Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9332 |
| ensemblid | ENSG00000177575.13 |
| hgncid | 1631 |
| symbol | CD163 |
| name | CD163 molecule |
| refseq_nuc | NM_203416.4 |
| refseq_prot | NP_981961.2 |
| ensembl_nuc | ENST00000432237.3 |
| ensembl_prot | ENSP00000403885.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 7470811 |
| end | 7503777 |
| strand | - |
| ver | v1.2 |
| region | chr12:7470811-7503777 |
| region5000 | chr12:7465811-7508777 |
| regionname0 | CD163_chr12_7470811_7503777 |
| regionname5000 | CD163_chr12_7465811_7508777 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1121 | 254 | 49 | 39 | 137 | 6 | 22 | 106 | CD163_chr12_7465811_7508777 | CD163 | MSKLR others(1116): Show |
chr12 | 7465811 | 7508777 |
| a0002 | 1/0 | 1121 | 120 | 30 | 15 | 67 | 2 | 5 | 53 | CD163_chr12_7465811_7508777 | CD163 | MSKLR others(1116): Show |
chr12 | 7465811 | 7508777 |
| a0003 | 0/0 | 1121 | 36 | 2 | 16 | 5 | 4 | 9 | 2 | CD163_chr12_7465811_7508777 | CD163 | MSKLR others(1116): Show |
chr12 | 7465811 | 7508777 |
| a0004 | 0/0 | 1121 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | MSKLR others(1116): Show |
chr12 | 7465811 | 7508777 |
| a0005 | 0/0 | 1121 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | MSKLR others(1116): Show |
chr12 | 7465811 | 7508777 |
| a0006 | 0/0 | 1121 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | MSKLR others(1116): Show |
chr12 | 7465811 | 7508777 |
| a0007 | 0/0 | 1121 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | MSKLR others(1116): Show |
chr12 | 7465811 | 7508777 |
| a0008 | 0/0 | 1121 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | MSKLR others(1116): Show |
chr12 | 7465811 | 7508777 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3363 | 116 | 3 | 26 | 67 | 5 | 14 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0001c0003 | 0/0 | 3363 | 111 | 41 | 10 | 52 | 1 | 7 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0001c0005 | 0/0 | 3363 | 18 | 0 | 0 | 18 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0001c0009 | 0/0 | 3363 | 5 | 1 | 3 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0001c0015 | 0/0 | 3363 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0001c0016 | 0/0 | 3363 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0001c0017 | 0/0 | 3363 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0001c0020 | 0/0 | 3363 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0002c0002 | 1/0 | 3363 | 113 | 24 | 14 | 67 | 2 | 5 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0002c0007 | 0/0 | 3363 | 7 | 6 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0003c0004 | 0/0 | 3363 | 22 | 1 | 11 | 4 | 1 | 5 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0003c0006 | 0/0 | 3363 | 12 | 0 | 4 | 1 | 3 | 4 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0003c0013 | 0/0 | 3363 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0003c0021 | 0/0 | 3363 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0004c0008 | 0/0 | 3363 | 5 | 5 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0004c0012 | 0/0 | 3363 | 2 | 2 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0004c0014 | 0/0 | 3363 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0004c0018 | 0/0 | 3363 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0005c0010 | 0/0 | 3363 | 4 | 3 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0006c0011 | 0/0 | 3363 | 3 | 0 | 0 | 3 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0007c0022 | 0/0 | 3363 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 | ||
| a0008c0019 | 0/0 | 3363 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | ATGAG others(3358): Show |
chr12 | 7465811 | 7508777 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4071 | 43 | 3 | 14 | 17 | 2 | 7 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0001c0001t0002 | 0/1 | 4071 | 72 | 0 | 12 | 49 | 3 | 7 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0001c0001t0005 | 0/0 | 4071 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0001c0003t0001 | 0/0 | 4071 | 102 | 40 | 9 | 45 | 1 | 7 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0001c0003t0002 | 0/0 | 4071 | 8 | 0 | 1 | 7 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0001c0003t0003 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0001c0005t0001 | 0/0 | 4071 | 17 | 0 | 0 | 17 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0001c0005t0002 | 0/0 | 4071 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0001c0009t0001 | 0/0 | 4071 | 4 | 0 | 3 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0001c0009t0003 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0001c0015t0001 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0001c0016t0001 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0001c0017t0001 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0001c0020t0008 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0002c0002t0001 | 1/0 | 4071 | 90 | 23 | 11 | 48 | 2 | 5 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0002c0002t0002 | 0/0 | 4071 | 21 | 0 | 2 | 19 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0002c0002t0006 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0002c0002t0007 | 0/0 | 4071 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0002c0007t0001 | 0/0 | 4071 | 7 | 6 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0003c0004t0001 | 0/0 | 4071 | 21 | 1 | 10 | 4 | 1 | 5 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0003c0004t0004 | 0/0 | 4071 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0003c0006t0001 | 0/0 | 4071 | 6 | 0 | 1 | 1 | 1 | 3 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0003c0006t0002 | 0/0 | 4071 | 6 | 0 | 3 | 0 | 2 | 1 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0003c0013t0001 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0003c0021t0001 | 0/0 | 4071 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0004c0008t0001 | 0/0 | 4071 | 5 | 5 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0004c0012t0001 | 0/0 | 4071 | 2 | 2 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0004c0014t0003 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0004c0018t0003 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0005c0010t0001 | 0/0 | 4071 | 4 | 3 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0006c0011t0001 | 0/0 | 4071 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0006c0011t0002 | 0/0 | 4071 | 2 | 0 | 0 | 2 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0007c0022t0002 | 0/0 | 4071 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| a0008c0019t0001 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | AGAAT others(4066): Show |
chr12 | 7465811 | 7508777 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0004 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0233 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0003 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0003t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0005t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0005t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0005t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0005t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0005t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0005t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0005t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0005t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0005t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0005t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0005t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0005t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0005t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0009t0001g0012 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0009t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0009t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0015t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0016t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0017t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0001c0020t0008g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0001 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0009 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0107 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0002g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0002g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0002t0007g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0007t0001g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0007t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0002c0007t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0004t0001g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0004t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0004t0001g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0004t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0004t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0004t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0004t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0004t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0004t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0004t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0004t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0004t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0004t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0004t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0004t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0004t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0004t0004g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0006t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0006t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0006t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0006t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0006t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0006t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0006t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0006t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0006t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0006t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0006t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0006t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0013t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0003c0021t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0004c0008t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0004c0008t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0004c0008t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0004c0008t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0004c0008t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0004c0012t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0004c0012t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0004c0014t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0004c0018t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0005c0010t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0005c0010t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0005c0010t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0005c0010t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0006c0011t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0006c0011t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0006c0011t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0007c0022t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| a0008c0019t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0328 | EUR | GBR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00099 | hp2 | a0003 | c0006 | t0001 | g0274 | EUR | GBR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00140 | hp1 | a0003 | c0006 | t0002 | g0271 | EUR | GBR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | GBR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | FIN | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0237 | EUR | FIN | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | CHS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | CHS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00423 | hp2 | a0003 | c0006 | t0001 | g0277 | EAS | CHS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | CHS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0075 | EAS | CHS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | CHS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | CHS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | CHS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00597 | hp1 | a0001 | c0003 | t0002 | g0084 | EAS | CHS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00597 | hp2 | a0006 | c0011 | t0002 | g0259 | EAS | CHS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00609 | hp2 | a0001 | c0003 | t0001 | g0051 | EAS | CHS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00621 | hp2 | a0001 | c0003 | t0001 | g0066 | EAS | CHS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0031 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0116 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0315 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00673 | hp1 | a0001 | c0003 | t0001 | g0330 | EAS | CHS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | CHS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00735 | hp2 | a0003 | c0004 | t0004 | g0289 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00738 | hp1 | a0003 | c0021 | t0001 | g0082 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0143 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG00741 | hp2 | a0007 | c0022 | t0002 | g0149 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01070 | hp1 | a0003 | c0006 | t0002 | g0273 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01070 | hp2 | a0001 | c0009 | t0001 | g0012 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01071 | hp2 | a0003 | c0006 | t0002 | g0276 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0021 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0132 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01106 | hp1 | a0001 | c0009 | t0001 | g0012 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01106 | hp2 | a0003 | c0004 | t0001 | g0010 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01109 | hp1 | a0003 | c0004 | t0001 | g0049 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01109 | hp2 | a0002 | c0002 | t0007 | g0103 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0032 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0072 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0032 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0017 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01192 | hp1 | a0003 | c0006 | t0001 | g0316 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0073 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01243 | hp2 | a0002 | c0007 | t0001 | g0131 | AMR | PUR | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | CLM | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | CLM | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | CLM | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01258 | hp2 | a0003 | c0004 | t0001 | g0010 | AMR | CLM | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01261 | hp1 | a0005 | c0010 | t0001 | g0209 | AMR | CLM | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01361 | hp1 | a0003 | c0004 | t0001 | g0287 | AMR | CLM | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01361 | hp2 | a0001 | c0009 | t0001 | g0083 | AMR | CLM | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01433 | hp1 | a0001 | c0003 | t0002 | g0071 | AMR | CLM | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01433 | hp2 | a0003 | c0004 | t0001 | g0048 | AMR | CLM | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0009 | EUR | IBS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01515 | hp2 | a0003 | c0006 | t0002 | g0272 | EUR | IBS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0009 | EUR | IBS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01517 | hp2 | a0003 | c0004 | t0001 | g0288 | EUR | IBS | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0151 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0199 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01891 | hp2 | a0001 | c0009 | t0003 | g0201 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01934 | hp2 | a0003 | c0004 | t0001 | g0269 | AMR | PEL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01952 | hp1 | a0003 | c0004 | t0001 | g0048 | AMR | PEL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0167 | AMR | PEL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0022 | AMR | PEL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0028 | AMR | PEL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01978 | hp1 | a0003 | c0004 | t0001 | g0010 | AMR | PEL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PEL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0022 | AMR | PEL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02015 | hp2 | a0001 | c0003 | t0001 | g0069 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02027 | hp1 | a0001 | c0005 | t0001 | g0207 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0202 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0137 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0203 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02080 | hp1 | a0003 | c0004 | t0001 | g0303 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02132 | hp1 | a0001 | c0003 | t0001 | g0064 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02132 | hp2 | a0001 | c0005 | t0001 | g0192 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02135 | hp1 | a0006 | c0011 | t0002 | g0261 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02135 | hp2 | a0001 | c0003 | t0001 | g0206 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02145 | hp1 | a0004 | c0012 | t0001 | g0140 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0138 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02148 | hp2 | a0003 | c0004 | t0001 | g0327 | AMR | PEL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0130 | EAS | CDX | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02155 | hp2 | a0001 | c0003 | t0001 | g0078 | EAS | CDX | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02165 | hp1 | a0001 | c0003 | t0001 | g0181 | EAS | CDX | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02165 | hp2 | a0003 | c0004 | t0001 | g0290 | EAS | CDX | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02257 | hp1 | a0001 | c0017 | t0001 | g0293 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02257 | hp2 | a0003 | c0013 | t0001 | g0215 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02258 | hp1 | a0004 | c0008 | t0001 | g0211 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0142 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0057 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0122 | AMR | PEL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02293 | hp2 | a0003 | c0004 | t0001 | g0010 | AMR | PEL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0011 | AMR | PEL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02451 | hp1 | a0005 | c0010 | t0001 | g0208 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02451 | hp2 | a0004 | c0008 | t0001 | g0158 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0177 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0081 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02622 | hp2 | a0002 | c0007 | t0001 | g0005 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0136 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0085 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02698 | hp2 | a0003 | c0004 | t0001 | g0323 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02717 | hp1 | a0004 | c0018 | t0003 | g0095 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02717 | hp2 | a0002 | c0002 | t0006 | g0102 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0174 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02738 | hp1 | a0003 | c0004 | t0001 | g0322 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02738 | hp2 | a0003 | c0006 | t0001 | g0317 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0109 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0172 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0176 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02886 | hp1 | a0004 | c0014 | t0003 | g0055 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0017 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02895 | hp1 | a0005 | c0010 | t0001 | g0169 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02922 | hp1 | a0004 | c0012 | t0001 | g0170 | AFR | ESN | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | ESN | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0104 | AFR | ESN | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | ESN | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02976 | hp1 | a0002 | c0007 | t0001 | g0159 | AFR | ESN | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | ESN | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0023 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0058 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03041 | hp2 | a0002 | c0007 | t0001 | g0005 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0164 | AFR | MSL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03098 | hp2 | a0001 | c0015 | t0001 | g0234 | AFR | MSL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0156 | AFR | ESN | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0153 | AFR | ESN | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0017 | AFR | ESN | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0194 | AFR | ESN | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | ESN | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0059 | AFR | ESN | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03209 | hp1 | a0001 | c0016 | t0001 | g0235 | AFR | MSL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0168 | AFR | MSL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | MSL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03239 | hp2 | a0003 | c0006 | t0001 | g0270 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0141 | AFR | MSL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03453 | hp2 | a0002 | c0007 | t0001 | g0005 | AFR | MSL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | MSL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0106 | AFR | MSL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03490 | hp1 | a0003 | c0006 | t0002 | g0278 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0023 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03516 | hp1 | a0008 | c0019 | t0001 | g0210 | AFR | ESN | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0166 | AFR | ESN | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0175 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0195 | AFR | GWD | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0031 | AFR | MSL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03579 | hp2 | a0001 | c0020 | t0008 | g0336 | AFR | MSL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03669 | hp1 | a0003 | c0004 | t0001 | g0236 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0065 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0076 | SAS | STU | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0093 | SAS | STU | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0115 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0226 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0152 | SAS | BEB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0088 | SAS | BEB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | BEB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0062 | SAS | BEB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03942 | hp2 | a0003 | c0006 | t0001 | g0275 | SAS | BEB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0302 | SAS | STU | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG04115 | hp2 | a0003 | c0004 | t0001 | g0320 | SAS | STU | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0087 | SAS | BEB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG04184 | hp2 | a0003 | c0004 | t0001 | g0222 | SAS | BEB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0092 | SAS | STU | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG04228 | hp2 | a0001 | c0009 | t0001 | g0012 | SAS | STU | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0161 | AFR | YRI | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | YRI | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | CHB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | CHB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0101 | AFR | YRI | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0110 | AFR | YRI | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18939 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18939 | hp2 | a0001 | c0003 | t0001 | g0182 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18940 | hp2 | a0001 | c0003 | t0001 | g0077 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18941 | hp2 | a0001 | c0003 | t0001 | g0186 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0184 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18943 | hp1 | a0001 | c0003 | t0001 | g0185 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18944 | hp2 | a0001 | c0005 | t0001 | g0190 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0128 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18947 | hp1 | a0001 | c0003 | t0001 | g0179 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18948 | hp1 | a0001 | c0005 | t0001 | g0006 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18951 | hp1 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18952 | hp2 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18957 | hp2 | a0001 | c0003 | t0001 | g0331 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18960 | hp1 | a0001 | c0005 | t0001 | g0006 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18960 | hp2 | a0006 | c0011 | t0001 | g0260 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0335 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18962 | hp1 | a0001 | c0003 | t0001 | g0052 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18962 | hp2 | a0003 | c0004 | t0001 | g0321 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18967 | hp1 | a0001 | c0003 | t0001 | g0334 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18968 | hp1 | a0001 | c0005 | t0001 | g0187 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18970 | hp1 | a0001 | c0003 | t0001 | g0079 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18970 | hp2 | a0001 | c0005 | t0001 | g0006 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0333 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18971 | hp2 | a0001 | c0003 | t0002 | g0183 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18979 | hp1 | a0001 | c0003 | t0001 | g0063 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18980 | hp2 | a0001 | c0003 | t0001 | g0053 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18981 | hp1 | a0001 | c0005 | t0001 | g0034 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18981 | hp2 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18982 | hp2 | a0001 | c0005 | t0001 | g0006 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18984 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18986 | hp1 | a0001 | c0003 | t0002 | g0332 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18988 | hp2 | a0001 | c0005 | t0001 | g0188 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18991 | hp1 | a0001 | c0003 | t0001 | g0090 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18995 | hp2 | a0001 | c0003 | t0001 | g0089 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19002 | hp1 | a0001 | c0003 | t0002 | g0070 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19003 | hp2 | a0001 | c0005 | t0001 | g0191 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19004 | hp1 | a0001 | c0005 | t0001 | g0034 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19004 | hp2 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19007 | hp1 | a0003 | c0004 | t0001 | g0319 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19009 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19010 | hp1 | a0001 | c0005 | t0001 | g0193 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0080 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19012 | hp2 | a0001 | c0003 | t0002 | g0067 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19030 | hp1 | a0005 | c0010 | t0001 | g0165 | AFR | LWK | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0160 | AFR | LWK | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0196 | AFR | LWK | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19043 | hp2 | a0001 | c0003 | t0003 | g0068 | AFR | LWK | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19054 | hp1 | a0001 | c0005 | t0002 | g0178 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19060 | hp1 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19060 | hp2 | a0001 | c0003 | t0001 | g0086 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19062 | hp2 | a0001 | c0003 | t0001 | g0091 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19065 | hp2 | a0001 | c0003 | t0001 | g0060 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19066 | hp2 | a0001 | c0005 | t0001 | g0200 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19070 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19078 | hp1 | a0001 | c0005 | t0001 | g0214 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19078 | hp2 | a0001 | c0001 | t0005 | g0241 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19079 | hp1 | a0001 | c0003 | t0001 | g0054 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19080 | hp1 | a0001 | c0003 | t0001 | g0180 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19081 | hp2 | a0001 | c0005 | t0001 | g0006 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19083 | hp2 | a0001 | c0003 | t0002 | g0329 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19084 | hp1 | a0001 | c0003 | t0001 | g0061 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19090 | hp2 | a0001 | c0003 | t0002 | g0204 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19091 | hp2 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0157 | AFR | YRI | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0171 | AFR | YRI | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0197 | AFR | ASW | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA20129 | hp2 | a0002 | c0007 | t0001 | g0005 | AFR | ASW | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0037 | EUR | TSI | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0056 | EUR | TSI | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG01123 | hp2 | a0003 | c0006 | t0002 | g0326 | AMR | CLM | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0205 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0163 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02486 | hp1 | a0004 | c0008 | t0001 | g0213 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0135 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02559 | hp1 | a0004 | c0008 | t0001 | g0173 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0021 | AFR | ACB | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03471 | hp1 | a0002 | c0007 | t0001 | g0005 | AFR | MSL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0074 | AFR | MSL | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18955 | hp1 | a0001 | c0005 | t0001 | g0189 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA20300 | hp1 | a0004 | c0008 | t0001 | g0212 | AFR | USA | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA20300 | hp2 | a0003 | c0004 | t0001 | g0049 | AFR | USA | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0162 | AFR | LWK | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0198 | AFR | LWK | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0233 | REF | REF | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0107 | REF | REF | CD163_chr12_7465811_7508777 | CD163 | chr12 | 7465811 | 7508777 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7482694 | C | T | 1 | a0008 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.3196G>A | p.Val1066Ile | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 14/17 | 3283/4071 | 3196/3366 | 1066/1121 | chr12 | 7482694 | |||
| chr12:7485136 | T | G | 1 | a0006 | 3 | HG00597.hp2 HG02135.hp1 NA18960.hp2 |
missense_variant | MODERATE | c.2739A>C | p.Arg913Ser | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/17 | 2826/4071 | 2739/3366 | 913/1121 | chr12 | 7485136 | |||
| chr12:7485173 | G | A | 1 | a0003 | 36 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(33): Show |
missense_variant | MODERATE | c.2702C>T | p.Thr901Met | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/17 | 2789/4071 | 2702/3366 | 901/1121 | chr12 | 7485173 | |||
| chr12:7487483 | A | T | 1 | a0004 | 9 | HG02145.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
missense_variant | MODERATE | c.1926T>A | p.Asn642Lys | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 8/17 | 2013/4071 | 1926/3366 | 642/1121 | chr12 | 7487483 | |||
| chr12:7487799 | C | T | 1 | a0005 | 4 | HG01261.hp1 HG02451.hp1 HG02895.hp1 others(1): Show |
missense_variant | MODERATE | c.1709G>A | p.Ser570Asn | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 7/17 | 1796/4071 | 1709/3366 | 570/1121 | chr12 | 7487799 | |||
| chr12:7496888 | T | C | 5 | a0001 a0003 a0005 others(2): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
missense_variant | MODERATE | c.1024A>G | p.Ile342Val | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/17 | 1111/4071 | 1024/3366 | 342/1121 | chr12 | 7496888 | |||
| chr12:7499111 | G | A | 1 | a0007 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.535C>T | p.Arg179Trp | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/17 | 622/4071 | 535/3366 | 179/1121 | chr12 | 7499111 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7483431 | A | G | 1 | a0002c0007 | 7 | HG01243.hp2 HG02622.hp2 HG02976.hp1 others(4): Show |
synonymous_variant | LOW | c.3024T>C | p.Cys1008Cys | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 12/17 | 3111/4071 | 3024/3366 | 1008/1121 | chr12 | 7483431 | |||
| chr12:7485112 | G | A | 1 | a0004c0018 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.2763C>T | p.Thr921Thr | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/17 | 2850/4071 | 2763/3366 | 921/1121 | chr12 | 7485112 | |||
| chr12:7485199 | A | G | 1 | a0001c0005 | 18 | HG02027.hp1 HG02132.hp2 NA18944.hp2 others(15): Show |
synonymous_variant | LOW | c.2676T>C | p.Asn892Asn | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/17 | 2763/4071 | 2676/3366 | 892/1121 | chr12 | 7485199 | |||
| chr12:7485276 | G | A | 3 | a0004c0008 a0004c0014 a0004c0018 |
7 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
synonymous_variant | LOW | c.2599C>T | p.Leu867Leu | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/17 | 2686/4071 | 2599/3366 | 867/1121 | chr12 | 7485276 | |||
| chr12:7487993 | C | T | 2 | a0003c0006 a0003c0021 |
13 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(10): Show |
synonymous_variant | LOW | c.1515G>A | p.Ser505Ser | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 7/17 | 1602/4071 | 1515/3366 | 505/1121 | chr12 | 7487993 | |||
| chr12:7495172 | G | A | 1 | a0001c0017 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.1329C>T | p.Asn443Asn | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/17 | 1416/4071 | 1329/3366 | 443/1121 | chr12 | 7495172 | |||
| chr12:7496952 | G | A | 2 | a0001c0016 a0001c0020 |
2 | HG03209.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.960C>T | p.Asn320Asn | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/17 | 1047/4071 | 960/3366 | 320/1121 | chr12 | 7496952 | |||
| chr12:7497057 | T | C | 8 | a0001c0001 a0001c0009 a0001c0017 others(5): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
synonymous_variant | LOW | c.855A>G | p.Gly285Gly | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/17 | 942/4071 | 855/3366 | 285/1121 | chr12 | 7497057 | |||
| chr12:7501374 | C | T | 1 | a0003c0013 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.222G>A | p.Thr74Thr | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/17 | 309/4071 | 222/3366 | 74/1121 | chr12 | 7501374 | |||
| chr12:7502541 | A | G | 9 | a0001c0001 a0001c0015 a0001c0016 others(6): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
synonymous_variant | LOW | c.70T>C | p.Leu24Leu | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 2/17 | 157/4071 | 70/3366 | 24/1121 | chr12 | 7502541 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7470891 | G | A | 1 | a0001c0001t0005 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*538C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 17/17 | 9000 | chr12 | 7470891 | ||||||
| chr12:7470921 | T | C | 1 | a0002c0002t0006 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*508A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 17/17 | 8970 | chr12 | 7470921 | ||||||
| chr12:7471001 | T | A | 4 | a0001c0003t0003 a0001c0009t0003 a0004c0014t0003 others(1): Show |
4 | HG01891.hp2 HG02717.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*428A>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 17/17 | 8890 | chr12 | 7471001 | ||||||
| chr12:7471044 | A | G | 1 | a0003c0004t0004 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*385T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 17/17 | 8847 | chr12 | 7471044 | ||||||
| chr12:7471128 | A | G | 7 | a0001c0001t0002 a0001c0003t0002 a0001c0005t0002 others(4): Show |
110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*301T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 17/17 | 8763 | chr12 | 7471128 | ||||||
| chr12:7471391 | G | A | 1 | a0002c0002t0007 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*38C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 17/17 | 8500 | chr12 | 7471391 | ||||||
| chr12:7503737 | T | A | 1 | a0001c0020t0008 | 1 | HG03579.hp2 | 5_prime_UTR_variant | MODIFIER | c.-47A>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 1/17 | 47 | chr12 | 7503737 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7471477 | C | T | 108 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(105): Show |
141 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.*32-80G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7471477 | |||||||
| chr12:7471517 | A | C | 2 | a0001c0001t0001g0314 a0003c0006t0001g0316 |
2 | HG01175.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.*32-120T>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7471517 | |||||||
| chr12:7471529 | AT | A | 58 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0001g0280 others(55): Show |
83 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.*32-133delA | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7471529 | |||||||
| chr12:7471584 | T | TAAGATTA others(308): Show |
1 | a0001c0003t0001g0186 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.*32-188_*32-187ins others(315): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7471584 | |||||||
| chr12:7471584 | T | TAAGATTA others(308): Show |
29 | a0001c0001t0001g0223 a0001c0001t0001g0242 a0001c0001t0001g0243 others(26): Show |
40 | HG00609.hp1 HG00639.hp2 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.*32-188_*32-187ins others(315): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7471584 | |||||||
| chr12:7471629 | T | C | 54 | a0001c0001t0001g0258 a0001c0001t0001g0285 a0001c0001t0001g0297 others(51): Show |
61 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.*32-232A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7471629 | |||||||
| chr12:7471835 | G | A | 2 | a0001c0001t0002g0251 a0002c0002t0002g0132 |
2 | HG01099.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.*32-438C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7471835 | |||||||
| chr12:7471861 | C | T | 1 | a0001c0003t0001g0018 | 3 | NA18951.hp1 NA18981.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.*32-464G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7471861 | |||||||
| chr12:7471962 | G | A | 1 | a0001c0001t0002g0268 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.*32-565C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7471962 | |||||||
| chr12:7471969 | A | T | 1 | a0001c0003t0001g0066 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.*32-572T>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7471969 | |||||||
| chr12:7471983 | G | A | 1 | a0003c0006t0001g0277 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.*32-586C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7471983 | |||||||
| chr12:7472115 | G | A | 1 | a0002c0002t0001g0136 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.*32-718C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7472115 | |||||||
| chr12:7472136 | G | A | 4 | a0001c0003t0001g0016 a0001c0003t0001g0143 a0005c0010t0001g0208 others(1): Show |
6 | HG00738.hp2 HG01261.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.*32-739C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7472136 | |||||||
| chr12:7472213 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.*32-816G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7472213 | |||||||
| chr12:7472218 | T | C | 54 | a0001c0001t0001g0258 a0001c0001t0001g0285 a0001c0001t0001g0297 others(51): Show |
61 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.*32-821A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7472218 | |||||||
| chr12:7472418 | T | C | 31 | a0001c0001t0001g0223 a0001c0001t0001g0242 a0001c0001t0001g0243 others(28): Show |
42 | HG00609.hp1 HG00639.hp2 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.*32-1021A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7472418 | |||||||
| chr12:7472550 | C | A | 5 | a0001c0003t0001g0163 a0001c0016t0001g0235 a0002c0002t0001g0026 others(2): Show |
6 | HG02055.hp2 HG02109.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.*32-1153G>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7472550 | |||||||
| chr12:7472557 | AC | A | 8 | a0001c0001t0001g0221 a0001c0003t0001g0033 a0002c0002t0001g0008 others(5): Show |
12 | HG02040.hp2 HG02083.hp1 NA18948.hp2 others(9): Show |
intron_variant | MODIFIER | c.*32-1161delG | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7472557 | |||||||
| chr12:7472578 | T | C | 114 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0001g0258 others(111): Show |
147 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(144): Show |
intron_variant | MODIFIER | c.*32-1181A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7472578 | |||||||
| chr12:7472596 | A | G | 1 | a0004c0008t0001g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.*32-1199T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7472596 | |||||||
| chr12:7472622 | A | C | 332 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(329): Show |
424 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(421): Show |
intron_variant | MODIFIER | c.*32-1225T>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7472622 | |||||||
| chr12:7472689 | G | C | 114 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0001g0258 others(111): Show |
147 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(144): Show |
intron_variant | MODIFIER | c.*32-1292C>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7472689 | |||||||
| chr12:7472821 | A | G | 131 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(128): Show |
172 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.*32-1424T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7472821 | |||||||
| chr12:7472947 | A | G | 1 | a0001c0001t0002g0238 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.*32-1550T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7472947 | |||||||
| chr12:7473258 | G | A | 113 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0001g0258 others(110): Show |
146 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(143): Show |
intron_variant | MODIFIER | c.*32-1861C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7473258 | |||||||
| chr12:7473328 | C | T | 1 | a0001c0003t0002g0183 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.*32-1931G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7473328 | |||||||
| chr12:7473444 | T | G | 1 | a0002c0002t0001g0133 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.*32-2047A>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7473444 | |||||||
| chr12:7473656 | A | T | 1 | a0002c0002t0001g0099 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.*32-2259T>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7473656 | |||||||
| chr12:7473761 | A | G | 33 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0227 others(30): Show |
37 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.*32-2364T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7473761 | |||||||
| chr12:7473920 | G | C | 4 | a0001c0003t0001g0016 a0001c0003t0001g0143 a0005c0010t0001g0208 others(1): Show |
6 | HG00738.hp2 HG01261.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.*32-2523C>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7473920 | |||||||
| chr12:7473986 | T | G | 322 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(319): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.*32-2589A>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7473986 | |||||||
| chr12:7474005 | G | C | 1 | a0001c0001t0002g0040 | 2 | NA19074.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.*32-2608C>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7474005 | |||||||
| chr12:7474076 | A | T | 3 | a0001c0003t0001g0018 a0001c0003t0001g0179 a0001c0003t0001g0203 |
5 | HG02056.hp2 NA18947.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.*32-2679T>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7474076 | |||||||
| chr12:7474128 | G | C | 1 | a0001c0001t0002g0244 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.*32-2731C>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7474128 | |||||||
| chr12:7474266 | A | T | 13 | a0001c0003t0001g0163 a0001c0016t0001g0235 a0002c0002t0001g0024 others(10): Show |
20 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.*32-2869T>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7474266 | |||||||
| chr12:7474657 | A | T | 1 | a0001c0005t0001g0192 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.*32-3260T>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7474657 | |||||||
| chr12:7474707 | G | A | 1 | a0002c0002t0001g0121 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.*32-3310C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7474707 | |||||||
| chr12:7474709 | C | G | 1 | a0002c0002t0001g0112 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.*32-3312G>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7474709 | |||||||
| chr12:7474715 | A | G | 32 | a0001c0001t0001g0223 a0001c0001t0001g0242 a0001c0001t0001g0243 others(29): Show |
43 | HG00609.hp1 HG00639.hp2 HG01123.hp1 others(40): Show |
intron_variant | MODIFIER | c.*32-3318T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7474715 | |||||||
| chr12:7474889 | G | A | 1 | a0002c0002t0002g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.*32-3492C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7474889 | |||||||
| chr12:7474916 | T | C | 1 | a0002c0002t0007g0103 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.*32-3519A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7474916 | |||||||
| chr12:7475035 | G | A | 1 | a0001c0003t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.*32-3638C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475035 | |||||||
| chr12:7475097 | C | CA | 107 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(104): Show |
140 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.*32-3701dupT | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475097 | |||||||
| chr12:7475097 | C | CAA | 105 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0221 others(102): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.*32-3702_*32-3701d others(4): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475097 | |||||||
| chr12:7475097 | C | CAAA | 13 | a0001c0001t0001g0256 a0001c0001t0001g0291 a0001c0001t0002g0246 others(10): Show |
15 | HG00735.hp1 HG01261.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.*32-3703_*32-3701d others(5): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475097 | |||||||
| chr12:7475097 | C | CAAAAAAA others(10): Show |
1 | a0005c0010t0001g0208 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.*32-3717_*32-3701d others(19): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475097 | |||||||
| chr12:7475097 | C | CAAAAAAA others(11): Show |
1 | a0005c0010t0001g0209 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.*32-3718_*32-3701d others(20): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475097 | |||||||
| chr12:7475097 | C | CAAAAAAA others(12): Show |
1 | a0001c0003t0001g0016 | 3 | HG01884.hp2 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.*32-3719_*32-3701d others(21): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475097 | |||||||
| chr12:7475097 | C | CAAAAAAA others(13): Show |
1 | a0001c0003t0001g0143 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.*32-3720_*32-3701d others(22): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475097 | |||||||
| chr12:7475097 | CA | C | 6 | a0001c0003t0001g0057 a0001c0003t0001g0186 a0001c0005t0001g0187 others(3): Show |
6 | HG02280.hp1 HG03516.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.*32-3701delT | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475097 | |||||||
| chr12:7475097 | CAA | C | 32 | a0001c0001t0001g0223 a0001c0001t0001g0242 a0001c0001t0001g0243 others(29): Show |
45 | HG00609.hp1 HG00639.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.*32-3702_*32-3701d others(4): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475097 | |||||||
| chr12:7475097 | CAAA | C | 48 | a0001c0001t0001g0258 a0001c0001t0001g0285 a0001c0001t0001g0297 others(45): Show |
53 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.*32-3703_*32-3701d others(5): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475097 | |||||||
| chr12:7475105 | A | T | 1 | a0001c0005t0001g0188 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.*32-3708T>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475105 | |||||||
| chr12:7475241 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.*32-3844C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475241 | |||||||
| chr12:7475282 | C | T | 1 | a0001c0003t0001g0077 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.*32-3885G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475282 | |||||||
| chr12:7475371 | C | T | 2 | a0001c0001t0002g0230 a0001c0003t0002g0071 |
2 | HG01256.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.*32-3974G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475371 | |||||||
| chr12:7475438 | G | A | 1 | a0001c0003t0001g0184 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.*32-4041C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475438 | |||||||
| chr12:7475490 | A | G | 3 | a0001c0003t0001g0058 a0001c0003t0001g0059 a0001c0003t0001g0196 |
3 | HG03041.hp1 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.*32-4093T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475490 | |||||||
| chr12:7475582 | C | T | 4 | a0001c0003t0001g0016 a0001c0003t0001g0143 a0005c0010t0001g0208 others(1): Show |
6 | HG00738.hp2 HG01261.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.*32-4185G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475582 | |||||||
| chr12:7475585 | A | G | 3 | a0001c0003t0001g0074 a0002c0002t0001g0106 a0002c0002t0001g0137 |
3 | HG02055.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.*32-4188T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475585 | |||||||
| chr12:7475612 | A | T | 2 | a0001c0003t0001g0160 a0001c0003t0001g0162 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.*32-4215T>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475612 | |||||||
| chr12:7475858 | C | T | 4 | a0001c0003t0001g0016 a0001c0003t0001g0143 a0005c0010t0001g0208 others(1): Show |
6 | HG00738.hp2 HG01261.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.*31+4002G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7475858 | |||||||
| chr12:7476117 | G | C | 4 | a0001c0003t0001g0172 a0001c0003t0001g0195 a0001c0015t0001g0234 others(1): Show |
4 | HG01109.hp2 HG02818.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*31+3743C>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7476117 | |||||||
| chr12:7476127 | A | G | 2 | a0004c0012t0001g0140 a0004c0012t0001g0170 |
2 | HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.*31+3733T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7476127 | |||||||
| chr12:7476194 | A | C | 2 | a0005c0010t0001g0208 a0005c0010t0001g0209 |
2 | HG01261.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.*31+3666T>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7476194 | |||||||
| chr12:7476201 | T | C | 2 | a0005c0010t0001g0208 a0005c0010t0001g0209 |
2 | HG01261.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.*31+3659A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7476201 | |||||||
| chr12:7476211 | T | G | 1 | a0001c0001t0001g0264 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.*31+3649A>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7476211 | |||||||
| chr12:7476319 | G | A | 2 | a0001c0003t0001g0172 a0001c0003t0001g0195 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.*31+3541C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7476319 | |||||||
| chr12:7476349 | A | G | 1 | a0001c0001t0001g0243 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.*31+3511T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7476349 | |||||||
| chr12:7476463 | C | A | 2 | a0005c0010t0001g0208 a0005c0010t0001g0209 |
2 | HG01261.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.*31+3397G>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7476463 | |||||||
| chr12:7476468 | C | T | 1 | a0004c0008t0001g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.*31+3392G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7476468 | |||||||
| chr12:7476594 | G | C | 1 | a0001c0003t0001g0080 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.*31+3266C>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7476594 | |||||||
| chr12:7476698 | C | T | 1 | a0002c0002t0006g0102 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.*31+3162G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7476698 | |||||||
| chr12:7477052 | C | A | 1 | a0004c0008t0001g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.*31+2808G>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7477052 | |||||||
| chr12:7477115 | T | C | 1 | a0001c0005t0001g0207 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.*31+2745A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7477115 | |||||||
| chr12:7477229 | C | CT | 32 | a0001c0001t0001g0223 a0001c0001t0001g0242 a0001c0001t0001g0243 others(29): Show |
43 | HG00609.hp1 HG00639.hp2 HG01123.hp1 others(40): Show |
intron_variant | MODIFIER | c.*31+2630_*31+2631i others(3): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7477229 | |||||||
| chr12:7477316 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.*31+2544C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7477316 | |||||||
| chr12:7477321 | G | C | 1 | a0001c0003t0001g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.*31+2539C>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7477321 | |||||||
| chr12:7477391 | G | A | 1 | a0002c0002t0001g0110 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.*31+2469C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7477391 | |||||||
| chr12:7477469 | A | C | 1 | a0001c0003t0001g0073 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.*31+2391T>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7477469 | |||||||
| chr12:7477493 | A | G | 1 | a0002c0002t0006g0102 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.*31+2367T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7477493 | |||||||
| chr12:7477503 | G | A | 1 | a0001c0001t0002g0225 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.*31+2357C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7477503 | |||||||
| chr12:7477585 | C | T | 1 | a0002c0002t0001g0150 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.*31+2275G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7477585 | |||||||
| chr12:7477664 | G | C | 60 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0001g0280 others(57): Show |
85 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.*31+2196C>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7477664 | |||||||
| chr12:7477696 | G | A | 1 | a0002c0002t0001g0115 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.*31+2164C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7477696 | |||||||
| chr12:7477917 | T | G | 1 | a0005c0010t0001g0169 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.*31+1943A>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7477917 | |||||||
| chr12:7477982 | T | C | 54 | a0001c0001t0001g0258 a0001c0001t0001g0285 a0001c0001t0001g0297 others(51): Show |
61 | HG00408.hp1 HG00544.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.*31+1878A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7477982 | |||||||
| chr12:7478030 | A | G | 8 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0239 others(5): Show |
10 | HG00544.hp2 NA18747.hp2 NA18953.hp1 others(7): Show |
intron_variant | MODIFIER | c.*31+1830T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7478030 | |||||||
| chr12:7478128 | A | C | 1 | a0001c0001t0001g0045 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.*31+1732T>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7478128 | |||||||
| chr12:7478237 | T | G | 60 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0001g0280 others(57): Show |
85 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.*31+1623A>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7478237 | |||||||
| chr12:7478348 | G | A | 1 | a0001c0001t0002g0247 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.*31+1512C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7478348 | |||||||
| chr12:7478594 | C | A | 129 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0001g0258 others(126): Show |
166 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.*31+1266G>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7478594 | |||||||
| chr12:7478629 | A | G | 60 | a0001c0001t0001g0221 a0001c0001t0001g0231 a0001c0001t0001g0280 others(57): Show |
85 | HG00558.hp2 HG00642.hp1 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.*31+1231T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7478629 | |||||||
| chr12:7478681 | G | T | 1 | a0002c0002t0002g0132 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.*31+1179C>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7478681 | |||||||
| chr12:7478687 | T | TAAGAGTT others(319): Show |
2 | a0001c0003t0001g0032 a0001c0003t0001g0198 |
3 | HG01167.hp1 HG01169.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.*31+1172_*31+1173i others(328): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7478687 | |||||||
| chr12:7478851 | C | T | 3 | a0001c0003t0001g0160 a0001c0003t0001g0162 a0005c0010t0001g0169 |
3 | HG02895.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.*31+1009G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7478851 | |||||||
| chr12:7478988 | TTA | T | 23 | a0001c0001t0001g0264 a0001c0001t0002g0226 a0001c0003t0001g0019 others(20): Show |
30 | HG02027.hp1 HG02258.hp1 HG02486.hp1 others(27): Show |
intron_variant | MODIFIER | c.*31+870_*31+871del others(2): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7478988 | |||||||
| chr12:7479100 | C | T | 2 | a0001c0003t0001g0057 a0001c0003t0001g0172 |
2 | HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.*31+760G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7479100 | |||||||
| chr12:7479141 | T | G | 5 | a0001c0020t0008g0336 a0004c0008t0001g0173 a0004c0008t0001g0211 others(2): Show |
5 | HG02258.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.*31+719A>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7479141 | |||||||
| chr12:7479287 | G | A | 264 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0216 others(261): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.*31+573C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7479287 | |||||||
| chr12:7479318 | C | T | 212 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0216 others(209): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.*31+542G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7479318 | |||||||
| chr12:7479342 | T | G | 13 | a0001c0001t0001g0044 a0001c0001t0001g0223 a0001c0003t0001g0003 others(10): Show |
22 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.*31+518A>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7479342 | |||||||
| chr12:7479387 | A | T | 2 | a0001c0003t0001g0057 a0001c0003t0001g0172 |
2 | HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.*31+473T>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7479387 | |||||||
| chr12:7479534 | C | T | 2 | a0003c0004t0001g0319 a0003c0004t0001g0321 |
2 | NA18962.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.*31+326G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7479534 | |||||||
| chr12:7479547 | T | C | 233 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0216 others(230): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.*31+313A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7479547 | |||||||
| chr12:7479780 | T | C | 44 | a0001c0001t0001g0291 a0001c0001t0001g0297 a0001c0003t0001g0011 others(41): Show |
48 | HG00544.hp1 HG00621.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.*31+80A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7479780 | |||||||
| chr12:7479799 | C | G | 1 | a0001c0009t0003g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.*31+61G>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 16/16 | chr12 | 7479799 | |||||||
| chr12:7479937 | G | T | 3 | a0005c0010t0001g0165 a0005c0010t0001g0208 a0005c0010t0001g0209 |
3 | HG01261.hp1 HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3344-24C>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 15/16 | chr12 | 7479937 | |||||||
| chr12:7479969 | C | T | 1 | a0001c0020t0008g0336 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3344-56G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 15/16 | chr12 | 7479969 | |||||||
| chr12:7480076 | A | C | 6 | a0001c0003t0001g0019 a0001c0003t0001g0184 a0001c0003t0001g0185 others(3): Show |
8 | NA18941.hp2 NA18942.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.3344-163T>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 15/16 | chr12 | 7480076 | |||||||
| chr12:7480077 | C | G | 13 | a0001c0005t0001g0006 a0001c0005t0001g0034 a0001c0005t0001g0187 others(10): Show |
18 | HG02027.hp1 NA18944.hp2 NA18948.hp1 others(15): Show |
intron_variant | MODIFIER | c.3344-164G>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 15/16 | chr12 | 7480077 | |||||||
| chr12:7480225 | T | C | 5 | a0004c0008t0001g0158 a0004c0008t0001g0173 a0004c0008t0001g0211 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3344-312A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 15/16 | chr12 | 7480225 | |||||||
| chr12:7480244 | C | T | 1 | a0001c0003t0002g0071 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3344-331G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 15/16 | chr12 | 7480244 | |||||||
| chr12:7480251 | A | G | 1 | a0003c0006t0002g0326 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3344-338T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 15/16 | chr12 | 7480251 | |||||||
| chr12:7480380 | G | A | 6 | a0001c0003t0001g0017 a0001c0003t0001g0031 a0001c0003t0001g0160 others(3): Show |
9 | HG00639.hp2 HG01175.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.3344-467C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 15/16 | chr12 | 7480380 | |||||||
| chr12:7480579 | C | T | 5 | a0004c0008t0001g0158 a0004c0008t0001g0173 a0004c0008t0001g0211 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3343+582G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 15/16 | chr12 | 7480579 | |||||||
| chr12:7480857 | T | C | 2 | a0005c0010t0001g0208 a0005c0010t0001g0209 |
2 | HG01261.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3343+304A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 15/16 | chr12 | 7480857 | |||||||
| chr12:7480905 | A | G | 4 | a0001c0003t0001g0174 a0001c0003t0001g0175 a0001c0003t0001g0176 others(1): Show |
4 | HG02109.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3343+256T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 15/16 | chr12 | 7480905 | |||||||
| chr12:7481072 | T | A | 22 | a0001c0003t0001g0003 a0001c0003t0001g0033 a0001c0003t0001g0074 others(19): Show |
33 | HG02027.hp1 HG02132.hp2 HG02258.hp2 others(30): Show |
intron_variant | MODIFIER | c.3343+89A>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 15/16 | chr12 | 7481072 | |||||||
| chr12:7481127 | C | A | 1 | a0001c0001t0001g0318 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3343+34G>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 15/16 | chr12 | 7481127 | |||||||
| chr12:7481312 | C | T | 1 | a0002c0007t0001g0131 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3248-56G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 14/16 | chr12 | 7481312 | |||||||
| chr12:7481351 | G | A | 3 | a0001c0016t0001g0235 a0001c0020t0008g0336 a0002c0002t0001g0110 |
3 | HG03209.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3248-95C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 14/16 | chr12 | 7481351 | |||||||
| chr12:7481412 | G | A | 2 | a0001c0003t0001g0199 a0001c0003t0001g0205 |
2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.3248-156C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 14/16 | chr12 | 7481412 | |||||||
| chr12:7481417 | C | G | 1 | a0002c0002t0001g0111 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3248-161G>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 14/16 | chr12 | 7481417 | |||||||
| chr12:7481603 | C | A | 1 | a0001c0003t0001g0077 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3248-347G>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 14/16 | chr12 | 7481603 | |||||||
| chr12:7481604 | A | T | 1 | a0001c0003t0001g0077 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3248-348T>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 14/16 | chr12 | 7481604 | |||||||
| chr12:7481605 | C | A | 1 | a0001c0003t0001g0077 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3248-349G>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 14/16 | chr12 | 7481605 | |||||||
| chr12:7481607 | T | A | 1 | a0001c0003t0001g0077 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3248-351A>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 14/16 | chr12 | 7481607 | |||||||
| chr12:7481608 | C | T | 1 | a0001c0003t0001g0077 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3248-352G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 14/16 | chr12 | 7481608 | |||||||
| chr12:7481610 | A | G | 1 | a0001c0003t0001g0077 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3248-354T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 14/16 | chr12 | 7481610 | |||||||
| chr12:7481611 | C | A | 1 | a0001c0003t0001g0077 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3248-355G>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 14/16 | chr12 | 7481611 | |||||||
| chr12:7482020 | A | G | 2 | a0001c0001t0001g0294 a0001c0001t0001g0296 |
2 | NA18612.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.3247+623T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 14/16 | chr12 | 7482020 | |||||||
| chr12:7482027 | T | C | 2 | a0001c0016t0001g0235 a0001c0020t0008g0336 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3247+616A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 14/16 | chr12 | 7482027 | |||||||
| chr12:7482027 | T | G | 1 | a0002c0002t0001g0139 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3247+616A>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 14/16 | chr12 | 7482027 | |||||||
| chr12:7482050 | A | G | 2 | a0005c0010t0001g0169 a0008c0019t0001g0210 |
2 | HG02895.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3247+593T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 14/16 | chr12 | 7482050 | |||||||
| chr12:7482085 | T | G | 1 | a0004c0008t0001g0173 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3247+558A>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 14/16 | chr12 | 7482085 | |||||||
| chr12:7482145 | C | A | 1 | a0001c0003t0001g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3247+498G>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 14/16 | chr12 | 7482145 | |||||||
| chr12:7482286 | G | A | 1 | a0001c0015t0001g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3247+357C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 14/16 | chr12 | 7482286 | |||||||
| chr12:7482442 | A | G | 245 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(242): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.3247+201T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 14/16 | chr12 | 7482442 | |||||||
| chr12:7483040 | T | C | 1 | a0001c0001t0001g0045 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3089-36A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 12/16 | chr12 | 7483040 | |||||||
| chr12:7483059 | G | A | 2 | a0005c0010t0001g0208 a0005c0010t0001g0209 |
2 | HG01261.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3089-55C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 12/16 | chr12 | 7483059 | |||||||
| chr12:7483197 | G | A | 215 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(212): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.3088+170C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 12/16 | chr12 | 7483197 | |||||||
| chr12:7483203 | T | C | 1 | a0001c0003t0001g0171 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3088+164A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 12/16 | chr12 | 7483203 | |||||||
| chr12:7483345 | A | G | 7 | a0001c0005t0001g0006 a0001c0005t0001g0188 a0001c0005t0001g0189 others(4): Show |
11 | HG02132.hp2 NA18944.hp2 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.3088+22T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 12/16 | chr12 | 7483345 | |||||||
| chr12:7483759 | T | G | 19 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0033 others(16): Show |
24 | HG00609.hp2 HG02040.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.2780-84A>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483759 | |||||||
| chr12:7483760 | T | TA | 7 | a0001c0001t0001g0300 a0001c0001t0002g0253 a0001c0005t0001g0214 others(4): Show |
7 | HG01934.hp1 HG02717.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2780-86dupT | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483760 | |||||||
| chr12:7483760 | TA | T | 11 | a0001c0001t0002g0220 a0001c0003t0001g0017 a0001c0003t0001g0031 others(8): Show |
14 | HG00639.hp2 HG01175.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2780-86delT | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483760 | |||||||
| chr12:7483795 | A | C | 4 | a0001c0003t0001g0032 a0001c0003t0001g0196 a0001c0003t0001g0197 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.2780-120T>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483795 | |||||||
| chr12:7483811 | T | TTA | 17 | a0001c0001t0001g0221 a0001c0001t0001g0258 a0001c0001t0001g0324 others(14): Show |
20 | HG00558.hp1 HG00673.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.2780-138_2780-137d others(4): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483811 | |||||||
| chr12:7483811 | T | TTATATAT others(9): Show |
2 | a0001c0003t0001g0051 a0001c0003t0001g0053 |
2 | HG00609.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.2780-137_2780-136i others(18): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483811 | |||||||
| chr12:7483813 | A | ATATATAT others(7): Show |
2 | a0001c0003t0001g0052 a0001c0003t0001g0054 |
2 | NA18962.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2780-139_2780-138i others(16): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483813 | |||||||
| chr12:7483815 | A | ATATATAT others(5): Show |
4 | a0001c0003t0001g0018 a0001c0003t0001g0180 a0001c0003t0001g0185 others(1): Show |
6 | HG02056.hp2 NA18943.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.2780-141_2780-140i others(14): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483815 | |||||||
| chr12:7483817 | A | ATATATAT others(3): Show |
5 | a0001c0003t0001g0019 a0001c0003t0001g0179 a0001c0003t0001g0186 others(2): Show |
7 | NA18941.hp2 NA18945.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.2780-143_2780-142i others(12): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483817 | |||||||
| chr12:7483823 | A | G | 1 | a0005c0010t0001g0165 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2780-148T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483823 | |||||||
| chr12:7483823 | ATG | A | 5 | a0004c0008t0001g0158 a0004c0008t0001g0173 a0004c0008t0001g0211 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2780-150_2780-149d others(4): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483823 | |||||||
| chr12:7483825 | G | A | 15 | a0001c0001t0005g0241 a0001c0003t0001g0018 a0001c0003t0001g0019 others(12): Show |
19 | HG00609.hp2 HG02056.hp2 NA18941.hp2 others(16): Show |
intron_variant | MODIFIER | c.2780-150C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483825 | |||||||
| chr12:7483825 | G | GTA | 5 | a0001c0003t0001g0016 a0001c0003t0001g0092 a0001c0003t0001g0143 others(2): Show |
7 | HG00738.hp2 HG01884.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2780-152_2780-151d others(4): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483825 | |||||||
| chr12:7483825 | G | GTATA | 20 | a0001c0001t0002g0238 a0001c0001t0002g0255 a0001c0003t0001g0003 others(17): Show |
22 | HG00673.hp1 HG01167.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.2780-154_2780-151d others(6): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483825 | |||||||
| chr12:7483825 | G | GTATATA | 9 | a0001c0001t0001g0279 a0001c0001t0001g0285 a0001c0001t0001g0292 others(6): Show |
10 | HG01891.hp2 HG01943.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.2780-156_2780-151d others(8): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483825 | |||||||
| chr12:7483825 | G | GTATATAT others(3): Show |
2 | a0001c0003t0001g0141 a0001c0003t0001g0195 |
2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2780-160_2780-151d others(12): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483825 | |||||||
| chr12:7483825 | G | GTATATAT others(9): Show |
1 | a0001c0003t0001g0172 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2780-166_2780-151d others(18): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483825 | |||||||
| chr12:7483829 | A | G | 5 | a0004c0008t0001g0158 a0004c0008t0001g0173 a0004c0008t0001g0211 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2780-154T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483829 | |||||||
| chr12:7483830 | T | TATATATA others(9): Show |
2 | a0005c0010t0001g0208 a0005c0010t0001g0209 |
2 | HG01261.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2780-156_2780-155i others(18): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483830 | |||||||
| chr12:7483841 | A | ATAT | 13 | a0001c0001t0001g0297 a0001c0003t0001g0003 a0001c0003t0001g0011 others(10): Show |
13 | HG00544.hp1 HG00621.hp2 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.2780-167_2780-166i others(5): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483841 | |||||||
| chr12:7483841 | A | ATATAT | 19 | a0001c0001t0001g0045 a0001c0001t0001g0264 a0001c0001t0001g0280 others(16): Show |
25 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.2780-167_2780-166i others(7): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483841 | |||||||
| chr12:7483841 | A | ATATATAT others(6): Show |
8 | a0001c0003t0001g0199 a0001c0005t0001g0034 a0001c0005t0001g0187 others(5): Show |
8 | HG01891.hp1 HG02027.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.2780-167_2780-166i others(15): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483841 | |||||||
| chr12:7483841 | A | ATATATAT others(8): Show |
2 | a0001c0005t0001g0034 a0001c0005t0002g0178 |
2 | NA19004.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.2780-167_2780-166i others(17): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483841 | |||||||
| chr12:7483841 | A | ATATATAT others(29): Show |
1 | a0001c0003t0001g0032 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2780-167_2780-166i others(38): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483841 | |||||||
| chr12:7483841 | A | ATATATAT others(25): Show |
1 | a0001c0003t0001g0197 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2780-167_2780-166i others(34): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483841 | |||||||
| chr12:7483841 | A | ATATATAT others(19): Show |
1 | a0001c0003t0001g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2780-167_2780-166i others(28): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483841 | |||||||
| chr12:7483841 | A | ATATATAT others(25): Show |
1 | a0001c0003t0001g0198 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2780-167_2780-166i others(34): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483841 | |||||||
| chr12:7483841 | A | ATATATAT others(8): Show |
1 | a0001c0005t0001g0006 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2780-167_2780-166i others(17): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483841 | |||||||
| chr12:7483841 | A | ATATATAT others(6): Show |
6 | a0001c0003t0001g0205 a0001c0005t0001g0006 a0001c0005t0001g0188 others(3): Show |
9 | HG02109.hp1 NA18948.hp1 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.2780-167_2780-166i others(15): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483841 | |||||||
| chr12:7483841 | A | ATATATAT others(3): Show |
4 | a0001c0003t0001g0181 a0001c0003t0001g0182 a0001c0003t0001g0202 others(1): Show |
4 | HG02040.hp1 HG02135.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.2780-167_2780-166i others(12): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483841 | |||||||
| chr12:7483841 | A | ATATATAT others(3): Show |
1 | a0001c0003t0001g0033 | 2 | NA18983.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.2780-167_2780-166i others(12): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483841 | |||||||
| chr12:7483841 | AT | A | 58 | a0001c0003t0001g0160 a0001c0003t0001g0161 a0001c0003t0001g0162 others(55): Show |
87 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.2780-167delA | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483841 | |||||||
| chr12:7483842 | T | TA | 9 | a0001c0003t0001g0080 a0002c0002t0001g0026 a0002c0002t0001g0104 others(6): Show |
10 | HG02055.hp2 HG02145.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.2780-168_2780-167i others(3): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483842 | |||||||
| chr12:7483842 | T | TATA | 8 | a0001c0003t0001g0021 a0001c0003t0001g0056 a0001c0003t0001g0062 others(5): Show |
9 | HG01074.hp1 HG02015.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2780-168_2780-167i others(5): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483842 | |||||||
| chr12:7483842 | T | TATACATA others(8): Show |
1 | a0005c0010t0001g0169 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2780-168_2780-167i others(17): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483842 | |||||||
| chr12:7483842 | T | TATATA | 97 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0216 others(94): Show |
118 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.2780-168_2780-167i others(7): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483842 | |||||||
| chr12:7483842 | T | TATATATA | 11 | a0001c0001t0001g0296 a0001c0001t0002g0302 a0001c0001t0002g0328 others(8): Show |
11 | HG00099.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.2780-168_2780-167i others(9): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483842 | |||||||
| chr12:7483842 | T | TATATATA others(10): Show |
1 | a0005c0010t0001g0165 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2780-168_2780-167i others(19): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483842 | |||||||
| chr12:7483842 | T | TATATATA others(24): Show |
1 | a0008c0019t0001g0210 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2780-168_2780-167i others(33): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483842 | |||||||
| chr12:7483843 | T | A | 33 | a0001c0001t0001g0285 a0001c0001t0002g0238 a0001c0001t0002g0255 others(30): Show |
39 | HG00639.hp2 HG01167.hp2 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.2780-168A>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483843 | |||||||
| chr12:7483844 | T | A | 66 | a0001c0001t0001g0231 a0001c0001t0001g0256 a0001c0001t0001g0258 others(63): Show |
97 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.2780-169A>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483844 | |||||||
| chr12:7483845 | T | A | 15 | a0001c0003t0001g0141 a0002c0002t0001g0029 a0002c0002t0001g0030 others(12): Show |
19 | HG01069.hp1 HG01261.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2780-170A>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483845 | |||||||
| chr12:7483846 | T | A | 8 | a0001c0001t0002g0040 a0001c0009t0001g0012 a0001c0009t0001g0083 others(5): Show |
11 | HG01070.hp2 HG01106.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.2780-171A>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483846 | |||||||
| chr12:7483847 | T | A | 2 | a0005c0010t0001g0208 a0005c0010t0001g0209 |
2 | HG01261.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2780-172A>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483847 | |||||||
| chr12:7483909 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG01099.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2780-234G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483909 | |||||||
| chr12:7483924 | T | C | 11 | a0001c0003t0001g0017 a0001c0003t0001g0031 a0001c0003t0001g0160 others(8): Show |
14 | HG00639.hp2 HG01175.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.2780-249A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483924 | |||||||
| chr12:7483985 | C | T | 1 | a0002c0002t0001g0105 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2780-310G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483985 | |||||||
| chr12:7483992 | C | T | 1 | a0005c0010t0001g0165 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2780-317G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7483992 | |||||||
| chr12:7484014 | G | T | 1 | a0001c0003t0001g0171 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2780-339C>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484014 | |||||||
| chr12:7484067 | C | T | 2 | a0004c0014t0003g0055 a0004c0018t0003g0095 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2780-392G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484067 | |||||||
| chr12:7484083 | G | A | 137 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(134): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.2780-408C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484083 | |||||||
| chr12:7484106 | C | T | 3 | a0005c0010t0001g0169 a0005c0010t0001g0208 a0005c0010t0001g0209 |
3 | HG01261.hp1 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2780-431G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484106 | |||||||
| chr12:7484117 | G | A | 2 | a0004c0012t0001g0140 a0004c0012t0001g0170 |
2 | HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2780-442C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484117 | |||||||
| chr12:7484157 | A | C | 1 | a0002c0002t0001g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2780-482T>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484157 | |||||||
| chr12:7484213 | G | A | 1 | a0002c0002t0001g0138 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2780-538C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484213 | |||||||
| chr12:7484214 | C | A | 1 | a0002c0002t0001g0138 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2780-539G>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484214 | |||||||
| chr12:7484352 | T | A | 2 | a0001c0016t0001g0235 a0001c0020t0008g0336 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2780-677A>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484352 | |||||||
| chr12:7484410 | C | T | 2 | a0004c0014t0003g0055 a0004c0018t0003g0095 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2779+686G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484410 | |||||||
| chr12:7484412 | G | A | 132 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(129): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.2779+684C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484412 | |||||||
| chr12:7484498 | G | A | 1 | a0001c0003t0001g0203 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2779+598C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484498 | |||||||
| chr12:7484509 | C | T | 1 | a0005c0010t0001g0165 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2779+587G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484509 | |||||||
| chr12:7484595 | C | T | 1 | a0002c0002t0001g0138 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2779+501G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484595 | |||||||
| chr12:7484638 | T | A | 2 | a0004c0012t0001g0140 a0004c0012t0001g0170 |
2 | HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2779+458A>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484638 | |||||||
| chr12:7484639 | C | CA | 14 | a0001c0001t0001g0227 a0001c0003t0001g0060 a0001c0003t0001g0075 others(11): Show |
14 | HG00323.hp1 HG00544.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.2779+456dupT | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484639 | |||||||
| chr12:7484639 | C | CAA | 108 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(105): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2779+455_2779+456d others(4): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484639 | |||||||
| chr12:7484639 | C | CAAA | 21 | a0001c0001t0001g0231 a0001c0001t0001g0258 a0001c0001t0001g0284 others(18): Show |
24 | HG00423.hp1 HG00621.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.2779+454_2779+456d others(5): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484639 | |||||||
| chr12:7484639 | CA | C | 46 | a0001c0003t0001g0016 a0001c0003t0001g0018 a0001c0003t0001g0019 others(43): Show |
58 | HG00609.hp2 HG01109.hp2 HG01261.hp1 others(55): Show |
intron_variant | MODIFIER | c.2779+456delT | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484639 | |||||||
| chr12:7484738 | T | C | 2 | a0002c0002t0001g0144 a0002c0002t0001g0145 |
2 | NA18950.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2779+358A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484738 | |||||||
| chr12:7484856 | G | A | 3 | a0001c0003t0001g0174 a0001c0003t0001g0175 a0001c0003t0001g0176 |
3 | HG02723.hp2 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2779+240C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484856 | |||||||
| chr12:7484893 | G | A | 5 | a0002c0002t0001g0030 a0002c0002t0001g0133 a0002c0002t0001g0134 others(2): Show |
8 | HG03831.hp2 NA18943.hp2 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.2779+203C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484893 | |||||||
| chr12:7484902 | C | T | 7 | a0001c0003t0001g0017 a0001c0003t0001g0031 a0001c0003t0001g0160 others(4): Show |
10 | HG00639.hp2 HG01175.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2779+194G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484902 | |||||||
| chr12:7484989 | C | T | 1 | a0004c0008t0001g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2779+107G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7484989 | |||||||
| chr12:7485052 | G | A | 6 | a0002c0002t0001g0015 a0002c0002t0001g0101 a0002c0002t0001g0135 others(3): Show |
8 | HG01952.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2779+44C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 11/16 | chr12 | 7485052 | |||||||
| chr12:7485424 | G | A | 131 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(128): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
splice_region_variant&intron_variant | LOW | c.2459-8C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 10/16 | chr12 | 7485424 | |||||||
| chr12:7485513 | T | C | 1 | a0003c0006t0002g0278 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2459-97A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 10/16 | chr12 | 7485513 | |||||||
| chr12:7485772 | A | G | 3 | a0003c0006t0002g0271 a0003c0006t0002g0272 a0003c0006t0002g0326 |
3 | HG00140.hp1 HG01123.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.2459-356T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 10/16 | chr12 | 7485772 | |||||||
| chr12:7485878 | G | A | 1 | a0001c0003t0001g0078 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2459-462C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 10/16 | chr12 | 7485878 | |||||||
| chr12:7485879 | A | C | 19 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0033 others(16): Show |
24 | HG00609.hp2 HG02040.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.2459-463T>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 10/16 | chr12 | 7485879 | |||||||
| chr12:7485891 | C | A | 1 | a0003c0013t0001g0215 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2459-475G>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 10/16 | chr12 | 7485891 | |||||||
| chr12:7485930 | C | T | 3 | a0005c0010t0001g0169 a0005c0010t0001g0208 a0005c0010t0001g0209 |
3 | HG01261.hp1 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2459-514G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 10/16 | chr12 | 7485930 | |||||||
| chr12:7485951 | A | G | 1 | a0001c0003t0001g0062 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2459-535T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 10/16 | chr12 | 7485951 | |||||||
| chr12:7485976 | T | G | 1 | a0002c0002t0001g0137 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2458+523A>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 10/16 | chr12 | 7485976 | |||||||
| chr12:7485996 | C | T | 2 | a0001c0001t0001g0232 a0001c0001t0002g0238 |
2 | HG01168.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.2458+503G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 10/16 | chr12 | 7485996 | |||||||
| chr12:7486051 | C | G | 13 | a0001c0003t0001g0018 a0001c0003t0001g0033 a0001c0003t0001g0051 others(10): Show |
16 | HG00609.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.2458+448G>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 10/16 | chr12 | 7486051 | |||||||
| chr12:7486458 | T | G | 7 | a0001c0003t0001g0017 a0001c0003t0001g0031 a0001c0003t0001g0160 others(4): Show |
10 | HG00639.hp2 HG01175.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2458+41A>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 10/16 | chr12 | 7486458 | |||||||
| chr12:7486997 | C | G | 1 | a0001c0001t0002g0305 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2051-11G>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 8/16 | chr12 | 7486997 | |||||||
| chr12:7487034 | G | C | 1 | a0001c0003t0001g0053 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2051-48C>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 8/16 | chr12 | 7487034 | |||||||
| chr12:7487109 | C | T | 19 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0033 others(16): Show |
24 | HG00609.hp2 HG02040.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.2051-123G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 8/16 | chr12 | 7487109 | |||||||
| chr12:7487223 | T | C | 1 | a0002c0002t0001g0138 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2050+136A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 8/16 | chr12 | 7487223 | |||||||
| chr12:7487250 | C | T | 1 | a0002c0007t0001g0159 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2050+109G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 8/16 | chr12 | 7487250 | |||||||
| chr12:7487740 | G | A | 7 | a0001c0003t0001g0017 a0001c0003t0001g0031 a0001c0003t0001g0160 others(4): Show |
10 | HG00639.hp2 HG01175.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1735+33C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 7/16 | chr12 | 7487740 | |||||||
| chr12:7488114 | G | C | 1 | a0001c0001t0001g0304 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1421-27C>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7488114 | |||||||
| chr12:7488217 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1421-130C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7488217 | |||||||
| chr12:7488242 | G | C | 1 | a0001c0003t0001g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1421-155C>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7488242 | |||||||
| chr12:7488576 | C | T | 4 | a0001c0003t0001g0032 a0001c0003t0001g0196 a0001c0003t0001g0197 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.1421-489G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7488576 | |||||||
| chr12:7488666 | C | T | 2 | a0004c0012t0001g0140 a0004c0012t0001g0170 |
2 | HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1421-579G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7488666 | |||||||
| chr12:7488855 | GC | G | 7 | a0001c0003t0001g0017 a0001c0003t0001g0031 a0001c0003t0001g0160 others(4): Show |
10 | HG00639.hp2 HG01175.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1421-769delG | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7488855 | |||||||
| chr12:7488939 | G | A | 4 | a0001c0001t0001g0314 a0001c0001t0002g0237 a0001c0001t0002g0262 others(1): Show |
4 | HG00099.hp1 HG00323.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1421-852C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7488939 | |||||||
| chr12:7489075 | T | A | 4 | a0001c0003t0001g0032 a0001c0003t0001g0196 a0001c0003t0001g0197 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.1421-988A>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7489075 | |||||||
| chr12:7489291 | A | C | 1 | a0001c0003t0001g0172 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1421-1204T>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7489291 | |||||||
| chr12:7489337 | G | A | 19 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0033 others(16): Show |
24 | HG00609.hp2 HG02040.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.1421-1250C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7489337 | |||||||
| chr12:7489372 | A | C | 1 | a0002c0002t0006g0102 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1421-1285T>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7489372 | |||||||
| chr12:7489414 | T | C | 2 | a0004c0012t0001g0140 a0004c0012t0001g0170 |
2 | HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1421-1327A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7489414 | |||||||
| chr12:7489472 | T | C | 1 | a0001c0003t0001g0079 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1421-1385A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7489472 | |||||||
| chr12:7489638 | C | T | 1 | a0002c0002t0001g0152 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1421-1551G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7489638 | |||||||
| chr12:7489678 | T | G | 7 | a0001c0003t0001g0017 a0001c0003t0001g0031 a0001c0003t0001g0160 others(4): Show |
10 | HG00639.hp2 HG01175.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1421-1591A>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7489678 | |||||||
| chr12:7489926 | G | A | 7 | a0001c0003t0001g0017 a0001c0003t0001g0031 a0001c0003t0001g0160 others(4): Show |
10 | HG00639.hp2 HG01175.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1421-1839C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7489926 | |||||||
| chr12:7489968 | T | C | 2 | a0004c0014t0003g0055 a0004c0018t0003g0095 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1421-1881A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7489968 | |||||||
| chr12:7490107 | C | G | 3 | a0005c0010t0001g0169 a0005c0010t0001g0208 a0005c0010t0001g0209 |
3 | HG01261.hp1 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1421-2020G>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7490107 | |||||||
| chr12:7490189 | A | C | 245 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(242): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1421-2102T>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7490189 | |||||||
| chr12:7490211 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1421-2124C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7490211 | |||||||
| chr12:7490303 | A | G | 56 | a0001c0001t0001g0297 a0001c0003t0001g0003 a0001c0003t0001g0011 others(53): Show |
65 | HG00544.hp1 HG00597.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1421-2216T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7490303 | |||||||
| chr12:7490396 | G | C | 1 | a0001c0003t0001g0185 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1421-2309C>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7490396 | |||||||
| chr12:7490469 | A | G | 3 | a0001c0003t0001g0061 a0001c0003t0001g0086 a0001c0003t0001g0090 |
3 | NA18991.hp1 NA19060.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1421-2382T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7490469 | |||||||
| chr12:7490493 | T | G | 2 | a0001c0003t0001g0141 a0001c0003t0001g0195 |
2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1421-2406A>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7490493 | |||||||
| chr12:7490558 | T | C | 2 | a0001c0001t0001g0297 a0001c0003t0001g0080 |
2 | NA19011.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1421-2471A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7490558 | |||||||
| chr12:7490562 | T | C | 1 | a0003c0004t0001g0323 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1421-2475A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7490562 | |||||||
| chr12:7490650 | C | T | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG00140.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.1421-2563G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7490650 | |||||||
| chr12:7490658 | G | A | 1 | a0008c0019t0001g0210 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1421-2571C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7490658 | |||||||
| chr12:7490703 | T | C | 2 | a0001c0016t0001g0235 a0001c0020t0008g0336 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1421-2616A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7490703 | |||||||
| chr12:7490712 | A | G | 13 | a0001c0005t0001g0006 a0001c0005t0001g0034 a0001c0005t0001g0187 others(10): Show |
18 | HG02027.hp1 HG02132.hp2 NA18944.hp2 others(15): Show |
intron_variant | MODIFIER | c.1421-2625T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7490712 | |||||||
| chr12:7490731 | G | A | 254 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(251): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1421-2644C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7490731 | |||||||
| chr12:7490778 | C | T | 4 | a0001c0003t0001g0032 a0001c0003t0001g0196 a0001c0003t0001g0197 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.1421-2691G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7490778 | |||||||
| chr12:7490836 | A | G | 3 | a0001c0003t0001g0174 a0001c0003t0001g0175 a0001c0003t0001g0176 |
3 | HG02723.hp2 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1421-2749T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7490836 | |||||||
| chr12:7490887 | A | G | 1 | a0001c0003t0001g0174 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1421-2800T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7490887 | |||||||
| chr12:7490977 | T | C | 7 | a0004c0008t0001g0158 a0004c0008t0001g0173 a0004c0008t0001g0211 others(4): Show |
7 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1421-2890A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7490977 | |||||||
| chr12:7491001 | A | G | 6 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(3): Show |
7 | HG00140.hp2 HG00323.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1421-2914T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7491001 | |||||||
| chr12:7491111 | A | G | 2 | a0001c0003t0001g0141 a0001c0003t0001g0195 |
2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1421-3024T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7491111 | |||||||
| chr12:7491134 | AAAAC | A | 7 | a0001c0003t0001g0017 a0001c0003t0001g0031 a0001c0003t0001g0160 others(4): Show |
10 | HG00639.hp2 HG01175.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1421-3051_1421-304 others(8): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7491134 | |||||||
| chr12:7491160 | TATTTTCT others(34): Show |
T | 1 | a0001c0001t0002g0268 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1421-3114_1421-307 others(45): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7491160 | |||||||
| chr12:7491273 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1421-3186G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7491273 | |||||||
| chr12:7491357 | G | T | 1 | a0001c0001t0001g0304 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1421-3270C>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7491357 | |||||||
| chr12:7491373 | C | T | 1 | a0004c0018t0003g0095 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1421-3286G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7491373 | |||||||
| chr12:7491407 | T | C | 1 | a0001c0003t0001g0081 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1421-3320A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7491407 | |||||||
| chr12:7491441 | TCTGA | T | 4 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0001c0003t0001g0053 others(1): Show |
4 | HG00609.hp2 NA18962.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1421-3358_1421-335 others(8): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7491441 | |||||||
| chr12:7491659 | A | G | 1 | a0001c0001t0001g0044 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1420+3422T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7491659 | |||||||
| chr12:7491779 | C | T | 3 | a0001c0003t0001g0016 a0001c0003t0001g0143 a0001c0003t0001g0177 |
5 | HG00738.hp2 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1420+3302G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7491779 | |||||||
| chr12:7491942 | A | T | 13 | a0001c0005t0001g0006 a0001c0005t0001g0034 a0001c0005t0001g0187 others(10): Show |
18 | HG02027.hp1 HG02132.hp2 NA18944.hp2 others(15): Show |
intron_variant | MODIFIER | c.1420+3139T>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7491942 | |||||||
| chr12:7491945 | C | T | 1 | a0003c0006t0001g0270 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1420+3136G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7491945 | |||||||
| chr12:7491971 | C | G | 1 | a0001c0003t0001g0060 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1420+3110G>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7491971 | |||||||
| chr12:7492017 | G | A | 4 | a0005c0010t0001g0165 a0005c0010t0001g0169 a0005c0010t0001g0208 others(1): Show |
4 | HG01261.hp1 HG02451.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420+3064C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7492017 | |||||||
| chr12:7492113 | A | G | 1 | a0002c0002t0001g0101 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1420+2968T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7492113 | |||||||
| chr12:7492459 | G | A | 2 | a0001c0001t0002g0263 a0001c0001t0002g0315 |
2 | HG00642.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1420+2622C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7492459 | |||||||
| chr12:7492563 | G | A | 2 | a0005c0010t0001g0208 a0005c0010t0001g0209 |
2 | HG01261.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1420+2518C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7492563 | |||||||
| chr12:7492666 | A | C | 133 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(130): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1420+2415T>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7492666 | |||||||
| chr12:7492666 | A | G | 112 | a0001c0003t0001g0003 a0001c0003t0001g0011 a0001c0003t0001g0016 others(109): Show |
137 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(134): Show |
intron_variant | MODIFIER | c.1420+2415T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7492666 | |||||||
| chr12:7492838 | T | A | 4 | a0001c0001t0001g0264 a0001c0001t0002g0043 a0001c0001t0002g0265 others(1): Show |
5 | NA18964.hp1 NA18972.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.1420+2243A>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7492838 | |||||||
| chr12:7492862 | T | C | 3 | a0005c0010t0001g0169 a0005c0010t0001g0208 a0005c0010t0001g0209 |
3 | HG01261.hp1 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1420+2219A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7492862 | |||||||
| chr12:7492904 | G | A | 2 | a0001c0003t0001g0199 a0001c0003t0001g0205 |
2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1420+2177C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7492904 | |||||||
| chr12:7492947 | C | T | 1 | a0005c0010t0001g0169 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1420+2134G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7492947 | |||||||
| chr12:7493181 | A | G | 133 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(130): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1420+1900T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7493181 | |||||||
| chr12:7493413 | G | A | 1 | a0001c0001t0002g0267 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1420+1668C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7493413 | |||||||
| chr12:7493518 | A | T | 1 | a0003c0004t0001g0269 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1420+1563T>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7493518 | |||||||
| chr12:7493653 | A | G | 3 | a0001c0003t0001g0057 a0001c0003t0001g0058 a0001c0003t0001g0059 |
3 | HG02280.hp1 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1420+1428T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7493653 | |||||||
| chr12:7493984 | A | C | 2 | a0001c0016t0001g0235 a0001c0020t0008g0336 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1420+1097T>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7493984 | |||||||
| chr12:7494086 | G | C | 1 | a0001c0015t0001g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1420+995C>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7494086 | |||||||
| chr12:7494129 | A | G | 215 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(212): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1420+952T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7494129 | |||||||
| chr12:7494170 | A | G | 1 | a0001c0003t0001g0171 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1420+911T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7494170 | |||||||
| chr12:7494260 | T | A | 1 | a0001c0003t0001g0172 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1420+821A>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7494260 | |||||||
| chr12:7494261 | A | T | 3 | a0001c0003t0001g0016 a0001c0003t0001g0143 a0001c0003t0001g0177 |
5 | HG00738.hp2 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1420+820T>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7494261 | |||||||
| chr12:7494373 | C | CCCCTATC others(34): Show |
1 | a0001c0001t0002g0268 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1420+707_1420+708i others(43): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7494373 | |||||||
| chr12:7494438 | C | T | 1 | a0001c0015t0001g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1420+643G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7494438 | |||||||
| chr12:7494446 | T | C | 1 | a0001c0003t0001g0186 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1420+635A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7494446 | |||||||
| chr12:7494503 | A | G | 133 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(130): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1420+578T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7494503 | |||||||
| chr12:7494591 | A | G | 78 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0227 others(75): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1420+490T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7494591 | |||||||
| chr12:7494768 | A | G | 1 | a0001c0015t0001g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1420+313T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7494768 | |||||||
| chr12:7494845 | T | G | 1 | a0001c0001t0001g0324 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1420+236A>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7494845 | |||||||
| chr12:7494858 | A | G | 2 | a0001c0016t0001g0235 a0001c0020t0008g0336 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1420+223T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7494858 | |||||||
| chr12:7494860 | C | G | 1 | a0005c0010t0001g0165 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1420+221G>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7494860 | |||||||
| chr12:7494974 | G | A | 1 | a0002c0002t0001g0139 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1420+107C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 6/16 | chr12 | 7494974 | |||||||
| chr12:7495431 | G | A | 1 | a0001c0003t0001g0172 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1100-30C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7495431 | |||||||
| chr12:7495484 | TG | T | 7 | a0001c0003t0001g0017 a0001c0003t0001g0031 a0001c0003t0001g0160 others(4): Show |
10 | HG00639.hp2 HG01175.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1100-84delC | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7495484 | |||||||
| chr12:7495545 | A | G | 2 | a0002c0002t0001g0146 a0002c0002t0002g0147 |
2 | NA18944.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.1100-144T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7495545 | |||||||
| chr12:7495690 | A | C | 11 | a0001c0003t0001g0017 a0001c0003t0001g0031 a0001c0003t0001g0160 others(8): Show |
14 | HG00639.hp2 HG01175.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.1100-289T>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7495690 | |||||||
| chr12:7495703 | G | T | 2 | a0003c0004t0001g0236 a0003c0004t0001g0303 |
2 | HG02080.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1100-302C>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7495703 | |||||||
| chr12:7495713 | CAT | C | 19 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0033 others(16): Show |
24 | HG00609.hp2 HG02040.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.1100-314_1100-313d others(4): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7495713 | |||||||
| chr12:7495813 | A | AGTCT | 7 | a0001c0003t0001g0017 a0001c0003t0001g0031 a0001c0003t0001g0160 others(4): Show |
10 | HG00639.hp2 HG01175.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1100-416_1100-413d others(6): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7495813 | |||||||
| chr12:7495831 | G | A | 4 | a0001c0003t0001g0016 a0001c0003t0001g0143 a0001c0003t0001g0177 others(1): Show |
6 | HG00738.hp2 HG01884.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1100-430C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7495831 | |||||||
| chr12:7495924 | T | C | 2 | a0004c0012t0001g0140 a0004c0012t0001g0170 |
2 | HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1100-523A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7495924 | |||||||
| chr12:7496081 | C | T | 4 | a0005c0010t0001g0165 a0005c0010t0001g0169 a0005c0010t0001g0208 others(1): Show |
4 | HG01261.hp1 HG02451.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1100-680G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7496081 | |||||||
| chr12:7496096 | C | T | 4 | a0005c0010t0001g0165 a0005c0010t0001g0169 a0005c0010t0001g0208 others(1): Show |
4 | HG01261.hp1 HG02451.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1100-695G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7496096 | |||||||
| chr12:7496265 | G | C | 4 | a0005c0010t0001g0165 a0005c0010t0001g0169 a0005c0010t0001g0208 others(1): Show |
4 | HG01261.hp1 HG02451.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099+548C>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7496265 | |||||||
| chr12:7496291 | C | G | 2 | a0001c0016t0001g0235 a0001c0020t0008g0336 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1099+522G>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7496291 | |||||||
| chr12:7496319 | G | A | 13 | a0001c0005t0001g0006 a0001c0005t0001g0034 a0001c0005t0001g0187 others(10): Show |
18 | HG02027.hp1 HG02132.hp2 NA18944.hp2 others(15): Show |
intron_variant | MODIFIER | c.1099+494C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7496319 | |||||||
| chr12:7496411 | T | C | 1 | a0001c0015t0001g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1099+402A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7496411 | |||||||
| chr12:7496452 | C | A | 7 | a0001c0005t0001g0006 a0001c0005t0001g0188 a0001c0005t0001g0189 others(4): Show |
11 | HG02132.hp2 NA18944.hp2 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.1099+361G>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7496452 | |||||||
| chr12:7496458 | C | T | 7 | a0001c0003t0001g0195 a0002c0002t0001g0096 a0002c0002t0001g0098 others(4): Show |
10 | HG03540.hp2 NA18747.hp1 NA18954.hp2 others(7): Show |
intron_variant | MODIFIER | c.1099+355G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7496458 | |||||||
| chr12:7496506 | A | T | 2 | a0004c0014t0003g0055 a0004c0018t0003g0095 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1099+307T>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7496506 | |||||||
| chr12:7496531 | G | A | 19 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0033 others(16): Show |
24 | HG00609.hp2 HG02040.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.1099+282C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7496531 | |||||||
| chr12:7496560 | G | C | 1 | a0005c0010t0001g0165 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1099+253C>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7496560 | |||||||
| chr12:7496667 | A | G | 3 | a0005c0010t0001g0169 a0005c0010t0001g0208 a0005c0010t0001g0209 |
3 | HG01261.hp1 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1099+146T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 5/16 | chr12 | 7496667 | |||||||
| chr12:7497156 | G | A | 1 | a0001c0003t0002g0084 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.779-23C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7497156 | |||||||
| chr12:7497162 | G | A | 1 | a0004c0012t0001g0170 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.779-29C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7497162 | |||||||
| chr12:7497260 | A | G | 1 | a0002c0002t0001g0144 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.779-127T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7497260 | |||||||
| chr12:7497297 | G | GGAGT | 13 | a0001c0001t0001g0223 a0001c0001t0001g0227 a0001c0001t0001g0228 others(10): Show |
15 | HG00140.hp2 HG00323.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.779-168_779-165dup others(4): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7497297 | |||||||
| chr12:7497357 | G | T | 1 | a0001c0003t0001g0171 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.779-224C>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7497357 | |||||||
| chr12:7497583 | TG | T | 4 | a0004c0008t0001g0158 a0004c0008t0001g0211 a0004c0008t0001g0212 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.779-451delC | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7497583 | |||||||
| chr12:7497635 | T | C | 1 | a0001c0001t0002g0325 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.779-502A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7497635 | |||||||
| chr12:7497738 | C | T | 1 | a0002c0002t0001g0022 | 2 | HG01975.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.779-605G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7497738 | |||||||
| chr12:7497754 | A | G | 1 | a0001c0003t0001g0056 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.779-621T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7497754 | |||||||
| chr12:7497863 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.779-730G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7497863 | |||||||
| chr12:7497900 | T | G | 7 | a0001c0003t0001g0032 a0001c0003t0001g0171 a0001c0003t0001g0174 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.779-767A>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7497900 | |||||||
| chr12:7497914 | C | T | 5 | a0001c0003t0001g0174 a0001c0003t0001g0175 a0001c0003t0001g0176 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.779-781G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7497914 | |||||||
| chr12:7497943 | T | G | 10 | a0001c0003t0001g0003 a0001c0003t0001g0016 a0001c0003t0001g0143 others(7): Show |
17 | HG00738.hp2 HG01261.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.779-810A>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7497943 | |||||||
| chr12:7498124 | T | TAC | 23 | a0001c0001t0001g0294 a0001c0001t0001g0296 a0001c0001t0002g0295 others(20): Show |
26 | HG00639.hp2 HG01175.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.778+742_778+743dup others(2): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498124 | |||||||
| chr12:7498124 | T | TACACACA others(3): Show |
2 | a0005c0010t0001g0208 a0005c0010t0001g0209 |
2 | HG01261.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.778+734_778+743dup others(10): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498124 | |||||||
| chr12:7498146 | C | CACACACA others(9): Show |
1 | a0005c0010t0001g0169 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.778+721_778+722ins others(16): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498146 | |||||||
| chr12:7498146 | C | CACACACA others(5): Show |
3 | a0001c0003t0001g0003 a0001c0003t0001g0168 a0002c0002t0001g0167 |
8 | HG01952.hp2 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.778+721_778+722ins others(12): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498146 | |||||||
| chr12:7498146 | C | CACACACA others(5): Show |
1 | a0001c0003t0001g0166 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.778+721_778+722ins others(12): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498146 | |||||||
| chr12:7498146 | C | CAG | 19 | a0001c0003t0001g0032 a0001c0003t0001g0174 a0001c0003t0001g0175 others(16): Show |
25 | HG01167.hp1 HG01169.hp2 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.778+720_778+721dup others(2): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498146 | |||||||
| chr12:7498146 | C | G | 1 | a0001c0001t0002g0225 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.778+722G>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498146 | |||||||
| chr12:7498148 | G | C | 85 | a0001c0001t0001g0297 a0001c0003t0001g0011 a0001c0003t0001g0017 others(82): Show |
99 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.778+720C>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498148 | |||||||
| chr12:7498150 | G | C | 30 | a0001c0003t0001g0017 a0001c0003t0001g0018 a0001c0003t0001g0019 others(27): Show |
38 | HG00609.hp2 HG00639.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.778+718C>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498150 | |||||||
| chr12:7498160 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.778+708C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498160 | |||||||
| chr12:7498187 | T | C | 2 | a0001c0005t0001g0200 a0001c0005t0001g0207 |
2 | HG02027.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.778+681A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498187 | |||||||
| chr12:7498243 | A | C | 1 | a0001c0003t0001g0032 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.778+625T>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498243 | |||||||
| chr12:7498277 | G | A | 1 | a0003c0006t0002g0326 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.778+591C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498277 | |||||||
| chr12:7498285 | G | A | 9 | a0001c0003t0001g0017 a0001c0003t0001g0031 a0001c0003t0001g0160 others(6): Show |
12 | HG00639.hp2 HG01175.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.778+583C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498285 | |||||||
| chr12:7498323 | T | G | 1 | a0003c0004t0001g0327 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.778+545A>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498323 | |||||||
| chr12:7498402 | T | C | 5 | a0001c0003t0001g0174 a0001c0003t0001g0175 a0001c0003t0001g0176 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.778+466A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498402 | |||||||
| chr12:7498531 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.778+337A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498531 | |||||||
| chr12:7498542 | A | T | 246 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(243): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.778+326T>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498542 | |||||||
| chr12:7498719 | T | C | 1 | a0001c0003t0001g0090 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.778+149A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498719 | |||||||
| chr12:7498728 | T | C | 1 | a0001c0001t0001g0299 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.778+140A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498728 | |||||||
| chr12:7498786 | T | TAAGAGTT others(217): Show |
1 | a0001c0001t0001g0300 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.778+81_778+82insTT others(222): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498786 | |||||||
| chr12:7498800 | C | G | 1 | a0001c0009t0003g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.778+68G>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 4/16 | chr12 | 7498800 | |||||||
| chr12:7499268 | T | C | 1 | a0002c0002t0001g0150 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.458-80A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7499268 | |||||||
| chr12:7499328 | G | A | 246 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(243): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.458-140C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7499328 | |||||||
| chr12:7499429 | CTGTTT | C | 48 | a0001c0003t0001g0011 a0001c0003t0001g0021 a0001c0003t0001g0050 others(45): Show |
54 | HG00544.hp1 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.458-246_458-242del others(5): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7499429 | |||||||
| chr12:7499448 | T | C | 210 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(207): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.458-260A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7499448 | |||||||
| chr12:7499729 | C | T | 1 | a0004c0018t0003g0095 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.458-541G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7499729 | |||||||
| chr12:7499829 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.458-641G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7499829 | |||||||
| chr12:7499836 | A | G | 1 | a0001c0003t0001g0171 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.458-648T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7499836 | |||||||
| chr12:7499864 | C | T | 1 | a0001c0005t0002g0178 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.458-676G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7499864 | |||||||
| chr12:7500130 | A | C | 1 | a0001c0001t0001g0223 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.458-942T>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7500130 | |||||||
| chr12:7500246 | C | A | 1 | a0004c0014t0003g0055 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.457+893G>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7500246 | |||||||
| chr12:7500350 | G | A | 1 | a0002c0002t0001g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.457+789C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7500350 | |||||||
| chr12:7500419 | C | A | 1 | a0001c0009t0003g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.457+720G>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7500419 | |||||||
| chr12:7500421 | C | CA | 15 | a0001c0003t0001g0171 a0001c0003t0001g0172 a0001c0003t0001g0174 others(12): Show |
15 | HG02027.hp1 HG02559.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+717dupT | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7500421 | |||||||
| chr12:7500421 | C | CAA | 83 | a0001c0003t0001g0003 a0001c0003t0001g0011 a0001c0003t0001g0018 others(80): Show |
104 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.457+716_457+717dup others(2): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7500421 | |||||||
| chr12:7500421 | C | CAAA | 14 | a0001c0003t0001g0086 a0001c0003t0001g0087 a0001c0003t0001g0088 others(11): Show |
14 | HG02040.hp1 HG02056.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.457+715_457+717dup others(3): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7500421 | |||||||
| chr12:7500421 | C | CAAAAA | 97 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(94): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.457+713_457+717dup others(5): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7500421 | |||||||
| chr12:7500421 | C | CAAAAAA | 29 | a0001c0001t0001g0304 a0001c0001t0001g0307 a0001c0001t0001g0312 others(26): Show |
30 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.457+712_457+717dup others(6): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7500421 | |||||||
| chr12:7500421 | C | CCA | 10 | a0001c0003t0001g0017 a0001c0003t0001g0031 a0001c0003t0001g0160 others(7): Show |
13 | HG00639.hp2 HG01175.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.457+717_457+718ins others(2): Show |
CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7500421 | |||||||
| chr12:7500472 | C | A | 1 | a0001c0003t0001g0206 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.457+667G>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7500472 | |||||||
| chr12:7500697 | G | A | 1 | a0001c0003t0001g0054 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.457+442C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7500697 | |||||||
| chr12:7500717 | T | C | 246 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(243): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.457+422A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7500717 | |||||||
| chr12:7500765 | T | A | 1 | a0004c0012t0001g0170 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.457+374A>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7500765 | |||||||
| chr12:7500987 | G | A | 1 | a0001c0005t0001g0207 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.457+152C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7500987 | |||||||
| chr12:7501074 | C | G | 1 | a0002c0002t0001g0094 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.457+65G>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7501074 | |||||||
| chr12:7501097 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.457+42G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7501097 | |||||||
| chr12:7501130 | A | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG01099.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.457+9T>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 3/16 | chr12 | 7501130 | |||||||
| chr12:7501630 | T | A | 1 | a0001c0005t0001g0214 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.134-168A>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 2/16 | chr12 | 7501630 | |||||||
| chr12:7501721 | T | A | 229 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(226): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.134-259A>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 2/16 | chr12 | 7501721 | |||||||
| chr12:7501766 | G | A | 2 | a0005c0010t0001g0208 a0005c0010t0001g0209 |
2 | HG01261.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.134-304C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 2/16 | chr12 | 7501766 | |||||||
| chr12:7501794 | T | C | 1 | a0001c0003t0001g0091 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.134-332A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 2/16 | chr12 | 7501794 | |||||||
| chr12:7501796 | G | T | 1 | a0001c0005t0001g0214 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.134-334C>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 2/16 | chr12 | 7501796 | |||||||
| chr12:7501992 | T | C | 1 | a0008c0019t0001g0210 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.133+486A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 2/16 | chr12 | 7501992 | |||||||
| chr12:7502006 | C | A | 2 | a0001c0003t0001g0092 a0001c0003t0001g0093 |
2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.133+472G>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 2/16 | chr12 | 7502006 | |||||||
| chr12:7502010 | T | C | 3 | a0004c0008t0001g0211 a0004c0008t0001g0212 a0004c0008t0001g0213 |
3 | HG02258.hp1 HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.133+468A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 2/16 | chr12 | 7502010 | |||||||
| chr12:7502025 | C | A | 1 | a0001c0005t0001g0214 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.133+453G>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 2/16 | chr12 | 7502025 | |||||||
| chr12:7502113 | C | T | 48 | a0001c0003t0001g0011 a0001c0003t0001g0021 a0001c0003t0001g0050 others(45): Show |
54 | HG00544.hp1 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.133+365G>A | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 2/16 | chr12 | 7502113 | |||||||
| chr12:7502154 | T | C | 1 | a0001c0001t0002g0328 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.133+324A>G | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 2/16 | chr12 | 7502154 | |||||||
| chr12:7502436 | A | G | 1 | a0001c0020t0008g0336 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.133+42T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 2/16 | chr12 | 7502436 | |||||||
| chr12:7502682 | T | A | 131 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0047 others(128): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.47-118A>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 1/16 | chr12 | 7502682 | |||||||
| chr12:7502983 | G | A | 7 | a0001c0003t0001g0050 a0001c0003t0001g0330 a0001c0003t0001g0331 others(4): Show |
8 | HG00673.hp1 NA18939.hp1 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.47-419C>T | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 1/16 | chr12 | 7502983 | |||||||
| chr12:7502990 | T | G | 1 | a0002c0002t0001g0335 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.47-426A>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 1/16 | chr12 | 7502990 | |||||||
| chr12:7503619 | A | G | 4 | a0001c0003t0001g0051 a0001c0003t0001g0052 a0001c0003t0001g0053 others(1): Show |
4 | HG00609.hp2 NA18962.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+26T>C | CD163 | ENSG00000177575.13 | transcript | ENST00000432237.3 | protein_coding | 1/16 | chr12 | 7503619 |