Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4345 |
| ensemblid | ENSG00000091972.18 |
| hgncid | 7203 |
| symbol | CD200 |
| name | CD200 molecule |
| refseq_nuc | NM_005944.7 |
| refseq_prot | NP_005935.4 |
| ensembl_nuc | ENST00000315711.12 |
| ensembl_prot | ENSP00000312766.8 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 112333156 |
| end | 112362812 |
| strand | + |
| ver | v1.2 |
| region | chr3:112333156-112362812 |
| region5000 | chr3:112328156-112367812 |
| regionname0 | CD200_chr3_112333156_112362812 |
| regionname5000 | CD200_chr3_112328156_112367812 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 269 | 272 | 77 | 45 | 116 | 11 | 22 | 90 | CD200_chr3_112328156_112367812 | CD200 | MERLV others(264): Show |
chr3 | 112328156 | 112367812 |
| a0002 | 0/0 | 269 | 73 | 10 | 19 | 31 | 4 | 9 | 24 | CD200_chr3_112328156_112367812 | CD200 | MERLV others(264): Show |
chr3 | 112328156 | 112367812 |
| a0003 | 1/0 | 269 | 61 | 9 | 12 | 29 | 1 | 9 | 22 | CD200_chr3_112328156_112367812 | CD200 | MERLV others(264): Show |
chr3 | 112328156 | 112367812 |
| a0004 | 0/0 | 269 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | MERLV others(264): Show |
chr3 | 112328156 | 112367812 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 807 | 182 | 48 | 39 | 73 | 11 | 10 | CD200_chr3_112328156_112367812 | CD200 | ATGGA others(802): Show |
chr3 | 112328156 | 112367812 | ||
| a0001c0002 | 0/0 | 807 | 88 | 28 | 6 | 42 | 0 | 12 | CD200_chr3_112328156_112367812 | CD200 | ATGGA others(802): Show |
chr3 | 112328156 | 112367812 | ||
| a0001c0008 | 0/0 | 807 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | ATGGA others(802): Show |
chr3 | 112328156 | 112367812 | ||
| a0001c0009 | 0/0 | 807 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | ATGGA others(802): Show |
chr3 | 112328156 | 112367812 | ||
| a0002c0003 | 0/0 | 807 | 73 | 10 | 19 | 31 | 4 | 9 | CD200_chr3_112328156_112367812 | CD200 | ATGGA others(802): Show |
chr3 | 112328156 | 112367812 | ||
| a0003c0004 | 1/0 | 807 | 51 | 3 | 12 | 27 | 1 | 7 | CD200_chr3_112328156_112367812 | CD200 | ATGGA others(802): Show |
chr3 | 112328156 | 112367812 | ||
| a0003c0005 | 0/0 | 807 | 6 | 6 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | ATGGA others(802): Show |
chr3 | 112328156 | 112367812 | ||
| a0003c0006 | 0/0 | 807 | 4 | 0 | 0 | 2 | 0 | 2 | CD200_chr3_112328156_112367812 | CD200 | ATGGA others(802): Show |
chr3 | 112328156 | 112367812 | ||
| a0004c0007 | 0/0 | 807 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | ATGGA others(802): Show |
chr3 | 112328156 | 112367812 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2131 | 149 | 23 | 38 | 66 | 11 | 10 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0001c0001t0002 | 0/0 | 2131 | 10 | 6 | 0 | 4 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0001c0001t0003 | 0/0 | 2125 | 2 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2120): Show |
chr3 | 112328156 | 112367812 |
| a0001c0001t0004 | 0/0 | 2129 | 7 | 7 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2124): Show |
chr3 | 112328156 | 112367812 |
| a0001c0001t0006 | 0/0 | 2131 | 4 | 3 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0001c0001t0008 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0001c0001t0009 | 0/0 | 2131 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0001c0001t0011 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2122): Show |
chr3 | 112328156 | 112367812 |
| a0001c0001t0013 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0001c0001t0015 | 0/0 | 2131 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0001c0001t0017 | 0/0 | 2129 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2124): Show |
chr3 | 112328156 | 112367812 |
| a0001c0001t0018 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0001c0001t0024 | 0/0 | 2125 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2120): Show |
chr3 | 112328156 | 112367812 |
| a0001c0001t0025 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2122): Show |
chr3 | 112328156 | 112367812 |
| a0001c0002t0001 | 0/0 | 2131 | 69 | 12 | 5 | 41 | 0 | 11 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0001c0002t0002 | 0/0 | 2131 | 8 | 7 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0001c0002t0003 | 0/0 | 2125 | 3 | 3 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2120): Show |
chr3 | 112328156 | 112367812 |
| a0001c0002t0004 | 0/0 | 2129 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2124): Show |
chr3 | 112328156 | 112367812 |
| a0001c0002t0014 | 0/0 | 2131 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0001c0002t0016 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0001c0002t0019 | 0/0 | 2131 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0001c0002t0020 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0001c0002t0021 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0001c0002t0022 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0001c0002t0023 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0001c0008t0001 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0001c0009t0001 | 0/0 | 2131 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0002c0003t0001 | 0/0 | 2131 | 65 | 6 | 19 | 27 | 4 | 9 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0002c0003t0002 | 0/0 | 2131 | 2 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0002c0003t0005 | 0/0 | 2131 | 4 | 0 | 0 | 4 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0002c0003t0008 | 0/0 | 2131 | 2 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0003c0004t0001 | 0/0 | 2131 | 33 | 2 | 12 | 13 | 1 | 5 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0003c0004t0002 | 0/0 | 2131 | 15 | 1 | 0 | 13 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0003c0004t0003 | 0/0 | 2125 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2120): Show |
chr3 | 112328156 | 112367812 |
| a0003c0004t0004 | 1/0 | 2129 | 1 | 0 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2124): Show |
chr3 | 112328156 | 112367812 |
| a0003c0004t0012 | 0/0 | 2131 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| a0003c0005t0003 | 0/0 | 2125 | 4 | 4 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2120): Show |
chr3 | 112328156 | 112367812 |
| a0003c0005t0010 | 0/0 | 2125 | 2 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2120): Show |
chr3 | 112328156 | 112367812 |
| a0003c0006t0007 | 0/0 | 2125 | 4 | 0 | 0 | 2 | 0 | 2 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2120): Show |
chr3 | 112328156 | 112367812 |
| a0004c0007t0001 | 0/0 | 2131 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | AGAGC others(2126): Show |
chr3 | 112328156 | 112367812 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 1 | 0 | 7 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0002 | 0/0 | 8 | 2 | 2 | 4 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0005 | 0/0 | 7 | 1 | 0 | 6 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0168 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0003g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0004g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0008g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0009g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0009g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0011g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0013g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0017g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0018g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0024g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0001t0025g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0014g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0016g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0019g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0020g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0021g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0022g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0002t0023g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0008t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0001c0009t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0009 | 0/0 | 6 | 0 | 2 | 0 | 2 | 2 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0013 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0049 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0050 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0002c0003t0008g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0001g0003 | 0/0 | 8 | 0 | 4 | 3 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0001g0004 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0001g0010 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0002g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0002g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0004g0236 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0004t0012g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0005t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0005t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0005t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0005t0010g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0005t0010g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0006t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0006t0007g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0006t0007g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0003c0006t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| a0004c0007t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00140 | hp2 | a0002 | c0003 | t0001 | g0270 | EUR | GBR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | FIN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | FIN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00323 | hp1 | a0002 | c0003 | t0001 | g0249 | EUR | FIN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00323 | hp2 | a0003 | c0004 | t0001 | g0003 | EUR | FIN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00438 | hp2 | a0003 | c0004 | t0002 | g0015 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00544 | hp1 | a0003 | c0006 | t0007 | g0177 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00544 | hp2 | a0002 | c0003 | t0001 | g0276 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00558 | hp1 | a0002 | c0003 | t0001 | g0278 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00597 | hp1 | a0002 | c0003 | t0001 | g0257 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00597 | hp2 | a0002 | c0003 | t0001 | g0052 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00609 | hp2 | a0003 | c0004 | t0002 | g0066 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00639 | hp2 | a0002 | c0003 | t0001 | g0268 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00673 | hp1 | a0002 | c0003 | t0001 | g0255 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00733 | hp1 | a0002 | c0003 | t0001 | g0023 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00738 | hp2 | a0003 | c0004 | t0001 | g0003 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00741 | hp1 | a0003 | c0004 | t0001 | g0003 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01074 | hp1 | a0002 | c0003 | t0001 | g0271 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0229 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01106 | hp1 | a0002 | c0003 | t0001 | g0009 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0114 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01109 | hp2 | a0003 | c0004 | t0001 | g0004 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01167 | hp2 | a0003 | c0004 | t0001 | g0010 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01168 | hp1 | a0003 | c0004 | t0001 | g0010 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01169 | hp2 | a0003 | c0004 | t0001 | g0010 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01175 | hp1 | a0002 | c0003 | t0001 | g0242 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01192 | hp1 | a0002 | c0003 | t0001 | g0241 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01256 | hp1 | a0004 | c0007 | t0001 | g0018 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01256 | hp2 | a0002 | c0003 | t0001 | g0009 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01257 | hp2 | a0003 | c0004 | t0001 | g0003 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01258 | hp1 | a0003 | c0004 | t0001 | g0003 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01258 | hp2 | a0004 | c0007 | t0001 | g0018 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01261 | hp2 | a0002 | c0003 | t0001 | g0273 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01346 | hp2 | a0002 | c0003 | t0001 | g0264 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0093 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01358 | hp2 | a0002 | c0003 | t0001 | g0244 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01361 | hp2 | a0003 | c0004 | t0001 | g0146 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01433 | hp1 | a0002 | c0003 | t0001 | g0049 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01516 | hp2 | a0002 | c0003 | t0001 | g0009 | EUR | IBS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01517 | hp2 | a0002 | c0003 | t0001 | g0009 | EUR | IBS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01884 | hp1 | a0002 | c0003 | t0001 | g0289 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0235 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0106 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01934 | hp2 | a0002 | c0003 | t0001 | g0023 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01943 | hp1 | a0002 | c0003 | t0001 | g0265 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01952 | hp1 | a0002 | c0003 | t0001 | g0267 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01978 | hp2 | a0003 | c0004 | t0001 | g0004 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01981 | hp2 | a0002 | c0003 | t0001 | g0023 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01993 | hp1 | a0002 | c0003 | t0001 | g0050 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02004 | hp1 | a0002 | c0003 | t0001 | g0013 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02004 | hp2 | a0002 | c0003 | t0001 | g0252 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02015 | hp1 | a0001 | c0001 | t0015 | g0001 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02040 | hp2 | a0002 | c0003 | t0001 | g0275 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02055 | hp1 | a0002 | c0003 | t0001 | g0290 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02056 | hp2 | a0003 | c0004 | t0002 | g0007 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02074 | hp2 | a0003 | c0004 | t0002 | g0131 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02129 | hp1 | a0003 | c0004 | t0002 | g0007 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02129 | hp2 | a0003 | c0004 | t0003 | g0239 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02145 | hp1 | a0001 | c0002 | t0020 | g0166 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02148 | hp1 | a0003 | c0004 | t0001 | g0031 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | CDX | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02257 | hp1 | a0003 | c0005 | t0003 | g0030 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02258 | hp1 | a0002 | c0003 | t0001 | g0243 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02258 | hp2 | a0001 | c0002 | t0021 | g0082 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0238 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02451 | hp2 | a0001 | c0002 | t0022 | g0217 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02523 | hp2 | a0002 | c0003 | t0001 | g0269 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02572 | hp1 | a0002 | c0003 | t0001 | g0288 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02572 | hp2 | a0001 | c0001 | t0017 | g0208 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02602 | hp1 | a0003 | c0004 | t0012 | g0015 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02602 | hp2 | a0002 | c0003 | t0001 | g0250 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02622 | hp1 | a0001 | c0002 | t0004 | g0116 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02622 | hp2 | a0001 | c0008 | t0001 | g0002 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02630 | hp1 | a0003 | c0005 | t0010 | g0128 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0138 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0232 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02698 | hp1 | a0003 | c0004 | t0001 | g0147 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02698 | hp2 | a0002 | c0003 | t0001 | g0253 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02717 | hp2 | a0003 | c0005 | t0010 | g0129 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02723 | hp1 | a0001 | c0001 | t0011 | g0019 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02735 | hp1 | a0003 | c0006 | t0007 | g0141 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0089 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02738 | hp1 | a0003 | c0004 | t0002 | g0015 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02809 | hp2 | a0001 | c0002 | t0003 | g0178 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0110 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02886 | hp1 | a0003 | c0005 | t0003 | g0135 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0059 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02896 | hp2 | a0002 | c0003 | t0008 | g0170 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02897 | hp2 | a0002 | c0003 | t0008 | g0171 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02922 | hp2 | a0001 | c0002 | t0023 | g0060 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02965 | hp1 | a0003 | c0005 | t0003 | g0030 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02970 | hp1 | a0002 | c0003 | t0002 | g0246 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02970 | hp2 | a0001 | c0001 | t0013 | g0161 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02976 | hp1 | a0001 | c0002 | t0003 | g0103 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0230 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0081 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03017 | hp2 | a0002 | c0003 | t0001 | g0279 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03041 | hp1 | a0003 | c0004 | t0001 | g0142 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0029 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0234 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0248 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03139 | hp1 | a0001 | c0002 | t0016 | g0064 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03195 | hp1 | a0002 | c0003 | t0002 | g0247 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03209 | hp2 | a0003 | c0004 | t0002 | g0231 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03225 | hp1 | a0001 | c0002 | t0003 | g0119 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0233 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03239 | hp1 | a0002 | c0003 | t0001 | g0291 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03453 | hp2 | a0002 | c0003 | t0001 | g0169 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03486 | hp1 | a0003 | c0005 | t0003 | g0134 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0045 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03491 | hp1 | a0002 | c0003 | t0001 | g0272 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0024 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0024 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0167 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0216 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0112 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0063 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03669 | hp1 | a0002 | c0003 | t0001 | g0009 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03688 | hp1 | a0003 | c0004 | t0001 | g0031 | SAS | STU | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0108 | SAS | STU | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03704 | hp1 | a0003 | c0004 | t0001 | g0010 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03710 | hp1 | a0002 | c0003 | t0001 | g0009 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0113 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03831 | hp2 | a0001 | c0002 | t0019 | g0094 | SAS | BEB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03834 | hp1 | a0003 | c0004 | t0001 | g0068 | SAS | BEB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03834 | hp2 | a0003 | c0004 | t0001 | g0133 | SAS | BEB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0107 | SAS | BEB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03927 | hp2 | a0002 | c0003 | t0001 | g0013 | SAS | BEB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0078 | SAS | BEB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0102 | SAS | BEB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | STU | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG04204 | hp1 | a0003 | c0006 | t0007 | g0140 | SAS | STU | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0029 | SAS | STU | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | STU | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG04228 | hp2 | a0002 | c0003 | t0001 | g0251 | SAS | STU | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | CHB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18906 | hp1 | a0003 | c0004 | t0001 | g0144 | AFR | YRI | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18940 | hp2 | a0002 | c0003 | t0005 | g0013 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18942 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18945 | hp1 | a0003 | c0004 | t0002 | g0007 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18946 | hp1 | a0003 | c0004 | t0002 | g0014 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18947 | hp1 | a0003 | c0004 | t0001 | g0259 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18947 | hp2 | a0002 | c0003 | t0001 | g0285 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18949 | hp1 | a0002 | c0003 | t0001 | g0277 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18952 | hp1 | a0003 | c0004 | t0002 | g0014 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18954 | hp1 | a0001 | c0001 | t0009 | g0197 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18956 | hp1 | a0003 | c0006 | t0007 | g0139 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18957 | hp1 | a0001 | c0002 | t0014 | g0092 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18959 | hp2 | a0002 | c0003 | t0001 | g0256 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18961 | hp1 | a0003 | c0004 | t0001 | g0260 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18963 | hp1 | a0002 | c0003 | t0001 | g0052 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18964 | hp2 | a0002 | c0003 | t0001 | g0049 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18968 | hp2 | a0002 | c0003 | t0005 | g0280 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18969 | hp2 | a0003 | c0004 | t0002 | g0007 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18970 | hp1 | a0002 | c0003 | t0001 | g0274 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18971 | hp1 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18974 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18975 | hp1 | a0002 | c0003 | t0001 | g0262 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18977 | hp2 | a0003 | c0004 | t0002 | g0014 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18979 | hp1 | a0003 | c0004 | t0001 | g0145 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18979 | hp2 | a0002 | c0003 | t0001 | g0048 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18981 | hp1 | a0002 | c0003 | t0001 | g0266 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18981 | hp2 | a0001 | c0001 | t0009 | g0194 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18982 | hp1 | a0002 | c0003 | t0001 | g0282 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18982 | hp2 | a0003 | c0004 | t0001 | g0007 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18983 | hp1 | a0003 | c0004 | t0001 | g0172 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18983 | hp2 | a0002 | c0003 | t0001 | g0051 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18985 | hp1 | a0003 | c0004 | t0002 | g0132 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18986 | hp1 | a0003 | c0004 | t0001 | g0258 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19000 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19000 | hp2 | a0002 | c0003 | t0001 | g0284 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19003 | hp1 | a0003 | c0004 | t0002 | g0007 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19004 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19005 | hp2 | a0002 | c0003 | t0005 | g0263 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19006 | hp1 | a0002 | c0003 | t0001 | g0254 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19007 | hp1 | a0002 | c0003 | t0001 | g0050 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19007 | hp2 | a0003 | c0004 | t0002 | g0067 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19009 | hp2 | a0002 | c0003 | t0001 | g0283 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0100 | AFR | LWK | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19043 | hp2 | a0001 | c0001 | t0025 | g0127 | AFR | LWK | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19056 | hp2 | a0002 | c0003 | t0001 | g0051 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19057 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19060 | hp1 | a0003 | c0004 | t0001 | g0003 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19072 | hp2 | a0002 | c0003 | t0001 | g0048 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19076 | hp2 | a0001 | c0009 | t0001 | g0025 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19078 | hp1 | a0002 | c0003 | t0005 | g0281 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19082 | hp2 | a0002 | c0003 | t0001 | g0240 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19083 | hp1 | a0002 | c0003 | t0001 | g0261 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19088 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | YRI | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA19240 | hp2 | a0001 | c0001 | t0024 | g0148 | AFR | YRI | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0149 | AFR | ASW | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | TSI | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | TSI | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | TSI | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | TSI | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01123 | hp1 | a0003 | c0004 | t0001 | g0004 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG01123 | hp2 | a0002 | c0003 | t0001 | g0237 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0181 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0130 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0077 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0104 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG06807 | hp1 | a0002 | c0003 | t0001 | g0245 | AFR | USA | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0109 | AFR | USA | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | USA | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0062 | AFR | USA | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA21309 | hp1 | a0001 | c0001 | t0018 | g0212 | AFR | LWK | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0168 | REF | REF | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| homoSapiens | grch38p0 | a0003 | c0004 | t0004 | g0236 | REF | REF | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:112340921 | C | G | 2 | a0001 a0004 |
273 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(270): Show |
missense_variant | MODERATE | c.32C>G | p.Ser11Cys | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/6 | 89/2129 | 32/810 | 11/269 | chr3 | 112340921 | |||
| chr3:112345003 | C | A | 1 | a0002 | 73 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(70): Show |
missense_variant | MODERATE | c.136C>A | p.Pro46Thr | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/6 | 193/2129 | 136/810 | 46/269 | chr3 | 112345003 | |||
| chr3:112347599 | C | T | 1 | a0004 | 2 | HG01256.hp1 HG01258.hp2 |
missense_variant | MODERATE | c.463C>T | p.His155Tyr | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/6 | 520/2129 | 463/810 | 155/269 | chr3 | 112347599 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:112345269 | G | A | 2 | a0001c0008 a0003c0006 |
5 | HG00544.hp1 HG02622.hp2 HG02735.hp1 others(2): Show |
synonymous_variant | LOW | c.402G>A | p.Thr134Thr | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/6 | 459/2129 | 402/810 | 134/269 | chr3 | 112345269 | |||
| chr3:112347715 | G | A | 3 | a0001c0002 a0001c0009 a0003c0005 |
95 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(92): Show |
synonymous_variant | LOW | c.579G>A | p.Thr193Thr | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/6 | 636/2129 | 579/810 | 193/269 | chr3 | 112347715 | |||
| chr3:112347820 | C | T | 1 | a0001c0009 | 1 | NA19076.hp2 | synonymous_variant | LOW | c.684C>T | p.Thr228Thr | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/6 | 741/2129 | 684/810 | 228/269 | chr3 | 112347820 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:112361551 | A | C | 8 | a0001c0001t0003 a0001c0001t0024 a0001c0001t0025 others(5): Show |
18 | HG00544.hp1 HG02129.hp2 HG02257.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 1 | chr3 | 112361551 | ||||||
| chr3:112361699 | C | A | 1 | a0003c0005t0010 | 2 | HG02630.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*149C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 149 | chr3 | 112361699 | ||||||
| chr3:112361719 | T | C | 1 | a0002c0003t0005 | 4 | NA18940.hp2 NA18968.hp2 NA19005.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*169T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 169 | chr3 | 112361719 | ||||||
| chr3:112361797 | T | C | 4 | a0001c0001t0003 a0001c0002t0003 a0003c0004t0003 others(1): Show |
10 | HG02129.hp2 HG02257.hp1 HG02809.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*247T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 247 | chr3 | 112361797 | ||||||
| chr3:112361818 | CTTAG | C | 9 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0024 others(6): Show |
19 | HG00544.hp1 HG02129.hp2 HG02257.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*274_*277delTAGT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 274 | INFO_REALIGN_3_PRIME | chr3 | 112361818 | |||||
| chr3:112361842 | G | A | 2 | a0001c0001t0008 a0002c0003t0008 |
3 | HG02630.hp2 HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*292G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 292 | chr3 | 112361842 | ||||||
| chr3:112361870 | G | C | 1 | a0003c0004t0012 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*320G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 320 | chr3 | 112361870 | ||||||
| chr3:112361882 | G | C | 1 | a0001c0001t0009 | 2 | NA18954.hp1 NA18981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*332G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 332 | chr3 | 112361882 | ||||||
| chr3:112361999 | G | A | 1 | a0001c0001t0013 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*449G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 449 | chr3 | 112361999 | ||||||
| chr3:112362159 | G | A | 1 | a0001c0002t0014 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*609G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 609 | chr3 | 112362159 | ||||||
| chr3:112362182 | A | G | 1 | a0001c0002t0023 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*632A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 632 | chr3 | 112362182 | ||||||
| chr3:112362247 | A | C | 1 | a0001c0001t0025 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*697A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 697 | chr3 | 112362247 | ||||||
| chr3:112362318 | C | A | 1 | a0001c0001t0015 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*768C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 768 | chr3 | 112362318 | ||||||
| chr3:112362348 | C | T | 7 | a0001c0001t0003 a0001c0001t0024 a0001c0002t0003 others(4): Show |
17 | HG00544.hp1 HG02129.hp2 HG02257.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*798C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 798 | chr3 | 112362348 | ||||||
| chr3:112362352 | C | A | 1 | a0001c0002t0016 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*802C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 802 | chr3 | 112362352 | ||||||
| chr3:112362511 | G | A | 6 | a0001c0001t0002 a0001c0001t0017 a0001c0002t0002 others(3): Show |
37 | HG00438.hp2 HG00609.hp2 HG01106.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*961G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 961 | chr3 | 112362511 | ||||||
| chr3:112362513 | G | A | 1 | a0001c0001t0018 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*963G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 963 | chr3 | 112362513 | ||||||
| chr3:112362538 | G | A | 2 | a0001c0001t0024 a0003c0005t0010 |
3 | HG02630.hp1 HG02717.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*988G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 988 | chr3 | 112362538 | ||||||
| chr3:112362550 | C | T | 1 | a0001c0002t0022 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1000C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 1000 | chr3 | 112362550 | ||||||
| chr3:112362667 | G | T | 1 | a0001c0002t0021 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1117G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 1117 | chr3 | 112362667 | ||||||
| chr3:112362672 | G | A | 1 | a0001c0002t0019 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1122G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 1122 | chr3 | 112362672 | ||||||
| chr3:112362696 | G | C | 7 | a0001c0001t0003 a0001c0001t0024 a0001c0002t0003 others(4): Show |
17 | HG00544.hp1 HG02129.hp2 HG02257.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1146G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 1146 | chr3 | 112362696 | ||||||
| chr3:112362713 | T | TTA | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(26): Show |
380 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(377): Show |
3_prime_UTR_variant | MODIFIER | c.*1176_*1177dupTA | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 1178 | INFO_REALIGN_3_PRIME | chr3 | 112362713 | |||||
| chr3:112362754 | C | A | 1 | a0001c0002t0020 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1204C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 1204 | chr3 | 112362754 | ||||||
| chr3:112362790 | C | A | 1 | a0001c0001t0006 | 4 | HG01081.hp2 HG01891.hp2 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1240C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 1240 | chr3 | 112362790 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:112333256 | G | T | 64 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0002t0001g0238 others(61): Show |
78 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.12+32G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112333256 | |||||||
| chr3:112333273 | G | A | 6 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(3): Show |
6 | HG00280.hp1 HG00738.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+49G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112333273 | |||||||
| chr3:112333288 | GGGCGGGC others(11): Show |
G | 1 | a0002c0003t0001g0237 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.12+69_12+86delGGCG others(14): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 112333288 | ||||||
| chr3:112333291 | C | A | 1 | a0001c0001t0001g0006 | 2 | NA19006.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.12+67C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112333291 | |||||||
| chr3:112333309 | C | A | 1 | a0002c0003t0001g0237 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.12+85C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112333309 | |||||||
| chr3:112333312 | G | C | 1 | a0002c0003t0001g0237 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.12+88G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112333312 | |||||||
| chr3:112333313 | G | C | 1 | a0002c0003t0001g0237 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.12+89G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112333313 | |||||||
| chr3:112333326 | T | C | 291 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(288): Show |
397 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(394): Show |
intron_variant | MODIFIER | c.12+102T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112333326 | |||||||
| chr3:112333798 | T | C | 2 | a0001c0002t0002g0059 a0001c0002t0023g0060 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.12+574T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112333798 | |||||||
| chr3:112333961 | G | A | 1 | a0001c0001t0006g0229 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.12+737G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112333961 | |||||||
| chr3:112333986 | G | A | 88 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0124 others(85): Show |
103 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.12+762G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112333986 | |||||||
| chr3:112334080 | G | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(114): Show |
176 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.12+856G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112334080 | |||||||
| chr3:112334237 | CA | C | 4 | a0001c0002t0001g0130 a0001c0002t0001g0238 a0001c0002t0002g0059 others(1): Show |
4 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.12+1014delA | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112334237 | |||||||
| chr3:112334399 | T | C | 147 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0124 others(144): Show |
176 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.12+1175T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112334399 | |||||||
| chr3:112334718 | G | A | 119 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(116): Show |
146 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.12+1494G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112334718 | |||||||
| chr3:112334748 | G | GA | 7 | a0001c0001t0001g0126 a0001c0002t0001g0061 a0001c0002t0001g0062 others(4): Show |
7 | HG02055.hp2 HG02074.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.12+1534dupA | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 112334748 | ||||||
| chr3:112334748 | GA | G | 53 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0002c0003t0001g0009 others(50): Show |
67 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.12+1534delA | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 112334748 | ||||||
| chr3:112334758 | AC | A | 5 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | NA18970.hp2 NA18974.hp1 NA19072.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+1536delC | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 112334758 | ||||||
| chr3:112334759 | C | A | 5 | a0001c0001t0001g0046 a0001c0001t0001g0196 a0001c0001t0002g0183 others(2): Show |
6 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+1535C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112334759 | |||||||
| chr3:112334904 | C | T | 119 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(116): Show |
146 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.12+1680C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112334904 | |||||||
| chr3:112335236 | A | C | 2 | a0001c0002t0002g0059 a0001c0002t0023g0060 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.12+2012A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335236 | |||||||
| chr3:112335277 | T | C | 6 | a0001c0001t0001g0137 a0001c0001t0004g0136 a0001c0001t0008g0138 others(3): Show |
7 | HG02257.hp1 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+2053T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335277 | |||||||
| chr3:112335371 | A | G | 2 | a0001c0002t0001g0130 a0001c0002t0001g0238 |
2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.12+2147A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335371 | |||||||
| chr3:112335376 | C | G | 3 | a0001c0001t0024g0148 a0003c0005t0010g0128 a0003c0005t0010g0129 |
3 | HG02630.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.12+2152C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335376 | |||||||
| chr3:112335387 | T | C | 6 | a0001c0001t0001g0137 a0001c0001t0004g0136 a0001c0001t0008g0138 others(3): Show |
7 | HG02257.hp1 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+2163T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335387 | |||||||
| chr3:112335389 | G | A | 6 | a0002c0003t0001g0023 a0002c0003t0001g0249 a0002c0003t0001g0250 others(3): Show |
8 | HG00323.hp1 HG00733.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.12+2165G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335389 | |||||||
| chr3:112335408 | G | A | 3 | a0002c0003t0001g0169 a0002c0003t0008g0170 a0002c0003t0008g0171 |
3 | HG02896.hp2 HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.12+2184G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335408 | |||||||
| chr3:112335666 | A | ACAT | 4 | a0001c0001t0001g0126 a0001c0001t0024g0148 a0003c0005t0010g0128 others(1): Show |
4 | HG02630.hp1 HG02717.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+2446_12+2448dup others(3): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 112335666 | ||||||
| chr3:112335678 | C | G | 1 | a0001c0002t0001g0125 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.12+2454C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335678 | |||||||
| chr3:112335688 | T | C | 3 | a0003c0006t0007g0139 a0003c0006t0007g0140 a0003c0006t0007g0141 |
3 | HG02735.hp1 HG04204.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.12+2464T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335688 | |||||||
| chr3:112335730 | A | G | 1 | a0001c0002t0001g0125 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.12+2506A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335730 | |||||||
| chr3:112335804 | A | T | 4 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(1): Show |
4 | NA18970.hp2 NA19072.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.12+2580A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335804 | |||||||
| chr3:112336092 | T | C | 1 | a0001c0001t0024g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.12+2868T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336092 | |||||||
| chr3:112336117 | C | G | 1 | a0001c0001t0001g0223 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.12+2893C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336117 | |||||||
| chr3:112336176 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(86): Show |
136 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.12+2952G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336176 | |||||||
| chr3:112336269 | C | T | 1 | a0002c0003t0001g0291 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.12+3045C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336269 | |||||||
| chr3:112336308 | G | C | 16 | a0001c0001t0001g0047 a0001c0001t0001g0137 a0001c0001t0004g0136 others(13): Show |
18 | HG00735.hp2 HG01081.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.12+3084G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336308 | |||||||
| chr3:112336370 | C | T | 3 | a0001c0001t0024g0148 a0003c0005t0010g0128 a0003c0005t0010g0129 |
3 | HG02630.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.12+3146C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336370 | |||||||
| chr3:112336525 | C | T | 1 | a0001c0002t0023g0060 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.12+3301C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336525 | |||||||
| chr3:112336789 | G | T | 3 | a0003c0006t0007g0139 a0003c0006t0007g0140 a0003c0006t0007g0141 |
3 | HG02735.hp1 HG04204.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.12+3565G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336789 | |||||||
| chr3:112336790 | G | C | 1 | a0001c0002t0001g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.12+3566G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336790 | |||||||
| chr3:112336864 | G | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(89): Show |
139 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.12+3640G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336864 | |||||||
| chr3:112336946 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(205): Show |
282 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.12+3722A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336946 | |||||||
| chr3:112336989 | A | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG01257.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.12+3765A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336989 | |||||||
| chr3:112336992 | A | T | 62 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0002t0002g0248 others(59): Show |
76 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.12+3768A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336992 | |||||||
| chr3:112337105 | A | G | 32 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(29): Show |
43 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.13-3797A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112337105 | |||||||
| chr3:112337567 | A | G | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(286): Show |
379 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.13-3335A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112337567 | |||||||
| chr3:112337661 | G | C | 2 | a0001c0002t0001g0130 a0001c0002t0001g0238 |
2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.13-3241G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112337661 | |||||||
| chr3:112337664 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.13-3238T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112337664 | |||||||
| chr3:112337784 | C | T | 4 | a0001c0001t0001g0126 a0001c0001t0024g0148 a0003c0005t0010g0128 others(1): Show |
4 | HG02630.hp1 HG02717.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-3118C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112337784 | |||||||
| chr3:112338070 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.13-2832A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112338070 | |||||||
| chr3:112338087 | A | G | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(286): Show |
379 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.13-2815A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112338087 | |||||||
| chr3:112338183 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.13-2719G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112338183 | |||||||
| chr3:112338261 | G | A | 1 | a0001c0002t0001g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.13-2641G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112338261 | |||||||
| chr3:112338288 | T | C | 119 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(116): Show |
146 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.13-2614T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112338288 | |||||||
| chr3:112338289 | G | A | 1 | a0001c0002t0016g0064 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.13-2613G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112338289 | |||||||
| chr3:112338346 | G | A | 8 | a0001c0001t0001g0047 a0001c0001t0006g0229 a0001c0001t0006g0232 others(5): Show |
9 | HG00735.hp2 HG01081.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.13-2556G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112338346 | |||||||
| chr3:112338388 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.13-2514C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112338388 | |||||||
| chr3:112338728 | G | A | 3 | a0001c0001t0024g0148 a0003c0005t0010g0128 a0003c0005t0010g0129 |
3 | HG02630.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.13-2174G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112338728 | |||||||
| chr3:112338766 | C | CAAT | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(102): Show |
154 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.13-2136_13-2135ins others(3): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112338766 | |||||||
| chr3:112339191 | A | G | 15 | a0001c0001t0001g0047 a0001c0001t0001g0137 a0001c0001t0004g0136 others(12): Show |
17 | HG00735.hp2 HG01081.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.13-1711A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112339191 | |||||||
| chr3:112339255 | A | G | 1 | a0003c0004t0001g0146 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.13-1647A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112339255 | |||||||
| chr3:112339298 | T | C | 1 | a0001c0002t0001g0065 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.13-1604T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112339298 | |||||||
| chr3:112339401 | G | A | 1 | a0003c0004t0001g0142 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.13-1501G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112339401 | |||||||
| chr3:112339581 | G | A | 2 | a0003c0005t0010g0128 a0003c0005t0010g0129 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.13-1321G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112339581 | |||||||
| chr3:112339604 | G | C | 10 | a0002c0003t0001g0048 a0002c0003t0001g0049 a0002c0003t0001g0254 others(7): Show |
12 | HG00597.hp1 HG00673.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.13-1298G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112339604 | |||||||
| chr3:112339875 | G | A | 1 | a0001c0001t0003g0032 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.13-1027G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112339875 | |||||||
| chr3:112339945 | A | G | 3 | a0002c0003t0001g0288 a0002c0003t0001g0289 a0002c0003t0001g0290 |
3 | HG01884.hp1 HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.13-957A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112339945 | |||||||
| chr3:112339971 | G | C | 3 | a0001c0001t0024g0148 a0003c0005t0010g0128 a0003c0005t0010g0129 |
3 | HG02630.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.13-931G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112339971 | |||||||
| chr3:112340063 | A | G | 3 | a0001c0001t0024g0148 a0003c0005t0010g0128 a0003c0005t0010g0129 |
3 | HG02630.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.13-839A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340063 | |||||||
| chr3:112340076 | A | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(84): Show |
134 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.13-826A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340076 | |||||||
| chr3:112340187 | A | G | 1 | a0001c0002t0001g0120 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.13-715A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340187 | |||||||
| chr3:112340260 | T | C | 1 | a0002c0003t0001g0262 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.13-642T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340260 | |||||||
| chr3:112340281 | T | A | 2 | a0001c0002t0001g0130 a0001c0002t0001g0238 |
2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.13-621T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340281 | |||||||
| chr3:112340286 | A | C | 1 | a0002c0003t0001g0261 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.13-616A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340286 | |||||||
| chr3:112340287 | G | A | 1 | a0002c0003t0001g0261 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.13-615G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340287 | |||||||
| chr3:112340288 | A | G | 1 | a0002c0003t0001g0261 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.13-614A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340288 | |||||||
| chr3:112340365 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.13-537C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340365 | |||||||
| chr3:112340366 | G | A | 62 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0002t0002g0248 others(59): Show |
76 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.13-536G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340366 | |||||||
| chr3:112340531 | T | G | 2 | a0001c0002t0001g0130 a0001c0002t0001g0238 |
2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.13-371T>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340531 | |||||||
| chr3:112340736 | A | G | 21 | a0001c0001t0001g0047 a0001c0001t0001g0137 a0001c0001t0003g0032 others(18): Show |
24 | HG00735.hp2 HG01081.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.13-166A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340736 | |||||||
| chr3:112341207 | T | A | 4 | a0003c0006t0007g0139 a0003c0006t0007g0140 a0003c0006t0007g0141 others(1): Show |
4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+224T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112341207 | |||||||
| chr3:112341399 | G | A | 4 | a0003c0006t0007g0139 a0003c0006t0007g0140 a0003c0006t0007g0141 others(1): Show |
4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+416G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112341399 | |||||||
| chr3:112341409 | A | C | 75 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(72): Show |
83 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.94+426A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112341409 | |||||||
| chr3:112341488 | C | T | 4 | a0003c0006t0007g0139 a0003c0006t0007g0140 a0003c0006t0007g0141 others(1): Show |
4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+505C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112341488 | |||||||
| chr3:112341541 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.94+558C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112341541 | |||||||
| chr3:112341911 | T | C | 155 | a0001c0001t0024g0148 a0001c0002t0001g0016 a0001c0002t0001g0017 others(152): Show |
185 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(182): Show |
intron_variant | MODIFIER | c.94+928T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112341911 | |||||||
| chr3:112342043 | A | G | 1 | a0001c0002t0001g0118 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.94+1060A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342043 | |||||||
| chr3:112342048 | T | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02015.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.94+1065T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342048 | |||||||
| chr3:112342064 | A | G | 3 | a0001c0002t0001g0130 a0001c0002t0001g0238 a0001c0002t0020g0166 |
3 | HG02109.hp2 HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.94+1081A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342064 | |||||||
| chr3:112342066 | C | A | 1 | a0001c0001t0024g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.94+1083C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342066 | |||||||
| chr3:112342271 | G | GTCCTTCC others(5): Show |
1 | a0001c0001t0001g0154 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.94+1314_94+1325dup others(12): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342271 | ||||||
| chr3:112342301 | CCTTCCTT others(24): Show |
C | 1 | a0003c0006t0007g0141 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.94+1322_94+1352del others(31): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342301 | ||||||
| chr3:112342301 | CCTTCCTT others(32): Show |
C | 1 | a0003c0006t0007g0177 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.94+1322_94+1360del others(39): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342301 | ||||||
| chr3:112342301 | CCTTCCTT others(36): Show |
C | 1 | a0003c0006t0007g0140 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.94+1322_94+1364del others(43): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342301 | ||||||
| chr3:112342303 | TTCCTTTC others(28): Show |
T | 1 | a0003c0006t0007g0139 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.94+1322_94+1356del others(35): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342303 | ||||||
| chr3:112342305 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.94+1322C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342305 | |||||||
| chr3:112342305 | CCTTTCTT others(32): Show |
C | 1 | a0001c0001t0001g0205 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.94+1330_94+1368del others(39): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342305 | ||||||
| chr3:112342305 | CCTTTCTT others(36): Show |
C | 2 | a0001c0001t0001g0012 a0003c0004t0001g0147 |
2 | HG02698.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.94+1330_94+1372del others(43): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342305 | ||||||
| chr3:112342305 | CCTTTCTT others(40): Show |
C | 1 | a0001c0001t0001g0039 | 2 | HG03239.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.94+1330_94+1376del others(47): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342305 | ||||||
| chr3:112342305 | CCTTTCTT others(44): Show |
C | 1 | a0001c0001t0001g0020 | 3 | NA18957.hp2 NA19004.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.94+1330_94+1380del others(51): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342305 | ||||||
| chr3:112342305 | CCTTTCTT others(48): Show |
C | 1 | a0003c0004t0001g0258 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.94+1330_94+1384del others(55): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342305 | ||||||
| chr3:112342306 | C | CTTCCTTC others(25): Show |
1 | a0001c0001t0006g0235 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.94+1325_94+1326ins others(32): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342306 | ||||||
| chr3:112342306 | CTTTCTTC others(5): Show |
C | 1 | a0002c0003t0005g0263 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.94+1326_94+1337del others(12): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342306 | ||||||
| chr3:112342306 | CTTTCTTC others(33): Show |
C | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.94+1326_94+1365del others(40): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342306 | ||||||
| chr3:112342306 | CTTTCTTC others(37): Show |
C | 1 | a0001c0001t0002g0123 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.94+1326_94+1369del others(44): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342306 | ||||||
| chr3:112342306 | CTTTCTTC others(41): Show |
C | 1 | a0001c0001t0001g0124 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.94+1326_94+1373del others(48): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342306 | ||||||
| chr3:112342306 | CTTTCTTC others(61): Show |
C | 1 | a0001c0001t0001g0209 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.94+1326_94+1393del others(68): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342306 | ||||||
| chr3:112342309 | T | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(259): Show |
341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.94+1326T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342309 | |||||||
| chr3:112342313 | C | CCTTCCTT others(9): Show |
1 | a0001c0001t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.94+1330_94+1331ins others(16): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | |||||||
| chr3:112342313 | C | T | 3 | a0001c0002t0001g0238 a0003c0004t0001g0142 a0003c0004t0001g0144 |
3 | HG02451.hp1 HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.94+1330C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | |||||||
| chr3:112342313 | CTTT | C | 20 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0035 others(17): Show |
22 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.94+1331_94+1333del others(3): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | |||||||
| chr3:112342313 | CTTTCTTT | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0037 others(3): Show |
7 | HG00642.hp2 HG00735.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+1331_94+1337del others(7): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | |||||||
| chr3:112342313 | CTTTCTTT others(4): Show |
C | 8 | a0001c0001t0001g0019 a0001c0001t0001g0038 a0001c0001t0001g0056 others(5): Show |
10 | HG00733.hp2 HG01192.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.94+1331_94+1341del others(11): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | |||||||
| chr3:112342313 | CTTTCTTT others(8): Show |
C | 5 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0126 others(2): Show |
5 | HG00735.hp2 HG01981.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+1331_94+1345del others(15): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | |||||||
| chr3:112342313 | CTTTCTTT others(20): Show |
C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0004g0045 others(7): Show |
12 | HG02080.hp1 HG02165.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.94+1331_94+1357del others(27): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | |||||||
| chr3:112342313 | CTTTCTTT others(24): Show |
C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0069 others(13): Show |
20 | HG00323.hp1 HG01175.hp1 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.94+1331_94+1361del others(31): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | |||||||
| chr3:112342313 | CTTTCTTT others(28): Show |
C | 17 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(14): Show |
19 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(16): Show |
intron_variant | MODIFIER | c.94+1331_94+1365del others(35): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | |||||||
| chr3:112342313 | CTTTCTTT others(32): Show |
C | 20 | a0001c0001t0001g0012 a0001c0001t0001g0041 a0001c0001t0001g0184 others(17): Show |
26 | HG00609.hp1 HG00741.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.94+1331_94+1369del others(39): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | |||||||
| chr3:112342313 | CTTTCTTT others(35): Show |
C | 1 | a0001c0001t0001g0046 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.94+1332_94+1373del others(42): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342313 | ||||||
| chr3:112342313 | CTTTCTTT others(36): Show |
C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0042 others(29): Show |
47 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.94+1331_94+1373del others(43): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | |||||||
| chr3:112342313 | CTTTCTTT others(38): Show |
C | 1 | a0001c0001t0001g0046 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94+1333_94+1377del others(45): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342313 | ||||||
| chr3:112342313 | CTTTCTTT others(40): Show |
C | 21 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0187 others(18): Show |
28 | HG00140.hp1 HG02040.hp1 HG02083.hp1 others(25): Show |
intron_variant | MODIFIER | c.94+1331_94+1377del others(47): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | |||||||
| chr3:112342313 | CTTTCTTT others(44): Show |
C | 16 | a0001c0001t0001g0021 a0001c0001t0001g0199 a0001c0001t0001g0200 others(13): Show |
18 | HG01071.hp1 HG01928.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.94+1331_94+1381del others(51): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | |||||||
| chr3:112342313 | CTTTCTTT others(48): Show |
C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0201 a0001c0002t0001g0063 others(6): Show |
15 | HG00438.hp1 HG01106.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.94+1331_94+1385del others(55): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | |||||||
| chr3:112342314 | T | C | 94 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0033 others(91): Show |
111 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.94+1331T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342314 | |||||||
| chr3:112342317 | C | T | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0165 others(1): Show |
4 | HG01346.hp1 HG02738.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+1334C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342317 | |||||||
| chr3:112342317 | CTTTCTTT others(16): Show |
C | 14 | a0001c0001t0001g0022 a0001c0001t0001g0211 a0001c0001t0001g0222 others(11): Show |
14 | HG00673.hp1 HG01358.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.94+1335_94+1357del others(23): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342317 | |||||||
| chr3:112342318 | T | C | 75 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0034 others(72): Show |
92 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.94+1335T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342318 | |||||||
| chr3:112342319 | T | C | 1 | a0003c0004t0002g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.94+1336T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342319 | |||||||
| chr3:112342319 | TTCTTTCT others(31): Show |
T | 1 | a0001c0001t0001g0207 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.94+1338_94+1375del others(38): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342319 | ||||||
| chr3:112342320 | T | C | 18 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0035 others(15): Show |
20 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.94+1337T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342320 | |||||||
| chr3:112342321 | C | CCTTCCTT others(5): Show |
1 | a0001c0001t0006g0229 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.94+1338_94+1339ins others(12): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342321 | |||||||
| chr3:112342321 | C | T | 1 | a0001c0001t0001g0033 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.94+1338C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342321 | |||||||
| chr3:112342321 | CTTTCTTT others(12): Show |
C | 2 | a0001c0001t0001g0204 a0001c0001t0011g0019 |
2 | HG02071.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.94+1339_94+1357del others(19): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342321 | |||||||
| chr3:112342321 | CTTTCTTT others(14): Show |
C | 2 | a0001c0001t0001g0228 a0001c0008t0001g0002 |
2 | HG02622.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.94+1341_94+1361del others(21): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342321 | ||||||
| chr3:112342321 | CTTTCTTT others(18): Show |
C | 1 | a0001c0001t0001g0173 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.94+1341_94+1365del others(25): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342321 | ||||||
| chr3:112342322 | T | C | 68 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0034 others(65): Show |
85 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.94+1339T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342322 | |||||||
| chr3:112342322 | TTTCTTTC others(9): Show |
T | 1 | a0003c0004t0001g0144 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.94+1355_94+1370del others(16): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342322 | ||||||
| chr3:112342324 | T | C | 19 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(16): Show |
23 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.94+1341T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342324 | |||||||
| chr3:112342325 | C | CCTTT | 3 | a0001c0001t0001g0054 a0001c0001t0001g0156 a0001c0001t0006g0232 |
3 | HG01496.hp1 HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.94+1342_94+1343ins others(4): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342325 | |||||||
| chr3:112342325 | C | T | 2 | a0001c0001t0001g0155 a0001c0002t0002g0059 |
2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.94+1342C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342325 | |||||||
| chr3:112342325 | CT | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0053 a0001c0001t0001g0157 |
4 | HG00738.hp1 HG01081.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+1345delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342325 | ||||||
| chr3:112342325 | CTTTCTTT others(8): Show |
C | 10 | a0001c0001t0024g0148 a0001c0002t0001g0115 a0001c0002t0004g0116 others(7): Show |
10 | HG01433.hp1 HG02074.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+1343_94+1357del others(15): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342325 | |||||||
| chr3:112342326 | T | C | 57 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0054 others(54): Show |
70 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.94+1343T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342326 | |||||||
| chr3:112342328 | T | C | 20 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0037 others(17): Show |
25 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.94+1345T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342328 | |||||||
| chr3:112342329 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0004g0136 |
4 | HG01255.hp2 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+1346C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342329 | |||||||
| chr3:112342329 | CT | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0160 a0001c0001t0004g0149 others(3): Show |
8 | HG00642.hp2 HG00735.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.94+1349delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342329 | ||||||
| chr3:112342329 | CTTTCTTT others(4): Show |
C | 1 | a0001c0002t0001g0062 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.94+1347_94+1357del others(11): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342329 | |||||||
| chr3:112342330 | T | C | 53 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0143 others(50): Show |
66 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.94+1347T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342330 | |||||||
| chr3:112342332 | T | C | 14 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0047 others(11): Show |
17 | HG00735.hp2 HG01175.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+1349T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342332 | |||||||
| chr3:112342333 | C | T | 1 | a0001c0001t0006g0233 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.94+1350C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342333 | |||||||
| chr3:112342333 | CT | C | 9 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0055 others(6): Show |
12 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+1353delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342333 | ||||||
| chr3:112342334 | T | C | 51 | a0001c0001t0001g0143 a0001c0001t0001g0154 a0001c0001t0006g0229 others(48): Show |
63 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.94+1351T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342334 | |||||||
| chr3:112342335 | T | C | 2 | a0002c0003t0001g0245 a0002c0003t0008g0171 |
2 | HG02897.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.94+1352T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342335 | |||||||
| chr3:112342336 | TC | T | 9 | a0001c0001t0001g0019 a0001c0001t0001g0047 a0001c0001t0001g0058 others(6): Show |
11 | HG00735.hp2 HG01192.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.94+1355delC | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342336 | ||||||
| chr3:112342337 | C | T | 20 | a0001c0002t0020g0166 a0002c0003t0001g0009 a0002c0003t0001g0023 others(17): Show |
27 | HG00544.hp2 HG00558.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.94+1354C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342337 | |||||||
| chr3:112342337 | CCTTCT | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0219 a0002c0003t0001g0289 others(1): Show |
5 | HG01175.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+1355_94+1359del others(5): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342337 | |||||||
| chr3:112342337 | CCTTCTTT others(7): Show |
C | 1 | a0002c0003t0001g0272 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.94+1355_94+1368del others(14): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342337 | |||||||
| chr3:112342338 | C | CTTCTTTC others(1): Show |
3 | a0003c0004t0001g0007 a0003c0004t0002g0014 a0003c0004t0002g0231 |
3 | HG03209.hp2 NA18977.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.94+1441_94+1448dup others(8): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | ||||||
| chr3:112342338 | C | CTTCTTTC others(9): Show |
1 | a0003c0004t0002g0007 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.94+1433_94+1448dup others(16): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | ||||||
| chr3:112342338 | C | CTTCTTTC others(17): Show |
1 | a0003c0004t0002g0132 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.94+1425_94+1448dup others(24): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | ||||||
| chr3:112342338 | C | T | 31 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0035 others(28): Show |
40 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.94+1355C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342338 | |||||||
| chr3:112342338 | CTTCT | C | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0003c0004t0001g0003 others(1): Show |
4 | HG02074.hp2 HG02738.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+1445_94+1448del others(4): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | ||||||
| chr3:112342338 | CTTCTTTC others(1): Show |
C | 6 | a0001c0001t0013g0161 a0003c0004t0001g0004 a0003c0004t0001g0010 others(3): Show |
6 | HG00438.hp2 HG00609.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+1441_94+1448del others(8): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | ||||||
| chr3:112342338 | CTTCTTTC others(5): Show |
C | 4 | a0003c0004t0001g0004 a0003c0004t0001g0068 a0003c0004t0001g0172 others(1): Show |
6 | HG01123.hp1 HG01978.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+1437_94+1448del others(12): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | ||||||
| chr3:112342338 | CTTCTTTC others(9): Show |
C | 5 | a0001c0001t0001g0165 a0003c0004t0001g0004 a0003c0004t0001g0010 others(2): Show |
7 | HG01168.hp1 HG01346.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+1433_94+1448del others(16): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | ||||||
| chr3:112342338 | CTTCTTTC others(13): Show |
C | 7 | a0003c0004t0001g0003 a0003c0004t0001g0010 a0003c0004t0001g0031 others(4): Show |
9 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.94+1429_94+1448del others(20): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | ||||||
| chr3:112342338 | CTTCTTTC others(17): Show |
C | 1 | a0003c0004t0001g0003 | 3 | HG00323.hp2 HG00738.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.94+1425_94+1448del others(24): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | ||||||
| chr3:112342338 | CTTCTTTC others(21): Show |
C | 1 | a0003c0004t0001g0003 | 2 | HG00741.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.94+1421_94+1448del others(28): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | ||||||
| chr3:112342338 | CTTCTTTC others(33): Show |
C | 1 | a0003c0004t0001g0003 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.94+1409_94+1448del others(40): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | ||||||
| chr3:112342341 | C | T | 13 | a0001c0002t0003g0178 a0002c0003t0001g0013 a0002c0003t0001g0051 others(10): Show |
17 | HG00597.hp1 HG00597.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.94+1358C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342341 | |||||||
| chr3:112342341 | CTTT | C | 4 | a0002c0003t0001g0048 a0002c0003t0001g0254 a0002c0003t0001g0261 others(1): Show |
5 | NA18975.hp1 NA18979.hp2 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+1359_94+1361del others(3): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342341 | |||||||
| chr3:112342341 | CTTTCTTT others(8): Show |
C | 3 | a0002c0003t0001g0240 a0002c0003t0001g0264 a0002c0003t0001g0265 |
3 | HG01346.hp2 HG01943.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.94+1359_94+1373del others(15): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342341 | |||||||
| chr3:112342341 | CTTTCTTT others(27): Show |
C | 1 | a0001c0002t0001g0118 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.94+1360_94+1393del others(34): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342341 | ||||||
| chr3:112342341 | CTTTCTTT others(36): Show |
C | 1 | a0001c0002t0001g0073 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.94+1359_94+1401del others(43): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342341 | |||||||
| chr3:112342341 | CTTTCTTT others(40): Show |
C | 1 | a0001c0002t0001g0072 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.94+1359_94+1405del others(47): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342341 | |||||||
| chr3:112342342 | T | C | 21 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0004g0136 others(18): Show |
27 | HG00597.hp1 HG00597.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.94+1359T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342342 | |||||||
| chr3:112342344 | T | C | 28 | a0001c0001t0008g0138 a0001c0001t0024g0148 a0001c0002t0001g0026 others(25): Show |
29 | HG00673.hp1 HG01358.hp2 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.94+1361T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342344 | |||||||
| chr3:112342345 | CT | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0204 others(4): Show |
9 | HG02071.hp2 HG02723.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+1365delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342345 | ||||||
| chr3:112342345 | CTTTCTTT others(6): Show |
C | 1 | a0002c0003t0001g0257 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.94+1365_94+1377del others(13): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342345 | ||||||
| chr3:112342346 | T | C | 17 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(14): Show |
20 | HG00738.hp1 HG01071.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.94+1363T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342346 | |||||||
| chr3:112342348 | T | C | 35 | a0001c0001t0001g0002 a0001c0001t0001g0205 a0001c0001t0001g0221 others(32): Show |
37 | HG00323.hp1 HG00673.hp1 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.94+1365T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342348 | |||||||
| chr3:112342349 | C | T | 1 | a0003c0006t0007g0141 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.94+1366C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342349 | |||||||
| chr3:112342349 | CT | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0069 others(11): Show |
17 | HG01433.hp1 HG01928.hp1 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.94+1369delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342349 | ||||||
| chr3:112342350 | T | C | 23 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(20): Show |
29 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.94+1367T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342350 | |||||||
| chr3:112342352 | T | C | 36 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0041 others(33): Show |
39 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.94+1369T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342352 | |||||||
| chr3:112342353 | C | T | 1 | a0003c0006t0007g0139 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.94+1370C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342353 | |||||||
| chr3:112342353 | CT | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0070 a0001c0001t0001g0180 others(11): Show |
16 | HG00408.hp1 HG00408.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.94+1373delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342353 | ||||||
| chr3:112342354 | T | C | 24 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0037 others(21): Show |
31 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.94+1371T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342354 | |||||||
| chr3:112342354 | TTTCTTTC others(4): Show |
T | 1 | a0003c0005t0003g0135 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.94+1374_94+1384del others(11): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342354 | ||||||
| chr3:112342356 | T | C | 35 | a0001c0001t0001g0039 a0001c0001t0001g0182 a0001c0001t0001g0184 others(32): Show |
43 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.94+1373T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342356 | |||||||
| chr3:112342357 | C | T | 2 | a0003c0005t0003g0030 a0003c0006t0007g0177 |
3 | HG00544.hp1 HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.94+1374C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342357 | |||||||
| chr3:112342357 | CT | C | 20 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0041 others(17): Show |
24 | HG00673.hp1 HG00673.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.94+1377delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342357 | ||||||
| chr3:112342358 | T | C | 26 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0037 others(23): Show |
31 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.94+1375T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342358 | |||||||
| chr3:112342360 | T | C | 46 | a0001c0001t0001g0020 a0001c0001t0001g0185 a0001c0001t0001g0224 others(43): Show |
55 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.94+1377T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342360 | |||||||
| chr3:112342361 | C | T | 2 | a0001c0002t0003g0178 a0003c0006t0007g0140 |
2 | HG02809.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.94+1378C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342361 | |||||||
| chr3:112342361 | CT | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0039 others(19): Show |
37 | HG00280.hp2 HG00621.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.94+1381delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342361 | ||||||
| chr3:112342362 | T | C | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0058 others(6): Show |
11 | HG01175.hp2 HG01192.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.94+1379T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342362 | |||||||
| chr3:112342364 | T | C | 50 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0002t0001g0016 others(47): Show |
57 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.94+1381T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342364 | |||||||
| chr3:112342365 | CT | C | 13 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0044 others(10): Show |
22 | HG00323.hp1 HG01175.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.94+1385delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342365 | ||||||
| chr3:112342366 | T | C | 5 | a0001c0001t0001g0018 a0001c0001t0003g0032 a0001c0001t0008g0138 others(2): Show |
7 | HG01175.hp2 HG01256.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+1383T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342366 | |||||||
| chr3:112342368 | T | C | 50 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(47): Show |
56 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.94+1385T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342368 | |||||||
| chr3:112342369 | C | T | 2 | a0003c0005t0003g0134 a0003c0005t0003g0135 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.94+1386C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342369 | |||||||
| chr3:112342369 | CT | C | 11 | a0001c0001t0001g0021 a0001c0001t0001g0187 a0001c0001t0001g0188 others(8): Show |
13 | HG00140.hp1 HG00639.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.94+1389delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342369 | ||||||
| chr3:112342370 | T | C | 2 | a0001c0001t0008g0138 a0001c0001t0011g0019 |
2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.94+1387T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342370 | |||||||
| chr3:112342372 | T | C | 46 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(43): Show |
52 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.94+1389T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342372 | |||||||
| chr3:112342373 | CT | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0201 a0003c0004t0001g0260 |
9 | HG00438.hp1 NA18952.hp2 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+1393delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342373 | ||||||
| chr3:112342374 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.94+1391T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342374 | |||||||
| chr3:112342376 | T | C | 29 | a0001c0002t0001g0016 a0001c0002t0001g0029 a0001c0002t0001g0063 others(26): Show |
31 | HG00558.hp2 HG01106.hp2 HG01928.hp2 others(28): Show |
intron_variant | MODIFIER | c.94+1393T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342376 | |||||||
| chr3:112342377 | C | T | 2 | a0003c0005t0010g0128 a0003c0005t0010g0129 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.94+1394C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342377 | |||||||
| chr3:112342378 | T | A | 1 | a0001c0002t0001g0098 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.94+1395T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342378 | |||||||
| chr3:112342380 | T | C | 18 | a0001c0002t0001g0029 a0001c0002t0001g0063 a0001c0002t0001g0096 others(15): Show |
18 | HG01106.hp2 HG01928.hp2 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.94+1397T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342380 | |||||||
| chr3:112342381 | CTTTCTTT others(6): Show |
C | 1 | a0003c0005t0003g0030 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.94+1401_94+1413del others(13): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342381 | ||||||
| chr3:112342382 | TTTCTTTC others(40): Show |
T | 1 | a0001c0002t0001g0238 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.94+1404_94+1450del others(47): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342382 | ||||||
| chr3:112342384 | T | C | 5 | a0001c0002t0001g0106 a0001c0002t0001g0120 a0001c0002t0002g0029 others(2): Show |
5 | HG01928.hp2 HG02451.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+1401T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342384 | |||||||
| chr3:112342388 | T | C | 1 | a0001c0002t0002g0029 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.94+1405T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342388 | |||||||
| chr3:112342393 | CT | C | 3 | a0002c0003t0001g0048 a0003c0005t0003g0134 a0003c0005t0003g0135 |
3 | HG02886.hp1 HG03486.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.94+1413delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342393 | ||||||
| chr3:112342398 | TTTCTTTC others(24): Show |
T | 3 | a0002c0003t0001g0251 a0002c0003t0001g0273 a0002c0003t0001g0274 |
3 | HG01261.hp2 HG04228.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.94+1420_94+1450del others(31): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342398 | ||||||
| chr3:112342402 | TTTCTTTC others(20): Show |
T | 5 | a0002c0003t0001g0009 a0002c0003t0001g0023 a0002c0003t0001g0252 others(2): Show |
6 | HG00544.hp2 HG01256.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+1424_94+1450del others(27): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342402 | ||||||
| chr3:112342406 | TTTCTTTC others(16): Show |
T | 9 | a0001c0002t0001g0071 a0001c0002t0020g0166 a0002c0003t0001g0009 others(6): Show |
10 | HG01106.hp1 HG01516.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+1428_94+1450del others(23): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342406 | ||||||
| chr3:112342410 | TTTCTTTC others(12): Show |
T | 7 | a0002c0003t0001g0013 a0002c0003t0001g0023 a0002c0003t0001g0051 others(4): Show |
7 | HG01123.hp2 HG01934.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+1432_94+1450del others(19): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342410 | ||||||
| chr3:112342414 | TTTCTTTC others(8): Show |
T | 3 | a0002c0003t0001g0023 a0002c0003t0001g0052 a0002c0003t0001g0284 |
3 | HG00597.hp2 HG00733.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.94+1436_94+1450del others(15): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342414 | ||||||
| chr3:112342418 | TTTCTTTC others(4): Show |
T | 7 | a0002c0003t0001g0050 a0002c0003t0001g0051 a0002c0003t0001g0256 others(4): Show |
7 | HG00558.hp1 HG03239.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+1440_94+1450del others(11): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342418 | ||||||
| chr3:112342422 | TTTCTTTC | T | 3 | a0002c0003t0001g0009 a0002c0003t0001g0013 a0002c0003t0001g0283 |
3 | HG03710.hp1 HG03927.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.94+1444_94+1450del others(7): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342422 | ||||||
| chr3:112342426 | TTTC | T | 27 | a0001c0001t0024g0148 a0001c0002t0001g0062 a0001c0002t0001g0115 others(24): Show |
30 | HG00597.hp1 HG01192.hp1 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.94+1448_94+1450del others(3): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342426 | ||||||
| chr3:112342427 | T | C | 2 | a0001c0002t0001g0167 a0001c0002t0001g0174 |
2 | HG03516.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.94+1444T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342427 | |||||||
| chr3:112342428 | T | C | 1 | a0001c0002t0001g0117 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.94+1445T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342428 | |||||||
| chr3:112342429 | C | T | 1 | a0001c0002t0001g0117 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.94+1446C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342429 | |||||||
| chr3:112342429 | CT | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0210 a0001c0002t0001g0167 others(2): Show |
5 | HG02622.hp2 HG03516.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+1448delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342429 | ||||||
| chr3:112342430 | T | C | 54 | a0001c0001t0024g0148 a0001c0002t0001g0062 a0001c0002t0001g0071 others(51): Show |
69 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.94+1447T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342430 | |||||||
| chr3:112342430 | T | TC | 89 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(86): Show |
97 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.94+1447_94+1448ins others(1): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342430 | |||||||
| chr3:112342439 | T | TC | 3 | a0001c0001t0001g0126 a0001c0001t0001g0207 a0003c0004t0001g0144 |
3 | HG03130.hp1 NA18906.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.94+1456_94+1457ins others(1): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342439 | |||||||
| chr3:112342661 | C | G | 147 | a0001c0001t0024g0148 a0001c0002t0001g0016 a0001c0002t0001g0017 others(144): Show |
170 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.94+1678C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342661 | |||||||
| chr3:112342675 | G | A | 1 | a0002c0003t0001g0252 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.94+1692G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342675 | |||||||
| chr3:112342703 | G | A | 6 | a0001c0002t0003g0178 a0003c0005t0003g0030 a0003c0005t0003g0134 others(3): Show |
7 | HG02257.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+1720G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342703 | |||||||
| chr3:112342740 | T | C | 47 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(44): Show |
59 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.94+1757T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342740 | |||||||
| chr3:112342790 | T | A | 4 | a0003c0006t0007g0139 a0003c0006t0007g0140 a0003c0006t0007g0141 others(1): Show |
4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+1807T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342790 | |||||||
| chr3:112342866 | C | T | 4 | a0001c0002t0001g0016 a0001c0002t0001g0118 a0003c0005t0010g0128 others(1): Show |
6 | HG02056.hp1 HG02080.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+1883C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342866 | |||||||
| chr3:112342884 | G | A | 147 | a0001c0001t0024g0148 a0001c0002t0001g0016 a0001c0002t0001g0017 others(144): Show |
170 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.94+1901G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342884 | |||||||
| chr3:112342926 | G | C | 74 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(71): Show |
82 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.94+1943G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342926 | |||||||
| chr3:112342991 | C | CTGTG | 4 | a0003c0006t0007g0139 a0003c0006t0007g0140 a0003c0006t0007g0141 others(1): Show |
4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-1962_95-1959dup others(4): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342991 | ||||||
| chr3:112342992 | T | C | 2 | a0001c0002t0001g0072 a0001c0002t0001g0073 |
2 | NA18747.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.95-1970T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342992 | |||||||
| chr3:112343192 | C | G | 1 | a0001c0001t0002g0214 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.95-1770C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343192 | |||||||
| chr3:112343194 | C | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(78): Show |
128 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.95-1768C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343194 | |||||||
| chr3:112343336 | C | T | 2 | a0002c0003t0005g0280 a0002c0003t0005g0281 |
2 | NA18968.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.95-1626C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343336 | |||||||
| chr3:112343377 | C | G | 59 | a0002c0003t0001g0009 a0002c0003t0001g0013 a0002c0003t0001g0023 others(56): Show |
73 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.95-1585C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343377 | |||||||
| chr3:112343440 | A | G | 4 | a0003c0006t0007g0139 a0003c0006t0007g0140 a0003c0006t0007g0141 others(1): Show |
4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-1522A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343440 | |||||||
| chr3:112343455 | C | T | 7 | a0001c0001t0025g0127 a0001c0002t0003g0178 a0003c0005t0003g0030 others(4): Show |
8 | HG02257.hp1 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-1507C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343455 | |||||||
| chr3:112343460 | C | T | 74 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(71): Show |
82 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.95-1502C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343460 | |||||||
| chr3:112343473 | T | C | 1 | a0002c0003t0001g0256 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.95-1489T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343473 | |||||||
| chr3:112343602 | T | C | 87 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(84): Show |
96 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.95-1360T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343602 | |||||||
| chr3:112343605 | T | C | 1 | a0002c0003t0001g0243 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.95-1357T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343605 | |||||||
| chr3:112343684 | T | C | 2 | a0001c0001t0001g0202 a0001c0001t0024g0148 |
2 | HG03704.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.95-1278T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343684 | |||||||
| chr3:112343881 | C | T | 1 | a0003c0004t0001g0145 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.95-1081C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343881 | |||||||
| chr3:112343989 | T | C | 2 | a0001c0002t0001g0130 a0001c0002t0001g0238 |
2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.95-973T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343989 | |||||||
| chr3:112344073 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(79): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.95-889C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344073 | |||||||
| chr3:112344207 | T | C | 2 | a0001c0002t0001g0130 a0001c0002t0001g0238 |
2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.95-755T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344207 | |||||||
| chr3:112344342 | A | T | 2 | a0002c0003t0001g0237 a0002c0003t0001g0279 |
2 | HG01123.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.95-620A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344342 | |||||||
| chr3:112344349 | T | G | 1 | a0001c0001t0001g0286 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.95-613T>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344349 | |||||||
| chr3:112344403 | C | T | 59 | a0001c0001t0024g0148 a0002c0003t0001g0009 a0002c0003t0001g0013 others(56): Show |
73 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.95-559C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344403 | |||||||
| chr3:112344424 | A | C | 39 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0025 others(36): Show |
45 | HG01255.hp1 HG01358.hp1 HG01496.hp2 others(42): Show |
intron_variant | MODIFIER | c.95-538A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344424 | |||||||
| chr3:112344482 | T | C | 1 | a0003c0004t0002g0066 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.95-480T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344482 | |||||||
| chr3:112344638 | T | C | 74 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(71): Show |
82 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.95-324T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344638 | |||||||
| chr3:112344667 | A | C | 4 | a0003c0006t0007g0139 a0003c0006t0007g0140 a0003c0006t0007g0141 others(1): Show |
4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-295A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344667 | |||||||
| chr3:112344667 | A | G | 2 | a0001c0002t0001g0107 a0001c0002t0001g0108 |
2 | HG03688.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.95-295A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344667 | |||||||
| chr3:112344816 | C | T | 7 | a0001c0002t0003g0178 a0002c0003t0001g0278 a0003c0005t0003g0030 others(4): Show |
8 | HG00558.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-146C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344816 | |||||||
| chr3:112344858 | T | C | 83 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(80): Show |
92 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.95-104T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344858 | |||||||
| chr3:112344907 | A | G | 1 | a0003c0004t0003g0239 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.95-55A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344907 | |||||||
| chr3:112344918 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.95-44G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344918 | |||||||
| chr3:112345352 | T | C | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0203 |
3 | HG02486.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.421+64T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345352 | |||||||
| chr3:112345401 | A | G | 4 | a0003c0006t0007g0139 a0003c0006t0007g0140 a0003c0006t0007g0141 others(1): Show |
4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+113A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345401 | |||||||
| chr3:112345416 | T | A | 87 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(84): Show |
96 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.421+128T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345416 | |||||||
| chr3:112345419 | T | C | 69 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(66): Show |
77 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.421+131T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345419 | |||||||
| chr3:112345479 | G | T | 3 | a0001c0002t0002g0059 a0001c0002t0002g0234 a0001c0002t0023g0060 |
3 | HG02886.hp2 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.421+191G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345479 | |||||||
| chr3:112345488 | A | G | 4 | a0003c0006t0007g0139 a0003c0006t0007g0140 a0003c0006t0007g0141 others(1): Show |
4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+200A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345488 | |||||||
| chr3:112345606 | C | A | 1 | a0001c0001t0001g0189 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.421+318C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345606 | |||||||
| chr3:112345629 | C | T | 4 | a0003c0006t0007g0139 a0003c0006t0007g0140 a0003c0006t0007g0141 others(1): Show |
4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+341C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345629 | |||||||
| chr3:112345774 | T | G | 1 | a0003c0004t0002g0067 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.421+486T>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345774 | |||||||
| chr3:112345812 | G | A | 1 | a0002c0003t0001g0273 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.421+524G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345812 | |||||||
| chr3:112345939 | G | T | 4 | a0001c0002t0001g0074 a0001c0002t0001g0075 a0001c0002t0001g0087 others(1): Show |
4 | NA18939.hp1 NA18942.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+651G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345939 | |||||||
| chr3:112345983 | C | T | 83 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(80): Show |
92 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.421+695C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345983 | |||||||
| chr3:112346032 | T | C | 83 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(80): Show |
92 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.421+744T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112346032 | |||||||
| chr3:112346065 | G | T | 4 | a0001c0001t0001g0124 a0001c0001t0002g0121 a0001c0001t0002g0122 others(1): Show |
4 | HG02280.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+777G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112346065 | |||||||
| chr3:112346119 | G | GCCAAAAG others(356): Show |
1 | a0001c0001t0002g0213 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.421+849_421+850ins others(363): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 112346119 | ||||||
| chr3:112346181 | T | C | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(286): Show |
379 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.421+893T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112346181 | |||||||
| chr3:112346390 | C | T | 1 | a0002c0003t0002g0247 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.421+1102C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112346390 | |||||||
| chr3:112346491 | C | T | 1 | a0001c0001t0018g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.422-1067C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112346491 | |||||||
| chr3:112346567 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.422-991C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112346567 | |||||||
| chr3:112346594 | T | C | 1 | a0002c0003t0001g0275 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.422-964T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112346594 | |||||||
| chr3:112346890 | G | T | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(286): Show |
379 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.422-668G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112346890 | |||||||
| chr3:112346971 | C | T | 9 | a0001c0002t0001g0130 a0001c0002t0001g0238 a0001c0002t0003g0178 others(6): Show |
10 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.422-587C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112346971 | |||||||
| chr3:112346988 | G | A | 3 | a0001c0002t0001g0167 a0001c0002t0003g0119 a0001c0002t0022g0217 |
3 | HG02451.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.422-570G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112346988 | |||||||
| chr3:112347042 | G | A | 1 | a0001c0002t0020g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.422-516G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112347042 | |||||||
| chr3:112347263 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.422-295A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112347263 | |||||||
| chr3:112347294 | C | T | 60 | a0001c0001t0024g0148 a0002c0003t0001g0009 a0002c0003t0001g0013 others(57): Show |
74 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.422-264C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112347294 | |||||||
| chr3:112347513 | C | T | 36 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(33): Show |
47 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.422-45C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112347513 | |||||||
| chr3:112347975 | C | A | 5 | a0001c0002t0001g0074 a0001c0002t0001g0075 a0001c0002t0001g0087 others(2): Show |
5 | HG06807.hp2 NA18939.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.694+145C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112347975 | |||||||
| chr3:112348239 | G | T | 1 | a0001c0002t0020g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.694+409G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112348239 | |||||||
| chr3:112348394 | C | T | 76 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(73): Show |
84 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.694+564C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112348394 | |||||||
| chr3:112348591 | C | G | 86 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(83): Show |
95 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.694+761C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112348591 | |||||||
| chr3:112348599 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.694+769C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112348599 | |||||||
| chr3:112348738 | T | C | 6 | a0001c0002t0003g0178 a0003c0005t0003g0030 a0003c0005t0003g0134 others(3): Show |
7 | HG02257.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.694+908T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112348738 | |||||||
| chr3:112348768 | G | A | 12 | a0001c0002t0001g0026 a0001c0002t0001g0065 a0001c0002t0001g0071 others(9): Show |
13 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.694+938G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112348768 | |||||||
| chr3:112348849 | GGAA | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(79): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.695-862_695-860del others(3): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112348849 | |||||||
| chr3:112348866 | A | G | 1 | a0001c0002t0002g0114 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.695-846A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112348866 | |||||||
| chr3:112348877 | C | CT | 91 | a0001c0001t0006g0232 a0001c0002t0001g0016 a0001c0002t0001g0017 others(88): Show |
100 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.695-825dupT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 112348877 | ||||||
| chr3:112348971 | CA | C | 77 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(74): Show |
85 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.695-735delA | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 112348971 | ||||||
| chr3:112348977 | A | T | 77 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(74): Show |
85 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.695-735A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112348977 | |||||||
| chr3:112349015 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.695-697A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349015 | |||||||
| chr3:112349016 | T | A | 1 | a0001c0001t0001g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.695-696T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349016 | |||||||
| chr3:112349017 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.695-695A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349017 | |||||||
| chr3:112349049 | G | A | 1 | a0001c0002t0020g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.695-663G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349049 | |||||||
| chr3:112349076 | A | G | 1 | a0002c0003t0001g0256 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.695-636A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349076 | |||||||
| chr3:112349089 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.695-623A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349089 | |||||||
| chr3:112349090 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.695-622G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349090 | |||||||
| chr3:112349217 | C | A | 90 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(87): Show |
99 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.695-495C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349217 | |||||||
| chr3:112349277 | T | G | 1 | a0001c0001t0001g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.695-435T>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349277 | |||||||
| chr3:112349298 | C | T | 36 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(33): Show |
47 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.695-414C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349298 | |||||||
| chr3:112349407 | T | C | 1 | a0001c0001t0001g0047 | 2 | HG00735.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.695-305T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349407 | |||||||
| chr3:112349439 | C | A | 1 | a0001c0001t0018g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.695-273C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349439 | |||||||
| chr3:112349501 | G | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0158 a0001c0001t0001g0160 |
3 | HG00642.hp2 HG02257.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.695-211G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349501 | |||||||
| chr3:112349509 | T | G | 1 | a0001c0001t0001g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.695-203T>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349509 | |||||||
| chr3:112349572 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.695-140T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349572 | |||||||
| chr3:112349593 | C | T | 86 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(83): Show |
95 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.695-119C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349593 | |||||||
| chr3:112349620 | A | C | 1 | a0001c0001t0001g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.695-92A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349620 | |||||||
| chr3:112349647 | T | TCTATTGC others(7): Show |
86 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(83): Show |
95 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.695-63_695-62insAT others(12): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 112349647 | ||||||
| chr3:112349656 | C | T | 1 | a0003c0004t0001g0010 | 4 | HG01167.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-56C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349656 | |||||||
| chr3:112349670 | C | T | 77 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0024 others(74): Show |
85 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.695-42C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349670 | |||||||
| chr3:112349828 | T | A | 4 | a0003c0006t0007g0139 a0003c0006t0007g0140 a0003c0006t0007g0141 others(1): Show |
4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+9T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112349828 | |||||||
| chr3:112349880 | T | C | 6 | a0001c0002t0003g0178 a0003c0005t0003g0030 a0003c0005t0003g0134 others(3): Show |
7 | HG02257.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.802+61T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112349880 | |||||||
| chr3:112349928 | T | C | 1 | a0001c0002t0002g0248 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.802+109T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112349928 | |||||||
| chr3:112349976 | G | A | 3 | a0001c0002t0001g0167 a0001c0002t0003g0119 a0001c0002t0022g0217 |
3 | HG02451.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.802+157G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112349976 | |||||||
| chr3:112350108 | C | T | 1 | a0001c0002t0001g0072 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.802+289C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112350108 | |||||||
| chr3:112350545 | T | C | 136 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(133): Show |
158 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.802+726T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112350545 | |||||||
| chr3:112350708 | G | A | 1 | a0001c0001t0003g0032 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.802+889G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112350708 | |||||||
| chr3:112350728 | G | T | 1 | a0001c0002t0002g0248 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.802+909G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112350728 | |||||||
| chr3:112350908 | T | C | 58 | a0002c0003t0001g0009 a0002c0003t0001g0013 a0002c0003t0001g0023 others(55): Show |
72 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.802+1089T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112350908 | |||||||
| chr3:112350918 | C | A | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(276): Show |
362 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.802+1099C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112350918 | |||||||
| chr3:112351037 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.802+1218C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351037 | |||||||
| chr3:112351076 | CTGTT | C | 4 | a0001c0001t0001g0182 a0001c0001t0001g0188 a0001c0001t0001g0221 others(1): Show |
4 | HG00140.hp1 HG00280.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+1260_802+1263d others(6): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112351076 | ||||||
| chr3:112351111 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.802+1292T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351111 | |||||||
| chr3:112351113 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.802+1294C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351113 | |||||||
| chr3:112351115 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.802+1296A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351115 | |||||||
| chr3:112351242 | A | G | 4 | a0001c0001t0001g0200 a0001c0001t0001g0220 a0001c0001t0009g0194 others(1): Show |
4 | NA18954.hp1 NA18981.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+1423A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351242 | |||||||
| chr3:112351613 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.802+1794G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351613 | |||||||
| chr3:112351640 | G | A | 16 | a0001c0001t0001g0047 a0001c0001t0001g0137 a0001c0001t0004g0136 others(13): Show |
17 | HG00544.hp1 HG00735.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.802+1821G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351640 | |||||||
| chr3:112351677 | G | GAATGTTC others(14): Show |
16 | a0001c0001t0001g0047 a0001c0001t0001g0137 a0001c0001t0004g0136 others(13): Show |
17 | HG00544.hp1 HG00735.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.802+1862_802+1863i others(23): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112351677 | ||||||
| chr3:112351729 | T | A | 52 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(49): Show |
64 | HG00280.hp1 HG00544.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.802+1910T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351729 | |||||||
| chr3:112351887 | G | A | 3 | a0001c0001t0002g0183 a0001c0001t0002g0190 a0001c0001t0002g0214 |
3 | NA18939.hp2 NA18941.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.802+2068G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351887 | |||||||
| chr3:112351911 | C | T | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.802+2092C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351911 | |||||||
| chr3:112351947 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.802+2128C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351947 | |||||||
| chr3:112352101 | T | C | 2 | a0001c0002t0001g0130 a0001c0002t0001g0238 |
2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.802+2282T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352101 | |||||||
| chr3:112352131 | T | C | 1 | a0001c0002t0002g0248 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.802+2312T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352131 | |||||||
| chr3:112352221 | C | A | 2 | a0001c0002t0002g0059 a0001c0002t0023g0060 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.802+2402C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352221 | |||||||
| chr3:112352348 | C | T | 3 | a0001c0002t0001g0130 a0001c0002t0001g0238 a0001c0002t0020g0166 |
3 | HG02109.hp2 HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.802+2529C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352348 | |||||||
| chr3:112352354 | A | G | 1 | a0001c0001t0024g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.802+2535A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352354 | |||||||
| chr3:112352382 | C | T | 1 | a0001c0002t0002g0248 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.802+2563C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352382 | |||||||
| chr3:112352435 | A | G | 36 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(33): Show |
47 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.802+2616A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352435 | |||||||
| chr3:112352451 | C | T | 4 | a0001c0001t0001g0046 a0001c0001t0002g0183 a0001c0001t0002g0190 others(1): Show |
5 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.802+2632C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352451 | |||||||
| chr3:112352540 | TGA | T | 68 | a0001c0001t0001g0042 a0001c0001t0003g0032 a0001c0002t0003g0178 others(65): Show |
85 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.802+2747_802+2748d others(4): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112352540 | ||||||
| chr3:112352540 | TGAGA | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(153): Show |
210 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.802+2745_802+2748d others(6): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112352540 | ||||||
| chr3:112352540 | TGAGAGA | T | 9 | a0001c0001t0001g0047 a0001c0001t0001g0137 a0001c0001t0001g0157 others(6): Show |
10 | HG00735.hp2 HG01081.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.802+2743_802+2748d others(8): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112352540 | ||||||
| chr3:112352540 | TGAGAGAG others(1): Show |
T | 43 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(40): Show |
54 | HG00280.hp1 HG00544.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.802+2741_802+2748d others(10): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112352540 | ||||||
| chr3:112352564 | AGAGT | A | 4 | a0001c0001t0001g0124 a0001c0001t0002g0121 a0001c0001t0002g0122 others(1): Show |
4 | HG02280.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+2747_802+2750d others(6): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112352564 | ||||||
| chr3:112352566 | A | T | 44 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(41): Show |
55 | HG00280.hp1 HG00544.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.802+2747A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352566 | |||||||
| chr3:112352629 | T | C | 3 | a0001c0002t0001g0216 a0001c0002t0003g0103 a0001c0002t0021g0082 |
3 | HG02258.hp2 HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.802+2810T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352629 | |||||||
| chr3:112352825 | G | A | 5 | a0001c0002t0001g0078 a0001c0002t0001g0107 a0001c0002t0001g0108 others(2): Show |
5 | HG02818.hp1 HG03471.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.802+3006G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352825 | |||||||
| chr3:112352837 | C | T | 1 | a0001c0001t0025g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.802+3018C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352837 | |||||||
| chr3:112352863 | TATAATGC others(8): Show |
T | 1 | a0001c0002t0001g0113 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.802+3047_802+3061d others(17): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112352863 | ||||||
| chr3:112352884 | G | A | 2 | a0003c0004t0001g0007 a0003c0004t0002g0007 |
6 | HG02056.hp2 HG02129.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+3065G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352884 | |||||||
| chr3:112352960 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.802+3141C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352960 | |||||||
| chr3:112353086 | C | T | 1 | a0001c0002t0001g0086 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.802+3267C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353086 | |||||||
| chr3:112353087 | G | A | 52 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(49): Show |
64 | HG00280.hp1 HG00544.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.802+3268G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353087 | |||||||
| chr3:112353184 | A | G | 4 | a0001c0001t0001g0124 a0001c0001t0002g0121 a0001c0001t0002g0122 others(1): Show |
4 | HG02280.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+3365A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353184 | |||||||
| chr3:112353249 | T | A | 1 | a0001c0001t0001g0180 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.802+3430T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353249 | |||||||
| chr3:112353309 | G | GTTTGC | 42 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(39): Show |
53 | HG00280.hp1 HG00544.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.802+3500_802+3504d others(7): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112353309 | ||||||
| chr3:112353324 | G | C | 52 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(49): Show |
64 | HG00280.hp1 HG00544.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.802+3505G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353324 | |||||||
| chr3:112353572 | A | C | 4 | a0001c0001t0001g0151 a0001c0001t0004g0149 a0001c0001t0004g0150 others(1): Show |
4 | HG01884.hp2 HG02280.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+3753A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353572 | |||||||
| chr3:112353613 | CA | C | 3 | a0001c0002t0001g0167 a0001c0002t0003g0119 a0001c0002t0022g0217 |
3 | HG02451.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.802+3796delA | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112353613 | ||||||
| chr3:112353621 | G | A | 1 | a0003c0004t0002g0131 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.802+3802G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353621 | |||||||
| chr3:112353753 | G | A | 3 | a0002c0003t0001g0262 a0002c0003t0001g0266 a0002c0003t0001g0283 |
3 | NA18975.hp1 NA18981.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.802+3934G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353753 | |||||||
| chr3:112353779 | C | T | 1 | a0002c0003t0001g0252 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.802+3960C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353779 | |||||||
| chr3:112353825 | T | C | 3 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0152 |
3 | HG02280.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.802+4006T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353825 | |||||||
| chr3:112353831 | C | T | 2 | a0001c0002t0003g0178 a0003c0005t0003g0135 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.802+4012C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353831 | |||||||
| chr3:112353980 | A | G | 4 | a0003c0006t0007g0139 a0003c0006t0007g0140 a0003c0006t0007g0141 others(1): Show |
4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+4161A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353980 | |||||||
| chr3:112353986 | G | A | 103 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(100): Show |
127 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.802+4167G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353986 | |||||||
| chr3:112353996 | T | G | 1 | a0001c0001t0024g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.802+4177T>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353996 | |||||||
| chr3:112354146 | C | T | 2 | a0002c0003t0001g0051 a0002c0003t0001g0052 |
4 | HG00597.hp2 NA18963.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+4327C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112354146 | |||||||
| chr3:112354182 | G | A | 1 | a0002c0003t0001g0288 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.802+4363G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112354182 | |||||||
| chr3:112354286 | T | C | 70 | a0001c0001t0001g0033 a0002c0003t0001g0009 a0002c0003t0001g0013 others(67): Show |
92 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.802+4467T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112354286 | |||||||
| chr3:112354520 | C | A | 1 | a0001c0002t0020g0166 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.802+4701C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112354520 | |||||||
| chr3:112354736 | A | C | 1 | a0001c0001t0003g0032 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.802+4917A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112354736 | |||||||
| chr3:112354809 | G | A | 1 | a0002c0003t0001g0051 | 2 | NA18983.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.802+4990G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112354809 | |||||||
| chr3:112354827 | C | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0184 a0001c0001t0001g0211 |
4 | HG01243.hp1 HG03669.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+5008C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112354827 | |||||||
| chr3:112354989 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.802+5170C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112354989 | |||||||
| chr3:112355031 | A | G | 1 | a0002c0003t0002g0247 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.802+5212A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355031 | |||||||
| chr3:112355040 | C | A | 5 | a0001c0002t0001g0028 a0001c0002t0001g0079 a0001c0002t0001g0083 others(2): Show |
6 | HG02132.hp2 NA18960.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+5221C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355040 | |||||||
| chr3:112355239 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0199 |
2 | HG01975.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.802+5420C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355239 | |||||||
| chr3:112355243 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.802+5424A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355243 | |||||||
| chr3:112355300 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(122): Show |
183 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.802+5481G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355300 | |||||||
| chr3:112355383 | C | G | 2 | a0003c0004t0001g0142 a0003c0004t0001g0144 |
2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.802+5564C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355383 | |||||||
| chr3:112355484 | C | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(124): Show |
185 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.802+5665C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355484 | |||||||
| chr3:112355732 | T | A | 2 | a0001c0002t0001g0130 a0001c0002t0001g0238 |
2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.803-5811T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355732 | |||||||
| chr3:112355761 | G | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(124): Show |
185 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.803-5782G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355761 | |||||||
| chr3:112355862 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.803-5681A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355862 | |||||||
| chr3:112355874 | T | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0173 a0001c0001t0001g0204 others(1): Show |
5 | HG00408.hp2 HG00673.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.803-5669T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355874 | |||||||
| chr3:112355874 | T | G | 2 | a0001c0002t0001g0130 a0001c0002t0001g0238 |
2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.803-5669T>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355874 | |||||||
| chr3:112355899 | CAATTT | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(79): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.803-5638_803-5634d others(7): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112355899 | ||||||
| chr3:112356091 | A | G | 4 | a0003c0006t0007g0139 a0003c0006t0007g0140 a0003c0006t0007g0141 others(1): Show |
4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-5452A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112356091 | |||||||
| chr3:112356130 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(81): Show |
131 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.803-5413A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112356130 | |||||||
| chr3:112356304 | T | C | 1 | a0001c0001t0024g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.803-5239T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112356304 | |||||||
| chr3:112356355 | AT | A | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(272): Show |
358 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.803-5181delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112356355 | ||||||
| chr3:112356357 | T | A | 1 | a0001c0001t0001g0220 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.803-5186T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112356357 | |||||||
| chr3:112356551 | C | T | 1 | a0001c0002t0001g0090 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.803-4992C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112356551 | |||||||
| chr3:112356619 | T | G | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.803-4924T>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112356619 | |||||||
| chr3:112356749 | T | A | 1 | a0001c0002t0021g0082 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.803-4794T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112356749 | |||||||
| chr3:112356807 | T | C | 1 | a0002c0003t0001g0051 | 2 | NA18983.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.803-4736T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112356807 | |||||||
| chr3:112356935 | A | G | 1 | a0001c0002t0016g0064 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.803-4608A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112356935 | |||||||
| chr3:112356945 | G | A | 1 | a0001c0002t0001g0080 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.803-4598G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112356945 | |||||||
| chr3:112357141 | G | A | 2 | a0001c0002t0001g0130 a0001c0002t0001g0238 |
2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.803-4402G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357141 | |||||||
| chr3:112357192 | C | T | 1 | a0001c0001t0025g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.803-4351C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357192 | |||||||
| chr3:112357239 | G | C | 67 | a0001c0001t0001g0033 a0001c0001t0001g0047 a0001c0001t0001g0154 others(64): Show |
83 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.803-4304G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357239 | |||||||
| chr3:112357253 | T | G | 5 | a0001c0002t0001g0028 a0001c0002t0001g0079 a0001c0002t0001g0083 others(2): Show |
6 | HG02132.hp2 NA18960.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.803-4290T>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357253 | |||||||
| chr3:112357258 | C | CA | 66 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0154 others(63): Show |
83 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.803-4269dupA | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112357258 | ||||||
| chr3:112357258 | C | CAA | 13 | a0001c0001t0001g0047 a0001c0001t0003g0032 a0001c0001t0006g0229 others(10): Show |
16 | HG00735.hp2 HG01081.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.803-4270_803-4269d others(4): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112357258 | ||||||
| chr3:112357271 | A | AAAAG | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(76): Show |
122 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.803-4252_803-4249d others(6): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112357271 | ||||||
| chr3:112357271 | A | AG | 6 | a0001c0002t0003g0178 a0003c0005t0003g0030 a0003c0005t0003g0134 others(3): Show |
7 | HG02257.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-4272_803-4271i others(3): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357271 | |||||||
| chr3:112357275 | G | A | 67 | a0001c0001t0001g0033 a0001c0001t0001g0047 a0001c0001t0001g0154 others(64): Show |
83 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.803-4268G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357275 | |||||||
| chr3:112357295 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.803-4248A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357295 | |||||||
| chr3:112357373 | C | G | 1 | a0002c0003t0001g0269 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.803-4170C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357373 | |||||||
| chr3:112357381 | T | C | 1 | a0001c0001t0001g0207 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.803-4162T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357381 | |||||||
| chr3:112357456 | C | T | 3 | a0001c0001t0024g0148 a0001c0002t0001g0130 a0001c0002t0001g0238 |
3 | HG02109.hp2 HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.803-4087C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357456 | |||||||
| chr3:112357697 | A | G | 1 | a0001c0001t0025g0127 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.803-3846A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357697 | |||||||
| chr3:112357720 | G | A | 1 | a0001c0002t0001g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.803-3823G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357720 | |||||||
| chr3:112357751 | T | C | 1 | a0001c0002t0002g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.803-3792T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357751 | |||||||
| chr3:112357754 | G | A | 1 | a0002c0003t0001g0265 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.803-3789G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357754 | |||||||
| chr3:112357786 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.803-3757A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357786 | |||||||
| chr3:112357798 | G | A | 2 | a0001c0001t0001g0191 a0003c0004t0001g0147 |
2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.803-3745G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357798 | |||||||
| chr3:112357924 | A | G | 5 | a0001c0002t0001g0074 a0001c0002t0001g0075 a0001c0002t0001g0087 others(2): Show |
5 | HG06807.hp2 NA18939.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-3619A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357924 | |||||||
| chr3:112357951 | G | A | 1 | a0003c0005t0010g0128 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.803-3592G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357951 | |||||||
| chr3:112358026 | G | C | 1 | a0003c0006t0007g0139 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.803-3517G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358026 | |||||||
| chr3:112358155 | T | A | 4 | a0003c0006t0007g0139 a0003c0006t0007g0140 a0003c0006t0007g0141 others(1): Show |
4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-3388T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358155 | |||||||
| chr3:112358219 | G | A | 1 | a0001c0002t0001g0102 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.803-3324G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358219 | |||||||
| chr3:112358262 | G | A | 123 | a0001c0001t0001g0033 a0001c0001t0001g0154 a0001c0001t0001g0158 others(120): Show |
146 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.803-3281G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358262 | |||||||
| chr3:112358366 | G | A | 7 | a0001c0002t0001g0167 a0001c0002t0002g0059 a0001c0002t0002g0234 others(4): Show |
7 | HG02451.hp2 HG02886.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-3177G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358366 | |||||||
| chr3:112358367 | TG | T | 124 | a0001c0001t0001g0033 a0001c0001t0001g0154 a0001c0001t0001g0158 others(121): Show |
148 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.803-3172delG | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112358367 | ||||||
| chr3:112358418 | C | A | 6 | a0001c0001t0001g0047 a0001c0001t0006g0229 a0001c0001t0006g0232 others(3): Show |
7 | HG00735.hp2 HG01081.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-3125C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358418 | |||||||
| chr3:112358428 | AATGAACT others(12): Show |
A | 1 | a0002c0003t0001g0245 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.803-3098_803-3080d others(21): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112358428 | ||||||
| chr3:112358487 | AG | A | 36 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0034 others(33): Show |
61 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.803-3055delG | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358487 | |||||||
| chr3:112358493 | A | T | 5 | a0001c0001t0001g0047 a0001c0001t0006g0229 a0001c0001t0006g0232 others(2): Show |
6 | HG00735.hp2 HG01081.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.803-3050A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358493 | |||||||
| chr3:112358610 | T | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(67): Show |
107 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.803-2933T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358610 | |||||||
| chr3:112358649 | C | T | 1 | a0001c0002t0001g0081 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.803-2894C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358649 | |||||||
| chr3:112358667 | G | A | 3 | a0001c0001t0024g0148 a0003c0005t0010g0128 a0003c0005t0010g0129 |
3 | HG02630.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.803-2876G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358667 | |||||||
| chr3:112358691 | C | G | 39 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0034 others(36): Show |
64 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.803-2852C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358691 | |||||||
| chr3:112358741 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.803-2802T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358741 | |||||||
| chr3:112358837 | C | T | 38 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0034 others(35): Show |
63 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.803-2706C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358837 | |||||||
| chr3:112358857 | C | A | 39 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0034 others(36): Show |
64 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.803-2686C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358857 | |||||||
| chr3:112358883 | C | A | 39 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0034 others(36): Show |
64 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.803-2660C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358883 | |||||||
| chr3:112358918 | GGAAAGAA others(7): Show |
G | 30 | a0001c0001t0001g0124 a0001c0001t0001g0137 a0001c0001t0002g0121 others(27): Show |
37 | HG00438.hp2 HG00609.hp2 HG02056.hp2 others(34): Show |
intron_variant | MODIFIER | c.803-2610_803-2597d others(16): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112358918 | ||||||
| chr3:112358931 | G | GAGAAAGA others(1): Show |
33 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0034 others(30): Show |
58 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.803-2608_803-2601d others(10): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112358931 | ||||||
| chr3:112358931 | G | GAGAAAGA others(5): Show |
4 | a0003c0006t0007g0139 a0003c0006t0007g0140 a0003c0006t0007g0141 others(1): Show |
4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-2601_803-2600i others(14): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112358931 | ||||||
| chr3:112359033 | G | A | 37 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0034 others(34): Show |
62 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.803-2510G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359033 | |||||||
| chr3:112359105 | T | C | 8 | a0001c0001t0003g0032 a0001c0002t0003g0103 a0001c0002t0003g0119 others(5): Show |
10 | HG02129.hp2 HG02257.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.803-2438T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359105 | |||||||
| chr3:112359247 | T | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(70): Show |
111 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.803-2296T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359247 | |||||||
| chr3:112359287 | A | G | 37 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0034 others(34): Show |
62 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.803-2256A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359287 | |||||||
| chr3:112359310 | C | T | 33 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0034 others(30): Show |
58 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.803-2233C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359310 | |||||||
| chr3:112359375 | G | A | 1 | a0001c0001t0017g0208 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.803-2168G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359375 | |||||||
| chr3:112359517 | A | G | 1 | a0001c0002t0001g0080 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.803-2026A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359517 | |||||||
| chr3:112359609 | T | A | 2 | a0001c0002t0001g0130 a0001c0002t0001g0238 |
2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.803-1934T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359609 | |||||||
| chr3:112359685 | T | C | 2 | a0002c0003t0008g0170 a0002c0003t0008g0171 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.803-1858T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359685 | |||||||
| chr3:112359721 | T | C | 33 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0034 others(30): Show |
58 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.803-1822T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359721 | |||||||
| chr3:112359749 | G | C | 2 | a0002c0003t0001g0267 a0002c0003t0001g0272 |
2 | HG01952.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.803-1794G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359749 | |||||||
| chr3:112359771 | G | T | 33 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0034 others(30): Show |
58 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.803-1772G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359771 | |||||||
| chr3:112359848 | A | T | 33 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0034 others(30): Show |
58 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.803-1695A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359848 | |||||||
| chr3:112359893 | T | A | 33 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0034 others(30): Show |
58 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.803-1650T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359893 | |||||||
| chr3:112359900 | AGG | A | 2 | a0003c0004t0001g0004 a0003c0004t0001g0146 |
8 | HG01109.hp2 HG01123.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.803-1641_803-1640d others(4): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112359900 | ||||||
| chr3:112360061 | C | T | 1 | a0002c0003t0001g0272 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.803-1482C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360061 | |||||||
| chr3:112360099 | A | T | 1 | a0003c0004t0002g0132 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.803-1444A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360099 | |||||||
| chr3:112360170 | A | T | 1 | a0001c0002t0001g0091 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.803-1373A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360170 | |||||||
| chr3:112360185 | G | T | 1 | a0001c0002t0001g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.803-1358G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360185 | |||||||
| chr3:112360241 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(93): Show |
141 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.803-1302T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360241 | |||||||
| chr3:112360284 | C | T | 4 | a0001c0001t0001g0126 a0001c0001t0004g0149 a0001c0001t0004g0150 others(1): Show |
4 | HG02280.hp2 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-1259C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360284 | |||||||
| chr3:112360308 | A | C | 1 | a0001c0001t0001g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.803-1235A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360308 | |||||||
| chr3:112360326 | T | TAAAAATA others(3): Show |
56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(53): Show |
92 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.803-1212_803-1211i others(12): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112360326 | ||||||
| chr3:112360326 | T | TAAAAATA others(4): Show |
2 | a0001c0001t0001g0184 a0001c0001t0001g0187 |
2 | HG02486.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.803-1212_803-1211i others(13): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112360326 | ||||||
| chr3:112360326 | T | TAAAAATA others(5): Show |
4 | a0001c0001t0001g0137 a0001c0002t0016g0064 a0003c0004t0001g0142 others(1): Show |
4 | HG02895.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-1212_803-1211i others(14): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112360326 | ||||||
| chr3:112360331 | A | ATAAAAAA others(5): Show |
4 | a0001c0001t0002g0121 a0001c0001t0017g0208 a0003c0004t0002g0015 others(1): Show |
5 | HG00438.hp2 HG02572.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-1212_803-1211i others(14): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360331 | |||||||
| chr3:112360331 | A | ATAAAAAA others(7): Show |
1 | a0002c0003t0002g0246 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.803-1212_803-1211i others(16): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360331 | |||||||
| chr3:112360331 | A | ATAAAAAA others(3): Show |
8 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0204 others(5): Show |
10 | HG00408.hp2 HG00673.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.803-1212_803-1211i others(12): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360331 | |||||||
| chr3:112360331 | A | ATAAAAAA others(5): Show |
19 | a0001c0001t0001g0124 a0001c0001t0002g0122 a0001c0001t0002g0123 others(16): Show |
25 | HG00609.hp2 HG02056.hp2 HG02074.hp2 others(22): Show |
intron_variant | MODIFIER | c.803-1212_803-1211i others(14): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360331 | |||||||
| chr3:112360331 | A | ATAAAAAA others(5): Show |
2 | a0001c0001t0002g0153 a0001c0002t0002g0059 |
2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.803-1212_803-1211i others(14): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360331 | |||||||
| chr3:112360333 | A | T | 53 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0022 others(50): Show |
77 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.803-1210A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360333 | |||||||
| chr3:112360334 | AT | A | 32 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0034 others(29): Show |
57 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.803-1208delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360334 | |||||||
| chr3:112360335 | T | A | 5 | a0001c0001t0001g0160 a0001c0001t0001g0173 a0001c0002t0001g0029 others(2): Show |
5 | HG00642.hp2 HG01256.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-1208T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360335 | |||||||
| chr3:112360358 | T | C | 2 | a0001c0001t0003g0032 a0001c0002t0003g0119 |
3 | HG02895.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.803-1185T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360358 | |||||||
| chr3:112360430 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(142): Show |
217 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.803-1113T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360430 | |||||||
| chr3:112360436 | A | T | 1 | a0002c0003t0001g0275 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.803-1107A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360436 | |||||||
| chr3:112360521 | A | G | 3 | a0001c0001t0001g0154 a0001c0001t0001g0158 a0001c0001t0001g0160 |
3 | HG00642.hp2 HG02257.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.803-1022A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360521 | |||||||
| chr3:112360569 | T | C | 1 | a0001c0001t0001g0228 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.803-974T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360569 | |||||||
| chr3:112360620 | T | A | 1 | a0001c0002t0001g0107 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.803-923T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360620 | |||||||
| chr3:112360777 | G | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0057 |
3 | HG00280.hp1 HG01361.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.803-766G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360777 | |||||||
| chr3:112360813 | A | T | 1 | a0001c0002t0001g0167 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.803-730A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360813 | |||||||
| chr3:112360933 | A | G | 33 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0034 others(30): Show |
58 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.803-610A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360933 | |||||||
| chr3:112360950 | C | T | 3 | a0001c0002t0001g0017 a0001c0002t0001g0093 a0001c0002t0001g0106 |
5 | HG01255.hp1 HG01358.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.803-593C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360950 | |||||||
| chr3:112361131 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.803-412A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112361131 | |||||||
| chr3:112361149 | G | A | 1 | a0001c0002t0002g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.803-394G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112361149 | |||||||
| chr3:112361202 | AT | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(119): Show |
171 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.803-330delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112361202 | ||||||
| chr3:112361262 | T | A | 1 | a0002c0003t0001g0284 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.803-281T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112361262 | |||||||
| chr3:112361293 | G | A | 1 | a0001c0002t0001g0083 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.803-250G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112361293 | |||||||
| chr3:112361295 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(93): Show |
141 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.803-248C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112361295 | |||||||
| chr3:112361311 | A | T | 1 | a0001c0001t0001g0160 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.803-232A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112361311 | |||||||
| chr3:112361314 | G | A | 5 | a0001c0001t0001g0047 a0001c0001t0006g0229 a0001c0001t0006g0232 others(2): Show |
6 | HG00735.hp2 HG01081.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.803-229G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112361314 | |||||||
| chr3:112361368 | C | T | 3 | a0001c0001t0024g0148 a0003c0005t0010g0128 a0003c0005t0010g0129 |
3 | HG02630.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.803-175C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112361368 | |||||||
| chr3:112361442 | ACT | A | 3 | a0001c0001t0024g0148 a0003c0005t0010g0128 a0003c0005t0010g0129 |
3 | HG02630.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.803-98_803-97delCT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112361442 |