Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10487 |
| ensemblid | ENSG00000131236.18 |
| hgncid | 20040 |
| symbol | CAP1 |
| name | cyclase associated actin cytoskeleton regulatory protein 1 |
| refseq_nuc | NM_006367.4 |
| refseq_prot | NP_006358.2 |
| ensembl_nuc | ENST00000372805.8 |
| ensembl_prot | ENSP00000361891.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 40040729 |
| end | 40072648 |
| strand | + |
| ver | v1.2 |
| region | chr1:40040729-40072648 |
| region5000 | chr1:40035729-40077648 |
| regionname0 | CAP1_chr1_40040729_40072648 |
| regionname5000 | CAP1_chr1_40035729_40077648 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 475 | 374 | 96 | 46 | 174 | 16 | 41 | 138 | CAP1_chr1_40035729_40077648 | CAP1 | MADMQ others(470): Show |
chr1 | 40035729 | 40077648 |
| a0002 | 0/0 | 475 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | MADMQ others(470): Show |
chr1 | 40035729 | 40077648 |
| a0003 | 0/0 | 475 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | MADMQ others(470): Show |
chr1 | 40035729 | 40077648 |
| a0004 | 0/1 | 475 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | MADMQ others(470): Show |
chr1 | 40035729 | 40077648 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1425 | 360 | 82 | 46 | 174 | 16 | 41 | CAP1_chr1_40035729_40077648 | CAP1 | ATGGC others(1420): Show |
chr1 | 40035729 | 40077648 | ||
| a0001c0002 | 0/0 | 1425 | 9 | 9 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | ATGGC others(1420): Show |
chr1 | 40035729 | 40077648 | ||
| a0001c0003 | 0/0 | 1425 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | ATGGC others(1420): Show |
chr1 | 40035729 | 40077648 | ||
| a0001c0005 | 0/0 | 1425 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | ATGGC others(1420): Show |
chr1 | 40035729 | 40077648 | ||
| a0001c0008 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | ATGGC others(1420): Show |
chr1 | 40035729 | 40077648 | ||
| a0002c0004 | 0/0 | 1425 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | ATGGC others(1420): Show |
chr1 | 40035729 | 40077648 | ||
| a0003c0007 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | ATGGC others(1420): Show |
chr1 | 40035729 | 40077648 | ||
| a0004c0006 | 0/1 | 1425 | 1 | 0 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | ATGGC others(1420): Show |
chr1 | 40035729 | 40077648 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2627 | 123 | 28 | 17 | 54 | 6 | 18 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2622): Show |
chr1 | 40035729 | 40077648 |
| a0001c0001t0002 | 0/0 | 2628 | 68 | 10 | 5 | 40 | 3 | 10 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2623): Show |
chr1 | 40035729 | 40077648 |
| a0001c0001t0003 | 0/0 | 2627 | 63 | 9 | 4 | 42 | 1 | 7 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2622): Show |
chr1 | 40035729 | 40077648 |
| a0001c0001t0004 | 1/0 | 2626 | 54 | 16 | 14 | 16 | 3 | 4 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2621): Show |
chr1 | 40035729 | 40077648 |
| a0001c0001t0005 | 0/0 | 2628 | 11 | 11 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2623): Show |
chr1 | 40035729 | 40077648 |
| a0001c0001t0006 | 0/0 | 2627 | 11 | 0 | 1 | 9 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2622): Show |
chr1 | 40035729 | 40077648 |
| a0001c0001t0007 | 0/0 | 2625 | 5 | 0 | 2 | 0 | 3 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2620): Show |
chr1 | 40035729 | 40077648 |
| a0001c0001t0008 | 0/0 | 2627 | 4 | 0 | 0 | 4 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2622): Show |
chr1 | 40035729 | 40077648 |
| a0001c0001t0009 | 0/0 | 2627 | 4 | 1 | 1 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2622): Show |
chr1 | 40035729 | 40077648 |
| a0001c0001t0011 | 0/0 | 2628 | 4 | 2 | 2 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2623): Show |
chr1 | 40035729 | 40077648 |
| a0001c0001t0012 | 0/0 | 2628 | 3 | 1 | 0 | 1 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2623): Show |
chr1 | 40035729 | 40077648 |
| a0001c0001t0014 | 0/0 | 2627 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2622): Show |
chr1 | 40035729 | 40077648 |
| a0001c0001t0016 | 0/0 | 2628 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2623): Show |
chr1 | 40035729 | 40077648 |
| a0001c0001t0017 | 0/0 | 2627 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2622): Show |
chr1 | 40035729 | 40077648 |
| a0001c0001t0018 | 0/0 | 2628 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2623): Show |
chr1 | 40035729 | 40077648 |
| a0001c0001t0019 | 0/0 | 2627 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2622): Show |
chr1 | 40035729 | 40077648 |
| a0001c0001t0020 | 0/0 | 2627 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2622): Show |
chr1 | 40035729 | 40077648 |
| a0001c0001t0021 | 0/0 | 2627 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2622): Show |
chr1 | 40035729 | 40077648 |
| a0001c0001t0022 | 0/0 | 2628 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2623): Show |
chr1 | 40035729 | 40077648 |
| a0001c0001t0023 | 0/0 | 2626 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2621): Show |
chr1 | 40035729 | 40077648 |
| a0001c0002t0010 | 0/0 | 2628 | 4 | 4 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2623): Show |
chr1 | 40035729 | 40077648 |
| a0001c0002t0013 | 0/0 | 2626 | 3 | 3 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2621): Show |
chr1 | 40035729 | 40077648 |
| a0001c0002t0015 | 0/0 | 2626 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2621): Show |
chr1 | 40035729 | 40077648 |
| a0001c0003t0004 | 0/0 | 2626 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2621): Show |
chr1 | 40035729 | 40077648 |
| a0001c0005t0004 | 0/0 | 2626 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2621): Show |
chr1 | 40035729 | 40077648 |
| a0001c0005t0005 | 0/0 | 2628 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2623): Show |
chr1 | 40035729 | 40077648 |
| a0001c0008t0001 | 0/0 | 2627 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2622): Show |
chr1 | 40035729 | 40077648 |
| a0002c0004t0004 | 0/0 | 2626 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2621): Show |
chr1 | 40035729 | 40077648 |
| a0003c0007t0001 | 0/0 | 2627 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2622): Show |
chr1 | 40035729 | 40077648 |
| a0004c0006t0001 | 0/1 | 2627 | 1 | 0 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | GAGAT others(2622): Show |
chr1 | 40035729 | 40077648 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 25 | 3 | 3 | 12 | 0 | 7 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0005 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0008 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0002 | 0/0 | 22 | 0 | 2 | 13 | 2 | 5 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0004 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0020 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0003 | 0/0 | 9 | 0 | 6 | 2 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0017 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0166 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0005g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0005g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0006g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0006g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0006g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0007g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0007g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0007g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0007g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0008g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0008g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0009g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0009g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0011g0013 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0011g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0012g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0012g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0012g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0014g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0016g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0017g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0018g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0019g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0020g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0021g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0022g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0001t0023g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0002t0010g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0002t0010g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0002t0013g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0002t0013g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0002t0015g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0003t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0003t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0005t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0005t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0001c0008t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0002c0004t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0003c0007t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| a0004c0006t0001g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | GBR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0003 | EUR | GBR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00140 | hp1 | a0001 | c0001 | t0007 | g0167 | EUR | GBR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0088 | EUR | GBR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0169 | EUR | FIN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | FIN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | CHS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00423 | hp2 | a0001 | c0001 | t0016 | g0007 | EAS | CHS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | CHS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | CHS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0158 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0164 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01071 | hp1 | a0001 | c0001 | t0011 | g0013 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0040 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0161 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0209 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0216 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01243 | hp1 | a0001 | c0001 | t0011 | g0013 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0174 | AMR | PUR | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | CLM | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01261 | hp2 | a0001 | c0001 | t0007 | g0145 | AMR | CLM | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0176 | AMR | CLM | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01496 | hp1 | a0001 | c0001 | t0006 | g0023 | AMR | CLM | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0155 | AMR | CLM | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01515 | hp1 | a0001 | c0001 | t0007 | g0003 | EUR | IBS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01517 | hp1 | a0001 | c0001 | t0007 | g0003 | EUR | IBS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01891 | hp1 | a0001 | c0005 | t0005 | g0022 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0153 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG01981 | hp2 | a0001 | c0001 | t0009 | g0168 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02027 | hp1 | a0001 | c0001 | t0006 | g0024 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02055 | hp2 | a0001 | c0005 | t0004 | g0063 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0154 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02145 | hp2 | a0001 | c0002 | t0013 | g0047 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CDX | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02257 | hp1 | a0001 | c0001 | t0021 | g0184 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0057 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0172 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0217 | AMR | PEL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02622 | hp1 | a0001 | c0002 | t0010 | g0045 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0009 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02647 | hp1 | a0002 | c0004 | t0004 | g0038 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02717 | hp1 | a0001 | c0002 | t0010 | g0046 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02717 | hp2 | a0001 | c0003 | t0004 | g0140 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02723 | hp1 | a0001 | c0002 | t0013 | g0047 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02723 | hp2 | a0001 | c0002 | t0015 | g0044 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02738 | hp1 | a0001 | c0001 | t0012 | g0192 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02809 | hp2 | a0001 | c0002 | t0015 | g0044 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02818 | hp1 | a0001 | c0003 | t0004 | g0138 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0144 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02922 | hp2 | a0001 | c0001 | t0011 | g0054 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0058 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0199 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03098 | hp1 | a0001 | c0002 | t0010 | g0046 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03130 | hp2 | a0001 | c0001 | t0011 | g0013 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03139 | hp1 | a0001 | c0001 | t0014 | g0037 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0165 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0204 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0060 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0059 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0202 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03516 | hp1 | a0001 | c0001 | t0012 | g0183 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | ESN | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03579 | hp1 | a0001 | c0008 | t0001 | g0188 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0019 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0173 | SAS | STU | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0017 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0162 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0160 | SAS | BEB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03927 | hp1 | a0003 | c0007 | t0001 | g0001 | SAS | BEB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0020 | SAS | BEB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0212 | SAS | BEB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG04199 | hp1 | a0001 | c0001 | t0006 | g0065 | SAS | STU | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | STU | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0020 | SAS | STU | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0182 | AFR | YRI | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | CHB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | CHB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | YRI | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18944 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18949 | hp1 | a0001 | c0001 | t0018 | g0225 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18949 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18950 | hp2 | a0001 | c0001 | t0017 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18954 | hp1 | a0001 | c0001 | t0012 | g0229 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18956 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18960 | hp2 | a0001 | c0001 | t0019 | g0231 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18975 | hp2 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18986 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18987 | hp1 | a0001 | c0001 | t0004 | g0156 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18993 | hp2 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19002 | hp1 | a0001 | c0001 | t0006 | g0064 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19003 | hp2 | a0001 | c0001 | t0008 | g0220 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0170 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | LWK | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19030 | hp2 | a0001 | c0001 | t0023 | g0053 | AFR | LWK | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19043 | hp1 | a0001 | c0002 | t0010 | g0045 | AFR | LWK | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | LWK | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19057 | hp1 | a0001 | c0001 | t0020 | g0195 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19059 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19059 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19064 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19064 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19065 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19066 | hp1 | a0001 | c0001 | t0006 | g0024 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19068 | hp2 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0146 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19085 | hp2 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | YRI | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | YRI | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ASW | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0180 | AFR | ASW | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0159 | EUR | TSI | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | TSI | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | TSI | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0185 | EUR | TSI | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0193 | SAS | GIH | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02559 | hp1 | a0001 | c0001 | t0014 | g0037 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | ACB | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0151 | AFR | MSL | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | USA | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | USA | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA18955 | hp2 | a0001 | c0001 | t0022 | g0002 | EAS | JPT | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA20300 | hp1 | a0001 | c0002 | t0013 | g0227 | AFR | USA | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | USA | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | LWK | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| NA21309 | hp2 | a0002 | c0004 | t0004 | g0038 | AFR | LWK | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| homoSapiens | chm13v2 | a0004 | c0006 | t0001 | g0107 | REF | REF | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0166 | REF | REF | CAP1_chr1_40035729_40077648 | CAP1 | chr1 | 40035729 | 40077648 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:40069786 | C | T | 1 | a0003 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.905C>T | p.Ala302Val | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 9/13 | 988/2626 | 905/1428 | 302/475 | chr1 | 40069786 | |||
| chr1:40070264 | A | G | 1 | a0002 | 2 | HG02647.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.1099A>G | p.Ile367Val | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 10/13 | 1182/2626 | 1099/1428 | 367/475 | chr1 | 40070264 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:40059439 | T | C | 2 | a0001c0003 a0002c0004 |
4 | HG02647.hp1 HG02717.hp2 HG02818.hp1 others(1): Show |
synonymous_variant | LOW | c.93T>C | p.Tyr31Tyr | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 2/13 | 176/2626 | 93/1428 | 31/475 | chr1 | 40059439 | |||
| chr1:40061737 | G | A | 1 | a0001c0002 | 9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
splice_region_variant&synonymous_variant | LOW | c.219G>A | p.Ala73Ala | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/13 | 302/2626 | 219/1428 | 73/475 | chr1 | 40061737 | |||
| chr1:40067587 | C | T | 1 | a0001c0008 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.678C>T | p.Ala226Ala | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/13 | 761/2626 | 678/1428 | 226/475 | chr1 | 40067587 | |||
| chr1:40070281 | A | T | 1 | a0001c0005 | 2 | HG01891.hp1 HG02055.hp2 |
splice_region_variant&synonymous_variant | LOW | c.1116A>T | p.Val372Val | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 10/13 | 1199/2626 | 1116/1428 | 372/475 | chr1 | 40070281 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:40040753 | G | C | 2 | a0001c0001t0006 a0001c0001t0016 |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-59G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/13 | 18594 | chr1 | 40040753 | ||||||
| chr1:40040758 | G | C | 1 | a0001c0001t0017 | 1 | NA18950.hp2 | 5_prime_UTR_variant | MODIFIER | c.-54G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/13 | 18589 | chr1 | 40040758 | ||||||
| chr1:40040779 | C | G | 1 | a0001c0002t0013 | 3 | HG02145.hp2 HG02723.hp1 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-33C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/13 | 18568 | chr1 | 40040779 | ||||||
| chr1:40040782 | A | G | 2 | a0001c0001t0011 a0001c0001t0023 |
5 | HG01071.hp1 HG01243.hp1 HG02922.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-30A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/13 | 18565 | chr1 | 40040782 | ||||||
| chr1:40071536 | G | A | 2 | a0001c0001t0008 a0001c0001t0018 |
5 | NA18949.hp1 NA18993.hp2 NA19003.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 3 | chr1 | 40071536 | ||||||
| chr1:40071759 | TC | T | 1 | a0001c0001t0007 | 5 | HG00140.hp1 HG00735.hp2 HG01261.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*227delC | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 227 | chr1 | 40071759 | ||||||
| chr1:40071893 | C | T | 2 | a0001c0001t0006 a0001c0001t0016 |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*360C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 360 | chr1 | 40071893 | ||||||
| chr1:40071944 | A | G | 3 | a0001c0002t0010 a0001c0002t0013 a0001c0002t0015 |
9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*411A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 411 | chr1 | 40071944 | ||||||
| chr1:40071991 | C | T | 1 | a0001c0001t0022 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*458C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 458 | chr1 | 40071991 | ||||||
| chr1:40072118 | A | G | 1 | a0001c0001t0014 | 2 | HG02559.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*585A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 585 | chr1 | 40072118 | ||||||
| chr1:40072252 | G | GA | 3 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0019 |
16 | HG01496.hp1 HG01981.hp2 HG02027.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*738dupA | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 739 | INFO_REALIGN_3_PRIME | chr1 | 40072252 | |||||
| chr1:40072252 | G | GAA | 5 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0016 others(2): Show |
21 | HG00423.hp2 HG01071.hp1 HG01243.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*737_*738dupAA | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 739 | INFO_REALIGN_3_PRIME | chr1 | 40072252 | |||||
| chr1:40072268 | A | AAC | 4 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0018 others(1): Show |
73 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*736_*737insCA | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 737 | INFO_REALIGN_3_PRIME | chr1 | 40072268 | |||||
| chr1:40072268 | A | AC | 9 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(6): Show |
197 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*735_*736insC | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 736 | chr1 | 40072268 | ||||||
| chr1:40072311 | C | T | 1 | a0001c0001t0021 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*778C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 778 | chr1 | 40072311 | ||||||
| chr1:40072429 | G | A | 7 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0012 others(4): Show |
74 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*896G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 896 | chr1 | 40072429 | ||||||
| chr1:40072555 | C | G | 1 | a0001c0001t0020 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1022C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 13/13 | 1022 | chr1 | 40072555 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:40040843 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0002g0048 |
2 | NA18979.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.-11+42G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40040843 | |||||||
| chr1:40040862 | G | T | 65 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(62): Show |
84 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(81): Show |
intron_variant | MODIFIER | c.-11+61G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40040862 | |||||||
| chr1:40040918 | G | A | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 |
3 | NA18960.hp1 NA18964.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-11+117G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40040918 | |||||||
| chr1:40041053 | G | A | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+252G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041053 | |||||||
| chr1:40041058 | G | C | 1 | a0001c0001t0023g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-11+257G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041058 | |||||||
| chr1:40041126 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-11+325C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041126 | |||||||
| chr1:40041440 | C | G | 5 | a0001c0001t0003g0228 a0001c0001t0003g0230 a0001c0001t0003g0232 others(2): Show |
5 | NA18950.hp1 NA18954.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+639C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041440 | |||||||
| chr1:40041473 | C | A | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+672C>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041473 | |||||||
| chr1:40041477 | C | G | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+676C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041477 | |||||||
| chr1:40041496 | A | G | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+695A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041496 | |||||||
| chr1:40041520 | A | G | 1 | a0001c0001t0002g0177 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-11+719A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041520 | |||||||
| chr1:40041550 | G | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(200): Show |
320 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(317): Show |
intron_variant | MODIFIER | c.-11+749G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041550 | |||||||
| chr1:40041552 | G | A | 1 | a0001c0001t0002g0055 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-11+751G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041552 | |||||||
| chr1:40041718 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-11+917T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041718 | |||||||
| chr1:40041734 | G | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0141 others(2): Show |
12 | HG00639.hp1 HG01884.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11+933G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041734 | |||||||
| chr1:40041892 | G | A | 7 | a0001c0001t0003g0041 a0001c0001t0003g0179 a0001c0001t0003g0180 others(4): Show |
8 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-11+1091G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041892 | |||||||
| chr1:40041978 | C | G | 5 | a0001c0002t0010g0045 a0001c0002t0010g0046 a0001c0002t0013g0047 others(2): Show |
9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+1177C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40041978 | |||||||
| chr1:40042033 | T | TTTAA | 86 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(83): Show |
116 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.-11+1235_-11+1238d others(6): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40042033 | ||||||
| chr1:40042074 | G | A | 1 | a0001c0001t0004g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11+1273G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40042074 | |||||||
| chr1:40042186 | G | T | 6 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(3): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+1385G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40042186 | |||||||
| chr1:40042245 | G | C | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0014 others(30): Show |
66 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11+1444G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40042245 | |||||||
| chr1:40042374 | A | G | 1 | a0001c0001t0002g0088 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-11+1573A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40042374 | |||||||
| chr1:40042394 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-11+1593G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40042394 | |||||||
| chr1:40042649 | T | C | 2 | a0001c0001t0002g0066 a0001c0001t0002g0067 |
2 | NA18973.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-11+1848T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40042649 | |||||||
| chr1:40042673 | G | T | 2 | a0001c0002t0013g0047 a0001c0002t0013g0227 |
3 | HG02145.hp2 HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-11+1872G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40042673 | |||||||
| chr1:40042733 | G | A | 12 | a0001c0001t0004g0010 a0001c0001t0004g0061 a0001c0001t0005g0010 others(9): Show |
15 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-11+1932G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40042733 | |||||||
| chr1:40043162 | AAAG | A | 6 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(3): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+2362_-11+2364d others(5): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40043162 | |||||||
| chr1:40043195 | T | TTTTG | 2 | a0001c0001t0002g0014 a0001c0001t0002g0068 |
4 | HG02027.hp2 NA18952.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+2410_-11+2413d others(6): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40043195 | ||||||
| chr1:40043415 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(195): Show |
314 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.-11+2614T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40043415 | |||||||
| chr1:40043424 | C | CT | 60 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(57): Show |
75 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(72): Show |
intron_variant | MODIFIER | c.-11+2624dupT | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40043424 | ||||||
| chr1:40043494 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(75): Show |
130 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-11+2693C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40043494 | |||||||
| chr1:40043596 | G | C | 4 | a0001c0001t0003g0041 a0001c0001t0003g0179 a0001c0001t0003g0180 others(1): Show |
5 | HG02559.hp2 HG02965.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+2795G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40043596 | |||||||
| chr1:40043618 | T | C | 1 | a0001c0002t0015g0044 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-11+2817T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40043618 | |||||||
| chr1:40043634 | T | G | 1 | a0001c0001t0004g0144 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-11+2833T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40043634 | |||||||
| chr1:40043737 | C | T | 5 | a0001c0002t0010g0045 a0001c0002t0010g0046 a0001c0002t0013g0047 others(2): Show |
9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+2936C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40043737 | |||||||
| chr1:40043874 | C | CA | 109 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(106): Show |
195 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.-11+3083dupA | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40043874 | ||||||
| chr1:40044224 | C | G | 5 | a0001c0001t0004g0061 a0001c0001t0005g0022 a0001c0001t0005g0062 others(2): Show |
5 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+3423C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044224 | |||||||
| chr1:40044236 | GA | G | 3 | a0001c0001t0011g0013 a0001c0001t0011g0054 a0001c0001t0023g0053 |
5 | HG01071.hp1 HG01243.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+3445delA | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40044236 | ||||||
| chr1:40044348 | A | C | 1 | a0001c0001t0004g0176 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-11+3547A>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044348 | |||||||
| chr1:40044620 | A | G | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0014 others(30): Show |
66 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11+3819A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044620 | |||||||
| chr1:40044705 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-11+3904C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044705 | |||||||
| chr1:40044760 | C | T | 18 | a0001c0001t0004g0010 a0001c0001t0004g0061 a0001c0001t0005g0010 others(15): Show |
27 | HG00423.hp2 HG01496.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.-11+3959C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044760 | |||||||
| chr1:40044788 | C | CT | 30 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0126 others(27): Show |
34 | HG01243.hp2 HG01433.hp1 HG01978.hp2 others(31): Show |
intron_variant | MODIFIER | c.-11+4013dupT | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40044788 | ||||||
| chr1:40044788 | CT | C | 49 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(46): Show |
87 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-11+4013delT | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40044788 | ||||||
| chr1:40044788 | CTT | C | 55 | a0001c0001t0002g0085 a0001c0001t0003g0006 a0001c0001t0003g0019 others(52): Show |
72 | HG00408.hp2 HG01071.hp1 HG01175.hp1 others(69): Show |
intron_variant | MODIFIER | c.-11+4012_-11+4013d others(4): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40044788 | ||||||
| chr1:40044788 | CTTT | C | 7 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0002t0010g0045 others(4): Show |
11 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+4011_-11+4013d others(5): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40044788 | ||||||
| chr1:40044788 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0007g0145 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-11+4003_-11+4013d others(13): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40044788 | ||||||
| chr1:40044803 | T | A | 1 | a0001c0001t0003g0185 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-11+4002T>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044803 | |||||||
| chr1:40044858 | A | G | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+4057A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044858 | |||||||
| chr1:40044928 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-11+4127C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044928 | |||||||
| chr1:40044931 | G | A | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+4130G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044931 | |||||||
| chr1:40044946 | G | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(56): Show |
74 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(71): Show |
intron_variant | MODIFIER | c.-11+4145G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044946 | |||||||
| chr1:40044987 | G | A | 5 | a0001c0002t0010g0045 a0001c0002t0010g0046 a0001c0002t0013g0047 others(2): Show |
9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+4186G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40044987 | |||||||
| chr1:40045035 | C | T | 1 | a0001c0008t0001g0188 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-11+4234C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045035 | |||||||
| chr1:40045036 | G | A | 3 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | NA18969.hp1 NA18970.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-11+4235G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045036 | |||||||
| chr1:40045216 | T | C | 5 | a0001c0002t0010g0045 a0001c0002t0010g0046 a0001c0002t0013g0047 others(2): Show |
9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+4415T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045216 | |||||||
| chr1:40045255 | G | A | 1 | a0001c0001t0023g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-11+4454G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045255 | |||||||
| chr1:40045317 | C | T | 60 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(57): Show |
75 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(72): Show |
intron_variant | MODIFIER | c.-11+4516C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045317 | |||||||
| chr1:40045340 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-11+4539G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045340 | |||||||
| chr1:40045350 | G | A | 4 | a0001c0001t0003g0189 a0001c0001t0003g0190 a0001c0001t0003g0191 others(1): Show |
4 | NA18943.hp2 NA18947.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+4549G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045350 | |||||||
| chr1:40045372 | A | G | 59 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(56): Show |
74 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(71): Show |
intron_variant | MODIFIER | c.-11+4571A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045372 | |||||||
| chr1:40045467 | T | C | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0014 others(30): Show |
66 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11+4666T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045467 | |||||||
| chr1:40045586 | T | C | 3 | a0001c0001t0011g0013 a0001c0001t0011g0054 a0001c0001t0023g0053 |
5 | HG01071.hp1 HG01243.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+4785T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045586 | |||||||
| chr1:40045595 | G | A | 59 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(56): Show |
74 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(71): Show |
intron_variant | MODIFIER | c.-11+4794G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045595 | |||||||
| chr1:40045627 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-11+4826C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045627 | |||||||
| chr1:40045842 | T | C | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+5041T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045842 | |||||||
| chr1:40045843 | G | A | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0014 others(30): Show |
66 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.-11+5042G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045843 | |||||||
| chr1:40045848 | C | T | 1 | a0001c0001t0003g0221 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-11+5047C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045848 | |||||||
| chr1:40045894 | C | T | 1 | a0001c0001t0002g0014 | 3 | HG02027.hp2 NA18952.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-11+5093C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045894 | |||||||
| chr1:40045968 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-11+5167A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40045968 | |||||||
| chr1:40046253 | C | T | 1 | a0001c0001t0004g0169 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-11+5452C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046253 | |||||||
| chr1:40046321 | T | C | 1 | a0001c0001t0011g0054 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-11+5520T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046321 | |||||||
| chr1:40046430 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-11+5629G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046430 | |||||||
| chr1:40046474 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-11+5673A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046474 | |||||||
| chr1:40046480 | CA | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(198): Show |
318 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.-11+5688delA | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40046480 | ||||||
| chr1:40046492 | A | G | 1 | a0001c0003t0004g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-11+5691A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046492 | |||||||
| chr1:40046510 | A | G | 7 | a0001c0001t0004g0010 a0001c0001t0005g0010 a0001c0001t0005g0021 others(4): Show |
10 | HG02258.hp2 HG02965.hp2 HG03195.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11+5709A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046510 | |||||||
| chr1:40046565 | G | T | 1 | a0001c0001t0001g0125 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-11+5764G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046565 | |||||||
| chr1:40046589 | C | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(56): Show |
74 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(71): Show |
intron_variant | MODIFIER | c.-11+5788C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046589 | |||||||
| chr1:40046711 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0002g0048 |
2 | NA18979.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.-11+5910A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046711 | |||||||
| chr1:40046773 | C | CT | 6 | a0001c0001t0002g0080 a0001c0001t0003g0181 a0001c0001t0003g0226 others(3): Show |
6 | HG00597.hp1 HG00597.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+5989dupT | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40046773 | ||||||
| chr1:40046773 | CT | C | 7 | a0001c0001t0001g0028 a0001c0001t0001g0096 a0001c0001t0002g0066 others(4): Show |
8 | HG02258.hp2 HG02273.hp1 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.-11+5989delT | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40046773 | ||||||
| chr1:40046836 | G | A | 3 | a0001c0001t0005g0022 a0001c0005t0004g0063 a0001c0005t0005g0022 |
3 | HG01891.hp1 HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-11+6035G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046836 | |||||||
| chr1:40046919 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(76): Show |
132 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-11+6118C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046919 | |||||||
| chr1:40046926 | C | A | 1 | a0001c0001t0003g0223 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-11+6125C>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40046926 | |||||||
| chr1:40047062 | C | T | 1 | a0001c0001t0014g0037 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-11+6261C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40047062 | |||||||
| chr1:40047101 | TTATAATC others(39): Show |
T | 86 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(83): Show |
116 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.-11+6316_-11+6361d others(48): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40047101 | ||||||
| chr1:40047192 | A | T | 1 | a0001c0001t0001g0090 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-11+6391A>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40047192 | |||||||
| chr1:40047433 | C | A | 1 | a0001c0001t0012g0192 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-11+6632C>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40047433 | |||||||
| chr1:40047649 | C | T | 60 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(57): Show |
75 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(72): Show |
intron_variant | MODIFIER | c.-11+6848C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40047649 | |||||||
| chr1:40047700 | T | G | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+6899T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40047700 | |||||||
| chr1:40047770 | C | T | 1 | a0001c0001t0009g0168 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-11+6969C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40047770 | |||||||
| chr1:40047880 | G | A | 4 | a0001c0001t0003g0041 a0001c0001t0003g0179 a0001c0001t0003g0180 others(1): Show |
5 | HG02559.hp2 HG02965.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+7079G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40047880 | |||||||
| chr1:40048038 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(74): Show |
129 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-11+7237T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048038 | |||||||
| chr1:40048162 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | NA19057.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-11+7361G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048162 | |||||||
| chr1:40048314 | ATTACAGG others(21): Show |
A | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+7543_-11+7570d others(30): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40048314 | ||||||
| chr1:40048394 | A | C | 60 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(57): Show |
75 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(72): Show |
intron_variant | MODIFIER | c.-11+7593A>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048394 | |||||||
| chr1:40048470 | T | C | 1 | a0001c0008t0001g0188 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-11+7669T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048470 | |||||||
| chr1:40048489 | G | A | 2 | a0001c0001t0011g0013 a0001c0001t0011g0054 |
4 | HG01071.hp1 HG01243.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+7688G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048489 | |||||||
| chr1:40048659 | T | C | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+7858T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048659 | |||||||
| chr1:40048673 | T | A | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+7872T>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048673 | |||||||
| chr1:40048693 | T | G | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+7892T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048693 | |||||||
| chr1:40048752 | C | A | 1 | a0001c0008t0001g0188 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-11+7951C>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048752 | |||||||
| chr1:40048872 | T | C | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+8071T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048872 | |||||||
| chr1:40048997 | A | G | 6 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(3): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+8196A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40048997 | |||||||
| chr1:40049178 | A | AT | 40 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0049 others(37): Show |
75 | HG00140.hp2 HG00597.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.-11+8403dupT | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | ||||||
| chr1:40049178 | A | ATT | 63 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(60): Show |
113 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.-11+8402_-11+8403d others(4): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | ||||||
| chr1:40049178 | A | ATTT | 23 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0092 others(20): Show |
34 | HG00408.hp2 HG00423.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-11+8401_-11+8403d others(5): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | ||||||
| chr1:40049178 | A | ATTTT | 6 | a0001c0001t0001g0124 a0001c0001t0004g0061 a0001c0001t0005g0059 others(3): Show |
8 | HG00741.hp2 HG01496.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11+8400_-11+8403d others(6): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | ||||||
| chr1:40049178 | A | ATTTTT | 4 | a0001c0001t0005g0062 a0001c0002t0010g0045 a0001c0002t0015g0044 others(1): Show |
6 | HG02055.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+8399_-11+8403d others(7): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | ||||||
| chr1:40049178 | A | ATTTTTT | 4 | a0001c0001t0005g0022 a0001c0002t0010g0046 a0001c0002t0013g0047 others(1): Show |
6 | HG01891.hp1 HG02145.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+8398_-11+8403d others(8): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | ||||||
| chr1:40049178 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0003g0186 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-11+8392_-11+8403d others(14): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | ||||||
| chr1:40049178 | A | ATTTTTTT others(6): Show |
25 | a0001c0001t0003g0006 a0001c0001t0003g0042 a0001c0001t0003g0180 others(22): Show |
34 | HG02280.hp1 HG03017.hp1 HG03209.hp2 others(31): Show |
intron_variant | MODIFIER | c.-11+8391_-11+8403d others(15): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | ||||||
| chr1:40049178 | A | ATTTTTTT others(7): Show |
14 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0003g0207 others(11): Show |
18 | HG00597.hp2 HG01175.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.-11+8390_-11+8403d others(16): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | ||||||
| chr1:40049178 | A | ATTTTTTT others(8): Show |
6 | a0001c0001t0003g0215 a0001c0001t0003g0216 a0001c0001t0003g0217 others(3): Show |
6 | HG01175.hp2 HG02135.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+8389_-11+8403d others(17): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | ||||||
| chr1:40049178 | A | ATTTTTTT others(9): Show |
2 | a0001c0001t0003g0043 a0001c0001t0012g0192 |
3 | HG02738.hp1 NA19007.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-11+8388_-11+8403d others(18): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | ||||||
| chr1:40049178 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0003g0218 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-11+8387_-11+8403d others(19): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | ||||||
| chr1:40049178 | A | ATTTTTTT others(11): Show |
2 | a0001c0001t0003g0191 a0001c0001t0003g0219 |
2 | NA18995.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-11+8386_-11+8403d others(20): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | ||||||
| chr1:40049178 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0127 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-11+8392_-11+8403d others(14): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40049178 | ||||||
| chr1:40049226 | G | A | 1 | a0001c0001t0023g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-11+8425G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049226 | |||||||
| chr1:40049269 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(76): Show |
132 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-11+8468C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049269 | |||||||
| chr1:40049351 | C | A | 2 | a0001c0002t0010g0045 a0001c0002t0010g0046 |
4 | HG02622.hp1 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+8550C>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049351 | |||||||
| chr1:40049362 | C | T | 1 | a0001c0001t0023g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-11+8561C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049362 | |||||||
| chr1:40049374 | T | C | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+8573T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049374 | |||||||
| chr1:40049453 | T | C | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+8652T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049453 | |||||||
| chr1:40049605 | G | A | 201 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(198): Show |
318 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.-11+8804G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049605 | |||||||
| chr1:40049615 | C | T | 1 | a0001c0001t0003g0232 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-11+8814C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049615 | |||||||
| chr1:40049674 | T | C | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-11+8873T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049674 | |||||||
| chr1:40049685 | T | G | 1 | a0001c0001t0003g0197 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-11+8884T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049685 | |||||||
| chr1:40049710 | C | T | 3 | a0001c0002t0010g0045 a0001c0002t0010g0046 a0001c0002t0015g0044 |
6 | HG02622.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+8909C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049710 | |||||||
| chr1:40049724 | C | A | 60 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(57): Show |
75 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(72): Show |
intron_variant | MODIFIER | c.-11+8923C>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049724 | |||||||
| chr1:40049747 | C | T | 7 | a0001c0001t0004g0010 a0001c0001t0005g0010 a0001c0001t0005g0021 others(4): Show |
10 | HG02258.hp2 HG02965.hp2 HG03195.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11+8946C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049747 | |||||||
| chr1:40049776 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-11+8975T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40049776 | |||||||
| chr1:40050064 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-11+9263A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40050064 | |||||||
| chr1:40050109 | C | G | 1 | a0001c0001t0007g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-10-9228C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40050109 | |||||||
| chr1:40050405 | T | TGAAATAT others(106): Show |
237 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(234): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.-10-8922_-10-8921i others(115): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40050405 | ||||||
| chr1:40050405 | T | TGAAATAT others(106): Show |
5 | a0001c0002t0010g0045 a0001c0002t0010g0046 a0001c0002t0013g0047 others(2): Show |
9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-8922_-10-8921i others(115): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40050405 | ||||||
| chr1:40050407 | A | AAATATCT others(106): Show |
1 | a0001c0001t0003g0224 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-10-8922_-10-8921i others(115): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40050407 | ||||||
| chr1:40050520 | G | A | 2 | a0001c0001t0001g0102 a0001c0008t0001g0188 |
2 | HG02273.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-10-8817G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40050520 | |||||||
| chr1:40050528 | G | A | 6 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(3): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10-8809G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40050528 | |||||||
| chr1:40050566 | G | A | 2 | a0001c0001t0004g0010 a0001c0001t0005g0010 |
4 | HG03195.hp2 HG06807.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-8771G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40050566 | |||||||
| chr1:40050724 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(75): Show |
131 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.-10-8613A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40050724 | |||||||
| chr1:40050768 | CTCCACA | C | 6 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(3): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10-8565_-10-8560d others(8): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40050768 | ||||||
| chr1:40050846 | T | G | 1 | a0001c0001t0002g0070 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-10-8491T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40050846 | |||||||
| chr1:40051395 | TAC | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(78): Show |
136 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.-10-7926_-10-7925d others(4): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40051395 | ||||||
| chr1:40051395 | TACAC | T | 65 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(62): Show |
84 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(81): Show |
intron_variant | MODIFIER | c.-10-7928_-10-7925d others(6): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40051395 | ||||||
| chr1:40051482 | G | T | 1 | a0001c0001t0007g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-10-7855G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051482 | |||||||
| chr1:40051494 | A | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0141 others(2): Show |
12 | HG00639.hp1 HG01884.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-7843A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051494 | |||||||
| chr1:40051529 | G | A | 1 | a0001c0001t0003g0207 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-10-7808G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051529 | |||||||
| chr1:40051566 | G | T | 69 | a0001c0001t0001g0118 a0001c0001t0003g0006 a0001c0001t0003g0019 others(66): Show |
90 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(87): Show |
intron_variant | MODIFIER | c.-10-7771G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051566 | |||||||
| chr1:40051575 | T | G | 1 | a0001c0001t0001g0093 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-10-7762T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051575 | |||||||
| chr1:40051626 | A | C | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-7711A>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051626 | |||||||
| chr1:40051629 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-10-7708G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051629 | |||||||
| chr1:40051640 | A | T | 5 | a0001c0002t0010g0045 a0001c0002t0010g0046 a0001c0002t0013g0047 others(2): Show |
9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-7697A>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051640 | |||||||
| chr1:40051692 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-10-7645C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051692 | |||||||
| chr1:40051696 | C | T | 4 | a0001c0001t0005g0021 a0001c0001t0005g0057 a0001c0001t0005g0059 others(1): Show |
5 | HG02258.hp2 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-7641C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051696 | |||||||
| chr1:40051742 | A | ATT | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-7588_-10-7587d others(4): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40051742 | ||||||
| chr1:40051773 | G | A | 7 | a0001c0001t0004g0010 a0001c0001t0005g0010 a0001c0001t0005g0021 others(4): Show |
10 | HG02258.hp2 HG02965.hp2 HG03195.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-7564G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051773 | |||||||
| chr1:40051787 | T | G | 1 | a0001c0001t0003g0193 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-10-7550T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051787 | |||||||
| chr1:40051794 | C | T | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-7543C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051794 | |||||||
| chr1:40051828 | C | G | 2 | a0001c0001t0004g0061 a0001c0001t0005g0062 |
2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-10-7509C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051828 | |||||||
| chr1:40051844 | C | T | 5 | a0001c0002t0010g0045 a0001c0002t0010g0046 a0001c0002t0013g0047 others(2): Show |
9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-7493C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051844 | |||||||
| chr1:40051858 | C | T | 1 | a0001c0001t0003g0206 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-10-7479C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051858 | |||||||
| chr1:40051880 | G | T | 1 | a0001c0001t0001g0056 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-10-7457G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051880 | |||||||
| chr1:40051907 | A | C | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-7430A>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051907 | |||||||
| chr1:40051945 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-10-7392C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40051945 | |||||||
| chr1:40052066 | T | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(73): Show |
127 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-10-7271T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052066 | |||||||
| chr1:40052128 | T | C | 2 | a0001c0001t0002g0071 a0001c0001t0002g0082 |
2 | NA18971.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-10-7209T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052128 | |||||||
| chr1:40052222 | C | T | 1 | a0001c0001t0007g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-10-7115C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052222 | |||||||
| chr1:40052291 | G | T | 1 | a0001c0001t0003g0214 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-10-7046G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052291 | |||||||
| chr1:40052431 | G | A | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-6906G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052431 | |||||||
| chr1:40052438 | C | G | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-6899C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052438 | |||||||
| chr1:40052494 | G | A | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-6843G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052494 | |||||||
| chr1:40052572 | A | G | 6 | a0001c0001t0004g0010 a0001c0001t0005g0010 a0001c0001t0005g0021 others(3): Show |
9 | HG02258.hp2 HG03195.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-6765A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052572 | |||||||
| chr1:40052818 | C | T | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-6519C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052818 | |||||||
| chr1:40052828 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG00099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-10-6509C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052828 | |||||||
| chr1:40052829 | G | A | 1 | a0001c0001t0003g0198 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-10-6508G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052829 | |||||||
| chr1:40052985 | G | A | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0014 others(30): Show |
66 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.-10-6352G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40052985 | |||||||
| chr1:40053035 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(238): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.-10-6302T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053035 | |||||||
| chr1:40053080 | C | T | 58 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(55): Show |
73 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(70): Show |
intron_variant | MODIFIER | c.-10-6257C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053080 | |||||||
| chr1:40053165 | A | G | 7 | a0001c0001t0004g0010 a0001c0001t0005g0010 a0001c0001t0005g0021 others(4): Show |
10 | HG02258.hp2 HG02965.hp2 HG03195.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-6172A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053165 | |||||||
| chr1:40053361 | A | G | 1 | a0001c0001t0003g0191 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-10-5976A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053361 | |||||||
| chr1:40053391 | A | G | 1 | a0001c0001t0003g0205 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-10-5946A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053391 | |||||||
| chr1:40053410 | C | T | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-5927C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053410 | |||||||
| chr1:40053472 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(195): Show |
314 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.-10-5865T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053472 | |||||||
| chr1:40053546 | G | C | 3 | a0001c0001t0011g0013 a0001c0001t0011g0054 a0001c0001t0023g0053 |
5 | HG01071.hp1 HG01243.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-5791G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053546 | |||||||
| chr1:40053555 | A | G | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-5782A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053555 | |||||||
| chr1:40053579 | C | T | 3 | a0001c0001t0003g0213 a0001c0001t0003g0216 a0001c0001t0003g0217 |
3 | HG01175.hp2 HG01255.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-10-5758C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053579 | |||||||
| chr1:40053631 | A | G | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-5706A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053631 | |||||||
| chr1:40053647 | A | G | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-5690A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053647 | |||||||
| chr1:40053681 | A | T | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-5656A>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053681 | |||||||
| chr1:40053725 | G | A | 1 | a0001c0001t0003g0224 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-10-5612G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053725 | |||||||
| chr1:40053727 | A | G | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-5610A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053727 | |||||||
| chr1:40053851 | A | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(75): Show |
131 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.-10-5486A>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053851 | |||||||
| chr1:40053971 | A | G | 1 | a0001c0008t0001g0188 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-10-5366A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40053971 | |||||||
| chr1:40054061 | T | TAAAAC | 6 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(3): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10-5259_-10-5255d others(7): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40054061 | ||||||
| chr1:40054061 | T | TAAAACAA others(3): Show |
1 | a0001c0001t0002g0069 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-10-5264_-10-5255d others(12): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40054061 | ||||||
| chr1:40054130 | AGAGT | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(76): Show |
132 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-10-5202_-10-5199d others(6): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40054130 | ||||||
| chr1:40054183 | G | A | 1 | a0001c0001t0004g0150 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-10-5154G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40054183 | |||||||
| chr1:40054193 | C | CTTTTTTT others(3): Show |
50 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(47): Show |
65 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(62): Show |
intron_variant | MODIFIER | c.-10-5139_-10-5130d others(12): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40054193 | ||||||
| chr1:40054193 | C | CTTTTTTT others(4): Show |
6 | a0001c0001t0003g0203 a0001c0001t0003g0204 a0001c0001t0003g0211 others(3): Show |
6 | HG01175.hp2 HG01255.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-5140_-10-5130d others(13): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40054193 | ||||||
| chr1:40054193 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0003g0212 a0001c0001t0003g0217 |
2 | HG02300.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-10-5141_-10-5130d others(14): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40054193 | ||||||
| chr1:40054193 | CTTTTTT | C | 5 | a0001c0002t0010g0045 a0001c0002t0010g0046 a0001c0002t0013g0047 others(2): Show |
9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-5135_-10-5130d others(8): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40054193 | ||||||
| chr1:40054222 | A | G | 66 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(63): Show |
86 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(83): Show |
intron_variant | MODIFIER | c.-10-5115A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40054222 | |||||||
| chr1:40054347 | C | T | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-4990C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40054347 | |||||||
| chr1:40054415 | A | G | 68 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(65): Show |
89 | HG00408.hp2 HG00597.hp2 HG01071.hp1 others(86): Show |
intron_variant | MODIFIER | c.-10-4922A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40054415 | |||||||
| chr1:40054428 | G | A | 1 | a0001c0001t0004g0146 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-10-4909G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40054428 | |||||||
| chr1:40054507 | T | G | 1 | a0001c0001t0002g0104 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-10-4830T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40054507 | |||||||
| chr1:40054519 | G | C | 1 | a0001c0003t0004g0138 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-10-4818G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40054519 | |||||||
| chr1:40054935 | C | T | 59 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(56): Show |
74 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(71): Show |
intron_variant | MODIFIER | c.-10-4402C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40054935 | |||||||
| chr1:40054938 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-10-4399G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40054938 | |||||||
| chr1:40054951 | C | G | 1 | a0001c0001t0004g0164 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-10-4386C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40054951 | |||||||
| chr1:40055043 | C | T | 1 | a0001c0001t0003g0202 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-10-4294C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055043 | |||||||
| chr1:40055102 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-10-4235G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055102 | |||||||
| chr1:40055117 | C | G | 5 | a0001c0002t0010g0045 a0001c0002t0010g0046 a0001c0002t0013g0047 others(2): Show |
9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-4220C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055117 | |||||||
| chr1:40055120 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-10-4217A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055120 | |||||||
| chr1:40055254 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(127): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.-10-4083A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055254 | |||||||
| chr1:40055259 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(75): Show |
131 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.-10-4078G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055259 | |||||||
| chr1:40055261 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-10-4076A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055261 | |||||||
| chr1:40055335 | TATC | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(127): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.-10-3999_-10-3997d others(5): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40055335 | ||||||
| chr1:40055423 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-10-3914A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055423 | |||||||
| chr1:40055446 | A | G | 2 | a0001c0001t0002g0077 a0001c0001t0002g0085 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-10-3891A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055446 | |||||||
| chr1:40055492 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-10-3845G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055492 | |||||||
| chr1:40055663 | T | C | 1 | a0001c0001t0004g0174 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-10-3674T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055663 | |||||||
| chr1:40055709 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(127): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.-10-3628A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055709 | |||||||
| chr1:40055722 | T | A | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0014 others(30): Show |
66 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.-10-3615T>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055722 | |||||||
| chr1:40055741 | T | A | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0014 others(30): Show |
66 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.-10-3596T>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055741 | |||||||
| chr1:40055845 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(127): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.-10-3492A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40055845 | |||||||
| chr1:40056085 | C | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(127): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.-10-3252C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40056085 | |||||||
| chr1:40056159 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-10-3178C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40056159 | |||||||
| chr1:40056242 | T | G | 1 | a0001c0001t0004g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-10-3095T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40056242 | |||||||
| chr1:40056279 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(73): Show |
127 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-10-3058C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40056279 | |||||||
| chr1:40056300 | A | ATT | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(112): Show |
207 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.-10-3025_-10-3024d others(4): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40056300 | ||||||
| chr1:40056300 | A | ATTT | 15 | a0001c0001t0001g0115 a0001c0001t0001g0123 a0001c0001t0002g0080 others(12): Show |
18 | HG00597.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-10-3026_-10-3024d others(5): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40056300 | ||||||
| chr1:40056776 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(127): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.-10-2561A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40056776 | |||||||
| chr1:40056897 | C | T | 1 | a0001c0001t0019g0231 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-10-2440C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40056897 | |||||||
| chr1:40056915 | A | AG | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(127): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.-10-2422_-10-2421i others(3): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40056915 | |||||||
| chr1:40056915 | A | C | 1 | a0001c0001t0004g0163 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-10-2422A>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40056915 | |||||||
| chr1:40057012 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-10-2325G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057012 | |||||||
| chr1:40057030 | G | A | 12 | a0001c0001t0004g0010 a0001c0001t0004g0061 a0001c0001t0005g0010 others(9): Show |
15 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10-2307G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057030 | |||||||
| chr1:40057258 | T | G | 2 | a0001c0001t0007g0145 a0001c0001t0007g0167 |
2 | HG00140.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.-10-2079T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057258 | |||||||
| chr1:40057299 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(127): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.-10-2038C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057299 | |||||||
| chr1:40057410 | T | C | 6 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(3): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10-1927T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057410 | |||||||
| chr1:40057427 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0114 |
2 | HG01516.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-10-1910C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057427 | |||||||
| chr1:40057444 | A | G | 1 | a0001c0001t0001g0027 | 2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-10-1893A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057444 | |||||||
| chr1:40057484 | A | G | 8 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0050 others(5): Show |
12 | HG02040.hp1 HG02135.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-1853A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057484 | |||||||
| chr1:40057485 | G | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(127): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.-10-1852G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057485 | |||||||
| chr1:40057561 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0114 |
2 | HG01516.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-10-1776T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057561 | |||||||
| chr1:40057606 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(127): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.-10-1731G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057606 | |||||||
| chr1:40057656 | A | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(109): Show |
198 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.-10-1681A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057656 | |||||||
| chr1:40057806 | C | T | 1 | a0001c0001t0003g0217 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-10-1531C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40057806 | |||||||
| chr1:40058142 | G | T | 1 | a0001c0001t0005g0058 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-10-1195G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40058142 | |||||||
| chr1:40058299 | A | C | 3 | a0001c0001t0011g0013 a0001c0001t0011g0054 a0001c0001t0023g0053 |
5 | HG01071.hp1 HG01243.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-1038A>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40058299 | |||||||
| chr1:40058299 | A | T | 29 | a0001c0001t0003g0020 a0001c0001t0003g0042 a0001c0001t0003g0185 others(26): Show |
34 | HG01175.hp1 HG02015.hp1 HG02129.hp2 others(31): Show |
intron_variant | MODIFIER | c.-10-1038A>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40058299 | |||||||
| chr1:40058497 | G | T | 1 | a0001c0001t0003g0210 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-10-840G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40058497 | |||||||
| chr1:40058528 | C | A | 1 | a0001c0001t0001g0027 | 2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-10-809C>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40058528 | |||||||
| chr1:40058759 | A | G | 12 | a0001c0001t0004g0010 a0001c0001t0004g0061 a0001c0001t0005g0010 others(9): Show |
15 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10-578A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40058759 | |||||||
| chr1:40058839 | G | T | 3 | a0001c0002t0010g0045 a0001c0002t0010g0046 a0001c0002t0015g0044 |
6 | HG02622.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-498G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40058839 | |||||||
| chr1:40058916 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0141 others(2): Show |
12 | HG00639.hp1 HG01884.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-421G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40058916 | |||||||
| chr1:40058976 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-10-361C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40058976 | |||||||
| chr1:40059014 | T | TTGCAAAT others(286): Show |
1 | a0001c0001t0021g0184 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-10-305_-10-304ins others(293): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40059014 | ||||||
| chr1:40059014 | T | TTGCAAAT others(299): Show |
22 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0041 others(19): Show |
32 | HG00408.hp2 HG00597.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10-305_-10-304ins others(306): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40059014 | ||||||
| chr1:40059014 | T | TTGCAAAT others(299): Show |
1 | a0001c0008t0001g0188 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-10-305_-10-304ins others(306): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40059014 | ||||||
| chr1:40059014 | T | TTGCAAAT others(302): Show |
1 | a0001c0001t0003g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-10-305_-10-304ins others(309): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40059014 | ||||||
| chr1:40059014 | T | TTGCAAAT others(300): Show |
30 | a0001c0001t0003g0020 a0001c0001t0003g0042 a0001c0001t0003g0179 others(27): Show |
35 | HG02015.hp1 HG02129.hp2 HG02135.hp2 others(32): Show |
intron_variant | MODIFIER | c.-10-305_-10-304ins others(307): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40059014 | ||||||
| chr1:40059014 | T | TTGCAAAT others(301): Show |
5 | a0001c0001t0003g0190 a0001c0001t0003g0201 a0001c0001t0003g0209 others(2): Show |
5 | HG01175.hp1 HG04184.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-305_-10-304ins others(308): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 40059014 | ||||||
| chr1:40059018 | A | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(127): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.-10-319A>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40059018 | |||||||
| chr1:40059194 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(127): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.-10-143T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40059194 | |||||||
| chr1:40059274 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-10-63T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 1/12 | chr1 | 40059274 | |||||||
| chr1:40059648 | AACACAAG others(3): Show |
A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0102 others(1): Show |
6 | HG01109.hp2 HG01952.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.112+191_112+200del others(10): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 2/12 | chr1 | 40059648 | |||||||
| chr1:40059754 | A | G | 1 | a0001c0001t0023g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.112+296A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 2/12 | chr1 | 40059754 | |||||||
| chr1:40059817 | A | T | 1 | a0001c0001t0003g0212 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.113-250A>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 2/12 | chr1 | 40059817 | |||||||
| chr1:40060321 | G | C | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0014 others(30): Show |
66 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.216+151G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40060321 | |||||||
| chr1:40060331 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(195): Show |
314 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.216+161T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40060331 | |||||||
| chr1:40060344 | G | A | 1 | a0001c0001t0023g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.216+174G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40060344 | |||||||
| chr1:40060636 | C | T | 1 | a0001c0001t0003g0222 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.216+466C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40060636 | |||||||
| chr1:40060722 | C | T | 5 | a0001c0002t0010g0045 a0001c0002t0010g0046 a0001c0002t0013g0047 others(2): Show |
9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.216+552C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40060722 | |||||||
| chr1:40060724 | A | G | 8 | a0001c0001t0004g0159 a0001c0001t0004g0160 a0001c0001t0004g0161 others(5): Show |
8 | HG00280.hp1 HG01109.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.216+554A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40060724 | |||||||
| chr1:40061013 | C | T | 1 | a0001c0001t0004g0162 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.217-722C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40061013 | |||||||
| chr1:40061156 | C | CT | 197 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(194): Show |
312 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.217-566dupT | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 40061156 | ||||||
| chr1:40061211 | T | G | 1 | a0001c0001t0001g0105 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.217-524T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40061211 | |||||||
| chr1:40061338 | T | G | 1 | a0001c0001t0001g0133 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.217-397T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40061338 | |||||||
| chr1:40061363 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.217-372C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40061363 | |||||||
| chr1:40061448 | C | T | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0014 others(30): Show |
66 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.217-287C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40061448 | |||||||
| chr1:40061540 | C | T | 1 | a0001c0001t0006g0064 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.217-195C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 3/12 | chr1 | 40061540 | |||||||
| chr1:40061858 | C | T | 3 | a0001c0001t0005g0022 a0001c0005t0004g0063 a0001c0005t0005g0022 |
3 | HG01891.hp1 HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.294+46C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40061858 | |||||||
| chr1:40062051 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.294+239T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062051 | |||||||
| chr1:40062222 | ACTCT | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(127): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.294+415_294+418del others(4): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062222 | ||||||
| chr1:40062234 | A | C | 59 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(56): Show |
74 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(71): Show |
intron_variant | MODIFIER | c.294+422A>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062234 | |||||||
| chr1:40062324 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.294+512G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062324 | |||||||
| chr1:40062523 | G | A | 2 | a0001c0001t0003g0041 a0001c0001t0003g0179 |
3 | HG02559.hp2 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.294+711G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062523 | |||||||
| chr1:40062578 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0004g0039 |
2 | HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.294+766C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062578 | |||||||
| chr1:40062639 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.294+827C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062639 | |||||||
| chr1:40062716 | G | C | 1 | a0001c0001t0023g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.294+904G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062716 | |||||||
| chr1:40062760 | C | A | 1 | a0001c0001t0001g0105 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.294+948C>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062760 | |||||||
| chr1:40062773 | T | TTGTGTG | 113 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(110): Show |
196 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.294+981_294+986dup others(6): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062773 | ||||||
| chr1:40062773 | T | TTGTGTGT others(1): Show |
14 | a0001c0001t0001g0032 a0001c0001t0001g0112 a0001c0001t0001g0114 others(11): Show |
20 | HG00735.hp1 HG01071.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.294+979_294+986dup others(8): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062773 | ||||||
| chr1:40062773 | T | TTGTGTGT others(3): Show |
2 | a0001c0001t0002g0025 a0001c0001t0023g0053 |
3 | HG03490.hp2 HG03492.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.294+977_294+986dup others(10): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062773 | ||||||
| chr1:40062773 | T | TTGTGTGT others(5): Show |
56 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(53): Show |
71 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(68): Show |
intron_variant | MODIFIER | c.294+975_294+986dup others(12): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062773 | ||||||
| chr1:40062773 | T | TTGTGTGT others(7): Show |
12 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0211 others(9): Show |
19 | HG02129.hp2 HG02145.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.294+973_294+986dup others(14): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062773 | ||||||
| chr1:40062773 | T | TTGTGTGT others(9): Show |
1 | a0001c0002t0013g0227 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.294+971_294+986dup others(16): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062773 | ||||||
| chr1:40062773 | T | TTGTGTGT others(11): Show |
12 | a0001c0001t0004g0137 a0001c0001t0004g0139 a0001c0001t0004g0143 others(9): Show |
13 | HG00280.hp1 HG01433.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.294+969_294+986dup others(18): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062773 | ||||||
| chr1:40062773 | T | TTGTGTGT others(13): Show |
7 | a0001c0001t0004g0150 a0001c0001t0004g0151 a0001c0001t0004g0154 others(4): Show |
7 | HG01109.hp1 HG01981.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+967_294+986dup others(20): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062773 | ||||||
| chr1:40062773 | T | TTGTGTGT others(15): Show |
13 | a0001c0001t0004g0003 a0001c0001t0004g0040 a0001c0001t0004g0146 others(10): Show |
24 | HG00099.hp2 HG00735.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.294+965_294+986dup others(22): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062773 | ||||||
| chr1:40062773 | T | TTGTGTGT others(17): Show |
2 | a0001c0001t0004g0157 a0001c0001t0007g0167 |
2 | HG00140.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.294+963_294+986dup others(24): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40062773 | ||||||
| chr1:40062927 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(127): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.294+1115A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062927 | |||||||
| chr1:40062953 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(127): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.294+1141C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062953 | |||||||
| chr1:40062992 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(132): Show |
234 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.294+1180T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40062992 | |||||||
| chr1:40063005 | A | T | 2 | a0001c0002t0013g0047 a0001c0002t0013g0227 |
3 | HG02145.hp2 HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.294+1193A>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063005 | |||||||
| chr1:40063016 | G | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(127): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.294+1204G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063016 | |||||||
| chr1:40063194 | C | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(195): Show |
314 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.295-1033C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063194 | |||||||
| chr1:40063212 | C | CT | 3 | a0001c0001t0008g0018 a0001c0001t0008g0220 a0001c0001t0018g0225 |
5 | NA18949.hp1 NA18993.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-1014dupT | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 40063212 | ||||||
| chr1:40063246 | C | T | 1 | a0001c0001t0004g0017 | 3 | HG02083.hp2 HG03471.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.295-981C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063246 | |||||||
| chr1:40063323 | A | T | 7 | a0001c0001t0004g0010 a0001c0001t0005g0010 a0001c0001t0005g0021 others(4): Show |
10 | HG02258.hp2 HG02965.hp2 HG03195.hp2 others(7): Show |
intron_variant | MODIFIER | c.295-904A>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063323 | |||||||
| chr1:40063357 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(75): Show |
131 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.295-870T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063357 | |||||||
| chr1:40063499 | G | T | 1 | a0001c0001t0004g0171 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.295-728G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063499 | |||||||
| chr1:40063561 | G | C | 2 | a0001c0002t0013g0047 a0001c0002t0013g0227 |
3 | HG02145.hp2 HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.295-666G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063561 | |||||||
| chr1:40063674 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | NA19057.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.295-553A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063674 | |||||||
| chr1:40063796 | G | A | 12 | a0001c0001t0004g0010 a0001c0001t0004g0061 a0001c0001t0005g0010 others(9): Show |
15 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.295-431G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063796 | |||||||
| chr1:40063817 | G | C | 1 | a0001c0002t0015g0044 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.295-410G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40063817 | |||||||
| chr1:40064076 | G | C | 2 | a0001c0001t0004g0137 a0001c0001t0004g0139 |
2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.295-151G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 4/12 | chr1 | 40064076 | |||||||
| chr1:40064450 | C | T | 1 | a0001c0001t0023g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.439-24C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 5/12 | chr1 | 40064450 | |||||||
| chr1:40064672 | C | G | 28 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0015 others(25): Show |
55 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.524+113C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40064672 | |||||||
| chr1:40064786 | G | C | 2 | a0001c0002t0013g0047 a0001c0002t0013g0227 |
3 | HG02145.hp2 HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.524+227G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40064786 | |||||||
| chr1:40064794 | C | G | 3 | a0001c0001t0003g0042 a0001c0001t0003g0187 a0001c0001t0003g0208 |
4 | NA18944.hp2 NA18999.hp1 NA19059.hp1 others(1): Show |
intron_variant | MODIFIER | c.524+235C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40064794 | |||||||
| chr1:40064880 | A | G | 4 | a0001c0001t0005g0021 a0001c0001t0005g0057 a0001c0001t0005g0059 others(1): Show |
5 | HG02258.hp2 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.524+321A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40064880 | |||||||
| chr1:40064935 | T | G | 1 | a0001c0001t0001g0129 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.524+376T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40064935 | |||||||
| chr1:40065038 | C | G | 1 | a0001c0001t0001g0111 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.524+479C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40065038 | |||||||
| chr1:40065142 | A | G | 59 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(56): Show |
74 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(71): Show |
intron_variant | MODIFIER | c.524+583A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40065142 | |||||||
| chr1:40065422 | A | G | 59 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(56): Show |
74 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(71): Show |
intron_variant | MODIFIER | c.525-793A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40065422 | |||||||
| chr1:40065451 | T | C | 1 | a0001c0001t0003g0213 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.525-764T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40065451 | |||||||
| chr1:40065485 | A | G | 7 | a0001c0001t0004g0010 a0001c0001t0005g0010 a0001c0001t0005g0021 others(4): Show |
10 | HG02258.hp2 HG02965.hp2 HG03195.hp2 others(7): Show |
intron_variant | MODIFIER | c.525-730A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40065485 | |||||||
| chr1:40065606 | G | A | 2 | a0001c0003t0004g0140 a0002c0004t0004g0038 |
3 | HG02647.hp1 HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.525-609G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40065606 | |||||||
| chr1:40065608 | T | G | 5 | a0001c0002t0010g0045 a0001c0002t0010g0046 a0001c0002t0013g0047 others(2): Show |
9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.525-607T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40065608 | |||||||
| chr1:40065655 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.525-560G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40065655 | |||||||
| chr1:40065822 | C | A | 12 | a0001c0001t0004g0010 a0001c0001t0004g0061 a0001c0001t0005g0010 others(9): Show |
15 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.525-393C>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40065822 | |||||||
| chr1:40065992 | G | C | 1 | a0001c0001t0001g0031 | 2 | HG00738.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.525-223G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40065992 | |||||||
| chr1:40066030 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.525-185T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40066030 | |||||||
| chr1:40066036 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG02040.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.525-179G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40066036 | |||||||
| chr1:40066128 | T | C | 1 | a0001c0001t0012g0192 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.525-87T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40066128 | |||||||
| chr1:40066172 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.525-43G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40066172 | |||||||
| chr1:40066178 | G | A | 6 | a0001c0001t0004g0010 a0001c0001t0005g0010 a0001c0001t0005g0021 others(3): Show |
9 | HG02258.hp2 HG03195.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.525-37G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 6/12 | chr1 | 40066178 | |||||||
| chr1:40066332 | C | A | 6 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(3): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.630+12C>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 7/12 | chr1 | 40066332 | |||||||
| chr1:40066356 | C | T | 18 | a0001c0001t0004g0010 a0001c0001t0004g0061 a0001c0001t0005g0010 others(15): Show |
27 | HG00423.hp2 HG01496.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.630+36C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 7/12 | chr1 | 40066356 | |||||||
| chr1:40066659 | A | C | 1 | a0001c0002t0015g0044 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.630+339A>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 7/12 | chr1 | 40066659 | |||||||
| chr1:40066667 | T | C | 1 | a0001c0001t0003g0200 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.630+347T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 7/12 | chr1 | 40066667 | |||||||
| chr1:40066760 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0141 others(2): Show |
12 | HG00639.hp1 HG01884.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.630+440G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 7/12 | chr1 | 40066760 | |||||||
| chr1:40067307 | A | G | 1 | a0001c0001t0003g0182 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.631-233A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 7/12 | chr1 | 40067307 | |||||||
| chr1:40067386 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0135 |
2 | NA18973.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.631-154A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 7/12 | chr1 | 40067386 | |||||||
| chr1:40067748 | TACA | T | 6 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(3): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.808+36_808+38delCA others(1): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 40067748 | ||||||
| chr1:40067772 | C | G | 5 | a0001c0002t0010g0045 a0001c0002t0010g0046 a0001c0002t0013g0047 others(2): Show |
9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.808+55C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40067772 | |||||||
| chr1:40067826 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.808+109C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40067826 | |||||||
| chr1:40067827 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.808+110G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40067827 | |||||||
| chr1:40067948 | T | G | 3 | a0001c0001t0011g0013 a0001c0001t0011g0054 a0001c0001t0023g0053 |
5 | HG01071.hp1 HG01243.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.808+231T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40067948 | |||||||
| chr1:40068223 | T | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(127): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.808+506T>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40068223 | |||||||
| chr1:40068286 | T | C | 3 | a0001c0001t0011g0013 a0001c0001t0011g0054 a0001c0001t0023g0053 |
5 | HG01071.hp1 HG01243.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.808+569T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40068286 | |||||||
| chr1:40068348 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(75): Show |
131 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.808+631G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40068348 | |||||||
| chr1:40068351 | A | G | 59 | a0001c0001t0003g0006 a0001c0001t0003g0019 a0001c0001t0003g0020 others(56): Show |
74 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(71): Show |
intron_variant | MODIFIER | c.808+634A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40068351 | |||||||
| chr1:40068401 | C | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(127): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.808+684C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40068401 | |||||||
| chr1:40068402 | C | T | 3 | a0001c0001t0008g0018 a0001c0001t0008g0220 a0001c0001t0018g0225 |
5 | NA18949.hp1 NA18993.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.808+685C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40068402 | |||||||
| chr1:40068429 | C | G | 1 | a0001c0001t0001g0089 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.808+712C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40068429 | |||||||
| chr1:40068443 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.808+726T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40068443 | |||||||
| chr1:40068639 | GA | G | 7 | a0001c0001t0001g0093 a0001c0001t0004g0156 a0001c0002t0010g0045 others(4): Show |
11 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.808+932delA | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 40068639 | ||||||
| chr1:40068751 | G | A | 1 | a0001c0001t0003g0204 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.809-939G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40068751 | |||||||
| chr1:40068826 | TTTTTA | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(76): Show |
132 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.809-849_809-845del others(5): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 40068826 | ||||||
| chr1:40068973 | C | T | 1 | a0001c0001t0004g0155 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.809-717C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40068973 | |||||||
| chr1:40069063 | A | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | NA19057.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.809-627A>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069063 | |||||||
| chr1:40069170 | T | A | 33 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0014 others(30): Show |
66 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.809-520T>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069170 | |||||||
| chr1:40069268 | A | T | 43 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0017 others(40): Show |
60 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.809-422A>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069268 | |||||||
| chr1:40069322 | G | C | 1 | a0001c0001t0003g0197 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.809-368G>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069322 | |||||||
| chr1:40069324 | G | T | 2 | a0001c0001t0002g0074 a0001c0001t0002g0076 |
2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.809-366G>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069324 | |||||||
| chr1:40069334 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(179): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.809-356C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069334 | |||||||
| chr1:40069395 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(128): Show |
226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.809-295T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069395 | |||||||
| chr1:40069405 | C | T | 2 | a0001c0001t0005g0057 a0001c0001t0005g0060 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.809-285C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069405 | |||||||
| chr1:40069420 | T | C | 1 | a0001c0001t0002g0072 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.809-270T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069420 | |||||||
| chr1:40069501 | T | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0141 others(3): Show |
13 | HG00639.hp1 HG01884.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.809-189T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069501 | |||||||
| chr1:40069667 | C | T | 6 | a0001c0001t0006g0007 a0001c0001t0006g0023 a0001c0001t0006g0024 others(3): Show |
12 | HG00423.hp2 HG01496.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.809-23C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 8/12 | chr1 | 40069667 | |||||||
| chr1:40069949 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0095 a0001c0001t0001g0120 |
6 | HG02109.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.993+75G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 9/12 | chr1 | 40069949 | |||||||
| chr1:40069973 | G | A | 32 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0014 others(29): Show |
65 | HG00597.hp1 HG00609.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.993+99G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 9/12 | chr1 | 40069973 | |||||||
| chr1:40069995 | C | T | 1 | a0001c0001t0023g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.993+121C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 9/12 | chr1 | 40069995 | |||||||
| chr1:40070003 | G | A | 1 | a0001c0001t0014g0037 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.993+129G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 9/12 | chr1 | 40070003 | |||||||
| chr1:40070071 | T | C | 5 | a0001c0001t0002g0026 a0001c0001t0002g0073 a0001c0001t0002g0079 others(2): Show |
6 | HG00597.hp1 NA18943.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.994-88T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 9/12 | chr1 | 40070071 | |||||||
| chr1:40070115 | G | A | 1 | a0001c0001t0003g0199 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.994-44G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 9/12 | chr1 | 40070115 | |||||||
| chr1:40070298 | T | G | 5 | a0001c0001t0004g0061 a0001c0001t0005g0022 a0001c0001t0005g0062 others(2): Show |
5 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1117+16T>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 10/12 | chr1 | 40070298 | |||||||
| chr1:40070402 | C | CT | 241 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(238): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.1118-28_1118-27ins others(1): Show |
CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 10/12 | chr1 | 40070402 | |||||||
| chr1:40070692 | C | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0113 a0001c0001t0001g0129 |
5 | HG00408.hp1 HG00673.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.1201-144C>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 11/12 | chr1 | 40070692 | |||||||
| chr1:40071130 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1344+151A>G | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 12/12 | chr1 | 40071130 | |||||||
| chr1:40071242 | G | A | 5 | a0001c0001t0004g0137 a0001c0001t0004g0139 a0001c0003t0004g0138 others(2): Show |
6 | HG02074.hp2 HG02523.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-208G>A | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 12/12 | chr1 | 40071242 | |||||||
| chr1:40071266 | CT | C | 5 | a0001c0002t0010g0045 a0001c0002t0010g0046 a0001c0002t0013g0047 others(2): Show |
9 | HG02145.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1345-182delT | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr1 | 40071266 | ||||||
| chr1:40071342 | C | T | 2 | a0001c0001t0011g0013 a0001c0001t0011g0054 |
4 | HG01071.hp1 HG01243.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-108C>T | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 12/12 | chr1 | 40071342 | |||||||
| chr1:40071434 | T | C | 2 | a0001c0001t0003g0194 a0001c0001t0020g0195 |
2 | NA18957.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1345-16T>C | CAP1 | ENSG00000131236.18 | transcript | ENST00000372805.8 | protein_coding | 12/12 | chr1 | 40071434 |