Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 914 |
| ensemblid | ENSG00000116824.5 |
| hgncid | 1639 |
| symbol | CD2 |
| name | CD2 molecule |
| refseq_nuc | NM_001767.5 |
| refseq_prot | NP_001758.2 |
| ensembl_nuc | ENST00000369478.4 |
| ensembl_prot | ENSP00000358490.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 116754430 |
| end | 116769229 |
| strand | + |
| ver | v1.2 |
| region | chr1:116754430-116769229 |
| region5000 | chr1:116749430-116774229 |
| regionname0 | CD2_chr1_116754430_116769229 |
| regionname5000 | CD2_chr1_116749430_116774229 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 351 | 292 | 29 | 51 | 151 | 14 | 45 | 119 | CD2_chr1_116749430_116774229 | CD2 | MSFPC others(346): Show |
chr1 | 116749430 | 116774229 |
| a0002 | 0/0 | 351 | 163 | 65 | 19 | 75 | 2 | 2 | 61 | CD2_chr1_116749430_116774229 | CD2 | MSFPC others(346): Show |
chr1 | 116749430 | 116774229 |
| a0003 | 0/0 | 351 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CD2_chr1_116749430_116774229 | CD2 | MSFPC others(346): Show |
chr1 | 116749430 | 116774229 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1053 | 292 | 29 | 51 | 151 | 14 | 45 | CD2_chr1_116749430_116774229 | CD2 | ATGAG others(1048): Show |
chr1 | 116749430 | 116774229 | ||
| a0002c0002 | 0/0 | 1053 | 156 | 58 | 19 | 75 | 2 | 2 | CD2_chr1_116749430_116774229 | CD2 | ATGAG others(1048): Show |
chr1 | 116749430 | 116774229 | ||
| a0002c0003 | 0/0 | 1053 | 7 | 7 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | ATGAG others(1048): Show |
chr1 | 116749430 | 116774229 | ||
| a0003c0004 | 0/0 | 1053 | 1 | 0 | 0 | 0 | 0 | 1 | CD2_chr1_116749430_116774229 | CD2 | ATGAG others(1048): Show |
chr1 | 116749430 | 116774229 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1565 | 291 | 29 | 51 | 151 | 13 | 45 | CD2_chr1_116749430_116774229 | CD2 | AGTCT others(1560): Show |
chr1 | 116749430 | 116774229 |
| a0001c0001t0005 | 0/0 | 1565 | 1 | 0 | 0 | 0 | 1 | 0 | CD2_chr1_116749430_116774229 | CD2 | AGTCT others(1560): Show |
chr1 | 116749430 | 116774229 |
| a0002c0002t0001 | 0/0 | 1565 | 141 | 55 | 19 | 63 | 2 | 2 | CD2_chr1_116749430_116774229 | CD2 | AGTCT others(1560): Show |
chr1 | 116749430 | 116774229 |
| a0002c0002t0002 | 0/0 | 1565 | 12 | 0 | 0 | 12 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | AGTCT others(1560): Show |
chr1 | 116749430 | 116774229 |
| a0002c0002t0003 | 0/0 | 1565 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | AGTCT others(1560): Show |
chr1 | 116749430 | 116774229 |
| a0002c0002t0004 | 0/0 | 1565 | 2 | 2 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | AGTCT others(1560): Show |
chr1 | 116749430 | 116774229 |
| a0002c0003t0003 | 0/0 | 1565 | 7 | 7 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | AGTCT others(1560): Show |
chr1 | 116749430 | 116774229 |
| a0003c0004t0001 | 0/0 | 1565 | 1 | 0 | 0 | 0 | 0 | 1 | CD2_chr1_116749430_116774229 | CD2 | AGTCT others(1560): Show |
chr1 | 116749430 | 116774229 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 1/0 | 32 | 1 | 7 | 14 | 3 | 6 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0003 | 0/0 | 26 | 1 | 5 | 17 | 1 | 2 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0004 | 0/0 | 24 | 0 | 2 | 18 | 1 | 3 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0005 | 0/0 | 19 | 0 | 4 | 15 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0008 | 0/0 | 10 | 0 | 2 | 5 | 1 | 2 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0009 | 0/0 | 9 | 1 | 5 | 0 | 1 | 2 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0010 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0011 | 0/0 | 8 | 1 | 5 | 0 | 0 | 2 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0012 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0013 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0014 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0015 | 0/1 | 6 | 0 | 2 | 0 | 1 | 2 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0016 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0018 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0024 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0034 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0035 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0037 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0054 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0059 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0001 | 0/0 | 40 | 2 | 6 | 32 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0006 | 0/0 | 12 | 3 | 1 | 5 | 2 | 1 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0007 | 0/0 | 12 | 10 | 2 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0019 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0022 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0023 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0058 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0002g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0002t0004g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0003t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0003t0003g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0003t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0003t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0002c0003t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| a0003c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | GBR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | GBR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0004 | EUR | FIN | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | CHS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | CHS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0092 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0058 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0089 | AMR | CLM | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | CLM | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | CLM | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | CLM | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | CLM | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | IBS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0006 | EUR | IBS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0006 | EUR | IBS | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0157 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01891 | hp2 | a0002 | c0003 | t0003 | g0138 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PEL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0060 | AMR | PEL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0047 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CDX | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CDX | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0115 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02280 | hp2 | a0002 | c0002 | t0004 | g0036 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02451 | hp1 | a0002 | c0003 | t0003 | g0148 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02451 | hp2 | a0002 | c0003 | t0003 | g0044 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0106 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0041 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02622 | hp1 | a0002 | c0003 | t0003 | g0137 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0155 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0109 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0047 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02723 | hp1 | a0002 | c0002 | t0003 | g0066 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0154 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02809 | hp2 | a0002 | c0003 | t0003 | g0044 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0150 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02896 | hp1 | a0002 | c0003 | t0003 | g0043 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0041 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02897 | hp1 | a0002 | c0003 | t0003 | g0043 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | ESN | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0073 | AFR | ESN | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0117 | AFR | ESN | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0099 | AFR | ESN | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0078 | AFR | MSL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0149 | AFR | MSL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | ESN | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0045 | AFR | ESN | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0140 | AFR | ESN | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | MSL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | MSL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | MSL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | MSL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0071 | AFR | MSL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0067 | AFR | MSL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0152 | AFR | GWD | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | MSL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03710 | hp2 | a0003 | c0004 | t0001 | g0070 | SAS | PJL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0061 | SAS | BEB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | STU | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | STU | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | YRI | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | CHB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0091 | AFR | YRI | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | LWK | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19075 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0124 | AFR | ASW | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ASW | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | GIH | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0045 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02486 | hp2 | a0002 | c0002 | t0004 | g0036 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | ACB | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | USA | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | USA | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0015 | REF | REF | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | CD2_chr1_116749430_116774229 | CD2 | chr1 | 116749430 | 116774229 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:116768525 | C | A | 1 | a0002 | 163 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(160): Show |
missense_variant | MODERATE | c.798C>A | p.His266Gln | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 5/5 | 861/1565 | 798/1056 | 266/351 | chr1 | 116768525 | |||
| chr1:116768769 | C | T | 1 | a0003 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.1042C>T | p.Pro348Ser | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 5/5 | 1105/1565 | 1042/1056 | 348/351 | chr1 | 116768769 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:116768672 | G | A | 1 | a0002c0003 | 7 | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(4): Show |
synonymous_variant | LOW | c.945G>A | p.Pro315Pro | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 5/5 | 1008/1565 | 945/1056 | 315/351 | chr1 | 116768672 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:116768815 | G | C | 1 | a0002c0002t0004 | 2 | HG02280.hp2 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*32G>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 5/5 | 32 | chr1 | 116768815 | ||||||
| chr1:116768915 | C | T | 1 | a0002c0002t0002 | 12 | NA18944.hp1 NA18950.hp1 NA18964.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*132C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 5/5 | 132 | chr1 | 116768915 | ||||||
| chr1:116769011 | G | A | 2 | a0002c0002t0003 a0002c0003t0003 |
8 | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*228G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 5/5 | 228 | chr1 | 116769011 | ||||||
| chr1:116769189 | A | G | 1 | a0001c0001t0005 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*406A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 5/5 | 406 | chr1 | 116769189 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:116755080 | A | G | 1 | a0002c0002t0001g0157 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.382+129A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116755080 | |||||||
| chr1:116755112 | A | G | 20 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0035 others(17): Show |
29 | HG00280.hp1 HG01123.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.382+161A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116755112 | |||||||
| chr1:116755115 | C | A | 2 | a0001c0001t0001g0020 a0002c0002t0001g0060 |
5 | HG01993.hp2 NA18953.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.382+164C>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116755115 | |||||||
| chr1:116755162 | A | G | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(48): Show |
152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.382+211A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116755162 | |||||||
| chr1:116755164 | A | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0156 a0002c0002t0001g0154 others(2): Show |
7 | HG01884.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.382+213A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116755164 | |||||||
| chr1:116755305 | T | C | 2 | a0001c0001t0001g0051 a0002c0002t0001g0061 |
3 | HG02698.hp1 HG02738.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.382+354T>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116755305 | |||||||
| chr1:116755351 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0052 others(6): Show |
34 | HG00423.hp2 HG00438.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.382+400G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116755351 | |||||||
| chr1:116755406 | G | A | 1 | a0001c0001t0001g0016 | 5 | HG01106.hp2 HG01261.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.382+455G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116755406 | |||||||
| chr1:116755420 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0110 |
4 | HG02074.hp2 NA18975.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+469A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116755420 | |||||||
| chr1:116755654 | G | A | 2 | a0002c0002t0001g0067 a0002c0002t0003g0066 |
2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.382+703G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116755654 | |||||||
| chr1:116755717 | G | A | 2 | a0001c0001t0001g0051 a0002c0002t0001g0061 |
3 | HG02698.hp1 HG02738.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.382+766G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116755717 | |||||||
| chr1:116755855 | G | A | 1 | a0002c0002t0001g0021 | 4 | HG02109.hp1 HG02145.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.382+904G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116755855 | |||||||
| chr1:116755902 | C | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0113 |
2 | HG03654.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.382+951C>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116755902 | |||||||
| chr1:116756054 | C | T | 23 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0016 others(20): Show |
51 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.382+1103C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116756054 | |||||||
| chr1:116756188 | G | C | 1 | a0001c0001t0001g0069 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.382+1237G>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116756188 | |||||||
| chr1:116756216 | G | C | 1 | a0002c0002t0004g0036 | 2 | HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.382+1265G>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116756216 | |||||||
| chr1:116756217 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.382+1266G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116756217 | |||||||
| chr1:116756232 | G | A | 1 | a0002c0002t0001g0022 | 4 | HG02257.hp2 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+1281G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116756232 | |||||||
| chr1:116756233 | C | T | 1 | a0002c0002t0001g0022 | 4 | HG02257.hp2 HG03130.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+1282C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116756233 | |||||||
| chr1:116756271 | A | G | 21 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0052 others(18): Show |
58 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.382+1320A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116756271 | |||||||
| chr1:116756341 | GCATTTAG others(2372): Show |
G | 3 | a0001c0001t0001g0100 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG02698.hp2 HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.382+1608_383-1465d others(2): Show |
CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 116756341 | ||||||
| chr1:116756798 | A | G | 41 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0027 others(38): Show |
122 | HG00140.hp1 HG00609.hp1 HG00735.hp1 others(119): Show |
intron_variant | MODIFIER | c.382+1847A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116756798 | |||||||
| chr1:116756850 | G | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(85): Show |
243 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(240): Show |
intron_variant | MODIFIER | c.382+1899G>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116756850 | |||||||
| chr1:116756969 | C | T | 2 | a0002c0002t0001g0025 a0002c0002t0001g0140 |
4 | HG02055.hp2 HG02818.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+2018C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116756969 | |||||||
| chr1:116756987 | TTC | T | 4 | a0001c0001t0001g0016 a0002c0002t0001g0109 a0002c0002t0001g0149 others(1): Show |
4 | HG01993.hp1 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.382+2040_382+2041d others(4): Show |
CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 116756987 | ||||||
| chr1:116756989 | CTCT | C | 20 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0016 others(17): Show |
47 | HG00733.hp1 HG01070.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.382+2040_382+2042d others(5): Show |
CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 116756989 | ||||||
| chr1:116756991 | CT | C | 17 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(14): Show |
21 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.382+2059delT | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 116756991 | ||||||
| chr1:116756993 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.382+2042T>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116756993 | |||||||
| chr1:116757031 | C | G | 1 | a0001c0001t0001g0005 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.382+2080C>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116757031 | |||||||
| chr1:116757095 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.382+2144C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116757095 | |||||||
| chr1:116757125 | T | C | 1 | a0002c0002t0001g0006 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.382+2174T>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116757125 | |||||||
| chr1:116757153 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382+2202C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116757153 | |||||||
| chr1:116757502 | C | T | 2 | a0002c0002t0001g0001 a0002c0002t0003g0066 |
7 | HG02723.hp1 NA18961.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.382+2551C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116757502 | |||||||
| chr1:116757503 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.382+2552G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116757503 | |||||||
| chr1:116757687 | G | A | 1 | a0001c0001t0001g0017 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.383-2715G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116757687 | |||||||
| chr1:116757740 | C | CAT | 11 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0037 others(8): Show |
24 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.383-2650_383-2649d others(4): Show |
CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 116757740 | ||||||
| chr1:116757750 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.383-2652T>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116757750 | |||||||
| chr1:116757750 | T | TAG | 3 | a0001c0001t0001g0048 a0002c0002t0001g0047 a0002c0002t0001g0150 |
3 | HG01978.hp1 HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.383-2651_383-2650i others(4): Show |
CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 116757750 | ||||||
| chr1:116757752 | T | G | 44 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(41): Show |
82 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.383-2650T>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116757752 | |||||||
| chr1:116757752 | T | TAG | 14 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(11): Show |
24 | HG00280.hp2 HG01070.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.383-2627_383-2626d others(4): Show |
CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 116757752 | ||||||
| chr1:116757754 | G | T | 57 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(54): Show |
149 | HG00408.hp2 HG00597.hp2 HG00609.hp1 others(146): Show |
intron_variant | MODIFIER | c.383-2648G>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116757754 | |||||||
| chr1:116757756 | G | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0127 others(9): Show |
29 | HG02109.hp1 HG02129.hp2 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.383-2646G>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116757756 | |||||||
| chr1:116757758 | G | T | 3 | a0002c0002t0001g0001 a0002c0002t0001g0021 a0002c0002t0001g0022 |
8 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.383-2644G>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116757758 | |||||||
| chr1:116757770 | G | A | 2 | a0002c0002t0001g0045 a0002c0002t0001g0149 |
3 | HG02109.hp2 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.383-2632G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116757770 | |||||||
| chr1:116757777 | G | A | 22 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0016 others(19): Show |
46 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.383-2625G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116757777 | |||||||
| chr1:116757915 | G | A | 2 | a0002c0002t0001g0007 a0002c0002t0001g0091 |
2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.383-2487G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116757915 | |||||||
| chr1:116758012 | G | A | 1 | a0002c0002t0001g0071 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.383-2390G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116758012 | |||||||
| chr1:116758211 | C | G | 1 | a0001c0001t0001g0011 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.383-2191C>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116758211 | |||||||
| chr1:116758243 | C | T | 1 | a0001c0001t0001g0002 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.383-2159C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116758243 | |||||||
| chr1:116758304 | G | A | 40 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0001g0088 others(37): Show |
126 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(123): Show |
intron_variant | MODIFIER | c.383-2098G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116758304 | |||||||
| chr1:116758367 | C | A | 1 | a0002c0002t0001g0041 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.383-2035C>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116758367 | |||||||
| chr1:116758421 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.383-1981C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116758421 | |||||||
| chr1:116758586 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.383-1816C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116758586 | |||||||
| chr1:116758596 | A | G | 2 | a0002c0002t0001g0021 a0002c0002t0001g0076 |
5 | HG02109.hp1 HG02132.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.383-1806A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116758596 | |||||||
| chr1:116758656 | G | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0052 others(3): Show |
10 | HG02647.hp2 HG02895.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.383-1746G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116758656 | |||||||
| chr1:116758678 | G | A | 2 | a0002c0002t0001g0109 a0002c0002t0003g0066 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.383-1724G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116758678 | |||||||
| chr1:116758720 | A | G | 22 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(19): Show |
65 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.383-1682A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116758720 | |||||||
| chr1:116758931 | TGGCAAGG others(28): Show |
T | 1 | a0003c0004t0001g0070 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.383-1470_383-1436d others(37): Show |
CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116758931 | |||||||
| chr1:116758963 | A | G | 22 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(19): Show |
65 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.383-1439A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116758963 | |||||||
| chr1:116759158 | G | A | 1 | a0002c0002t0001g0071 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.383-1244G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116759158 | |||||||
| chr1:116759191 | T | G | 1 | a0002c0002t0002g0072 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.383-1211T>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116759191 | |||||||
| chr1:116759257 | T | C | 2 | a0002c0002t0001g0025 a0002c0002t0001g0140 |
4 | HG02055.hp2 HG02818.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-1145T>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116759257 | |||||||
| chr1:116759374 | A | C | 2 | a0002c0002t0001g0071 a0002c0002t0001g0099 |
2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.383-1028A>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116759374 | |||||||
| chr1:116759428 | GA | G | 38 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0093 others(35): Show |
120 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(117): Show |
intron_variant | MODIFIER | c.383-962delA | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 116759428 | ||||||
| chr1:116759591 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.383-811A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116759591 | |||||||
| chr1:116759745 | G | T | 2 | a0002c0002t0001g0030 a0002c0002t0001g0130 |
4 | NA18967.hp2 NA18973.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-657G>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116759745 | |||||||
| chr1:116759761 | A | T | 1 | a0001c0001t0001g0086 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.383-641A>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116759761 | |||||||
| chr1:116759821 | C | A | 1 | a0001c0001t0001g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.383-581C>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116759821 | |||||||
| chr1:116759877 | C | A | 1 | a0002c0002t0001g0073 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.383-525C>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116759877 | |||||||
| chr1:116759920 | C | A | 1 | a0002c0002t0001g0124 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.383-482C>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116759920 | |||||||
| chr1:116759991 | A | G | 40 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0069 others(37): Show |
127 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(124): Show |
intron_variant | MODIFIER | c.383-411A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116759991 | |||||||
| chr1:116760089 | A | G | 2 | a0002c0002t0001g0033 a0002c0002t0001g0042 |
5 | NA18940.hp1 NA18951.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.383-313A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116760089 | |||||||
| chr1:116760121 | G | A | 21 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0016 others(18): Show |
48 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.383-281G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116760121 | |||||||
| chr1:116760253 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.383-149A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116760253 | |||||||
| chr1:116760366 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.383-36T>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 2/4 | chr1 | 116760366 | |||||||
| chr1:116760749 | A | G | 1 | a0002c0003t0003g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.613+117A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116760749 | |||||||
| chr1:116760778 | C | T | 21 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0016 others(18): Show |
48 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.613+146C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116760778 | |||||||
| chr1:116760875 | C | T | 62 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(59): Show |
190 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(187): Show |
intron_variant | MODIFIER | c.613+243C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116760875 | |||||||
| chr1:116760915 | G | A | 1 | a0002c0002t0001g0089 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.613+283G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116760915 | |||||||
| chr1:116761129 | G | A | 1 | a0002c0002t0001g0149 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.613+497G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116761129 | |||||||
| chr1:116761294 | G | C | 2 | a0002c0002t0001g0071 a0002c0002t0001g0099 |
2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.613+662G>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116761294 | |||||||
| chr1:116761478 | G | A | 86 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(83): Show |
247 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(244): Show |
intron_variant | MODIFIER | c.613+846G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116761478 | |||||||
| chr1:116761561 | G | A | 1 | a0002c0002t0001g0090 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.613+929G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116761561 | |||||||
| chr1:116761610 | C | T | 1 | a0002c0002t0001g0067 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.613+978C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116761610 | |||||||
| chr1:116761674 | C | A | 1 | a0001c0001t0001g0143 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.613+1042C>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116761674 | |||||||
| chr1:116761740 | G | A | 1 | a0002c0002t0001g0126 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.613+1108G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116761740 | |||||||
| chr1:116761812 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.613+1180A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116761812 | |||||||
| chr1:116761883 | T | G | 2 | a0002c0002t0001g0045 a0002c0002t0001g0149 |
3 | HG02109.hp2 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.613+1251T>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116761883 | |||||||
| chr1:116761926 | G | A | 1 | a0002c0002t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.613+1294G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116761926 | |||||||
| chr1:116762049 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.613+1417C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116762049 | |||||||
| chr1:116762115 | T | C | 88 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(85): Show |
252 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(249): Show |
intron_variant | MODIFIER | c.613+1483T>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116762115 | |||||||
| chr1:116762120 | G | C | 1 | a0002c0002t0001g0067 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.613+1488G>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116762120 | |||||||
| chr1:116762308 | T | C | 1 | a0002c0002t0001g0150 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.613+1676T>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116762308 | |||||||
| chr1:116762309 | G | C | 1 | a0002c0002t0001g0150 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.613+1677G>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116762309 | |||||||
| chr1:116762310 | G | T | 1 | a0002c0002t0001g0150 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.613+1678G>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116762310 | |||||||
| chr1:116762311 | A | ATTTTTCA others(5): Show |
1 | a0002c0002t0001g0150 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.613+1679_613+1680i others(14): Show |
CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116762311 | |||||||
| chr1:116762312 | G | A | 1 | a0002c0002t0001g0150 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.613+1680G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116762312 | |||||||
| chr1:116762313 | C | T | 1 | a0002c0002t0001g0150 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.613+1681C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116762313 | |||||||
| chr1:116762314 | C | A | 1 | a0002c0002t0001g0150 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.613+1682C>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116762314 | |||||||
| chr1:116762432 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.613+1800A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116762432 | |||||||
| chr1:116762454 | C | T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(39): Show |
112 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.613+1822C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116762454 | |||||||
| chr1:116762517 | C | T | 2 | a0002c0002t0001g0021 a0002c0002t0001g0076 |
5 | HG02109.hp1 HG02132.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.613+1885C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116762517 | |||||||
| chr1:116762595 | G | C | 1 | a0002c0002t0001g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.614-1889G>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116762595 | |||||||
| chr1:116762661 | A | C | 36 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0127 others(33): Show |
122 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(119): Show |
intron_variant | MODIFIER | c.614-1823A>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116762661 | |||||||
| chr1:116762667 | A | C | 51 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(48): Show |
129 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.614-1817A>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116762667 | |||||||
| chr1:116762754 | T | G | 1 | a0002c0002t0001g0152 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.614-1730T>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116762754 | |||||||
| chr1:116762919 | T | C | 5 | a0002c0002t0001g0007 a0002c0002t0001g0041 a0002c0002t0001g0091 others(2): Show |
17 | HG01109.hp2 HG01175.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.614-1565T>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116762919 | |||||||
| chr1:116762960 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.614-1524G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116762960 | |||||||
| chr1:116763001 | G | C | 1 | a0001c0001t0001g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.614-1483G>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116763001 | |||||||
| chr1:116763089 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | NA19003.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.614-1395C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116763089 | |||||||
| chr1:116763198 | G | T | 1 | a0001c0001t0001g0144 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.614-1286G>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116763198 | |||||||
| chr1:116763294 | C | T | 15 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0016 others(12): Show |
41 | HG00733.hp1 HG01070.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.614-1190C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116763294 | |||||||
| chr1:116763356 | T | C | 2 | a0002c0002t0001g0071 a0002c0002t0001g0099 |
2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.614-1128T>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116763356 | |||||||
| chr1:116763391 | G | A | 1 | a0002c0002t0001g0076 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.614-1093G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116763391 | |||||||
| chr1:116763509 | C | T | 34 | a0001c0001t0001g0097 a0002c0002t0001g0001 a0002c0002t0001g0006 others(31): Show |
120 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(117): Show |
intron_variant | MODIFIER | c.614-975C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116763509 | |||||||
| chr1:116763544 | C | T | 1 | a0001c0001t0001g0040 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.614-940C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116763544 | |||||||
| chr1:116763860 | C | T | 5 | a0002c0003t0003g0043 a0002c0003t0003g0044 a0002c0003t0003g0137 others(2): Show |
7 | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.614-624C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116763860 | |||||||
| chr1:116763872 | G | A | 2 | a0002c0002t0001g0025 a0002c0002t0001g0140 |
4 | HG02055.hp2 HG02818.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.614-612G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116763872 | |||||||
| chr1:116763967 | C | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0116 |
2 | HG00140.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.614-517C>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116763967 | |||||||
| chr1:116764018 | C | T | 1 | a0002c0002t0001g0098 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.614-466C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116764018 | |||||||
| chr1:116764019 | G | GAGAGCAG others(28): Show |
1 | a0003c0004t0001g0070 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.614-452_614-451ins others(35): Show |
CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 116764019 | ||||||
| chr1:116764130 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.614-354A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116764130 | |||||||
| chr1:116764167 | A | C | 2 | a0001c0001t0001g0083 a0001c0001t0001g0088 |
2 | HG03710.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.614-317A>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116764167 | |||||||
| chr1:116764243 | T | C | 1 | a0001c0001t0001g0046 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.614-241T>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116764243 | |||||||
| chr1:116764331 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.614-153C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 3/4 | chr1 | 116764331 | |||||||
| chr1:116764633 | G | A | 6 | a0002c0002t0003g0066 a0002c0003t0003g0043 a0002c0003t0003g0044 others(3): Show |
8 | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.736+27G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116764633 | |||||||
| chr1:116764735 | G | A | 1 | a0002c0002t0001g0071 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.736+129G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116764735 | |||||||
| chr1:116764736 | T | C | 61 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(58): Show |
159 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(156): Show |
intron_variant | MODIFIER | c.736+130T>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116764736 | |||||||
| chr1:116764740 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.736+134C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116764740 | |||||||
| chr1:116764993 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.736+387A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116764993 | |||||||
| chr1:116765086 | T | C | 2 | a0002c0002t0001g0022 a0002c0002t0001g0106 |
5 | HG02257.hp2 HG02572.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.736+480T>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116765086 | |||||||
| chr1:116765194 | G | A | 1 | a0002c0002t0001g0152 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.736+588G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116765194 | |||||||
| chr1:116765264 | G | T | 1 | a0002c0002t0001g0071 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.736+658G>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116765264 | |||||||
| chr1:116765266 | G | C | 11 | a0001c0001t0001g0013 a0001c0001t0001g0031 a0001c0001t0001g0057 others(8): Show |
22 | HG00423.hp1 HG00438.hp2 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.736+660G>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116765266 | |||||||
| chr1:116765295 | C | T | 5 | a0002c0003t0003g0043 a0002c0003t0003g0044 a0002c0003t0003g0137 others(2): Show |
7 | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.736+689C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116765295 | |||||||
| chr1:116765296 | G | A | 1 | a0002c0002t0001g0094 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.736+690G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116765296 | |||||||
| chr1:116765343 | G | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0119 others(7): Show |
21 | HG00558.hp1 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.736+737G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116765343 | |||||||
| chr1:116765343 | G | T | 2 | a0002c0002t0001g0021 a0002c0002t0001g0076 |
5 | HG02109.hp1 HG02132.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.736+737G>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116765343 | |||||||
| chr1:116765539 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736+933C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116765539 | |||||||
| chr1:116765566 | C | A | 2 | a0002c0002t0001g0022 a0002c0002t0001g0106 |
5 | HG02257.hp2 HG02572.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.736+960C>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116765566 | |||||||
| chr1:116765616 | A | C | 42 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(39): Show |
131 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(128): Show |
intron_variant | MODIFIER | c.736+1010A>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116765616 | |||||||
| chr1:116765618 | C | G | 1 | a0002c0002t0001g0099 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.736+1012C>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116765618 | |||||||
| chr1:116765620 | C | T | 6 | a0002c0002t0003g0066 a0002c0003t0003g0043 a0002c0003t0003g0044 others(3): Show |
8 | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.736+1014C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116765620 | |||||||
| chr1:116765692 | T | A | 1 | a0001c0001t0001g0121 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.736+1086T>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116765692 | |||||||
| chr1:116765694 | C | G | 1 | a0001c0001t0001g0108 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.736+1088C>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116765694 | |||||||
| chr1:116765920 | A | C | 1 | a0001c0001t0001g0056 | 2 | NA18990.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.736+1314A>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116765920 | |||||||
| chr1:116766036 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.736+1430C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116766036 | |||||||
| chr1:116766153 | G | T | 3 | a0002c0002t0001g0047 a0002c0002t0001g0150 a0002c0002t0001g0155 |
4 | HG02055.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.736+1547G>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116766153 | |||||||
| chr1:116766191 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.736+1585C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116766191 | |||||||
| chr1:116766208 | T | A | 42 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(39): Show |
131 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(128): Show |
intron_variant | MODIFIER | c.736+1602T>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116766208 | |||||||
| chr1:116766231 | G | A | 2 | a0002c0002t0001g0045 a0002c0002t0001g0149 |
3 | HG02109.hp2 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.736+1625G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116766231 | |||||||
| chr1:116766550 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0039 others(6): Show |
23 | HG00558.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.737-1914G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116766550 | |||||||
| chr1:116766568 | T | C | 9 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0053 others(6): Show |
21 | HG00438.hp1 HG02015.hp1 HG02523.hp1 others(18): Show |
intron_variant | MODIFIER | c.737-1896T>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116766568 | |||||||
| chr1:116766622 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.737-1842G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116766622 | |||||||
| chr1:116766695 | T | TA | 6 | a0002c0002t0001g0045 a0002c0002t0001g0047 a0002c0002t0001g0128 others(3): Show |
8 | HG02055.hp1 HG02109.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.737-1759dupA | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 116766695 | ||||||
| chr1:116766774 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.737-1690A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116766774 | |||||||
| chr1:116766857 | G | C | 1 | a0002c0002t0001g0067 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.737-1607G>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116766857 | |||||||
| chr1:116766991 | G | A | 4 | a0002c0002t0001g0021 a0002c0002t0001g0067 a0002c0002t0001g0076 others(1): Show |
7 | HG02109.hp1 HG02132.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.737-1473G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116766991 | |||||||
| chr1:116767018 | T | C | 1 | a0002c0002t0001g0152 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.737-1446T>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116767018 | |||||||
| chr1:116767034 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0048 a0001c0001t0001g0114 |
8 | HG01106.hp2 HG01261.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.737-1430A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116767034 | |||||||
| chr1:116767067 | A | T | 1 | a0002c0002t0001g0140 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.737-1397A>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116767067 | |||||||
| chr1:116767245 | A | T | 1 | a0001c0001t0001g0040 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.737-1219A>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116767245 | |||||||
| chr1:116767321 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.737-1143C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116767321 | |||||||
| chr1:116767344 | AGCACTTT others(5): Show |
A | 6 | a0002c0002t0003g0066 a0002c0003t0003g0043 a0002c0003t0003g0044 others(3): Show |
8 | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.737-1117_737-1106d others(14): Show |
CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 116767344 | ||||||
| chr1:116767385 | A | G | 40 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(37): Show |
124 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(121): Show |
intron_variant | MODIFIER | c.737-1079A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116767385 | |||||||
| chr1:116767390 | G | A | 1 | a0002c0003t0003g0043 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.737-1074G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116767390 | |||||||
| chr1:116767417 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0133 |
2 | NA19002.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.737-1047C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116767417 | |||||||
| chr1:116767429 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.737-1035T>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116767429 | |||||||
| chr1:116767447 | C | T | 1 | a0002c0002t0001g0041 | 2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.737-1017C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116767447 | |||||||
| chr1:116767448 | G | A | 1 | a0002c0002t0001g0091 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.737-1016G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116767448 | |||||||
| chr1:116767467 | T | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0121 a0001c0001t0001g0134 |
8 | NA18939.hp2 NA18943.hp1 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.737-997T>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116767467 | |||||||
| chr1:116767497 | A | G | 1 | a0002c0002t0003g0066 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.737-967A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116767497 | |||||||
| chr1:116767513 | C | T | 5 | a0002c0002t0001g0045 a0002c0002t0001g0047 a0002c0002t0001g0149 others(2): Show |
7 | HG02055.hp1 HG02109.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.737-951C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116767513 | |||||||
| chr1:116767546 | G | A | 1 | a0002c0002t0001g0071 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.737-918G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116767546 | |||||||
| chr1:116767591 | CA | C | 22 | a0001c0001t0001g0055 a0001c0001t0001g0063 a0001c0001t0001g0083 others(19): Show |
35 | HG00558.hp1 HG01496.hp1 HG01515.hp1 others(32): Show |
intron_variant | MODIFIER | c.737-856delA | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 116767591 | ||||||
| chr1:116767591 | CAA | C | 6 | a0002c0002t0003g0066 a0002c0003t0003g0043 a0002c0003t0003g0044 others(3): Show |
8 | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.737-857_737-856del others(2): Show |
CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 116767591 | ||||||
| chr1:116767666 | T | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(17): Show |
64 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.737-798T>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116767666 | |||||||
| chr1:116767674 | C | T | 60 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0007 others(57): Show |
156 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(153): Show |
intron_variant | MODIFIER | c.737-790C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116767674 | |||||||
| chr1:116767920 | G | T | 6 | a0002c0002t0003g0066 a0002c0003t0003g0043 a0002c0003t0003g0044 others(3): Show |
8 | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.737-544G>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116767920 | |||||||
| chr1:116767932 | T | C | 1 | a0002c0002t0001g0095 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.737-532T>C | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116767932 | |||||||
| chr1:116767940 | G | A | 1 | a0002c0002t0001g0096 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.737-524G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116767940 | |||||||
| chr1:116768027 | A | G | 2 | a0002c0002t0001g0022 a0002c0002t0001g0106 |
5 | HG02257.hp2 HG02572.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.737-437A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116768027 | |||||||
| chr1:116768080 | C | T | 3 | a0002c0002t0001g0019 a0002c0002t0001g0060 a0002c0002t0001g0089 |
7 | HG00738.hp1 HG01255.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.737-384C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116768080 | |||||||
| chr1:116768136 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.737-328G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116768136 | |||||||
| chr1:116768170 | C | T | 1 | a0002c0002t0001g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.737-294C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116768170 | |||||||
| chr1:116768179 | C | T | 1 | a0002c0002t0001g0067 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.737-285C>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116768179 | |||||||
| chr1:116768180 | G | A | 1 | a0002c0002t0001g0092 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.737-284G>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116768180 | |||||||
| chr1:116768224 | C | G | 1 | a0001c0001t0001g0153 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.737-240C>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116768224 | |||||||
| chr1:116768257 | C | A | 1 | a0002c0002t0002g0129 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.737-207C>A | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116768257 | |||||||
| chr1:116768312 | A | T | 1 | a0001c0001t0001g0082 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.737-152A>T | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116768312 | |||||||
| chr1:116768392 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.737-72A>G | CD2 | ENSG00000116824.5 | transcript | ENST00000369478.4 | protein_coding | 4/4 | chr1 | 116768392 |