8): Show |
11 | HG00544.hp2 HG00621.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.143-7711_143-7709d others(5): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47367748 | |||||||
| chr11:47367748 | AT | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(52): Show |
92 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.143-7709delA | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47367748 | |||||||
| chr11:47367748 | ATT | A | 18 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0031 others(15): Show |
22 | HG00323.hp2 HG00642.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.143-7710_143-7709d others(4): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47367748 | |||||||
| chr11:47367748 | ATTT | A | 25 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(22): Show |
38 | HG00280.hp1 HG00735.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.143-7711_143-7709d others(5): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47367748 | |||||||
| chr11:47367748 | ATTTT | A | 68 | a0001c0001t0001g0201 a0001c0001t0001g0207 a0001c0001t0002g0003 others(65): Show |
98 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.143-7712_143-7709d others(6): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47367748 | |||||||
| chr11:47367748 | ATTTTT | A | 7 | a0001c0001t0001g0200 a0001c0001t0002g0037 a0001c0001t0002g0159 others(4): Show |
8 | HG01884.hp2 HG02055.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.143-7713_143-7709d others(7): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47367748 | |||||||
| chr11:47368019 | A | G | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.142+7614T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47368019 | |||||||
| chr11:47368087 | C | T | 48 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(45): Show |
79 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.142+7546G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47368087 | |||||||
| chr11:47368125 | C | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(170): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.142+7508G>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47368125 | |||||||
| chr11:47368136 | C | T | 2 | a0001c0001t0002g0174 a0001c0001t0002g0182 |
2 | HG00639.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.142+7497G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47368136 | |||||||
| chr11:47368220 | C | G | 1 | a0001c0001t0001g0083 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.142+7413G>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47368220 | |||||||
| chr11:47368278 | T | A | 1 | a0001c0001t0002g0042 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.142+7355A>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47368278 | |||||||
| chr11:47368470 | G | A | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.142+7163C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47368470 | |||||||
| chr11:47368515 | G | A | 1 | a0001c0001t0002g0211 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.142+7118C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47368515 | |||||||
| chr11:47368836 | G | A | 1 | a0001c0001t0003g0129 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.142+6797C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47368836 | |||||||
| chr11:47368872 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.142+6761C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47368872 | |||||||
| chr11:47368921 | G | T | 1 | a0001c0001t0002g0172 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.142+6712C>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47368921 | |||||||
| chr11:47369062 | A | T | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0025 others(5): Show |
14 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.142+6571T>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47369062 | |||||||
| chr11:47369108 | CA | C | 2 | a0001c0001t0002g0042 a0001c0001t0002g0202 |
3 | HG01109.hp1 HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.142+6524delT | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47369108 | |||||||
| chr11:47369109 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.142+6524T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47369109 | |||||||
| chr11:47369141 | A | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(170): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.142+6492T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47369141 | |||||||
| chr11:47369488 | C | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(167): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.142+6145G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47369488 | |||||||
| chr11:47369560 | G | GA | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(157): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.142+6072dupT | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47369560 | |||||||
| chr11:47369560 | G | GAGA | 89 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(86): Show |
121 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.142+6072_142+6073i others(5): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47369560 | |||||||
| chr11:47369570 | A | AC | 5 | a0001c0001t0001g0036 a0001c0001t0001g0071 a0001c0001t0001g0124 others(2): Show |
6 | HG02109.hp1 HG02572.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+6062_142+6063i others(3): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47369570 | |||||||
| chr11:47369570 | A | C | 1 | a0001c0001t0002g0181 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.142+6063T>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47369570 | |||||||
| chr11:47369573 | C | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0067 |
2 | HG00423.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.142+6060G>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47369573 | |||||||
| chr11:47369623 | G | A | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(255): Show |
383 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.142+6010C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47369623 | |||||||
| chr11:47370141 | G | A | 1 | a0001c0001t0002g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.142+5492C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47370141 | |||||||
| chr11:47370194 | G | A | 86 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0207 others(83): Show |
118 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.142+5439C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47370194 | |||||||
| chr11:47370328 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(167): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.142+5305C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47370328 | |||||||
| chr11:47370397 | G | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(76): Show |
118 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.142+5236C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47370397 | |||||||
| chr11:47370502 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.142+5131C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47370502 | |||||||
| chr11:47370522 | C | T | 1 | a0001c0001t0002g0180 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.142+5111G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47370522 | |||||||
| chr11:47370523 | G | A | 1 | a0001c0001t0002g0225 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.142+5110C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47370523 | |||||||
| chr11:47370559 | G | T | 1 | a0001c0001t0001g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.142+5074C>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47370559 | |||||||
| chr11:47370563 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(170): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.142+5070C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47370563 | |||||||
| chr11:47370570 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.142+5063G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47370570 | |||||||
| chr11:47370600 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.142+5033C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47370600 | |||||||
| chr11:47370681 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.142+4952C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47370681 | |||||||
| chr11:47370879 | A | AGTGT | 29 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0035 others(26): Show |
33 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.142+4750_142+4753d others(6): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47370879 | |||||||
| chr11:47371017 | C | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(68): Show |
115 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.142+4616G>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371017 | |||||||
| chr11:47371058 | C | A | 2 | a0001c0001t0002g0176 a0001c0001t0002g0203 |
2 | NA19056.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.142+4575G>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371058 | |||||||
| chr11:47371155 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.142+4478A>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371155 | |||||||
| chr11:47371275 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0068 a0001c0001t0002g0172 |
5 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+4358C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371275 | |||||||
| chr11:47371351 | G | C | 1 | a0001c0001t0002g0168 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.142+4282C>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371351 | |||||||
| chr11:47371354 | C | CATCTCAA others(1990): Show |
2 | a0001c0001t0002g0217 a0001c0001t0002g0218 |
2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.142+4278_142+4279i others(1999): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371354 | |||||||
| chr11:47371354 | C | CATCTCAA others(1990): Show |
7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0254 others(4): Show |
9 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.142+4278_142+4279i others(1999): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371354 | |||||||
| chr11:47371354 | C | CATCTCAA others(1990): Show |
10 | a0001c0001t0001g0032 a0001c0001t0001g0080 a0001c0001t0001g0089 others(7): Show |
11 | HG01978.hp2 HG02027.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.142+4278_142+4279i others(1999): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371354 | |||||||
| chr11:47371354 | C | CATCTCAA others(1990): Show |
2 | a0001c0001t0001g0079 a0001c0001t0001g0116 |
2 | HG00423.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.142+4278_142+4279i others(1999): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371354 | |||||||
| chr11:47371354 | C | CATCTCAA others(1990): Show |
1 | a0001c0001t0002g0212 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.142+4278_142+4279i others(1999): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371354 | |||||||
| chr11:47371354 | C | CATCTCAA others(1990): Show |
18 | a0001c0001t0001g0207 a0001c0001t0002g0055 a0001c0001t0002g0056 others(15): Show |
18 | HG00438.hp1 HG01192.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.142+4278_142+4279i others(1999): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371354 | |||||||
| chr11:47371354 | C | CATCTCAA others(1990): Show |
1 | a0001c0001t0001g0063 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.142+4278_142+4279i others(1999): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371354 | |||||||
| chr11:47371359 | C | CAAAAAAA others(1991): Show |
2 | a0001c0001t0002g0220 a0001c0001t0002g0221 |
2 | HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.142+4273_142+4274i others(2000): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371359 | |||||||
| chr11:47371359 | C | CAAAAAAA others(1991): Show |
1 | a0001c0001t0002g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.142+4273_142+4274i others(2000): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371359 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1984): Show |
1 | a0001c0001t0001g0154 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.142+4272_142+4273i others(1993): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1989): Show |
1 | a0001c0001t0001g0152 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.142+4272_142+4273i others(1998): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1988): Show |
1 | a0001c0001t0001g0113 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.142+4272_142+4273i others(1997): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1989): Show |
1 | a0001c0001t0001g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.142+4272_142+4273i others(1998): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1989): Show |
1 | a0001c0001t0001g0115 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.142+4272_142+4273i others(1998): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1989): Show |
47 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(44): Show |
82 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.142+4272_142+4273i others(1998): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1989): Show |
1 | a0001c0001t0001g0073 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.142+4272_142+4273i others(1998): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1989): Show |
44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(41): Show |
82 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.142+4272_142+4273i others(1998): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1989): Show |
3 | a0001c0001t0001g0015 a0001c0001t0001g0091 a0001c0001t0001g0092 |
5 | HG00408.hp1 NA18947.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+4272_142+4273i others(1998): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1989): Show |
1 | a0001c0001t0001g0016 | 3 | HG02109.hp2 HG02698.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.142+4272_142+4273i others(1998): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1989): Show |
3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 |
3 | HG02080.hp2 HG02523.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.142+4272_142+4273i others(1998): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1989): Show |
14 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0028 others(11): Show |
22 | HG00280.hp1 HG00642.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.142+4272_142+4273i others(1998): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1989): Show |
1 | a0001c0001t0001g0093 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.142+4272_142+4273i others(1998): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1989): Show |
1 | a0001c0001t0001g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.142+4272_142+4273i others(1998): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1989): Show |
1 | a0001c0001t0002g0024 | 3 | HG01934.hp2 HG01943.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.142+4272_142+4273i others(1998): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1989): Show |
59 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0002g0003 others(56): Show |
89 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.142+4272_142+4273i others(1998): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1989): Show |
1 | a0001c0001t0002g0227 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.142+4272_142+4273i others(1998): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1989): Show |
2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG02056.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.142+4272_142+4273i others(1998): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1989): Show |
1 | a0001c0001t0002g0176 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.142+4272_142+4273i others(1998): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1989): Show |
1 | a0001c0001t0002g0178 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.142+4272_142+4273i others(1998): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371360 | A | AAAAAAAA others(1992): Show |
1 | a0001c0001t0002g0177 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.142+4272_142+4273i others(2001): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371360 | |||||||
| chr11:47371361 | A | AAAAAAAA others(1988): Show |
2 | a0001c0001t0002g0069 a0001c0001t0002g0070 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.142+4271_142+4272i others(1997): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371361 | |||||||
| chr11:47371361 | A | AAAAAAAA others(1988): Show |
1 | a0001c0001t0001g0156 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.142+4271_142+4272i others(1997): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371361 | |||||||
| chr11:47371361 | A | AAAAAAAA others(1988): Show |
2 | a0001c0001t0001g0036 a0001c0001t0001g0153 |
3 | HG02109.hp1 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.142+4271_142+4272i others(1997): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371361 | |||||||
| chr11:47371361 | A | AAAAAAAA others(1988): Show |
19 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0035 others(16): Show |
23 | HG00099.hp1 HG00544.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.142+4271_142+4272i others(1997): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371361 | |||||||
| chr11:47371361 | A | AAAAAAAA others(1988): Show |
1 | a0001c0001t0001g0124 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142+4271_142+4272i others(1997): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371361 | |||||||
| chr11:47371361 | A | AAAAAAAA others(1988): Show |
1 | a0001c0001t0001g0151 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.142+4271_142+4272i others(1997): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371361 | |||||||
| chr11:47371361 | A | AAAAAAAA others(1988): Show |
1 | a0001c0001t0001g0136 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.142+4271_142+4272i others(1997): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371361 | |||||||
| chr11:47371361 | A | AAAAAAAA others(1989): Show |
1 | a0001c0001t0001g0137 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.142+4271_142+4272i others(1998): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371361 | |||||||
| chr11:47371361 | A | AAAAAAAA others(1988): Show |
1 | a0001c0001t0003g0125 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.142+4271_142+4272i others(1997): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371361 | |||||||
| chr11:47371361 | A | AAAAAAAA others(1988): Show |
2 | a0001c0001t0002g0174 a0001c0001t0002g0175 |
2 | HG00639.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.142+4271_142+4272i others(1997): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371361 | |||||||
| chr11:47371362 | A | AAAAAAAA others(1987): Show |
1 | a0001c0001t0001g0155 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.142+4270_142+4271i others(1996): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371362 | |||||||
| chr11:47371362 | A | AAAAAAAA others(1987): Show |
1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.142+4270_142+4271i others(1996): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371362 | |||||||
| chr11:47371411 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.142+4222T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371411 | |||||||
| chr11:47371470 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.142+4163G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371470 | |||||||
| chr11:47371515 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.142+4118T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371515 | |||||||
| chr11:47371667 | T | TA | 85 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(82): Show |
139 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.142+3965dupT | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371667 | |||||||
| chr11:47371667 | TA | T | 12 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0263 others(9): Show |
15 | HG01069.hp2 HG01070.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.142+3965delT | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371667 | |||||||
| chr11:47371752 | A | T | 86 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0207 others(83): Show |
118 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.142+3881T>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371752 | |||||||
| chr11:47371943 | C | T | 17 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0019 others(14): Show |
27 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.142+3690G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47371943 | |||||||
| chr11:47372087 | T | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(170): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.142+3546A>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47372087 | |||||||
| chr11:47372105 | C | CT | 13 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00597.hp2 HG02976.hp1 HG04204.hp1 others(10): Show |
intron_variant | MODIFIER | c.142+3527dupA | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47372105 | |||||||
| chr11:47372196 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.142+3437G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47372196 | |||||||
| chr11:47372381 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.142+3252G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47372381 | |||||||
| chr11:47372391 | T | A | 1 | a0001c0001t0002g0213 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.142+3242A>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47372391 | |||||||
| chr11:47372456 | C | G | 1 | a0001c0001t0001g0076 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.142+3177G>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47372456 | |||||||
| chr11:47372502 | C | T | 1 | a0001c0001t0002g0169 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.142+3131G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47372502 | |||||||
| chr11:47372706 | G | A | 1 | a0001c0001t0002g0041 | 2 | HG02129.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.142+2927C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47372706 | |||||||
| chr11:47372747 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.142+2886G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47372747 | |||||||
| chr11:47372754 | C | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(71): Show |
107 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.142+2879G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47372754 | |||||||
| chr11:47372766 | G | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0025 others(5): Show |
14 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.142+2867C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47372766 | |||||||
| chr11:47372766 | G | T | 1 | a0001c0001t0002g0167 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.142+2867C>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47372766 | |||||||
| chr11:47372787 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(167): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.142+2846A>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47372787 | |||||||
| chr11:47373277 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0123 |
3 | HG00280.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.142+2356C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47373277 | |||||||
| chr11:47373326 | C | T | 3 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 |
3 | HG02257.hp2 HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.142+2307G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47373326 | |||||||
| chr11:47373609 | C | T | 1 | a0001c0001t0002g0042 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.142+2024G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47373609 | |||||||
| chr11:47373658 | A | G | 6 | a0001c0001t0001g0043 a0001c0001t0001g0228 a0001c0001t0001g0229 others(3): Show |
7 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+1975T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47373658 | |||||||
| chr11:47373663 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.142+1970T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47373663 | |||||||
| chr11:47373689 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(167): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.142+1944C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47373689 | |||||||
| chr11:47373861 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.142+1772C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47373861 | |||||||
| chr11:47373979 | G | A | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG01069.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.142+1654C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47373979 | |||||||
| chr11:47374038 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.142+1595G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47374038 | |||||||
| chr11:47374082 | G | A | 1 | a0001c0001t0002g0214 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.142+1551C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47374082 | |||||||
| chr11:47374121 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0228 |
3 | HG01069.hp1 HG01071.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.142+1512G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47374121 | |||||||
| chr11:47374642 | G | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0124 a0001c0001t0001g0152 others(1): Show |
5 | HG02109.hp1 HG02572.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+991C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47374642 | |||||||
| chr11:47374748 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0003g0125 a0001c0001t0003g0126 others(3): Show |
8 | HG00323.hp2 HG01070.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+885C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47374748 | |||||||
| chr11:47374813 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.142+820G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47374813 | |||||||
| chr11:47374961 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.142+672G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47374961 | |||||||
| chr11:47375095 | C | A | 1 | a0001c0001t0002g0225 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.142+538G>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47375095 | |||||||
| chr11:47375103 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(81): Show |
138 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.142+530C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47375103 | |||||||
| chr11:47375152 | A | G | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(232): Show |
358 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(355): Show |
intron_variant | MODIFIER | c.142+481T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47375152 | |||||||
| chr11:47375200 | G | A | 3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0259 |
3 | HG01261.hp2 HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.142+433C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47375200 | |||||||
| chr11:47375389 | G | A | 1 | a0001c0001t0002g0042 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.142+244C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47375389 | |||||||
| chr11:47375396 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.142+237G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47375396 | |||||||
| chr11:47375454 | G | A | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | HG02698.hp2 HG02735.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.142+179C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47375454 | |||||||
| chr11:47375625 | G | A | 1 | a0001c0001t0002g0159 | 1 | HG02055.hp1 | splice_region_variant&intron_variant | LOW | c.142+8C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 2/4 | chr11 | 47375625 | |||||||
| chr11:47375802 | G | A | 77 | a0001c0001t0001g0036 a0001c0001t0001g0151 a0001c0001t0001g0152 others(74): Show |
107 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.46-73C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47375802 | |||||||
| chr11:47375993 | A | G | 1 | a0001c0001t0002g0164 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.46-264T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47375993 | |||||||
| chr11:47376065 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.46-336T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47376065 | |||||||
| chr11:47376149 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.46-420G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47376149 | |||||||
| chr11:47376153 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.46-424G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47376153 | |||||||
| chr11:47376163 | C | G | 83 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(80): Show |
112 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.46-434G>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47376163 | |||||||
| chr11:47376281 | C | T | 1 | a0001c0001t0002g0163 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.46-552G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47376281 | |||||||
| chr11:47376481 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0002g0160 |
2 | HG00423.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.46-752G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47376481 | |||||||
| chr11:47376507 | T | A | 1 | a0001c0001t0001g0154 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.46-778A>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47376507 | |||||||
| chr11:47376569 | G | A | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG01069.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.46-840C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47376569 | |||||||
| chr11:47376635 | GTCC | G | 5 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0056 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-909_46-907delGG others(1): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47376635 | |||||||
| chr11:47376643 | T | C | 1 | a0001c0001t0002g0216 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.46-914A>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47376643 | |||||||
| chr11:47376749 | G | C | 1 | a0001c0001t0001g0226 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.46-1020C>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47376749 | |||||||
| chr11:47376968 | AGACAGT | A | 3 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0001c0001t0002g0162 |
3 | HG02818.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.46-1245_46-1240del others(6): Show |
SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47376968 | |||||||
| chr11:47376991 | T | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.46-1262A>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47376991 | |||||||
| chr11:47377053 | G | A | 8 | a0001c0001t0002g0020 a0001c0001t0002g0037 a0001c0001t0002g0157 others(5): Show |
11 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.45+1256C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47377053 | |||||||
| chr11:47377284 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.45+1025T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47377284 | |||||||
| chr11:47377412 | G | A | 74 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0207 others(71): Show |
103 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.45+897C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47377412 | |||||||
| chr11:47377507 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0053 |
3 | HG02723.hp1 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.45+802G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47377507 | |||||||
| chr11:47377589 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.45+720T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47377589 | |||||||
| chr11:47377663 | G | A | 5 | a0001c0001t0002g0010 a0001c0001t0002g0222 a0001c0001t0002g0223 others(2): Show |
8 | HG00733.hp1 HG00735.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+646C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47377663 | |||||||
| chr11:47377672 | T | C | 5 | a0001c0001t0002g0010 a0001c0001t0002g0222 a0001c0001t0002g0223 others(2): Show |
8 | HG00733.hp1 HG00735.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+637A>G | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47377672 | |||||||
| chr11:47377763 | C | G | 1 | a0001c0001t0002g0052 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.45+546G>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47377763 | |||||||
| chr11:47377811 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.45+498C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47377811 | |||||||
| chr11:47377813 | G | T | 1 | a0001c0001t0001g0051 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.45+496C>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47377813 | |||||||
| chr11:47377832 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.45+477C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47377832 | |||||||
| chr11:47378027 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.45+282T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47378027 | |||||||
| chr11:47378051 | G | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0043 others(41): Show |
73 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.45+258C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47378051 | |||||||
| chr11:47378145 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.45+164T>C | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47378145 | |||||||
| chr11:47378225 | G | A | 1 | a0001c0001t0002g0265 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.45+84C>T | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47378225 | |||||||
| chr11:47378299 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.45+10G>A | SPI1 | ENSG00000066336.13 | transcript | ENST00000378538.8 | protein_coding | 1/4 | chr11 | 47378299 |