Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 283316 |
|---|---|
| ensemblid | ENSG00000177675.9 |
| hgncid | 30375 |
| symbol | CD163L1 |
| name | CD163 molecule like 1 |
| refseq_nuc | NM_174941.6 |
| refseq_prot | NP_777601.3 |
| ensembl_nuc | ENST00000313599.8 |
| ensembl_prot | ENSP00000315945.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 7354960 |
| end | 7444153 |
| strand | - |
| ver | v1.2 |
| region | chr12:7354960-7444153 |
| region5000 | chr12:7349960-7449153 |
| regionname0 | CD163L1_chr12_7354960_7444153 |
| regionname5000 | CD163L1_chr12_7349960_7449153 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1453 | 250 | 37 | 56 | 123 | 13 | 20 | 100 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0002 | 0/0 | 1453 | 55 | 22 | 4 | 22 | 0 | 7 | 16 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0003 | 0/0 | 1453 | 21 | 8 | 1 | 9 | 0 | 3 | 7 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0004 | 0/0 | 1453 | 15 | 8 | 0 | 5 | 0 | 2 | 4 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0005 | 0/0 | 1453 | 7 | 6 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0006 | 0/0 | 1453 | 7 | 5 | 2 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0007 | 0/0 | 1455 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0008 | 1/0 | 1453 | 3 | 2 | 0 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0009 | 0/0 | 1453 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0010 | 0/0 | 1453 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0011 | 0/0 | 1453 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0012 | 0/0 | 1453 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0013 | 0/0 | 1453 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0014 | 0/0 | 1453 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0015 | 0/0 | 834 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0016 | 0/0 | 1453 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0017 | 0/0 | 1453 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0018 | 0/0 | 1453 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0019 | 0/0 | 1453 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0020 | 0/0 | 1453 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0021 | 0/0 | 1453 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0022 | 0/0 | 1453 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0023 | 0/0 | 1453 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0024 | 0/0 | 1453 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0025 | 0/0 | 1453 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 4362 | 138 | 19 | 27 | 78 | 3 | 10 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0002 | 0/0 | 4362 | 67 | 0 | 19 | 41 | 2 | 5 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0003 | 0/0 | 4362 | 54 | 21 | 4 | 22 | 0 | 7 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0004 | 0/0 | 4362 | 21 | 4 | 4 | 2 | 6 | 5 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0005 | 0/0 | 4362 | 20 | 7 | 1 | 9 | 0 | 3 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0006 | 0/0 | 4362 | 11 | 4 | 0 | 5 | 0 | 2 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0007 | 0/0 | 4362 | 9 | 4 | 3 | 0 | 2 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0008 | 0/0 | 4362 | 7 | 6 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0009 | 0/0 | 4362 | 6 | 4 | 2 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0010 | 0/0 | 4368 | 5 | 0 | 0 | 5 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0011 | 1/0 | 4362 | 3 | 2 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0012 | 0/0 | 4362 | 3 | 3 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0013 | 0/0 | 4362 | 3 | 3 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0014 | 0/0 | 4362 | 3 | 3 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0015 | 0/0 | 4362 | 2 | 0 | 1 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0016 | 0/0 | 4362 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0017 | 0/0 | 4362 | 2 | 0 | 2 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0018 | 0/0 | 4362 | 2 | 1 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0019 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0020 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0021 | 0/0 | 4362 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0022 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0023 | 0/0 | 4362 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0024 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0025 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0026 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0027 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0028 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0029 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0030 | 0/0 | 4362 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0031 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0032 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0033 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0034 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0035 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0036 | 0/0 | 4362 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0037 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0038 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0039 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0040 | 0/0 | 4362 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0041 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0042 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0043 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| c0044 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 222 | 262 | 55 | 37 | 146 | 6 | 17 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| t0002 | 0/0 | 222 | 94 | 39 | 19 | 21 | 3 | 12 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| t0003 | 0/1 | 222 | 27 | 0 | 10 | 4 | 5 | 7 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| t0004 | 0/0 | 222 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0002 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0234 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 4362 | 138 | 19 | 27 | 78 | 3 | 10 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0002 | 0/0 | 4362 | 67 | 0 | 19 | 41 | 2 | 5 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0004 | 0/0 | 4362 | 21 | 4 | 4 | 2 | 6 | 5 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0007 | 0/0 | 4362 | 9 | 4 | 3 | 0 | 2 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0008 | 0/0 | 4362 | 7 | 6 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0017 | 0/0 | 4362 | 2 | 0 | 2 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0025 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0026 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0027 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0029 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0039 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0041 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0002c0003 | 0/0 | 4362 | 54 | 21 | 4 | 22 | 0 | 7 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0002c0032 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0003c0005 | 0/0 | 4362 | 20 | 7 | 1 | 9 | 0 | 3 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0003c0033 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0004c0006 | 0/0 | 4362 | 11 | 4 | 0 | 5 | 0 | 2 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0004c0012 | 0/0 | 4362 | 3 | 3 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0004c0028 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0005c0013 | 0/0 | 4362 | 3 | 3 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0005c0014 | 0/0 | 4362 | 3 | 3 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0005c0030 | 0/0 | 4362 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0006c0009 | 0/0 | 4362 | 6 | 4 | 2 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0006c0034 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0007c0010 | 0/0 | 4368 | 5 | 0 | 0 | 5 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0008c0011 | 1/0 | 4362 | 3 | 2 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0009c0018 | 0/0 | 4362 | 2 | 1 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0010c0042 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0010c0043 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0011c0015 | 0/0 | 4362 | 2 | 0 | 1 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0012c0016 | 0/0 | 4362 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0013c0044 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0014c0019 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0015c0020 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0016c0021 | 0/0 | 4362 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0017c0022 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0018c0031 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0019c0035 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0020c0023 | 0/0 | 4362 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0021c0038 | 0/0 | 4362 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0022c0024 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0023c0037 | 0/0 | 4362 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0024c0036 | 0/0 | 4362 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0025c0040 | 0/0 | 4362 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4583 | 104 | 12 | 17 | 64 | 2 | 9 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0001t0002 | 0/0 | 4583 | 26 | 7 | 5 | 13 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0001t0003 | 0/1 | 4583 | 7 | 0 | 5 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0001t0004 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0002t0001 | 0/0 | 4583 | 52 | 0 | 13 | 35 | 0 | 4 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0002t0002 | 0/0 | 4583 | 9 | 0 | 3 | 5 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0002t0003 | 0/0 | 4583 | 6 | 0 | 3 | 1 | 2 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0004t0001 | 0/0 | 4583 | 7 | 2 | 0 | 2 | 3 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0004t0002 | 0/0 | 4583 | 11 | 2 | 3 | 0 | 2 | 4 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0004t0003 | 0/0 | 4583 | 3 | 0 | 1 | 0 | 1 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0007t0001 | 0/0 | 4583 | 6 | 4 | 1 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0007t0002 | 0/0 | 4583 | 2 | 0 | 1 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0007t0003 | 0/0 | 4583 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0008t0001 | 0/0 | 4583 | 3 | 3 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0008t0002 | 0/0 | 4583 | 4 | 3 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0017t0002 | 0/0 | 4583 | 2 | 0 | 2 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0025t0002 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0026t0002 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0027t0002 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0029t0001 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0039t0001 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0001c0041t0001 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0002c0003t0001 | 0/0 | 4583 | 33 | 10 | 2 | 21 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0002c0003t0002 | 0/0 | 4583 | 18 | 11 | 2 | 1 | 0 | 4 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0002c0003t0003 | 0/0 | 4583 | 3 | 0 | 0 | 0 | 0 | 3 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0002c0032t0001 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0003c0005t0001 | 0/0 | 4583 | 14 | 4 | 1 | 7 | 0 | 2 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0003c0005t0002 | 0/0 | 4583 | 4 | 3 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0003c0005t0003 | 0/0 | 4583 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0003c0033t0002 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0004c0006t0001 | 0/0 | 4583 | 8 | 2 | 0 | 5 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0004c0006t0002 | 0/0 | 4583 | 2 | 2 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0004c0006t0003 | 0/0 | 4583 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0004c0012t0001 | 0/0 | 4583 | 2 | 2 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0004c0012t0002 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0004c0028t0001 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0005c0013t0001 | 0/0 | 4583 | 2 | 2 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0005c0013t0002 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0005c0014t0001 | 0/0 | 4583 | 2 | 2 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0005c0014t0002 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0005c0030t0003 | 0/0 | 4583 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0006c0009t0001 | 0/0 | 4583 | 3 | 3 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0006c0009t0002 | 0/0 | 4583 | 3 | 1 | 2 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0006c0034t0001 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0007c0010t0001 | 0/0 | 4589 | 4 | 0 | 0 | 4 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0007c0010t0003 | 0/0 | 4589 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0008c0011t0001 | 1/0 | 4583 | 2 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0008c0011t0002 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0009c0018t0001 | 0/0 | 4583 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0009c0018t0002 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0010c0042t0002 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0010c0043t0001 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0011c0015t0001 | 0/0 | 4583 | 2 | 0 | 1 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0012c0016t0001 | 0/0 | 4583 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0013c0044t0002 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0014c0019t0001 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0015c0020t0001 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0016c0021t0003 | 0/0 | 4583 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0017c0022t0001 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0018c0031t0001 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0019c0035t0002 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0020c0023t0003 | 0/0 | 4583 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0021c0038t0001 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0022c0024t0001 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0023c0037t0001 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0024c0036t0002 | 0/0 | 4583 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| a0025c0040t0001 | 0/0 | 4583 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | copy fasta | chr12 | 7349960 | 7449153 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0003g0234 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0002t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0004t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0004t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0004t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0004t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0004t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0004t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0004t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0004t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0004t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0004t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0004t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0004t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0004t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0004t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0004t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0004t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0004t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0004t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0004t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0004t0003g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0007t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0007t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0007t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0007t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0007t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0007t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0007t0002g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0007t0003g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0008t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0008t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0008t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0008t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0008t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0008t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0017t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0025t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0026t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0027t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0029t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0039t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0001c0041t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0002c0032t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0003c0005t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0003c0005t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0003c0005t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0003c0005t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0003c0005t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0003c0005t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0003c0005t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0003c0005t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0003c0005t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0003c0005t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0003c0005t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0003c0005t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0003c0005t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0003c0005t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0003c0005t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0003c0005t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0003c0005t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0003c0005t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0003c0005t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0003c0033t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0004c0006t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0004c0006t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0004c0006t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0004c0006t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0004c0006t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0004c0006t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0004c0006t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0004c0006t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0004c0006t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0004c0006t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0004c0006t0003g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0004c0012t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0004c0012t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0004c0012t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0004c0028t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0005c0013t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0005c0013t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0005c0013t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0005c0014t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0005c0014t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0005c0014t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0005c0030t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0006c0009t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0006c0009t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0006c0009t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0006c0009t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0006c0009t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0006c0034t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0007c0010t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0007c0010t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0007c0010t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0007c0010t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0008c0011t0001g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0008c0011t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0008c0011t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0009c0018t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0009c0018t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0010c0042t0002g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0010c0043t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0011c0015t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0011c0015t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0012c0016t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0012c0016t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0013c0044t0002g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0014c0019t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0015c0020t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0016c0021t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0017c0022t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0018c0031t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0019c0035t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0020c0023t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0021c0038t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0022c0024t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0023c0037t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0024c0036t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| a0025c0040t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0001 | g0323 | EUR | GBR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00099 | hp2 | a0001 | c0002 | t0003 | g0297 | EUR | GBR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00140 | hp1 | a0005 | c0030 | t0003 | g0309 | EUR | GBR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | GBR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00408 | hp1 | a0002 | c0003 | t0001 | g0094 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00423 | hp1 | a0003 | c0005 | t0001 | g0044 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00423 | hp2 | a0001 | c0002 | t0003 | g0284 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00544 | hp1 | a0022 | c0024 | t0001 | g0296 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0302 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00639 | hp2 | a0001 | c0007 | t0001 | g0339 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00673 | hp1 | a0002 | c0003 | t0001 | g0054 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00673 | hp2 | a0023 | c0037 | t0001 | g0346 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0287 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00738 | hp1 | a0002 | c0003 | t0002 | g0084 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG00738 | hp2 | a0001 | c0004 | t0002 | g0308 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01069 | hp2 | a0002 | c0003 | t0001 | g0029 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0292 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01074 | hp1 | a0001 | c0004 | t0002 | g0318 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01099 | hp1 | a0003 | c0005 | t0001 | g0006 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0328 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01106 | hp1 | a0001 | c0002 | t0003 | g0289 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01109 | hp2 | a0001 | c0004 | t0002 | g0330 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01167 | hp1 | a0006 | c0009 | t0002 | g0010 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0256 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01168 | hp1 | a0001 | c0017 | t0002 | g0015 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0095 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01169 | hp1 | a0006 | c0009 | t0002 | g0010 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01169 | hp2 | a0001 | c0017 | t0002 | g0015 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01175 | hp1 | a0001 | c0008 | t0002 | g0236 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01175 | hp2 | a0001 | c0004 | t0003 | g0320 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0281 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01243 | hp1 | a0025 | c0040 | t0001 | g0069 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0278 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01256 | hp1 | a0001 | c0002 | t0003 | g0286 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01256 | hp2 | a0001 | c0007 | t0002 | g0013 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01261 | hp1 | a0009 | c0018 | t0001 | g0355 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0254 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01515 | hp1 | a0001 | c0007 | t0002 | g0013 | EUR | IBS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01515 | hp2 | a0001 | c0004 | t0001 | g0322 | EUR | IBS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01516 | hp1 | a0001 | c0004 | t0001 | g0311 | EUR | IBS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0242 | EUR | IBS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01517 | hp1 | a0001 | c0004 | t0002 | g0310 | EUR | IBS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01517 | hp2 | a0001 | c0007 | t0001 | g0152 | EUR | IBS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01884 | hp1 | a0004 | c0006 | t0002 | g0333 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01884 | hp2 | a0002 | c0003 | t0002 | g0075 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01891 | hp1 | a0008 | c0011 | t0001 | g0122 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01891 | hp2 | a0003 | c0033 | t0002 | g0123 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0300 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01943 | hp1 | a0002 | c0003 | t0001 | g0030 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0276 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0275 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0273 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0290 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02015 | hp2 | a0001 | c0004 | t0001 | g0316 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02027 | hp1 | a0001 | c0025 | t0002 | g0307 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02055 | hp2 | a0002 | c0003 | t0001 | g0079 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02056 | hp2 | a0002 | c0003 | t0001 | g0093 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02074 | hp2 | a0002 | c0003 | t0001 | g0092 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02083 | hp1 | a0001 | c0041 | t0001 | g0106 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02129 | hp1 | a0003 | c0005 | t0003 | g0058 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02129 | hp2 | a0014 | c0019 | t0001 | g0129 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02132 | hp2 | a0002 | c0003 | t0001 | g0055 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02145 | hp2 | a0010 | c0043 | t0001 | g0353 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0209 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02165 | hp2 | a0002 | c0003 | t0001 | g0043 | EAS | CDX | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02257 | hp1 | a0002 | c0003 | t0002 | g0047 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0315 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02258 | hp1 | a0002 | c0003 | t0002 | g0083 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02258 | hp2 | a0006 | c0009 | t0001 | g0032 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02280 | hp1 | a0013 | c0044 | t0002 | g0357 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02280 | hp2 | a0002 | c0003 | t0002 | g0071 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0291 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02300 | hp2 | a0002 | c0003 | t0002 | g0046 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02451 | hp1 | a0009 | c0018 | t0002 | g0356 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0331 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02572 | hp1 | a0008 | c0011 | t0002 | g0120 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02572 | hp2 | a0005 | c0013 | t0001 | g0244 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02615 | hp1 | a0002 | c0003 | t0002 | g0085 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02615 | hp2 | a0002 | c0003 | t0001 | g0024 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02622 | hp1 | a0002 | c0003 | t0001 | g0082 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02622 | hp2 | a0004 | c0006 | t0002 | g0096 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02630 | hp1 | a0004 | c0012 | t0002 | g0332 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02630 | hp2 | a0001 | c0039 | t0001 | g0201 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02647 | hp1 | a0006 | c0009 | t0002 | g0226 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02647 | hp2 | a0002 | c0003 | t0002 | g0078 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02698 | hp1 | a0011 | c0015 | t0001 | g0267 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02698 | hp2 | a0002 | c0003 | t0002 | g0040 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02717 | hp1 | a0001 | c0007 | t0001 | g0126 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02723 | hp1 | a0001 | c0008 | t0002 | g0225 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02723 | hp2 | a0002 | c0032 | t0001 | g0036 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02735 | hp1 | a0020 | c0023 | t0003 | g0299 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02735 | hp2 | a0001 | c0004 | t0002 | g0314 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0301 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02809 | hp1 | a0015 | c0020 | t0001 | g0313 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02809 | hp2 | a0002 | c0003 | t0002 | g0068 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02818 | hp1 | a0002 | c0003 | t0001 | g0034 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02818 | hp2 | a0001 | c0004 | t0002 | g0115 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02886 | hp1 | a0005 | c0013 | t0001 | g0352 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02886 | hp2 | a0004 | c0006 | t0001 | g0336 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02895 | hp1 | a0003 | c0005 | t0001 | g0025 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0080 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02897 | hp2 | a0002 | c0003 | t0001 | g0074 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02922 | hp1 | a0010 | c0042 | t0002 | g0354 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02922 | hp2 | a0001 | c0008 | t0002 | g0017 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02970 | hp1 | a0004 | c0012 | t0001 | g0335 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03017 | hp2 | a0002 | c0003 | t0003 | g0066 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03041 | hp1 | a0001 | c0008 | t0001 | g0240 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03041 | hp2 | a0002 | c0003 | t0002 | g0081 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03098 | hp2 | a0001 | c0007 | t0001 | g0338 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03130 | hp1 | a0002 | c0003 | t0001 | g0067 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03130 | hp2 | a0005 | c0014 | t0001 | g0109 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03139 | hp2 | a0004 | c0006 | t0001 | g0337 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03195 | hp1 | a0001 | c0007 | t0001 | g0097 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03195 | hp2 | a0001 | c0008 | t0002 | g0017 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03209 | hp1 | a0003 | c0005 | t0001 | g0193 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03209 | hp2 | a0002 | c0003 | t0002 | g0087 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03453 | hp1 | a0001 | c0008 | t0001 | g0206 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03453 | hp2 | a0003 | c0005 | t0001 | g0073 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03486 | hp2 | a0003 | c0005 | t0002 | g0026 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03491 | hp2 | a0001 | c0004 | t0002 | g0020 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0350 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03492 | hp2 | a0001 | c0004 | t0002 | g0020 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03516 | hp1 | a0021 | c0038 | t0001 | g0127 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03516 | hp2 | a0002 | c0003 | t0001 | g0077 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03540 | hp1 | a0002 | c0003 | t0002 | g0035 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03540 | hp2 | a0001 | c0027 | t0002 | g0023 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03579 | hp1 | a0006 | c0009 | t0001 | g0111 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03579 | hp2 | a0001 | c0007 | t0001 | g0342 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03654 | hp2 | a0003 | c0005 | t0002 | g0042 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03669 | hp1 | a0002 | c0003 | t0002 | g0061 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03669 | hp2 | a0004 | c0006 | t0001 | g0341 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03688 | hp1 | a0002 | c0003 | t0003 | g0051 | SAS | STU | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03688 | hp2 | a0001 | c0004 | t0003 | g0321 | SAS | STU | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03704 | hp2 | a0016 | c0021 | t0003 | g0260 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0285 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03831 | hp1 | a0024 | c0036 | t0002 | g0198 | SAS | BEB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | BEB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | BEB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03927 | hp2 | a0001 | c0004 | t0002 | g0319 | SAS | BEB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG04115 | hp1 | a0002 | c0003 | t0002 | g0041 | SAS | STU | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0277 | SAS | STU | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG04184 | hp1 | a0003 | c0005 | t0001 | g0062 | SAS | BEB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG04199 | hp1 | a0004 | c0006 | t0003 | g0340 | SAS | STU | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG04204 | hp1 | a0002 | c0003 | t0002 | g0037 | SAS | STU | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG04228 | hp1 | a0002 | c0003 | t0003 | g0050 | SAS | STU | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG04228 | hp2 | a0003 | c0005 | t0001 | g0006 | SAS | STU | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18522 | hp1 | a0002 | c0003 | t0002 | g0076 | AFR | YRI | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18522 | hp2 | a0004 | c0012 | t0001 | g0334 | AFR | YRI | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18612 | hp2 | a0004 | c0006 | t0001 | g0343 | EAS | CHB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18747 | hp1 | a0007 | c0010 | t0001 | g0014 | EAS | CHB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | CHB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | YRI | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18906 | hp2 | a0003 | c0005 | t0002 | g0086 | AFR | YRI | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18939 | hp2 | a0004 | c0006 | t0001 | g0347 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18941 | hp2 | a0002 | c0003 | t0001 | g0060 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18943 | hp2 | a0002 | c0003 | t0001 | g0091 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18944 | hp1 | a0001 | c0004 | t0001 | g0351 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18946 | hp1 | a0012 | c0016 | t0001 | g0031 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18956 | hp1 | a0003 | c0005 | t0001 | g0326 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18960 | hp2 | a0004 | c0006 | t0001 | g0344 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18962 | hp2 | a0002 | c0003 | t0001 | g0057 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0266 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18967 | hp1 | a0004 | c0006 | t0001 | g0348 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18967 | hp2 | a0002 | c0003 | t0001 | g0022 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18968 | hp1 | a0003 | c0005 | t0001 | g0327 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18970 | hp2 | a0003 | c0005 | t0001 | g0065 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18975 | hp1 | a0018 | c0031 | t0001 | g0053 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18979 | hp1 | a0002 | c0003 | t0001 | g0039 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18979 | hp2 | a0007 | c0010 | t0001 | g0174 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18983 | hp2 | a0002 | c0003 | t0001 | g0090 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18984 | hp2 | a0002 | c0003 | t0001 | g0049 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18991 | hp2 | a0002 | c0003 | t0001 | g0064 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18994 | hp1 | a0012 | c0016 | t0001 | g0056 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18998 | hp1 | a0007 | c0010 | t0003 | g0175 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19003 | hp1 | a0004 | c0006 | t0001 | g0345 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19009 | hp2 | a0003 | c0005 | t0001 | g0028 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19010 | hp2 | a0003 | c0005 | t0001 | g0048 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19011 | hp1 | a0002 | c0003 | t0001 | g0089 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19030 | hp1 | a0005 | c0014 | t0002 | g0110 | AFR | LWK | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | LWK | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19043 | hp1 | a0001 | c0008 | t0001 | g0241 | AFR | LWK | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19043 | hp2 | a0005 | c0014 | t0001 | g0098 | AFR | LWK | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19058 | hp1 | a0017 | c0022 | t0001 | g0261 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19060 | hp1 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0288 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19062 | hp2 | a0002 | c0003 | t0001 | g0038 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19063 | hp2 | a0007 | c0010 | t0001 | g0014 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19064 | hp2 | a0002 | c0003 | t0001 | g0052 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19068 | hp2 | a0002 | c0003 | t0002 | g0059 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19074 | hp1 | a0019 | c0035 | t0002 | g0218 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19078 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19081 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19083 | hp2 | a0007 | c0010 | t0001 | g0176 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19084 | hp1 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19085 | hp2 | a0003 | c0005 | t0003 | g0045 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19087 | hp1 | a0003 | c0005 | t0001 | g0325 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19240 | hp1 | a0001 | c0029 | t0001 | g0117 | AFR | YRI | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA19240 | hp2 | a0001 | c0004 | t0001 | g0116 | AFR | YRI | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA20129 | hp1 | a0001 | c0026 | t0002 | g0102 | AFR | ASW | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ASW | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA20752 | hp1 | a0001 | c0004 | t0002 | g0324 | EUR | TSI | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA20752 | hp2 | a0001 | c0002 | t0003 | g0257 | EUR | TSI | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA20805 | hp1 | a0001 | c0004 | t0003 | g0312 | EUR | TSI | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | TSI | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01123 | hp1 | a0011 | c0015 | t0001 | g0282 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG01123 | hp2 | a0001 | c0007 | t0003 | g0349 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02109 | hp1 | a0004 | c0028 | t0001 | g0121 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02109 | hp2 | a0002 | c0003 | t0001 | g0072 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02486 | hp2 | a0003 | c0005 | t0001 | g0063 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02559 | hp1 | a0001 | c0004 | t0002 | g0317 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG02559 | hp2 | a0006 | c0009 | t0001 | g0033 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03471 | hp1 | a0002 | c0003 | t0001 | g0070 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG06807 | hp1 | a0005 | c0013 | t0002 | g0243 | AFR | USA | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | USA | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | USA | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA20300 | hp2 | a0003 | c0005 | t0002 | g0027 | AFR | USA | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | LWK | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| NA21309 | hp2 | a0006 | c0034 | t0001 | g0118 | AFR | LWK | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0234 | REF | REF | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| homoSapiens_grch38 | hp1 | a0008 | c0011 | t0001 | g0119 | REF | REF | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7355130
|
T | G | 8 | a0001a0002a0003others(5): Show | 27 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(24): Show |
splice_region_variant | LOW | c.*25A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 20/20 | chr12 | 7355130 | ||||||
| chr12:7369536
|
A | C | 1 | a0020 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.3860T>G | p.Leu1287Arg | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 15/20 | 3886/4583 | 3860/4362 | 1287/1453 | chr12 | 7369536 | ||
| chr12:7369561
|
C | T | 1 | a0023 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.3835G>A | p.Glu1279Lys | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 15/20 | 3861/4583 | 3835/4362 | 1279/1453 | chr12 | 7369561 | ||
| chr12:7373488
|
C | T | 1 | a0021 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.3562G>A | p.Glu1188Lys | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/20 | 3588/4583 | 3562/4362 | 1188/1453 | chr12 | 7373488 | ||
| chr12:7373524
|
T | C | 1 | a0014 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.3526A>G | p.Ile1176Val | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/20 | 3552/4583 | 3526/4362 | 1176/1453 | chr12 | 7373524 | ||
| chr12:7374505
|
G | A | 1 | a0022 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.3346C>T | p.Pro1116Ser | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 13/20 | 3372/4583 | 3346/4362 | 1116/1453 | chr12 | 7374505 | ||
| chr12:7374528
|
A | G | 7 | a0003a0004a0006others(4): Show | 49 | HG00423.hp1 HG00673.hp2 HG01099.hp1 others(46): Show |
missense_variant | MODERATE | c.3323T>C | p.Met1108Thr | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 13/20 | 3349/4583 | 3323/4362 | 1108/1453 | chr12 | 7374528 | ||
| chr12:7374688
|
C | T | 1 | a0011 | 2 | HG01123.hp1 HG02698.hp1 |
missense_variant | MODERATE | c.3163G>A | p.Gly1055Ser | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 13/20 | 3189/4583 | 3163/4362 | 1055/1453 | chr12 | 7374688 | ||
| chr12:7375445
|
G | A | 1 | a0012 | 2 | NA18946.hp1 NA18994.hp1 |
missense_variant | MODERATE | c.2837C>T | p.Ala946Val | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 11/20 | 2863/4583 | 2837/4362 | 946/1453 | chr12 | 7375445 | ||
| chr12:7375582
|
G | GACAGAT | 1 | a0007 | 5 | NA18747.hp1 NA18979.hp2 NA18998.hp1 others(2): Show |
disruptive_inframe_insertion | MODERATE | c.2699_2700insATCTGT | p.Val900_Arg901insSe others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 11/20 | 2725/4583 | 2699/4362 | 900/1453 | chr12 | 7375582 | ||
| chr12:7375883
|
C | A | 1 | a0015 | 1 | HG02809.hp1 | stop_gained | HIGH | c.2503G>T | p.Glu835* | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 10/20 | 2529/4583 | 2503/4362 | 835/1453 | chr12 | 7375883 | ||
| chr12:7379176
|
C | G | 1 | a0024 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.2173G>C | p.Glu725Gln | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/20 | 2199/4583 | 2173/4362 | 725/1453 | chr12 | 7379176 | ||
| chr12:7379218
|
C | T | 1 | a0019 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.2131G>A | p.Val711Met | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/20 | 2157/4583 | 2131/4362 | 711/1453 | chr12 | 7379218 | ||
| chr12:7396338
|
G | A | 1 | a0005 | 7 | HG00140.hp1 HG02572.hp2 HG02886.hp1 others(4): Show |
missense_variant | MODERATE | c.1807C>T | p.Arg603Trp | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/20 | 1833/4583 | 1807/4362 | 603/1453 | chr12 | 7396338 | ||
| chr12:7396350
|
A | T | 1 | a0009 | 2 | HG01261.hp1 HG02451.hp1 |
missense_variant | MODERATE | c.1795T>A | p.Tyr599Asn | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/20 | 1821/4583 | 1795/4362 | 599/1453 | chr12 | 7396350 | ||
| chr12:7396400
|
C | G | 7 | a0002a0003a0009others(4): Show | 84 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(81): Show |
missense_variant | MODERATE | c.1745G>C | p.Gly582Ala | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/20 | 1771/4583 | 1745/4362 | 582/1453 | chr12 | 7396400 | ||
| chr12:7396413
|
C | T | 8 | a0002a0003a0006others(5): Show | 91 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(88): Show |
missense_variant&splice_region_variant | MODERATE | c.1732G>A | p.Asp578Asn | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/20 | 1758/4583 | 1732/4362 | 578/1453 | chr12 | 7396413 | ||
| chr12:7398398
|
T | C | 1 | a0025 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.1595A>G | p.Lys532Arg | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/20 | 1621/4583 | 1595/4362 | 532/1453 | chr12 | 7398398 | ||
| chr12:7398426
|
A | T | 24 | a0001a0002a0003others(21): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
missense_variant | MODERATE | c.1567T>A | p.Leu523Met | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/20 | 1593/4583 | 1567/4362 | 523/1453 | chr12 | 7398426 | ||
| chr12:7398482
|
C | T | 1 | a0018 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.1511G>A | p.Arg504Lys | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/20 | 1537/4583 | 1511/4362 | 504/1453 | chr12 | 7398482 | ||
| chr12:7398533
|
C | T | 1 | a0017 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.1460G>A | p.Gly487Glu | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/20 | 1486/4583 | 1460/4362 | 487/1453 | chr12 | 7398533 | ||
| chr12:7403681
|
C | T | 1 | a0016 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.1262G>A | p.Arg421His | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/20 | 1288/4583 | 1262/4362 | 421/1453 | chr12 | 7403681 | ||
| chr12:7433523
|
C | T | 1 | a0015 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.296G>A | p.Arg99His | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/20 | 322/4583 | 296/4362 | 99/1453 | chr12 | 7433523 | ||
| chr12:7433550
|
C | G | 1 | a0014 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.269G>C | p.Gly90Ala | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/20 | 295/4583 | 269/4362 | 90/1453 | chr12 | 7433550 | ||
| chr12:7444117
|
G | A | 3 | a0009a0010a0013 | 5 | HG01261.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
missense_variant | MODERATE | c.11C>T | p.Pro4Leu | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/20 | 37/4583 | 11/4362 | 4/1453 | chr12 | 7444117 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7368175
|
G | A | 13 | a0001c0008a0001c0027a0001c0039others(10): Show | 26 | HG01175.hp1 HG01261.hp1 HG01891.hp2 others(23): Show |
synonymous_variant | LOW | c.4095C>T | p.Ser1365Ser | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 17/20 | 4121/4583 | 4095/4362 | 1365/1453 | chr12 | 7368175 | ||
| chr12:7369556
|
C | T | 3 | a0001c0039a0002c0032a0005c0013 | 5 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(2): Show |
synonymous_variant | LOW | c.3840G>A | p.Ala1280Ala | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 15/20 | 3866/4583 | 3840/4362 | 1280/1453 | chr12 | 7369556 | ||
| chr12:7374713
|
G | A | 3 | a0009c0018a0010c0042a0010c0043 | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
synonymous_variant | LOW | c.3138C>T | p.Ala1046Ala | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 13/20 | 3164/4583 | 3138/4362 | 1046/1453 | chr12 | 7374713 | ||
| chr12:7375396
|
C | T | 1 | a0013c0044 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.2886G>A | p.Val962Val | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 11/20 | 2912/4583 | 2886/4362 | 962/1453 | chr12 | 7375396 | ||
| chr12:7375875
|
G | A | 25 | a0001c0001a0001c0008a0001c0017others(22): Show | 210 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(207): Show |
synonymous_variant | LOW | c.2511C>T | p.Asn837Asn | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 10/20 | 2537/4583 | 2511/4362 | 837/1453 | chr12 | 7375875 | ||
| chr12:7379291
|
C | T | 1 | a0001c0026 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.2058G>A | p.Ser686Ser | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/20 | 2084/4583 | 2058/4362 | 686/1453 | chr12 | 7379291 | ||
| chr12:7398454
|
A | C | 43 | a0001c0001a0001c0002a0001c0004others(40): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
synonymous_variant | LOW | c.1539T>G | p.Val513Val | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/20 | 1565/4583 | 1539/4362 | 513/1453 | chr12 | 7398454 | ||
| chr12:7432651
|
T | C | 29 | a0001c0001a0001c0007a0001c0008others(26): Show | 280 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(277): Show |
synonymous_variant | LOW | c.531A>G | p.Gly177Gly | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/20 | 557/4583 | 531/4362 | 177/1453 | chr12 | 7432651 | ||
| chr12:7433375
|
A | G | 8 | a0001c0002a0001c0025a0011c0015others(5): Show | 75 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
splice_region_variant&synonymous_variant | LOW | c.444T>C | p.Tyr148Tyr | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/20 | 470/4583 | 444/4362 | 148/1453 | chr12 | 7433375 | ||
| chr12:7433381
|
G | A | 1 | a0001c0017 | 2 | HG01168.hp1 HG01169.hp2 |
synonymous_variant | LOW | c.438C>T | p.Asn146Asn | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/20 | 464/4583 | 438/4362 | 146/1453 | chr12 | 7433381 | ||
| chr12:7433510
|
G | A | 1 | a0001c0041 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.309C>T | p.Ala103Ala | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/20 | 335/4583 | 309/4362 | 103/1453 | chr12 | 7433510 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7355059
|
C | T | 1 | a0001c0001t0004 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*96G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 20/20 | 2345 | chr12 | 7355059 | |||||
| chr12:7355061
|
T | C | 23 | a0001c0001t0002a0001c0002t0002a0001c0004t0002others(20): Show | 94 | HG00558.hp1 HG00558.hp2 HG00735.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*94A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 20/20 | 2343 | chr12 | 7355061 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7355238
|
C | A | 6 | a0001c0001t0001g0103a0001c0001t0001g0161a0001c0001t0001g0164others(3): Show | 6 | NA18942.hp1 NA18968.hp2 NA19009.hp1 others(3): Show |
intron_variant | MODIFIER | c.*25-108G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7355238 | ||||||
| chr12:7355282
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG00609.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.*25-152C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7355282 | ||||||
| chr12:7355597
|
G | A | 1 | a0005c0013t0001g0352 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.*25-467C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7355597 | ||||||
| chr12:7355741
|
T | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0229a0006c0009t0001g0033 | 4 | HG02559.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.*25-611A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7355741 | ||||||
| chr12:7356060
|
G | A | 39 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0001g0142others(36): Show | 42 | HG00408.hp1 HG00639.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.*25-930C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7356060 | ||||||
| chr12:7356214
|
G | T | 4 | a0001c0002t0001g0255a0001c0002t0001g0279a0001c0002t0001g0283others(1): Show | 4 | NA18943.hp2 NA18980.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.*25-1084C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7356214 | ||||||
| chr12:7356272
|
A | G | 4 | a0001c0001t0002g0331a0001c0008t0002g0017a0001c0008t0002g0225others(1): Show | 5 | HG02451.hp2 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.*24+1108T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7356272 | ||||||
| chr12:7356462
|
T | C | 1 | a0001c0001t0002g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.*24+918A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7356462 | ||||||
| chr12:7356570
|
G | C | 3 | a0001c0001t0001g0197a0005c0014t0001g0098a0015c0020t0001g0313 | 3 | HG02809.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.*24+810C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7356570 | ||||||
| chr12:7356574
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.*24+806G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7356574 | ||||||
| chr12:7356709
|
G | T | 1 | a0001c0002t0001g0291 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.*24+671C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7356709 | ||||||
| chr12:7356732
|
A | T | 1 | a0004c0012t0002g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.*24+648T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7356732 | ||||||
| chr12:7356841
|
C | T | 46 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(43): Show | 54 | HG00544.hp1 HG00609.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.*24+539G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7356841 | ||||||
| chr12:7356850
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0135 | 3 | NA18951.hp1 NA18981.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.*24+530C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7356850 | ||||||
| chr12:7357267
|
T | G | 4 | a0001c0002t0001g0251a0002c0003t0001g0090a0017c0022t0001g0261others(1): Show | 4 | NA18945.hp2 NA18975.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.*24+113A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7357267 | ||||||
| chr12:7357306
|
A | C | 1 | a0001c0001t0002g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.*24+74T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7357306 | ||||||
| chr12:7357372
|
C | T | 2 | a0001c0004t0002g0310a0001c0007t0002g0013 | 3 | HG01256.hp2 HG01515.hp1 HG01517.hp1 |
splice_region_variant&intron_variant | LOW | c.*24+8G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7357372 | ||||||
| chr12:7357541
|
G | A | 1 | a0021c0038t0001g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4280-55C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7357541 | ||||||
| chr12:7357648
|
T | C | 66 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0001g0142others(63): Show | 69 | HG00408.hp1 HG00639.hp2 HG01074.hp2 others(66): Show |
intron_variant | MODIFIER | c.4280-162A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7357648 | ||||||
| chr12:7357668
|
A | T | 8 | a0001c0001t0001g0101a0001c0001t0001g0125a0001c0007t0001g0097others(5): Show | 8 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.4280-182T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7357668 | ||||||
| chr12:7357927
|
A | G | 88 | a0001c0001t0002g0100a0001c0001t0002g0131a0001c0001t0002g0151others(85): Show | 93 | HG00558.hp1 HG00558.hp2 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.4280-441T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7357927 | ||||||
| chr12:7358122
|
A | C | 1 | a0001c0001t0001g0138 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.4280-636T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7358122 | ||||||
| chr12:7358179
|
A | C | 47 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0001g0142others(44): Show | 50 | HG00408.hp1 HG00639.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.4280-693T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7358179 | ||||||
| chr12:7358405
|
G | A | 3 | a0001c0001t0001g0197a0005c0014t0001g0098a0015c0020t0001g0313 | 3 | HG02809.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4280-919C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7358405 | ||||||
| chr12:7358605
|
A | G | 14 | a0001c0001t0001g0016a0001c0001t0001g0191a0001c0001t0001g0204others(11): Show | 15 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.4280-1119T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7358605 | ||||||
| chr12:7358715
|
T | C | 5 | a0001c0001t0002g0202a0002c0003t0002g0047a0002c0003t0002g0068others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.4280-1229A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7358715 | ||||||
| chr12:7358908
|
A | G | 94 | a0001c0001t0001g0099a0001c0001t0001g0114a0001c0001t0001g0124others(91): Show | 96 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.4280-1422T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7358908 | ||||||
| chr12:7358910
|
T | C | 1 | a0002c0003t0001g0089 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.4280-1424A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7358910 | ||||||
| chr12:7358948
|
G | A | 1 | a0002c0003t0001g0057 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.4280-1462C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7358948 | ||||||
| chr12:7358972
|
C | G | 1 | a0002c0003t0001g0034 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4280-1486G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7358972 | ||||||
| chr12:7359151
|
A | G | 1 | a0001c0002t0002g0256 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.4280-1665T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7359151 | ||||||
| chr12:7359430
|
A | C | 341 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(338): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.4280-1944T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7359430 | ||||||
| chr12:7359448
|
G | T | 353 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(350): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.4280-1962C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7359448 | ||||||
| chr12:7359477
|
A | G | 2 | a0001c0001t0002g0167a0001c0001t0002g0173 | 2 | NA18982.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.4280-1991T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7359477 | ||||||
| chr12:7359935
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4280-2449A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7359935 | ||||||
| chr12:7359998
|
T | G | 4 | a0001c0001t0002g0232a0004c0006t0002g0333a0006c0009t0002g0226others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.4280-2512A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7359998 | ||||||
| chr12:7360383
|
T | C | 8 | a0001c0001t0001g0101a0001c0001t0001g0125a0001c0007t0001g0097others(5): Show | 8 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.4280-2897A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7360383 | ||||||
| chr12:7360671
|
A | G | 1 | a0003c0005t0001g0326 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.4280-3185T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7360671 | ||||||
| chr12:7360687
|
G | A | 11 | a0001c0002t0001g0285a0001c0002t0001g0287a0001c0004t0001g0315others(8): Show | 11 | HG00099.hp1 HG00733.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.4280-3201C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7360687 | ||||||
| chr12:7360859
|
G | T | 1 | a0005c0013t0002g0243 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4280-3373C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7360859 | ||||||
| chr12:7360945
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0130a0001c0001t0001g0135others(1): Show | 5 | NA18951.hp1 NA18981.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.4280-3459C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7360945 | ||||||
| chr12:7360953
|
TTTTGGTT others(4): Show |
T | 55 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(52): Show | 65 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.4280-3478_4280-346 others(15): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7360953 | ||||||
| chr12:7360964
|
C | CTTTGT | 89 | a0001c0001t0001g0099a0001c0001t0001g0114a0001c0001t0001g0124others(86): Show | 91 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.4280-3483_4280-347 others(9): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7360964 | ||||||
| chr12:7360964
|
C | CTTTGTTT others(3): Show |
1 | a0003c0005t0001g0044 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.4280-3488_4280-347 others(14): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7360964 | ||||||
| chr12:7361197
|
T | C | 89 | a0001c0001t0002g0100a0001c0001t0002g0131a0001c0001t0002g0151others(86): Show | 94 | HG00558.hp1 HG00558.hp2 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.4280-3711A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361197 | ||||||
| chr12:7361321
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4280-3835A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361321 | ||||||
| chr12:7361497
|
TC | T | 3 | a0001c0001t0002g0100a0001c0001t0002g0186a0003c0005t0002g0026 | 3 | HG03471.hp2 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4280-4012delG | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361497 | ||||||
| chr12:7361544
|
T | C | 89 | a0001c0001t0002g0100a0001c0001t0002g0131a0001c0001t0002g0151others(86): Show | 94 | HG00558.hp1 HG00558.hp2 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.4280-4058A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361544 | ||||||
| chr12:7361546
|
T | C | 12 | a0001c0001t0001g0101a0001c0001t0001g0125a0001c0001t0001g0215others(9): Show | 12 | HG01168.hp2 HG01243.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.4280-4060A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361546 | ||||||
| chr12:7361608
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0183 | 2 | NA18961.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.4280-4122G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361608 | ||||||
| chr12:7361616
|
C | T | 12 | a0001c0001t0001g0191a0001c0001t0001g0204a0001c0001t0001g0205others(9): Show | 12 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.4280-4130G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361616 | ||||||
| chr12:7361636
|
C | T | 39 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0001g0142others(36): Show | 42 | HG00408.hp1 HG00639.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.4280-4150G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361636 | ||||||
| chr12:7361720
|
T | C | 6 | a0001c0001t0001g0134a0001c0002t0001g0265a0002c0003t0001g0005others(3): Show | 7 | NA18946.hp1 NA18970.hp2 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.4280-4234A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361720 | ||||||
| chr12:7361837
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.4280-4351C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361837 | ||||||
| chr12:7361910
|
C | T | 4 | a0001c0001t0002g0232a0004c0006t0002g0333a0006c0009t0002g0226others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.4280-4424G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361910 | ||||||
| chr12:7362217
|
AT | A | 85 | a0001c0001t0002g0100a0001c0001t0002g0131a0001c0001t0002g0151others(82): Show | 90 | HG00558.hp1 HG00558.hp2 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.4280-4732delA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362217 | ||||||
| chr12:7362256
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(104): Show | 121 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.4280-4770C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362256 | ||||||
| chr12:7362294
|
T | C | 1 | a0002c0003t0001g0077 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4280-4808A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362294 | ||||||
| chr12:7362346
|
T | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(104): Show | 121 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.4280-4860A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362346 | ||||||
| chr12:7362440
|
A | G | 3 | a0004c0006t0001g0336a0004c0006t0001g0337a0004c0028t0001g0121 | 3 | HG02109.hp1 HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.4279+4796T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362440 | ||||||
| chr12:7362526
|
A | G | 1 | a0004c0006t0001g0343 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.4279+4710T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362526 | ||||||
| chr12:7362617
|
A | G | 55 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(52): Show | 65 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.4279+4619T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362617 | ||||||
| chr12:7362669
|
A | G | 3 | a0001c0001t0001g0215a0001c0002t0001g0021a0001c0002t0001g0274 | 3 | HG06807.hp2 NA19005.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.4279+4567T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362669 | ||||||
| chr12:7362705
|
T | C | 40 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0001g0142others(37): Show | 43 | HG00408.hp1 HG00639.hp2 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.4279+4531A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362705 | ||||||
| chr12:7362807
|
T | C | 16 | a0001c0001t0002g0202a0001c0026t0002g0102a0002c0003t0002g0035others(13): Show | 17 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.4279+4429A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362807 | ||||||
| chr12:7362974
|
T | A | 1 | a0006c0009t0001g0033 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4279+4262A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362974 | ||||||
| chr12:7362975
|
A | T | 2 | a0001c0004t0001g0116a0002c0003t0001g0067 | 2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4279+4261T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362975 | ||||||
| chr12:7363030
|
C | G | 1 | a0001c0001t0002g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4279+4206G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7363030 | ||||||
| chr12:7363043
|
G | A | 3 | a0002c0003t0002g0037a0002c0003t0002g0040a0002c0003t0002g0041 | 3 | HG02698.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.4279+4193C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7363043 | ||||||
| chr12:7363347
|
G | A | 1 | a0001c0004t0001g0315 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4279+3889C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7363347 | ||||||
| chr12:7363418
|
A | AAATAAT | 41 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0001g0142others(38): Show | 44 | HG00408.hp1 HG00639.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.4279+3812_4279+381 others(10): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7363418 | ||||||
| chr12:7363701
|
T | C | 1 | a0001c0002t0001g0294 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.4279+3535A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7363701 | ||||||
| chr12:7363718
|
C | T | 8 | a0001c0001t0001g0101a0001c0001t0001g0125a0001c0007t0001g0097others(5): Show | 8 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.4279+3518G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7363718 | ||||||
| chr12:7363790
|
G | GA | 341 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(338): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.4279+3445dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7363790 | ||||||
| chr12:7364109
|
C | T | 37 | a0001c0001t0001g0001a0001c0001t0001g0088a0001c0001t0001g0103others(34): Show | 43 | HG00099.hp1 HG00733.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.4279+3127G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7364109 | ||||||
| chr12:7364240
|
G | A | 1 | a0001c0017t0002g0015 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.4279+2996C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7364240 | ||||||
| chr12:7364294
|
T | C | 1 | a0001c0002t0001g0302 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4279+2942A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7364294 | ||||||
| chr12:7364446
|
A | G | 2 | a0012c0016t0001g0031a0012c0016t0001g0056 | 2 | NA18946.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.4279+2790T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7364446 | ||||||
| chr12:7364547
|
C | T | 3 | a0001c0001t0003g0209a0001c0002t0003g0278a0001c0004t0003g0321 | 3 | HG01243.hp2 HG02148.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.4279+2689G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7364547 | ||||||
| chr12:7364832
|
A | G | 1 | a0001c0002t0001g0292 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.4279+2404T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7364832 | ||||||
| chr12:7364863
|
C | T | 1 | a0003c0005t0003g0058 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4279+2373G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7364863 | ||||||
| chr12:7365011
|
C | G | 1 | a0002c0003t0001g0039 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4279+2225G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7365011 | ||||||
| chr12:7365182
|
C | T | 3 | a0001c0001t0001g0197a0005c0014t0001g0098a0015c0020t0001g0313 | 3 | HG02809.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4279+2054G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7365182 | ||||||
| chr12:7365294
|
A | G | 14 | a0001c0001t0001g0016a0001c0001t0001g0191a0001c0001t0001g0204others(11): Show | 15 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.4279+1942T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7365294 | ||||||
| chr12:7365346
|
T | C | 1 | a0021c0038t0001g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4279+1890A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7365346 | ||||||
| chr12:7365732
|
A | G | 1 | a0005c0013t0001g0352 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4279+1504T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7365732 | ||||||
| chr12:7365742
|
T | C | 2 | a0004c0006t0001g0337a0004c0028t0001g0121 | 2 | HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4279+1494A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7365742 | ||||||
| chr12:7365787
|
G | C | 107 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0001g0142others(104): Show | 115 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.4279+1449C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7365787 | ||||||
| chr12:7365794
|
C | T | 1 | a0002c0003t0002g0071 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4279+1442G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7365794 | ||||||
| chr12:7365826
|
G | T | 106 | a0001c0001t0001g0138a0001c0001t0001g0141a0001c0001t0001g0142others(103): Show | 114 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.4279+1410C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7365826 | ||||||
| chr12:7365909
|
G | A | 2 | a0001c0001t0001g0185a0001c0002t0001g0268 | 2 | NA18942.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.4279+1327C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7365909 | ||||||
| chr12:7366161
|
T | C | 11 | a0002c0003t0001g0024a0002c0003t0001g0082a0002c0003t0002g0047others(8): Show | 12 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.4279+1075A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7366161 | ||||||
| chr12:7366179
|
T | G | 10 | a0001c0001t0001g0099a0001c0001t0001g0197a0001c0001t0002g0331others(7): Show | 10 | HG01884.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.4279+1057A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7366179 | ||||||
| chr12:7366293
|
A | G | 3 | a0002c0003t0001g0072a0002c0003t0001g0074a0002c0003t0001g0080 | 3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4279+943T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7366293 | ||||||
| chr12:7366421
|
A | G | 1 | a0001c0001t0001g0002 | 3 | HG03017.hp1 HG03491.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.4279+815T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7366421 | ||||||
| chr12:7366537
|
T | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 171 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.4279+699A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7366537 | ||||||
| chr12:7366724
|
T | C | 1 | a0006c0034t0001g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4279+512A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7366724 | ||||||
| chr12:7366889
|
T | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.4279+347A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7366889 | ||||||
| chr12:7366918
|
G | A | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0183 | 3 | NA18961.hp2 NA18981.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.4279+318C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7366918 | ||||||
| chr12:7367117
|
G | A | 1 | a0001c0002t0001g0095 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.4279+119C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7367117 | ||||||
| chr12:7367177
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | NA19003.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.4279+59G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7367177 | ||||||
| chr12:7367230
|
A | G | 38 | a0001c0001t0001g0088a0001c0001t0001g0108a0001c0001t0001g0112others(35): Show | 39 | HG00558.hp2 HG00609.hp2 HG00735.hp2 others(36): Show |
splice_region_variant&intron_variant | LOW | c.4279+6T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7367230 | ||||||
| chr12:7367528
|
C | G | 15 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0130others(12): Show | 17 | HG00544.hp2 HG02040.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.4184-197G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 17/19 | chr12 | 7367528 | ||||||
| chr12:7368039
|
T | G | 1 | a0001c0002t0002g0290 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4183+48A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 17/19 | chr12 | 7368039 | ||||||
| chr12:7368435
|
G | A | 25 | a0001c0008t0001g0206a0001c0008t0001g0240a0001c0008t0001g0241others(22): Show | 26 | HG01175.hp1 HG01261.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.4073-238C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 16/19 | chr12 | 7368435 | ||||||
| chr12:7368529
|
C | CT | 33 | a0001c0001t0001g0199a0001c0001t0002g0100a0001c0001t0002g0186others(30): Show | 35 | HG00558.hp2 HG00673.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.4073-333dupA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 16/19 | chr12 | 7368529 | ||||||
| chr12:7368529
|
C | CTT | 28 | a0001c0001t0001g0088a0001c0001t0001g0108a0001c0001t0001g0112others(25): Show | 28 | HG00609.hp2 HG00735.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.4073-334_4073-333d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 16/19 | chr12 | 7368529 | ||||||
| chr12:7368584
|
T | C | 1 | a0001c0002t0001g0306 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.4072+349A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 16/19 | chr12 | 7368584 | ||||||
| chr12:7368703
|
AG | A | 5 | a0001c0004t0002g0115a0002c0003t0001g0074a0002c0003t0001g0080others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.4072+229delC | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 16/19 | chr12 | 7368703 | ||||||
| chr12:7368708
|
A | T | 5 | a0001c0004t0002g0115a0002c0003t0001g0074a0002c0003t0001g0080others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.4072+225T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 16/19 | chr12 | 7368708 | ||||||
| chr12:7368908
|
A | G | 2 | a0008c0011t0001g0122a0008c0011t0002g0120 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.4072+25T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 16/19 | chr12 | 7368908 | ||||||
| chr12:7368967
|
T | TGA | 7 | a0001c0001t0001g0099a0001c0001t0001g0180a0001c0004t0001g0116others(4): Show | 7 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.4040-4_4040-3dupTC | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 15/19 | chr12 | 7368967 | ||||||
| chr12:7368967
|
T | TGAGA | 6 | a0001c0007t0001g0126a0001c0008t0001g0240a0001c0008t0002g0236others(3): Show | 6 | HG01175.hp1 HG01261.hp1 HG02451.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.4040-6_4040-3dupTC others(2): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 15/19 | chr12 | 7368967 | ||||||
| chr12:7368979
|
A | G | 1 | a0005c0030t0003g0309 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4040-14T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 15/19 | chr12 | 7368979 | ||||||
| chr12:7369277
|
A | G | 1 | a0002c0003t0001g0054 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4039+80T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 15/19 | chr12 | 7369277 | ||||||
| chr12:7369280
|
C | A | 2 | a0001c0001t0002g0331a0002c0003t0001g0024 | 2 | HG02451.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.4039+77G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 15/19 | chr12 | 7369280 | ||||||
| chr12:7369752
|
G | A | 4 | a0001c0004t0002g0115a0002c0003t0001g0074a0002c0003t0001g0080others(1): Show | 4 | HG02647.hp1 HG02818.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.3731-87C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7369752 | ||||||
| chr12:7370072
|
T | C | 1 | a0001c0004t0001g0316 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3731-407A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370072 | ||||||
| chr12:7370179
|
A | G | 5 | a0001c0039t0001g0201a0002c0032t0001g0036a0005c0013t0001g0244others(2): Show | 5 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.3731-514T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370179 | ||||||
| chr12:7370367
|
T | A | 3 | a0002c0003t0001g0024a0008c0011t0001g0122a0008c0011t0002g0120 | 3 | HG01891.hp1 HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3731-702A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370367 | ||||||
| chr12:7370393
|
T | C | 2 | a0009c0018t0001g0355a0009c0018t0002g0356 | 2 | HG01261.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3731-728A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370393 | ||||||
| chr12:7370413
|
T | C | 2 | a0003c0005t0001g0193a0003c0005t0002g0086 | 2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3731-748A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370413 | ||||||
| chr12:7370602
|
G | A | 2 | a0003c0005t0001g0048a0003c0005t0001g0065 | 2 | NA18970.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.3731-937C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370602 | ||||||
| chr12:7370636
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3731-971T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370636 | ||||||
| chr12:7370757
|
C | T | 17 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0130others(14): Show | 19 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.3731-1092G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370757 | ||||||
| chr12:7370866
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3731-1201C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370866 | ||||||
| chr12:7370905
|
G | C | 1 | a0002c0003t0001g0024 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3731-1240C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370905 | ||||||
| chr12:7370956
|
G | T | 4 | a0006c0009t0001g0111a0006c0009t0002g0010a0006c0009t0002g0226others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3731-1291C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370956 | ||||||
| chr12:7371026
|
A | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(51): Show | 63 | HG00558.hp1 HG00735.hp1 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.3731-1361T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7371026 | ||||||
| chr12:7371103
|
C | T | 152 | a0001c0002t0001g0004a0001c0002t0001g0008a0001c0002t0001g0009others(149): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.3731-1438G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7371103 | ||||||
| chr12:7371447
|
A | G | 3 | a0002c0003t0001g0024a0008c0011t0001g0122a0008c0011t0002g0120 | 3 | HG01891.hp1 HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3731-1782T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7371447 | ||||||
| chr12:7371614
|
T | C | 1 | a0008c0011t0001g0122 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3730+1706A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7371614 | ||||||
| chr12:7371775
|
A | C | 2 | a0001c0004t0001g0116a0001c0027t0002g0023 | 2 | HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3730+1545T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7371775 | ||||||
| chr12:7371835
|
G | C | 32 | a0001c0001t0002g0331a0002c0003t0001g0034a0002c0003t0002g0035others(29): Show | 33 | HG00423.hp1 HG01099.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.3730+1485C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7371835 | ||||||
| chr12:7371882
|
T | G | 1 | a0004c0006t0001g0348 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3730+1438A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7371882 | ||||||
| chr12:7371895
|
T | C | 1 | a0003c0005t0001g0062 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3730+1425A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7371895 | ||||||
| chr12:7371898
|
A | T | 17 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0130others(14): Show | 19 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.3730+1422T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7371898 | ||||||
| chr12:7371976
|
T | C | 2 | a0010c0042t0002g0354a0010c0043t0001g0353 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3730+1344A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7371976 | ||||||
| chr12:7372055
|
AAAG | A | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.3730+1262_3730+126 others(7): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7372055 | ||||||
| chr12:7372079
|
T | C | 5 | a0002c0032t0001g0036a0005c0013t0001g0244a0005c0013t0001g0352others(2): Show | 5 | HG02572.hp2 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.3730+1241A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7372079 | ||||||
| chr12:7372130
|
C | A | 1 | a0001c0002t0003g0297 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3730+1190G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7372130 | ||||||
| chr12:7372308
|
T | C | 1 | a0001c0002t0001g0265 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3730+1012A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7372308 | ||||||
| chr12:7372314
|
C | G | 343 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(340): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.3730+1006G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7372314 | ||||||
| chr12:7372809
|
T | C | 3 | a0003c0005t0001g0025a0003c0005t0001g0073a0025c0040t0001g0069 | 3 | HG01243.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3730+511A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7372809 | ||||||
| chr12:7372958
|
T | A | 1 | a0001c0004t0002g0330 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3730+362A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7372958 | ||||||
| chr12:7373199
|
C | T | 277 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0088others(274): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.3730+121G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7373199 | ||||||
| chr12:7373209
|
T | C | 1 | a0001c0007t0001g0126 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3730+111A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7373209 | ||||||
| chr12:7373269
|
G | C | 178 | a0001c0002t0001g0004a0001c0002t0001g0008a0001c0002t0001g0009others(175): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.3730+51C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7373269 | ||||||
| chr12:7373711
|
A | AT | 65 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0088others(62): Show | 69 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.3410-72dupA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 13/19 | chr12 | 7373711 | ||||||
| chr12:7373903
|
C | G | 1 | a0019c0035t0002g0218 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3410-263G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 13/19 | chr12 | 7373903 | ||||||
| chr12:7374043
|
C | A | 2 | a0010c0042t0002g0354a0010c0043t0001g0353 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3409+399G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 13/19 | chr12 | 7374043 | ||||||
| chr12:7374142
|
C | T | 1 | a0008c0011t0001g0122 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3409+300G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 13/19 | chr12 | 7374142 | ||||||
| chr12:7374263
|
C | G | 1 | a0001c0001t0001g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3409+179G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 13/19 | chr12 | 7374263 | ||||||
| chr12:7374404
|
G | A | 1 | a0001c0007t0001g0126 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3409+38C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 13/19 | chr12 | 7374404 | ||||||
| chr12:7374794
|
T | C | 18 | a0003c0005t0001g0006a0003c0005t0001g0025a0003c0005t0001g0028others(15): Show | 19 | HG00423.hp1 HG01099.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.3094+37A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 12/19 | chr12 | 7374794 | ||||||
| chr12:7374987
|
T | C | 2 | a0001c0001t0001g0179a0001c0001t0001g0183 | 2 | NA18961.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.3002-64A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 11/19 | chr12 | 7374987 | ||||||
| chr12:7375064
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3002-141A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 11/19 | chr12 | 7375064 | ||||||
| chr12:7375255
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3001+26C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 11/19 | chr12 | 7375255 | ||||||
| chr12:7376313
|
C | T | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2372-299G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7376313 | ||||||
| chr12:7376330
|
A | G | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2372-316T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7376330 | ||||||
| chr12:7376467
|
G | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 210 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(207): Show |
intron_variant | MODIFIER | c.2372-453C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7376467 | ||||||
| chr12:7376577
|
A | G | 5 | a0004c0006t0002g0096a0004c0006t0002g0333a0004c0012t0001g0334others(2): Show | 5 | HG01884.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2372-563T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7376577 | ||||||
| chr12:7376960
|
A | G | 23 | a0003c0005t0001g0006a0003c0005t0001g0025a0003c0005t0001g0028others(20): Show | 24 | HG00423.hp1 HG01099.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.2372-946T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7376960 | ||||||
| chr12:7377088
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 210 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(207): Show |
intron_variant | MODIFIER | c.2372-1074G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377088 | ||||||
| chr12:7377104
|
T | C | 19 | a0003c0005t0001g0193a0003c0005t0002g0086a0004c0006t0001g0336others(16): Show | 19 | HG00673.hp2 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2372-1090A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377104 | ||||||
| chr12:7377126
|
A | G | 1 | a0024c0036t0002g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2372-1112T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377126 | ||||||
| chr12:7377291
|
T | C | 149 | a0001c0002t0001g0004a0001c0002t0001g0008a0001c0002t0001g0009others(146): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.2372-1277A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377291 | ||||||
| chr12:7377295
|
T | A | 1 | a0001c0001t0001g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2372-1281A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377295 | ||||||
| chr12:7377326
|
C | T | 16 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0130others(13): Show | 18 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.2372-1312G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377326 | ||||||
| chr12:7377355
|
C | T | 1 | a0013c0044t0002g0357 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2372-1341G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377355 | ||||||
| chr12:7377487
|
C | T | 2 | a0001c0002t0001g0285a0001c0002t0003g0286 | 2 | HG01256.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2372-1473G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377487 | ||||||
| chr12:7377730
|
C | A | 1 | a0001c0008t0002g0236 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2371+1248G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377730 | ||||||
| chr12:7377749
|
C | T | 1 | a0001c0002t0001g0252 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2371+1229G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377749 | ||||||
| chr12:7377764
|
C | T | 2 | a0006c0009t0001g0032a0006c0009t0001g0033 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2371+1214G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377764 | ||||||
| chr12:7377912
|
G | A | 47 | a0003c0005t0001g0006a0003c0005t0001g0025a0003c0005t0001g0028others(44): Show | 49 | HG00423.hp1 HG00673.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.2371+1066C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377912 | ||||||
| chr12:7377940
|
T | C | 3 | a0001c0004t0001g0116a0001c0004t0002g0115a0001c0027t0002g0023 | 3 | HG02818.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2371+1038A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377940 | ||||||
| chr12:7378041
|
C | T | 1 | a0003c0005t0001g0063 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2371+937G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378041 | ||||||
| chr12:7378155
|
T | A | 1 | a0001c0002t0001g0272 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2371+823A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378155 | ||||||
| chr12:7378225
|
CT | C | 3 | a0004c0006t0002g0333a0004c0012t0001g0334a0004c0012t0001g0335 | 3 | HG01884.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2371+752delA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378225 | ||||||
| chr12:7378266
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2371+712C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378266 | ||||||
| chr12:7378268
|
A | G | 18 | a0003c0005t0001g0006a0003c0005t0001g0025a0003c0005t0001g0028others(15): Show | 19 | HG00423.hp1 HG01099.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.2371+710T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378268 | ||||||
| chr12:7378302
|
G | A | 1 | a0001c0002t0001g0274 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2371+676C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378302 | ||||||
| chr12:7378369
|
C | T | 4 | a0001c0004t0001g0116a0001c0004t0002g0115a0001c0007t0001g0126others(1): Show | 4 | HG02717.hp1 HG02818.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2371+609G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378369 | ||||||
| chr12:7378396
|
A | G | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0133others(6): Show | 11 | HG00544.hp2 HG02056.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.2371+582T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378396 | ||||||
| chr12:7378407
|
A | C | 1 | a0001c0004t0002g0330 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2371+571T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378407 | ||||||
| chr12:7378422
|
T | C | 16 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0130others(13): Show | 18 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.2371+556A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378422 | ||||||
| chr12:7378612
|
TA | T | 6 | a0006c0009t0001g0032a0006c0009t0001g0033a0006c0009t0001g0111others(3): Show | 7 | HG01167.hp1 HG01169.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2371+365delT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378612 | ||||||
| chr12:7379313
|
C | T | 1 | a0001c0001t0002g0227 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2051-15G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7379313 | ||||||
| chr12:7379373
|
C | T | 1 | a0003c0005t0001g0063 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2051-75G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7379373 | ||||||
| chr12:7379420
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2051-122C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7379420 | ||||||
| chr12:7379736
|
G | C | 1 | a0001c0001t0001g0157 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2051-438C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7379736 | ||||||
| chr12:7379803
|
A | G | 1 | a0021c0038t0001g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2051-505T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7379803 | ||||||
| chr12:7379867
|
G | GT | 5 | a0001c0001t0001g0207a0001c0001t0002g0248a0001c0008t0002g0017others(2): Show | 6 | HG02723.hp1 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2051-570dupA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7379867 | ||||||
| chr12:7379867
|
G | GTT | 58 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0088others(55): Show | 61 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.2051-571_2051-570d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7379867 | ||||||
| chr12:7379867
|
GT | G | 17 | a0004c0006t0001g0336a0004c0006t0001g0337a0004c0006t0001g0341others(14): Show | 17 | HG00673.hp2 HG01884.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2051-570delA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7379867 | ||||||
| chr12:7380205
|
A | T | 2 | a0009c0018t0001g0355a0009c0018t0002g0356 | 2 | HG01261.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2051-907T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380205 | ||||||
| chr12:7380210
|
G | A | 2 | a0006c0009t0001g0032a0006c0009t0001g0033 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2051-912C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380210 | ||||||
| chr12:7380234
|
C | T | 1 | a0001c0002t0001g0285 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2051-936G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380234 | ||||||
| chr12:7380273
|
T | C | 2 | a0006c0009t0001g0032a0006c0009t0001g0033 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2051-975A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380273 | ||||||
| chr12:7380274
|
GGT | G | 16 | a0001c0004t0001g0315a0001c0004t0001g0316a0001c0004t0001g0322others(13): Show | 16 | HG00099.hp1 HG01074.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2051-978_2051-977d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380274 | ||||||
| chr12:7380274
|
GGTGT | G | 148 | a0001c0002t0001g0004a0001c0002t0001g0008a0001c0002t0001g0009others(145): Show | 157 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2051-980_2051-977d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380274 | ||||||
| chr12:7380274
|
GGTGTGT | G | 6 | a0001c0001t0001g0107a0001c0001t0001g0181a0001c0001t0001g0182others(3): Show | 7 | HG01167.hp1 HG01169.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.2051-982_2051-977d others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380274 | ||||||
| chr12:7380274
|
GGTGTGTG others(1): Show |
G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(171): Show | 191 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(188): Show |
intron_variant | MODIFIER | c.2051-984_2051-977d others(10): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380274 | ||||||
| chr12:7380287
|
GTGTGTGT others(57): Show |
G | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051-1053_2051-990 others(67): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380287 | ||||||
| chr12:7380287
|
GTGTGTGT others(85): Show |
G | 1 | a0001c0001t0001g0130 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2051-1081_2051-990 others(95): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380287 | ||||||
| chr12:7380291
|
GTGTGTGT others(29): Show |
G | 2 | a0003c0005t0001g0062a0006c0009t0002g0226 | 2 | HG02647.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2051-1029_2051-994 others(39): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380291 | ||||||
| chr12:7380293
|
G | GTATACAC others(13): Show |
1 | a0004c0012t0002g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2051-996_2051-995i others(22): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380293 | ||||||
| chr12:7380295
|
G | A | 1 | a0004c0012t0002g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2051-997C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380295 | ||||||
| chr12:7380295
|
G | GTGTATAC others(17): Show |
2 | a0001c0002t0001g0105a0001c0002t0002g0250 | 2 | HG02135.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2051-998_2051-997i others(26): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380295 | ||||||
| chr12:7380299
|
G | A | 3 | a0001c0002t0001g0105a0001c0002t0002g0250a0004c0012t0002g0332 | 3 | HG02135.hp1 HG02630.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2051-1001C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380299 | ||||||
| chr12:7380301
|
G | A | 1 | a0001c0004t0002g0330 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2051-1003C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380301 | ||||||
| chr12:7380307
|
A | G | 21 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0132others(18): Show | 23 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.2051-1009T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380307 | ||||||
| chr12:7380309
|
A | G | 11 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0104others(8): Show | 13 | HG02135.hp1 HG02630.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.2051-1011T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380309 | ||||||
| chr12:7380316
|
T | C | 1 | a0001c0029t0001g0117 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2051-1018A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380316 | ||||||
| chr12:7380321
|
A | G | 21 | a0001c0002t0001g0105a0001c0002t0002g0250a0003c0005t0001g0006others(18): Show | 22 | HG00423.hp1 HG01099.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.2051-1023T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380321 | ||||||
| chr12:7380327
|
A | ATGTATAC others(21): Show |
1 | a0006c0009t0001g0111 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2051-1030_2051-102 others(32): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380327 | ||||||
| chr12:7380327
|
A | ATGTATAC others(21): Show |
2 | a0001c0002t0001g0258a0001c0002t0001g0269 | 2 | NA19063.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2051-1030_2051-102 others(32): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380327 | ||||||
| chr12:7380327
|
A | G | 21 | a0001c0001t0001g0143a0001c0002t0001g0104a0001c0002t0001g0105others(18): Show | 22 | HG00423.hp1 HG01099.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.2051-1029T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380327 | ||||||
| chr12:7380327
|
ATGTATAC others(21): Show |
A | 2 | a0006c0009t0001g0032a0006c0009t0001g0033 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2051-1057_2051-103 others(32): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380327 | ||||||
| chr12:7380335
|
A | ACGTATAC others(49): Show |
2 | a0001c0004t0001g0322a0001c0004t0001g0323 | 2 | HG00099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.2051-1038_2051-103 others(60): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380335 | ||||||
| chr12:7380335
|
A | ACGTATAC others(21): Show |
138 | a0001c0002t0001g0004a0001c0002t0001g0008a0001c0002t0001g0009others(135): Show | 147 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.2051-1065_2051-103 others(32): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380335 | ||||||
| chr12:7380335
|
A | ACGTATAC others(49): Show |
3 | a0002c0003t0001g0064a0011c0015t0001g0267a0011c0015t0001g0282 | 3 | HG01123.hp1 HG02698.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.2051-1038_2051-103 others(60): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380335 | ||||||
| chr12:7380335
|
A | ACGTATAC others(77): Show |
1 | a0022c0024t0001g0296 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2051-1038_2051-103 others(88): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380335 | ||||||
| chr12:7380335
|
A | G | 10 | a0001c0001t0001g0143a0001c0002t0001g0105a0001c0002t0001g0258others(7): Show | 11 | HG01167.hp1 HG01169.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.2051-1037T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380335 | ||||||
| chr12:7380335
|
ACGTATAC others(21): Show |
A | 15 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0132others(12): Show | 17 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.2051-1065_2051-103 others(32): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380335 | ||||||
| chr12:7380337
|
G | A | 2 | a0003c0005t0001g0062a0006c0009t0002g0226 | 2 | HG02647.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2051-1039C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380337 | ||||||
| chr12:7380344
|
T | C | 4 | a0006c0009t0001g0111a0006c0009t0002g0010a0006c0009t0002g0226others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2051-1046A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380344 | ||||||
| chr12:7380344
|
T | TACATGTA others(21): Show |
1 | a0001c0002t0003g0257 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2051-1047_2051-104 others(32): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380344 | ||||||
| chr12:7380349
|
G | A | 1 | a0006c0009t0002g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2051-1051C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380349 | ||||||
| chr12:7380363
|
G | A | 6 | a0003c0005t0001g0006a0003c0005t0001g0062a0009c0018t0001g0355others(3): Show | 7 | HG01099.hp1 HG01261.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2051-1065C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380363 | ||||||
| chr12:7380365
|
G | A | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051-1067C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380365 | ||||||
| chr12:7380372
|
T | C | 17 | a0001c0001t0001g0150a0001c0001t0001g0153a0001c0001t0001g0154others(14): Show | 18 | HG01167.hp1 HG01169.hp1 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.2051-1074A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380372 | ||||||
| chr12:7380372
|
T | TACATGTA others(21): Show |
2 | a0001c0002t0001g0279a0017c0022t0001g0261 | 2 | NA19058.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2051-1075_2051-107 others(32): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380372 | ||||||
| chr12:7380372
|
T | TACATGTA others(49): Show |
1 | a0002c0003t0003g0066 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2051-1075_2051-107 others(60): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380372 | ||||||
| chr12:7380372
|
TACATGTA others(21): Show |
T | 15 | a0003c0005t0001g0006a0003c0005t0001g0025a0003c0005t0001g0028others(12): Show | 16 | HG00423.hp1 HG01099.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.2051-1102_2051-107 others(32): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380372 | ||||||
| chr12:7380390
|
T | C | 18 | a0001c0004t0001g0116a0001c0004t0002g0115a0001c0007t0001g0126others(15): Show | 18 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.2051-1092A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380390 | ||||||
| chr12:7380391
|
G | A | 1 | a0003c0005t0001g0062 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2051-1093C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380391 | ||||||
| chr12:7380400
|
C | T | 2 | a0003c0005t0001g0062a0003c0033t0002g0123 | 2 | HG01891.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2051-1102G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380400 | ||||||
| chr12:7380413
|
G | GTA | 7 | a0002c0032t0001g0036a0005c0013t0001g0244a0005c0013t0001g0352others(4): Show | 7 | HG02572.hp2 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2051-1117_2051-111 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380413 | ||||||
| chr12:7380415
|
A | G | 1 | a0001c0002t0003g0289 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2051-1117T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380415 | ||||||
| chr12:7380493
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2051-1195A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380493 | ||||||
| chr12:7380757
|
T | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2051-1459A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380757 | ||||||
| chr12:7380793
|
A | T | 4 | a0006c0009t0001g0111a0006c0009t0002g0010a0006c0009t0002g0226others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2051-1495T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380793 | ||||||
| chr12:7380799
|
G | T | 13 | a0001c0001t0001g0191a0001c0001t0001g0233a0001c0001t0001g0238others(10): Show | 14 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.2051-1501C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380799 | ||||||
| chr12:7380806
|
C | T | 2 | a0001c0001t0003g0235a0001c0007t0001g0338 | 2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2051-1508G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380806 | ||||||
| chr12:7380825
|
T | C | 1 | a0002c0003t0001g0064 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2051-1527A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380825 | ||||||
| chr12:7380833
|
G | C | 1 | a0001c0008t0001g0206 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2051-1535C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380833 | ||||||
| chr12:7380883
|
C | T | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG00609.hp2 HG02015.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051-1585G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380883 | ||||||
| chr12:7380903
|
A | T | 1 | a0001c0001t0001g0231 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2051-1605T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380903 | ||||||
| chr12:7381130
|
C | A | 2 | a0003c0005t0001g0006a0003c0005t0001g0062 | 3 | HG01099.hp1 HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2051-1832G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7381130 | ||||||
| chr12:7381440
|
C | T | 4 | a0006c0009t0001g0111a0006c0009t0002g0010a0006c0009t0002g0226others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2051-2142G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7381440 | ||||||
| chr12:7381926
|
A | G | 3 | a0004c0006t0001g0336a0004c0006t0001g0337a0004c0028t0001g0121 | 3 | HG02109.hp1 HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2051-2628T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7381926 | ||||||
| chr12:7381961
|
AAT | A | 15 | a0003c0005t0001g0006a0003c0005t0001g0025a0003c0005t0001g0028others(12): Show | 16 | HG00423.hp1 HG01099.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.2051-2665_2051-266 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7381961 | ||||||
| chr12:7381962
|
AT | A | 65 | a0001c0001t0001g0199a0001c0002t0002g0288a0001c0007t0001g0097others(62): Show | 67 | HG00408.hp1 HG00673.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.2051-2665delA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7381962 | ||||||
| chr12:7381963
|
T | A | 6 | a0006c0009t0001g0032a0006c0009t0001g0033a0006c0009t0001g0111others(3): Show | 7 | HG01167.hp1 HG01169.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2051-2665A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7381963 | ||||||
| chr12:7381965
|
T | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2051-2667A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7381965 | ||||||
| chr12:7382018
|
T | A | 1 | a0002c0003t0002g0047 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2051-2720A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7382018 | ||||||
| chr12:7382079
|
T | C | 1 | a0001c0008t0002g0236 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2051-2781A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7382079 | ||||||
| chr12:7382132
|
A | G | 1 | a0004c0012t0002g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2051-2834T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7382132 | ||||||
| chr12:7382270
|
T | C | 1 | a0001c0001t0003g0018 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2051-2972A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7382270 | ||||||
| chr12:7382457
|
G | A | 1 | a0002c0003t0001g0082 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2051-3159C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7382457 | ||||||
| chr12:7382551
|
T | C | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2051-3253A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7382551 | ||||||
| chr12:7382702
|
C | A | 1 | a0001c0002t0001g0306 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2051-3404G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7382702 | ||||||
| chr12:7382758
|
G | A | 21 | a0001c0007t0001g0338a0001c0007t0001g0339a0001c0007t0001g0342others(18): Show | 21 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.2051-3460C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7382758 | ||||||
| chr12:7382785
|
T | C | 1 | a0002c0003t0003g0066 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2051-3487A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7382785 | ||||||
| chr12:7383095
|
A | G | 1 | a0013c0044t0002g0357 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2051-3797T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383095 | ||||||
| chr12:7383286
|
C | T | 16 | a0001c0007t0001g0338a0001c0007t0001g0339a0001c0007t0001g0342others(13): Show | 16 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.2051-3988G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383286 | ||||||
| chr12:7383302
|
G | A | 1 | a0001c0002t0001g0306 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2051-4004C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383302 | ||||||
| chr12:7383334
|
C | A | 1 | a0001c0027t0002g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2051-4036G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383334 | ||||||
| chr12:7383360
|
G | A | 4 | a0004c0006t0002g0333a0004c0012t0001g0334a0004c0012t0001g0335others(1): Show | 4 | HG01884.hp1 HG02630.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051-4062C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383360 | ||||||
| chr12:7383402
|
G | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0088others(58): Show | 65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.2051-4104C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383402 | ||||||
| chr12:7383408
|
A | G | 1 | a0002c0003t0001g0055 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2051-4110T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383408 | ||||||
| chr12:7383441
|
C | T | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0133others(5): Show | 10 | HG00544.hp2 HG02056.hp1 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.2051-4143G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383441 | ||||||
| chr12:7383445
|
C | G | 1 | a0001c0001t0001g0128 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2051-4147G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383445 | ||||||
| chr12:7383532
|
G | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0144others(9): Show | 18 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2051-4234C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383532 | ||||||
| chr12:7383622
|
G | A | 1 | a0001c0001t0003g0234 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2051-4324C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383622 | ||||||
| chr12:7383697
|
A | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(46): Show | 58 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.2051-4399T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383697 | ||||||
| chr12:7383762
|
C | G | 1 | a0001c0007t0001g0126 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2051-4464G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383762 | ||||||
| chr12:7383951
|
C | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(76): Show | 91 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.2051-4653G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383951 | ||||||
| chr12:7383984
|
G | A | 1 | a0001c0029t0001g0117 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2051-4686C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383984 | ||||||
| chr12:7384053
|
T | A | 1 | a0013c0044t0002g0357 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2051-4755A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7384053 | ||||||
| chr12:7384171
|
T | TA | 11 | a0003c0033t0002g0123a0006c0009t0001g0032a0006c0009t0001g0033others(8): Show | 12 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.2051-4874dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7384171 | ||||||
| chr12:7384171
|
T | TAA | 74 | a0001c0007t0001g0097a0002c0003t0001g0005a0002c0003t0001g0007others(71): Show | 77 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.2051-4875_2051-487 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7384171 | ||||||
| chr12:7384353
|
A | G | 1 | a0002c0003t0002g0047 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2051-5055T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7384353 | ||||||
| chr12:7384499
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2051-5201G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7384499 | ||||||
| chr12:7384519
|
A | C | 1 | a0001c0001t0001g0149 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2051-5221T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7384519 | ||||||
| chr12:7384687
|
C | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2051-5389G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7384687 | ||||||
| chr12:7384772
|
T | C | 1 | a0001c0004t0001g0316 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2051-5474A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7384772 | ||||||
| chr12:7384860
|
A | G | 1 | a0001c0001t0002g0131 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2051-5562T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7384860 | ||||||
| chr12:7384868
|
A | G | 2 | a0006c0009t0001g0032a0006c0009t0001g0033 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2051-5570T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7384868 | ||||||
| chr12:7385034
|
C | A | 1 | a0001c0002t0001g0306 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2051-5736G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7385034 | ||||||
| chr12:7385186
|
G | T | 4 | a0001c0002t0001g0249a0001c0002t0001g0303a0001c0002t0001g0304others(1): Show | 4 | NA18951.hp2 NA18984.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051-5888C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7385186 | ||||||
| chr12:7385250
|
T | TA | 79 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0016others(76): Show | 85 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.2051-5953dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7385250 | ||||||
| chr12:7385250
|
TA | T | 6 | a0001c0004t0003g0320a0002c0032t0001g0036a0009c0018t0001g0355others(3): Show | 6 | HG01175.hp2 HG01261.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.2051-5953delT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7385250 | ||||||
| chr12:7385348
|
C | T | 1 | a0001c0002t0002g0256 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2051-6050G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7385348 | ||||||
| chr12:7385356
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2051-6058A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7385356 | ||||||
| chr12:7385755
|
A | C | 1 | a0015c0020t0001g0313 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2051-6457T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7385755 | ||||||
| chr12:7385930
|
A | T | 16 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0130others(13): Show | 18 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.2051-6632T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7385930 | ||||||
| chr12:7386014
|
A | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(59): Show | 72 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.2051-6716T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386014 | ||||||
| chr12:7386087
|
TAAAAG | T | 3 | a0006c0009t0001g0111a0006c0009t0002g0010a0006c0034t0001g0118 | 4 | HG01167.hp1 HG01169.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051-6794_2051-679 others(9): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386087 | ||||||
| chr12:7386125
|
A | G | 4 | a0006c0009t0001g0111a0006c0009t0002g0010a0006c0009t0002g0226others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2051-6827T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386125 | ||||||
| chr12:7386190
|
C | T | 5 | a0001c0004t0002g0317a0004c0006t0002g0333a0004c0012t0001g0334others(2): Show | 5 | HG01884.hp1 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2051-6892G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386190 | ||||||
| chr12:7386246
|
G | C | 1 | a0001c0026t0002g0102 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2051-6948C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386246 | ||||||
| chr12:7386346
|
A | AC | 4 | a0004c0006t0002g0333a0004c0012t0001g0334a0004c0012t0001g0335others(1): Show | 4 | HG01884.hp1 HG02630.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051-7049dupG | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386346 | ||||||
| chr12:7386403
|
A | G | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2051-7105T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386403 | ||||||
| chr12:7386536
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2051-7238T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386536 | ||||||
| chr12:7386604
|
C | CA | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(115): Show | 129 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(126): Show |
intron_variant | MODIFIER | c.2051-7307dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386604 | ||||||
| chr12:7386604
|
CA | C | 205 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(202): Show | 219 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.2051-7307delT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386604 | ||||||
| chr12:7386619
|
A | C | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2051-7321T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386619 | ||||||
| chr12:7386664
|
T | C | 76 | a0001c0007t0001g0097a0002c0003t0001g0005a0002c0003t0001g0007others(73): Show | 79 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.2051-7366A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386664 | ||||||
| chr12:7386971
|
C | T | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2051-7673G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386971 | ||||||
| chr12:7387253
|
C | A | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051-7955G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7387253 | ||||||
| chr12:7387362
|
G | A | 11 | a0001c0002t0001g0019a0001c0002t0001g0251a0001c0002t0001g0258others(8): Show | 12 | HG00544.hp1 NA18747.hp2 NA18945.hp2 others(9): Show |
intron_variant | MODIFIER | c.2051-8064C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7387362 | ||||||
| chr12:7387427
|
T | C | 3 | a0002c0003t0002g0037a0002c0003t0002g0040a0002c0003t0002g0041 | 3 | HG02698.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2051-8129A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7387427 | ||||||
| chr12:7387641
|
C | T | 6 | a0006c0009t0001g0032a0006c0009t0001g0033a0006c0009t0001g0111others(3): Show | 7 | HG01167.hp1 HG01169.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2051-8343G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7387641 | ||||||
| chr12:7387759
|
C | T | 1 | a0001c0007t0001g0126 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2050+8336G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7387759 | ||||||
| chr12:7387881
|
A | G | 80 | a0001c0007t0001g0097a0002c0003t0001g0005a0002c0003t0001g0007others(77): Show | 83 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.2050+8214T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7387881 | ||||||
| chr12:7387923
|
A | C | 1 | a0002c0003t0002g0040 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2050+8172T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7387923 | ||||||
| chr12:7387934
|
T | G | 7 | a0002c0032t0001g0036a0005c0013t0001g0244a0005c0013t0001g0352others(4): Show | 7 | HG02572.hp2 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2050+8161A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7387934 | ||||||
| chr12:7388137
|
T | C | 1 | a0001c0002t0003g0286 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2050+7958A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388137 | ||||||
| chr12:7388163
|
A | G | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2050+7932T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388163 | ||||||
| chr12:7388236
|
A | C | 1 | a0006c0009t0002g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2050+7859T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388236 | ||||||
| chr12:7388294
|
T | C | 1 | a0003c0005t0003g0058 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2050+7801A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388294 | ||||||
| chr12:7388321
|
G | T | 1 | a0004c0006t0001g0341 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2050+7774C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388321 | ||||||
| chr12:7388339
|
G | A | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2050+7756C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388339 | ||||||
| chr12:7388509
|
A | AC | 8 | a0001c0004t0001g0315a0001c0004t0001g0316a0001c0004t0001g0322others(5): Show | 8 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050+7585_2050+758 others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388509 | ||||||
| chr12:7388510
|
A | T | 8 | a0001c0004t0001g0315a0001c0004t0001g0316a0001c0004t0001g0322others(5): Show | 8 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050+7585T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388510 | ||||||
| chr12:7388511
|
G | T | 8 | a0001c0004t0001g0315a0001c0004t0001g0316a0001c0004t0001g0322others(5): Show | 8 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050+7584C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388511 | ||||||
| chr12:7388515
|
G | C | 8 | a0001c0004t0001g0315a0001c0004t0001g0316a0001c0004t0001g0322others(5): Show | 8 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050+7580C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388515 | ||||||
| chr12:7388516
|
G | C | 8 | a0001c0004t0001g0315a0001c0004t0001g0316a0001c0004t0001g0322others(5): Show | 8 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050+7579C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388516 | ||||||
| chr12:7388517
|
C | CG | 8 | a0001c0004t0001g0315a0001c0004t0001g0316a0001c0004t0001g0322others(5): Show | 8 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050+7577_2050+757 others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388517 | ||||||
| chr12:7388518
|
A | G | 8 | a0001c0004t0001g0315a0001c0004t0001g0316a0001c0004t0001g0322others(5): Show | 8 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050+7577T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388518 | ||||||
| chr12:7388625
|
T | C | 1 | a0001c0007t0001g0126 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2050+7470A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388625 | ||||||
| chr12:7388677
|
G | A | 16 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0130others(13): Show | 18 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.2050+7418C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388677 | ||||||
| chr12:7388743
|
C | CA | 68 | a0001c0001t0001g0101a0001c0001t0001g0162a0001c0001t0001g0170others(65): Show | 70 | HG00140.hp2 HG00639.hp2 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.2050+7351dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388743 | ||||||
| chr12:7388743
|
C | CAA | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(44): Show | 56 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.2050+7350_2050+735 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388743 | ||||||
| chr12:7388766
|
G | GC | 16 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0130others(13): Show | 18 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.2050+7328_2050+732 others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388766 | ||||||
| chr12:7388771
|
G | GT | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2050+7323_2050+732 others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388771 | ||||||
| chr12:7388816
|
G | A | 12 | a0001c0004t0001g0315a0001c0004t0001g0316a0001c0004t0001g0322others(9): Show | 12 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.2050+7279C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388816 | ||||||
| chr12:7389001
|
A | G | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2050+7094T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389001 | ||||||
| chr12:7389094
|
T | A | 13 | a0001c0001t0001g0191a0001c0001t0001g0233a0001c0001t0001g0238others(10): Show | 14 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.2050+7001A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389094 | ||||||
| chr12:7389118
|
C | T | 1 | a0001c0002t0001g0350 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2050+6977G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389118 | ||||||
| chr12:7389174
|
C | T | 1 | a0001c0002t0001g0258 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2050+6921G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389174 | ||||||
| chr12:7389340
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(46): Show | 58 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.2050+6755G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389340 | ||||||
| chr12:7389944
|
T | TTTTATAT others(7): Show |
5 | a0002c0003t0001g0024a0002c0003t0001g0082a0003c0005t0001g0025others(2): Show | 5 | HG02615.hp2 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2050+6137_2050+615 others(18): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389944 | ||||||
| chr12:7389946
|
T | TTATATAT others(5): Show |
2 | a0001c0001t0001g0187a0024c0036t0002g0198 | 2 | HG03831.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.2050+6137_2050+614 others(16): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389946 | ||||||
| chr12:7389946
|
T | TTATATAT others(7): Show |
1 | a0001c0001t0001g0195 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2050+6148_2050+614 others(18): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389946 | ||||||
| chr12:7389946
|
T | TTATATAT others(25): Show |
1 | a0001c0001t0001g0189 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2050+6148_2050+614 others(36): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389946 | ||||||
| chr12:7389948
|
A | ATATATAT others(5): Show |
1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2050+6135_2050+614 others(16): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389948 | ||||||
| chr12:7389950
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0002g0247 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2050+6144_2050+614 others(16): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389950 | ||||||
| chr12:7389960
|
T | A | 8 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0001g0195others(5): Show | 8 | HG00558.hp2 HG03831.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050+6135A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | ||||||
| chr12:7389960
|
T | TTA | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0128others(54): Show | 68 | HG00099.hp1 HG00609.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.2050+6133_2050+613 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | ||||||
| chr12:7389960
|
T | TTATA | 49 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(46): Show | 53 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.2050+6131_2050+613 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | ||||||
| chr12:7389960
|
T | TTATATA | 49 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(46): Show | 51 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.2050+6129_2050+613 others(10): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | ||||||
| chr12:7389960
|
T | TTATATAT others(1): Show |
4 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0182others(1): Show | 4 | HG02040.hp2 NA18946.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.2050+6127_2050+613 others(12): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | ||||||
| chr12:7389960
|
T | TTATATAT others(3): Show |
1 | a0004c0006t0003g0340 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2050+6125_2050+613 others(14): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | ||||||
| chr12:7389960
|
T | TTATATAT others(5): Show |
1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2050+6123_2050+613 others(16): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | ||||||
| chr12:7389960
|
T | TTATATAT others(7): Show |
1 | a0001c0041t0001g0106 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2050+6121_2050+613 others(18): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | ||||||
| chr12:7389960
|
T | TTATATAT others(9): Show |
2 | a0009c0018t0001g0355a0009c0018t0002g0356 | 2 | HG01261.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2050+6119_2050+613 others(20): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | ||||||
| chr12:7389960
|
T | TTATATAT others(23): Show |
1 | a0001c0001t0001g0199 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2050+6134_2050+613 others(34): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | ||||||
| chr12:7389960
|
T | TTATATAT others(23): Show |
1 | a0001c0029t0001g0117 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2050+6134_2050+613 others(34): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | ||||||
| chr12:7389960
|
T | TTATATAT others(9): Show |
8 | a0006c0009t0001g0032a0006c0009t0001g0033a0006c0009t0001g0111others(5): Show | 9 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2050+6134_2050+613 others(20): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | ||||||
| chr12:7389962
|
A | ATATATAT others(6): Show |
1 | a0002c0003t0001g0022 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2050+6120_2050+613 others(17): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389962 | ||||||
| chr12:7389962
|
A | ATATATAT others(5): Show |
69 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0029others(66): Show | 72 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.2050+6132_2050+613 others(16): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389962 | ||||||
| chr12:7389964
|
A | ATATATAT others(3): Show |
1 | a0002c0003t0003g0066 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2050+6130_2050+613 others(14): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389964 | ||||||
| chr12:7390128
|
C | T | 87 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(84): Show | 91 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.2050+5967G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7390128 | ||||||
| chr12:7390212
|
A | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(257): Show | 280 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.2050+5883T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7390212 | ||||||
| chr12:7390865
|
A | G | 1 | a0001c0004t0002g0317 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2050+5230T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7390865 | ||||||
| chr12:7391013
|
C | T | 1 | a0001c0002t0001g0270 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2050+5082G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391013 | ||||||
| chr12:7391019
|
A | G | 1 | a0004c0028t0001g0121 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2050+5076T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391019 | ||||||
| chr12:7391420
|
T | C | 1 | a0006c0009t0002g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2050+4675A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391420 | ||||||
| chr12:7391542
|
C | T | 20 | a0001c0007t0001g0338a0001c0007t0001g0339a0001c0007t0001g0342others(17): Show | 20 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.2050+4553G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391542 | ||||||
| chr12:7391655
|
G | A | 2 | a0001c0007t0001g0126a0021c0038t0001g0127 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2050+4440C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391655 | ||||||
| chr12:7391659
|
G | T | 4 | a0001c0001t0002g0232a0001c0007t0001g0097a0001c0008t0001g0240others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2050+4436C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391659 | ||||||
| chr12:7391712
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2050+4383A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391712 | ||||||
| chr12:7391765
|
G | A | 60 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(57): Show | 62 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.2050+4330C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391765 | ||||||
| chr12:7391805
|
C | A | 6 | a0006c0009t0001g0032a0006c0009t0001g0033a0006c0009t0001g0111others(3): Show | 7 | HG01167.hp1 HG01169.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2050+4290G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391805 | ||||||
| chr12:7391830
|
C | T | 60 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(57): Show | 62 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.2050+4265G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391830 | ||||||
| chr12:7391990
|
CCACT | C | 87 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(84): Show | 91 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.2050+4101_2050+410 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391990 | ||||||
| chr12:7391992
|
A | T | 90 | a0001c0002t0001g0004a0001c0002t0001g0008a0001c0002t0001g0009others(87): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.2050+4103T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391992 | ||||||
| chr12:7392100
|
C | T | 1 | a0001c0029t0001g0117 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2050+3995G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392100 | ||||||
| chr12:7392116
|
T | C | 20 | a0001c0007t0001g0338a0001c0007t0001g0339a0001c0007t0001g0342others(17): Show | 20 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.2050+3979A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392116 | ||||||
| chr12:7392121
|
AT | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(14): Show | 21 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.2050+3973delA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392121 | ||||||
| chr12:7392224
|
C | T | 60 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(57): Show | 62 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.2050+3871G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392224 | ||||||
| chr12:7392230
|
G | C | 2 | a0006c0009t0002g0010a0006c0034t0001g0118 | 3 | HG01167.hp1 HG01169.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2050+3865C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392230 | ||||||
| chr12:7392238
|
C | T | 1 | a0001c0002t0001g0328 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2050+3857G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392238 | ||||||
| chr12:7392248
|
T | C | 1 | a0001c0002t0001g0328 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2050+3847A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392248 | ||||||
| chr12:7392335
|
A | G | 20 | a0001c0007t0001g0338a0001c0007t0001g0339a0001c0007t0001g0342others(17): Show | 20 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.2050+3760T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392335 | ||||||
| chr12:7392349
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2050+3746T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392349 | ||||||
| chr12:7392418
|
T | G | 2 | a0001c0007t0001g0126a0021c0038t0001g0127 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2050+3677A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392418 | ||||||
| chr12:7392460
|
C | T | 1 | a0002c0003t0001g0039 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2050+3635G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392460 | ||||||
| chr12:7392663
|
T | C | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2050+3432A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392663 | ||||||
| chr12:7392896
|
C | T | 1 | a0013c0044t0002g0357 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2050+3199G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392896 | ||||||
| chr12:7392914
|
A | G | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0019c0035t0002g0218 | 3 | NA18950.hp2 NA18994.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2050+3181T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392914 | ||||||
| chr12:7392998
|
G | T | 2 | a0003c0005t0001g0006a0003c0005t0001g0062 | 3 | HG01099.hp1 HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2050+3097C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392998 | ||||||
| chr12:7393175
|
A | C | 1 | a0003c0005t0001g0063 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2050+2920T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7393175 | ||||||
| chr12:7393191
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2050+2904C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7393191 | ||||||
| chr12:7393231
|
A | G | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0104others(2): Show | 7 | HG02135.hp1 NA18948.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.2050+2864T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7393231 | ||||||
| chr12:7393309
|
G | A | 1 | a0001c0002t0001g0306 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2050+2786C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7393309 | ||||||
| chr12:7393329
|
T | C | 6 | a0001c0002t0001g0004a0001c0002t0001g0095a0001c0002t0001g0300others(3): Show | 8 | HG00639.hp1 HG01074.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050+2766A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7393329 | ||||||
| chr12:7393853
|
C | T | 4 | a0001c0002t0001g0249a0001c0002t0001g0303a0001c0002t0001g0304others(1): Show | 4 | NA18951.hp2 NA18984.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.2050+2242G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7393853 | ||||||
| chr12:7393975
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(46): Show | 58 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.2050+2120G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7393975 | ||||||
| chr12:7394081
|
G | A | 4 | a0006c0009t0001g0111a0006c0009t0002g0010a0006c0009t0002g0226others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2050+2014C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7394081 | ||||||
| chr12:7394106
|
C | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(46): Show | 58 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.2050+1989G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7394106 | ||||||
| chr12:7394123
|
A | AC | 86 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(83): Show | 90 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.2050+1971_2050+197 others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7394123 | ||||||
| chr12:7394123
|
A | C | 1 | a0006c0009t0002g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2050+1972T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7394123 | ||||||
| chr12:7394474
|
T | C | 66 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(63): Show | 68 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.2050+1621A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7394474 | ||||||
| chr12:7394695
|
C | G | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2050+1400G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7394695 | ||||||
| chr12:7394774
|
G | T | 2 | a0006c0009t0001g0032a0006c0009t0001g0033 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2050+1321C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7394774 | ||||||
| chr12:7394868
|
G | C | 1 | a0001c0002t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2050+1227C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7394868 | ||||||
| chr12:7395158
|
G | A | 6 | a0006c0009t0001g0032a0006c0009t0001g0033a0006c0009t0001g0111others(3): Show | 7 | HG01167.hp1 HG01169.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2050+937C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7395158 | ||||||
| chr12:7395179
|
G | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | NA18943.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2050+916C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7395179 | ||||||
| chr12:7395358
|
A | AC | 12 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0144others(9): Show | 18 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2050+736dupG | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7395358 | ||||||
| chr12:7395579
|
A | G | 1 | a0013c0044t0002g0357 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2050+516T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7395579 | ||||||
| chr12:7395587
|
G | A | 3 | a0001c0001t0001g0215a0001c0001t0002g0224a0001c0001t0003g0209 | 3 | HG00735.hp2 HG02148.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2050+508C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7395587 | ||||||
| chr12:7396017
|
TACTG | T | 11 | a0001c0002t0001g0252a0001c0002t0001g0253a0001c0002t0001g0259others(8): Show | 11 | HG00408.hp2 NA18947.hp1 NA18965.hp2 others(8): Show |
intron_variant | MODIFIER | c.2050+74_2050+77del others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7396017 | ||||||
| chr12:7396494
|
C | A | 2 | a0001c0007t0001g0126a0021c0038t0001g0127 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1730-79G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396494 | ||||||
| chr12:7396494
|
C | T | 1 | a0001c0004t0001g0316 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1730-79G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396494 | ||||||
| chr12:7396495
|
C | G | 91 | a0001c0002t0001g0004a0001c0002t0001g0008a0001c0002t0001g0009others(88): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.1730-80G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396495 | ||||||
| chr12:7396559
|
C | G | 1 | a0001c0001t0001g0178 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1730-144G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396559 | ||||||
| chr12:7396629
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1730-214A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396629 | ||||||
| chr12:7396742
|
C | G | 1 | a0001c0002t0002g0288 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1730-327G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396742 | ||||||
| chr12:7396770
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1730-355G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396770 | ||||||
| chr12:7396856
|
C | A | 60 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(57): Show | 62 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1730-441G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396856 | ||||||
| chr12:7396856
|
C | CAGAG | 61 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(58): Show | 71 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.1730-445_1730-442d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396856 | ||||||
| chr12:7396856
|
C | G | 4 | a0001c0004t0001g0116a0001c0004t0001g0351a0001c0004t0002g0115others(1): Show | 4 | HG02818.hp2 HG03540.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.1730-441G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396856 | ||||||
| chr12:7396874
|
A | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(59): Show | 72 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.1730-459T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396874 | ||||||
| chr12:7396924
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(46): Show | 58 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.1730-509G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396924 | ||||||
| chr12:7397083
|
A | C | 1 | a0004c0006t0002g0096 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1730-668T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7397083 | ||||||
| chr12:7397083
|
A | G | 16 | a0001c0004t0001g0315a0001c0004t0001g0316a0001c0004t0001g0322others(13): Show | 17 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.1730-668T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7397083 | ||||||
| chr12:7397166
|
C | T | 2 | a0001c0001t0001g0213a0001c0001t0002g0211 | 2 | HG00558.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1730-751G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7397166 | ||||||
| chr12:7397184
|
T | C | 20 | a0001c0007t0001g0338a0001c0007t0001g0339a0001c0007t0001g0342others(17): Show | 20 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1730-769A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7397184 | ||||||
| chr12:7397294
|
A | C | 60 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(57): Show | 62 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1730-879T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7397294 | ||||||
| chr12:7397346
|
C | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1729+918G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7397346 | ||||||
| chr12:7397536
|
AC | A | 3 | a0001c0007t0001g0097a0001c0008t0001g0240a0001c0008t0001g0241 | 3 | HG03041.hp1 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1729+727delG | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7397536 | ||||||
| chr12:7397576
|
C | A | 3 | a0002c0003t0001g0034a0002c0003t0002g0035a0002c0032t0001g0036 | 3 | HG02723.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1729+688G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7397576 | ||||||
| chr12:7397590
|
G | A | 87 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(84): Show | 91 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.1729+674C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7397590 | ||||||
| chr12:7397925
|
G | C | 3 | a0002c0003t0001g0034a0002c0003t0002g0035a0002c0032t0001g0036 | 3 | HG02723.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1729+339C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7397925 | ||||||
| chr12:7398626
|
G | C | 87 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(84): Show | 91 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.1409-42C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7398626 | ||||||
| chr12:7398711
|
A | G | 87 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(84): Show | 91 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.1409-127T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7398711 | ||||||
| chr12:7398760
|
G | A | 1 | a0001c0002t0001g0281 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1409-176C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7398760 | ||||||
| chr12:7398792
|
G | A | 2 | a0009c0018t0001g0355a0009c0018t0002g0356 | 2 | HG01261.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1409-208C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7398792 | ||||||
| chr12:7399143
|
TCTTC | T | 3 | a0004c0006t0002g0333a0004c0012t0001g0334a0004c0012t0001g0335 | 3 | HG01884.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1409-563_1409-560d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399143 | ||||||
| chr12:7399172
|
C | T | 1 | a0018c0031t0001g0053 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1409-588G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399172 | ||||||
| chr12:7399207
|
CT | C | 17 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(14): Show | 21 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.1409-624delA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399207 | ||||||
| chr12:7399300
|
C | CCT | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 278 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(275): Show |
intron_variant | MODIFIER | c.1409-718_1409-717d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399300 | ||||||
| chr12:7399319
|
TTC | T | 32 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(29): Show | 34 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.1409-737_1409-736d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399319 | ||||||
| chr12:7399321
|
C | CTCTCTCT others(8): Show |
2 | a0001c0001t0001g0016a0001c0001t0001g0229 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1409-752_1409-738d others(17): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399321 | ||||||
| chr12:7399321
|
CTCTCTCT others(8): Show |
C | 8 | a0004c0006t0001g0341a0004c0006t0001g0343a0004c0006t0001g0344others(5): Show | 8 | HG00673.hp2 HG03669.hp2 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.1409-752_1409-738d others(17): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399321 | ||||||
| chr12:7399389
|
TTTTC | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(21): Show | 28 | HG00544.hp2 HG00609.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1409-809_1409-806d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399389 | ||||||
| chr12:7399430
|
T | TCTTCTTC others(83): Show |
1 | a0001c0002t0001g0306 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1409-847_1409-846i others(92): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399430 | ||||||
| chr12:7399430
|
T | TCTTCTTC others(41): Show |
187 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(184): Show | 193 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.1409-894_1409-847d others(50): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399430 | ||||||
| chr12:7399430
|
T | TCTTCTTC others(83): Show |
2 | a0001c0002t0001g0258a0001c0002t0001g0269 | 2 | NA19063.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1409-847_1409-846i others(92): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399430 | ||||||
| chr12:7399430
|
T | TCTTCTTC others(89): Show |
78 | a0001c0002t0001g0004a0001c0002t0001g0008a0001c0002t0001g0009others(75): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.1409-847_1409-846i others(98): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399430 | ||||||
| chr12:7399441
|
C | CTCTTCCT others(83): Show |
1 | a0001c0025t0002g0307 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1409-858_1409-857i others(92): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399441 | ||||||
| chr12:7399550
|
G | T | 41 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0108others(38): Show | 41 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1409-966C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399550 | ||||||
| chr12:7399550
|
GCTTT | G | 22 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0101others(19): Show | 24 | HG00558.hp2 HG01358.hp1 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.1409-970_1409-967d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399550 | ||||||
| chr12:7399554
|
T | G | 39 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0108others(36): Show | 39 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1409-970A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399554 | ||||||
| chr12:7399554
|
T | TCTTTCTT others(2): Show |
3 | a0001c0002t0001g0275a0001c0002t0001g0276a0002c0003t0001g0049 | 3 | HG01975.hp1 HG01978.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1409-979_1409-971d others(11): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399554 | ||||||
| chr12:7399584
|
C | T | 4 | a0006c0009t0001g0111a0006c0009t0002g0010a0006c0009t0002g0226others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1409-1000G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399584 | ||||||
| chr12:7399703
|
T | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1409-1119A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399703 | ||||||
| chr12:7399881
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1409-1297G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399881 | ||||||
| chr12:7400017
|
C | A | 88 | a0001c0002t0001g0004a0001c0002t0001g0008a0001c0002t0001g0009others(85): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.1409-1433G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7400017 | ||||||
| chr12:7400259
|
A | G | 85 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(82): Show | 89 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1409-1675T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7400259 | ||||||
| chr12:7400325
|
C | T | 85 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(82): Show | 89 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1409-1741G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7400325 | ||||||
| chr12:7400455
|
G | T | 85 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(82): Show | 89 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1409-1871C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7400455 | ||||||
| chr12:7400614
|
C | T | 1 | a0001c0002t0001g0301 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1409-2030G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7400614 | ||||||
| chr12:7400720
|
A | G | 1 | a0002c0003t0001g0052 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1409-2136T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7400720 | ||||||
| chr12:7400734
|
T | C | 1 | a0001c0002t0001g0287 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1409-2150A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7400734 | ||||||
| chr12:7400899
|
T | A | 1 | a0001c0001t0001g0144 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1409-2315A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7400899 | ||||||
| chr12:7400951
|
A | C | 6 | a0005c0013t0001g0244a0005c0013t0001g0352a0005c0013t0002g0243others(3): Show | 6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1409-2367T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7400951 | ||||||
| chr12:7400968
|
C | A | 1 | a0001c0001t0001g0130 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1409-2384G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7400968 | ||||||
| chr12:7401029
|
G | C | 86 | a0001c0004t0002g0330a0002c0003t0001g0005a0002c0003t0001g0007others(83): Show | 90 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.1409-2445C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7401029 | ||||||
| chr12:7401039
|
A | T | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1409-2455T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7401039 | ||||||
| chr12:7401101
|
A | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1408+2434T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7401101 | ||||||
| chr12:7401145
|
T | C | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1408+2390A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7401145 | ||||||
| chr12:7401223
|
C | A | 89 | a0001c0002t0001g0004a0001c0002t0001g0008a0001c0002t0001g0009others(86): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.1408+2312G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7401223 | ||||||
| chr12:7401645
|
G | A | 1 | a0004c0006t0002g0096 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1408+1890C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7401645 | ||||||
| chr12:7401790
|
A | T | 1 | a0002c0003t0002g0046 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1408+1745T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7401790 | ||||||
| chr12:7401792
|
C | T | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1408+1743G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7401792 | ||||||
| chr12:7401816
|
AT | A | 8 | a0001c0002t0001g0021a0001c0002t0001g0255a0001c0002t0001g0274others(5): Show | 8 | HG01975.hp1 HG01978.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.1408+1718delA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7401816 | ||||||
| chr12:7402004
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1408+1531G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7402004 | ||||||
| chr12:7402190
|
A | T | 2 | a0001c0007t0001g0126a0021c0038t0001g0127 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1408+1345T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7402190 | ||||||
| chr12:7402362
|
A | G | 4 | a0006c0009t0001g0111a0006c0009t0002g0010a0006c0009t0002g0226others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1408+1173T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7402362 | ||||||
| chr12:7402369
|
T | TTG | 18 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(15): Show | 22 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.1408+1164_1408+116 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7402369 | ||||||
| chr12:7402638
|
A | AT | 13 | a0001c0004t0001g0315a0001c0004t0001g0316a0001c0004t0001g0322others(10): Show | 13 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1408+896dupA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7402638 | ||||||
| chr12:7402638
|
AT | A | 100 | a0001c0001t0001g0016a0001c0001t0001g0197a0001c0001t0001g0203others(97): Show | 106 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(103): Show |
intron_variant | MODIFIER | c.1408+896delA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7402638 | ||||||
| chr12:7402820
|
G | C | 81 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(78): Show | 84 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(81): Show |
intron_variant | MODIFIER | c.1408+715C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7402820 | ||||||
| chr12:7402921
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1408+614G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7402921 | ||||||
| chr12:7402930
|
G | A | 1 | a0001c0029t0001g0117 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1408+605C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7402930 | ||||||
| chr12:7403040
|
A | G | 92 | a0001c0001t0001g0215a0001c0002t0001g0004a0001c0002t0001g0008others(89): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.1408+495T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7403040 | ||||||
| chr12:7403100
|
A | G | 1 | a0001c0002t0001g0285 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1408+435T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7403100 | ||||||
| chr12:7403198
|
TA | T | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 280 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.1408+336delT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7403198 | ||||||
| chr12:7403295
|
G | C | 6 | a0005c0013t0001g0244a0005c0013t0001g0352a0005c0013t0002g0243others(3): Show | 6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1408+240C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7403295 | ||||||
| chr12:7403375
|
T | C | 4 | a0006c0009t0001g0111a0006c0009t0002g0010a0006c0009t0002g0226others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1408+160A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7403375 | ||||||
| chr12:7403505
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1408+30C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7403505 | ||||||
| chr12:7403863
|
G | A | 1 | a0001c0029t0001g0117 | 1 | NA19240.hp1 | splice_region_variant&intron_variant | LOW | c.1088-8C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7403863 | ||||||
| chr12:7404007
|
AATTTTAA others(17): Show |
A | 1 | a0003c0005t0001g0063 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1088-176_1088-153d others(26): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404007 | ||||||
| chr12:7404194
|
A | G | 4 | a0006c0009t0001g0111a0006c0009t0002g0010a0006c0009t0002g0226others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1088-339T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404194 | ||||||
| chr12:7404370
|
T | TTCTCATA others(330): Show |
1 | a0001c0004t0001g0323 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1088-516_1088-515i others(339): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404370 | ||||||
| chr12:7404370
|
T | TTCTCATA others(340): Show |
1 | a0001c0004t0001g0322 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1088-516_1088-515i others(349): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404370 | ||||||
| chr12:7404377
|
A | G | 1 | a0004c0006t0002g0096 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1088-522T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404377 | ||||||
| chr12:7404388
|
C | T | 1 | a0001c0002t0001g0252 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1088-533G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404388 | ||||||
| chr12:7404487
|
C | T | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1088-632G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404487 | ||||||
| chr12:7404538
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0229 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1088-683T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404538 | ||||||
| chr12:7404622
|
T | G | 1 | a0001c0029t0001g0117 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1088-767A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404622 | ||||||
| chr12:7404653
|
C | T | 7 | a0001c0001t0001g0238a0001c0001t0002g0237a0001c0001t0003g0018others(4): Show | 8 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1088-798G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404653 | ||||||
| chr12:7404876
|
T | C | 1 | a0002c0032t0001g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1088-1021A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404876 | ||||||
| chr12:7404896
|
G | C | 1 | a0013c0044t0002g0357 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1088-1041C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404896 | ||||||
| chr12:7404966
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG04184.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1088-1111A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404966 | ||||||
| chr12:7405039
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1088-1184C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7405039 | ||||||
| chr12:7405158
|
T | C | 12 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(9): Show | 13 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1088-1303A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7405158 | ||||||
| chr12:7405229
|
T | C | 1 | a0002c0003t0001g0043 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1087+1303A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7405229 | ||||||
| chr12:7405283
|
T | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 184 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.1087+1249A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7405283 | ||||||
| chr12:7405412
|
T | C | 1 | a0003c0005t0001g0025 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1087+1120A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7405412 | ||||||
| chr12:7405563
|
G | A | 4 | a0001c0001t0002g0232a0001c0007t0001g0097a0001c0008t0001g0240others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+969C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7405563 | ||||||
| chr12:7405979
|
T | C | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+553A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7405979 | ||||||
| chr12:7406410
|
A | T | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+122T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7406410 | ||||||
| chr12:7406991
|
C | A | 4 | a0006c0009t0001g0111a0006c0009t0002g0010a0006c0009t0002g0226others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.767-139G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7406991 | ||||||
| chr12:7407171
|
A | T | 1 | a0017c0022t0001g0261 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.767-319T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407171 | ||||||
| chr12:7407205
|
G | A | 62 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(59): Show | 64 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.767-353C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407205 | ||||||
| chr12:7407214
|
T | G | 1 | a0001c0029t0001g0117 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.767-362A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407214 | ||||||
| chr12:7407328
|
C | T | 2 | a0006c0009t0001g0032a0006c0009t0001g0033 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.767-476G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407328 | ||||||
| chr12:7407509
|
G | T | 1 | a0001c0001t0003g0235 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.767-657C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407509 | ||||||
| chr12:7407541
|
C | A | 3 | a0004c0006t0002g0333a0004c0012t0001g0334a0004c0012t0001g0335 | 3 | HG01884.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.767-689G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407541 | ||||||
| chr12:7407565
|
T | A | 1 | a0013c0044t0002g0357 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.767-713A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407565 | ||||||
| chr12:7407652
|
C | T | 4 | a0006c0009t0001g0111a0006c0009t0002g0010a0006c0009t0002g0226others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.767-800G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407652 | ||||||
| chr12:7407674
|
C | T | 84 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(81): Show | 88 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.767-822G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407674 | ||||||
| chr12:7407688
|
T | C | 19 | a0001c0007t0001g0338a0001c0007t0001g0339a0001c0007t0001g0342others(16): Show | 19 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.767-836A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407688 | ||||||
| chr12:7407692
|
G | C | 1 | a0013c0044t0002g0357 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.767-840C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407692 | ||||||
| chr12:7407782
|
T | TAC | 70 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0103others(67): Show | 81 | HG00733.hp1 HG00735.hp1 HG01069.hp1 others(78): Show |
intron_variant | MODIFIER | c.767-932_767-931dup others(2): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407782 | ||||||
| chr12:7407782
|
T | TACAC | 18 | a0001c0001t0001g0233a0001c0007t0001g0152a0001c0007t0001g0338others(15): Show | 19 | HG00140.hp2 HG00639.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.767-934_767-931dup others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407782 | ||||||
| chr12:7407782
|
TAC | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(29): Show | 37 | HG01099.hp1 HG01256.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.767-932_767-931del others(2): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407782 | ||||||
| chr12:7407816
|
C | A | 62 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(59): Show | 64 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.767-964G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407816 | ||||||
| chr12:7407828
|
T | C | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-976A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407828 | ||||||
| chr12:7407872
|
C | T | 71 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(68): Show | 74 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.767-1020G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407872 | ||||||
| chr12:7408076
|
C | CAT | 81 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(78): Show | 88 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.767-1226_767-1225d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7408076 | ||||||
| chr12:7408076
|
CAT | C | 22 | a0001c0004t0001g0116a0001c0004t0002g0115a0001c0007t0001g0338others(19): Show | 22 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.767-1226_767-1225d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7408076 | ||||||
| chr12:7408093
|
A | ATATC | 84 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(81): Show | 88 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.767-1242_767-1241i others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7408093 | ||||||
| chr12:7408205
|
T | C | 1 | a0002c0003t0002g0071 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.767-1353A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7408205 | ||||||
| chr12:7408388
|
GTAT | G | 19 | a0001c0007t0001g0338a0001c0007t0001g0339a0001c0007t0001g0342others(16): Show | 19 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.767-1539_767-1537d others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7408388 | ||||||
| chr12:7408432
|
C | T | 84 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(81): Show | 88 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.767-1580G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7408432 | ||||||
| chr12:7408492
|
G | T | 1 | a0001c0004t0001g0351 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.767-1640C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7408492 | ||||||
| chr12:7408615
|
C | A | 4 | a0006c0009t0001g0111a0006c0009t0002g0010a0006c0009t0002g0226others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.767-1763G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7408615 | ||||||
| chr12:7408663
|
C | T | 353 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(350): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.767-1811G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7408663 | ||||||
| chr12:7408870
|
G | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0133others(5): Show | 10 | HG00544.hp2 HG02056.hp1 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.767-2018C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7408870 | ||||||
| chr12:7409109
|
C | T | 1 | a0001c0004t0001g0315 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.767-2257G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7409109 | ||||||
| chr12:7409137
|
C | T | 3 | a0001c0004t0001g0116a0001c0004t0002g0115a0001c0027t0002g0023 | 3 | HG02818.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.767-2285G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7409137 | ||||||
| chr12:7409276
|
G | A | 1 | a0006c0009t0001g0111 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.767-2424C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7409276 | ||||||
| chr12:7409294
|
T | C | 1 | a0004c0006t0001g0348 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.767-2442A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7409294 | ||||||
| chr12:7409423
|
C | G | 19 | a0001c0007t0001g0338a0001c0007t0001g0339a0001c0007t0001g0342others(16): Show | 19 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.767-2571G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7409423 | ||||||
| chr12:7409478
|
T | C | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.767-2626A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7409478 | ||||||
| chr12:7409651
|
G | A | 1 | a0001c0004t0003g0320 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.767-2799C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7409651 | ||||||
| chr12:7410018
|
T | A | 1 | a0001c0001t0002g0151 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.767-3166A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410018 | ||||||
| chr12:7410243
|
A | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.767-3391T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410243 | ||||||
| chr12:7410572
|
C | A | 1 | a0001c0001t0001g0130 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.767-3720G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410572 | ||||||
| chr12:7410573
|
C | A | 1 | a0001c0001t0001g0130 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.767-3721G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410573 | ||||||
| chr12:7410604
|
C | CA | 19 | a0001c0007t0001g0338a0001c0007t0001g0339a0001c0007t0001g0342others(16): Show | 19 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.767-3753dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410604 | ||||||
| chr12:7410604
|
CA | C | 79 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.767-3753delT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410604 | ||||||
| chr12:7410648
|
G | A | 71 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(68): Show | 74 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.767-3796C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410648 | ||||||
| chr12:7410760
|
G | T | 2 | a0006c0009t0001g0032a0006c0009t0001g0033 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.767-3908C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410760 | ||||||
| chr12:7410794
|
C | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.767-3942G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410794 | ||||||
| chr12:7410813
|
G | C | 3 | a0001c0002t0002g0254a0001c0002t0002g0256a0001c0002t0002g0277 | 3 | HG01167.hp2 HG01361.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.767-3961C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410813 | ||||||
| chr12:7410817
|
G | A | 3 | a0001c0004t0001g0116a0001c0004t0002g0115a0001c0027t0002g0023 | 3 | HG02818.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.767-3965C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410817 | ||||||
| chr12:7411539
|
C | A | 3 | a0001c0004t0001g0116a0001c0004t0002g0115a0001c0027t0002g0023 | 3 | HG02818.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.767-4687G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7411539 | ||||||
| chr12:7411671
|
A | T | 1 | a0001c0001t0002g0168 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.767-4819T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7411671 | ||||||
| chr12:7411886
|
A | T | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.767-5034T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7411886 | ||||||
| chr12:7411969
|
C | T | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.767-5117G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7411969 | ||||||
| chr12:7412007
|
A | G | 1 | a0006c0009t0001g0111 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.767-5155T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7412007 | ||||||
| chr12:7412144
|
G | A | 63 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(60): Show | 65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.767-5292C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7412144 | ||||||
| chr12:7412162
|
C | T | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.767-5310G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7412162 | ||||||
| chr12:7412300
|
T | C | 1 | a0013c0044t0002g0357 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.767-5448A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7412300 | ||||||
| chr12:7412425
|
T | C | 84 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(81): Show | 88 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.767-5573A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7412425 | ||||||
| chr12:7412620
|
T | C | 84 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(81): Show | 88 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.767-5768A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7412620 | ||||||
| chr12:7412752
|
C | T | 1 | a0003c0005t0001g0025 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.767-5900G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7412752 | ||||||
| chr12:7412824
|
C | T | 5 | a0001c0007t0001g0126a0006c0009t0001g0111a0006c0009t0002g0010others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.767-5972G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7412824 | ||||||
| chr12:7412862
|
C | T | 21 | a0002c0003t0001g0067a0002c0003t0001g0070a0002c0003t0001g0072others(18): Show | 21 | HG00738.hp1 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.767-6010G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7412862 | ||||||
| chr12:7412988
|
C | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.767-6136G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7412988 | ||||||
| chr12:7413011
|
G | A | 1 | a0001c0001t0002g0212 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.767-6159C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413011 | ||||||
| chr12:7413044
|
C | T | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-6192G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413044 | ||||||
| chr12:7413091
|
C | CA | 64 | a0001c0001t0001g0107a0001c0001t0001g0128a0001c0001t0001g0135others(61): Show | 67 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.767-6240dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413091 | ||||||
| chr12:7413091
|
C | CAA | 81 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0108others(78): Show | 83 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.767-6241_767-6240d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413091 | ||||||
| chr12:7413091
|
C | CAAA | 6 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0191others(3): Show | 6 | HG01358.hp1 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.767-6242_767-6240d others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413091 | ||||||
| chr12:7413091
|
CAAAAAAA others(5): Show |
C | 4 | a0004c0006t0002g0333a0004c0012t0001g0334a0004c0012t0001g0335others(1): Show | 4 | HG01884.hp1 HG02630.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-6251_767-6240d others(14): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413091 | ||||||
| chr12:7413311
|
A | G | 13 | a0001c0004t0001g0315a0001c0004t0001g0316a0001c0004t0001g0322others(10): Show | 13 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.767-6459T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413311 | ||||||
| chr12:7413534
|
C | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.767-6682G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413534 | ||||||
| chr12:7413552
|
C | A | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-6700G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413552 | ||||||
| chr12:7413562
|
T | C | 1 | a0016c0021t0003g0260 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.767-6710A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413562 | ||||||
| chr12:7413694
|
C | T | 1 | a0003c0005t0001g0073 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.767-6842G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413694 | ||||||
| chr12:7413825
|
T | C | 3 | a0001c0004t0001g0116a0001c0004t0002g0115a0001c0027t0002g0023 | 3 | HG02818.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.767-6973A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413825 | ||||||
| chr12:7414266
|
T | C | 2 | a0001c0001t0001g0238a0001c0001t0003g0239 | 2 | HG00733.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.767-7414A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7414266 | ||||||
| chr12:7414325
|
T | G | 1 | a0001c0007t0001g0126 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.767-7473A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7414325 | ||||||
| chr12:7414545
|
AAATT | A | 80 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(77): Show | 83 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.767-7697_767-7694d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7414545 | ||||||
| chr12:7414724
|
A | G | 6 | a0005c0013t0001g0244a0005c0013t0001g0352a0005c0013t0002g0243others(3): Show | 6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.767-7872T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7414724 | ||||||
| chr12:7414799
|
G | A | 2 | a0002c0003t0002g0087a0003c0005t0002g0086 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.767-7947C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7414799 | ||||||
| chr12:7414827
|
A | G | 1 | a0001c0004t0002g0330 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.767-7975T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7414827 | ||||||
| chr12:7414866
|
T | A | 1 | a0008c0011t0001g0122 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.767-8014A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7414866 | ||||||
| chr12:7414960
|
G | T | 89 | a0001c0002t0001g0004a0001c0002t0001g0008a0001c0002t0001g0009others(86): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.767-8108C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7414960 | ||||||
| chr12:7415141
|
T | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.767-8289A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7415141 | ||||||
| chr12:7415152
|
T | C | 5 | a0001c0007t0001g0126a0006c0009t0001g0111a0006c0009t0002g0010others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.767-8300A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7415152 | ||||||
| chr12:7415286
|
T | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(47): Show | 60 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.767-8434A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7415286 | ||||||
| chr12:7415608
|
G | A | 1 | a0001c0002t0001g0298 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.767-8756C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7415608 | ||||||
| chr12:7415762
|
G | A | 1 | a0001c0025t0002g0307 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.767-8910C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7415762 | ||||||
| chr12:7415798
|
G | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(47): Show | 60 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.767-8946C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7415798 | ||||||
| chr12:7416195
|
A | G | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-9343T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7416195 | ||||||
| chr12:7416428
|
T | A | 63 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(60): Show | 65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.767-9576A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7416428 | ||||||
| chr12:7416664
|
C | T | 80 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(77): Show | 83 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.767-9812G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7416664 | ||||||
| chr12:7416849
|
C | T | 13 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(10): Show | 14 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.767-9997G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7416849 | ||||||
| chr12:7417039
|
C | A | 2 | a0006c0009t0001g0032a0006c0009t0001g0033 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.767-10187G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7417039 | ||||||
| chr12:7417086
|
T | C | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-10234A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7417086 | ||||||
| chr12:7417234
|
C | G | 2 | a0003c0005t0002g0026a0003c0005t0002g0027 | 2 | HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.767-10382G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7417234 | ||||||
| chr12:7417382
|
C | T | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.767-10530G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7417382 | ||||||
| chr12:7417422
|
G | T | 19 | a0001c0007t0001g0338a0001c0007t0001g0339a0001c0007t0001g0342others(16): Show | 19 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.767-10570C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7417422 | ||||||
| chr12:7417476
|
C | A | 90 | a0001c0002t0001g0004a0001c0002t0001g0008a0001c0002t0001g0009others(87): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.767-10624G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7417476 | ||||||
| chr12:7417802
|
G | A | 1 | a0004c0006t0001g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.767-10950C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7417802 | ||||||
| chr12:7417825
|
T | A | 6 | a0005c0013t0001g0244a0005c0013t0001g0352a0005c0013t0002g0243others(3): Show | 6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.767-10973A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7417825 | ||||||
| chr12:7417886
|
G | A | 2 | a0001c0002t0001g0292a0001c0002t0003g0297 | 2 | HG00099.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.767-11034C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7417886 | ||||||
| chr12:7417961
|
A | C | 1 | a0001c0001t0001g0130 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.767-11109T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7417961 | ||||||
| chr12:7418001
|
T | TA | 143 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(140): Show | 148 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.767-11150dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418001 | ||||||
| chr12:7418096
|
C | T | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.767-11244G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418096 | ||||||
| chr12:7418117
|
T | C | 1 | a0001c0004t0001g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.767-11265A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418117 | ||||||
| chr12:7418141
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.767-11289G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418141 | ||||||
| chr12:7418234
|
C | G | 2 | a0001c0007t0001g0126a0021c0038t0001g0127 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.767-11382G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418234 | ||||||
| chr12:7418322
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0229 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.767-11470T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418322 | ||||||
| chr12:7418347
|
C | G | 1 | a0001c0004t0002g0324 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.767-11495G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418347 | ||||||
| chr12:7418351
|
C | T | 2 | a0006c0009t0001g0032a0006c0009t0001g0033 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.767-11499G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418351 | ||||||
| chr12:7418416
|
G | A | 63 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(60): Show | 65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.767-11564C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418416 | ||||||
| chr12:7418861
|
A | G | 4 | a0005c0013t0001g0244a0005c0013t0001g0352a0005c0013t0002g0243others(1): Show | 4 | HG02572.hp2 HG02886.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-12009T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418861 | ||||||
| chr12:7418904
|
A | G | 75 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(72): Show | 78 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.767-12052T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418904 | ||||||
| chr12:7418957
|
G | T | 1 | a0003c0005t0001g0025 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.767-12105C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418957 | ||||||
| chr12:7419021
|
C | A | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.767-12169G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7419021 | ||||||
| chr12:7419044
|
T | G | 1 | a0001c0001t0001g0141 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.767-12192A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7419044 | ||||||
| chr12:7419114
|
C | CAAAACAC others(300): Show |
1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.767-12263_767-1226 others(311): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7419114 | ||||||
| chr12:7419391
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.767-12539T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7419391 | ||||||
| chr12:7419409
|
T | C | 63 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(60): Show | 65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.767-12557A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7419409 | ||||||
| chr12:7419462
|
C | T | 1 | a0003c0005t0001g0048 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.767-12610G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7419462 | ||||||
| chr12:7419479
|
T | C | 2 | a0006c0009t0001g0032a0006c0009t0001g0033 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.767-12627A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7419479 | ||||||
| chr12:7419585
|
T | C | 1 | a0001c0004t0002g0330 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.767-12733A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7419585 | ||||||
| chr12:7419657
|
G | C | 17 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(14): Show | 21 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.766+12759C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7419657 | ||||||
| chr12:7419736
|
G | A | 1 | a0025c0040t0001g0069 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.766+12680C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7419736 | ||||||
| chr12:7420184
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.766+12232G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420184 | ||||||
| chr12:7420375
|
A | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.766+12041T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420375 | ||||||
| chr12:7420415
|
C | G | 4 | a0005c0013t0001g0244a0005c0013t0001g0352a0005c0013t0002g0243others(1): Show | 4 | HG02572.hp2 HG02886.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+12001G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420415 | ||||||
| chr12:7420460
|
C | T | 4 | a0001c0007t0001g0338a0001c0007t0001g0339a0001c0007t0001g0342others(1): Show | 4 | HG00639.hp2 HG01123.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+11956G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420460 | ||||||
| chr12:7420475
|
T | A | 80 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(77): Show | 83 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.766+11941A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420475 | ||||||
| chr12:7420519
|
A | C | 17 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(14): Show | 21 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.766+11897T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420519 | ||||||
| chr12:7420550
|
A | C | 90 | a0001c0002t0001g0004a0001c0002t0001g0008a0001c0002t0001g0009others(87): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.766+11866T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420550 | ||||||
| chr12:7420553
|
C | G | 4 | a0001c0007t0001g0338a0001c0007t0001g0339a0001c0007t0001g0342others(1): Show | 4 | HG00639.hp2 HG01123.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+11863G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420553 | ||||||
| chr12:7420757
|
A | C | 1 | a0001c0001t0001g0233 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.766+11659T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420757 | ||||||
| chr12:7420892
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.766+11524G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420892 | ||||||
| chr12:7420902
|
T | C | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0329 | 3 | NA18943.hp1 NA19009.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.766+11514A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420902 | ||||||
| chr12:7420983
|
T | TGGTATAT others(57): Show |
1 | a0014c0019t0001g0129 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.766+11369_766+1143 others(68): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420983 | ||||||
| chr12:7420998
|
T | TATATATA others(77): Show |
1 | a0001c0001t0001g0125 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.766+11417_766+1141 others(88): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420998 | ||||||
| chr12:7420998
|
T | TATATATA others(77): Show |
1 | a0001c0001t0001g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.766+11417_766+1141 others(88): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420998 | ||||||
| chr12:7420998
|
TATATATA others(19): Show |
T | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+11392_766+1141 others(30): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420998 | ||||||
| chr12:7421001
|
ATATATAT others(79): Show |
A | 75 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(72): Show | 78 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.766+11329_766+1141 others(90): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421001 | ||||||
| chr12:7421022
|
T | C | 1 | a0005c0014t0001g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.766+11394A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421022 | ||||||
| chr12:7421024
|
C | CAT | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(150): Show | 166 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.766+11390_766+1139 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421024 | ||||||
| chr12:7421024
|
C | CATATATA others(23): Show |
2 | a0001c0001t0003g0234a0013c0044t0002g0357 | 2 | HG02280.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.766+11391_766+1139 others(34): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421024 | ||||||
| chr12:7421024
|
C | CATATATA others(29): Show |
1 | a0001c0007t0001g0342 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.766+11391_766+1139 others(40): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421024 | ||||||
| chr12:7421025
|
A | G | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11391T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421025 | ||||||
| chr12:7421029
|
ATATATAC others(13): Show |
A | 1 | a0001c0025t0002g0307 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.766+11367_766+1138 others(24): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421029 | ||||||
| chr12:7421030
|
T | C | 2 | a0001c0002t0001g0259a0001c0002t0002g0266 | 2 | NA18965.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.766+11386A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421030 | ||||||
| chr12:7421034
|
T | C | 1 | a0001c0004t0001g0351 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.766+11382A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421034 | ||||||
| chr12:7421036
|
C | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0002g0224others(1): Show | 4 | HG00735.hp2 HG03831.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+11380G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421036 | ||||||
| chr12:7421037
|
G | A | 4 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0002g0224others(1): Show | 4 | HG00735.hp2 HG03831.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+11379C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421037 | ||||||
| chr12:7421038
|
T | C | 4 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0002g0224others(1): Show | 4 | HG00735.hp2 HG03831.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+11378A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421038 | ||||||
| chr12:7421039
|
G | A | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11377C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421039 | ||||||
| chr12:7421041
|
A | ATATATAT others(19): Show |
2 | a0001c0001t0001g0210a0001c0001t0001g0228 | 2 | NA18961.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.766+11374_766+1137 others(30): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421041 | ||||||
| chr12:7421041
|
A | G | 4 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0002g0224others(1): Show | 4 | HG00735.hp2 HG03831.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+11375T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421041 | ||||||
| chr12:7421045
|
A | ATATACAT others(47): Show |
3 | a0001c0001t0001g0192a0001c0001t0001g0204a0001c0001t0001g0215 | 3 | HG02135.hp2 HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.766+11370_766+1137 others(58): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421045 | ||||||
| chr12:7421045
|
A | ATATACAT others(107): Show |
2 | a0006c0009t0001g0032a0006c0009t0001g0033 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.766+11370_766+1137 others(118): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421045 | ||||||
| chr12:7421045
|
A | ATATACAT others(79): Show |
1 | a0001c0001t0001g0101 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.766+11370_766+1137 others(90): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421045 | ||||||
| chr12:7421045
|
A | ATATACAT others(51): Show |
2 | a0001c0001t0001g0099a0001c0001t0002g0100 | 2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.766+11370_766+1137 others(62): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421045 | ||||||
| chr12:7421045
|
A | ATATACAT others(49): Show |
47 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0107others(44): Show | 49 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.766+11370_766+1137 others(60): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421045 | ||||||
| chr12:7421045
|
A | ATATACAT others(81): Show |
2 | a0001c0001t0001g0205a0001c0001t0001g0213 | 2 | HG01952.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.766+11370_766+1137 others(92): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421045 | ||||||
| chr12:7421045
|
A | ATATATAC others(51): Show |
1 | a0001c0001t0002g0190 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.766+11370_766+1137 others(62): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421045 | ||||||
| chr12:7421045
|
A | G | 3 | a0004c0006t0002g0333a0004c0012t0001g0334a0004c0012t0001g0335 | 3 | HG01884.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.766+11371T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421045 | ||||||
| chr12:7421047
|
A | ATACATAT others(49): Show |
1 | a0004c0012t0002g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.766+11368_766+1136 others(60): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421047 | ||||||
| chr12:7421048
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.766+11368A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421048 | ||||||
| chr12:7421049
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0016others(107): Show | 122 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(119): Show |
intron_variant | MODIFIER | c.766+11367C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421049 | ||||||
| chr12:7421049
|
G | GTATATAC others(23): Show |
1 | a0001c0029t0001g0117 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.766+11366_766+1136 others(34): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421049 | ||||||
| chr12:7421049
|
G | GTATATAC others(23): Show |
1 | a0001c0001t0001g0130 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.766+11337_766+1136 others(34): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421049 | ||||||
| chr12:7421049
|
G | GTATATAC others(139): Show |
2 | a0006c0009t0002g0010a0006c0034t0001g0118 | 3 | HG01167.hp1 HG01169.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.766+11366_766+1136 others(150): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421049 | ||||||
| chr12:7421049
|
G | GTATATAC others(65): Show |
2 | a0001c0007t0001g0126a0021c0038t0001g0127 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.766+11366_766+1136 others(76): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421049 | ||||||
| chr12:7421050
|
T | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(47): Show | 60 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.766+11366A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421050 | ||||||
| chr12:7421055
|
ACG | A | 2 | a0001c0007t0001g0152a0001c0007t0002g0013 | 3 | HG01256.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.766+11359_766+1136 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421055 | ||||||
| chr12:7421056
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(46): Show | 58 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.766+11360G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421056 | ||||||
| chr12:7421057
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(45): Show | 57 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+11359C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421057 | ||||||
| chr12:7421057
|
G | GTA | 57 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(54): Show | 59 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.766+11357_766+1135 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421057 | ||||||
| chr12:7421057
|
G | GTATATAT others(49): Show |
1 | a0001c0001t0001g0195 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.766+11358_766+1135 others(60): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421057 | ||||||
| chr12:7421057
|
G | GTATATAT others(87): Show |
1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.766+11358_766+1135 others(98): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421057 | ||||||
| chr12:7421057
|
G | GTATATAT others(27): Show |
1 | a0001c0001t0002g0224 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.766+11358_766+1135 others(38): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421057 | ||||||
| chr12:7421057
|
G | GTATATAT others(57): Show |
2 | a0001c0001t0001g0189a0024c0036t0002g0198 | 2 | HG03831.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.766+11358_766+1135 others(68): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421057 | ||||||
| chr12:7421062
|
T | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(45): Show | 57 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+11354A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421062 | ||||||
| chr12:7421063
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(45): Show | 57 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+11353T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421063 | ||||||
| chr12:7421064
|
T | C | 2 | a0001c0007t0001g0152a0001c0007t0002g0013 | 3 | HG01256.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.766+11352A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421064 | ||||||
| chr12:7421064
|
T | TGTATATA others(57): Show |
1 | a0001c0001t0001g0187 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.766+11351_766+1135 others(68): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421064 | ||||||
| chr12:7421065
|
G | A | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11351C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421065 | ||||||
| chr12:7421067
|
A | G | 2 | a0001c0007t0001g0152a0001c0007t0002g0013 | 3 | HG01256.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.766+11349T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421067 | ||||||
| chr12:7421073
|
ACG | A | 2 | a0001c0007t0001g0152a0001c0007t0002g0013 | 3 | HG01256.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.766+11341_766+1134 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421073 | ||||||
| chr12:7421073
|
ACGTATAT others(41): Show |
A | 48 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(45): Show | 57 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+11295_766+1134 others(52): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421073 | ||||||
| chr12:7421074
|
CGT | C | 15 | a0001c0007t0001g0338a0001c0007t0001g0339a0001c0007t0001g0342others(12): Show | 15 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.766+11340_766+1134 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421074 | ||||||
| chr12:7421075
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.766+11341C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421075 | ||||||
| chr12:7421077
|
A | ATATATAC others(19): Show |
3 | a0004c0006t0002g0333a0004c0012t0001g0334a0004c0012t0001g0335 | 3 | HG01884.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.766+11338_766+1133 others(30): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421077 | ||||||
| chr12:7421077
|
A | ATATATAT others(23): Show |
2 | a0001c0001t0001g0210a0001c0001t0001g0228 | 2 | NA18961.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.766+11338_766+1133 others(34): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421077 | ||||||
| chr12:7421080
|
T | C | 2 | a0001c0007t0001g0152a0001c0007t0002g0013 | 3 | HG01256.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.766+11336A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421080 | ||||||
| chr12:7421085
|
ACG | A | 2 | a0001c0007t0001g0152a0001c0007t0002g0013 | 3 | HG01256.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.766+11329_766+1133 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421085 | ||||||
| chr12:7421087
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.766+11329C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421087 | ||||||
| chr12:7421089
|
A | ATATATGT others(227): Show |
1 | a0006c0009t0001g0111 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.766+11326_766+1132 others(238): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421089 | ||||||
| chr12:7421093
|
A | T | 75 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(72): Show | 78 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.766+11323T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421093 | ||||||
| chr12:7421094
|
T | C | 2 | a0001c0007t0001g0152a0001c0007t0002g0013 | 3 | HG01256.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.766+11322A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421094 | ||||||
| chr12:7421095
|
A | G | 77 | a0001c0007t0001g0152a0001c0007t0002g0013a0002c0003t0001g0005others(74): Show | 81 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.766+11321T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421095 | ||||||
| chr12:7421096
|
T | TACGTATA others(109): Show |
1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11319_766+1132 others(120): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421096 | ||||||
| chr12:7421097
|
G | A | 75 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(72): Show | 78 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.766+11319C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421097 | ||||||
| chr12:7421105
|
ACATTTGG others(9): Show |
A | 2 | a0001c0007t0001g0152a0001c0007t0002g0013 | 3 | HG01256.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.766+11295_766+1131 others(20): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421105 | ||||||
| chr12:7421123
|
A | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(47): Show | 60 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.766+11293T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421123 | ||||||
| chr12:7421139
|
G | GTA | 353 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(350): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.766+11275_766+1127 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421139 | ||||||
| chr12:7421153
|
A | T | 1 | a0002c0003t0001g0057 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.766+11263T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421153 | ||||||
| chr12:7421154
|
A | T | 2 | a0002c0003t0001g0090a0002c0003t0001g0091 | 2 | NA18943.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.766+11262T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421154 | ||||||
| chr12:7421195
|
G | GTA | 5 | a0001c0001t0001g0103a0001c0001t0001g0160a0001c0001t0001g0161others(2): Show | 5 | NA18945.hp1 NA18952.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.766+11219_766+1122 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421195 | ||||||
| chr12:7421241
|
T | C | 1 | a0001c0002t0002g0295 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.766+11175A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421241 | ||||||
| chr12:7421271
|
A | ATG | 5 | a0002c0003t0001g0024a0002c0003t0001g0072a0003c0005t0001g0025others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.766+11143_766+1114 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421271 | ||||||
| chr12:7421274
|
T | C | 1 | a0001c0004t0002g0330 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.766+11142A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421274 | ||||||
| chr12:7421277
|
GTA | G | 8 | a0001c0001t0002g0232a0001c0007t0001g0097a0001c0008t0001g0240others(5): Show | 8 | HG02572.hp2 HG02886.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.766+11137_766+1113 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421277 | ||||||
| chr12:7421287
|
A | ATG | 74 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(71): Show | 77 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.766+11127_766+1112 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421287 | ||||||
| chr12:7421287
|
A | G | 5 | a0002c0003t0001g0024a0002c0003t0001g0072a0003c0005t0001g0025others(2): Show | 5 | HG02109.hp2 HG02615.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.766+11129T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421287 | ||||||
| chr12:7421291
|
GTGTATAT others(47): Show |
G | 18 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(15): Show | 22 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.766+11071_766+1112 others(58): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421291 | ||||||
| chr12:7421298
|
TATGTATA others(39): Show |
T | 1 | a0001c0001t0001g0128 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.766+11072_766+1111 others(50): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421298 | ||||||
| chr12:7421304
|
TATATACA others(74): Show |
T | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+11031_766+1111 others(85): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421304 | ||||||
| chr12:7421328
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.766+11088C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421328 | ||||||
| chr12:7421329
|
T | C | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.766+11087A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421329 | ||||||
| chr12:7421330
|
A | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0220 | 2 | HG01975.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.766+11086T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421330 | ||||||
| chr12:7421347
|
G | GTA | 43 | a0002c0003t0001g0034a0002c0003t0001g0043a0002c0003t0001g0057others(40): Show | 43 | HG00423.hp1 HG00738.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.766+11067_766+1106 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421347 | ||||||
| chr12:7421352
|
T | C | 2 | a0006c0009t0001g0032a0006c0009t0001g0033 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.766+11064A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421352 | ||||||
| chr12:7421355
|
ATGTG | A | 15 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(12): Show | 16 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.766+11057_766+1106 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421355 | ||||||
| chr12:7421357
|
G | A | 31 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(28): Show | 34 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.766+11059C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421357 | ||||||
| chr12:7421359
|
G | A | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11057C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421359 | ||||||
| chr12:7421360
|
T | C | 14 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(11): Show | 15 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.766+11056A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421360 | ||||||
| chr12:7421361
|
A | G | 31 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(28): Show | 34 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.766+11055T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421361 | ||||||
| chr12:7421365
|
A | G | 1 | a0003c0005t0001g0048 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.766+11051T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421365 | ||||||
| chr12:7421366
|
TGTATATA others(37): Show |
T | 31 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(28): Show | 34 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.766+11006_766+1104 others(48): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421366 | ||||||
| chr12:7421368
|
T | TAC | 13 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(10): Show | 14 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.766+11047_766+1104 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421368 | ||||||
| chr12:7421370
|
T | C | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.766+11046A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421370 | ||||||
| chr12:7421372
|
TATACATT others(31): Show |
T | 1 | a0003c0005t0001g0048 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.766+11006_766+1104 others(42): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421372 | ||||||
| chr12:7421375
|
ACATTTGG others(31): Show |
A | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.766+11003_766+1104 others(42): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421375 | ||||||
| chr12:7421376
|
CATTTGGA others(4): Show |
C | 43 | a0002c0003t0001g0034a0002c0003t0001g0043a0002c0003t0001g0057others(40): Show | 43 | HG00423.hp1 HG00738.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.766+11029_766+1103 others(15): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421376 | ||||||
| chr12:7421378
|
TTTGGA | T | 13 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(10): Show | 14 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.766+11033_766+1103 others(9): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421378 | ||||||
| chr12:7421379
|
T | A | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11037A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421379 | ||||||
| chr12:7421382
|
G | T | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11034C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421382 | ||||||
| chr12:7421385
|
G | T | 14 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(11): Show | 15 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.766+11031C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421385 | ||||||
| chr12:7421387
|
T | C | 14 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(11): Show | 15 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.766+11029A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421387 | ||||||
| chr12:7421396
|
A | G | 67 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(64): Show | 69 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.766+11020T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421396 | ||||||
| chr12:7421397
|
T | C | 57 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(54): Show | 58 | HG00140.hp2 HG00423.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.766+11019A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421397 | ||||||
| chr12:7421398
|
ATATATCT others(8): Show |
A | 1 | a0002c0003t0002g0047 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.766+11003_766+1101 others(19): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421398 | ||||||
| chr12:7421400
|
ATATCTTC others(6): Show |
A | 42 | a0002c0003t0001g0034a0002c0003t0001g0043a0002c0003t0001g0057others(39): Show | 42 | HG00423.hp1 HG00738.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.766+11003_766+1101 others(17): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421400 | ||||||
| chr12:7421403
|
TCTTCCAA | T | 17 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(14): Show | 18 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.766+11006_766+1101 others(11): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421403 | ||||||
| chr12:7421404
|
C | A | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11012G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421404 | ||||||
| chr12:7421406
|
T | A | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11010A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421406 | ||||||
| chr12:7421408
|
C | T | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11008G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421408 | ||||||
| chr12:7421410
|
A | T | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11006T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421410 | ||||||
| chr12:7421412
|
T | C | 13 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(10): Show | 14 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.766+11004A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421412 | ||||||
| chr12:7421413
|
G | A | 13 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(10): Show | 14 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.766+11003C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421413 | ||||||
| chr12:7421416
|
T | C | 4 | a0001c0001t0002g0331a0002c0003t0001g0034a0002c0003t0002g0035others(1): Show | 4 | HG02451.hp2 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+11000A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421416 | ||||||
| chr12:7421416
|
TATATACA others(17): Show |
T | 1 | a0001c0025t0002g0307 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.766+10976_766+1099 others(28): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421416 | ||||||
| chr12:7421420
|
T | C | 1 | a0003c0005t0001g0065 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.766+10996A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421420 | ||||||
| chr12:7421427
|
A | G | 1 | a0002c0003t0002g0071 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.766+10989T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421427 | ||||||
| chr12:7421434
|
TATATAC | T | 17 | a0001c0001t0001g0192a0001c0001t0001g0233a0001c0001t0001g0238others(14): Show | 18 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.766+10976_766+1098 others(10): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421434 | ||||||
| chr12:7421438
|
TAC | T | 23 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(20): Show | 25 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.766+10976_766+1097 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421438 | ||||||
| chr12:7421440
|
C | CATATACA others(21): Show |
4 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0214others(1): Show | 4 | HG01975.hp2 HG02004.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+10948_766+1097 others(32): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421440 | ||||||
| chr12:7421440
|
C | T | 2 | a0002c0003t0003g0050a0002c0003t0003g0051 | 2 | HG03688.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.766+10976G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421440 | ||||||
| chr12:7421453
|
G | A | 13 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(10): Show | 14 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.766+10963C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421453 | ||||||
| chr12:7421454
|
T | C | 13 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(10): Show | 14 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.766+10962A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421454 | ||||||
| chr12:7421456
|
C | T | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+10960G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421456 | ||||||
| chr12:7421456
|
CAT | C | 4 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0002g0247others(1): Show | 4 | HG00558.hp2 NA18964.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+10958_766+1095 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421456 | ||||||
| chr12:7421458
|
TATATACA others(37): Show |
T | 1 | a0002c0003t0001g0049 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.766+10914_766+1095 others(48): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421458 | ||||||
| chr12:7421461
|
A | ATG | 5 | a0001c0007t0001g0126a0006c0009t0001g0111a0006c0009t0002g0010others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.766+10954_766+1095 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421461 | ||||||
| chr12:7421461
|
A | G | 2 | a0003c0033t0002g0123a0011c0015t0001g0267 | 2 | HG01891.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.766+10955T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421461 | ||||||
| chr12:7421462
|
TAC | T | 7 | a0002c0003t0001g0024a0003c0005t0002g0026a0003c0005t0002g0027others(4): Show | 7 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.766+10952_766+1095 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421462 | ||||||
| chr12:7421463
|
A | G | 12 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(9): Show | 13 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.766+10953T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421463 | ||||||
| chr12:7421464
|
C | CAT | 6 | a0001c0002t0002g0256a0005c0013t0001g0244a0005c0013t0001g0352others(3): Show | 6 | HG01167.hp2 HG02572.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.766+10950_766+1095 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421464 | ||||||
| chr12:7421464
|
C | T | 12 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(9): Show | 13 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.766+10952G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421464 | ||||||
| chr12:7421464
|
CAT | C | 20 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(17): Show | 24 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.766+10950_766+1095 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421464 | ||||||
| chr12:7421464
|
CATAT | C | 76 | a0001c0001t0001g0016a0001c0001t0001g0229a0001c0002t0002g0295others(73): Show | 80 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.766+10948_766+1095 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421464 | ||||||
| chr12:7421464
|
CATATATA others(55): Show |
C | 3 | a0002c0003t0001g0034a0002c0003t0002g0035a0002c0032t0001g0036 | 3 | HG02723.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.766+10890_766+1095 others(66): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421464 | ||||||
| chr12:7421466
|
T | C | 12 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(9): Show | 13 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.766+10950A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421466 | ||||||
| chr12:7421467
|
ATATATAC others(7): Show |
A | 1 | a0001c0002t0001g0293 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.766+10935_766+1094 others(18): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421467 | ||||||
| chr12:7421468
|
T | C | 7 | a0002c0003t0001g0024a0003c0005t0002g0026a0003c0005t0002g0027others(4): Show | 7 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.766+10948A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421468 | ||||||
| chr12:7421468
|
T | TAC | 5 | a0001c0007t0001g0126a0006c0009t0001g0111a0006c0009t0002g0010others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.766+10947_766+1094 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421468 | ||||||
| chr12:7421468
|
T | TATATATA others(1): Show |
3 | a0001c0001t0001g0146a0001c0001t0001g0158a0007c0010t0001g0176 | 3 | HG01433.hp2 HG01993.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.766+10947_766+1094 others(12): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421468 | ||||||
| chr12:7421470
|
T | C | 3 | a0001c0001t0001g0222a0001c0002t0003g0278a0005c0030t0003g0309 | 3 | HG00140.hp1 HG01243.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.766+10946A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421470 | ||||||
| chr12:7421471
|
A | G | 1 | a0001c0008t0001g0240 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.766+10945T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421471 | ||||||
| chr12:7421472
|
TAC | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(38): Show | 51 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.766+10942_766+1094 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421472 | ||||||
| chr12:7421474
|
CATAT | C | 17 | a0001c0007t0001g0338a0001c0007t0001g0339a0001c0007t0003g0349others(14): Show | 17 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.766+10938_766+1094 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421474 | ||||||
| chr12:7421477
|
ATATG | A | 6 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(3): Show | 6 | HG02148.hp1 NA18954.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.766+10935_766+1093 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421477 | ||||||
| chr12:7421478
|
T | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(38): Show | 51 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.766+10938A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421478 | ||||||
| chr12:7421481
|
G | A | 41 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(38): Show | 51 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.766+10935C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421481 | ||||||
| chr12:7421484
|
C | CATATATA others(21): Show |
1 | a0001c0001t0001g0158 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.766+10931_766+1093 others(32): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421484 | ||||||
| chr12:7421486
|
T | C | 1 | a0001c0008t0001g0240 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.766+10930A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421486 | ||||||
| chr12:7421486
|
T | TATATAC | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0104others(2): Show | 7 | HG02135.hp1 NA18948.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.766+10924_766+1092 others(10): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421486 | ||||||
| chr12:7421486
|
TATATACA others(9): Show |
T | 28 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(25): Show | 30 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.766+10914_766+1092 others(20): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421486 | ||||||
| chr12:7421490
|
T | C | 12 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(9): Show | 13 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.766+10926A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421490 | ||||||
| chr12:7421491
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(44): Show | 57 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+10925T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421491 | ||||||
| chr12:7421492
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(44): Show | 57 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+10924G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421492 | ||||||
| chr12:7421492
|
CATATATG others(27): Show |
C | 41 | a0002c0003t0001g0043a0002c0003t0001g0057a0002c0003t0001g0067others(38): Show | 42 | HG00423.hp1 HG00738.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.766+10890_766+1092 others(38): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421492 | ||||||
| chr12:7421494
|
T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(44): Show | 57 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+10922A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421494 | ||||||
| chr12:7421494
|
T | TATATATA others(5): Show |
1 | a0001c0001t0001g0146 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.766+10921_766+1092 others(16): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421494 | ||||||
| chr12:7421494
|
TATATGTA others(7): Show |
T | 18 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(15): Show | 22 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.766+10908_766+1092 others(18): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421494 | ||||||
| chr12:7421496
|
TATGTACA others(5): Show |
T | 28 | a0001c0002t0001g0303a0001c0002t0001g0306a0001c0002t0002g0295others(25): Show | 29 | HG00140.hp1 HG00639.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.766+10908_766+1091 others(16): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421496 | ||||||
| chr12:7421499
|
G | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0016others(121): Show | 138 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.766+10917C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421499 | ||||||
| chr12:7421502
|
C | CAT | 5 | a0002c0003t0001g0024a0003c0005t0001g0025a0003c0005t0002g0026others(2): Show | 5 | HG02109.hp1 HG02615.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.766+10912_766+1091 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421502 | ||||||
| chr12:7421502
|
C | CATATATG others(5): Show |
2 | a0001c0001t0001g0101a0001c0001t0002g0100 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.766+10913_766+1091 others(16): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421502 | ||||||
| chr12:7421502
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.766+10914G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421502 | ||||||
| chr12:7421504
|
T | TATATAC | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0104others(2): Show | 7 | HG02135.hp1 NA18948.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.766+10911_766+1091 others(10): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421504 | ||||||
| chr12:7421505
|
A | G | 1 | a0004c0006t0001g0343 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.766+10911T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421505 | ||||||
| chr12:7421506
|
T | TATGTAC | 3 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0229 | 4 | HG02055.hp1 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+10909_766+1091 others(10): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421506 | ||||||
| chr12:7421506
|
TAC | T | 4 | a0001c0002t0001g0293a0002c0003t0001g0070a0003c0005t0001g0048others(1): Show | 4 | HG01891.hp2 HG03471.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+10908_766+1090 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421506 | ||||||
| chr12:7421508
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0016others(52): Show | 68 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(65): Show |
intron_variant | MODIFIER | c.766+10908G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421508 | ||||||
| chr12:7421511
|
A | ATATACAT others(5): Show |
1 | a0004c0006t0001g0343 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.766+10904_766+1090 others(16): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421511 | ||||||
| chr12:7421511
|
A | G | 2 | a0002c0003t0001g0070a0003c0005t0001g0048 | 2 | HG03471.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.766+10905T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421511 | ||||||
| chr12:7421512
|
T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(44): Show | 57 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+10904A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421512 | ||||||
| chr12:7421516
|
T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(44): Show | 57 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+10900A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421516 | ||||||
| chr12:7421521
|
G | A | 2 | a0006c0009t0001g0032a0006c0009t0001g0033 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.766+10895C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421521 | ||||||
| chr12:7421522
|
TAC | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(44): Show | 57 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+10892_766+1089 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421522 | ||||||
| chr12:7421523
|
A | G | 12 | a0001c0002t0001g0252a0001c0002t0001g0253a0001c0002t0001g0259others(9): Show | 12 | HG00408.hp2 HG00423.hp2 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.766+10893T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421523 | ||||||
| chr12:7421526
|
T | C | 6 | a0002c0003t0001g0024a0002c0003t0001g0070a0003c0005t0001g0025others(3): Show | 6 | HG02615.hp2 HG02895.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.766+10890A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421526 | ||||||
| chr12:7421526
|
T | TATAC | 3 | a0001c0001t0001g0016a0001c0001t0001g0220a0001c0001t0001g0229 | 4 | HG02004.hp1 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+10889_766+1089 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421526 | ||||||
| chr12:7421529
|
A | ATGTACAT others(53): Show |
1 | a0001c0001t0001g0099 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.766+10886_766+1088 others(64): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421529 | ||||||
| chr12:7421536
|
TACGTACA others(1): Show |
T | 9 | a0001c0001t0001g0197a0001c0001t0001g0203a0001c0001t0001g0204others(6): Show | 9 | HG01952.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.766+10872_766+1087 others(12): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421536 | ||||||
| chr12:7421537
|
ACG | A | 13 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0104others(10): Show | 16 | HG00140.hp1 HG00544.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.766+10877_766+1087 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421537 | ||||||
| chr12:7421538
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(217): Show | 239 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(236): Show |
intron_variant | MODIFIER | c.766+10878G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421538 | ||||||
| chr12:7421538
|
CGTACACA others(25): Show |
C | 4 | a0002c0003t0001g0024a0003c0005t0001g0025a0003c0005t0002g0026others(1): Show | 4 | HG02615.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+10846_766+1087 others(36): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421538 | ||||||
| chr12:7421539
|
G | A | 2 | a0001c0001t0001g0146a0007c0010t0001g0176 | 2 | HG01993.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.766+10877C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421539 | ||||||
| chr12:7421540
|
TAC | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 151 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.766+10874_766+1087 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421540 | ||||||
| chr12:7421542
|
C | CACACATA others(19): Show |
2 | a0001c0001t0001g0146a0007c0010t0001g0176 | 2 | HG01993.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.766+10873_766+1087 others(30): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421542 | ||||||
| chr12:7421542
|
C | CATATACA others(31): Show |
4 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0001g0195others(1): Show | 4 | HG03831.hp1 NA18966.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+10873_766+1087 others(42): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421542 | ||||||
| chr12:7421542
|
C | CATATACA others(25): Show |
1 | a0001c0004t0002g0115 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.766+10873_766+1087 others(36): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421542 | ||||||
| chr12:7421542
|
C | T | 13 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0104others(10): Show | 16 | HG00140.hp1 HG00544.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.766+10874G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421542 | ||||||
| chr12:7421544
|
C | T | 7 | a0001c0001t0001g0016a0001c0001t0001g0229a0003c0033t0002g0123others(4): Show | 8 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.766+10872G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421544 | ||||||
| chr12:7421547
|
A | G | 8 | a0001c0001t0001g0197a0001c0001t0001g0203a0001c0001t0001g0204others(5): Show | 8 | HG01952.hp1 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.766+10869T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421547 | ||||||
| chr12:7421550
|
C | T | 8 | a0001c0001t0001g0197a0001c0001t0001g0203a0001c0001t0001g0204others(5): Show | 8 | HG01952.hp1 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.766+10866G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421550 | ||||||
| chr12:7421556
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0229 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.766+10860G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421556 | ||||||
| chr12:7421557
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0229 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.766+10859T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421557 | ||||||
| chr12:7421559
|
A | G | 71 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(68): Show | 74 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.766+10857T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421559 | ||||||
| chr12:7421560
|
T | C | 1 | a0001c0002t0002g0290 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.766+10856A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421560 | ||||||
| chr12:7421560
|
TATGTACA others(7): Show |
T | 2 | a0003c0005t0001g0006a0003c0005t0001g0062 | 3 | HG01099.hp1 HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.766+10842_766+1085 others(18): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421560 | ||||||
| chr12:7421562
|
T | C | 12 | a0001c0001t0001g0158a0001c0001t0001g0197a0001c0001t0001g0203others(9): Show | 12 | HG01433.hp2 HG01952.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.766+10854A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421562 | ||||||
| chr12:7421563
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0229 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.766+10853C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421563 | ||||||
| chr12:7421565
|
A | G | 5 | a0001c0001t0001g0166a0007c0010t0001g0014a0007c0010t0001g0174others(2): Show | 6 | HG02027.hp2 NA18747.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.766+10851T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421565 | ||||||
| chr12:7421568
|
T | C | 9 | a0001c0001t0001g0158a0001c0001t0001g0197a0001c0001t0001g0203others(6): Show | 9 | HG01433.hp2 HG01952.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.766+10848A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421568 | ||||||
| chr12:7421570
|
TATAC | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0229 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.766+10842_766+1084 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421570 | ||||||
| chr12:7421573
|
A | G | 4 | a0002c0003t0001g0024a0003c0005t0001g0025a0003c0005t0002g0026others(1): Show | 4 | HG02615.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+10843T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421573 | ||||||
| chr12:7421574
|
C | CATATACA others(3): Show |
4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+10841_766+1084 others(14): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421574 | ||||||
| chr12:7421574
|
C | T | 4 | a0002c0003t0001g0024a0003c0005t0001g0025a0003c0005t0002g0026others(1): Show | 4 | HG02615.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+10842G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421574 | ||||||
| chr12:7421576
|
T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0229 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.766+10840A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421576 | ||||||
| chr12:7421576
|
T | TATAC | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 176 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(173): Show |
intron_variant | MODIFIER | c.766+10839_766+1084 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421576 | ||||||
| chr12:7421577
|
G | A | 9 | a0001c0001t0001g0158a0001c0001t0001g0197a0001c0001t0001g0203others(6): Show | 9 | HG01433.hp2 HG01952.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.766+10839C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421577 | ||||||
| chr12:7421582
|
T | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(161): Show | 183 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(180): Show |
intron_variant | MODIFIER | c.766+10834A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421582 | ||||||
| chr12:7421584
|
TATAC | T | 9 | a0001c0001t0001g0158a0001c0001t0001g0197a0001c0001t0001g0203others(6): Show | 9 | HG01433.hp2 HG01952.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.766+10828_766+1083 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421584 | ||||||
| chr12:7421588
|
CATATACA others(29): Show |
C | 103 | a0001c0001t0001g0101a0001c0001t0001g0233a0001c0001t0001g0238others(100): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.766+10792_766+1082 others(40): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421588 | ||||||
| chr12:7421590
|
T | A | 6 | a0004c0006t0001g0343a0004c0006t0001g0344a0004c0006t0001g0345others(3): Show | 6 | HG00673.hp2 NA18612.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.766+10826A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421590 | ||||||
| chr12:7421591
|
A | G | 9 | a0001c0001t0001g0158a0001c0001t0001g0197a0001c0001t0001g0203others(6): Show | 9 | HG01433.hp2 HG01952.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.766+10825T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421591 | ||||||
| chr12:7421597
|
A | G | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+10819T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421597 | ||||||
| chr12:7421600
|
TGTAC | T | 9 | a0001c0001t0001g0158a0001c0001t0001g0197a0001c0001t0001g0203others(6): Show | 9 | HG01433.hp2 HG01952.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.766+10812_766+1081 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421600 | ||||||
| chr12:7421606
|
C | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(160): Show | 182 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.766+10810G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421606 | ||||||
| chr12:7421609
|
A | G | 9 | a0001c0001t0001g0158a0001c0001t0001g0197a0001c0001t0001g0203others(6): Show | 9 | HG01433.hp2 HG01952.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.766+10807T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421609 | ||||||
| chr12:7421610
|
TACATATA others(23): Show |
T | 48 | a0002c0003t0001g0024a0002c0003t0001g0034a0002c0003t0001g0043others(45): Show | 48 | HG00423.hp1 HG00738.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.766+10776_766+1080 others(34): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421610 | ||||||
| chr12:7421613
|
A | ATG | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 181 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(178): Show |
intron_variant | MODIFIER | c.766+10802_766+1080 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421613 | ||||||
| chr12:7421616
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 181 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(178): Show |
intron_variant | MODIFIER | c.766+10800A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421616 | ||||||
| chr12:7421616
|
T | TAC | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+10799_766+1080 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421616 | ||||||
| chr12:7421618
|
T | C | 30 | a0001c0004t0001g0116a0001c0004t0002g0115a0001c0027t0002g0023others(27): Show | 33 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.766+10798A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421618 | ||||||
| chr12:7421618
|
TGTAC | T | 9 | a0001c0001t0001g0158a0001c0001t0001g0197a0001c0001t0001g0203others(6): Show | 9 | HG01433.hp2 HG01952.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.766+10794_766+1079 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421618 | ||||||
| chr12:7421619
|
G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 215 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(212): Show |
intron_variant | MODIFIER | c.766+10797C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421619 | ||||||
| chr12:7421622
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 215 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(212): Show |
intron_variant | MODIFIER | c.766+10794G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421622 | ||||||
| chr12:7421624
|
T | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(172): Show | 194 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(191): Show |
intron_variant | MODIFIER | c.766+10792A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421624 | ||||||
| chr12:7421624
|
T | TATATACA others(85): Show |
1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+10791_766+1079 others(96): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421624 | ||||||
| chr12:7421624
|
TATATACA others(11): Show |
T | 1 | a0001c0002t0001g0283 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.766+10774_766+1079 others(22): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421624 | ||||||
| chr12:7421625
|
A | G | 27 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(24): Show | 30 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.766+10791T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421625 | ||||||
| chr12:7421626
|
T | C | 1 | a0005c0014t0001g0109 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.766+10790A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421626 | ||||||
| chr12:7421628
|
T | C | 27 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(24): Show | 30 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.766+10788A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421628 | ||||||
| chr12:7421634
|
TATGTAC | T | 27 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(24): Show | 30 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.766+10776_766+1078 others(10): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421634 | ||||||
| chr12:7421640
|
C | CACATAT | 3 | a0003c0033t0002g0123a0010c0042t0002g0354a0010c0043t0001g0353 | 3 | HG01891.hp2 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.766+10770_766+1077 others(10): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421640 | ||||||
| chr12:7421654
|
T | C | 1 | a0001c0002t0001g0283 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.766+10762A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421654 | ||||||
| chr12:7421657
|
A | G | 1 | a0001c0002t0001g0283 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.766+10759T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421657 | ||||||
| chr12:7421686
|
T | C | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+10730A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421686 | ||||||
| chr12:7421686
|
TATAC | T | 4 | a0005c0013t0001g0244a0005c0013t0001g0352a0005c0013t0002g0243others(1): Show | 4 | HG02572.hp2 HG02886.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+10726_766+1072 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421686 | ||||||
| chr12:7421720
|
C | T | 3 | a0001c0004t0001g0116a0001c0004t0002g0115a0001c0027t0002g0023 | 3 | HG02818.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.766+10696G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421720 | ||||||
| chr12:7421745
|
GTA | G | 5 | a0001c0001t0002g0331a0001c0002t0001g0279a0003c0033t0002g0123others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.766+10669_766+1067 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421745 | ||||||
| chr12:7421745
|
GTATA | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(240): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.766+10667_766+1067 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421745 | ||||||
| chr12:7421745
|
GTATATA | G | 7 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0134others(4): Show | 9 | HG01358.hp1 HG02280.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.766+10665_766+1067 others(10): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421745 | ||||||
| chr12:7421747
|
A | G | 7 | a0001c0007t0001g0126a0002c0003t0001g0089a0003c0005t0001g0044others(4): Show | 8 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.766+10669T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421747 | ||||||
| chr12:7421749
|
A | G | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+10667T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421749 | ||||||
| chr12:7421760
|
TATATA | T | 5 | a0001c0001t0001g0233a0001c0001t0002g0232a0001c0007t0001g0097others(2): Show | 5 | HG00140.hp2 HG03041.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.766+10651_766+1065 others(9): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421760 | ||||||
| chr12:7421760
|
TATATATA others(2): Show |
T | 17 | a0002c0003t0001g0024a0002c0003t0001g0038a0002c0003t0001g0043others(14): Show | 17 | HG00408.hp1 HG01243.hp1 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.766+10647_766+1065 others(13): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421760 | ||||||
| chr12:7421761
|
ATATATAT others(2): Show |
A | 54 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(51): Show | 57 | HG00423.hp1 HG00673.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.766+10646_766+1065 others(13): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421761 | ||||||
| chr12:7421761
|
ATATATAT others(3): Show |
A | 1 | a0002c0003t0002g0083 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.766+10645_766+1065 others(14): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421761 | ||||||
| chr12:7421762
|
TATATA | T | 10 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0238others(7): Show | 11 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.766+10649_766+1065 others(9): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421762 | ||||||
| chr12:7421762
|
TATATATA | T | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+10647_766+1065 others(11): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421762 | ||||||
| chr12:7421763
|
ATATATAT others(2): Show |
A | 3 | a0002c0003t0001g0057a0002c0003t0002g0084a0003c0005t0003g0058 | 3 | HG00738.hp1 HG02129.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.766+10644_766+1065 others(13): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421763 | ||||||
| chr12:7421764
|
TATA | T | 3 | a0006c0009t0001g0111a0006c0009t0002g0010a0006c0034t0001g0118 | 4 | HG01167.hp1 HG01169.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+10649_766+1065 others(7): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421764 | ||||||
| chr12:7421765
|
A | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0103a0001c0001t0001g0128others(47): Show | 58 | HG00099.hp2 HG00423.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.766+10651T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421765 | ||||||
| chr12:7421767
|
A | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0016others(199): Show | 217 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.766+10649T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421767 | ||||||
| chr12:7421769
|
A | T | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.766+10647T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421769 | ||||||
| chr12:7421776
|
C | T | 79 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.766+10640G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421776 | ||||||
| chr12:7421785
|
G | A | 79 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.766+10631C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421785 | ||||||
| chr12:7421865
|
T | G | 10 | a0001c0001t0001g0103a0001c0001t0001g0143a0001c0001t0001g0160others(7): Show | 10 | NA18941.hp1 NA18943.hp1 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.766+10551A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421865 | ||||||
| chr12:7421886
|
T | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(28): Show | 36 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.766+10530A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421886 | ||||||
| chr12:7422056
|
T | G | 79 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.766+10360A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422056 | ||||||
| chr12:7422072
|
G | A | 1 | a0001c0004t0001g0323 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.766+10344C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422072 | ||||||
| chr12:7422108
|
T | C | 1 | a0001c0002t0001g0255 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.766+10308A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422108 | ||||||
| chr12:7422111
|
C | G | 2 | a0001c0001t0002g0186a0001c0001t0002g0188 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.766+10305G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422111 | ||||||
| chr12:7422112
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.766+10304G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422112 | ||||||
| chr12:7422139
|
T | C | 356 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(353): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.766+10277A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422139 | ||||||
| chr12:7422148
|
A | G | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.766+10268T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422148 | ||||||
| chr12:7422225
|
G | A | 79 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.766+10191C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422225 | ||||||
| chr12:7422257
|
G | C | 6 | a0005c0013t0001g0244a0005c0013t0001g0352a0005c0013t0002g0243others(3): Show | 6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.766+10159C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422257 | ||||||
| chr12:7422361
|
C | T | 1 | a0001c0001t0002g0248 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.766+10055G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422361 | ||||||
| chr12:7422373
|
A | T | 1 | a0001c0001t0002g0248 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.766+10043T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422373 | ||||||
| chr12:7422375
|
A | G | 1 | a0001c0001t0002g0248 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.766+10041T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422375 | ||||||
| chr12:7422412
|
CAAGGGCA others(13): Show |
C | 1 | a0001c0001t0002g0248 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.766+9984_766+10003 others(23): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422412 | ||||||
| chr12:7422435
|
T | A | 1 | a0001c0001t0002g0248 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.766+9981A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422435 | ||||||
| chr12:7422439
|
T | G | 1 | a0001c0001t0002g0248 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.766+9977A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422439 | ||||||
| chr12:7422639
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG04184.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.766+9777T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422639 | ||||||
| chr12:7422643
|
CATAT | C | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+9769_766+9772d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422643 | ||||||
| chr12:7422751
|
A | ATG | 9 | a0001c0001t0001g0003a0001c0001t0001g0108a0001c0001t0001g0169others(6): Show | 11 | HG02040.hp2 NA18948.hp1 NA18955.hp2 others(8): Show |
intron_variant | MODIFIER | c.766+9663_766+9664d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422751 | ||||||
| chr12:7422751
|
ATG | A | 204 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(201): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.766+9663_766+9664d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422751 | ||||||
| chr12:7422751
|
ATGTG | A | 19 | a0001c0007t0001g0338a0001c0007t0001g0339a0001c0007t0001g0342others(16): Show | 19 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.766+9661_766+9664d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422751 | ||||||
| chr12:7422771
|
GTGTA | G | 3 | a0002c0003t0001g0038a0002c0003t0001g0039a0004c0012t0002g0332 | 3 | HG02630.hp1 NA18979.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.766+9641_766+9644d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422771 | ||||||
| chr12:7422773
|
G | A | 2 | a0006c0009t0001g0111a0014c0019t0001g0129 | 2 | HG02129.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.766+9643C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422773 | ||||||
| chr12:7422773
|
GTA | G | 8 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0004t0001g0311others(5): Show | 8 | HG01516.hp1 HG01517.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.766+9641_766+9642d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422773 | ||||||
| chr12:7423272
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.766+9144A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7423272 | ||||||
| chr12:7423347
|
T | G | 5 | a0001c0007t0001g0126a0006c0009t0001g0111a0006c0009t0002g0010others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.766+9069A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7423347 | ||||||
| chr12:7423538
|
G | T | 71 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(68): Show | 74 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.766+8878C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7423538 | ||||||
| chr12:7423656
|
G | A | 2 | a0002c0003t0001g0060a0002c0003t0002g0059 | 2 | NA18941.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.766+8760C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7423656 | ||||||
| chr12:7423800
|
A | G | 1 | a0001c0007t0001g0126 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.766+8616T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7423800 | ||||||
| chr12:7423883
|
C | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.766+8533G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7423883 | ||||||
| chr12:7423927
|
T | C | 1 | a0011c0015t0001g0282 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.766+8489A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7423927 | ||||||
| chr12:7424074
|
T | C | 80 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(77): Show | 83 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.766+8342A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424074 | ||||||
| chr12:7424205
|
A | T | 5 | a0001c0007t0001g0126a0006c0009t0001g0111a0006c0009t0002g0010others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.766+8211T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424205 | ||||||
| chr12:7424288
|
TA | T | 303 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(300): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.766+8127delT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424288 | ||||||
| chr12:7424434
|
G | C | 8 | a0001c0001t0001g0124a0001c0001t0001g0125a0005c0013t0001g0244others(5): Show | 8 | HG02572.hp2 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.766+7982C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424434 | ||||||
| chr12:7424496
|
G | A | 1 | a0001c0002t0001g0306 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.766+7920C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424496 | ||||||
| chr12:7424497
|
C | A | 1 | a0001c0002t0001g0306 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.766+7919G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424497 | ||||||
| chr12:7424506
|
G | T | 1 | a0001c0002t0001g0306 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.766+7910C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424506 | ||||||
| chr12:7424512
|
A | T | 1 | a0001c0002t0001g0306 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.766+7904T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424512 | ||||||
| chr12:7424546
|
G | C | 1 | a0001c0001t0001g0144 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.766+7870C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424546 | ||||||
| chr12:7424686
|
C | T | 1 | a0001c0002t0003g0257 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.766+7730G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424686 | ||||||
| chr12:7424941
|
T | C | 6 | a0005c0013t0001g0244a0005c0013t0001g0352a0005c0013t0002g0243others(3): Show | 6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.766+7475A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424941 | ||||||
| chr12:7424944
|
C | G | 1 | a0001c0029t0001g0117 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.766+7472G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424944 | ||||||
| chr12:7425042
|
A | T | 1 | a0013c0044t0002g0357 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.766+7374T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7425042 | ||||||
| chr12:7425304
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.766+7112G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7425304 | ||||||
| chr12:7425422
|
G | A | 2 | a0001c0004t0001g0322a0001c0004t0001g0323 | 2 | HG00099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.766+6994C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7425422 | ||||||
| chr12:7426028
|
C | A | 1 | a0001c0002t0003g0284 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.766+6388G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426028 | ||||||
| chr12:7426098
|
A | C | 63 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(60): Show | 65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.766+6318T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426098 | ||||||
| chr12:7426123
|
G | A | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+6293C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426123 | ||||||
| chr12:7426142
|
G | A | 1 | a0019c0035t0002g0218 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.766+6274C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426142 | ||||||
| chr12:7426338
|
G | A | 1 | a0006c0009t0002g0010 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.766+6078C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426338 | ||||||
| chr12:7426439
|
C | A | 1 | a0001c0001t0001g0143 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.766+5977G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426439 | ||||||
| chr12:7426445
|
C | T | 1 | a0001c0001t0002g0167 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.766+5971G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426445 | ||||||
| chr12:7426477
|
T | C | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.766+5939A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426477 | ||||||
| chr12:7426519
|
G | A | 2 | a0001c0002t0001g0285a0001c0002t0003g0286 | 2 | HG01256.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.766+5897C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426519 | ||||||
| chr12:7426666
|
C | T | 2 | a0001c0001t0001g0130a0002c0003t0001g0089 | 2 | NA19011.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.766+5750G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426666 | ||||||
| chr12:7426667
|
G | A | 2 | a0003c0005t0001g0006a0003c0005t0001g0062 | 3 | HG01099.hp1 HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.766+5749C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426667 | ||||||
| chr12:7426671
|
T | C | 63 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(60): Show | 65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.766+5745A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426671 | ||||||
| chr12:7426681
|
C | A | 79 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.766+5735G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426681 | ||||||
| chr12:7427058
|
G | A | 98 | a0001c0007t0001g0338a0001c0007t0001g0339a0001c0007t0001g0342others(95): Show | 101 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.766+5358C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7427058 | ||||||
| chr12:7427170
|
G | A | 1 | a0001c0001t0003g0209 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.766+5246C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7427170 | ||||||
| chr12:7427176
|
GAAC | G | 79 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.766+5237_766+5239d others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7427176 | ||||||
| chr12:7427519
|
G | A | 18 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(15): Show | 22 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.766+4897C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7427519 | ||||||
| chr12:7427698
|
T | C | 3 | a0004c0006t0002g0333a0004c0012t0001g0334a0004c0012t0001g0335 | 3 | HG01884.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.766+4718A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7427698 | ||||||
| chr12:7427723
|
C | T | 355 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(352): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.766+4693G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7427723 | ||||||
| chr12:7428153
|
T | A | 63 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(60): Show | 65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.766+4263A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7428153 | ||||||
| chr12:7428209
|
A | C | 3 | a0001c0004t0001g0116a0001c0004t0002g0115a0001c0027t0002g0023 | 3 | HG02818.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.766+4207T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7428209 | ||||||
| chr12:7428220
|
G | A | 4 | a0001c0004t0001g0116a0001c0004t0002g0115a0001c0027t0002g0023others(1): Show | 4 | HG02818.hp2 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+4196C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7428220 | ||||||
| chr12:7428285
|
A | T | 1 | a0003c0005t0001g0063 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.766+4131T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7428285 | ||||||
| chr12:7428288
|
T | C | 3 | a0003c0005t0001g0325a0003c0005t0001g0326a0003c0005t0001g0327 | 3 | NA18956.hp1 NA18968.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.766+4128A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7428288 | ||||||
| chr12:7428463
|
C | T | 1 | a0001c0026t0002g0102 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.766+3953G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7428463 | ||||||
| chr12:7428602
|
T | C | 6 | a0005c0013t0001g0244a0005c0013t0001g0352a0005c0013t0002g0243others(3): Show | 6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.766+3814A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7428602 | ||||||
| chr12:7428735
|
G | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(14): Show | 21 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.766+3681C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7428735 | ||||||
| chr12:7428963
|
C | T | 63 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(60): Show | 65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.766+3453G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7428963 | ||||||
| chr12:7429011
|
A | C | 1 | a0002c0003t0002g0037 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.766+3405T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7429011 | ||||||
| chr12:7429182
|
A | C | 39 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0108others(36): Show | 39 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.766+3234T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7429182 | ||||||
| chr12:7429517
|
C | T | 79 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.766+2899G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7429517 | ||||||
| chr12:7429581
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.766+2835A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7429581 | ||||||
| chr12:7429696
|
A | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0145 | 2 | HG01934.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.766+2720T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7429696 | ||||||
| chr12:7429877
|
C | A | 2 | a0006c0009t0001g0032a0006c0009t0001g0033 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.766+2539G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7429877 | ||||||
| chr12:7430177
|
T | C | 1 | a0003c0005t0001g0063 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.766+2239A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7430177 | ||||||
| chr12:7430222
|
A | G | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.766+2194T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7430222 | ||||||
| chr12:7430503
|
T | C | 1 | a0006c0009t0001g0111 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.766+1913A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7430503 | ||||||
| chr12:7430824
|
A | G | 3 | a0002c0003t0001g0034a0002c0003t0002g0035a0002c0032t0001g0036 | 3 | HG02723.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.766+1592T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7430824 | ||||||
| chr12:7430870
|
G | C | 1 | a0001c0001t0003g0239 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.766+1546C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7430870 | ||||||
| chr12:7430934
|
A | G | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+1482T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7430934 | ||||||
| chr12:7431101
|
C | T | 79 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.766+1315G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431101 | ||||||
| chr12:7431102
|
T | G | 1 | a0002c0003t0001g0064 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.766+1314A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431102 | ||||||
| chr12:7431159
|
A | T | 5 | a0001c0007t0001g0126a0006c0009t0001g0111a0006c0009t0002g0010others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.766+1257T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431159 | ||||||
| chr12:7431160
|
C | G | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.766+1256G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431160 | ||||||
| chr12:7431160
|
C | T | 5 | a0001c0007t0001g0126a0006c0009t0001g0111a0006c0009t0002g0010others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.766+1256G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431160 | ||||||
| chr12:7431161
|
G | A | 4 | a0005c0013t0001g0244a0005c0013t0001g0352a0005c0013t0002g0243others(1): Show | 4 | HG02572.hp2 HG02886.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+1255C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431161 | ||||||
| chr12:7431274
|
G | A | 1 | a0006c0009t0001g0033 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.766+1142C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431274 | ||||||
| chr12:7431288
|
G | T | 1 | a0002c0003t0003g0066 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.766+1128C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431288 | ||||||
| chr12:7431335
|
C | T | 1 | a0013c0044t0002g0357 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.766+1081G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431335 | ||||||
| chr12:7431420
|
C | T | 3 | a0003c0005t0001g0325a0003c0005t0001g0326a0003c0005t0001g0327 | 3 | NA18956.hp1 NA18968.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.766+996G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431420 | ||||||
| chr12:7431427
|
C | CA | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 280 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.766+988dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431427 | ||||||
| chr12:7431480
|
T | A | 1 | a0004c0006t0002g0333 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.766+936A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431480 | ||||||
| chr12:7431608
|
G | C | 1 | a0001c0002t0003g0286 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.766+808C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431608 | ||||||
| chr12:7431730
|
C | T | 79 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.766+686G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431730 | ||||||
| chr12:7431731
|
T | G | 79 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.766+685A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431731 | ||||||
| chr12:7432317
|
G | A | 1 | a0001c0002t0001g0287 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.766+99C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7432317 | ||||||
| chr12:7432740
|
C | T | 3 | a0001c0001t0001g0144a0006c0009t0001g0032a0006c0009t0001g0033 | 3 | HG02258.hp2 HG02559.hp2 NA20805.hp2 |
splice_region_variant&intron_variant | LOW | c.446-4G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/19 | chr12 | 7432740 | ||||||
| chr12:7432808
|
G | T | 1 | a0001c0026t0002g0102 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.446-72C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/19 | chr12 | 7432808 | ||||||
| chr12:7432847
|
T | TA | 39 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0108others(36): Show | 39 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.446-112dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/19 | chr12 | 7432847 | ||||||
| chr12:7433011
|
T | C | 2 | a0006c0009t0001g0032a0006c0009t0001g0033 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.446-275A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/19 | chr12 | 7433011 | ||||||
| chr12:7433137
|
G | A | 1 | a0002c0003t0002g0085 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.445+237C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/19 | chr12 | 7433137 | ||||||
| chr12:7433150
|
G | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0228 | 2 | NA18961.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.445+224C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/19 | chr12 | 7433150 | ||||||
| chr12:7433329
|
G | A | 1 | a0021c0038t0001g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.445+45C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/19 | chr12 | 7433329 | ||||||
| chr12:7433331
|
G | T | 2 | a0001c0004t0001g0311a0001c0004t0002g0310 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.445+43C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/19 | chr12 | 7433331 | ||||||
| chr12:7433838
|
T | G | 1 | a0001c0001t0001g0164 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.125-144A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7433838 | ||||||
| chr12:7433902
|
C | T | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-208G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7433902 | ||||||
| chr12:7433990
|
G | C | 6 | a0005c0013t0001g0244a0005c0013t0001g0352a0005c0013t0002g0243others(3): Show | 6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-296C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7433990 | ||||||
| chr12:7433999
|
T | C | 89 | a0001c0002t0001g0004a0001c0002t0001g0008a0001c0002t0001g0009others(86): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.125-305A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7433999 | ||||||
| chr12:7434033
|
A | G | 4 | a0002c0003t0001g0024a0003c0005t0001g0025a0003c0005t0002g0026others(1): Show | 4 | HG02615.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-339T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434033 | ||||||
| chr12:7434221
|
C | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.125-527G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434221 | ||||||
| chr12:7434226
|
CAGG | C | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-535_125-533del others(3): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434226 | ||||||
| chr12:7434367
|
T | C | 1 | a0001c0002t0002g0288 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.125-673A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434367 | ||||||
| chr12:7434374
|
T | C | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.125-680A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434374 | ||||||
| chr12:7434703
|
A | C | 1 | a0001c0041t0001g0106 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.125-1009T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434703 | ||||||
| chr12:7434706
|
AAGAG | A | 63 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(60): Show | 65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.125-1016_125-1013d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434706 | ||||||
| chr12:7434724
|
G | C | 1 | a0001c0001t0001g0165 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.125-1030C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434724 | ||||||
| chr12:7434784
|
T | G | 2 | a0001c0004t0001g0311a0001c0004t0002g0310 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.125-1090A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434784 | ||||||
| chr12:7434805
|
A | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.125-1111T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434805 | ||||||
| chr12:7434884
|
G | T | 1 | a0013c0044t0002g0357 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.125-1190C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434884 | ||||||
| chr12:7434906
|
T | C | 1 | a0003c0005t0001g0065 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.125-1212A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434906 | ||||||
| chr12:7434938
|
T | C | 72 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0099others(69): Show | 75 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.125-1244A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434938 | ||||||
| chr12:7435031
|
G | C | 79 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.125-1337C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435031 | ||||||
| chr12:7435047
|
A | G | 2 | a0001c0007t0001g0126a0021c0038t0001g0127 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.125-1353T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435047 | ||||||
| chr12:7435089
|
TAC | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(47): Show | 60 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.125-1397_125-1396d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435089 | ||||||
| chr12:7435121
|
A | T | 1 | a0006c0034t0001g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.125-1427T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435121 | ||||||
| chr12:7435156
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.125-1462C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435156 | ||||||
| chr12:7435240
|
TAAAGAA | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(47): Show | 60 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.125-1552_125-1547d others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435240 | ||||||
| chr12:7435346
|
T | C | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0019c0035t0002g0218 | 3 | NA18950.hp2 NA18994.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.125-1652A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435346 | ||||||
| chr12:7435595
|
A | G | 4 | a0009c0018t0001g0355a0009c0018t0002g0356a0010c0042t0002g0354others(1): Show | 4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-1901T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435595 | ||||||
| chr12:7435598
|
T | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.125-1904A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435598 | ||||||
| chr12:7435707
|
T | C | 2 | a0002c0003t0002g0087a0003c0005t0002g0086 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.125-2013A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435707 | ||||||
| chr12:7435866
|
C | T | 2 | a0004c0006t0001g0343a0004c0006t0001g0344 | 2 | NA18612.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.125-2172G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435866 | ||||||
| chr12:7436039
|
T | C | 1 | a0013c0044t0002g0357 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.125-2345A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7436039 | ||||||
| chr12:7436068
|
G | A | 1 | a0002c0003t0003g0066 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.125-2374C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7436068 | ||||||
| chr12:7436280
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.125-2586C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7436280 | ||||||
| chr12:7436363
|
C | T | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 280 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.125-2669G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7436363 | ||||||
| chr12:7436471
|
C | T | 1 | a0001c0002t0002g0256 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.125-2777G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7436471 | ||||||
| chr12:7436508
|
A | G | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0104others(2): Show | 7 | HG02135.hp1 NA18948.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-2814T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7436508 | ||||||
| chr12:7436572
|
G | C | 75 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(72): Show | 78 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.125-2878C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7436572 | ||||||
| chr12:7436716
|
TAAC | T | 89 | a0001c0002t0001g0004a0001c0002t0001g0008a0001c0002t0001g0009others(86): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.125-3025_125-3023d others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7436716 | ||||||
| chr12:7436892
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0002g0331 | 2 | HG02451.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.125-3198T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7436892 | ||||||
| chr12:7436997
|
T | C | 1 | a0004c0012t0001g0334 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.125-3303A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7436997 | ||||||
| chr12:7437009
|
T | C | 2 | a0003c0005t0002g0026a0003c0005t0002g0027 | 2 | HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.125-3315A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437009 | ||||||
| chr12:7437117
|
T | C | 1 | a0001c0002t0003g0289 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.125-3423A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437117 | ||||||
| chr12:7437131
|
TTTTA | T | 79 | a0001c0002t0001g0252a0002c0003t0001g0005a0002c0003t0001g0007others(76): Show | 82 | HG00423.hp1 HG00673.hp1 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.125-3441_125-3438d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437131 | ||||||
| chr12:7437136
|
T | TTTA | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(177): Show | 198 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(195): Show |
intron_variant | MODIFIER | c.125-3445_125-3443d others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437136 | ||||||
| chr12:7437166
|
T | TTAAG | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(254): Show | 278 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(275): Show |
intron_variant | MODIFIER | c.125-3473_125-3472i others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437166 | ||||||
| chr12:7437183
|
ATTTTTAT others(84): Show |
A | 79 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.125-3580_125-3490d others(93): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437183 | ||||||
| chr12:7437204
|
CTTT | C | 4 | a0001c0004t0001g0116a0001c0004t0002g0115a0001c0027t0002g0023others(1): Show | 4 | HG02818.hp2 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-3513_125-3511d others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437204 | ||||||
| chr12:7437205
|
TTTTTTAT others(62): Show |
T | 2 | a0004c0028t0001g0121a0008c0011t0001g0122 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.125-3580_125-3512d others(71): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437205 | ||||||
| chr12:7437235
|
T | TAAATACT others(150): Show |
1 | a0001c0027t0002g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.125-3542_125-3541i others(159): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437235 | ||||||
| chr12:7437235
|
T | TAAATACT others(140): Show |
1 | a0001c0029t0001g0117 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.125-3542_125-3541i others(149): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437235 | ||||||
| chr12:7437235
|
T | TAAATACT others(151): Show |
1 | a0001c0004t0002g0115 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.125-3542_125-3541i others(160): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437235 | ||||||
| chr12:7437235
|
T | TAAATACT others(96): Show |
1 | a0001c0004t0001g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.125-3542_125-3541i others(105): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437235 | ||||||
| chr12:7437237
|
C | A | 4 | a0001c0004t0001g0116a0001c0004t0002g0115a0001c0027t0002g0023others(1): Show | 4 | HG02818.hp2 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-3543G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437237 | ||||||
| chr12:7437238
|
T | TTTTAAAT others(92): Show |
1 | a0001c0002t0003g0297 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.125-3545_125-3544i others(101): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437238 | ||||||
| chr12:7437238
|
T | TTTTAAAT others(92): Show |
6 | a0001c0002t0001g0019a0001c0002t0001g0292a0001c0002t0001g0293others(3): Show | 7 | HG00544.hp1 HG01071.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.125-3545_125-3544i others(101): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437238 | ||||||
| chr12:7437238
|
T | TTTTAAAT others(92): Show |
42 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0021others(39): Show | 44 | HG00408.hp2 HG00423.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.125-3545_125-3544i others(101): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437238 | ||||||
| chr12:7437238
|
T | TTTTAAAT others(81): Show |
1 | a0001c0002t0001g0252 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.125-3545_125-3544i others(90): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437238 | ||||||
| chr12:7437238
|
T | TTTTAAAT others(125): Show |
1 | a0001c0002t0001g0255 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.125-3545_125-3544i others(134): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437238 | ||||||
| chr12:7437238
|
T | TTTTAAAT others(81): Show |
1 | a0001c0002t0002g0290 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.125-3545_125-3544i others(90): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437238 | ||||||
| chr12:7437238
|
T | TTTTAAAT others(59): Show |
1 | a0001c0002t0001g0253 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.125-3545_125-3544i others(68): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437238 | ||||||
| chr12:7437238
|
T | TTTTAAAT others(92): Show |
1 | a0001c0002t0001g0291 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.125-3545_125-3544i others(101): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437238 | ||||||
| chr12:7437238
|
T | TTTTAAAT others(70): Show |
1 | a0001c0002t0002g0254 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.125-3545_125-3544i others(79): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437238 | ||||||
| chr12:7437239
|
T | A | 4 | a0001c0004t0001g0116a0001c0004t0002g0115a0001c0027t0002g0023others(1): Show | 4 | HG02818.hp2 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-3545A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(102): Show |
1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(111): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(58): Show |
4 | a0001c0007t0001g0126a0006c0009t0001g0111a0006c0034t0001g0118others(1): Show | 4 | HG02717.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(67): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(80): Show |
1 | a0006c0009t0002g0010 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(89): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(107): Show |
2 | a0006c0009t0001g0032a0006c0009t0001g0033 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(116): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(212): Show |
1 | a0001c0025t0002g0307 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(221): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(58): Show |
48 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(45): Show | 58 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(67): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(146): Show |
1 | a0001c0004t0002g0324 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(155): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(234): Show |
1 | a0001c0002t0001g0298 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(243): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(102): Show |
2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(111): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(146): Show |
10 | a0001c0004t0001g0315a0001c0004t0001g0316a0001c0004t0001g0322others(7): Show | 10 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(155): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(157): Show |
6 | a0001c0004t0001g0311a0001c0004t0001g0351a0001c0004t0002g0020others(3): Show | 7 | HG00140.hp1 HG00738.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(166): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(157): Show |
1 | a0001c0002t0001g0306 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(166): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(201): Show |
1 | a0015c0020t0001g0313 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(210): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(300): Show |
1 | a0001c0002t0001g0305 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(309): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(212): Show |
3 | a0001c0002t0001g0249a0001c0002t0001g0303a0001c0002t0001g0304 | 3 | NA18951.hp2 NA18984.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(221): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(47): Show |
6 | a0005c0013t0001g0244a0005c0013t0001g0352a0005c0013t0002g0243others(3): Show | 6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(56): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(124): Show |
1 | a0001c0004t0002g0330 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(133): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(190): Show |
1 | a0001c0026t0002g0102 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(199): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(91): Show |
6 | a0001c0002t0001g0004a0001c0002t0001g0095a0001c0002t0001g0300others(3): Show | 8 | HG00639.hp1 HG01074.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(100): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(69): Show |
2 | a0001c0007t0003g0349a0013c0044t0002g0357 | 2 | HG01123.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(78): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(58): Show |
3 | a0001c0001t0001g0166a0004c0006t0001g0336a0004c0006t0001g0337 | 3 | HG02027.hp2 HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(67): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(146): Show |
1 | a0001c0004t0003g0312 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(155): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(168): Show |
3 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0002g0100 | 3 | HG02055.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(177): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(80): Show |
3 | a0004c0006t0002g0333a0004c0012t0001g0334a0004c0012t0001g0335 | 3 | HG01884.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(89): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(69): Show |
24 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(21): Show | 28 | HG00544.hp2 HG00609.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(78): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(256): Show |
1 | a0008c0011t0002g0120 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(265): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(190): Show |
1 | a0001c0001t0002g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(199): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(58): Show |
10 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(7): Show | 11 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(67): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(80): Show |
3 | a0004c0006t0001g0343a0004c0006t0001g0344a0004c0006t0001g0345 | 3 | NA18612.hp2 NA18960.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(89): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(124): Show |
1 | a0001c0001t0001g0195 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(133): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(146): Show |
1 | a0001c0001t0002g0224 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(155): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(157): Show |
4 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG01496.hp1 HG01943.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(166): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(157): Show |
1 | a0001c0001t0001g0194 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(166): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(190): Show |
1 | a0001c0001t0002g0186 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(199): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(69): Show |
3 | a0001c0007t0001g0097a0001c0008t0001g0240a0001c0008t0001g0241 | 3 | HG03041.hp1 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(78): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(135): Show |
1 | a0001c0001t0001g0108 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(144): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(124): Show |
1 | a0001c0001t0002g0246 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(133): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(91): Show |
3 | a0004c0006t0001g0347a0004c0006t0001g0348a0023c0037t0001g0346 | 3 | HG00673.hp2 NA18939.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(100): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(135): Show |
7 | a0001c0001t0001g0088a0001c0001t0001g0112a0001c0001t0001g0197others(4): Show | 7 | HG02165.hp1 HG02738.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(144): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(124): Show |
1 | a0001c0001t0001g0187 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(133): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(168): Show |
1 | a0001c0001t0002g0223 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(177): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(146): Show |
1 | a0001c0001t0001g0228 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(155): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(135): Show |
3 | a0001c0001t0002g0247a0001c0001t0002g0248a0001c0008t0002g0225 | 3 | HG00558.hp2 HG02723.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(144): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(146): Show |
14 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0203others(11): Show | 14 | HG00609.hp2 HG01952.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(155): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(146): Show |
1 | a0001c0001t0001g0185 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(155): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(168): Show |
1 | a0001c0001t0002g0227 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(177): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(146): Show |
1 | a0001c0008t0002g0017 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(155): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(135): Show |
1 | a0001c0001t0001g0189 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(144): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(168): Show |
1 | a0001c0001t0001g0107 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(177): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(157): Show |
8 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(5): Show | 8 | HG00558.hp1 HG01361.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(166): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(146): Show |
2 | a0001c0001t0001g0016a0001c0001t0001g0229 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(155): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(157): Show |
1 | a0006c0009t0002g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(166): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(146): Show |
1 | a0001c0001t0002g0190 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(155): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(168): Show |
1 | a0001c0001t0002g0219 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(177): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(113): Show |
1 | a0001c0001t0002g0245 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(122): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(157): Show |
2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG01358.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(166): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437239
|
T | TTTAAATA others(179): Show |
1 | a0003c0005t0001g0193 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(188): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | ||||||
| chr12:7437244
|
ATAGTATT others(1469): Show |
A | 1 | a0001c0001t0001g0184 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.124+2434_125-3551d others(2): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437244 | ||||||
| chr12:7437247
|
G | GTATTTAA others(4): Show |
1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.125-3554_125-3553i others(13): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437247 | ||||||
| chr12:7437247
|
G | GTATTTAA others(92): Show |
1 | a0001c0002t0001g0105 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.125-3554_125-3553i others(101): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437247 | ||||||
| chr12:7437258
|
G | C | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.125-3564C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437258 | ||||||
| chr12:7437315
|
ATTATTT | A | 19 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(16): Show | 23 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.125-3627_125-3622d others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437315 | ||||||
| chr12:7437318
|
ATTT | A | 79 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.125-3627_125-3625d others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437318 | ||||||
| chr12:7437324
|
ATTT | A | 6 | a0005c0013t0001g0244a0005c0013t0001g0352a0005c0013t0002g0243others(3): Show | 6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-3633_125-3631d others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437324 | ||||||
| chr12:7437350
|
ATATT | A | 79 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.125-3660_125-3657d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437350 | ||||||
| chr12:7437370
|
T | C | 2 | a0006c0009t0001g0032a0006c0009t0001g0033 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.125-3676A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437370 | ||||||
| chr12:7437373
|
ATGTGCAC others(10): Show |
A | 2 | a0006c0009t0001g0032a0006c0009t0001g0033 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.125-3696_125-3680d others(19): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437373 | ||||||
| chr12:7437402
|
T | C | 1 | a0003c0033t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.125-3708A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437402 | ||||||
| chr12:7437581
|
C | T | 13 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(10): Show | 14 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.124+3573G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437581 | ||||||
| chr12:7437630
|
C | T | 1 | a0002c0003t0001g0024 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.124+3524G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437630 | ||||||
| chr12:7437670
|
CT | C | 46 | a0001c0001t0001g0229a0001c0001t0002g0230a0001c0001t0002g0331others(43): Show | 46 | HG00639.hp2 HG00673.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.124+3483delA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437670 | ||||||
| chr12:7437898
|
T | TA | 20 | a0001c0001t0001g0003a0001c0001t0001g0166a0001c0001t0001g0169others(17): Show | 23 | HG02027.hp2 NA18612.hp1 NA18747.hp1 others(20): Show |
intron_variant | MODIFIER | c.124+3255dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437898 | ||||||
| chr12:7437898
|
TA | T | 6 | a0001c0007t0001g0126a0003c0033t0002g0123a0006c0009t0001g0111others(3): Show | 7 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+3255delT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437898 | ||||||
| chr12:7437967
|
T | C | 6 | a0006c0009t0001g0032a0006c0009t0001g0033a0009c0018t0001g0355others(3): Show | 6 | HG01261.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.124+3187A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437967 | ||||||
| chr12:7437988
|
G | T | 6 | a0005c0013t0001g0244a0005c0013t0001g0352a0005c0013t0002g0243others(3): Show | 6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.124+3166C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437988 | ||||||
| chr12:7438181
|
T | C | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.124+2973A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7438181 | ||||||
| chr12:7438218
|
C | G | 75 | a0002c0003t0001g0005a0002c0003t0001g0007a0002c0003t0001g0022others(72): Show | 78 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.124+2936G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7438218 | ||||||
| chr12:7438464
|
T | C | 5 | a0001c0007t0001g0126a0006c0009t0001g0111a0006c0009t0002g0010others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.124+2690A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7438464 | ||||||
| chr12:7438593
|
T | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0002g0100 | 3 | HG02055.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.124+2561A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7438593 | ||||||
| chr12:7438681
|
T | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0103others(46): Show | 59 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.124+2473A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7438681 | ||||||
| chr12:7438718
|
T | C | 1 | a0001c0001t0003g0242 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.124+2436A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7438718 | ||||||
| chr12:7438741
|
T | A | 1 | a0001c0001t0001g0231 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.124+2413A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7438741 | ||||||
| chr12:7438771
|
C | T | 1 | a0001c0002t0001g0251 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.124+2383G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7438771 | ||||||
| chr12:7438940
|
T | A | 84 | a0001c0001t0001g0088a0001c0001t0002g0331a0001c0027t0002g0023others(81): Show | 87 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(84): Show |
intron_variant | MODIFIER | c.124+2214A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7438940 | ||||||
| chr12:7438968
|
T | C | 1 | a0001c0017t0002g0015 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.124+2186A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7438968 | ||||||
| chr12:7439085
|
G | A | 15 | a0001c0007t0001g0338a0001c0007t0001g0339a0001c0007t0001g0342others(12): Show | 15 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.124+2069C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439085 | ||||||
| chr12:7439119
|
T | G | 76 | a0001c0001t0001g0088a0002c0003t0001g0005a0002c0003t0001g0007others(73): Show | 79 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.124+2035A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439119 | ||||||
| chr12:7439147
|
A | C | 1 | a0014c0019t0001g0129 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.124+2007T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439147 | ||||||
| chr12:7439213
|
C | T | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0104others(2): Show | 7 | HG02135.hp1 NA18948.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+1941G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439213 | ||||||
| chr12:7439439
|
G | T | 93 | a0001c0002t0001g0004a0001c0002t0001g0008a0001c0002t0001g0009others(90): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.124+1715C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439439 | ||||||
| chr12:7439543
|
G | A | 93 | a0001c0002t0001g0004a0001c0002t0001g0008a0001c0002t0001g0009others(90): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.124+1611C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439543 | ||||||
| chr12:7439598
|
T | C | 80 | a0001c0001t0001g0088a0001c0001t0002g0331a0002c0003t0001g0005others(77): Show | 83 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.124+1556A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439598 | ||||||
| chr12:7439629
|
C | T | 1 | a0005c0013t0002g0243 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.124+1525G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439629 | ||||||
| chr12:7439783
|
A | G | 79 | a0001c0001t0001g0088a0002c0003t0001g0005a0002c0003t0001g0007others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.124+1371T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439783 | ||||||
| chr12:7439815
|
C | A | 2 | a0001c0002t0001g0009a0001c0002t0001g0105 | 3 | NA18959.hp1 NA18983.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.124+1339G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439815 | ||||||
| chr12:7439849
|
G | C | 92 | a0001c0002t0001g0004a0001c0002t0001g0008a0001c0002t0001g0009others(89): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.124+1305C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439849 | ||||||
| chr12:7439900
|
CCTT | C | 62 | a0001c0001t0001g0016a0001c0001t0001g0099a0001c0001t0001g0101others(59): Show | 64 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.124+1251_124+1253d others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439900 | ||||||
| chr12:7439943
|
A | T | 91 | a0001c0002t0001g0004a0001c0002t0001g0008a0001c0002t0001g0009others(88): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.124+1211T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439943 | ||||||
| chr12:7439998
|
T | C | 1 | a0021c0038t0001g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.124+1156A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439998 | ||||||
| chr12:7440038
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.124+1116G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440038 | ||||||
| chr12:7440090
|
G | A | 1 | a0004c0012t0001g0335 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.124+1064C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440090 | ||||||
| chr12:7440233
|
G | T | 88 | a0001c0002t0001g0004a0001c0002t0001g0019a0001c0002t0001g0021others(85): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.124+921C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440233 | ||||||
| chr12:7440280
|
G | C | 79 | a0001c0001t0001g0088a0002c0003t0001g0005a0002c0003t0001g0007others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.124+874C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440280 | ||||||
| chr12:7440364
|
G | C | 79 | a0001c0001t0001g0088a0002c0003t0001g0005a0002c0003t0001g0007others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.124+790C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440364 | ||||||
| chr12:7440377
|
C | G | 12 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0004t0001g0116others(9): Show | 13 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.124+777G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440377 | ||||||
| chr12:7440568
|
T | C | 13 | a0001c0001t0001g0233a0001c0001t0001g0238a0001c0001t0002g0232others(10): Show | 14 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.124+586A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440568 | ||||||
| chr12:7440627
|
T | A | 10 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0002g0247others(7): Show | 10 | HG00558.hp2 HG02572.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.124+527A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440627 | ||||||
| chr12:7440629
|
CT | C | 331 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(328): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.124+524delA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440629 | ||||||
| chr12:7440882
|
C | G | 4 | a0001c0004t0001g0116a0001c0004t0002g0115a0001c0027t0002g0023others(1): Show | 4 | HG02818.hp2 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+272G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440882 | ||||||
| chr12:7440922
|
C | T | 4 | a0001c0004t0001g0116a0001c0004t0002g0115a0001c0027t0002g0023others(1): Show | 4 | HG02818.hp2 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+232G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440922 | ||||||
| chr12:7441062
|
A | G | 2 | a0002c0003t0001g0029a0002c0003t0001g0030 | 2 | HG01069.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.124+92T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7441062 | ||||||
| chr12:7441433
|
G | C | 4 | a0004c0006t0002g0333a0004c0012t0001g0334a0004c0012t0001g0335others(1): Show | 4 | HG01884.hp1 HG02630.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.32-187C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7441433 | ||||||
| chr12:7441579
|
C | T | 79 | a0001c0001t0001g0088a0002c0003t0001g0005a0002c0003t0001g0007others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.32-333G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7441579 | ||||||
| chr12:7441618
|
C | A | 15 | a0001c0007t0001g0338a0001c0007t0001g0339a0001c0007t0001g0342others(12): Show | 15 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.32-372G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7441618 | ||||||
| chr12:7441758
|
T | C | 89 | a0001c0001t0001g0329a0001c0002t0001g0004a0001c0002t0001g0019others(86): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.32-512A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7441758 | ||||||
| chr12:7441790
|
A | G | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114 | 3 | HG00609.hp2 HG02165.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.32-544T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7441790 | ||||||
| chr12:7441812
|
A | T | 1 | a0006c0009t0001g0111 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.32-566T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7441812 | ||||||
| chr12:7442036
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.32-790C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442036 | ||||||
| chr12:7442207
|
C | T | 2 | a0005c0014t0001g0109a0005c0014t0002g0110 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32-961G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442207 | ||||||
| chr12:7442242
|
G | T | 7 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0002t0001g0008others(4): Show | 9 | HG02040.hp2 HG02083.hp1 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.32-996C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442242 | ||||||
| chr12:7442380
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.32-1134T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442380 | ||||||
| chr12:7442429
|
A | G | 1 | a0001c0026t0002g0102 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.32-1183T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442429 | ||||||
| chr12:7442506
|
T | TA | 19 | a0001c0007t0001g0338a0001c0007t0001g0339a0001c0007t0001g0342others(16): Show | 19 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.32-1261_32-1260ins others(1): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442506 | ||||||
| chr12:7442535
|
C | T | 1 | a0003c0005t0001g0028 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.32-1289G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442535 | ||||||
| chr12:7442555
|
A | G | 4 | a0002c0003t0001g0024a0003c0005t0001g0025a0003c0005t0002g0026others(1): Show | 4 | HG02615.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-1309T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442555 | ||||||
| chr12:7442600
|
A | G | 3 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0002g0100 | 3 | HG02055.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.32-1354T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442600 | ||||||
| chr12:7442605
|
G | A | 8 | a0002c0003t0001g0007a0002c0003t0001g0022a0002c0003t0001g0089others(5): Show | 9 | HG00408.hp1 HG02056.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.32-1359C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442605 | ||||||
| chr12:7442619
|
A | G | 1 | a0005c0014t0001g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32-1373T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442619 | ||||||
| chr12:7442627
|
C | T | 1 | a0001c0007t0001g0097 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.32-1381G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442627 | ||||||
| chr12:7442983
|
T | A | 1 | a0004c0006t0002g0096 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.31+1114A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442983 | ||||||
| chr12:7443004
|
A | G | 1 | a0004c0006t0002g0096 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.31+1093T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7443004 | ||||||
| chr12:7443054
|
A | T | 1 | a0001c0002t0001g0095 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.31+1043T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7443054 | ||||||
| chr12:7443138
|
T | C | 1 | a0001c0002t0001g0350 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.31+959A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7443138 | ||||||
| chr12:7443240
|
C | T | 79 | a0001c0001t0001g0088a0002c0003t0001g0005a0002c0003t0001g0007others(76): Show | 82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.31+857G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7443240 | ||||||
| chr12:7443267
|
A | C | 1 | a0001c0027t0002g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.31+830T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7443267 | ||||||
| chr12:7443783
|
T | A | 1 | a0001c0004t0001g0351 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.31+314A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7443783 | ||||||
| chr12:7443973
|
A | G | 1 | a0002c0003t0001g0022 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.31+124T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7443973 | ||||||
| chr12:7443987
|
G | C | 1 | a0005c0013t0001g0352 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.31+110C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7443987 | ||||||
| chr12:7444081
|
A | C | 1 | a0001c0002t0001g0021 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.31+16T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7444081 |