Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 940 |
| ensemblid | ENSG00000178562.18 |
| hgncid | 1653 |
| symbol | CD28 |
| name | CD28 molecule |
| refseq_nuc | NM_006139.4 |
| refseq_prot | NP_006130.1 |
| ensembl_nuc | ENST00000324106.9 |
| ensembl_prot | ENSP00000324890.7 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 203706639 |
| end | 203738912 |
| strand | + |
| ver | v1.2 |
| region | chr2:203706639-203738912 |
| region5000 | chr2:203701639-203743912 |
| regionname0 | CD28_chr2_203706639_203738912 |
| regionname5000 | CD28_chr2_203701639_203743912 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 220 | 387 | 87 | 66 | 176 | 16 | 40 | 135 | CD28_chr2_203701639_203743912 | CD28 | MLRLL others(215): Show |
chr2 | 203701639 | 203743912 |
| a0002 | 0/0 | 220 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | MLRLL others(215): Show |
chr2 | 203701639 | 203743912 |
| a0003 | 0/0 | 220 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | MLRLL others(215): Show |
chr2 | 203701639 | 203743912 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 660 | 383 | 87 | 64 | 174 | 16 | 40 | CD28_chr2_203701639_203743912 | CD28 | ATGCT others(655): Show |
chr2 | 203701639 | 203743912 | ||
| a0001c0002 | 0/0 | 660 | 2 | 0 | 2 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ATGCT others(655): Show |
chr2 | 203701639 | 203743912 | ||
| a0001c0005 | 0/0 | 660 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ATGCT others(655): Show |
chr2 | 203701639 | 203743912 | ||
| a0001c0006 | 0/0 | 660 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ATGCT others(655): Show |
chr2 | 203701639 | 203743912 | ||
| a0002c0003 | 0/0 | 660 | 2 | 0 | 0 | 2 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ATGCT others(655): Show |
chr2 | 203701639 | 203743912 | ||
| a0003c0004 | 0/0 | 660 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ATGCT others(655): Show |
chr2 | 203701639 | 203743912 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4721 | 207 | 53 | 39 | 82 | 6 | 26 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0002 | 0/0 | 4720 | 89 | 11 | 13 | 60 | 0 | 5 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4715): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0003 | 0/0 | 4737 | 18 | 1 | 4 | 7 | 4 | 2 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4732): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0004 | 1/0 | 4721 | 12 | 3 | 4 | 0 | 2 | 2 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0005 | 0/0 | 4719 | 10 | 0 | 0 | 10 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4714): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0006 | 0/0 | 4734 | 9 | 2 | 0 | 3 | 2 | 2 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4729): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0007 | 0/0 | 4724 | 5 | 4 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4719): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0008 | 0/0 | 4721 | 3 | 0 | 0 | 3 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0009 | 0/0 | 4727 | 3 | 3 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4722): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0010 | 0/0 | 4721 | 2 | 0 | 0 | 2 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0011 | 0/0 | 4720 | 2 | 0 | 0 | 0 | 2 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4715): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0012 | 0/0 | 4722 | 2 | 2 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4717): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0013 | 0/0 | 4721 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0014 | 0/0 | 4721 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0015 | 0/0 | 4721 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0016 | 0/0 | 4721 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0017 | 0/0 | 4721 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0018 | 0/0 | 4721 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0019 | 0/0 | 4721 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0020 | 0/0 | 4721 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0021 | 0/0 | 4721 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0022 | 0/0 | 4720 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4715): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0023 | 0/0 | 4721 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0024 | 0/0 | 4723 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4718): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0025 | 0/0 | 4721 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0026 | 0/0 | 4721 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0027 | 0/0 | 4719 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4714): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0028 | 0/0 | 4734 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4729): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0029 | 0/0 | 4740 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4735): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0030 | 0/0 | 4743 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4738): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0031 | 0/0 | 4720 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4715): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0032 | 0/0 | 4721 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0001c0001t0033 | 0/0 | 4721 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0001c0002t0001 | 0/0 | 4721 | 2 | 0 | 2 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0001c0005t0002 | 0/0 | 4720 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4715): Show |
chr2 | 203701639 | 203743912 |
| a0001c0006t0001 | 0/0 | 4721 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0002c0003t0001 | 0/0 | 4721 | 2 | 0 | 0 | 2 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| a0003c0004t0001 | 0/0 | 4721 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | ACACT others(4716): Show |
chr2 | 203701639 | 203743912 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 46 | 11 | 7 | 26 | 0 | 2 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0003 | 0/1 | 37 | 0 | 13 | 18 | 3 | 2 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0004 | 0/0 | 17 | 0 | 2 | 13 | 0 | 2 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0006 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0002 | 0/0 | 43 | 1 | 1 | 36 | 0 | 5 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0005 | 0/0 | 7 | 0 | 5 | 2 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0003g0011 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0004g0012 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0004g0013 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0004g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0004g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0005g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0005g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0006g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0006g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0006g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0006g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0007g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0007g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0007g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0008g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0008g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0009g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0010g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0011g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0011g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0012g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0012g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0013g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0014g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0015g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0016g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0017g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0018g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0019g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0020g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0021g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0022g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0023g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0024g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0025g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0026g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0027g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0028g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0029g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0030g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0031g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0032g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0001t0033g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0005t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0001c0006t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0002c0003t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| a0003c0004t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0130 | EUR | GBR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | GBR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00140 | hp1 | a0001 | c0001 | t0011 | g0108 | EUR | GBR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0030 | EUR | FIN | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0032 | EUR | FIN | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00323 | hp2 | a0001 | c0001 | t0011 | g0002 | EUR | FIN | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0018 | EAS | CHS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00597 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | CHS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | CHS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01168 | hp2 | a0001 | c0001 | t0030 | g0132 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0013 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01256 | hp2 | a0001 | c0001 | t0024 | g0017 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01496 | hp1 | a0001 | c0001 | t0017 | g0055 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0013 | EUR | IBS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0129 | EUR | IBS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0124 | EUR | IBS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0013 | EUR | IBS | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01884 | hp1 | a0001 | c0001 | t0033 | g0167 | AFR | ACB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01975 | hp2 | a0001 | c0001 | t0020 | g0164 | AMR | PEL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PEL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02055 | hp1 | a0001 | c0001 | t0025 | g0170 | AFR | ACB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | KHV | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02074 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | KHV | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | KHV | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02080 | hp2 | a0001 | c0001 | t0006 | g0127 | EAS | KHV | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02083 | hp1 | a0001 | c0001 | t0019 | g0003 | EAS | KHV | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02129 | hp2 | a0001 | c0001 | t0028 | g0122 | EAS | KHV | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | KHV | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02155 | hp1 | a0001 | c0001 | t0005 | g0112 | EAS | CDX | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | CDX | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02165 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | CDX | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0133 | AFR | ACB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0027 | AFR | ACB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02886 | hp1 | a0001 | c0001 | t0014 | g0012 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0044 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | ESN | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | ESN | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02970 | hp1 | a0001 | c0001 | t0009 | g0026 | AFR | ESN | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | MSL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03130 | hp1 | a0001 | c0001 | t0012 | g0076 | AFR | ESN | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | ESN | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0134 | AFR | ESN | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0026 | AFR | ESN | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03195 | hp2 | a0001 | c0001 | t0031 | g0090 | AFR | ESN | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | MSL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03225 | hp1 | a0001 | c0001 | t0026 | g0091 | AFR | MSL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | MSL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0027 | AFR | MSL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | MSL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0034 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0034 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03516 | hp1 | a0001 | c0001 | t0012 | g0077 | AFR | ESN | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | MSL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0128 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0131 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | STU | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | STU | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03704 | hp2 | a0001 | c0001 | t0006 | g0030 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03710 | hp2 | a0001 | c0001 | t0018 | g0003 | SAS | PJL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG04184 | hp1 | a0001 | c0001 | t0006 | g0031 | SAS | BEB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG04204 | hp2 | a0001 | c0001 | t0016 | g0015 | SAS | STU | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18612 | hp2 | a0001 | c0001 | t0005 | g0126 | EAS | CHB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18906 | hp1 | a0001 | c0001 | t0013 | g0109 | AFR | YRI | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18947 | hp2 | a0001 | c0005 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18949 | hp2 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18950 | hp1 | a0001 | c0001 | t0032 | g0060 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18956 | hp1 | a0001 | c0001 | t0021 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18961 | hp2 | a0001 | c0001 | t0008 | g0080 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18962 | hp1 | a0001 | c0006 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18963 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0031 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18966 | hp2 | a0001 | c0001 | t0029 | g0162 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18986 | hp1 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18987 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18993 | hp2 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | LWK | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | LWK | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19064 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19078 | hp1 | a0001 | c0001 | t0022 | g0110 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19087 | hp1 | a0001 | c0001 | t0006 | g0121 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | YRI | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0032 | EUR | TSI | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA20905 | hp1 | a0001 | c0001 | t0023 | g0015 | SAS | GIH | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | GIH | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02109 | hp2 | a0003 | c0004 | t0001 | g0064 | AFR | ACB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0028 | AFR | ACB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG03471 | hp2 | a0001 | c0001 | t0015 | g0086 | AFR | MSL | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0028 | AFR | USA | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | USA | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | USA | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | USA | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0141 | AFR | LWK | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| NA21309 | hp2 | a0001 | c0001 | t0027 | g0169 | AFR | LWK | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0003 | REF | REF | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0012 | REF | REF | CD28_chr2_203701639_203743912 | CD28 | chr2 | 203701639 | 203743912 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:203726852 | G | A | 1 | a0003 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.272G>A | p.Gly91Asp | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/4 | 330/4721 | 272/663 | 91/220 | chr2 | 203726852 | |||
| chr2:203734841 | C | T | 1 | a0002 | 2 | HG00597.hp2 NA19064.hp1 |
missense_variant | MODERATE | c.592C>T | p.Arg198Cys | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 650/4721 | 592/663 | 198/220 | chr2 | 203734841 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:203726790 | G | A | 1 | a0001c0002 | 2 | HG01070.hp2 HG01071.hp2 |
synonymous_variant | LOW | c.210G>A | p.Gly70Gly | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/4 | 268/4721 | 210/663 | 70/220 | chr2 | 203726790 | |||
| chr2:203729679 | C | A | 1 | a0001c0005 | 1 | NA18947.hp2 | synonymous_variant | LOW | c.441C>A | p.Pro147Pro | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/4 | 499/4721 | 441/663 | 147/220 | chr2 | 203729679 | |||
| chr2:203729688 | T | G | 1 | a0001c0006 | 1 | NA18962.hp1 | synonymous_variant | LOW | c.450T>G | p.Ser150Ser | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/4 | 508/4721 | 450/663 | 150/220 | chr2 | 203729688 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:203735088 | A | C | 1 | a0001c0001t0033 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*176A>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 176 | chr2 | 203735088 | ||||||
| chr2:203735265 | G | A | 1 | a0001c0001t0013 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*353G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 353 | chr2 | 203735265 | ||||||
| chr2:203735426 | A | C | 1 | a0001c0001t0032 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*514A>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 514 | chr2 | 203735426 | ||||||
| chr2:203735533 | C | T | 1 | a0001c0001t0031 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*621C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 621 | chr2 | 203735533 | ||||||
| chr2:203735734 | G | T | 7 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(4): Show |
41 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*822G>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 822 | chr2 | 203735734 | ||||||
| chr2:203735772 | T | G | 2 | a0001c0001t0005 a0001c0001t0027 |
11 | HG00438.hp1 HG00609.hp1 HG02071.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*860T>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 860 | chr2 | 203735772 | ||||||
| chr2:203735902 | A | G | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(33): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
3_prime_UTR_variant | MODIFIER | c.*990A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 990 | chr2 | 203735902 | ||||||
| chr2:203735957 | G | A | 1 | a0001c0001t0005 | 10 | HG00438.hp1 HG00609.hp1 HG02071.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1045G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 1045 | chr2 | 203735957 | ||||||
| chr2:203735980 | C | T | 2 | a0001c0001t0025 a0001c0001t0026 |
2 | HG02055.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1068C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 1068 | chr2 | 203735980 | ||||||
| chr2:203735987 | G | A | 1 | a0001c0001t0015 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1075G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 1075 | chr2 | 203735987 | ||||||
| chr2:203736007 | C | CCAACAA | 1 | a0001c0001t0009 | 3 | HG02886.hp2 HG02970.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1095_*1096insCAAC others(2): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 1096 | chr2 | 203736007 | ||||||
| chr2:203736007 | C | CCAACAAC others(5): Show |
2 | a0001c0001t0006 a0001c0001t0028 |
10 | HG00280.hp1 HG00323.hp1 HG02080.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1095_*1096insCAAC others(8): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 1096 | chr2 | 203736007 | ||||||
| chr2:203736007 | C | CCAACAAC others(8): Show |
1 | a0001c0001t0003 | 18 | HG00099.hp1 HG00735.hp2 HG01099.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1095_*1096insCAAC others(11): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 1096 | chr2 | 203736007 | ||||||
| chr2:203736007 | C | CCAACAAC others(11): Show |
1 | a0001c0001t0029 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1095_*1096insCAAC others(14): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 1096 | chr2 | 203736007 | ||||||
| chr2:203736007 | C | CCAACAAC others(14): Show |
1 | a0001c0001t0030 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1095_*1096insCAAC others(17): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 1096 | chr2 | 203736007 | ||||||
| chr2:203736008 | A | AAAC | 2 | a0001c0001t0007 a0001c0001t0024 |
6 | HG01256.hp2 HG02074.hp1 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1126_*1128dupCAA | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 1129 | INFO_REALIGN_3_PRIME | chr2 | 203736008 | |||||
| chr2:203736008 | A | C | 8 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0009 others(5): Show |
36 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1096A>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 1096 | chr2 | 203736008 | ||||||
| chr2:203736008 | AAAC | A | 2 | a0001c0001t0005 a0001c0001t0027 |
11 | HG00438.hp1 HG00609.hp1 HG02071.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1126_*1128delCAA | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 1126 | INFO_REALIGN_3_PRIME | chr2 | 203736008 | |||||
| chr2:203736621 | G | C | 2 | a0001c0001t0025 a0001c0001t0026 |
2 | HG02055.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1709G>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 1709 | chr2 | 203736621 | ||||||
| chr2:203736638 | C | T | 2 | a0001c0001t0009 a0001c0001t0033 |
4 | HG01884.hp1 HG02886.hp2 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1726C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 1726 | chr2 | 203736638 | ||||||
| chr2:203736701 | C | T | 1 | a0001c0001t0023 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1789C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 1789 | chr2 | 203736701 | ||||||
| chr2:203736878 | A | G | 1 | a0001c0001t0011 | 2 | HG00140.hp1 HG00323.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1966A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 1966 | chr2 | 203736878 | ||||||
| chr2:203737054 | A | G | 2 | a0001c0001t0009 a0001c0001t0033 |
4 | HG01884.hp1 HG02886.hp2 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2142A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 2142 | chr2 | 203737054 | ||||||
| chr2:203737067 | T | C | 1 | a0001c0001t0016 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2155T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 2155 | chr2 | 203737067 | ||||||
| chr2:203737137 | T | A | 1 | a0001c0001t0009 | 3 | HG02886.hp2 HG02970.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2225T>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 2225 | chr2 | 203737137 | ||||||
| chr2:203737185 | C | T | 1 | a0001c0001t0028 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2273C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 2273 | chr2 | 203737185 | ||||||
| chr2:203737187 | G | T | 5 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0022 others(2): Show |
94 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*2275G>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 2275 | chr2 | 203737187 | ||||||
| chr2:203737404 | A | C | 1 | a0001c0001t0021 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2492A>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 2492 | chr2 | 203737404 | ||||||
| chr2:203737430 | C | CT | 8 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(5): Show |
43 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2526dupT | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 2527 | INFO_REALIGN_3_PRIME | chr2 | 203737430 | |||||
| chr2:203737488 | GA | G | 6 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0022 others(3): Show |
95 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*2581delA | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 2581 | INFO_REALIGN_3_PRIME | chr2 | 203737488 | |||||
| chr2:203737636 | C | T | 1 | a0001c0001t0033 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2724C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 2724 | chr2 | 203737636 | ||||||
| chr2:203737912 | G | A | 1 | a0001c0001t0017 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3000G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 3000 | chr2 | 203737912 | ||||||
| chr2:203738028 | A | C | 1 | a0001c0001t0012 | 2 | HG03130.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3116A>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 3116 | chr2 | 203738028 | ||||||
| chr2:203738089 | C | T | 1 | a0001c0001t0020 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3177C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 3177 | chr2 | 203738089 | ||||||
| chr2:203738191 | C | T | 1 | a0001c0001t0019 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3279C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 3279 | chr2 | 203738191 | ||||||
| chr2:203738206 | G | C | 5 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0028 others(2): Show |
30 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3294G>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 3294 | chr2 | 203738206 | ||||||
| chr2:203738224 | C | T | 1 | a0001c0001t0026 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3312C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 3312 | chr2 | 203738224 | ||||||
| chr2:203738309 | G | A | 2 | a0001c0001t0005 a0001c0001t0027 |
11 | HG00438.hp1 HG00609.hp1 HG02071.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3397G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 3397 | chr2 | 203738309 | ||||||
| chr2:203738473 | G | A | 1 | a0001c0001t0010 | 2 | NA18949.hp2 NA18993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3561G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 3561 | chr2 | 203738473 | ||||||
| chr2:203738493 | T | G | 1 | a0001c0001t0014 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3581T>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 3581 | chr2 | 203738493 | ||||||
| chr2:203738518 | G | T | 1 | a0001c0001t0018 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3606G>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 3606 | chr2 | 203738518 | ||||||
| chr2:203738537 | A | G | 1 | a0001c0001t0022 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3625A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 3625 | chr2 | 203738537 | ||||||
| chr2:203738598 | C | T | 2 | a0001c0001t0009 a0001c0001t0033 |
4 | HG01884.hp1 HG02886.hp2 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3686C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 3686 | chr2 | 203738598 | ||||||
| chr2:203738782 | A | G | 1 | a0001c0001t0031 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3870A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 3870 | chr2 | 203738782 | ||||||
| chr2:203738908 | G | C | 1 | a0001c0001t0008 | 3 | NA18961.hp2 NA18963.hp1 NA18987.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3996G>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 4/4 | 3996 | chr2 | 203738908 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:203706985 | A | T | 2 | a0001c0001t0025g0170 a0001c0001t0027g0169 |
2 | HG02055.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.52+237A>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203706985 | |||||||
| chr2:203707028 | G | T | 1 | a0001c0001t0002g0168 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.52+280G>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203707028 | |||||||
| chr2:203707059 | G | A | 1 | a0001c0001t0001g0020 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.52+311G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203707059 | |||||||
| chr2:203707186 | T | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(59): Show |
135 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.52+438T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203707186 | |||||||
| chr2:203707283 | G | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(133): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.52+535G>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203707283 | |||||||
| chr2:203707311 | C | G | 7 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0081 others(4): Show |
11 | HG00099.hp2 HG01069.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.52+563C>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203707311 | |||||||
| chr2:203707334 | A | T | 62 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(59): Show |
135 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.52+586A>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203707334 | |||||||
| chr2:203707346 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.52+598G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203707346 | |||||||
| chr2:203707417 | A | C | 27 | a0001c0001t0002g0017 a0001c0001t0002g0119 a0001c0001t0002g0123 others(24): Show |
40 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.52+669A>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203707417 | |||||||
| chr2:203707417 | A | T | 2 | a0001c0001t0006g0133 a0001c0001t0006g0134 |
2 | HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.52+669A>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203707417 | |||||||
| chr2:203707522 | T | C | 1 | a0001c0001t0015g0086 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.52+774T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203707522 | |||||||
| chr2:203707544 | T | G | 1 | a0001c0001t0001g0135 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.52+796T>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203707544 | |||||||
| chr2:203707552 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
8 | HG02145.hp1 HG02293.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.52+804G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203707552 | |||||||
| chr2:203707742 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.52+994G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203707742 | |||||||
| chr2:203707930 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.52+1182G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203707930 | |||||||
| chr2:203707954 | G | C | 2 | a0001c0001t0001g0043 a0001c0001t0031g0090 |
2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.52+1206G>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203707954 | |||||||
| chr2:203707954 | G | T | 49 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0087 others(46): Show |
116 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.52+1206G>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203707954 | |||||||
| chr2:203707997 | T | A | 3 | a0001c0001t0001g0165 a0001c0001t0015g0086 a0001c0001t0031g0090 |
3 | HG02976.hp2 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.52+1249T>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203707997 | |||||||
| chr2:203707998 | G | A | 1 | a0001c0001t0002g0099 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.52+1250G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203707998 | |||||||
| chr2:203708336 | C | A | 2 | a0001c0001t0001g0045 a0001c0001t0009g0044 |
2 | HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.52+1588C>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203708336 | |||||||
| chr2:203708453 | A | C | 1 | a0001c0001t0020g0164 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.52+1705A>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203708453 | |||||||
| chr2:203708480 | G | A | 1 | a0001c0001t0004g0033 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.52+1732G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203708480 | |||||||
| chr2:203708519 | A | T | 1 | a0001c0001t0002g0163 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.52+1771A>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203708519 | |||||||
| chr2:203708579 | A | G | 33 | a0001c0001t0001g0084 a0001c0001t0002g0017 a0001c0001t0002g0119 others(30): Show |
46 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.52+1831A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203708579 | |||||||
| chr2:203708595 | A | G | 1 | a0001c0001t0027g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.52+1847A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203708595 | |||||||
| chr2:203708644 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0159 a0001c0001t0001g0160 others(1): Show |
7 | HG02615.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+1896A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203708644 | |||||||
| chr2:203708659 | T | A | 1 | a0001c0001t0001g0046 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.52+1911T>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203708659 | |||||||
| chr2:203708669 | C | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(67): Show |
151 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.52+1921C>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203708669 | |||||||
| chr2:203708925 | G | A | 1 | a0001c0001t0026g0091 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.52+2177G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203708925 | |||||||
| chr2:203708927 | C | T | 1 | a0001c0001t0027g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.52+2179C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203708927 | |||||||
| chr2:203709040 | T | A | 2 | a0001c0001t0007g0027 a0001c0001t0007g0028 |
4 | HG02451.hp2 HG02486.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+2292T>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203709040 | |||||||
| chr2:203709046 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0083 |
3 | HG00099.hp2 HG01069.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.52+2298C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203709046 | |||||||
| chr2:203709109 | C | CA | 63 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0049 others(60): Show |
119 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.52+2376dupA | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 203709109 | ||||||
| chr2:203709109 | C | CAA | 5 | a0001c0001t0002g0005 a0001c0001t0002g0092 a0001c0001t0002g0100 others(2): Show |
11 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.52+2375_52+2376dup others(2): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 203709109 | ||||||
| chr2:203709109 | C | CAAA | 3 | a0001c0001t0001g0006 a0001c0001t0001g0087 a0001c0001t0001g0088 |
7 | HG02145.hp1 HG02293.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+2374_52+2376dup others(3): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 203709109 | ||||||
| chr2:203709364 | G | T | 1 | a0001c0001t0002g0094 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.52+2616G>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203709364 | |||||||
| chr2:203709704 | T | C | 1 | a0001c0001t0031g0090 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.52+2956T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203709704 | |||||||
| chr2:203709874 | G | A | 3 | a0001c0001t0003g0116 a0001c0001t0003g0117 a0001c0001t0029g0162 |
3 | NA18966.hp2 NA19002.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.52+3126G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203709874 | |||||||
| chr2:203709966 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0160 a0001c0001t0001g0161 |
6 | HG02615.hp2 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+3218C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203709966 | |||||||
| chr2:203710121 | G | C | 5 | a0001c0001t0001g0048 a0001c0001t0001g0102 a0001c0001t0001g0136 others(2): Show |
5 | HG02055.hp1 HG03516.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+3373G>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203710121 | |||||||
| chr2:203710167 | T | C | 29 | a0001c0001t0001g0084 a0001c0001t0002g0017 a0001c0001t0002g0119 others(26): Show |
36 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.52+3419T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203710167 | |||||||
| chr2:203710290 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0087 a0001c0001t0001g0088 |
7 | HG02145.hp1 HG02293.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+3542C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203710290 | |||||||
| chr2:203710398 | T | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0087 a0001c0001t0001g0088 |
7 | HG02145.hp1 HG02293.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+3650T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203710398 | |||||||
| chr2:203710976 | CT | C | 1 | a0001c0001t0005g0018 | 3 | HG00438.hp1 NA18970.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.52+4229delT | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203710976 | |||||||
| chr2:203711228 | A | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.52+4480A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203711228 | |||||||
| chr2:203711264 | T | G | 1 | a0001c0001t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.52+4516T>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203711264 | |||||||
| chr2:203711358 | A | G | 1 | a0001c0001t0008g0080 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.52+4610A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203711358 | |||||||
| chr2:203711397 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.52+4649C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203711397 | |||||||
| chr2:203711489 | A | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0096 others(1): Show |
6 | HG02809.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+4741A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203711489 | |||||||
| chr2:203712053 | G | A | 34 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0084 others(31): Show |
43 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.52+5305G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203712053 | |||||||
| chr2:203712194 | C | CAA | 2 | a0001c0001t0007g0027 a0001c0001t0007g0028 |
4 | HG02451.hp2 HG02486.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+5447_52+5448dup others(2): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 203712194 | ||||||
| chr2:203712197 | C | A | 29 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0043 others(26): Show |
41 | HG00280.hp1 HG01081.hp2 HG01256.hp2 others(38): Show |
intron_variant | MODIFIER | c.52+5449C>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203712197 | |||||||
| chr2:203712200 | C | A | 39 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0043 others(36): Show |
54 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.52+5452C>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203712200 | |||||||
| chr2:203712200 | C | CA | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(85): Show |
208 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.52+5460dupA | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 203712200 | ||||||
| chr2:203712202 | A | AC | 9 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(6): Show |
10 | HG00544.hp1 HG01361.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.52+5454_52+5455ins others(1): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203712202 | |||||||
| chr2:203712203 | A | C | 3 | a0001c0001t0005g0008 a0001c0001t0005g0018 a0001c0001t0005g0126 |
9 | HG00438.hp1 HG00609.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.52+5455A>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203712203 | |||||||
| chr2:203712324 | G | A | 2 | a0001c0001t0006g0133 a0001c0001t0006g0134 |
2 | HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.52+5576G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203712324 | |||||||
| chr2:203712481 | G | A | 34 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0084 others(31): Show |
43 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.52+5733G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203712481 | |||||||
| chr2:203712674 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.52+5926A>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203712674 | |||||||
| chr2:203712686 | G | T | 1 | a0001c0001t0022g0110 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.52+5938G>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203712686 | |||||||
| chr2:203712719 | G | A | 1 | a0001c0001t0017g0055 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.52+5971G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203712719 | |||||||
| chr2:203712806 | A | G | 3 | a0001c0001t0002g0115 a0001c0001t0009g0026 a0001c0001t0009g0044 |
4 | HG02886.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+6058A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203712806 | |||||||
| chr2:203712812 | A | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0087 a0001c0001t0001g0088 |
7 | HG02145.hp1 HG02293.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+6064A>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203712812 | |||||||
| chr2:203712836 | A | G | 34 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0084 others(31): Show |
43 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.52+6088A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203712836 | |||||||
| chr2:203713046 | C | T | 1 | a0001c0001t0003g0131 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.52+6298C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203713046 | |||||||
| chr2:203713182 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(91): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.52+6434C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203713182 | |||||||
| chr2:203713236 | T | C | 1 | a0001c0001t0006g0030 | 2 | HG00280.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.52+6488T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203713236 | |||||||
| chr2:203713548 | A | G | 3 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0078 |
3 | HG01361.hp2 NA19070.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.52+6800A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203713548 | |||||||
| chr2:203713852 | G | GGA | 26 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0019 others(23): Show |
69 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.52+7127_52+7128dup others(2): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 203713852 | ||||||
| chr2:203713852 | G | GGAGA | 4 | a0001c0001t0001g0036 a0001c0001t0001g0153 a0001c0001t0002g0037 others(1): Show |
7 | HG00673.hp2 HG02622.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+7125_52+7128dup others(4): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 203713852 | ||||||
| chr2:203713852 | G | GGAGAGAG others(1): Show |
5 | a0001c0001t0001g0038 a0001c0001t0001g0155 a0001c0001t0002g0154 others(2): Show |
6 | HG02280.hp2 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+7121_52+7128dup others(8): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 203713852 | ||||||
| chr2:203713852 | G | GGAGAGAG others(3): Show |
1 | a0001c0001t0001g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.52+7119_52+7128dup others(10): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 203713852 | ||||||
| chr2:203713852 | GGA | G | 3 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0002g0111 |
3 | NA19030.hp1 NA19078.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.52+7127_52+7128del others(2): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 203713852 | ||||||
| chr2:203713852 | GGAGA | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(58): Show |
134 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.52+7125_52+7128del others(4): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 203713852 | ||||||
| chr2:203713873 | G | C | 35 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0089 others(32): Show |
46 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.52+7125G>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203713873 | |||||||
| chr2:203713875 | GAC | G | 35 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0089 others(32): Show |
46 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.52+7129_52+7130del others(2): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 203713875 | ||||||
| chr2:203713877 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.52+7129C>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203713877 | |||||||
| chr2:203713879 | G | C | 1 | a0001c0001t0001g0142 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.52+7131G>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203713879 | |||||||
| chr2:203713886 | A | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0089 others(5): Show |
12 | HG01884.hp1 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.52+7138A>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203713886 | |||||||
| chr2:203713888 | A | T | 40 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0043 others(37): Show |
56 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.52+7140A>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203713888 | |||||||
| chr2:203713935 | G | T | 1 | a0001c0001t0015g0086 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.52+7187G>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203713935 | |||||||
| chr2:203714074 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.52+7326A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203714074 | |||||||
| chr2:203714098 | G | A | 2 | a0001c0001t0002g0047 a0001c0001t0002g0168 |
2 | HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.52+7350G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203714098 | |||||||
| chr2:203714315 | T | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG01433.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.52+7567T>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203714315 | |||||||
| chr2:203714390 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.52+7642T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203714390 | |||||||
| chr2:203714496 | CCT | C | 27 | a0001c0001t0002g0017 a0001c0001t0002g0119 a0001c0001t0002g0123 others(24): Show |
34 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.52+7753_52+7754del others(2): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 203714496 | ||||||
| chr2:203714616 | A | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0083 |
3 | HG00099.hp2 HG01069.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.52+7868A>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203714616 | |||||||
| chr2:203714654 | A | G | 2 | a0001c0001t0007g0027 a0001c0001t0007g0028 |
4 | HG02451.hp2 HG02486.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+7906A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203714654 | |||||||
| chr2:203714711 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0166 |
2 | NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.52+7963G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203714711 | |||||||
| chr2:203714731 | A | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0087 a0001c0001t0001g0088 |
7 | HG02145.hp1 HG02293.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+7983A>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203714731 | |||||||
| chr2:203714877 | T | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.52+8129T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203714877 | |||||||
| chr2:203715064 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.52+8316G>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203715064 | |||||||
| chr2:203715072 | C | G | 1 | a0001c0001t0003g0124 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.52+8324C>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203715072 | |||||||
| chr2:203715130 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.52+8382G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203715130 | |||||||
| chr2:203715357 | A | C | 2 | a0001c0001t0007g0027 a0001c0001t0007g0028 |
4 | HG02451.hp2 HG02486.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+8609A>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203715357 | |||||||
| chr2:203715399 | T | A | 1 | a0001c0001t0006g0133 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.52+8651T>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203715399 | |||||||
| chr2:203715410 | A | T | 1 | a0001c0001t0002g0101 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.52+8662A>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203715410 | |||||||
| chr2:203715531 | G | C | 2 | a0001c0001t0007g0027 a0001c0001t0007g0028 |
4 | HG02451.hp2 HG02486.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+8783G>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203715531 | |||||||
| chr2:203715579 | G | T | 1 | a0001c0001t0007g0028 | 2 | HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.52+8831G>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203715579 | |||||||
| chr2:203715811 | G | A | 1 | a0001c0001t0017g0055 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.52+9063G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203715811 | |||||||
| chr2:203715830 | C | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0089 others(3): Show |
8 | HG01884.hp1 HG02559.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.52+9082C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203715830 | |||||||
| chr2:203715960 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.52+9212T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203715960 | |||||||
| chr2:203716050 | A | G | 2 | a0001c0001t0003g0116 a0001c0001t0003g0117 |
2 | NA19002.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.52+9302A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203716050 | |||||||
| chr2:203716104 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.52+9356A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203716104 | |||||||
| chr2:203716251 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.52+9503C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203716251 | |||||||
| chr2:203716472 | A | G | 33 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0096 others(30): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.52+9724A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203716472 | |||||||
| chr2:203716491 | GA | G | 2 | a0001c0001t0007g0027 a0001c0001t0007g0028 |
4 | HG02451.hp2 HG02486.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+9745delA | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 203716491 | ||||||
| chr2:203716510 | G | A | 1 | a0001c0001t0026g0091 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.52+9762G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203716510 | |||||||
| chr2:203716542 | C | T | 1 | a0001c0001t0003g0130 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.52+9794C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203716542 | |||||||
| chr2:203716949 | G | C | 3 | a0001c0001t0002g0115 a0001c0001t0009g0026 a0001c0001t0009g0044 |
4 | HG02886.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-9684G>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203716949 | |||||||
| chr2:203717055 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.53-9578C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203717055 | |||||||
| chr2:203717492 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.53-9141C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203717492 | |||||||
| chr2:203717667 | A | C | 1 | a0001c0001t0001g0042 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.53-8966A>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203717667 | |||||||
| chr2:203717900 | T | C | 26 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(23): Show |
79 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.53-8733T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203717900 | |||||||
| chr2:203717922 | T | C | 2 | a0001c0001t0007g0027 a0001c0001t0007g0028 |
4 | HG02451.hp2 HG02486.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-8711T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203717922 | |||||||
| chr2:203717956 | T | C | 33 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0096 others(30): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.53-8677T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203717956 | |||||||
| chr2:203718070 | A | T | 1 | a0001c0001t0001g0088 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.53-8563A>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203718070 | |||||||
| chr2:203718361 | G | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0096 others(2): Show |
7 | HG01884.hp1 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-8272G>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203718361 | |||||||
| chr2:203718440 | G | A | 33 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0096 others(30): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.53-8193G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203718440 | |||||||
| chr2:203718628 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.53-8005A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203718628 | |||||||
| chr2:203718837 | A | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0087 others(5): Show |
14 | HG01884.hp1 HG02145.hp1 HG02293.hp2 others(11): Show |
intron_variant | MODIFIER | c.53-7796A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203718837 | |||||||
| chr2:203718874 | T | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.53-7759T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203718874 | |||||||
| chr2:203719100 | A | G | 1 | a0001c0001t0011g0108 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.53-7533A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203719100 | |||||||
| chr2:203719244 | C | CT | 42 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0043 others(39): Show |
57 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.53-7382dupT | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 203719244 | ||||||
| chr2:203719362 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.53-7271A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203719362 | |||||||
| chr2:203719392 | T | C | 1 | a0001c0001t0002g0025 | 2 | NA18944.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.53-7241T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203719392 | |||||||
| chr2:203719406 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.53-7227C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203719406 | |||||||
| chr2:203719413 | A | G | 1 | a0001c0001t0033g0167 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.53-7220A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203719413 | |||||||
| chr2:203719449 | A | G | 7 | a0001c0001t0001g0016 a0001c0001t0001g0089 a0001c0001t0001g0096 others(4): Show |
11 | HG01884.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-7184A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203719449 | |||||||
| chr2:203719596 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
5 | HG00642.hp2 HG01069.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-7037T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203719596 | |||||||
| chr2:203719657 | G | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.53-6976G>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203719657 | |||||||
| chr2:203719733 | A | T | 30 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(27): Show |
84 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.53-6900A>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203719733 | |||||||
| chr2:203720036 | T | C | 36 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(33): Show |
96 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.53-6597T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203720036 | |||||||
| chr2:203720168 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.53-6465A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203720168 | |||||||
| chr2:203720277 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.53-6356C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203720277 | |||||||
| chr2:203720318 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.53-6315G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203720318 | |||||||
| chr2:203720470 | A | G | 5 | a0001c0001t0001g0043 a0001c0001t0007g0027 a0001c0001t0007g0028 others(2): Show |
7 | HG01884.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.53-6163A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203720470 | |||||||
| chr2:203720719 | A | T | 5 | a0001c0001t0001g0043 a0001c0001t0007g0027 a0001c0001t0007g0028 others(2): Show |
7 | HG01884.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.53-5914A>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203720719 | |||||||
| chr2:203720779 | T | C | 33 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(30): Show |
40 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.53-5854T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203720779 | |||||||
| chr2:203720834 | C | T | 3 | a0001c0001t0002g0115 a0001c0001t0009g0026 a0001c0001t0009g0044 |
4 | HG02886.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-5799C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203720834 | |||||||
| chr2:203720994 | A | G | 1 | a0001c0001t0002g0107 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.53-5639A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203720994 | |||||||
| chr2:203721219 | A | G | 2 | a0001c0001t0007g0027 a0001c0001t0007g0028 |
4 | HG02451.hp2 HG02486.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-5414A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203721219 | |||||||
| chr2:203721233 | T | A | 36 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0007 others(33): Show |
96 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.53-5400T>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203721233 | |||||||
| chr2:203721313 | G | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0089 others(3): Show |
8 | HG01884.hp2 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.53-5320G>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203721313 | |||||||
| chr2:203721314 | C | G | 32 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(29): Show |
39 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.53-5319C>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203721314 | |||||||
| chr2:203721353 | G | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(129): Show |
316 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.53-5280G>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203721353 | |||||||
| chr2:203721462 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.53-5171C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203721462 | |||||||
| chr2:203721505 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.53-5128C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203721505 | |||||||
| chr2:203721571 | C | A | 1 | a0001c0001t0004g0034 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.53-5062C>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203721571 | |||||||
| chr2:203721666 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.53-4967C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203721666 | |||||||
| chr2:203721792 | G | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0041 a0001c0001t0001g0042 others(15): Show |
36 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.53-4841G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203721792 | |||||||
| chr2:203721868 | C | T | 3 | a0001c0001t0002g0115 a0001c0001t0009g0026 a0001c0001t0009g0044 |
4 | HG02886.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-4765C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203721868 | |||||||
| chr2:203721953 | C | T | 27 | a0001c0001t0002g0017 a0001c0001t0002g0119 a0001c0001t0002g0123 others(24): Show |
34 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.53-4680C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203721953 | |||||||
| chr2:203722073 | C | T | 1 | a0001c0001t0002g0114 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.53-4560C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203722073 | |||||||
| chr2:203722309 | A | G | 1 | a0001c0001t0002g0107 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.53-4324A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203722309 | |||||||
| chr2:203722418 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.53-4215A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203722418 | |||||||
| chr2:203722439 | G | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.53-4194G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203722439 | |||||||
| chr2:203722546 | C | A | 36 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0052 others(33): Show |
45 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.53-4087C>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203722546 | |||||||
| chr2:203722639 | G | T | 5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
5 | HG02109.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-3994G>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203722639 | |||||||
| chr2:203723145 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.53-3488A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203723145 | |||||||
| chr2:203723266 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.53-3367C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203723266 | |||||||
| chr2:203723312 | C | A | 3 | a0001c0001t0001g0043 a0001c0001t0015g0086 a0001c0001t0033g0167 |
3 | HG01884.hp1 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.53-3321C>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203723312 | |||||||
| chr2:203723489 | TA | T | 62 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(59): Show |
137 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.53-3132delA | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 203723489 | ||||||
| chr2:203723492 | A | T | 1 | a0001c0001t0001g0166 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.53-3141A>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203723492 | |||||||
| chr2:203723616 | A | C | 1 | a0001c0001t0026g0091 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.53-3017A>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203723616 | |||||||
| chr2:203723659 | A | G | 33 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(30): Show |
40 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.53-2974A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203723659 | |||||||
| chr2:203723749 | C | T | 1 | a0001c0001t0002g0105 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.53-2884C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203723749 | |||||||
| chr2:203723757 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.53-2876G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203723757 | |||||||
| chr2:203723804 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.53-2829T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203723804 | |||||||
| chr2:203724055 | A | C | 1 | a0001c0001t0001g0148 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.53-2578A>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203724055 | |||||||
| chr2:203724144 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.53-2489C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203724144 | |||||||
| chr2:203724199 | T | C | 2 | a0001c0001t0007g0027 a0001c0001t0007g0028 |
4 | HG02451.hp2 HG02486.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-2434T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203724199 | |||||||
| chr2:203724335 | T | TA | 2 | a0001c0001t0007g0027 a0001c0001t0007g0028 |
4 | HG02451.hp2 HG02486.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-2292dupA | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 203724335 | ||||||
| chr2:203724538 | C | T | 1 | a0001c0001t0025g0170 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.53-2095C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203724538 | |||||||
| chr2:203724558 | G | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
326 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.53-2075G>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203724558 | |||||||
| chr2:203724756 | A | C | 1 | a0001c0001t0009g0044 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.53-1877A>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203724756 | |||||||
| chr2:203724794 | A | G | 4 | a0001c0001t0001g0043 a0001c0001t0007g0027 a0001c0001t0007g0028 others(1): Show |
6 | HG02451.hp2 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-1839A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203724794 | |||||||
| chr2:203724858 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.53-1775C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203724858 | |||||||
| chr2:203725014 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.53-1619G>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203725014 | |||||||
| chr2:203725017 | G | A | 1 | a0003c0004t0001g0064 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.53-1616G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203725017 | |||||||
| chr2:203725028 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0007g0027 a0001c0001t0007g0028 others(1): Show |
6 | HG02451.hp2 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-1605C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203725028 | |||||||
| chr2:203725047 | T | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.53-1586T>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203725047 | |||||||
| chr2:203725221 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.53-1412C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203725221 | |||||||
| chr2:203725245 | G | A | 2 | a0001c0001t0007g0027 a0001c0001t0007g0028 |
4 | HG02451.hp2 HG02486.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-1388G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203725245 | |||||||
| chr2:203725277 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.53-1356C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203725277 | |||||||
| chr2:203725285 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
211 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.53-1348C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203725285 | |||||||
| chr2:203725293 | GA | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
317 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.53-1325delA | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 203725293 | ||||||
| chr2:203725348 | C | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.53-1285C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203725348 | |||||||
| chr2:203725387 | T | G | 4 | a0001c0001t0001g0043 a0001c0001t0007g0027 a0001c0001t0007g0028 others(1): Show |
6 | HG02451.hp2 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-1246T>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203725387 | |||||||
| chr2:203725489 | G | GA | 38 | a0001c0001t0001g0043 a0001c0001t0002g0002 a0001c0001t0002g0005 others(35): Show |
98 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.53-1133dupA | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 203725489 | ||||||
| chr2:203725517 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.53-1116G>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203725517 | |||||||
| chr2:203725612 | T | A | 27 | a0001c0001t0002g0017 a0001c0001t0002g0119 a0001c0001t0002g0123 others(24): Show |
34 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.53-1021T>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203725612 | |||||||
| chr2:203725690 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0015g0086 |
2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.53-943T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203725690 | |||||||
| chr2:203725744 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.53-889C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203725744 | |||||||
| chr2:203725845 | AT | A | 27 | a0001c0001t0002g0017 a0001c0001t0002g0119 a0001c0001t0002g0123 others(24): Show |
34 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.53-787delT | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203725845 | |||||||
| chr2:203725935 | A | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
211 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.53-698A>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203725935 | |||||||
| chr2:203726074 | G | A | 1 | a0001c0001t0001g0009 | 4 | HG02071.hp2 NA18948.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-559G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203726074 | |||||||
| chr2:203726276 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.53-357A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203726276 | |||||||
| chr2:203726322 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.53-311A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203726322 | |||||||
| chr2:203726324 | T | A | 1 | a0001c0001t0001g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.53-309T>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203726324 | |||||||
| chr2:203726423 | T | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0087 a0001c0001t0001g0088 |
7 | HG02145.hp1 HG02293.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.53-210T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203726423 | |||||||
| chr2:203726430 | A | C | 27 | a0001c0001t0002g0017 a0001c0001t0002g0119 a0001c0001t0002g0123 others(24): Show |
34 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.53-203A>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203726430 | |||||||
| chr2:203726443 | T | C | 5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
5 | HG02109.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-190T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203726443 | |||||||
| chr2:203726444 | G | A | 5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
5 | HG02109.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-189G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203726444 | |||||||
| chr2:203726500 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.53-133G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203726500 | |||||||
| chr2:203726534 | T | C | 3 | a0001c0001t0002g0115 a0001c0001t0009g0026 a0001c0001t0009g0044 |
4 | HG02886.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-99T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203726534 | |||||||
| chr2:203726558 | T | G | 1 | a0001c0001t0027g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.53-75T>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203726558 | |||||||
| chr2:203726606 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.53-27T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 1/3 | chr2 | 203726606 | |||||||
| chr2:203727162 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.409+173G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203727162 | |||||||
| chr2:203727298 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.409+309G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203727298 | |||||||
| chr2:203727389 | C | A | 1 | a0001c0001t0025g0170 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.409+400C>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203727389 | |||||||
| chr2:203727430 | T | TTTCC | 3 | a0001c0001t0001g0138 a0001c0001t0004g0033 a0001c0001t0004g0141 |
4 | HG00438.hp2 HG03098.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.409+476_409+479dup others(4): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 203727430 | ||||||
| chr2:203727430 | T | TTTCCTTC others(5): Show |
8 | a0001c0001t0002g0123 a0001c0001t0003g0011 a0001c0001t0003g0117 others(5): Show |
11 | HG00735.hp2 HG01099.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.409+468_409+479dup others(12): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 203727430 | ||||||
| chr2:203727430 | T | TTTCCTTC others(9): Show |
12 | a0001c0001t0001g0102 a0001c0001t0002g0017 a0001c0001t0003g0032 others(9): Show |
14 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.409+464_409+479dup others(16): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 203727430 | ||||||
| chr2:203727430 | T | TTTCCTTC others(13): Show |
4 | a0001c0001t0002g0119 a0001c0001t0003g0029 a0001c0001t0003g0129 others(1): Show |
6 | HG00280.hp1 HG01358.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.409+460_409+479dup others(20): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 203727430 | ||||||
| chr2:203727430 | T | TTTCCTTC others(17): Show |
4 | a0001c0001t0001g0053 a0001c0001t0001g0166 a0001c0001t0003g0118 others(1): Show |
4 | HG02155.hp2 HG03139.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.409+456_409+479dup others(24): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 203727430 | ||||||
| chr2:203727430 | T | TTTCCTTC others(21): Show |
2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.409+452_409+479dup others(28): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 203727430 | ||||||
| chr2:203727430 | TTTCC | T | 1 | a0001c0001t0004g0013 | 4 | HG01167.hp2 HG01169.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.409+476_409+479del others(4): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 203727430 | ||||||
| chr2:203727442 | C | CTTCT | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.409+456_409+457ins others(4): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 203727442 | ||||||
| chr2:203727535 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.409+546A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203727535 | |||||||
| chr2:203727572 | C | T | 1 | a0001c0001t0002g0104 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.409+583C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203727572 | |||||||
| chr2:203727604 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0007g0027 a0001c0001t0007g0028 others(1): Show |
6 | HG02451.hp2 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.409+615C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203727604 | |||||||
| chr2:203727623 | G | GT | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.409+634_409+635ins others(1): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203727623 | |||||||
| chr2:203727627 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.409+638C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203727627 | |||||||
| chr2:203727686 | AT | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.409+708delT | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 203727686 | ||||||
| chr2:203728090 | G | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.409+1101G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203728090 | |||||||
| chr2:203728214 | C | A | 1 | a0001c0001t0001g0009 | 4 | HG02071.hp2 NA18948.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.409+1225C>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203728214 | |||||||
| chr2:203728400 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.410-1248G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203728400 | |||||||
| chr2:203728555 | G | T | 2 | a0001c0001t0007g0027 a0001c0001t0007g0028 |
4 | HG02451.hp2 HG02486.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.410-1093G>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203728555 | |||||||
| chr2:203728735 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.410-913G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203728735 | |||||||
| chr2:203728764 | C | A | 4 | a0001c0001t0001g0043 a0001c0001t0007g0027 a0001c0001t0007g0028 others(1): Show |
6 | HG02451.hp2 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.410-884C>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203728764 | |||||||
| chr2:203728784 | A | G | 1 | a0001c0001t0033g0167 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.410-864A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203728784 | |||||||
| chr2:203728954 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.410-694A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203728954 | |||||||
| chr2:203729003 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.410-645G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203729003 | |||||||
| chr2:203729082 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.410-566T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203729082 | |||||||
| chr2:203729139 | C | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.410-509C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203729139 | |||||||
| chr2:203729335 | C | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.410-313C>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203729335 | |||||||
| chr2:203729436 | C | T | 5 | a0001c0001t0005g0008 a0001c0001t0005g0018 a0001c0001t0005g0112 others(2): Show |
11 | HG00438.hp1 HG00609.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.410-212C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203729436 | |||||||
| chr2:203729524 | C | G | 3 | a0001c0001t0002g0154 a0001c0001t0002g0156 a0001c0001t0002g0163 |
3 | HG02922.hp1 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.410-124C>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203729524 | |||||||
| chr2:203729597 | C | T | 5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
5 | HG02109.hp1 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.410-51C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 2/3 | chr2 | 203729597 | |||||||
| chr2:203729789 | T | C | 27 | a0001c0001t0003g0011 a0001c0001t0003g0029 a0001c0001t0003g0032 others(24): Show |
39 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.534+17T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203729789 | |||||||
| chr2:203729824 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.534+52T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203729824 | |||||||
| chr2:203729838 | A | G | 1 | a0001c0001t0032g0060 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.534+66A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203729838 | |||||||
| chr2:203729977 | T | C | 1 | a0001c0001t0002g0007 | 5 | NA18968.hp2 NA18971.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.534+205T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203729977 | |||||||
| chr2:203730387 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.534+615G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203730387 | |||||||
| chr2:203730429 | A | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+657A>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203730429 | |||||||
| chr2:203730486 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.534+714C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203730486 | |||||||
| chr2:203730497 | C | A | 24 | a0001c0001t0003g0011 a0001c0001t0003g0029 a0001c0001t0003g0032 others(21): Show |
30 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.534+725C>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203730497 | |||||||
| chr2:203730600 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.534+828A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203730600 | |||||||
| chr2:203730796 | T | C | 23 | a0001c0001t0003g0011 a0001c0001t0003g0029 a0001c0001t0003g0032 others(20): Show |
29 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.534+1024T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203730796 | |||||||
| chr2:203730874 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(143): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.534+1102A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203730874 | |||||||
| chr2:203731108 | CAA | C | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+1338_534+1339d others(4): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 203731108 | ||||||
| chr2:203731498 | C | T | 2 | a0001c0001t0012g0076 a0001c0001t0012g0077 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.534+1726C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203731498 | |||||||
| chr2:203731534 | A | G | 5 | a0001c0001t0005g0008 a0001c0001t0005g0018 a0001c0001t0005g0112 others(2): Show |
11 | HG00438.hp1 HG00609.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.534+1762A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203731534 | |||||||
| chr2:203731698 | C | CTCACTTT others(17): Show |
2 | a0001c0001t0001g0102 a0001c0001t0001g0166 |
2 | NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.534+1937_534+1960d others(26): Show |
CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 203731698 | ||||||
| chr2:203731721 | G | T | 3 | a0001c0001t0001g0015 a0001c0001t0016g0015 a0001c0001t0023g0015 |
3 | HG02738.hp1 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.534+1949G>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203731721 | |||||||
| chr2:203731765 | C | A | 1 | a0001c0001t0001g0019 | 3 | HG02132.hp2 HG02523.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.534+1993C>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203731765 | |||||||
| chr2:203731782 | T | C | 5 | a0001c0001t0005g0008 a0001c0001t0005g0018 a0001c0001t0005g0112 others(2): Show |
11 | HG00438.hp1 HG00609.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.534+2010T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203731782 | |||||||
| chr2:203731852 | C | A | 1 | a0001c0001t0012g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.534+2080C>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203731852 | |||||||
| chr2:203731853 | C | A | 1 | a0001c0001t0012g0076 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.534+2081C>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203731853 | |||||||
| chr2:203731886 | C | G | 1 | a0001c0001t0001g0020 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.534+2114C>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203731886 | |||||||
| chr2:203732006 | A | G | 27 | a0001c0001t0003g0011 a0001c0001t0003g0029 a0001c0001t0003g0032 others(24): Show |
34 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.534+2234A>G | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203732006 | |||||||
| chr2:203732045 | G | C | 5 | a0001c0001t0005g0008 a0001c0001t0005g0018 a0001c0001t0005g0112 others(2): Show |
11 | HG00438.hp1 HG00609.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.534+2273G>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203732045 | |||||||
| chr2:203732073 | T | C | 1 | a0001c0001t0002g0103 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.534+2301T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203732073 | |||||||
| chr2:203732173 | G | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0098 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.534+2401G>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203732173 | |||||||
| chr2:203732310 | G | C | 23 | a0001c0001t0003g0011 a0001c0001t0003g0029 a0001c0001t0003g0032 others(20): Show |
29 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.535-2474G>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203732310 | |||||||
| chr2:203732774 | G | A | 2 | a0001c0001t0025g0170 a0001c0001t0026g0091 |
2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.535-2010G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203732774 | |||||||
| chr2:203732783 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.535-2001C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203732783 | |||||||
| chr2:203732808 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.535-1976C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203732808 | |||||||
| chr2:203732818 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.535-1966G>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203732818 | |||||||
| chr2:203732965 | C | A | 24 | a0001c0001t0003g0011 a0001c0001t0003g0029 a0001c0001t0003g0032 others(21): Show |
30 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.535-1819C>A | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203732965 | |||||||
| chr2:203733011 | C | T | 1 | a0001c0001t0028g0122 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.535-1773C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203733011 | |||||||
| chr2:203733936 | T | C | 2 | a0001c0001t0002g0047 a0001c0001t0002g0168 |
2 | HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.535-848T>C | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203733936 | |||||||
| chr2:203734432 | C | T | 2 | a0001c0001t0009g0026 a0001c0001t0009g0044 |
3 | HG02886.hp2 HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.535-352C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203734432 | |||||||
| chr2:203734642 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.535-142C>T | CD28 | ENSG00000178562.18 | transcript | ENST00000324106.9 | protein_coding | 3/3 | chr2 | 203734642 |