Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 822 |
| ensemblid | ENSG00000042493.16 |
| hgncid | 1474 |
| symbol | CAPG |
| name | capping actin protein, gelsolin like |
| refseq_nuc | NM_001747.4 |
| refseq_prot | NP_001738.2 |
| ensembl_nuc | ENST00000263867.9 |
| ensembl_prot | ENSP00000263867.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 85394753 |
| end | 85410366 |
| strand | - |
| ver | v1.2 |
| region | chr2:85394753-85410366 |
| region5000 | chr2:85389753-85415366 |
| regionname0 | CAPG_chr2_85394753_85410366 |
| regionname5000 | CAPG_chr2_85389753_85415366 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 348 | 205 | 61 | 24 | 91 | 7 | 21 | 71 | CAPG_chr2_85389753_85415366 | CAPG | MYTAI others(343): Show |
chr2 | 85389753 | 85415366 |
| a0002 | 1/0 | 348 | 162 | 21 | 44 | 68 | 6 | 22 | 54 | CAPG_chr2_85389753_85415366 | CAPG | MYTAI others(343): Show |
chr2 | 85389753 | 85415366 |
| a0003 | 0/0 | 348 | 29 | 6 | 7 | 7 | 4 | 5 | 6 | CAPG_chr2_85389753_85415366 | CAPG | MYTAI others(343): Show |
chr2 | 85389753 | 85415366 |
| a0004 | 0/0 | 348 | 11 | 0 | 0 | 11 | 0 | 0 | 6 | CAPG_chr2_85389753_85415366 | CAPG | MYTAI others(343): Show |
chr2 | 85389753 | 85415366 |
| a0005 | 0/0 | 348 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | MYTAI others(343): Show |
chr2 | 85389753 | 85415366 |
| a0006 | 0/0 | 348 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | MYTAI others(343): Show |
chr2 | 85389753 | 85415366 |
| a0007 | 0/0 | 7 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | MCGGW others(2): Show |
chr2 | 85389753 | 85415366 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/1 | 1044 | 139 | 31 | 17 | 76 | 3 | 11 | CAPG_chr2_85389753_85415366 | CAPG | ATGTA others(1039): Show |
chr2 | 85389753 | 85415366 | ||
| a0001c0003 | 0/0 | 1044 | 65 | 29 | 7 | 15 | 4 | 10 | CAPG_chr2_85389753_85415366 | CAPG | ATGTA others(1039): Show |
chr2 | 85389753 | 85415366 | ||
| a0001c0010 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | ATGTA others(1039): Show |
chr2 | 85389753 | 85415366 | ||
| a0002c0001 | 1/0 | 1044 | 161 | 21 | 43 | 68 | 6 | 22 | CAPG_chr2_85389753_85415366 | CAPG | ATGTA others(1039): Show |
chr2 | 85389753 | 85415366 | ||
| a0002c0011 | 0/0 | 1044 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | ATGTA others(1039): Show |
chr2 | 85389753 | 85415366 | ||
| a0003c0004 | 0/0 | 1044 | 19 | 6 | 5 | 5 | 1 | 2 | CAPG_chr2_85389753_85415366 | CAPG | ATGTA others(1039): Show |
chr2 | 85389753 | 85415366 | ||
| a0003c0006 | 0/0 | 1044 | 9 | 0 | 1 | 2 | 3 | 3 | CAPG_chr2_85389753_85415366 | CAPG | ATGTA others(1039): Show |
chr2 | 85389753 | 85415366 | ||
| a0003c0008 | 0/0 | 1044 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | ATGTA others(1039): Show |
chr2 | 85389753 | 85415366 | ||
| a0004c0005 | 0/0 | 1044 | 11 | 0 | 0 | 11 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | ATGTA others(1039): Show |
chr2 | 85389753 | 85415366 | ||
| a0005c0009 | 0/0 | 1044 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | ATGTA others(1039): Show |
chr2 | 85389753 | 85415366 | ||
| a0006c0012 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | ATGTA others(1039): Show |
chr2 | 85389753 | 85415366 | ||
| a0007c0007 | 0/0 | 1044 | 1 | 0 | 0 | 0 | 1 | 0 | CAPG_chr2_85389753_85415366 | CAPG | ATATA others(1039): Show |
chr2 | 85389753 | 85415366 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/1 | 1250 | 139 | 31 | 17 | 76 | 3 | 11 | CAPG_chr2_85389753_85415366 | CAPG | GAGAA others(1245): Show |
chr2 | 85389753 | 85415366 |
| a0001c0003t0001 | 0/0 | 1250 | 63 | 27 | 7 | 15 | 4 | 10 | CAPG_chr2_85389753_85415366 | CAPG | GAGAA others(1245): Show |
chr2 | 85389753 | 85415366 |
| a0001c0003t0002 | 0/0 | 1250 | 2 | 2 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | GAGAA others(1245): Show |
chr2 | 85389753 | 85415366 |
| a0001c0010t0001 | 0/0 | 1250 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | GAGAA others(1245): Show |
chr2 | 85389753 | 85415366 |
| a0002c0001t0001 | 1/0 | 1250 | 161 | 21 | 43 | 68 | 6 | 22 | CAPG_chr2_85389753_85415366 | CAPG | GAGAA others(1245): Show |
chr2 | 85389753 | 85415366 |
| a0002c0011t0001 | 0/0 | 1250 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | GAGAA others(1245): Show |
chr2 | 85389753 | 85415366 |
| a0003c0004t0001 | 0/0 | 1250 | 19 | 6 | 5 | 5 | 1 | 2 | CAPG_chr2_85389753_85415366 | CAPG | GAGAA others(1245): Show |
chr2 | 85389753 | 85415366 |
| a0003c0006t0001 | 0/0 | 1250 | 9 | 0 | 1 | 2 | 3 | 3 | CAPG_chr2_85389753_85415366 | CAPG | GAGAA others(1245): Show |
chr2 | 85389753 | 85415366 |
| a0003c0008t0001 | 0/0 | 1250 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | GAGAA others(1245): Show |
chr2 | 85389753 | 85415366 |
| a0004c0005t0001 | 0/0 | 1250 | 11 | 0 | 0 | 11 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | GAGAA others(1245): Show |
chr2 | 85389753 | 85415366 |
| a0005c0009t0001 | 0/0 | 1250 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | GAGAA others(1245): Show |
chr2 | 85389753 | 85415366 |
| a0006c0012t0001 | 0/0 | 1250 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | GAGAA others(1245): Show |
chr2 | 85389753 | 85415366 |
| a0007c0007t0001 | 0/0 | 1250 | 1 | 0 | 0 | 0 | 1 | 0 | CAPG_chr2_85389753_85415366 | CAPG | GAGAA others(1245): Show |
chr2 | 85389753 | 85415366 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0002 | 0/0 | 14 | 0 | 0 | 12 | 0 | 2 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0005 | 0/0 | 7 | 3 | 0 | 4 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0008 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0015 | 0/0 | 5 | 4 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0022 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0023 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0030 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0034 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0035 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0046 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0051 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0052 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0011 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0016 | 0/0 | 5 | 0 | 0 | 0 | 3 | 2 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0020 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0032 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0033 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0055 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0057 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0058 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0003t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0001c0010t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0001 | 0/0 | 28 | 2 | 6 | 15 | 0 | 5 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0003 | 0/0 | 12 | 0 | 2 | 10 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0004 | 0/0 | 9 | 4 | 3 | 1 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0009 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0013 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0014 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0018 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0019 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0024 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0025 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0027 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0028 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0149 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0002c0011t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0003c0004t0001g0007 | 0/0 | 6 | 3 | 0 | 3 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0003c0004t0001g0012 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0003c0004t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0003c0004t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0003c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0003c0004t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0003c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0003c0004t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0003c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0003c0004t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0003c0006t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0003c0006t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0003c0006t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0003c0006t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0003c0006t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0003c0006t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0003c0006t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0003c0006t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0003c0008t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0004c0005t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0004c0005t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0004c0005t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0004c0005t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0004c0005t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0005c0009t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0006c0012t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| a0007c0007t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0035 | EUR | GBR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0023 | EUR | GBR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0016 | EUR | GBR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00140 | hp2 | a0001 | c0003 | t0001 | g0057 | EUR | GBR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0016 | EUR | FIN | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00280 | hp2 | a0002 | c0001 | t0001 | g0040 | EUR | FIN | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00323 | hp1 | a0003 | c0004 | t0001 | g0082 | EUR | FIN | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0016 | EUR | FIN | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00408 | hp1 | a0004 | c0005 | t0001 | g0010 | EAS | CHS | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00408 | hp2 | a0002 | c0001 | t0001 | g0106 | EAS | CHS | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00423 | hp1 | a0004 | c0005 | t0001 | g0166 | EAS | CHS | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00423 | hp2 | a0002 | c0001 | t0001 | g0019 | EAS | CHS | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00438 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | CHS | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00558 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | CHS | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | CHS | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | CHS | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | CHS | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00639 | hp1 | a0002 | c0001 | t0001 | g0018 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0047 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00642 | hp1 | a0003 | c0004 | t0001 | g0012 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00642 | hp2 | a0002 | c0001 | t0001 | g0013 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00673 | hp1 | a0002 | c0001 | t0001 | g0027 | EAS | CHS | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00733 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00735 | hp1 | a0005 | c0009 | t0001 | g0215 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00735 | hp2 | a0003 | c0004 | t0001 | g0012 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00738 | hp2 | a0002 | c0001 | t0001 | g0003 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG00741 | hp2 | a0002 | c0001 | t0001 | g0019 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01069 | hp1 | a0002 | c0001 | t0001 | g0004 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0191 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01070 | hp2 | a0002 | c0001 | t0001 | g0024 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01071 | hp1 | a0002 | c0001 | t0001 | g0004 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0192 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01074 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01081 | hp1 | a0002 | c0001 | t0001 | g0132 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0047 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01099 | hp1 | a0002 | c0001 | t0001 | g0018 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01099 | hp2 | a0003 | c0004 | t0001 | g0012 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01106 | hp2 | a0002 | c0001 | t0001 | g0041 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01109 | hp1 | a0002 | c0001 | t0001 | g0144 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01109 | hp2 | a0001 | c0003 | t0001 | g0020 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0142 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01168 | hp1 | a0003 | c0008 | t0001 | g0074 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01168 | hp2 | a0002 | c0001 | t0001 | g0099 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01169 | hp1 | a0002 | c0001 | t0001 | g0125 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0093 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01175 | hp1 | a0002 | c0001 | t0001 | g0019 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01175 | hp2 | a0002 | c0001 | t0001 | g0108 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0193 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01243 | hp2 | a0002 | c0011 | t0001 | g0151 | AMR | PUR | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01255 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01255 | hp2 | a0003 | c0006 | t0001 | g0079 | AMR | CLM | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01256 | hp1 | a0002 | c0001 | t0001 | g0039 | AMR | CLM | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0150 | AMR | CLM | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01257 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01257 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0163 | AMR | CLM | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01261 | hp2 | a0002 | c0001 | t0001 | g0004 | AMR | CLM | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | CLM | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0173 | AMR | CLM | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | CLM | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01358 | hp2 | a0002 | c0001 | t0001 | g0025 | AMR | CLM | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0019 | AMR | CLM | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01433 | hp2 | a0002 | c0001 | t0001 | g0009 | AMR | CLM | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01515 | hp1 | a0002 | c0001 | t0001 | g0025 | EUR | IBS | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01515 | hp2 | a0002 | c0001 | t0001 | g0103 | EUR | IBS | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01516 | hp1 | a0003 | c0006 | t0001 | g0076 | EUR | IBS | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01516 | hp2 | a0002 | c0001 | t0001 | g0028 | EUR | IBS | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01517 | hp1 | a0002 | c0001 | t0001 | g0025 | EUR | IBS | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01517 | hp2 | a0003 | c0006 | t0001 | g0075 | EUR | IBS | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01884 | hp1 | a0003 | c0004 | t0001 | g0094 | AFR | ACB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0058 | AFR | ACB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01891 | hp1 | a0002 | c0001 | t0001 | g0160 | AFR | ACB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0033 | AFR | ACB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01928 | hp1 | a0002 | c0001 | t0001 | g0044 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01928 | hp2 | a0002 | c0001 | t0001 | g0014 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01952 | hp1 | a0002 | c0001 | t0001 | g0044 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01952 | hp2 | a0002 | c0001 | t0001 | g0043 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0208 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01975 | hp2 | a0002 | c0001 | t0001 | g0009 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01978 | hp1 | a0002 | c0001 | t0001 | g0118 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01978 | hp2 | a0002 | c0001 | t0001 | g0003 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01981 | hp2 | a0002 | c0001 | t0001 | g0009 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01993 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01993 | hp2 | a0002 | c0001 | t0001 | g0014 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02004 | hp1 | a0001 | c0003 | t0001 | g0207 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0009 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02015 | hp1 | a0002 | c0001 | t0001 | g0129 | EAS | KHV | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | KHV | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02040 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | KHV | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | KHV | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02055 | hp1 | a0002 | c0001 | t0001 | g0105 | AFR | ACB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0204 | AFR | ACB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02056 | hp1 | a0002 | c0001 | t0001 | g0039 | EAS | KHV | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02056 | hp2 | a0004 | c0005 | t0001 | g0175 | EAS | KHV | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02071 | hp1 | a0002 | c0001 | t0001 | g0013 | EAS | KHV | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | KHV | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02074 | hp1 | a0002 | c0001 | t0001 | g0101 | EAS | KHV | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | KHV | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | KHV | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02083 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | KHV | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | KHV | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02132 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02132 | hp2 | a0004 | c0005 | t0001 | g0048 | EAS | KHV | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | KHV | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02135 | hp2 | a0002 | c0001 | t0001 | g0096 | EAS | KHV | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | ACB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0213 | AFR | ACB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02148 | hp1 | a0003 | c0004 | t0001 | g0012 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02148 | hp2 | a0002 | c0001 | t0001 | g0009 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | CDX | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02155 | hp2 | a0004 | c0005 | t0001 | g0010 | EAS | CDX | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02165 | hp1 | a0003 | c0006 | t0001 | g0037 | EAS | CDX | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | CDX | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0020 | AFR | ACB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0049 | AFR | ACB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0153 | AFR | ACB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02258 | hp2 | a0002 | c0001 | t0001 | g0028 | AFR | ACB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02273 | hp1 | a0002 | c0001 | t0001 | g0009 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02273 | hp2 | a0002 | c0001 | t0001 | g0014 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02293 | hp1 | a0002 | c0001 | t0001 | g0187 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02293 | hp2 | a0002 | c0001 | t0001 | g0100 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02300 | hp1 | a0002 | c0001 | t0001 | g0043 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0057 | AMR | PEL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | ACB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02451 | hp2 | a0003 | c0004 | t0001 | g0186 | AFR | ACB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | KHV | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0080 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02572 | hp2 | a0002 | c0001 | t0001 | g0133 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02602 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0224 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0206 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02622 | hp1 | a0002 | c0001 | t0001 | g0004 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0033 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02630 | hp2 | a0002 | c0001 | t0001 | g0001 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0218 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02647 | hp2 | a0002 | c0001 | t0001 | g0130 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0209 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02683 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0214 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02698 | hp2 | a0003 | c0006 | t0001 | g0078 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02717 | hp1 | a0003 | c0004 | t0001 | g0007 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02717 | hp2 | a0002 | c0001 | t0001 | g0001 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0199 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0020 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02735 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02735 | hp2 | a0003 | c0006 | t0001 | g0061 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0011 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0212 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0020 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0045 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0045 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0141 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02886 | hp2 | a0001 | c0003 | t0002 | g0226 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0219 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02895 | hp2 | a0001 | c0003 | t0002 | g0227 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0220 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | ESN | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | ESN | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02965 | hp1 | a0002 | c0001 | t0001 | g0098 | AFR | ESN | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0164 | AFR | ESN | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02970 | hp1 | a0002 | c0001 | t0001 | g0029 | AFR | ESN | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | ESN | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02976 | hp1 | a0002 | c0001 | t0001 | g0131 | AFR | ESN | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02976 | hp2 | a0002 | c0001 | t0001 | g0004 | AFR | ESN | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03017 | hp1 | a0002 | c0001 | t0001 | g0102 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0051 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0184 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0159 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0217 | AFR | MSL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0182 | AFR | MSL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03130 | hp1 | a0002 | c0001 | t0001 | g0029 | AFR | ESN | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03130 | hp2 | a0003 | c0004 | t0001 | g0007 | AFR | ESN | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03139 | hp1 | a0002 | c0001 | t0001 | g0027 | AFR | ESN | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0033 | AFR | ESN | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03195 | hp1 | a0002 | c0001 | t0001 | g0027 | AFR | ESN | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0183 | AFR | ESN | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03225 | hp1 | a0002 | c0001 | t0001 | g0042 | AFR | MSL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | MSL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03239 | hp1 | a0002 | c0001 | t0001 | g0091 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03239 | hp2 | a0002 | c0001 | t0001 | g0223 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0225 | AFR | MSL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | MSL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03486 | hp1 | a0002 | c0001 | t0001 | g0004 | AFR | MSL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0154 | AFR | MSL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0038 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03490 | hp2 | a0001 | c0003 | t0001 | g0032 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03491 | hp1 | a0001 | c0003 | t0001 | g0055 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0216 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0055 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0038 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0171 | AFR | ESN | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03516 | hp2 | a0002 | c0001 | t0001 | g0004 | AFR | ESN | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0197 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0147 | AFR | GWD | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03579 | hp1 | a0002 | c0001 | t0001 | g0042 | AFR | MSL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03579 | hp2 | a0001 | c0010 | t0001 | g0176 | AFR | MSL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03654 | hp1 | a0002 | c0001 | t0001 | g0114 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03654 | hp2 | a0002 | c0001 | t0001 | g0040 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03669 | hp1 | a0002 | c0001 | t0001 | g0111 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03669 | hp2 | a0002 | c0001 | t0001 | g0189 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03688 | hp1 | a0002 | c0001 | t0001 | g0026 | SAS | STU | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03688 | hp2 | a0002 | c0001 | t0001 | g0095 | SAS | STU | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03704 | hp1 | a0003 | c0006 | t0001 | g0077 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03704 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03710 | hp1 | a0002 | c0001 | t0001 | g0041 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03710 | hp2 | a0001 | c0003 | t0001 | g0200 | SAS | PJL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03831 | hp1 | a0002 | c0001 | t0001 | g0026 | SAS | BEB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0201 | SAS | BEB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0030 | SAS | BEB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03834 | hp2 | a0002 | c0001 | t0001 | g0134 | SAS | BEB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0016 | SAS | BEB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03942 | hp2 | a0002 | c0001 | t0001 | g0026 | SAS | BEB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG04115 | hp1 | a0002 | c0001 | t0001 | g0145 | SAS | STU | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG04115 | hp2 | a0003 | c0004 | t0001 | g0084 | SAS | STU | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0032 | SAS | BEB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG04184 | hp2 | a0002 | c0001 | t0001 | g0089 | SAS | BEB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0190 | SAS | STU | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG04199 | hp2 | a0003 | c0004 | t0001 | g0083 | SAS | STU | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG04204 | hp1 | a0002 | c0001 | t0001 | g0004 | SAS | STU | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG04204 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | STU | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG04228 | hp1 | a0002 | c0001 | t0001 | g0115 | SAS | STU | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0016 | SAS | STU | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0222 | AFR | YRI | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0170 | AFR | YRI | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | CHB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18612 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | CHB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0194 | AFR | YRI | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0155 | AFR | YRI | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18940 | hp1 | a0002 | c0001 | t0001 | g0013 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18942 | hp1 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18943 | hp1 | a0002 | c0001 | t0001 | g0143 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18944 | hp2 | a0002 | c0001 | t0001 | g0128 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18945 | hp2 | a0003 | c0004 | t0001 | g0126 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18947 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18948 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18948 | hp2 | a0003 | c0004 | t0001 | g0007 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18949 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18949 | hp2 | a0004 | c0005 | t0001 | g0010 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18950 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18951 | hp1 | a0002 | c0001 | t0001 | g0024 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18951 | hp2 | a0003 | c0004 | t0001 | g0007 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18953 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18954 | hp1 | a0002 | c0001 | t0001 | g0024 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18954 | hp2 | a0004 | c0005 | t0001 | g0010 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18956 | hp1 | a0002 | c0001 | t0001 | g0088 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18957 | hp2 | a0002 | c0001 | t0001 | g0123 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18959 | hp2 | a0002 | c0001 | t0001 | g0221 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18960 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18960 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18961 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18962 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18962 | hp2 | a0003 | c0006 | t0001 | g0037 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18963 | hp1 | a0002 | c0001 | t0001 | g0119 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18963 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18964 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18965 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18966 | hp2 | a0002 | c0001 | t0001 | g0109 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18967 | hp2 | a0004 | c0005 | t0001 | g0048 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18968 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18970 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0056 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18972 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18973 | hp1 | a0004 | c0005 | t0001 | g0010 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18975 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18977 | hp1 | a0002 | c0001 | t0001 | g0135 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18977 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18979 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18980 | hp1 | a0002 | c0001 | t0001 | g0013 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18982 | hp2 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18983 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18987 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18988 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18990 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18990 | hp2 | a0004 | c0005 | t0001 | g0010 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18991 | hp1 | a0002 | c0001 | t0001 | g0122 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18993 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18997 | hp1 | a0001 | c0003 | t0001 | g0059 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18997 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18998 | hp2 | a0002 | c0001 | t0001 | g0013 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19002 | hp1 | a0003 | c0004 | t0001 | g0085 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19005 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19007 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19009 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19010 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19011 | hp1 | a0002 | c0001 | t0001 | g0110 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19011 | hp2 | a0003 | c0004 | t0001 | g0007 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19012 | hp2 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19030 | hp1 | a0003 | c0004 | t0001 | g0081 | AFR | LWK | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0196 | AFR | LWK | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0086 | AFR | LWK | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19043 | hp2 | a0002 | c0001 | t0001 | g0029 | AFR | LWK | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19054 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19056 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19056 | hp2 | a0002 | c0001 | t0001 | g0104 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19060 | hp1 | a0006 | c0012 | t0001 | g0116 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19062 | hp2 | a0002 | c0001 | t0001 | g0188 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19064 | hp2 | a0002 | c0001 | t0001 | g0112 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0202 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19065 | hp2 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19066 | hp1 | a0001 | c0003 | t0001 | g0056 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19067 | hp2 | a0002 | c0001 | t0001 | g0120 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19070 | hp2 | a0002 | c0001 | t0001 | g0117 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19072 | hp1 | a0004 | c0005 | t0001 | g0165 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19072 | hp2 | a0002 | c0001 | t0001 | g0097 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19076 | hp1 | a0002 | c0001 | t0001 | g0121 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19077 | hp1 | a0002 | c0001 | t0001 | g0113 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19077 | hp2 | a0002 | c0001 | t0001 | g0107 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19083 | hp2 | a0002 | c0001 | t0001 | g0124 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19084 | hp1 | a0002 | c0001 | t0001 | g0138 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19085 | hp2 | a0002 | c0001 | t0001 | g0087 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19088 | hp1 | a0002 | c0001 | t0001 | g0127 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19090 | hp2 | a0002 | c0001 | t0001 | g0140 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0198 | AFR | YRI | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | YRI | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA20752 | hp1 | a0002 | c0001 | t0001 | g0139 | EUR | TSI | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA20752 | hp2 | a0007 | c0007 | t0001 | g0185 | EUR | TSI | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0023 | EUR | TSI | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA20805 | hp2 | a0003 | c0006 | t0001 | g0060 | EUR | TSI | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA20905 | hp1 | a0001 | c0003 | t0001 | g0032 | SAS | GIH | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | GIH | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01123 | hp1 | a0003 | c0004 | t0001 | g0012 | AMR | CLM | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG01123 | hp2 | a0002 | c0001 | t0001 | g0028 | AMR | CLM | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02109 | hp2 | a0003 | c0004 | t0001 | g0007 | AFR | ACB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02559 | hp1 | a0002 | c0001 | t0001 | g0137 | AFR | ACB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | ACB | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0049 | AFR | MSL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0152 | AFR | MSL | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | USA | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0205 | AFR | USA | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18955 | hp1 | a0002 | c0001 | t0001 | g0136 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA18955 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0058 | AFR | USA | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0046 | AFR | USA | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0034 | REF | REF | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| homoSapiens | grch38p0 | a0002 | c0001 | t0001 | g0149 | REF | REF | CAPG_chr2_85389753_85415366 | CAPG | chr2 | 85389753 | 85415366 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:85394936 | T | C | 5 | a0001 a0003 a0004 others(2): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
missense_variant | MODERATE | c.1004A>G | p.His335Arg | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 10/10 | 1067/1250 | 1004/1047 | 335/348 | chr2 | 85394936 | |||
| chr2:85398769 | T | C | 1 | a0004 | 11 | HG00408.hp1 HG00423.hp1 HG02056.hp2 others(8): Show |
missense_variant | MODERATE | c.680A>G | p.Lys227Arg | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 7/10 | 743/1250 | 680/1047 | 227/348 | chr2 | 85398769 | |||
| chr2:85401533 | T | C | 1 | a0006 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.347A>G | p.Tyr116Cys | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 4/10 | 410/1250 | 347/1047 | 116/348 | chr2 | 85401533 | |||
| chr2:85401581 | C | T | 1 | a0005 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.299G>A | p.Gly100Asp | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 4/10 | 362/1250 | 299/1047 | 100/348 | chr2 | 85401581 | |||
| chr2:85401860 | C | T | 2 | a0003 a0004 |
40 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(37): Show |
missense_variant | MODERATE | c.121G>A | p.Val41Ile | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 3/10 | 184/1250 | 121/1047 | 41/348 | chr2 | 85401860 | |||
| chr2:85402143 | C | T | 1 | a0007 | 1 | NA20752.hp2 | start_lost | HIGH | c.3G>A | p.Met1? | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 2/10 | 66/1250 | 3/1047 | 1/348 | chr2 | 85402143 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:85398051 | G | A | 1 | a0003c0008 | 1 | HG01168.hp1 | synonymous_variant | LOW | c.861C>T | p.Asn287Asn | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/10 | 924/1250 | 861/1047 | 287/348 | chr2 | 85398051 | |||
| chr2:85398099 | T | G | 6 | a0001c0003 a0002c0011 a0003c0004 others(3): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
synonymous_variant | LOW | c.813A>C | p.Pro271Pro | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/10 | 876/1250 | 813/1047 | 271/348 | chr2 | 85398099 | |||
| chr2:85399181 | C | T | 1 | a0001c0010 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.621G>A | p.Gln207Gln | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 6/10 | 684/1250 | 621/1047 | 207/348 | chr2 | 85399181 | |||
| chr2:85401622 | C | T | 1 | a0003c0004 | 19 | HG00323.hp1 HG00642.hp1 HG00735.hp2 others(16): Show |
synonymous_variant | LOW | c.258G>A | p.Thr86Thr | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 4/10 | 321/1250 | 258/1047 | 86/348 | chr2 | 85401622 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:85410326 | G | A | 1 | a0001c0003t0002 | 2 | HG02886.hp2 HG02895.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-23C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/10 | chr2 | 85410326 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:85395194 | T | C | 55 | a0001c0002t0001g0170 a0001c0002t0001g0199 a0001c0002t0001g0203 others(52): Show |
95 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.982-236A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 9/9 | chr2 | 85395194 | |||||||
| chr2:85395460 | C | A | 12 | a0001c0003t0001g0020 a0001c0003t0001g0080 a0001c0003t0001g0141 others(9): Show |
15 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.981+78G>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 9/9 | chr2 | 85395460 | |||||||
| chr2:85395665 | C | T | 1 | a0001c0002t0001g0147 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.893-39G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85395665 | |||||||
| chr2:85395767 | G | C | 15 | a0001c0003t0001g0020 a0001c0003t0001g0049 a0001c0003t0001g0080 others(12): Show |
19 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.893-141C>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85395767 | |||||||
| chr2:85395794 | G | A | 1 | a0001c0002t0001g0218 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.893-168C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85395794 | |||||||
| chr2:85395803 | G | T | 5 | a0004c0005t0001g0010 a0004c0005t0001g0048 a0004c0005t0001g0165 others(2): Show |
11 | HG00408.hp1 HG00423.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.893-177C>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85395803 | |||||||
| chr2:85395846 | C | T | 1 | a0002c0001t0001g0026 | 3 | HG03688.hp1 HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.893-220G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85395846 | |||||||
| chr2:85395847 | G | A | 1 | a0001c0003t0001g0058 | 2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.893-221C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85395847 | |||||||
| chr2:85395974 | C | T | 9 | a0003c0004t0001g0007 a0003c0004t0001g0012 a0003c0004t0001g0081 others(6): Show |
18 | HG00323.hp1 HG00642.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.893-348G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85395974 | |||||||
| chr2:85396116 | T | C | 2 | a0001c0003t0001g0045 a0001c0003t0001g0159 |
3 | HG02809.hp2 HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.893-490A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85396116 | |||||||
| chr2:85396187 | T | C | 34 | a0001c0002t0001g0199 a0001c0002t0001g0203 a0001c0002t0001g0204 others(31): Show |
58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.893-561A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85396187 | |||||||
| chr2:85396199 | T | C | 11 | a0001c0003t0001g0219 a0001c0003t0001g0220 a0003c0004t0001g0007 others(8): Show |
20 | HG00323.hp1 HG00642.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.893-573A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85396199 | |||||||
| chr2:85396237 | G | A | 20 | a0001c0002t0001g0199 a0001c0002t0001g0203 a0001c0002t0001g0204 others(17): Show |
41 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(38): Show |
intron_variant | MODIFIER | c.893-611C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85396237 | |||||||
| chr2:85396244 | G | C | 50 | a0001c0002t0001g0170 a0001c0002t0001g0199 a0001c0002t0001g0203 others(47): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.893-618C>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85396244 | |||||||
| chr2:85396254 | C | T | 9 | a0003c0006t0001g0037 a0003c0006t0001g0060 a0003c0006t0001g0061 others(6): Show |
10 | HG01168.hp1 HG01255.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.893-628G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85396254 | |||||||
| chr2:85396291 | T | C | 3 | a0001c0003t0001g0049 a0001c0003t0001g0163 a0001c0003t0001g0171 |
4 | HG01261.hp1 HG02257.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.893-665A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85396291 | |||||||
| chr2:85396334 | C | T | 15 | a0001c0003t0001g0020 a0001c0003t0001g0049 a0001c0003t0001g0080 others(12): Show |
19 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.893-708G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85396334 | |||||||
| chr2:85396362 | G | GT | 11 | a0001c0002t0001g0068 a0001c0002t0001g0070 a0001c0002t0001g0193 others(8): Show |
11 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.893-737dupA | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85396362 | |||||||
| chr2:85396362 | G | T | 21 | a0001c0002t0001g0021 a0001c0002t0001g0038 a0001c0002t0001g0047 others(18): Show |
28 | HG00639.hp2 HG01081.hp2 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.893-736C>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85396362 | |||||||
| chr2:85396362 | GT | G | 63 | a0001c0002t0001g0170 a0001c0002t0001g0199 a0001c0002t0001g0203 others(60): Show |
107 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.893-737delA | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85396362 | |||||||
| chr2:85396364 | T | G | 2 | a0001c0002t0001g0170 a0003c0004t0001g0186 |
2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.893-738A>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85396364 | |||||||
| chr2:85396374 | T | C | 3 | a0001c0003t0001g0020 a0001c0003t0001g0080 a0001c0003t0001g0155 |
6 | HG01109.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.893-748A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85396374 | |||||||
| chr2:85396448 | G | A | 2 | a0001c0002t0001g0170 a0003c0004t0001g0186 |
2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.893-822C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85396448 | |||||||
| chr2:85396679 | C | G | 1 | a0001c0002t0001g0156 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.893-1053G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85396679 | |||||||
| chr2:85396848 | T | A | 1 | a0001c0003t0001g0205 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.892+1172A>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85396848 | |||||||
| chr2:85396851 | C | T | 2 | a0001c0003t0001g0045 a0001c0003t0001g0159 |
3 | HG02809.hp2 HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.892+1169G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85396851 | |||||||
| chr2:85396916 | G | C | 28 | a0001c0003t0001g0020 a0001c0003t0001g0045 a0001c0003t0001g0049 others(25): Show |
35 | HG01109.hp2 HG01167.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.892+1104C>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85396916 | |||||||
| chr2:85397115 | T | C | 1 | a0001c0002t0001g0161 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.892+905A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85397115 | |||||||
| chr2:85397187 | C | G | 21 | a0001c0002t0001g0199 a0001c0002t0001g0203 a0001c0002t0001g0204 others(18): Show |
42 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.892+833G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85397187 | |||||||
| chr2:85397305 | G | A | 1 | a0001c0003t0001g0086 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.892+715C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85397305 | |||||||
| chr2:85397398 | A | T | 1 | a0002c0001t0001g0123 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.892+622T>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85397398 | |||||||
| chr2:85397420 | A | G | 1 | a0001c0002t0001g0168 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.892+600T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85397420 | |||||||
| chr2:85397431 | C | T | 10 | a0001c0003t0001g0086 a0003c0006t0001g0037 a0003c0006t0001g0060 others(7): Show |
11 | HG01168.hp1 HG01255.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.892+589G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85397431 | |||||||
| chr2:85397432 | G | A | 2 | a0001c0003t0001g0045 a0001c0003t0001g0159 |
3 | HG02809.hp2 HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.892+588C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85397432 | |||||||
| chr2:85397506 | C | T | 2 | a0001c0003t0001g0153 a0001c0003t0001g0154 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.892+514G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85397506 | |||||||
| chr2:85397704 | A | AAAAG | 9 | a0001c0002t0001g0172 a0001c0003t0001g0049 a0001c0003t0001g0152 others(6): Show |
10 | HG01243.hp2 HG01261.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.892+312_892+315dup others(4): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85397704 | |||||||
| chr2:85397704 | A | AAAAGAAA others(1): Show |
3 | a0001c0003t0001g0086 a0001c0003t0001g0153 a0001c0003t0001g0154 |
3 | HG02258.hp1 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.892+308_892+315dup others(8): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85397704 | |||||||
| chr2:85397704 | A | AAAAGAAA others(13): Show |
2 | a0001c0003t0001g0142 a0003c0008t0001g0074 |
2 | HG01167.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.892+296_892+315dup others(20): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85397704 | |||||||
| chr2:85397704 | A | AAAAGAAA others(17): Show |
4 | a0001c0003t0001g0020 a0001c0003t0001g0080 a0001c0003t0001g0141 others(1): Show |
7 | HG01109.hp2 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.892+292_892+315dup others(24): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85397704 | |||||||
| chr2:85397704 | A | AAAAGAAA others(21): Show |
2 | a0003c0006t0001g0037 a0003c0006t0001g0060 |
3 | HG02165.hp1 NA18962.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.892+315_892+316ins others(28): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85397704 | |||||||
| chr2:85397704 | A | AAAAGAAA others(25): Show |
4 | a0003c0006t0001g0061 a0003c0006t0001g0075 a0003c0006t0001g0076 others(1): Show |
4 | HG01255.hp2 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.892+315_892+316ins others(32): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85397704 | |||||||
| chr2:85397704 | A | AAAAGAAA others(33): Show |
1 | a0003c0006t0001g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.892+315_892+316ins others(40): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85397704 | |||||||
| chr2:85397704 | A | AAAAGAAA others(37): Show |
1 | a0003c0006t0001g0078 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.892+315_892+316ins others(44): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85397704 | |||||||
| chr2:85397704 | AAAAG | A | 29 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0209 others(26): Show |
54 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.892+312_892+315del others(4): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85397704 | |||||||
| chr2:85397774 | C | G | 17 | a0001c0003t0001g0219 a0001c0003t0001g0220 a0003c0004t0001g0007 others(14): Show |
32 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.892+246G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85397774 | |||||||
| chr2:85397835 | T | G | 1 | a0001c0003t0001g0217 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.892+185A>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85397835 | |||||||
| chr2:85397970 | G | A | 1 | a0001c0002t0001g0038 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.892+50C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 8/9 | chr2 | 85397970 | |||||||
| chr2:85398164 | G | C | 1 | a0001c0003t0001g0016 | 5 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(2): Show |
intron_variant | MODIFIER | c.760-12C>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 7/9 | chr2 | 85398164 | |||||||
| chr2:85398187 | C | T | 1 | a0001c0003t0001g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.760-35G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 7/9 | chr2 | 85398187 | |||||||
| chr2:85398193 | C | G | 4 | a0002c0001t0001g0104 a0002c0001t0001g0110 a0002c0001t0001g0117 others(1): Show |
4 | NA19011.hp1 NA19056.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.760-41G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 7/9 | chr2 | 85398193 | |||||||
| chr2:85398221 | G | A | 2 | a0002c0001t0001g0099 a0002c0001t0001g0125 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.760-69C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 7/9 | chr2 | 85398221 | |||||||
| chr2:85398233 | C | T | 1 | a0001c0003t0001g0058 | 2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.760-81G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 7/9 | chr2 | 85398233 | |||||||
| chr2:85398316 | T | G | 10 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0209 others(7): Show |
13 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.760-164A>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 7/9 | chr2 | 85398316 | |||||||
| chr2:85398390 | T | A | 71 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(68): Show |
124 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.760-238A>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 7/9 | chr2 | 85398390 | |||||||
| chr2:85398396 | C | A | 2 | a0001c0003t0001g0045 a0001c0003t0001g0159 |
3 | HG02809.hp2 HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.760-244G>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 7/9 | chr2 | 85398396 | |||||||
| chr2:85398446 | G | A | 1 | a0001c0003t0001g0086 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.759+244C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 7/9 | chr2 | 85398446 | |||||||
| chr2:85398515 | G | A | 1 | a0003c0004t0001g0186 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.759+175C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 7/9 | chr2 | 85398515 | |||||||
| chr2:85398661 | G | A | 16 | a0001c0003t0001g0020 a0001c0003t0001g0049 a0001c0003t0001g0058 others(13): Show |
21 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.759+29C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 7/9 | chr2 | 85398661 | |||||||
| chr2:85398791 | G | A | 1 | a0001c0003t0001g0058 | 2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.667-9C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 6/9 | chr2 | 85398791 | |||||||
| chr2:85398853 | G | A | 3 | a0001c0003t0001g0049 a0001c0003t0001g0163 a0001c0003t0001g0171 |
4 | HG01261.hp1 HG02257.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-71C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 6/9 | chr2 | 85398853 | |||||||
| chr2:85398953 | G | A | 1 | a0002c0001t0001g0134 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.667-171C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 6/9 | chr2 | 85398953 | |||||||
| chr2:85399033 | C | T | 4 | a0001c0002t0001g0036 a0001c0002t0001g0062 a0001c0002t0001g0065 others(1): Show |
5 | NA18940.hp2 NA18966.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.666+103G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 6/9 | chr2 | 85399033 | |||||||
| chr2:85399063 | C | T | 1 | a0002c0001t0001g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.666+73G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 6/9 | chr2 | 85399063 | |||||||
| chr2:85399331 | C | A | 9 | a0003c0004t0001g0007 a0003c0004t0001g0012 a0003c0004t0001g0081 others(6): Show |
18 | HG00323.hp1 HG00642.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.517-46G>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85399331 | |||||||
| chr2:85399356 | G | C | 58 | a0001c0003t0001g0006 a0001c0003t0001g0011 a0001c0003t0001g0016 others(55): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.517-71C>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85399356 | |||||||
| chr2:85399401 | C | T | 24 | a0003c0004t0001g0007 a0003c0004t0001g0012 a0003c0004t0001g0081 others(21): Show |
40 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.517-116G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85399401 | |||||||
| chr2:85399449 | C | T | 2 | a0001c0002t0001g0224 a0001c0002t0001g0225 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.517-164G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85399449 | |||||||
| chr2:85399458 | A | T | 149 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(146): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.517-173T>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85399458 | |||||||
| chr2:85399483 | G | A | 18 | a0001c0003t0001g0006 a0001c0003t0001g0011 a0001c0003t0001g0016 others(15): Show |
39 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.517-198C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85399483 | |||||||
| chr2:85399583 | T | C | 139 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(136): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.517-298A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85399583 | |||||||
| chr2:85399598 | G | A | 9 | a0003c0004t0001g0007 a0003c0004t0001g0012 a0003c0004t0001g0081 others(6): Show |
18 | HG00323.hp1 HG00642.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.517-313C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85399598 | |||||||
| chr2:85399614 | T | C | 1 | a0002c0001t0001g0112 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.517-329A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85399614 | |||||||
| chr2:85399633 | G | C | 1 | a0001c0003t0001g0086 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.517-348C>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85399633 | |||||||
| chr2:85399696 | C | A | 1 | a0001c0003t0001g0201 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.517-411G>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85399696 | |||||||
| chr2:85399724 | A | G | 1 | a0005c0009t0001g0215 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.517-439T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85399724 | |||||||
| chr2:85399740 | C | CT | 12 | a0001c0002t0001g0002 a0001c0002t0001g0031 a0001c0002t0001g0168 others(9): Show |
15 | HG00735.hp1 HG01261.hp1 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.517-456dupA | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85399740 | |||||||
| chr2:85399740 | CT | C | 59 | a0001c0002t0001g0005 a0001c0002t0001g0046 a0001c0002t0001g0064 others(56): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.517-456delA | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85399740 | |||||||
| chr2:85399740 | CTTTTTTT others(7): Show |
C | 1 | a0002c0001t0001g0189 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.517-469_517-456del others(14): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85399740 | |||||||
| chr2:85399761 | G | A | 9 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0209 others(6): Show |
12 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.517-476C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85399761 | |||||||
| chr2:85399798 | A | G | 12 | a0001c0003t0001g0020 a0001c0003t0001g0080 a0001c0003t0001g0141 others(9): Show |
15 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.517-513T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85399798 | |||||||
| chr2:85399907 | A | G | 1 | a0002c0001t0001g0139 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.517-622T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85399907 | |||||||
| chr2:85399955 | G | A | 1 | a0001c0003t0001g0086 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.517-670C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85399955 | |||||||
| chr2:85399969 | G | A | 1 | a0001c0003t0001g0045 | 2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.517-684C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85399969 | |||||||
| chr2:85400075 | T | C | 1 | a0003c0006t0001g0060 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.517-790A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85400075 | |||||||
| chr2:85400087 | T | G | 2 | a0001c0003t0001g0045 a0001c0003t0001g0159 |
3 | HG02809.hp2 HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.517-802A>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85400087 | |||||||
| chr2:85400188 | C | T | 9 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0209 others(6): Show |
12 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.517-903G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85400188 | |||||||
| chr2:85400206 | G | A | 1 | a0002c0001t0001g0113 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.517-921C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85400206 | |||||||
| chr2:85400228 | G | A | 1 | a0003c0004t0001g0186 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.516+937C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85400228 | |||||||
| chr2:85400341 | G | A | 2 | a0002c0001t0001g0114 a0002c0001t0001g0115 |
2 | HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.516+824C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85400341 | |||||||
| chr2:85400538 | C | T | 2 | a0001c0002t0001g0212 a0001c0002t0001g0213 |
2 | HG02145.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.516+627G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85400538 | |||||||
| chr2:85400558 | C | T | 1 | a0002c0001t0001g0189 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.516+607G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85400558 | |||||||
| chr2:85400591 | C | A | 9 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0210 others(6): Show |
12 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.516+574G>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85400591 | |||||||
| chr2:85400696 | C | T | 1 | a0001c0003t0001g0086 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.516+469G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85400696 | |||||||
| chr2:85400843 | T | G | 1 | a0002c0001t0001g0088 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.516+322A>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85400843 | |||||||
| chr2:85401043 | G | C | 2 | a0001c0002t0001g0196 a0001c0002t0001g0197 |
2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.516+122C>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85401043 | |||||||
| chr2:85401050 | C | T | 4 | a0002c0001t0001g0018 a0002c0001t0001g0044 a0002c0001t0001g0100 others(1): Show |
8 | HG00639.hp1 HG01099.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.516+115G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 5/9 | chr2 | 85401050 | |||||||
| chr2:85401433 | A | G | 19 | a0003c0004t0001g0007 a0003c0004t0001g0012 a0003c0004t0001g0081 others(16): Show |
29 | HG00323.hp1 HG00642.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.351+96T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 4/9 | chr2 | 85401433 | |||||||
| chr2:85401441 | G | A | 1 | a0001c0003t0001g0142 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.351+88C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 4/9 | chr2 | 85401441 | |||||||
| chr2:85401981 | A | G | 1 | a0001c0003t0001g0164 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.24-24T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 2/9 | chr2 | 85401981 | |||||||
| chr2:85402065 | G | C | 1 | a0001c0002t0001g0064 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.23+58C>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 2/9 | chr2 | 85402065 | |||||||
| chr2:85402207 | C | A | 9 | a0003c0006t0001g0037 a0003c0006t0001g0060 a0003c0006t0001g0061 others(6): Show |
10 | HG01168.hp1 HG01255.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13-49G>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85402207 | |||||||
| chr2:85402398 | G | A | 1 | a0001c0002t0001g0192 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-13-240C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85402398 | |||||||
| chr2:85402530 | G | A | 1 | a0001c0002t0001g0218 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-13-372C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85402530 | |||||||
| chr2:85402532 | T | C | 1 | a0001c0003t0001g0086 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-13-374A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85402532 | |||||||
| chr2:85402578 | G | A | 9 | a0003c0004t0001g0007 a0003c0004t0001g0012 a0003c0004t0001g0081 others(6): Show |
18 | HG00323.hp1 HG00642.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.-13-420C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85402578 | |||||||
| chr2:85402694 | A | G | 149 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(146): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.-13-536T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85402694 | |||||||
| chr2:85402799 | C | G | 1 | a0001c0002t0001g0177 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-13-641G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85402799 | |||||||
| chr2:85402800 | T | A | 1 | a0001c0002t0001g0177 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-13-642A>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85402800 | |||||||
| chr2:85402801 | C | G | 1 | a0001c0002t0001g0177 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-13-643G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85402801 | |||||||
| chr2:85402810 | A | G | 5 | a0002c0001t0001g0003 a0002c0001t0001g0014 a0002c0001t0001g0136 others(2): Show |
6 | HG00558.hp1 NA18943.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-652T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85402810 | |||||||
| chr2:85402849 | C | T | 1 | a0002c0001t0001g0025 | 3 | HG01358.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-13-691G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85402849 | |||||||
| chr2:85402889 | G | A | 2 | a0002c0001t0001g0108 a0002c0001t0001g0223 |
2 | HG01175.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-13-731C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85402889 | |||||||
| chr2:85402927 | C | T | 1 | a0001c0003t0001g0058 | 2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-13-769G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85402927 | |||||||
| chr2:85403009 | G | A | 1 | a0001c0003t0001g0058 | 2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-13-851C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403009 | |||||||
| chr2:85403015 | C | T | 2 | a0003c0006t0001g0077 a0003c0006t0001g0078 |
2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-13-857G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403015 | |||||||
| chr2:85403018 | G | A | 1 | a0002c0001t0001g0089 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-13-860C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403018 | |||||||
| chr2:85403046 | C | T | 18 | a0001c0003t0001g0006 a0001c0003t0001g0011 a0001c0003t0001g0016 others(15): Show |
39 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.-13-888G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403046 | |||||||
| chr2:85403140 | A | G | 1 | a0001c0003t0001g0086 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-13-982T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403140 | |||||||
| chr2:85403239 | A | G | 1 | a0002c0001t0001g0109 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-13-1081T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403239 | |||||||
| chr2:85403300 | A | C | 1 | a0002c0001t0001g0123 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-13-1142T>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403300 | |||||||
| chr2:85403311 | A | G | 1 | a0001c0002t0001g0218 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-13-1153T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403311 | |||||||
| chr2:85403320 | G | A | 9 | a0003c0006t0001g0037 a0003c0006t0001g0060 a0003c0006t0001g0061 others(6): Show |
10 | HG01168.hp1 HG01255.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13-1162C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403320 | |||||||
| chr2:85403326 | A | G | 14 | a0001c0003t0001g0020 a0001c0003t0001g0045 a0001c0003t0001g0080 others(11): Show |
18 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-13-1168T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403326 | |||||||
| chr2:85403371 | C | G | 1 | a0002c0001t0001g0123 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-13-1213G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403371 | |||||||
| chr2:85403372 | G | C | 1 | a0002c0001t0001g0123 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-13-1214C>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403372 | |||||||
| chr2:85403421 | T | C | 16 | a0001c0003t0001g0020 a0001c0003t0001g0045 a0001c0003t0001g0058 others(13): Show |
21 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-13-1263A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403421 | |||||||
| chr2:85403488 | A | G | 1 | a0001c0002t0001g0210 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-13-1330T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403488 | |||||||
| chr2:85403580 | A | G | 12 | a0001c0003t0001g0020 a0001c0003t0001g0080 a0001c0003t0001g0141 others(9): Show |
15 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.-13-1422T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403580 | |||||||
| chr2:85403617 | G | A | 9 | a0003c0004t0001g0007 a0003c0004t0001g0012 a0003c0004t0001g0081 others(6): Show |
18 | HG00323.hp1 HG00642.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.-13-1459C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403617 | |||||||
| chr2:85403628 | C | T | 21 | a0001c0002t0001g0199 a0001c0002t0001g0203 a0001c0002t0001g0204 others(18): Show |
42 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.-13-1470G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403628 | |||||||
| chr2:85403751 | G | A | 1 | a0007c0007t0001g0185 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-13-1593C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403751 | |||||||
| chr2:85403859 | C | T | 1 | a0001c0002t0001g0146 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-13-1701G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403859 | |||||||
| chr2:85403886 | C | CA | 16 | a0001c0002t0001g0031 a0001c0002t0001g0067 a0001c0002t0001g0069 others(13): Show |
24 | HG00609.hp1 HG00642.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.-13-1729dupT | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403886 | |||||||
| chr2:85403886 | CA | C | 49 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0054 others(46): Show |
78 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.-13-1729delT | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403886 | |||||||
| chr2:85403886 | CAA | C | 17 | a0001c0002t0001g0210 a0001c0002t0001g0212 a0001c0002t0001g0213 others(14): Show |
24 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(21): Show |
intron_variant | MODIFIER | c.-13-1730_-13-1729d others(4): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403886 | |||||||
| chr2:85403886 | CAAA | C | 18 | a0001c0003t0001g0020 a0001c0003t0001g0080 a0001c0003t0001g0141 others(15): Show |
30 | HG00642.hp1 HG00735.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.-13-1731_-13-1729d others(5): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403886 | |||||||
| chr2:85403954 | T | A | 1 | a0002c0001t0001g0123 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-13-1796A>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403954 | |||||||
| chr2:85403955 | A | T | 1 | a0002c0001t0001g0123 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-13-1797T>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403955 | |||||||
| chr2:85403960 | A | AT | 11 | a0001c0003t0001g0219 a0001c0003t0001g0220 a0003c0004t0001g0007 others(8): Show |
20 | HG00323.hp1 HG00642.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.-13-1803dupA | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403960 | |||||||
| chr2:85403984 | C | T | 2 | a0002c0001t0001g0103 a0002c0001t0001g0189 |
2 | HG01515.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-13-1826G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85403984 | |||||||
| chr2:85404043 | C | A | 2 | a0001c0002t0001g0157 a0001c0002t0001g0181 |
2 | NA18967.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-13-1885G>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404043 | |||||||
| chr2:85404155 | A | G | 5 | a0004c0005t0001g0010 a0004c0005t0001g0048 a0004c0005t0001g0165 others(2): Show |
11 | HG00408.hp1 HG00423.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13-1997T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404155 | |||||||
| chr2:85404176 | T | C | 1 | a0001c0003t0001g0059 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-13-2018A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404176 | |||||||
| chr2:85404201 | T | A | 21 | a0001c0002t0001g0199 a0001c0002t0001g0203 a0001c0002t0001g0204 others(18): Show |
42 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.-13-2043A>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404201 | |||||||
| chr2:85404273 | C | CA | 28 | a0001c0002t0001g0072 a0001c0002t0001g0093 a0001c0002t0001g0172 others(25): Show |
53 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.-13-2116dupT | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404273 | |||||||
| chr2:85404273 | CA | C | 12 | a0001c0003t0001g0020 a0001c0003t0001g0080 a0001c0003t0001g0141 others(9): Show |
15 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.-13-2116delT | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404273 | |||||||
| chr2:85404274 | A | C | 7 | a0003c0004t0001g0007 a0003c0004t0001g0012 a0003c0004t0001g0082 others(4): Show |
16 | HG00323.hp1 HG00642.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.-13-2116T>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404274 | |||||||
| chr2:85404292 | C | A | 1 | a0002c0001t0001g0123 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-13-2134G>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404292 | |||||||
| chr2:85404294 | A | C | 1 | a0002c0001t0001g0123 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-13-2136T>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404294 | |||||||
| chr2:85404298 | T | A | 5 | a0002c0001t0001g0009 a0002c0001t0001g0043 a0002c0001t0001g0118 others(2): Show |
11 | HG01433.hp2 HG01952.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13-2140A>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404298 | |||||||
| chr2:85404517 | G | A | 3 | a0002c0001t0001g0040 a0002c0001t0001g0095 a0002c0001t0001g0102 |
4 | HG00280.hp2 HG03017.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-2359C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404517 | |||||||
| chr2:85404620 | C | T | 21 | a0001c0002t0001g0199 a0001c0002t0001g0203 a0001c0002t0001g0204 others(18): Show |
42 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.-13-2462G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404620 | |||||||
| chr2:85404628 | A | G | 1 | a0001c0003t0001g0150 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-13-2470T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404628 | |||||||
| chr2:85404696 | T | C | 63 | a0001c0002t0001g0199 a0001c0002t0001g0203 a0001c0002t0001g0204 others(60): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.-13-2538A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404696 | |||||||
| chr2:85404786 | A | C | 1 | a0002c0001t0001g0123 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-13-2628T>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404786 | |||||||
| chr2:85404851 | G | A | 1 | a0001c0002t0001g0183 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-13-2693C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404851 | |||||||
| chr2:85404907 | A | G | 1 | a0002c0001t0001g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-13-2749T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404907 | |||||||
| chr2:85404935 | C | CA | 11 | a0001c0003t0001g0219 a0001c0003t0001g0220 a0002c0001t0001g0119 others(8): Show |
17 | HG01884.hp1 HG02109.hp2 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.-13-2778dupT | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404935 | |||||||
| chr2:85404935 | CA | C | 34 | a0001c0002t0001g0168 a0001c0002t0001g0199 a0001c0003t0001g0006 others(31): Show |
56 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.-13-2778delT | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404935 | |||||||
| chr2:85404936 | A | C | 1 | a0001c0002t0001g0030 | 2 | HG02451.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-13-2778T>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404936 | |||||||
| chr2:85404950 | AAT | A | 21 | a0001c0002t0001g0021 a0001c0002t0001g0038 a0001c0002t0001g0047 others(18): Show |
28 | HG00639.hp2 HG01081.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.-13-2794_-13-2793d others(4): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404950 | |||||||
| chr2:85404951 | A | T | 1 | a0001c0003t0001g0086 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-13-2793T>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404951 | |||||||
| chr2:85404951 | AT | A | 69 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(66): Show |
119 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.-13-2794delA | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404951 | |||||||
| chr2:85404952 | T | A | 1 | a0001c0003t0001g0058 | 2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-13-2794A>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404952 | |||||||
| chr2:85404961 | T | A | 1 | a0002c0001t0001g0121 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-13-2803A>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85404961 | |||||||
| chr2:85405050 | T | C | 1 | a0002c0001t0001g0122 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-13-2892A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85405050 | |||||||
| chr2:85405220 | A | T | 12 | a0001c0003t0001g0020 a0001c0003t0001g0080 a0001c0003t0001g0141 others(9): Show |
15 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.-13-3062T>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85405220 | |||||||
| chr2:85405263 | C | T | 1 | a0001c0002t0001g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-13-3105G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85405263 | |||||||
| chr2:85405299 | G | A | 2 | a0001c0003t0001g0045 a0001c0003t0001g0159 |
3 | HG02809.hp2 HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-13-3141C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85405299 | |||||||
| chr2:85405367 | G | A | 1 | a0001c0003t0001g0086 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-13-3209C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85405367 | |||||||
| chr2:85405697 | T | C | 1 | a0002c0001t0001g0145 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-13-3539A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85405697 | |||||||
| chr2:85405729 | A | G | 22 | a0001c0003t0001g0086 a0001c0003t0001g0219 a0001c0003t0001g0220 others(19): Show |
32 | HG00323.hp1 HG00642.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.-13-3571T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85405729 | |||||||
| chr2:85405735 | C | G | 61 | a0001c0002t0001g0199 a0001c0002t0001g0203 a0001c0002t0001g0204 others(58): Show |
103 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.-13-3577G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85405735 | |||||||
| chr2:85405805 | G | A | 21 | a0001c0002t0001g0199 a0001c0002t0001g0203 a0001c0002t0001g0204 others(18): Show |
42 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.-13-3647C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85405805 | |||||||
| chr2:85405819 | C | G | 6 | a0001c0002t0001g0023 a0001c0002t0001g0054 a0001c0002t0001g0190 others(3): Show |
10 | HG00099.hp2 HG00733.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13-3661G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85405819 | |||||||
| chr2:85405853 | C | G | 5 | a0004c0005t0001g0010 a0004c0005t0001g0048 a0004c0005t0001g0165 others(2): Show |
11 | HG00408.hp1 HG00423.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13-3695G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85405853 | |||||||
| chr2:85405866 | T | A | 1 | a0002c0001t0001g0123 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-13-3708A>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85405866 | |||||||
| chr2:85405930 | T | C | 21 | a0001c0002t0001g0199 a0001c0002t0001g0203 a0001c0002t0001g0204 others(18): Show |
42 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.-13-3772A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85405930 | |||||||
| chr2:85406056 | C | T | 2 | a0001c0003t0001g0045 a0001c0003t0001g0159 |
3 | HG02809.hp2 HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-13-3898G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85406056 | |||||||
| chr2:85406251 | CA | C | 6 | a0001c0002t0001g0158 a0001c0003t0001g0164 a0002c0001t0001g0097 others(3): Show |
6 | HG01168.hp1 HG01516.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14+4065delT | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85406251 | |||||||
| chr2:85406259 | A | AAAAAAGA others(4): Show |
20 | a0001c0002t0001g0199 a0001c0002t0001g0203 a0001c0002t0001g0204 others(17): Show |
41 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(38): Show |
intron_variant | MODIFIER | c.-14+4047_-14+4057d others(13): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85406259 | |||||||
| chr2:85406259 | A | AAAAAGAA others(3): Show |
1 | a0001c0003t0001g0200 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-14+4057_-14+4058i others(12): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85406259 | |||||||
| chr2:85406287 | T | C | 63 | a0001c0002t0001g0199 a0001c0002t0001g0203 a0001c0002t0001g0204 others(60): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.-14+4030A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85406287 | |||||||
| chr2:85406377 | C | A | 21 | a0001c0002t0001g0199 a0001c0002t0001g0203 a0001c0002t0001g0204 others(18): Show |
42 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.-14+3940G>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85406377 | |||||||
| chr2:85406408 | G | A | 1 | a0003c0004t0001g0186 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-14+3909C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85406408 | |||||||
| chr2:85406612 | A | C | 1 | a0002c0001t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-14+3705T>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85406612 | |||||||
| chr2:85406630 | G | A | 2 | a0001c0003t0001g0152 a0002c0011t0001g0151 |
2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-14+3687C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85406630 | |||||||
| chr2:85406654 | T | C | 1 | a0001c0003t0001g0058 | 2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-14+3663A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85406654 | |||||||
| chr2:85406934 | C | CT | 38 | a0001c0002t0001g0199 a0001c0002t0001g0203 a0001c0002t0001g0204 others(35): Show |
66 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.-14+3382dupA | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85406934 | |||||||
| chr2:85406934 | CT | C | 12 | a0001c0002t0001g0023 a0001c0003t0001g0020 a0001c0003t0001g0080 others(9): Show |
15 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.-14+3382delA | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85406934 | |||||||
| chr2:85406935 | T | C | 1 | a0001c0002t0001g0158 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-14+3382A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85406935 | |||||||
| chr2:85407017 | G | A | 1 | a0001c0002t0001g0047 | 2 | HG00639.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.-14+3300C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407017 | |||||||
| chr2:85407067 | T | C | 9 | a0003c0006t0001g0037 a0003c0006t0001g0060 a0003c0006t0001g0061 others(6): Show |
10 | HG01168.hp1 HG01255.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14+3250A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407067 | |||||||
| chr2:85407215 | G | A | 10 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0209 others(7): Show |
13 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14+3102C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407215 | |||||||
| chr2:85407321 | A | G | 1 | a0001c0003t0001g0200 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-14+2996T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407321 | |||||||
| chr2:85407475 | G | C | 21 | a0001c0002t0001g0199 a0001c0002t0001g0203 a0001c0002t0001g0204 others(18): Show |
42 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.-14+2842C>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407475 | |||||||
| chr2:85407520 | C | T | 1 | a0001c0002t0001g0158 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-14+2797G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407520 | |||||||
| chr2:85407521 | T | G | 1 | a0001c0002t0001g0158 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-14+2796A>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407521 | |||||||
| chr2:85407531 | G | A | 19 | a0003c0004t0001g0007 a0003c0004t0001g0012 a0003c0004t0001g0081 others(16): Show |
29 | HG00323.hp1 HG00642.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-14+2786C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407531 | |||||||
| chr2:85407550 | A | G | 1 | a0001c0003t0001g0055 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-14+2767T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407550 | |||||||
| chr2:85407581 | C | T | 1 | a0002c0001t0001g0103 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-14+2736G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407581 | |||||||
| chr2:85407661 | C | T | 3 | a0001c0002t0001g0182 a0001c0002t0001g0183 a0001c0010t0001g0176 |
3 | HG03098.hp2 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-14+2656G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407661 | |||||||
| chr2:85407712 | C | CA | 69 | a0001c0003t0001g0016 a0001c0003t0001g0032 a0001c0003t0001g0033 others(66): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.-14+2604dupT | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407712 | |||||||
| chr2:85407712 | C | CAA | 5 | a0002c0001t0001g0028 a0002c0001t0001g0124 a0002c0001t0001g0134 others(2): Show |
7 | HG01123.hp2 HG01516.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+2603_-14+2604d others(4): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407712 | |||||||
| chr2:85407712 | CA | C | 97 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0008 others(94): Show |
166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-14+2604delT | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407712 | |||||||
| chr2:85407712 | CAA | C | 5 | a0001c0002t0001g0022 a0001c0002t0001g0191 a0001c0003t0001g0153 others(2): Show |
8 | HG01069.hp2 HG01884.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14+2603_-14+2604d others(4): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407712 | |||||||
| chr2:85407712 | CAAA | C | 10 | a0001c0003t0001g0020 a0001c0003t0001g0080 a0001c0003t0001g0141 others(7): Show |
13 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.-14+2602_-14+2604d others(5): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407712 | |||||||
| chr2:85407724 | A | C | 1 | a0004c0005t0001g0175 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-14+2593T>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407724 | |||||||
| chr2:85407749 | TA | T | 59 | a0001c0002t0001g0167 a0002c0001t0001g0001 a0002c0001t0001g0003 others(56): Show |
126 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.-14+2567delT | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407749 | |||||||
| chr2:85407879 | T | C | 1 | a0001c0003t0001g0155 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-14+2438A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407879 | |||||||
| chr2:85407881 | C | A | 9 | a0003c0006t0001g0037 a0003c0006t0001g0060 a0003c0006t0001g0061 others(6): Show |
10 | HG01168.hp1 HG01255.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14+2436G>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407881 | |||||||
| chr2:85407892 | G | C | 1 | a0001c0003t0001g0163 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-14+2425C>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407892 | |||||||
| chr2:85407986 | G | A | 1 | a0002c0001t0001g0135 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-14+2331C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85407986 | |||||||
| chr2:85408113 | C | T | 2 | a0001c0003t0001g0045 a0001c0003t0001g0159 |
3 | HG02809.hp2 HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-14+2204G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408113 | |||||||
| chr2:85408304 | T | C | 62 | a0001c0002t0001g0038 a0001c0002t0001g0199 a0001c0002t0001g0203 others(59): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.-14+2013A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408304 | |||||||
| chr2:85408328 | G | C | 21 | a0001c0002t0001g0199 a0001c0002t0001g0203 a0001c0002t0001g0204 others(18): Show |
42 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.-14+1989C>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408328 | |||||||
| chr2:85408338 | T | TCA | 12 | a0001c0002t0001g0030 a0001c0002t0001g0156 a0001c0002t0001g0157 others(9): Show |
22 | HG00408.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.-14+1977_-14+1978d others(4): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408338 | |||||||
| chr2:85408338 | T | TCACA | 19 | a0001c0002t0001g0021 a0001c0002t0001g0023 a0001c0002t0001g0046 others(16): Show |
29 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-14+1975_-14+1978d others(6): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408338 | |||||||
| chr2:85408338 | T | TCACACA | 20 | a0001c0002t0001g0002 a0001c0002t0001g0022 a0001c0002t0001g0031 others(17): Show |
41 | HG00438.hp2 HG00558.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.-14+1973_-14+1978d others(8): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408338 | |||||||
| chr2:85408338 | T | TCACACAC others(1): Show |
22 | a0001c0002t0001g0005 a0001c0002t0001g0017 a0001c0002t0001g0034 others(19): Show |
34 | HG00609.hp1 HG00621.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14+1971_-14+1978d others(10): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408338 | |||||||
| chr2:85408338 | T | TCACACAC others(3): Show |
12 | a0001c0002t0001g0015 a0001c0002t0001g0036 a0001c0002t0001g0053 others(9): Show |
19 | HG02074.hp2 HG02129.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-14+1969_-14+1978d others(12): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408338 | |||||||
| chr2:85408338 | T | TCACACAC others(5): Show |
10 | a0001c0002t0001g0073 a0001c0002t0001g0198 a0001c0002t0001g0214 others(7): Show |
10 | HG00609.hp2 HG01168.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14+1967_-14+1978d others(14): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408338 | |||||||
| chr2:85408338 | T | TCACACAC others(7): Show |
4 | a0001c0002t0001g0035 a0001c0003t0001g0057 a0003c0006t0001g0061 others(1): Show |
7 | HG00099.hp1 HG00140.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14+1965_-14+1978d others(16): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408338 | |||||||
| chr2:85408338 | T | TCACACAC others(9): Show |
4 | a0001c0002t0001g0216 a0001c0003t0001g0208 a0003c0006t0001g0079 others(1): Show |
4 | HG00735.hp1 HG01255.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+1963_-14+1978d others(18): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408338 | |||||||
| chr2:85408338 | TCA | T | 21 | a0001c0002t0001g0199 a0001c0002t0001g0224 a0001c0003t0001g0006 others(18): Show |
53 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.-14+1977_-14+1978d others(4): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408338 | |||||||
| chr2:85408338 | TCACA | T | 59 | a0002c0001t0001g0001 a0002c0001t0001g0004 a0002c0001t0001g0009 others(56): Show |
123 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.-14+1975_-14+1978d others(6): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408338 | |||||||
| chr2:85408338 | TCACACA | T | 6 | a0001c0002t0001g0038 a0002c0001t0001g0095 a0003c0004t0001g0012 others(3): Show |
11 | HG00323.hp1 HG00642.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14+1973_-14+1978d others(8): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408338 | |||||||
| chr2:85408338 | TCACACAC others(1): Show |
T | 8 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0003t0001g0219 others(5): Show |
13 | HG01169.hp2 HG01884.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-14+1971_-14+1978d others(10): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408338 | |||||||
| chr2:85408338 | TCACACAC others(3): Show |
T | 2 | a0001c0002t0001g0008 a0001c0002t0001g0090 |
7 | HG00741.hp1 HG01167.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14+1969_-14+1978d others(12): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408338 | |||||||
| chr2:85408338 | TCACACAC others(7): Show |
T | 3 | a0002c0001t0001g0087 a0002c0001t0001g0088 a0002c0001t0001g0089 |
3 | HG04184.hp2 NA18956.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-14+1965_-14+1978d others(16): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408338 | |||||||
| chr2:85408338 | TCACACAC others(9): Show |
T | 1 | a0001c0003t0001g0086 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-14+1963_-14+1978d others(18): Show |
CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408338 | |||||||
| chr2:85408344 | A | G | 1 | a0002c0001t0001g0096 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-14+1973T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408344 | |||||||
| chr2:85408368 | A | T | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1949T>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408368 | |||||||
| chr2:85408370 | A | T | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1947T>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408370 | |||||||
| chr2:85408372 | A | T | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1945T>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408372 | |||||||
| chr2:85408375 | C | A | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1942G>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408375 | |||||||
| chr2:85408376 | A | C | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1941T>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408376 | |||||||
| chr2:85408377 | C | A | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1940G>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408377 | |||||||
| chr2:85408389 | T | C | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1928A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408389 | |||||||
| chr2:85408391 | T | A | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1926A>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408391 | |||||||
| chr2:85408393 | C | G | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1924G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408393 | |||||||
| chr2:85408394 | T | G | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1923A>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408394 | |||||||
| chr2:85408395 | T | A | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1922A>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408395 | |||||||
| chr2:85408396 | C | G | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1921G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408396 | |||||||
| chr2:85408397 | C | G | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1920G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408397 | |||||||
| chr2:85408402 | C | A | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1915G>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408402 | |||||||
| chr2:85408403 | C | G | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1914G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408403 | |||||||
| chr2:85408405 | T | A | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1912A>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408405 | |||||||
| chr2:85408407 | T | A | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1910A>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408407 | |||||||
| chr2:85408408 | C | A | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1909G>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408408 | |||||||
| chr2:85408409 | A | G | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1908T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408409 | |||||||
| chr2:85408412 | C | A | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1905G>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408412 | |||||||
| chr2:85408413 | C | G | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1904G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408413 | |||||||
| chr2:85408414 | C | A | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1903G>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408414 | |||||||
| chr2:85408415 | C | G | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1902G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408415 | |||||||
| chr2:85408417 | G | T | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1900C>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408417 | |||||||
| chr2:85408420 | G | C | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1897C>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408420 | |||||||
| chr2:85408426 | G | C | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1891C>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408426 | |||||||
| chr2:85408427 | G | A | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1890C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408427 | |||||||
| chr2:85408432 | T | A | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1885A>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408432 | |||||||
| chr2:85408433 | T | A | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1884A>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408433 | |||||||
| chr2:85408435 | C | G | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1882G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408435 | |||||||
| chr2:85408440 | C | G | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1877G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408440 | |||||||
| chr2:85408441 | A | G | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1876T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408441 | |||||||
| chr2:85408442 | T | A | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1875A>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408442 | |||||||
| chr2:85408443 | T | A | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1874A>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408443 | |||||||
| chr2:85408447 | T | A | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1870A>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408447 | |||||||
| chr2:85408453 | C | A | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1864G>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408453 | |||||||
| chr2:85408454 | C | G | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1863G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408454 | |||||||
| chr2:85408455 | G | A | 2 | a0002c0001t0001g0187 a0003c0004t0001g0186 |
2 | HG02293.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-14+1862C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408455 | |||||||
| chr2:85408456 | C | G | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1861G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408456 | |||||||
| chr2:85408457 | C | A | 1 | a0002c0001t0001g0187 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14+1860G>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408457 | |||||||
| chr2:85408463 | T | A | 1 | a0002c0001t0001g0188 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-14+1854A>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408463 | |||||||
| chr2:85408506 | C | T | 21 | a0001c0002t0001g0199 a0001c0002t0001g0203 a0001c0002t0001g0204 others(18): Show |
42 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.-14+1811G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408506 | |||||||
| chr2:85408822 | C | CG | 8 | a0001c0002t0001g0038 a0003c0004t0001g0007 a0003c0004t0001g0012 others(5): Show |
18 | HG00323.hp1 HG00642.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.-14+1494dupC | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408822 | |||||||
| chr2:85408825 | G | A | 1 | a0002c0001t0001g0189 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-14+1492C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408825 | |||||||
| chr2:85408999 | C | G | 1 | a0001c0003t0001g0080 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-14+1318G>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85408999 | |||||||
| chr2:85409069 | G | A | 11 | a0001c0002t0001g0023 a0001c0002t0001g0054 a0001c0002t0001g0190 others(8): Show |
15 | HG00099.hp2 HG00733.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.-14+1248C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85409069 | |||||||
| chr2:85409072 | T | C | 32 | a0001c0002t0001g0034 a0001c0002t0001g0035 a0001c0002t0001g0199 others(29): Show |
57 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.-14+1245A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85409072 | |||||||
| chr2:85409261 | A | G | 9 | a0003c0006t0001g0037 a0003c0006t0001g0060 a0003c0006t0001g0061 others(6): Show |
10 | HG01168.hp1 HG01255.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14+1056T>C | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85409261 | |||||||
| chr2:85409309 | G | A | 1 | a0001c0003t0001g0217 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-14+1008C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85409309 | |||||||
| chr2:85409417 | C | T | 1 | a0001c0002t0001g0218 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-14+900G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85409417 | |||||||
| chr2:85409465 | C | T | 14 | a0001c0002t0001g0017 a0001c0002t0001g0036 a0001c0002t0001g0062 others(11): Show |
18 | HG00609.hp2 HG02129.hp2 HG02155.hp1 others(15): Show |
intron_variant | MODIFIER | c.-14+852G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85409465 | |||||||
| chr2:85409497 | C | T | 2 | a0003c0006t0001g0060 a0003c0006t0001g0061 |
2 | HG02735.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-14+820G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85409497 | |||||||
| chr2:85409705 | T | C | 3 | a0001c0002t0001g0218 a0001c0003t0001g0219 a0001c0003t0001g0220 |
3 | HG02647.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-14+612A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85409705 | |||||||
| chr2:85409820 | T | C | 1 | a0002c0001t0001g0221 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-14+497A>G | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85409820 | |||||||
| chr2:85409953 | C | A | 1 | a0001c0002t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-14+364G>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85409953 | |||||||
| chr2:85410062 | G | A | 1 | a0002c0001t0001g0223 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-14+255C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85410062 | |||||||
| chr2:85410200 | C | T | 2 | a0001c0003t0001g0006 a0001c0003t0001g0059 |
7 | NA18947.hp1 NA18960.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14+117G>A | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85410200 | |||||||
| chr2:85410256 | G | A | 2 | a0001c0002t0001g0224 a0001c0002t0001g0225 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-14+61C>T | CAPG | ENSG00000042493.16 | transcript | ENST00000263867.9 | protein_coding | 1/9 | chr2 | 85410256 |