Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 926 |
| ensemblid | ENSG00000172116.23 |
| hgncid | 1707 |
| symbol | CD8B |
| name | CD8 subunit beta |
| refseq_nuc | NM_004931.5 |
| refseq_prot | NP_004922.1 |
| ensembl_nuc | ENST00000390655.12 |
| ensembl_prot | ENSP00000375070.6 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 86838167 |
| end | 86861886 |
| strand | - |
| ver | v1.2 |
| region | chr2:86838167-86861886 |
| region5000 | chr2:86833167-86866886 |
| regionname0 | CD8B_chr2_86838167_86861886 |
| regionname5000 | CD8B_chr2_86833167_86866886 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 210 | 310 | 83 | 49 | 133 | 11 | 32 | 100 | CD8B_chr2_86833167_86866886 | CD8B | MRPRL others(205): Show |
chr2 | 86833167 | 86866886 |
| a0002 | 0/0 | 210 | 74 | 4 | 23 | 37 | 3 | 7 | 32 | CD8B_chr2_86833167_86866886 | CD8B | MRPRL others(205): Show |
chr2 | 86833167 | 86866886 |
| a0003 | 0/0 | 210 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | MRPRL others(205): Show |
chr2 | 86833167 | 86866886 |
| a0004 | 0/0 | 210 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | MRPRL others(205): Show |
chr2 | 86833167 | 86866886 |
| a0005 | 0/0 | 28 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CD8B_chr2_86833167_86866886 | CD8B | MRPRL others(23): Show |
chr2 | 86833167 | 86866886 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 630 | 191 | 57 | 21 | 86 | 5 | 22 | CD8B_chr2_86833167_86866886 | CD8B | ATGCG others(625): Show |
chr2 | 86833167 | 86866886 | ||
| a0001c0002 | 1/1 | 630 | 111 | 18 | 28 | 47 | 6 | 10 | CD8B_chr2_86833167_86866886 | CD8B | ATGCG others(625): Show |
chr2 | 86833167 | 86866886 | ||
| a0001c0004 | 0/0 | 630 | 8 | 8 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | ATGCG others(625): Show |
chr2 | 86833167 | 86866886 | ||
| a0002c0003 | 0/0 | 630 | 67 | 4 | 18 | 35 | 3 | 7 | CD8B_chr2_86833167_86866886 | CD8B | ATGCG others(625): Show |
chr2 | 86833167 | 86866886 | ||
| a0002c0006 | 0/0 | 630 | 5 | 0 | 5 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | ATGCG others(625): Show |
chr2 | 86833167 | 86866886 | ||
| a0002c0007 | 0/0 | 630 | 2 | 0 | 0 | 2 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | ATGCG others(625): Show |
chr2 | 86833167 | 86866886 | ||
| a0003c0005 | 0/0 | 630 | 6 | 5 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | ATGCG others(625): Show |
chr2 | 86833167 | 86866886 | ||
| a0004c0009 | 0/0 | 630 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | ATGCG others(625): Show |
chr2 | 86833167 | 86866886 | ||
| a0005c0008 | 0/0 | 446 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | ATGCG others(441): Show |
chr2 | 86833167 | 86866886 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4794 | 103 | 20 | 10 | 56 | 3 | 14 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0001t0002 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0001t0004 | 0/0 | 4794 | 33 | 2 | 5 | 22 | 0 | 4 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0001t0005 | 0/0 | 4794 | 20 | 18 | 2 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0001t0006 | 0/0 | 4794 | 9 | 6 | 2 | 0 | 1 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0001t0009 | 0/0 | 4794 | 5 | 5 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0001t0011 | 0/0 | 4794 | 3 | 0 | 0 | 3 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0001t0013 | 0/0 | 4794 | 2 | 1 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0001t0014 | 0/0 | 4794 | 2 | 2 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0001t0015 | 0/0 | 4794 | 2 | 0 | 1 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0001t0024 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0001t0026 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0001t0027 | 0/0 | 4794 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0001t0029 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0001t0030 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0001t0032 | 0/0 | 4794 | 1 | 0 | 0 | 0 | 1 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0001t0033 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0001t0034 | 0/0 | 4794 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0001t0035 | 0/0 | 4794 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0001t0036 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0001t0042 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0002t0001 | 0/0 | 4794 | 10 | 0 | 2 | 8 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0002t0002 | 1/1 | 4794 | 78 | 9 | 18 | 36 | 3 | 10 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0002t0004 | 0/0 | 4794 | 2 | 1 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0002t0006 | 0/0 | 4794 | 2 | 2 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0002t0010 | 0/0 | 4794 | 4 | 0 | 3 | 0 | 1 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0002t0012 | 0/0 | 4794 | 3 | 1 | 1 | 0 | 1 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0002t0013 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0002t0016 | 0/0 | 4794 | 2 | 0 | 2 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0002t0023 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0002t0025 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0002t0028 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0002t0031 | 0/0 | 4794 | 1 | 0 | 0 | 0 | 1 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0002t0038 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0002t0039 | 0/0 | 4778 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4773): Show |
chr2 | 86833167 | 86866886 |
| a0001c0002t0040 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0002t0041 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0002t0043 | 0/0 | 4794 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0001c0004t0007 | 0/0 | 4794 | 8 | 8 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0002c0003t0003 | 0/0 | 4794 | 61 | 2 | 17 | 33 | 3 | 6 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0002c0003t0017 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0002c0003t0018 | 0/0 | 4794 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0002c0003t0019 | 0/0 | 4794 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0002c0003t0020 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0002c0003t0021 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0002c0003t0022 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0002c0006t0003 | 0/0 | 4794 | 5 | 0 | 5 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0002c0007t0003 | 0/0 | 4794 | 2 | 0 | 0 | 2 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0003c0005t0008 | 0/0 | 4794 | 5 | 4 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0003c0005t0037 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0004c0009t0002 | 0/0 | 4794 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4789): Show |
chr2 | 86833167 | 86866886 |
| a0005c0008t0002 | 0/0 | 4610 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | AGGTG others(4605): Show |
chr2 | 86833167 | 86866886 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 13 | 6 | 0 | 6 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 1 | 3 | 1 | 2 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0004g0005 | 0/0 | 10 | 0 | 0 | 8 | 0 | 2 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0004g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0004g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0005g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0005g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0005g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0005g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0006g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0006g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0006g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0006g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0009g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0009g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0011g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0011g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0011g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0013g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0013g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0014g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0014g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0015g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0015g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0024g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0026g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0027g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0029g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0030g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0032g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0033g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0034g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0035g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0036g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0001t0042g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0001 | 0/0 | 24 | 0 | 0 | 23 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0002 | 0/0 | 17 | 3 | 5 | 4 | 0 | 5 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0007 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0009 | 1/0 | 5 | 0 | 3 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0184 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0010g0015 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0012g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0012g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0013g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0016g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0023g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0025g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0028g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0031g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0038g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0039g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0040g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0041g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0002t0043g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0004t0007g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0004t0007g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0001c0004t0007g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0003 | 0/0 | 16 | 0 | 4 | 5 | 2 | 5 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0017g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0018g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0019g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0020g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0021g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0003t0022g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0006t0003g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0006t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0006t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0007t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0002c0007t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0003c0005t0008g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0003c0005t0008g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0003c0005t0008g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0003c0005t0008g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0003c0005t0037g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0004c0009t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| a0005c0008t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00099 | hp2 | a0001 | c0002 | t0010 | g0015 | EUR | GBR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | GBR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0216 | EUR | GBR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00280 | hp2 | a0002 | c0003 | t0003 | g0003 | EUR | FIN | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0215 | EUR | FIN | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00323 | hp2 | a0002 | c0003 | t0003 | g0003 | EUR | FIN | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00423 | hp2 | a0001 | c0001 | t0030 | g0148 | EAS | CHS | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00438 | hp1 | a0002 | c0003 | t0003 | g0229 | EAS | CHS | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00438 | hp2 | a0002 | c0003 | t0003 | g0226 | EAS | CHS | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | CHS | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | CHS | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | CHS | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0079 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0046 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00642 | hp2 | a0002 | c0003 | t0003 | g0198 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0046 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00735 | hp2 | a0001 | c0001 | t0015 | g0097 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00738 | hp1 | a0002 | c0003 | t0019 | g0204 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0054 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00741 | hp1 | a0002 | c0003 | t0003 | g0205 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG00741 | hp2 | a0002 | c0003 | t0003 | g0014 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0063 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01070 | hp2 | a0002 | c0003 | t0003 | g0207 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0182 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0159 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01099 | hp1 | a0004 | c0009 | t0002 | g0221 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01106 | hp2 | a0002 | c0003 | t0003 | g0003 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0072 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01167 | hp1 | a0003 | c0005 | t0008 | g0235 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01167 | hp2 | a0002 | c0006 | t0003 | g0017 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01169 | hp2 | a0002 | c0006 | t0003 | g0065 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01175 | hp1 | a0002 | c0003 | t0003 | g0206 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01175 | hp2 | a0002 | c0003 | t0003 | g0178 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0138 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01255 | hp2 | a0002 | c0003 | t0003 | g0003 | AMR | CLM | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01257 | hp2 | a0002 | c0006 | t0003 | g0017 | AMR | CLM | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0158 | AMR | CLM | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0036 | AMR | CLM | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01346 | hp2 | a0001 | c0002 | t0012 | g0044 | AMR | CLM | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01358 | hp1 | a0002 | c0003 | t0003 | g0003 | AMR | CLM | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01358 | hp2 | a0001 | c0001 | t0013 | g0131 | AMR | CLM | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01433 | hp1 | a0002 | c0003 | t0003 | g0014 | AMR | CLM | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01496 | hp1 | a0001 | c0002 | t0004 | g0212 | AMR | CLM | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01496 | hp2 | a0002 | c0003 | t0003 | g0003 | AMR | CLM | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0036 | EUR | IBS | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01517 | hp2 | a0001 | c0002 | t0031 | g0210 | EUR | IBS | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01884 | hp1 | a0001 | c0002 | t0006 | g0238 | AFR | ACB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0077 | AFR | ACB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01891 | hp1 | a0003 | c0005 | t0008 | g0237 | AFR | ACB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0183 | AFR | ACB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01928 | hp1 | a0002 | c0003 | t0003 | g0040 | AMR | PEL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01928 | hp2 | a0001 | c0002 | t0043 | g0220 | AMR | PEL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0026 | AMR | PEL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0222 | AMR | PEL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01943 | hp1 | a0001 | c0002 | t0010 | g0015 | AMR | PEL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01943 | hp2 | a0001 | c0002 | t0016 | g0045 | AMR | PEL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01978 | hp2 | a0002 | c0003 | t0003 | g0193 | AMR | PEL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01981 | hp1 | a0002 | c0003 | t0003 | g0014 | AMR | PEL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01981 | hp2 | a0002 | c0003 | t0003 | g0200 | AMR | PEL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01993 | hp1 | a0002 | c0006 | t0003 | g0066 | AMR | PEL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01993 | hp2 | a0001 | c0002 | t0016 | g0045 | AMR | PEL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02015 | hp2 | a0002 | c0003 | t0003 | g0003 | EAS | KHV | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | KHV | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0177 | EAS | KHV | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02055 | hp1 | a0002 | c0003 | t0003 | g0195 | AFR | ACB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | KHV | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | KHV | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02074 | hp1 | a0002 | c0003 | t0022 | g0191 | EAS | KHV | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02080 | hp2 | a0001 | c0002 | t0023 | g0173 | EAS | KHV | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02129 | hp2 | a0002 | c0003 | t0003 | g0010 | EAS | KHV | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | KHV | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02135 | hp1 | a0001 | c0001 | t0036 | g0149 | EAS | KHV | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02145 | hp1 | a0001 | c0002 | t0038 | g0218 | AFR | ACB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02145 | hp2 | a0002 | c0003 | t0017 | g0231 | AFR | ACB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02148 | hp1 | a0002 | c0006 | t0003 | g0017 | AMR | PEL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02148 | hp2 | a0001 | c0002 | t0010 | g0015 | AMR | PEL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CDX | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02257 | hp1 | a0001 | c0004 | t0007 | g0008 | AFR | ACB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0024 | AFR | ACB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0013 | AFR | ACB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02293 | hp1 | a0001 | c0002 | t0010 | g0015 | AMR | PEL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02293 | hp2 | a0002 | c0003 | t0003 | g0040 | AMR | PEL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02300 | hp2 | a0002 | c0003 | t0003 | g0014 | AMR | PEL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02451 | hp1 | a0001 | c0001 | t0014 | g0123 | AFR | ACB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0168 | EAS | KHV | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02523 | hp2 | a0001 | c0002 | t0025 | g0224 | EAS | KHV | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02572 | hp2 | a0001 | c0002 | t0041 | g0219 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0146 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02615 | hp2 | a0003 | c0005 | t0037 | g0232 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02622 | hp1 | a0001 | c0004 | t0007 | g0008 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02630 | hp1 | a0001 | c0002 | t0013 | g0180 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02683 | hp2 | a0002 | c0003 | t0018 | g0202 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0022 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02723 | hp2 | a0001 | c0004 | t0007 | g0233 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0005 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02738 | hp1 | a0001 | c0001 | t0027 | g0102 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02738 | hp2 | a0001 | c0001 | t0035 | g0147 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02809 | hp1 | a0003 | c0005 | t0008 | g0236 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0074 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02818 | hp1 | a0001 | c0004 | t0007 | g0008 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02818 | hp2 | a0001 | c0001 | t0009 | g0013 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02895 | hp1 | a0003 | c0005 | t0008 | g0047 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0076 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02897 | hp2 | a0003 | c0005 | t0008 | g0047 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0013 | AFR | ESN | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02965 | hp1 | a0002 | c0003 | t0003 | g0194 | AFR | ESN | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0081 | AFR | ESN | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02970 | hp2 | a0001 | c0001 | t0013 | g0130 | AFR | ESN | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0161 | AFR | ESN | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ESN | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03041 | hp1 | a0001 | c0002 | t0006 | g0162 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03041 | hp2 | a0001 | c0002 | t0012 | g0044 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03098 | hp2 | a0001 | c0002 | t0028 | g0211 | AFR | MSL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0075 | AFR | ESN | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | ESN | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03139 | hp2 | a0001 | c0004 | t0007 | g0008 | AFR | ESN | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | ESN | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03209 | hp1 | a0001 | c0004 | t0007 | g0008 | AFR | MSL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | MSL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0239 | AFR | MSL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0071 | AFR | MSL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0061 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03490 | hp2 | a0002 | c0003 | t0003 | g0003 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0176 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03492 | hp2 | a0002 | c0003 | t0003 | g0003 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0157 | AFR | ESN | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03516 | hp2 | a0001 | c0004 | t0007 | g0234 | AFR | ESN | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0022 | AFR | GWD | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03579 | hp1 | a0001 | c0001 | t0033 | g0080 | AFR | MSL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0156 | AFR | MSL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03654 | hp1 | a0002 | c0003 | t0003 | g0003 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0217 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03669 | hp2 | a0001 | c0001 | t0015 | g0111 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0225 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03831 | hp2 | a0002 | c0003 | t0003 | g0003 | SAS | BEB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | BEB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03942 | hp1 | a0002 | c0003 | t0003 | g0192 | SAS | BEB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0009 | SAS | STU | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG04115 | hp2 | a0001 | c0001 | t0034 | g0105 | SAS | STU | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | STU | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG04199 | hp2 | a0002 | c0003 | t0003 | g0003 | SAS | STU | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG04228 | hp1 | a0005 | c0008 | t0002 | g0163 | SAS | STU | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18522 | hp1 | a0001 | c0001 | t0014 | g0126 | AFR | YRI | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | YRI | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | CHB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | YRI | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18939 | hp2 | a0001 | c0002 | t0039 | g0172 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18943 | hp1 | a0002 | c0003 | t0003 | g0186 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18946 | hp1 | a0002 | c0003 | t0003 | g0187 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0145 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18949 | hp1 | a0002 | c0003 | t0003 | g0197 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18950 | hp1 | a0002 | c0003 | t0003 | g0227 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18952 | hp1 | a0002 | c0003 | t0003 | g0003 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18954 | hp2 | a0002 | c0003 | t0003 | g0003 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18966 | hp1 | a0002 | c0003 | t0003 | g0003 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18967 | hp1 | a0002 | c0003 | t0003 | g0189 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18968 | hp1 | a0002 | c0003 | t0003 | g0190 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18973 | hp2 | a0002 | c0003 | t0003 | g0039 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18975 | hp1 | a0002 | c0003 | t0003 | g0037 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18980 | hp1 | a0001 | c0001 | t0029 | g0103 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18983 | hp2 | a0002 | c0003 | t0003 | g0037 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18987 | hp1 | a0001 | c0001 | t0042 | g0090 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18987 | hp2 | a0002 | c0003 | t0003 | g0041 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18994 | hp1 | a0002 | c0003 | t0003 | g0010 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18995 | hp1 | a0002 | c0003 | t0003 | g0039 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19001 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19002 | hp1 | a0002 | c0003 | t0020 | g0230 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19003 | hp2 | a0002 | c0003 | t0003 | g0010 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19004 | hp1 | a0002 | c0003 | t0003 | g0196 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19009 | hp1 | a0002 | c0003 | t0003 | g0038 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19011 | hp2 | a0002 | c0003 | t0003 | g0179 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19012 | hp2 | a0002 | c0007 | t0003 | g0051 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0214 | AFR | LWK | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0150 | AFR | LWK | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19055 | hp2 | a0002 | c0003 | t0003 | g0228 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19056 | hp1 | a0002 | c0003 | t0003 | g0185 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19060 | hp2 | a0002 | c0003 | t0003 | g0010 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19063 | hp2 | a0002 | c0003 | t0003 | g0199 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19064 | hp1 | a0002 | c0003 | t0003 | g0188 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19067 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19067 | hp2 | a0001 | c0001 | t0026 | g0083 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19068 | hp1 | a0001 | c0001 | t0011 | g0087 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19078 | hp1 | a0001 | c0001 | t0011 | g0125 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19079 | hp2 | a0002 | c0003 | t0003 | g0041 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19080 | hp2 | a0002 | c0003 | t0003 | g0010 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19084 | hp1 | a0002 | c0003 | t0003 | g0003 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19088 | hp2 | a0002 | c0007 | t0003 | g0086 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19089 | hp2 | a0002 | c0003 | t0003 | g0201 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19091 | hp1 | a0001 | c0001 | t0011 | g0143 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0013 | AFR | YRI | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0069 | AFR | YRI | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA20129 | hp1 | a0002 | c0003 | t0021 | g0167 | AFR | ASW | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA20129 | hp2 | a0001 | c0002 | t0040 | g0165 | AFR | ASW | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0140 | EUR | TSI | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA20752 | hp2 | a0002 | c0003 | t0003 | g0203 | EUR | TSI | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA20805 | hp1 | a0001 | c0001 | t0032 | g0144 | EUR | TSI | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA20805 | hp2 | a0001 | c0002 | t0012 | g0166 | EUR | TSI | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0005 | SAS | GIH | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | GIH | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0122 | AMR | CLM | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | ACB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0121 | AFR | ACB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0073 | AFR | ACB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02559 | hp1 | a0001 | c0004 | t0007 | g0008 | AFR | ACB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0078 | AFR | ACB | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | MSL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG03471 | hp2 | a0001 | c0001 | t0024 | g0128 | AFR | MSL | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG06807 | hp1 | a0001 | c0002 | t0004 | g0209 | AFR | USA | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | USA | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA18955 | hp2 | a0002 | c0003 | t0003 | g0038 | EAS | JPT | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | USA | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | USA | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0048 | AFR | LWK | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0184 | REF | REF | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0009 | REF | REF | CD8B_chr2_86833167_86866886 | CD8B | chr2 | 86833167 | 86866886 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:86842308 | C | T | 2 | a0001 a0002 |
282 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(279): Show |
stop_retained_variant | LOW | c.632G>A | p.Ter211Ter | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 653/4794 | 632/633 | 211/210 | chr2 | 86842308 | |||
| chr2:86844934 | C | T | 1 | a0003 | 6 | HG01167.hp1 HG01891.hp1 HG02615.hp2 others(3): Show |
missense_variant | MODERATE | c.608G>A | p.Arg203His | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/6 | 629/4794 | 608/633 | 203/210 | chr2 | 86844934 | |||
| chr2:86844955 | C | T | 1 | a0004 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.587G>A | p.Arg196Gln | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/6 | 608/4794 | 587/633 | 196/210 | chr2 | 86844955 | |||
| chr2:86846729 | C | T | 1 | a0002 | 74 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(71): Show |
missense_variant | MODERATE | c.538G>A | p.Val180Ile | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 4/6 | 559/4794 | 538/633 | 180/210 | chr2 | 86846729 | |||
| chr2:86858232 | TGCGGAAT others(181): Show |
T | 1 | a0005 | 1 | HG04228.hp1 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.44-4_227del | p.Val15fs | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/6 | 248/4794 | 44/633 | 15/210 | chr2 | 86858232 | |||
| chr2:86858278 | G | A | 1 | a0001 | 4 | HG01243.hp2 HG01261.hp1 HG02897.hp1 others(1): Show |
missense_variant | MODERATE | c.182C>T | p.Pro61Leu | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/6 | 203/4794 | 182/633 | 61/210 | chr2 | 86858278 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:86858166 | C | T | 1 | a0002c0006 | 5 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(2): Show |
synonymous_variant | LOW | c.294G>A | p.Arg98Arg | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/6 | 315/4794 | 294/633 | 98/210 | chr2 | 86858166 | |||
| chr2:86858217 | G | A | 1 | a0001c0004 | 8 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
synonymous_variant | LOW | c.243C>T | p.His81His | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/6 | 264/4794 | 243/633 | 81/210 | chr2 | 86858217 | |||
| chr2:86861841 | A | G | 3 | a0001c0001 a0002c0006 a0002c0007 |
198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
synonymous_variant | LOW | c.25T>C | p.Leu9Leu | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/6 | 46/4794 | 25/633 | 9/210 | chr2 | 86861841 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:86838194 | T | C | 1 | a0001c0002t0025 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4113A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 4113 | chr2 | 86838194 | ||||||
| chr2:86838308 | G | A | 1 | a0001c0001t0005 | 20 | HG01109.hp1 HG01884.hp2 HG01934.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3999C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 3999 | chr2 | 86838308 | ||||||
| chr2:86838400 | G | T | 1 | a0001c0001t0014 | 2 | HG02451.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3907C>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 3907 | chr2 | 86838400 | ||||||
| chr2:86838474 | G | A | 1 | a0002c0003t0020 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3833C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 3833 | chr2 | 86838474 | ||||||
| chr2:86838487 | C | A | 1 | a0001c0002t0002 | 3 | HG03927.hp2 NA18974.hp2 NA18981.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3820G>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 3820 | chr2 | 86838487 | ||||||
| chr2:86838487 | CAAG | C | 8 | a0001c0001t0013 a0002c0003t0003 a0002c0003t0018 others(5): Show |
73 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*3817_*3819delCTT | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 3817 | chr2 | 86838487 | ||||||
| chr2:86838490 | G | C | 1 | a0002c0003t0021 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3817C>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 3817 | chr2 | 86838490 | ||||||
| chr2:86838659 | C | A | 1 | a0001c0001t0026 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3648G>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 3648 | chr2 | 86838659 | ||||||
| chr2:86838660 | A | G | 1 | a0001c0001t0026 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3647T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 3647 | chr2 | 86838660 | ||||||
| chr2:86838661 | G | A | 1 | a0001c0001t0026 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3646C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 3646 | chr2 | 86838661 | ||||||
| chr2:86838730 | G | C | 1 | a0002c0003t0017 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3577C>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 3577 | chr2 | 86838730 | ||||||
| chr2:86838851 | C | T | 1 | a0001c0002t0031 | 1 | HG01517.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3456G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 3456 | chr2 | 86838851 | ||||||
| chr2:86839087 | G | A | 1 | a0002c0003t0022 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3220C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 3220 | chr2 | 86839087 | ||||||
| chr2:86839335 | G | C | 2 | a0001c0001t0013 a0001c0002t0013 |
3 | HG01358.hp2 HG02630.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2972C>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 2972 | chr2 | 86839335 | ||||||
| chr2:86839552 | C | T | 3 | a0001c0001t0009 a0001c0001t0013 a0001c0002t0013 |
8 | HG01358.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2755G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 2755 | chr2 | 86839552 | ||||||
| chr2:86839555 | C | T | 1 | a0001c0002t0028 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2752G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 2752 | chr2 | 86839555 | ||||||
| chr2:86839581 | C | T | 3 | a0001c0001t0009 a0001c0001t0013 a0001c0002t0013 |
8 | HG01358.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2726G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 2726 | chr2 | 86839581 | ||||||
| chr2:86839727 | A | T | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(29): Show |
280 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(277): Show |
3_prime_UTR_variant | MODIFIER | c.*2580T>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 2580 | chr2 | 86839727 | ||||||
| chr2:86839738 | G | T | 1 | a0002c0003t0019 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2569C>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 2569 | chr2 | 86839738 | ||||||
| chr2:86839740 | C | T | 4 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0030 others(1): Show |
9 | HG00423.hp2 HG01358.hp2 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2567G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 2567 | chr2 | 86839740 | ||||||
| chr2:86839810 | G | A | 1 | a0001c0001t0027 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2497C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 2497 | chr2 | 86839810 | ||||||
| chr2:86839850 | C | T | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(29): Show |
280 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(277): Show |
3_prime_UTR_variant | MODIFIER | c.*2457G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 2457 | chr2 | 86839850 | ||||||
| chr2:86839937 | A | G | 1 | a0001c0002t0040 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2370T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 2370 | chr2 | 86839937 | ||||||
| chr2:86840079 | GTGCTGAA others(9): Show |
G | 1 | a0001c0002t0039 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2212_*2227delTCTC others(12): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 2212 | chr2 | 86840079 | ||||||
| chr2:86840100 | T | C | 1 | a0001c0002t0010 | 4 | HG00099.hp2 HG01943.hp1 HG02148.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2207A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 2207 | chr2 | 86840100 | ||||||
| chr2:86840231 | C | T | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(29): Show |
280 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(277): Show |
3_prime_UTR_variant | MODIFIER | c.*2076G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 2076 | chr2 | 86840231 | ||||||
| chr2:86840290 | G | A | 4 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0033 others(1): Show |
32 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2017C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 2017 | chr2 | 86840290 | ||||||
| chr2:86840399 | C | A | 1 | a0001c0001t0015 | 2 | HG00735.hp2 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1908G>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 1908 | chr2 | 86840399 | ||||||
| chr2:86840423 | A | G | 1 | a0003c0005t0037 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1884T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 1884 | chr2 | 86840423 | ||||||
| chr2:86840497 | C | T | 3 | a0001c0001t0009 a0001c0001t0013 a0001c0002t0013 |
8 | HG01358.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1810G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 1810 | chr2 | 86840497 | ||||||
| chr2:86840498 | G | A | 2 | a0001c0002t0028 a0001c0004t0007 |
9 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1809C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 1809 | chr2 | 86840498 | ||||||
| chr2:86840607 | T | C | 2 | a0001c0001t0032 a0001c0002t0041 |
2 | HG02572.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1700A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 1700 | chr2 | 86840607 | ||||||
| chr2:86841110 | G | A | 1 | a0001c0001t0029 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1197C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 1197 | chr2 | 86841110 | ||||||
| chr2:86841261 | C | A | 1 | a0001c0001t0011 | 3 | NA19068.hp1 NA19078.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1046G>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 1046 | chr2 | 86841261 | ||||||
| chr2:86841328 | C | T | 1 | a0002c0003t0018 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*979G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 979 | chr2 | 86841328 | ||||||
| chr2:86841347 | C | T | 1 | a0001c0001t0024 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*960G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 960 | chr2 | 86841347 | ||||||
| chr2:86841404 | T | C | 1 | a0001c0001t0033 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*903A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 903 | chr2 | 86841404 | ||||||
| chr2:86841457 | C | T | 1 | a0003c0005t0037 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*850G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 850 | chr2 | 86841457 | ||||||
| chr2:86841486 | G | A | 10 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(7): Show |
71 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*821C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 821 | chr2 | 86841486 | ||||||
| chr2:86841525 | G | T | 36 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(33): Show |
289 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*782C>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 782 | chr2 | 86841525 | ||||||
| chr2:86841635 | A | G | 1 | a0001c0002t0038 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*672T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 672 | chr2 | 86841635 | ||||||
| chr2:86841659 | T | G | 29 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(26): Show |
217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*648A>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 648 | chr2 | 86841659 | ||||||
| chr2:86841704 | G | A | 10 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(7): Show |
71 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*603C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 603 | chr2 | 86841704 | ||||||
| chr2:86841723 | T | G | 2 | a0001c0002t0016 a0001c0002t0043 |
3 | HG01928.hp2 HG01943.hp2 HG01993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*584A>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 584 | chr2 | 86841723 | ||||||
| chr2:86841795 | C | T | 1 | a0001c0001t0034 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*512G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 512 | chr2 | 86841795 | ||||||
| chr2:86841855 | C | T | 1 | a0001c0002t0012 | 3 | HG01346.hp2 HG03041.hp2 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*452G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 452 | chr2 | 86841855 | ||||||
| chr2:86841901 | C | G | 1 | a0002c0003t0017 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*406G>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 406 | chr2 | 86841901 | ||||||
| chr2:86841932 | A | G | 2 | a0003c0005t0008 a0003c0005t0037 |
6 | HG01167.hp1 HG01891.hp1 HG02615.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*375T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 375 | chr2 | 86841932 | ||||||
| chr2:86842041 | C | A | 1 | a0001c0002t0043 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*266G>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 266 | chr2 | 86842041 | ||||||
| chr2:86842074 | G | A | 1 | a0001c0001t0034 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*233C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 233 | chr2 | 86842074 | ||||||
| chr2:86842086 | G | A | 1 | a0001c0002t0002 | 3 | HG02717.hp2 HG03195.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*221C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 221 | chr2 | 86842086 | ||||||
| chr2:86842217 | T | A | 1 | a0001c0001t0035 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*90A>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 90 | chr2 | 86842217 | ||||||
| chr2:86842256 | G | A | 34 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(31): Show |
282 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*51C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 51 | chr2 | 86842256 | ||||||
| chr2:86842296 | G | A | 1 | a0001c0001t0036 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 6/6 | 11 | chr2 | 86842296 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:86842589 | A | C | 18 | a0002c0003t0003g0010 a0002c0003t0003g0037 a0002c0003t0003g0038 others(15): Show |
25 | HG00438.hp1 HG00438.hp2 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.621-270T>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86842589 | |||||||
| chr2:86842845 | C | G | 2 | a0002c0003t0003g0205 a0002c0003t0019g0204 |
2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.621-526G>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86842845 | |||||||
| chr2:86842859 | G | T | 1 | a0001c0002t0039g0172 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.621-540C>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86842859 | |||||||
| chr2:86842888 | C | T | 18 | a0002c0003t0003g0010 a0002c0003t0003g0037 a0002c0003t0003g0038 others(15): Show |
25 | HG00438.hp1 HG00438.hp2 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.621-569G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86842888 | |||||||
| chr2:86842961 | T | C | 1 | a0001c0002t0039g0172 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.621-642A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86842961 | |||||||
| chr2:86842962 | C | T | 1 | a0001c0002t0039g0172 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.621-643G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86842962 | |||||||
| chr2:86843217 | C | T | 1 | a0001c0001t0013g0130 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.621-898G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86843217 | |||||||
| chr2:86843220 | GTAGCTGG others(7): Show |
G | 5 | a0001c0001t0009g0013 a0001c0001t0009g0161 a0001c0001t0013g0130 others(2): Show |
8 | HG01358.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.621-915_621-902del others(14): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86843220 | |||||||
| chr2:86843464 | G | A | 191 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(188): Show |
282 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.621-1145C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86843464 | |||||||
| chr2:86843824 | G | T | 1 | a0002c0003t0003g0190 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.620+1098C>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86843824 | |||||||
| chr2:86843829 | G | A | 1 | a0003c0005t0008g0047 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.620+1093C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86843829 | |||||||
| chr2:86843876 | G | A | 1 | a0001c0001t0004g0049 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.620+1046C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86843876 | |||||||
| chr2:86844108 | C | T | 1 | a0005c0008t0002g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.620+814G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86844108 | |||||||
| chr2:86844174 | G | T | 4 | a0001c0001t0009g0013 a0001c0001t0009g0161 a0001c0001t0013g0130 others(1): Show |
7 | HG01358.hp2 HG02280.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.620+748C>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86844174 | |||||||
| chr2:86844176 | G | A | 1 | a0001c0002t0004g0212 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.620+746C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86844176 | |||||||
| chr2:86844228 | T | G | 197 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(194): Show |
291 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.620+694A>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86844228 | |||||||
| chr2:86844279 | T | C | 1 | a0001c0001t0004g0160 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.620+643A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86844279 | |||||||
| chr2:86844351 | A | G | 197 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(194): Show |
291 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.620+571T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86844351 | |||||||
| chr2:86844507 | G | A | 1 | a0001c0002t0002g0174 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.620+415C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86844507 | |||||||
| chr2:86844597 | G | A | 2 | a0001c0002t0002g0214 a0001c0002t0006g0162 |
2 | HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.620+325C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86844597 | |||||||
| chr2:86844764 | T | G | 1 | a0002c0003t0017g0231 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.620+158A>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86844764 | |||||||
| chr2:86844803 | C | G | 1 | a0001c0002t0002g0171 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.620+119G>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 5/5 | chr2 | 86844803 | |||||||
| chr2:86845128 | A | T | 1 | a0002c0003t0017g0231 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.584-170T>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 4/5 | chr2 | 86845128 | |||||||
| chr2:86845199 | A | C | 1 | a0001c0001t0013g0131 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.584-241T>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 4/5 | chr2 | 86845199 | |||||||
| chr2:86845355 | G | T | 1 | a0002c0003t0003g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.584-397C>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 4/5 | chr2 | 86845355 | |||||||
| chr2:86845432 | CA | C | 5 | a0001c0001t0009g0013 a0001c0001t0009g0161 a0001c0001t0013g0130 others(2): Show |
8 | HG01358.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.584-475delT | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 4/5 | chr2 | 86845432 | |||||||
| chr2:86845893 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.583+791G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 4/5 | chr2 | 86845893 | |||||||
| chr2:86845916 | C | T | 1 | a0001c0002t0002g0217 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.583+768G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 4/5 | chr2 | 86845916 | |||||||
| chr2:86846090 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.583+594G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 4/5 | chr2 | 86846090 | |||||||
| chr2:86846286 | A | C | 3 | a0002c0003t0003g0197 a0002c0003t0003g0199 a0002c0003t0003g0201 |
3 | NA18949.hp1 NA19063.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.583+398T>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 4/5 | chr2 | 86846286 | |||||||
| chr2:86846522 | C | T | 45 | a0002c0003t0003g0003 a0002c0003t0003g0010 a0002c0003t0003g0014 others(42): Show |
74 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.583+162G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 4/5 | chr2 | 86846522 | |||||||
| chr2:86846544 | CCTCTGGA others(11): Show |
C | 1 | a0002c0003t0003g0197 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.583+122_583+139del others(18): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 4/5 | chr2 | 86846544 | |||||||
| chr2:86846620 | A | G | 197 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(194): Show |
291 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.583+64T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 4/5 | chr2 | 86846620 | |||||||
| chr2:86846657 | C | T | 17 | a0002c0003t0003g0010 a0002c0003t0003g0037 a0002c0003t0003g0038 others(14): Show |
24 | HG00438.hp1 HG00438.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.583+27G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 4/5 | chr2 | 86846657 | |||||||
| chr2:86846672 | G | GAGACAAC others(53): Show |
1 | a0001c0001t0001g0106 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.535_583+11dupGGCGT others(55): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 4/5 | chr2 | 86846672 | |||||||
| chr2:86846798 | G | A | 45 | a0002c0003t0003g0003 a0002c0003t0003g0010 a0002c0003t0003g0014 others(42): Show |
74 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.494-25C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86846798 | |||||||
| chr2:86846831 | G | A | 1 | a0001c0001t0006g0078 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.494-58C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86846831 | |||||||
| chr2:86846925 | G | GTC | 29 | a0001c0001t0013g0130 a0002c0003t0003g0003 a0002c0003t0003g0010 others(26): Show |
56 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.494-153_494-152ins others(2): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86846925 | |||||||
| chr2:86846925 | G | GTCT | 15 | a0001c0001t0013g0131 a0002c0003t0003g0040 a0002c0003t0003g0041 others(12): Show |
17 | HG00438.hp1 HG00438.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.494-153_494-152ins others(3): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86846925 | |||||||
| chr2:86846925 | GTATTTTT others(9): Show |
G | 2 | a0001c0001t0009g0013 a0001c0001t0009g0161 |
5 | HG02280.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-168_494-153del others(16): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86846925 | |||||||
| chr2:86846926 | TA | T | 110 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(107): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.494-154delT | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86846926 | |||||||
| chr2:86846927 | A | AT | 10 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(7): Show |
16 | HG00140.hp2 HG00735.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.494-155dupA | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86846927 | |||||||
| chr2:86846927 | A | C | 30 | a0001c0001t0001g0029 a0001c0001t0001g0056 a0001c0001t0001g0068 others(27): Show |
33 | HG00609.hp1 HG00609.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.494-154T>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86846927 | |||||||
| chr2:86846927 | A | T | 49 | a0001c0001t0013g0130 a0001c0001t0013g0131 a0001c0002t0006g0162 others(46): Show |
78 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.494-154T>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86846927 | |||||||
| chr2:86846928 | T | C | 110 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(107): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.494-155A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86846928 | |||||||
| chr2:86846929 | T | C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0137 a0001c0001t0001g0155 others(2): Show |
5 | HG02451.hp1 HG02897.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-156A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86846929 | |||||||
| chr2:86846943 | T | C | 2 | a0001c0001t0009g0013 a0001c0001t0009g0161 |
5 | HG02280.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-170A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86846943 | |||||||
| chr2:86846985 | C | T | 27 | a0001c0001t0004g0049 a0001c0001t0005g0018 a0001c0001t0005g0024 others(24): Show |
33 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.494-212G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86846985 | |||||||
| chr2:86847023 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.494-250G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86847023 | |||||||
| chr2:86847163 | C | T | 5 | a0001c0001t0009g0013 a0001c0001t0009g0161 a0001c0001t0013g0130 others(2): Show |
8 | HG01358.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.494-390G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86847163 | |||||||
| chr2:86847169 | T | C | 5 | a0001c0001t0009g0013 a0001c0001t0009g0161 a0001c0001t0013g0130 others(2): Show |
8 | HG01358.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.494-396A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86847169 | |||||||
| chr2:86847512 | T | G | 5 | a0001c0001t0009g0013 a0001c0001t0009g0161 a0001c0001t0013g0130 others(2): Show |
8 | HG01358.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.494-739A>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86847512 | |||||||
| chr2:86847527 | T | G | 197 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(194): Show |
291 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.494-754A>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86847527 | |||||||
| chr2:86847532 | A | G | 1 | a0001c0002t0002g0239 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.494-759T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86847532 | |||||||
| chr2:86847546 | C | T | 1 | a0001c0001t0001g0021 | 3 | HG00408.hp2 NA18999.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.494-773G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86847546 | |||||||
| chr2:86847547 | G | A | 5 | a0001c0001t0009g0013 a0001c0001t0009g0161 a0001c0001t0013g0130 others(2): Show |
8 | HG01358.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.494-774C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86847547 | |||||||
| chr2:86847653 | C | T | 2 | a0001c0001t0009g0013 a0001c0001t0009g0161 |
5 | HG02280.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-880G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86847653 | |||||||
| chr2:86847714 | C | T | 4 | a0001c0002t0028g0211 a0001c0004t0007g0008 a0001c0004t0007g0233 others(1): Show |
9 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.494-941G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86847714 | |||||||
| chr2:86847767 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.494-994G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86847767 | |||||||
| chr2:86847920 | T | C | 46 | a0001c0002t0006g0162 a0002c0003t0003g0003 a0002c0003t0003g0010 others(43): Show |
75 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.494-1147A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86847920 | |||||||
| chr2:86847936 | T | C | 45 | a0001c0002t0006g0162 a0002c0003t0003g0003 a0002c0003t0003g0010 others(42): Show |
74 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.494-1163A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86847936 | |||||||
| chr2:86848024 | T | A | 1 | a0001c0002t0002g0036 | 2 | HG01346.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.494-1251A>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848024 | |||||||
| chr2:86848079 | ACT | A | 46 | a0001c0002t0006g0162 a0002c0003t0003g0003 a0002c0003t0003g0010 others(43): Show |
75 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.494-1308_494-1307d others(4): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848079 | |||||||
| chr2:86848118 | A | G | 46 | a0001c0002t0006g0162 a0002c0003t0003g0003 a0002c0003t0003g0010 others(43): Show |
75 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.494-1345T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848118 | |||||||
| chr2:86848257 | T | C | 46 | a0001c0002t0006g0162 a0002c0003t0003g0003 a0002c0003t0003g0010 others(43): Show |
75 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.494-1484A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848257 | |||||||
| chr2:86848275 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0070 |
4 | HG02922.hp1 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-1502T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848275 | |||||||
| chr2:86848393 | C | T | 1 | a0001c0001t0013g0130 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.494-1620G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848393 | |||||||
| chr2:86848537 | T | C | 2 | a0001c0001t0009g0013 a0001c0001t0009g0161 |
5 | HG02280.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-1764A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848537 | |||||||
| chr2:86848577 | G | A | 3 | a0001c0001t0006g0121 a0001c0001t0006g0122 a0003c0005t0037g0232 |
3 | HG01123.hp2 HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.494-1804C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848577 | |||||||
| chr2:86848700 | A | AATTATTT others(22): Show |
1 | a0002c0003t0003g0197 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.494-1928_494-1927i others(31): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848700 | |||||||
| chr2:86848701 | A | ATTAATAT others(11): Show |
1 | a0001c0001t0004g0108 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.494-1929_494-1928i others(20): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848701 | |||||||
| chr2:86848701 | A | ATTAATTA others(13): Show |
1 | a0001c0001t0004g0049 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.494-1929_494-1928i others(22): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848701 | |||||||
| chr2:86848701 | A | ATTAATTA others(9): Show |
1 | a0001c0001t0004g0127 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.494-1929_494-1928i others(18): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848701 | |||||||
| chr2:86848701 | A | ATTAATTA others(13): Show |
9 | a0001c0001t0001g0053 a0001c0001t0001g0109 a0001c0001t0001g0110 others(6): Show |
9 | HG00642.hp1 HG01884.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.494-1929_494-1928i others(22): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848701 | |||||||
| chr2:86848701 | A | ATTAATTA others(17): Show |
2 | a0001c0001t0001g0124 a0001c0001t0001g0133 |
2 | HG02970.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.494-1929_494-1928i others(26): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848701 | |||||||
| chr2:86848701 | A | ATTAATTA others(5): Show |
6 | a0001c0001t0005g0027 a0001c0001t0024g0128 a0001c0002t0028g0211 others(3): Show |
12 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.494-1929_494-1928i others(14): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848701 | |||||||
| chr2:86848701 | A | ATTAATTA others(9): Show |
25 | a0001c0001t0001g0030 a0001c0001t0001g0088 a0001c0001t0001g0096 others(22): Show |
38 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.494-1929_494-1928i others(18): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848701 | |||||||
| chr2:86848701 | A | ATTAATTA others(18): Show |
1 | a0002c0003t0003g0186 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.494-1929_494-1928i others(27): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848701 | |||||||
| chr2:86848701 | A | ATTAATTA others(13): Show |
64 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0019 others(61): Show |
86 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.494-1929_494-1928i others(22): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848701 | |||||||
| chr2:86848701 | A | ATTAATTA others(22): Show |
34 | a0001c0002t0006g0162 a0002c0003t0003g0003 a0002c0003t0003g0010 others(31): Show |
59 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.494-1929_494-1928i others(31): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848701 | |||||||
| chr2:86848701 | A | ATTAATTA others(26): Show |
2 | a0002c0003t0003g0194 a0002c0003t0003g0195 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.494-1929_494-1928i others(35): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848701 | |||||||
| chr2:86848701 | A | ATTAATTA others(17): Show |
18 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0033 others(15): Show |
37 | HG00423.hp1 HG00621.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.494-1929_494-1928i others(26): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848701 | |||||||
| chr2:86848701 | A | ATTAATTA others(21): Show |
7 | a0001c0001t0001g0020 a0001c0001t0001g0070 a0001c0001t0001g0135 others(4): Show |
9 | HG01261.hp1 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.494-1929_494-1928i others(30): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848701 | |||||||
| chr2:86848701 | A | ATTATTTA others(1): Show |
32 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(29): Show |
86 | HG00099.hp2 HG00544.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.494-1936_494-1929d others(10): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848701 | |||||||
| chr2:86848701 | A | ATTATTTA others(5): Show |
4 | a0001c0001t0001g0112 a0001c0002t0002g0170 a0001c0002t0002g0216 others(1): Show |
4 | HG00140.hp2 HG01891.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-1940_494-1929d others(14): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848701 | |||||||
| chr2:86848701 | A | ATTATTTA others(9): Show |
5 | a0001c0001t0001g0107 a0001c0001t0009g0013 a0001c0001t0013g0130 others(2): Show |
8 | HG01358.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.494-1944_494-1929d others(18): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848701 | |||||||
| chr2:86848701 | A | ATTATTTA others(13): Show |
6 | a0001c0001t0001g0064 a0001c0001t0001g0091 a0001c0001t0006g0140 others(3): Show |
7 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.494-1948_494-1929d others(22): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848701 | |||||||
| chr2:86848701 | A | ATTATTTA others(22): Show |
8 | a0002c0003t0003g0014 a0002c0003t0003g0040 a0002c0003t0003g0193 others(5): Show |
12 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.494-1929_494-1928i others(31): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848701 | |||||||
| chr2:86848701 | A | ATTATTTA others(17): Show |
8 | a0001c0001t0001g0089 a0001c0001t0001g0093 a0001c0001t0005g0077 others(5): Show |
8 | HG01123.hp2 HG01167.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.494-1952_494-1929d others(26): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848701 | |||||||
| chr2:86848705 | T | A | 1 | a0001c0001t0026g0083 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.494-1932A>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848705 | |||||||
| chr2:86848728 | A | ATTTATTT others(10): Show |
1 | a0001c0001t0026g0083 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.494-1956_494-1955i others(19): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848728 | |||||||
| chr2:86848787 | A | G | 5 | a0001c0001t0009g0013 a0001c0001t0009g0161 a0001c0001t0013g0130 others(2): Show |
8 | HG01358.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.494-2014T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848787 | |||||||
| chr2:86848932 | G | C | 46 | a0001c0002t0006g0162 a0002c0003t0003g0003 a0002c0003t0003g0010 others(43): Show |
75 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.494-2159C>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848932 | |||||||
| chr2:86848983 | C | T | 1 | a0001c0002t0013g0180 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.494-2210G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86848983 | |||||||
| chr2:86849154 | A | G | 4 | a0001c0002t0028g0211 a0001c0004t0007g0008 a0001c0004t0007g0233 others(1): Show |
9 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.494-2381T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86849154 | |||||||
| chr2:86849375 | T | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0113 |
3 | HG00597.hp2 NA18949.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.494-2602A>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86849375 | |||||||
| chr2:86849397 | C | A | 2 | a0001c0001t0009g0013 a0001c0001t0009g0161 |
5 | HG02280.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-2624G>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86849397 | |||||||
| chr2:86849607 | C | T | 1 | a0001c0002t0002g0177 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.494-2834G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86849607 | |||||||
| chr2:86849651 | A | G | 1 | a0001c0002t0040g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.494-2878T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86849651 | |||||||
| chr2:86849657 | A | C | 1 | a0001c0002t0002g0215 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.494-2884T>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86849657 | |||||||
| chr2:86849703 | G | GT | 151 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(148): Show |
220 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.494-2931dupA | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86849703 | |||||||
| chr2:86849703 | G | GTT | 13 | a0001c0001t0001g0052 a0001c0001t0001g0089 a0001c0001t0001g0093 others(10): Show |
13 | HG00140.hp1 HG00597.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.494-2932_494-2931d others(4): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86849703 | |||||||
| chr2:86849752 | G | A | 1 | a0003c0005t0037g0232 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.494-2979C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86849752 | |||||||
| chr2:86849892 | C | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0067 a0001c0001t0001g0089 others(5): Show |
11 | HG01099.hp2 HG01109.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.493+3105G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86849892 | |||||||
| chr2:86850017 | A | G | 1 | a0001c0002t0002g0213 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.493+2980T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86850017 | |||||||
| chr2:86850068 | G | T | 1 | a0002c0003t0017g0231 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.493+2929C>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86850068 | |||||||
| chr2:86850241 | C | T | 2 | a0002c0003t0003g0194 a0002c0003t0003g0195 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.493+2756G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86850241 | |||||||
| chr2:86850310 | C | T | 1 | a0002c0003t0003g0198 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.493+2687G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86850310 | |||||||
| chr2:86850318 | T | C | 197 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(194): Show |
291 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.493+2679A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86850318 | |||||||
| chr2:86850701 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.493+2296G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86850701 | |||||||
| chr2:86850723 | C | T | 18 | a0002c0003t0003g0010 a0002c0003t0003g0037 a0002c0003t0003g0038 others(15): Show |
25 | HG00438.hp1 HG00438.hp2 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.493+2274G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86850723 | |||||||
| chr2:86850811 | C | T | 1 | a0002c0003t0003g0188 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.493+2186G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86850811 | |||||||
| chr2:86851082 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.493+1915G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86851082 | |||||||
| chr2:86851090 | C | CA | 44 | a0001c0001t0001g0116 a0001c0002t0006g0162 a0002c0003t0003g0003 others(41): Show |
74 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.493+1906dupT | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86851090 | |||||||
| chr2:86851090 | CA | C | 10 | a0001c0001t0001g0055 a0001c0001t0001g0082 a0001c0001t0004g0141 others(7): Show |
13 | HG01070.hp1 HG01358.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.493+1906delT | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86851090 | |||||||
| chr2:86851091 | A | G | 4 | a0001c0002t0028g0211 a0001c0004t0007g0008 a0001c0004t0007g0233 others(1): Show |
9 | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.493+1906T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86851091 | |||||||
| chr2:86851125 | A | T | 1 | a0001c0001t0006g0074 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.493+1872T>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86851125 | |||||||
| chr2:86851282 | C | A | 1 | a0002c0003t0017g0231 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.493+1715G>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86851282 | |||||||
| chr2:86851338 | C | G | 25 | a0001c0001t0005g0018 a0001c0001t0005g0024 a0001c0001t0005g0026 others(22): Show |
31 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.493+1659G>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86851338 | |||||||
| chr2:86851376 | C | T | 2 | a0002c0003t0003g0194 a0002c0003t0003g0195 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.493+1621G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86851376 | |||||||
| chr2:86851385 | C | T | 2 | a0001c0002t0004g0209 a0001c0002t0031g0210 |
2 | HG01517.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.493+1612G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86851385 | |||||||
| chr2:86851435 | G | T | 197 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(194): Show |
291 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.493+1562C>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86851435 | |||||||
| chr2:86851543 | A | G | 1 | a0002c0003t0017g0231 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.493+1454T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86851543 | |||||||
| chr2:86851632 | G | A | 5 | a0001c0001t0009g0013 a0001c0001t0009g0161 a0001c0001t0013g0130 others(2): Show |
8 | HG01358.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.493+1365C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86851632 | |||||||
| chr2:86851783 | C | T | 1 | a0001c0001t0036g0149 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.493+1214G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86851783 | |||||||
| chr2:86851910 | A | C | 5 | a0001c0001t0009g0013 a0001c0001t0009g0161 a0001c0001t0013g0130 others(2): Show |
8 | HG01358.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.493+1087T>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86851910 | |||||||
| chr2:86851916 | A | G | 1 | a0001c0001t0005g0073 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.493+1081T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86851916 | |||||||
| chr2:86852146 | C | T | 1 | a0001c0001t0001g0028 | 2 | NA18967.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.493+851G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86852146 | |||||||
| chr2:86852165 | C | T | 2 | a0001c0001t0005g0071 a0001c0001t0005g0072 |
2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.493+832G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86852165 | |||||||
| chr2:86852166 | G | A | 1 | a0001c0001t0011g0087 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.493+831C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86852166 | |||||||
| chr2:86852237 | G | T | 2 | a0001c0001t0004g0158 a0001c0001t0004g0159 |
2 | HG01074.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.493+760C>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86852237 | |||||||
| chr2:86852295 | C | T | 1 | a0002c0003t0003g0227 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.493+702G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86852295 | |||||||
| chr2:86852685 | A | G | 9 | a0002c0003t0003g0010 a0002c0003t0003g0037 a0002c0003t0003g0185 others(6): Show |
14 | HG00438.hp1 HG00438.hp2 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.493+312T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86852685 | |||||||
| chr2:86852705 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.493+292C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 3/5 | chr2 | 86852705 | |||||||
| chr2:86853101 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.404-15G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86853101 | |||||||
| chr2:86853201 | C | T | 1 | a0001c0001t0011g0087 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.404-115G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86853201 | |||||||
| chr2:86853314 | T | G | 5 | a0001c0001t0009g0013 a0001c0001t0009g0161 a0001c0001t0013g0130 others(2): Show |
8 | HG01358.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.404-228A>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86853314 | |||||||
| chr2:86853320 | C | T | 1 | a0002c0003t0003g0193 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.404-234G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86853320 | |||||||
| chr2:86853377 | G | A | 1 | a0001c0001t0004g0138 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.404-291C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86853377 | |||||||
| chr2:86853419 | A | G | 51 | a0001c0001t0009g0013 a0001c0001t0009g0161 a0001c0001t0013g0130 others(48): Show |
83 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.404-333T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86853419 | |||||||
| chr2:86853536 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.404-450C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86853536 | |||||||
| chr2:86853538 | C | T | 146 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(143): Show |
208 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.404-452G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86853538 | |||||||
| chr2:86853680 | C | T | 2 | a0001c0001t0009g0013 a0001c0001t0009g0161 |
5 | HG02280.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.404-594G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86853680 | |||||||
| chr2:86853775 | G | C | 1 | a0001c0001t0001g0119 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.404-689C>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86853775 | |||||||
| chr2:86853884 | G | A | 2 | a0002c0003t0003g0206 a0002c0003t0003g0207 |
2 | HG01070.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.404-798C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86853884 | |||||||
| chr2:86853989 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.404-903G>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86853989 | |||||||
| chr2:86854275 | C | T | 1 | a0001c0002t0040g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.404-1189G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86854275 | |||||||
| chr2:86854342 | T | C | 4 | a0001c0001t0009g0013 a0001c0001t0009g0161 a0001c0001t0013g0130 others(1): Show |
7 | HG01358.hp2 HG02280.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-1256A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86854342 | |||||||
| chr2:86854406 | T | C | 2 | a0001c0001t0004g0146 a0001c0001t0035g0147 |
2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.404-1320A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86854406 | |||||||
| chr2:86854415 | C | T | 4 | a0001c0001t0009g0013 a0001c0001t0009g0161 a0001c0001t0013g0130 others(1): Show |
7 | HG01358.hp2 HG02280.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-1329G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86854415 | |||||||
| chr2:86854729 | T | C | 1 | a0001c0001t0006g0150 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.404-1643A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86854729 | |||||||
| chr2:86854806 | GA | G | 85 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(82): Show |
122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.404-1721delT | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86854806 | |||||||
| chr2:86854814 | A | G | 1 | a0001c0001t0004g0049 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.404-1728T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86854814 | |||||||
| chr2:86855000 | A | C | 18 | a0002c0003t0003g0010 a0002c0003t0003g0037 a0002c0003t0003g0038 others(15): Show |
25 | HG00438.hp1 HG00438.hp2 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.404-1914T>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86855000 | |||||||
| chr2:86855112 | G | A | 4 | a0001c0001t0009g0013 a0001c0001t0009g0161 a0001c0001t0013g0130 others(1): Show |
7 | HG01358.hp2 HG02280.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-2026C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86855112 | |||||||
| chr2:86855182 | T | G | 1 | a0004c0009t0002g0221 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.404-2096A>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86855182 | |||||||
| chr2:86855333 | A | G | 2 | a0001c0001t0013g0130 a0001c0001t0013g0131 |
2 | HG01358.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.404-2247T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86855333 | |||||||
| chr2:86855493 | A | C | 1 | a0001c0002t0013g0180 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.404-2407T>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86855493 | |||||||
| chr2:86855556 | C | T | 143 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(140): Show |
202 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.404-2470G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86855556 | |||||||
| chr2:86855679 | C | G | 1 | a0002c0003t0017g0231 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.403+2378G>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86855679 | |||||||
| chr2:86855695 | C | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0026g0083 |
3 | NA18942.hp1 NA19066.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.403+2362G>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86855695 | |||||||
| chr2:86855772 | G | A | 1 | a0002c0003t0017g0231 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.403+2285C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86855772 | |||||||
| chr2:86855882 | G | T | 47 | a0001c0002t0006g0162 a0001c0002t0013g0180 a0002c0003t0003g0003 others(44): Show |
76 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.403+2175C>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86855882 | |||||||
| chr2:86855938 | T | G | 1 | a0002c0003t0021g0167 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.403+2119A>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86855938 | |||||||
| chr2:86856021 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.403+2036C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86856021 | |||||||
| chr2:86856031 | T | C | 4 | a0001c0001t0009g0013 a0001c0001t0009g0161 a0001c0001t0013g0130 others(1): Show |
7 | HG01358.hp2 HG02280.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+2026A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86856031 | |||||||
| chr2:86856104 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG00642.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.403+1953C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86856104 | |||||||
| chr2:86856178 | T | C | 5 | a0001c0001t0001g0033 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
6 | HG01243.hp2 HG01261.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.403+1879A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86856178 | |||||||
| chr2:86856222 | C | G | 5 | a0001c0001t0001g0019 a0001c0001t0001g0082 a0001c0001t0001g0084 others(2): Show |
7 | HG00408.hp1 NA18942.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+1835G>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86856222 | |||||||
| chr2:86856257 | G | A | 5 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(2): Show |
5 | NA18953.hp1 NA18963.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.403+1800C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86856257 | |||||||
| chr2:86856420 | C | T | 2 | a0001c0001t0004g0138 a0001c0004t0007g0233 |
2 | HG01192.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.403+1637G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86856420 | |||||||
| chr2:86856561 | T | C | 1 | a0001c0002t0002g0176 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.403+1496A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86856561 | |||||||
| chr2:86856569 | G | A | 1 | a0001c0002t0002g0175 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.403+1488C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86856569 | |||||||
| chr2:86856758 | G | T | 2 | a0001c0002t0002g0007 a0001c0002t0002g0036 |
8 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.403+1299C>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86856758 | |||||||
| chr2:86856772 | A | G | 147 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(144): Show |
212 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.403+1285T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86856772 | |||||||
| chr2:86856800 | G | A | 1 | a0001c0002t0002g0222 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.403+1257C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86856800 | |||||||
| chr2:86856915 | A | G | 21 | a0001c0001t0001g0070 a0001c0001t0005g0018 a0001c0001t0005g0024 others(18): Show |
27 | HG00639.hp1 HG01109.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.403+1142T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86856915 | |||||||
| chr2:86856985 | T | C | 138 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(135): Show |
195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.403+1072A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86856985 | |||||||
| chr2:86857099 | C | T | 1 | a0001c0002t0013g0180 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.403+958G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86857099 | |||||||
| chr2:86857145 | T | C | 1 | a0001c0001t0004g0061 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.403+912A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86857145 | |||||||
| chr2:86857247 | C | T | 1 | a0002c0003t0003g0179 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.403+810G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86857247 | |||||||
| chr2:86857274 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.403+783T>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86857274 | |||||||
| chr2:86857457 | G | T | 6 | a0001c0001t0006g0150 a0003c0005t0008g0047 a0003c0005t0008g0235 others(3): Show |
7 | HG01167.hp1 HG01891.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+600C>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86857457 | |||||||
| chr2:86857471 | C | T | 1 | a0002c0003t0003g0226 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.403+586G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86857471 | |||||||
| chr2:86857612 | C | T | 1 | a0002c0003t0003g0178 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.403+445G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86857612 | |||||||
| chr2:86857725 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.403+332T>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86857725 | |||||||
| chr2:86857793 | T | C | 138 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(135): Show |
198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.403+264A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86857793 | |||||||
| chr2:86857795 | G | C | 2 | a0001c0001t0009g0013 a0001c0001t0009g0161 |
5 | HG02280.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.403+262C>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86857795 | |||||||
| chr2:86857881 | A | G | 1 | a0001c0002t0002g0168 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.403+176T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86857881 | |||||||
| chr2:86857926 | T | C | 1 | a0003c0005t0037g0232 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.403+131A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86857926 | |||||||
| chr2:86858040 | T | C | 2 | a0001c0001t0005g0048 a0001c0002t0002g0022 |
4 | HG02717.hp2 HG03195.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.403+17A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 2/5 | chr2 | 86858040 | |||||||
| chr2:86858444 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.44-28T>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86858444 | |||||||
| chr2:86858475 | T | C | 138 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(135): Show |
198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.44-59A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86858475 | |||||||
| chr2:86858518 | G | A | 138 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(135): Show |
198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.44-102C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86858518 | |||||||
| chr2:86858619 | G | C | 139 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(136): Show |
199 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.44-203C>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86858619 | |||||||
| chr2:86858723 | G | A | 20 | a0001c0001t0001g0062 a0001c0001t0004g0005 a0001c0001t0004g0012 others(17): Show |
33 | HG00423.hp2 HG00544.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.44-307C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86858723 | |||||||
| chr2:86858739 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.44-323C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86858739 | |||||||
| chr2:86858777 | C | T | 1 | a0001c0001t0004g0063 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.44-361G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86858777 | |||||||
| chr2:86858850 | A | T | 1 | a0001c0002t0002g0177 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.44-434T>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86858850 | |||||||
| chr2:86859003 | T | G | 2 | a0001c0001t0009g0013 a0001c0001t0009g0161 |
5 | HG02280.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-587A>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86859003 | |||||||
| chr2:86859046 | T | C | 1 | a0001c0001t0036g0149 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.44-630A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86859046 | |||||||
| chr2:86859060 | C | G | 137 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(134): Show |
194 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.44-644G>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86859060 | |||||||
| chr2:86859089 | C | A | 4 | a0003c0005t0008g0047 a0003c0005t0008g0235 a0003c0005t0008g0236 others(1): Show |
5 | HG01167.hp1 HG01891.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.44-673G>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86859089 | |||||||
| chr2:86859108 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.44-692C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86859108 | |||||||
| chr2:86859139 | C | T | 1 | a0001c0002t0002g0176 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.44-723G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86859139 | |||||||
| chr2:86859174 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.44-758G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86859174 | |||||||
| chr2:86859415 | T | G | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | NA18939.hp1 NA19004.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.44-999A>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86859415 | |||||||
| chr2:86859490 | G | T | 1 | a0001c0001t0004g0061 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.44-1074C>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86859490 | |||||||
| chr2:86859585 | G | T | 11 | a0001c0002t0001g0169 a0001c0002t0002g0001 a0001c0002t0002g0035 others(8): Show |
36 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.44-1169C>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86859585 | |||||||
| chr2:86859641 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.44-1225G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86859641 | |||||||
| chr2:86859682 | T | C | 1 | a0001c0002t0002g0046 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.44-1266A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86859682 | |||||||
| chr2:86859699 | T | C | 1 | a0001c0002t0002g0225 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.44-1283A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86859699 | |||||||
| chr2:86859721 | A | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0055 a0001c0001t0001g0056 others(3): Show |
7 | NA18950.hp2 NA18953.hp1 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-1305T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86859721 | |||||||
| chr2:86859741 | T | C | 140 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(137): Show |
200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.44-1325A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86859741 | |||||||
| chr2:86859881 | G | C | 1 | a0001c0001t0009g0161 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.44-1465C>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86859881 | |||||||
| chr2:86859939 | G | A | 2 | a0001c0001t0005g0156 a0001c0001t0005g0157 |
2 | HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.44-1523C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86859939 | |||||||
| chr2:86860097 | T | C | 140 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(137): Show |
200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.44-1681A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86860097 | |||||||
| chr2:86860138 | C | A | 6 | a0002c0003t0003g0010 a0002c0003t0003g0226 a0002c0003t0003g0227 others(3): Show |
10 | HG00438.hp1 HG00438.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.43+1685G>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86860138 | |||||||
| chr2:86860378 | A | G | 1 | a0002c0003t0021g0167 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.43+1445T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86860378 | |||||||
| chr2:86860689 | T | C | 150 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(147): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.43+1134A>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86860689 | |||||||
| chr2:86860709 | C | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
7 | HG00738.hp2 NA18973.hp1 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.43+1114G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86860709 | |||||||
| chr2:86860728 | C | T | 1 | a0001c0002t0012g0166 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.43+1095G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86860728 | |||||||
| chr2:86860763 | C | T | 1 | a0001c0002t0040g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.43+1060G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86860763 | |||||||
| chr2:86860887 | C | T | 2 | a0001c0001t0002g0050 a0001c0001t0004g0049 |
2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.43+936G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86860887 | |||||||
| chr2:86861077 | C | T | 136 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0011 others(133): Show |
193 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.43+746G>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86861077 | |||||||
| chr2:86861135 | G | T | 1 | a0001c0001t0005g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.43+688C>A | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86861135 | |||||||
| chr2:86861227 | A | AGATGCCC others(181): Show |
1 | a0005c0008t0002g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.43+595_43+596insGC others(186): Show |
CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86861227 | |||||||
| chr2:86861323 | G | A | 3 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 |
3 | HG01074.hp2 HG01261.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.43+500C>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86861323 | |||||||
| chr2:86861408 | G | C | 1 | a0001c0002t0002g0239 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.43+415C>G | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86861408 | |||||||
| chr2:86861414 | A | G | 1 | a0001c0002t0006g0162 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.43+409T>C | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86861414 | |||||||
| chr2:86861698 | C | A | 2 | a0001c0001t0009g0013 a0001c0001t0009g0161 |
5 | HG02280.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+125G>T | CD8B | ENSG00000172116.23 | transcript | ENST00000390655.12 | protein_coding | 1/5 | chr2 | 86861698 |