Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2159 |
| ensemblid | ENSG00000126218.12 |
| hgncid | 3528 |
| symbol | F10 |
| name | coagulation factor X |
| refseq_nuc | NM_000504.4 |
| refseq_prot | NP_000495.1 |
| ensembl_nuc | ENST00000375559.8 |
| ensembl_prot | ENSP00000364709.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 113122799 |
| end | 113149529 |
| strand | + |
| ver | v1.2 |
| region | chr13:113122799-113149529 |
| region5000 | chr13:113117799-113154529 |
| regionname0 | F10_chr13_113122799_113149529 |
| regionname5000 | F10_chr13_113117799_113154529 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 488 | 392 | 75 | 79 | 182 | 18 | 36 | 134 | F10_chr13_113117799_113154529 | F10 | MGRPL others(483): Show |
chr13 | 113117799 | 113154529 |
| a0002 | 0/0 | 488 | 13 | 11 | 2 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | MGRPL others(483): Show |
chr13 | 113117799 | 113154529 |
| a0003 | 0/0 | 488 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | MGRPL others(483): Show |
chr13 | 113117799 | 113154529 |
| a0004 | 0/0 | 488 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | MGRPL others(483): Show |
chr13 | 113117799 | 113154529 |
| a0005 | 0/0 | 488 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | MGRPL others(483): Show |
chr13 | 113117799 | 113154529 |
| a0006 | 0/0 | 488 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | MGRPL others(483): Show |
chr13 | 113117799 | 113154529 |
| a0007 | 0/0 | 488 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | MGRPL others(483): Show |
chr13 | 113117799 | 113154529 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1464 | 254 | 45 | 54 | 116 | 16 | 22 | F10_chr13_113117799_113154529 | F10 | ATGGG others(1459): Show |
chr13 | 113117799 | 113154529 | ||
| a0001c0002 | 1/0 | 1464 | 122 | 21 | 21 | 64 | 1 | 14 | F10_chr13_113117799_113154529 | F10 | ATGGG others(1459): Show |
chr13 | 113117799 | 113154529 | ||
| a0001c0004 | 0/0 | 1464 | 8 | 7 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | ATGGG others(1459): Show |
chr13 | 113117799 | 113154529 | ||
| a0001c0006 | 0/0 | 1464 | 3 | 0 | 2 | 0 | 1 | 0 | F10_chr13_113117799_113154529 | F10 | ATGGG others(1459): Show |
chr13 | 113117799 | 113154529 | ||
| a0001c0007 | 0/0 | 1464 | 2 | 2 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | ATGGG others(1459): Show |
chr13 | 113117799 | 113154529 | ||
| a0001c0009 | 0/0 | 1464 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | ATGGG others(1459): Show |
chr13 | 113117799 | 113154529 | ||
| a0001c0012 | 0/0 | 1464 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | ATGGG others(1459): Show |
chr13 | 113117799 | 113154529 | ||
| a0001c0015 | 0/0 | 1464 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | ATGGG others(1459): Show |
chr13 | 113117799 | 113154529 | ||
| a0002c0003 | 0/0 | 1464 | 12 | 10 | 2 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | ATGGG others(1459): Show |
chr13 | 113117799 | 113154529 | ||
| a0002c0008 | 0/0 | 1464 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | ATGGG others(1459): Show |
chr13 | 113117799 | 113154529 | ||
| a0003c0005 | 0/0 | 1464 | 3 | 3 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | ATGGG others(1459): Show |
chr13 | 113117799 | 113154529 | ||
| a0004c0010 | 0/0 | 1464 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | ATGGG others(1459): Show |
chr13 | 113117799 | 113154529 | ||
| a0005c0013 | 0/0 | 1464 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | ATGGG others(1459): Show |
chr13 | 113117799 | 113154529 | ||
| a0006c0011 | 0/0 | 1464 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | ATGGG others(1459): Show |
chr13 | 113117799 | 113154529 | ||
| a0007c0014 | 0/0 | 1464 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | ATGGG others(1459): Show |
chr13 | 113117799 | 113154529 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1536 | 251 | 45 | 53 | 116 | 16 | 20 | F10_chr13_113117799_113154529 | F10 | GACTT others(1531): Show |
chr13 | 113117799 | 113154529 |
| a0001c0001t0002 | 0/0 | 1536 | 3 | 0 | 1 | 0 | 0 | 2 | F10_chr13_113117799_113154529 | F10 | GACTT others(1531): Show |
chr13 | 113117799 | 113154529 |
| a0001c0002t0001 | 1/0 | 1536 | 121 | 21 | 21 | 64 | 1 | 13 | F10_chr13_113117799_113154529 | F10 | GACTT others(1531): Show |
chr13 | 113117799 | 113154529 |
| a0001c0002t0002 | 0/0 | 1536 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | GACTT others(1531): Show |
chr13 | 113117799 | 113154529 |
| a0001c0004t0001 | 0/0 | 1536 | 8 | 7 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | GACTT others(1531): Show |
chr13 | 113117799 | 113154529 |
| a0001c0006t0001 | 0/0 | 1536 | 3 | 0 | 2 | 0 | 1 | 0 | F10_chr13_113117799_113154529 | F10 | GACTT others(1531): Show |
chr13 | 113117799 | 113154529 |
| a0001c0007t0001 | 0/0 | 1536 | 2 | 2 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | GACTT others(1531): Show |
chr13 | 113117799 | 113154529 |
| a0001c0009t0001 | 0/0 | 1536 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | GACTT others(1531): Show |
chr13 | 113117799 | 113154529 |
| a0001c0012t0001 | 0/0 | 1536 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | GACTT others(1531): Show |
chr13 | 113117799 | 113154529 |
| a0001c0015t0001 | 0/0 | 1536 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | GACTT others(1531): Show |
chr13 | 113117799 | 113154529 |
| a0002c0003t0001 | 0/0 | 1536 | 12 | 10 | 2 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | GACTT others(1531): Show |
chr13 | 113117799 | 113154529 |
| a0002c0008t0001 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | GACTT others(1531): Show |
chr13 | 113117799 | 113154529 |
| a0003c0005t0001 | 0/0 | 1536 | 3 | 3 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | GACTT others(1531): Show |
chr13 | 113117799 | 113154529 |
| a0004c0010t0001 | 0/0 | 1536 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | GACTT others(1531): Show |
chr13 | 113117799 | 113154529 |
| a0005c0013t0001 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | GACTT others(1531): Show |
chr13 | 113117799 | 113154529 |
| a0006c0011t0001 | 0/0 | 1536 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | GACTT others(1531): Show |
chr13 | 113117799 | 113154529 |
| a0007c0014t0001 | 0/0 | 1536 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | GACTT others(1531): Show |
chr13 | 113117799 | 113154529 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0002 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0069 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0004t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0004t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0004t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0004t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0004t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0004t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0004t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0004t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0006t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0006t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0007t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0007t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0009t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0012t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0001c0015t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0002c0003t0001g0003 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0002c0003t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0002c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0002c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0002c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0002c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0002c0003t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0002c0003t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0002c0008t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0003c0005t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0003c0005t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0003c0005t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0004c0010t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0005c0013t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0006c0011t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| a0007c0014t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0237 | EUR | GBR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | GBR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | GBR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | GBR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0302 | EUR | FIN | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | FIN | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | FIN | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | FIN | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0330 | EAS | CHS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | CHS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | CHS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0300 | EAS | CHS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | CHS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | CHS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0225 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00735 | hp2 | a0001 | c0015 | t0001 | g0009 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0206 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0307 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01069 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01070 | hp2 | a0001 | c0006 | t0001 | g0025 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01071 | hp2 | a0001 | c0006 | t0001 | g0025 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0109 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0276 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0343 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0077 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0084 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0078 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01243 | hp2 | a0001 | c0004 | t0001 | g0292 | AMR | PUR | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0305 | AMR | CLM | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | CLM | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0347 | AMR | CLM | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | CLM | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0144 | AMR | CLM | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0362 | AMR | CLM | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0345 | EUR | IBS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0348 | EUR | IBS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | IBS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0363 | AFR | ACB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0359 | AFR | ACB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0274 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0172 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0059 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0044 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0102 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0299 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0331 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0317 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0335 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0358 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02145 | hp2 | a0001 | c0004 | t0001 | g0289 | AFR | ACB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0341 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0333 | EAS | CDX | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | CDX | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CDX | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02273 | hp2 | a0004 | c0010 | t0001 | g0014 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02280 | hp1 | a0001 | c0004 | t0001 | g0295 | AFR | ACB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02280 | hp2 | a0005 | c0013 | t0001 | g0070 | AFR | ACB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | KHV | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0038 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0271 | SAS | PJL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0048 | SAS | PJL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02622 | hp2 | a0002 | c0003 | t0001 | g0279 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0284 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02723 | hp2 | a0001 | c0004 | t0001 | g0365 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0165 | SAS | PJL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0075 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0281 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0288 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02895 | hp1 | a0002 | c0003 | t0001 | g0277 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02895 | hp2 | a0002 | c0003 | t0001 | g0285 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | ESN | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02976 | hp1 | a0001 | c0004 | t0001 | g0293 | AFR | ESN | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0247 | SAS | PJL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0145 | SAS | PJL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0150 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0272 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | MSL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03098 | hp2 | a0003 | c0005 | t0001 | g0366 | AFR | MSL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03130 | hp2 | a0003 | c0005 | t0001 | g0361 | AFR | ESN | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0367 | AFR | ESN | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | ESN | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0290 | AFR | ESN | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0296 | AFR | MSL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03225 | hp1 | a0002 | c0003 | t0001 | g0280 | AFR | MSL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | MSL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0339 | SAS | PJL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0171 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03540 | hp2 | a0002 | c0003 | t0001 | g0003 | AFR | GWD | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03579 | hp2 | a0002 | c0003 | t0001 | g0023 | AFR | MSL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | STU | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0160 | SAS | PJL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | BEB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0094 | SAS | BEB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0349 | SAS | BEB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0136 | SAS | BEB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0270 | SAS | BEB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0139 | SAS | STU | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0162 | SAS | STU | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | STU | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18522 | hp1 | a0002 | c0003 | t0001 | g0003 | AFR | YRI | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18522 | hp2 | a0001 | c0007 | t0001 | g0051 | AFR | YRI | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | CHB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | CHB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | CHB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0329 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0369 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0368 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0319 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18979 | hp1 | a0001 | c0012 | t0001 | g0134 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0351 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18994 | hp1 | a0001 | c0009 | t0001 | g0055 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0350 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0322 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0327 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | LWK | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19043 | hp1 | a0002 | c0008 | t0001 | g0278 | AFR | LWK | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19062 | hp2 | a0006 | c0011 | t0001 | g0184 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19065 | hp1 | a0007 | c0014 | t0001 | g0133 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0328 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0337 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19240 | hp1 | a0002 | c0003 | t0001 | g0023 | AFR | YRI | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | YRI | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ASW | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0087 | AFR | ASW | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0340 | EUR | TSI | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA20752 | hp2 | a0001 | c0006 | t0001 | g0287 | EUR | TSI | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | GIH | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | GIH | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02109 | hp2 | a0002 | c0003 | t0001 | g0360 | AFR | ACB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | ACB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0294 | AFR | ACB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG02559 | hp2 | a0003 | c0005 | t0001 | g0034 | AFR | ACB | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0364 | AFR | MSL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0169 | AFR | MSL | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | USA | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | USA | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | USA | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | USA | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| NA21309 | hp2 | a0001 | c0007 | t0001 | g0164 | AFR | LWK | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0090 | REF | REF | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0069 | REF | REF | F10_chr13_113117799_113154529 | F10 | chr13 | 113117799 | 113154529 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113129471 | G | C | 1 | a0003 | 3 | HG02559.hp2 HG03098.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.90G>C | p.Gln30His | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/8 | 147/1536 | 90/1467 | 30/488 | chr13 | 113129471 | |||
| chr13:113129496 | A | C | 1 | a0007 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.115A>C | p.Thr39Pro | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/8 | 172/1536 | 115/1467 | 39/488 | chr13 | 113129496 | |||
| chr13:113143922 | G | A | 1 | a0002 | 13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
missense_variant | MODERATE | c.574G>A | p.Gly192Arg | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/8 | 631/1536 | 574/1467 | 192/488 | chr13 | 113143922 | |||
| chr13:113149018 | T | C | 1 | a0006 | 1 | NA19062.hp2 | missense_variant | MODERATE | c.968T>C | p.Ile323Thr | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 8/8 | 1025/1536 | 968/1467 | 323/488 | chr13 | 113149018 | |||
| chr13:113149165 | G | C | 1 | a0005 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.1115G>C | p.Arg372Pro | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 8/8 | 1172/1536 | 1115/1467 | 372/488 | chr13 | 113149165 | |||
| chr13:113149489 | A | C | 1 | a0004 | 1 | HG02273.hp2 | missense_variant | MODERATE | c.1439A>C | p.Glu480Ala | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 8/8 | 1496/1536 | 1439/1467 | 480/488 | chr13 | 113149489 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113122915 | C | T | 1 | a0001c0015 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.60C>T | p.Leu20Leu | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/8 | 117/1536 | 60/1467 | 20/488 | chr13 | 113122915 | |||
| chr13:113140944 | C | T | 1 | a0001c0007 | 2 | NA18522.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.396C>T | p.Asp132Asp | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/8 | 453/1536 | 396/1467 | 132/488 | chr13 | 113140944 | |||
| chr13:113140947 | C | T | 2 | a0001c0004 a0001c0006 |
11 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(8): Show |
synonymous_variant | LOW | c.399C>T | p.Asn133Asn | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/8 | 456/1536 | 399/1467 | 133/488 | chr13 | 113140947 | |||
| chr13:113147423 | C | T | 8 | a0001c0001 a0001c0006 a0001c0012 others(5): Show |
262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
synonymous_variant | LOW | c.792C>T | p.Thr264Thr | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/8 | 849/1536 | 792/1467 | 264/488 | chr13 | 113147423 | |||
| chr13:113149055 | C | A | 1 | a0001c0009 | 1 | NA18994.hp1 | synonymous_variant | LOW | c.1005C>A | p.Arg335Arg | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 8/8 | 1062/1536 | 1005/1467 | 335/488 | chr13 | 113149055 | |||
| chr13:113149106 | G | A | 1 | a0001c0012 | 1 | NA18979.hp1 | synonymous_variant | LOW | c.1056G>A | p.Thr352Thr | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 8/8 | 1113/1536 | 1056/1467 | 352/488 | chr13 | 113149106 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113122816 | C | T | 2 | a0001c0001t0002 a0001c0002t0002 |
4 | HG01256.hp1 HG03239.hp1 HG03490.hp1 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-40C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/8 | chr13 | 113122816 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113123018 | C | T | 3 | a0001c0001t0001g0030 a0001c0002t0001g0368 a0001c0002t0001g0369 |
4 | NA18951.hp2 NA18954.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+93C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113123018 | |||||||
| chr13:113123195 | A | G | 82 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0026 others(79): Show |
91 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.70+270A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113123195 | |||||||
| chr13:113123216 | A | G | 1 | a0001c0002t0001g0367 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.70+291A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113123216 | |||||||
| chr13:113123308 | A | G | 1 | a0003c0005t0001g0366 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.70+383A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113123308 | |||||||
| chr13:113123408 | C | G | 3 | a0001c0004t0001g0294 a0001c0004t0001g0295 a0001c0004t0001g0365 |
3 | HG02280.hp1 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.70+483C>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113123408 | |||||||
| chr13:113123413 | G | T | 30 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0286 others(27): Show |
35 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.70+488G>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113123413 | |||||||
| chr13:113123475 | C | T | 1 | a0001c0002t0001g0276 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.70+550C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113123475 | |||||||
| chr13:113123495 | G | A | 1 | a0001c0002t0001g0031 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.70+570G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113123495 | |||||||
| chr13:113123567 | G | A | 1 | a0001c0002t0001g0032 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.70+642G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113123567 | |||||||
| chr13:113123639 | C | A | 10 | a0001c0001t0001g0282 a0001c0002t0001g0281 a0002c0003t0001g0003 others(7): Show |
14 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.70+714C>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113123639 | |||||||
| chr13:113123689 | G | C | 3 | a0001c0001t0001g0033 a0001c0001t0001g0283 a0001c0002t0001g0284 |
3 | HG02630.hp1 HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.70+764G>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113123689 | |||||||
| chr13:113123710 | T | C | 24 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0037 others(21): Show |
28 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.70+785T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113123710 | |||||||
| chr13:113123725 | G | T | 1 | a0001c0001t0001g0275 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.70+800G>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113123725 | |||||||
| chr13:113123866 | C | T | 1 | a0001c0002t0001g0274 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.70+941C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113123866 | |||||||
| chr13:113123874 | C | T | 2 | a0001c0001t0001g0282 a0001c0002t0001g0281 |
2 | HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.70+949C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113123874 | |||||||
| chr13:113124027 | C | T | 1 | a0001c0002t0001g0273 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.70+1102C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113124027 | |||||||
| chr13:113124107 | G | A | 2 | a0001c0001t0001g0297 a0001c0002t0001g0298 |
2 | NA18967.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.70+1182G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113124107 | |||||||
| chr13:113124110 | A | G | 18 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0039 others(15): Show |
22 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.70+1185A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113124110 | |||||||
| chr13:113124124 | TGAGGCCC others(21): Show |
T | 1 | a0001c0001t0001g0043 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.70+1222_70+1249del others(28): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113124124 | ||||||
| chr13:113124276 | C | T | 3 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0358 |
3 | HG02135.hp1 HG02602.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.70+1351C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113124276 | |||||||
| chr13:113124373 | G | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
6 | HG00639.hp2 HG01109.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+1448G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113124373 | |||||||
| chr13:113124444 | T | C | 1 | a0001c0002t0001g0048 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.70+1519T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113124444 | |||||||
| chr13:113124493 | G | A | 1 | a0001c0002t0001g0044 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.70+1568G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113124493 | |||||||
| chr13:113124673 | C | T | 4 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 others(1): Show |
4 | HG00544.hp2 NA18975.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+1748C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113124673 | |||||||
| chr13:113124720 | G | T | 4 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0002t0001g0350 others(1): Show |
4 | NA18982.hp2 NA18989.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+1795G>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113124720 | |||||||
| chr13:113124775 | C | T | 1 | a0001c0001t0001g0364 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.70+1850C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113124775 | |||||||
| chr13:113124898 | C | T | 29 | a0001c0001t0001g0022 a0001c0001t0001g0254 a0001c0001t0001g0255 others(26): Show |
30 | HG01099.hp1 HG01243.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.70+1973C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113124898 | |||||||
| chr13:113124910 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | NA18960.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.70+1985G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113124910 | |||||||
| chr13:113124923 | A | G | 174 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(171): Show |
190 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.70+1998A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113124923 | |||||||
| chr13:113124963 | T | C | 1 | a0001c0007t0001g0051 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70+2038T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113124963 | |||||||
| chr13:113125010 | AGAAGGAC others(10): Show |
A | 1 | a0001c0002t0001g0253 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.70+2087_70+2103del others(17): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113125010 | ||||||
| chr13:113125160 | G | C | 1 | a0001c0006t0001g0025 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.70+2235G>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113125160 | |||||||
| chr13:113125283 | C | T | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG01978.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.70+2358C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113125283 | |||||||
| chr13:113125502 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.70+2577T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113125502 | |||||||
| chr13:113125553 | C | A | 1 | a0001c0002t0001g0299 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.70+2628C>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113125553 | |||||||
| chr13:113125646 | C | T | 1 | a0001c0002t0001g0160 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.70+2721C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113125646 | |||||||
| chr13:113125704 | C | T | 2 | a0001c0001t0001g0159 a0001c0002t0001g0362 |
2 | HG01496.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.70+2779C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113125704 | |||||||
| chr13:113125727 | T | C | 48 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0039 others(45): Show |
53 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(50): Show |
intron_variant | MODIFIER | c.70+2802T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113125727 | |||||||
| chr13:113125738 | C | T | 1 | a0001c0001t0001g0364 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.70+2813C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113125738 | |||||||
| chr13:113125782 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.70+2857G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113125782 | |||||||
| chr13:113126067 | G | T | 1 | a0001c0001t0001g0269 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.70+3142G>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113126067 | |||||||
| chr13:113126311 | A | G | 7 | a0001c0004t0001g0288 a0001c0004t0001g0289 a0001c0004t0001g0290 others(4): Show |
7 | HG02145.hp2 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.71-3141A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113126311 | |||||||
| chr13:113126394 | T | C | 1 | a0001c0001t0001g0364 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.71-3058T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113126394 | |||||||
| chr13:113126435 | A | C | 1 | a0001c0001t0001g0269 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.71-3017A>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113126435 | |||||||
| chr13:113126469 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.71-2983A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113126469 | |||||||
| chr13:113126475 | T | C | 1 | a0001c0001t0001g0364 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.71-2977T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113126475 | |||||||
| chr13:113126483 | A | C | 3 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0348 |
3 | HG00738.hp2 HG01358.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.71-2969A>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113126483 | |||||||
| chr13:113126505 | G | C | 1 | a0001c0002t0001g0362 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.71-2947G>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113126505 | |||||||
| chr13:113126596 | T | C | 40 | a0001c0001t0001g0163 a0001c0001t0001g0166 a0001c0001t0001g0167 others(37): Show |
41 | HG00673.hp2 HG01243.hp2 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.71-2856T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113126596 | |||||||
| chr13:113126704 | G | A | 86 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(83): Show |
96 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.71-2748G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113126704 | |||||||
| chr13:113126737 | A | G | 2 | a0001c0001t0001g0364 a0001c0002t0001g0362 |
2 | HG01496.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.71-2715A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113126737 | |||||||
| chr13:113126741 | G | A | 3 | a0001c0001t0001g0242 a0001c0002t0001g0053 a0001c0002t0001g0243 |
3 | HG02080.hp1 NA18994.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.71-2711G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113126741 | |||||||
| chr13:113127180 | T | C | 2 | a0001c0001t0001g0254 a0001c0001t0001g0255 |
2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.71-2272T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113127180 | |||||||
| chr13:113127281 | G | A | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG02717.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-2171G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113127281 | |||||||
| chr13:113127293 | G | C | 17 | a0001c0001t0001g0022 a0001c0001t0001g0173 a0001c0001t0001g0258 others(14): Show |
18 | HG01099.hp1 HG02135.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.71-2159G>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113127293 | |||||||
| chr13:113127402 | T | A | 2 | a0001c0004t0001g0294 a0001c0004t0001g0365 |
2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.71-2050T>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113127402 | |||||||
| chr13:113127464 | G | T | 1 | a0001c0002t0001g0172 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.71-1988G>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113127464 | |||||||
| chr13:113127628 | A | C | 23 | a0001c0001t0001g0163 a0001c0001t0001g0166 a0001c0001t0001g0167 others(20): Show |
24 | HG00673.hp2 HG01952.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.71-1824A>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113127628 | |||||||
| chr13:113127843 | G | A | 1 | a0001c0002t0001g0031 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.71-1609G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113127843 | |||||||
| chr13:113127968 | T | C | 10 | a0001c0002t0001g0363 a0001c0004t0001g0288 a0001c0004t0001g0289 others(7): Show |
10 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.71-1484T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113127968 | |||||||
| chr13:113127988 | T | C | 1 | a0001c0002t0001g0362 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.71-1464T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113127988 | |||||||
| chr13:113128810 | G | A | 2 | a0001c0004t0001g0292 a0001c0004t0001g0293 |
2 | HG01243.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.71-642G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113128810 | |||||||
| chr13:113128874 | C | T | 1 | a0001c0002t0001g0241 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.71-578C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113128874 | |||||||
| chr13:113128886 | G | GA | 41 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0056 others(38): Show |
43 | HG00280.hp1 HG00597.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.71-541dupA | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113128886 | ||||||
| chr13:113128886 | G | GAA | 9 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0002t0001g0162 others(6): Show |
9 | HG00423.hp2 HG01496.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.71-542_71-541dupAA | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113128886 | ||||||
| chr13:113128886 | GA | G | 27 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(24): Show |
27 | HG00099.hp1 HG01070.hp1 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.71-541delA | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113128886 | ||||||
| chr13:113128886 | GAA | G | 22 | a0001c0001t0001g0022 a0001c0001t0001g0173 a0001c0001t0001g0254 others(19): Show |
23 | HG01099.hp1 HG02135.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.71-542_71-541delAA | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113128886 | ||||||
| chr13:113128889 | A | G | 1 | a0001c0001t0001g0364 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.71-563A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113128889 | |||||||
| chr13:113128890 | A | G | 22 | a0001c0001t0001g0022 a0001c0001t0001g0173 a0001c0001t0001g0254 others(19): Show |
23 | HG01099.hp1 HG02135.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.71-562A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113128890 | |||||||
| chr13:113128925 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
6 | HG00639.hp2 HG01109.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-527C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113128925 | |||||||
| chr13:113129194 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.71-258G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113129194 | |||||||
| chr13:113129276 | AG | A | 4 | a0001c0002t0001g0035 a0003c0005t0001g0034 a0003c0005t0001g0361 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-174delG | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113129276 | ||||||
| chr13:113129358 | T | C | 1 | a0001c0001t0001g0306 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.71-94T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | chr13 | 113129358 | |||||||
| chr13:113129397 | G | GGGAGCCT others(9): Show |
32 | a0001c0001t0001g0010 a0001c0001t0001g0163 a0001c0001t0001g0166 others(29): Show |
34 | HG00438.hp1 HG00673.hp2 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.71-42_71-41insAGAG others(12): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113129397 | ||||||
| chr13:113129676 | C | T | 100 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(97): Show |
110 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.231+64C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113129676 | |||||||
| chr13:113129701 | G | A | 58 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(55): Show |
64 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.231+89G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113129701 | |||||||
| chr13:113129727 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.231+115G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113129727 | |||||||
| chr13:113129739 | GGGCGGGG others(19): Show |
G | 10 | a0001c0004t0001g0288 a0001c0004t0001g0289 a0001c0004t0001g0290 others(7): Show |
11 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.231+133_231+158del others(26): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113129739 | ||||||
| chr13:113129772 | G | A | 1 | a0001c0001t0001g0364 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.231+160G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113129772 | |||||||
| chr13:113129798 | G | GC | 7 | a0001c0001t0001g0124 a0001c0001t0001g0190 a0001c0001t0001g0254 others(4): Show |
7 | HG00741.hp2 HG01496.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.231+191dupC | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113129798 | ||||||
| chr13:113129856 | C | T | 2 | a0001c0001t0001g0009 a0001c0015t0001g0009 |
3 | HG00735.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.231+244C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113129856 | |||||||
| chr13:113129907 | T | G | 32 | a0001c0001t0001g0163 a0001c0001t0001g0166 a0001c0001t0001g0167 others(29): Show |
33 | HG00438.hp1 HG00673.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.231+295T>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113129907 | |||||||
| chr13:113130003 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.231+391T>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113130003 | |||||||
| chr13:113130033 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.231+421C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113130033 | |||||||
| chr13:113130077 | ACGAACCC others(46): Show |
A | 10 | a0001c0004t0001g0288 a0001c0004t0001g0289 a0001c0004t0001g0290 others(7): Show |
11 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.231+473_231+525del others(53): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113130077 | ||||||
| chr13:113130093 | T | G | 310 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(307): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.231+481T>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113130093 | |||||||
| chr13:113130129 | G | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(214): Show |
236 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.231+517G>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113130129 | |||||||
| chr13:113130226 | A | C | 11 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(8): Show |
11 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.231+614A>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113130226 | |||||||
| chr13:113130274 | A | G | 32 | a0001c0001t0001g0114 a0001c0001t0001g0163 a0001c0001t0001g0166 others(29): Show |
33 | HG00438.hp1 HG00673.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.231+662A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113130274 | |||||||
| chr13:113130330 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0113 others(12): Show |
18 | HG00642.hp2 HG00735.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.231+718C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113130330 | |||||||
| chr13:113130406 | A | G | 34 | a0001c0001t0001g0163 a0001c0001t0001g0166 a0001c0001t0001g0167 others(31): Show |
35 | HG00438.hp1 HG00673.hp2 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.231+794A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113130406 | |||||||
| chr13:113130657 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.231+1045C>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113130657 | |||||||
| chr13:113130684 | G | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(63): Show |
74 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.231+1072G>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113130684 | |||||||
| chr13:113130718 | C | G | 1 | a0001c0002t0001g0061 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.231+1106C>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113130718 | |||||||
| chr13:113130792 | C | G | 1 | a0001c0001t0001g0189 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.231+1180C>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113130792 | |||||||
| chr13:113130892 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.231+1280C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113130892 | |||||||
| chr13:113130896 | G | C | 1 | a0001c0001t0001g0364 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.231+1284G>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113130896 | |||||||
| chr13:113131002 | C | G | 2 | a0001c0001t0001g0233 a0001c0002t0001g0234 |
2 | NA18966.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.231+1390C>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113131002 | |||||||
| chr13:113131151 | C | T | 2 | a0001c0007t0001g0051 a0001c0007t0001g0164 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.231+1539C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113131151 | |||||||
| chr13:113131686 | T | G | 1 | a0001c0002t0001g0350 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.231+2074T>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113131686 | |||||||
| chr13:113131721 | ATCTC | A | 3 | a0001c0004t0001g0289 a0001c0004t0001g0290 a0001c0004t0001g0295 |
3 | HG02145.hp2 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.231+2113_231+2116d others(6): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113131721 | ||||||
| chr13:113131876 | T | C | 1 | a0001c0002t0001g0261 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.231+2264T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113131876 | |||||||
| chr13:113131891 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG00733.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.231+2279C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113131891 | |||||||
| chr13:113131892 | G | A | 2 | a0001c0001t0001g0291 a0001c0002t0001g0362 |
2 | HG01496.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.231+2280G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113131892 | |||||||
| chr13:113131893 | C | T | 1 | a0001c0002t0001g0169 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.231+2281C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113131893 | |||||||
| chr13:113131910 | C | T | 2 | a0001c0001t0001g0282 a0001c0002t0001g0281 |
2 | HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.231+2298C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113131910 | |||||||
| chr13:113131991 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0316 |
2 | NA18963.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.231+2379T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113131991 | |||||||
| chr13:113132085 | A | G | 10 | a0001c0004t0001g0288 a0001c0004t0001g0289 a0001c0004t0001g0290 others(7): Show |
11 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.231+2473A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113132085 | |||||||
| chr13:113132359 | C | A | 3 | a0001c0002t0001g0035 a0003c0005t0001g0034 a0003c0005t0001g0361 |
3 | HG02559.hp2 HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.231+2747C>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113132359 | |||||||
| chr13:113132469 | T | C | 2 | a0001c0007t0001g0051 a0001c0007t0001g0164 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.231+2857T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113132469 | |||||||
| chr13:113132613 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.231+3001T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113132613 | |||||||
| chr13:113132633 | C | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(303): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.231+3021C>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113132633 | |||||||
| chr13:113132651 | C | T | 9 | a0002c0003t0001g0003 a0002c0003t0001g0023 a0002c0003t0001g0277 others(6): Show |
13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.231+3039C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113132651 | |||||||
| chr13:113132963 | C | T | 12 | a0001c0004t0001g0288 a0001c0004t0001g0289 a0001c0004t0001g0290 others(9): Show |
13 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.231+3351C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113132963 | |||||||
| chr13:113133145 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(167): Show |
189 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.231+3533A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113133145 | |||||||
| chr13:113133507 | G | A | 306 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(303): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.231+3895G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113133507 | |||||||
| chr13:113133564 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.231+3952T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113133564 | |||||||
| chr13:113133571 | A | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0291 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.231+3959A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113133571 | |||||||
| chr13:113133739 | C | A | 2 | a0001c0001t0001g0354 a0001c0001t0001g0355 |
2 | HG00544.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.231+4127C>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113133739 | |||||||
| chr13:113133931 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0347 |
3 | HG01257.hp2 HG01258.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.231+4319G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113133931 | |||||||
| chr13:113134044 | A | T | 4 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0188 others(1): Show |
4 | HG00438.hp1 HG00673.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.232-4413A>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113134044 | |||||||
| chr13:113134359 | T | C | 2 | a0001c0007t0001g0051 a0001c0007t0001g0164 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.232-4098T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113134359 | |||||||
| chr13:113134374 | A | G | 1 | a0001c0002t0001g0228 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.232-4083A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113134374 | |||||||
| chr13:113134640 | G | A | 306 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(303): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.232-3817G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113134640 | |||||||
| chr13:113134816 | T | C | 2 | a0001c0007t0001g0051 a0001c0007t0001g0164 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.232-3641T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113134816 | |||||||
| chr13:113134915 | T | C | 9 | a0002c0003t0001g0003 a0002c0003t0001g0023 a0002c0003t0001g0277 others(6): Show |
13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.232-3542T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113134915 | |||||||
| chr13:113134968 | C | T | 16 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0079 others(13): Show |
16 | HG00140.hp1 HG00323.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.232-3489C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113134968 | |||||||
| chr13:113134969 | G | A | 1 | a0001c0001t0001g0364 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.232-3488G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113134969 | |||||||
| chr13:113135183 | C | T | 2 | a0001c0001t0001g0227 a0001c0002t0001g0226 |
2 | HG00438.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.232-3274C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113135183 | |||||||
| chr13:113135219 | G | C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG00741.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.232-3238G>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113135219 | |||||||
| chr13:113135244 | C | CA | 17 | a0001c0001t0001g0126 a0001c0001t0001g0174 a0001c0001t0001g0180 others(14): Show |
21 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.232-3200dupA | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113135244 | ||||||
| chr13:113135460 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.232-2997C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113135460 | |||||||
| chr13:113135517 | C | T | 2 | a0001c0002t0001g0077 a0001c0002t0001g0078 |
2 | HG01106.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.232-2940C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113135517 | |||||||
| chr13:113135655 | T | A | 1 | a0001c0001t0001g0056 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.232-2802T>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113135655 | |||||||
| chr13:113135681 | A | G | 1 | a0001c0001t0001g0364 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.232-2776A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113135681 | |||||||
| chr13:113135955 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
239 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.232-2502T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113135955 | |||||||
| chr13:113136038 | A | G | 2 | a0001c0004t0001g0294 a0001c0004t0001g0365 |
2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.232-2419A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113136038 | |||||||
| chr13:113136047 | A | G | 1 | a0001c0002t0001g0225 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.232-2410A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113136047 | |||||||
| chr13:113136064 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(303): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.232-2393T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113136064 | |||||||
| chr13:113136181 | C | T | 3 | a0001c0004t0001g0289 a0001c0004t0001g0290 a0001c0004t0001g0295 |
3 | HG02145.hp2 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.232-2276C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113136181 | |||||||
| chr13:113136305 | GA | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0039 |
3 | HG02451.hp2 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.232-2148delA | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113136305 | ||||||
| chr13:113136448 | C | CT | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(82): Show |
97 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.232-1994dupT | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113136448 | ||||||
| chr13:113136448 | CT | C | 26 | a0001c0001t0001g0163 a0001c0001t0001g0166 a0001c0001t0001g0167 others(23): Show |
27 | HG00438.hp1 HG00673.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.232-1994delT | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113136448 | ||||||
| chr13:113136494 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.232-1963G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113136494 | |||||||
| chr13:113136536 | C | G | 1 | a0001c0002t0001g0171 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.232-1921C>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113136536 | |||||||
| chr13:113136622 | TAATTCTT others(320): Show |
T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(303): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.232-1819_232-1493d others(2): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113136622 | ||||||
| chr13:113136633 | C | CT | 18 | a0001c0001t0001g0030 a0001c0001t0001g0043 a0001c0001t0001g0052 others(15): Show |
18 | HG00280.hp1 HG01168.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.232-1789dupT | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113136633 | ||||||
| chr13:113136633 | C | CTT | 18 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0065 others(15): Show |
19 | HG00140.hp1 HG00323.hp2 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.232-1790_232-1789d others(4): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113136633 | ||||||
| chr13:113136633 | C | CTTTT | 8 | a0001c0001t0001g0026 a0001c0001t0001g0159 a0001c0001t0001g0345 others(5): Show |
9 | HG00741.hp2 HG01106.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.232-1792_232-1789d others(6): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113136633 | ||||||
| chr13:113136633 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0039 |
3 | HG02451.hp2 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.232-1800_232-1789d others(14): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113136633 | ||||||
| chr13:113137031 | C | T | 1 | a0001c0002t0001g0161 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.232-1426C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113137031 | |||||||
| chr13:113137068 | A | G | 1 | a0001c0001t0001g0364 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.232-1389A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113137068 | |||||||
| chr13:113137230 | T | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0291 a0001c0002t0001g0362 |
3 | HG01496.hp2 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.232-1227T>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113137230 | |||||||
| chr13:113137564 | C | T | 4 | a0001c0001t0001g0334 a0001c0001t0001g0336 a0001c0002t0001g0335 others(1): Show |
4 | HG02129.hp1 HG02132.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.232-893C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113137564 | |||||||
| chr13:113137605 | C | T | 1 | a0001c0002t0001g0224 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.232-852C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113137605 | |||||||
| chr13:113137731 | C | T | 1 | a0001c0002t0001g0333 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.232-726C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113137731 | |||||||
| chr13:113137732 | G | A | 3 | a0001c0004t0001g0289 a0001c0004t0001g0290 a0001c0004t0001g0295 |
3 | HG02145.hp2 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.232-725G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113137732 | |||||||
| chr13:113137764 | G | C | 1 | a0001c0001t0001g0364 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.232-693G>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113137764 | |||||||
| chr13:113137768 | T | G | 1 | a0001c0001t0001g0052 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.232-689T>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113137768 | |||||||
| chr13:113137777 | G | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0002t0001g0038 |
3 | HG01891.hp2 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.232-680G>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113137777 | |||||||
| chr13:113137838 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.232-619C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113137838 | |||||||
| chr13:113137856 | T | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
239 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.232-601T>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113137856 | |||||||
| chr13:113137894 | G | A | 2 | a0001c0002t0001g0161 a0001c0002t0001g0363 |
2 | HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.232-563G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113137894 | |||||||
| chr13:113137956 | A | C | 1 | a0001c0001t0001g0364 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.232-501A>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113137956 | |||||||
| chr13:113138007 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.232-450A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113138007 | |||||||
| chr13:113138076 | G | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
190 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.232-381G>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113138076 | |||||||
| chr13:113138153 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0291 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.232-304G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113138153 | |||||||
| chr13:113138237 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.232-220A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113138237 | |||||||
| chr13:113138251 | A | G | 3 | a0001c0001t0001g0030 a0001c0002t0001g0368 a0001c0002t0001g0369 |
4 | NA18951.hp2 NA18954.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.232-206A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113138251 | |||||||
| chr13:113138440 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(303): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.232-17T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 2/7 | chr13 | 113138440 | |||||||
| chr13:113138579 | C | A | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(275): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.256+98C>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 3/7 | chr13 | 113138579 | |||||||
| chr13:113138768 | A | G | 1 | a0001c0002t0001g0362 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.256+287A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 3/7 | chr13 | 113138768 | |||||||
| chr13:113138874 | C | T | 1 | a0001c0002t0001g0331 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.256+393C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 3/7 | chr13 | 113138874 | |||||||
| chr13:113138989 | T | C | 1 | a0001c0002t0001g0349 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.257-368T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 3/7 | chr13 | 113138989 | |||||||
| chr13:113139269 | C | T | 2 | a0001c0001t0001g0266 a0001c0002t0001g0267 |
2 | NA18960.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.257-88C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 3/7 | chr13 | 113139269 | |||||||
| chr13:113139535 | G | A | 30 | a0001c0001t0001g0163 a0001c0001t0001g0166 a0001c0001t0001g0167 others(27): Show |
31 | HG00438.hp1 HG00673.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.370+65G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 4/7 | chr13 | 113139535 | |||||||
| chr13:113139899 | T | A | 3 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0268 |
3 | HG02145.hp1 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.370+429T>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 4/7 | chr13 | 113139899 | |||||||
| chr13:113139987 | G | A | 10 | a0001c0004t0001g0288 a0001c0004t0001g0289 a0001c0004t0001g0290 others(7): Show |
11 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.370+517G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 4/7 | chr13 | 113139987 | |||||||
| chr13:113140073 | C | CT | 15 | a0001c0001t0001g0011 a0001c0001t0001g0089 a0001c0001t0001g0188 others(12): Show |
16 | HG00438.hp1 HG01069.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.370+621dupT | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr13 | 113140073 | ||||||
| chr13:113140073 | C | CTT | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
184 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.370+620_370+621dup others(2): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr13 | 113140073 | ||||||
| chr13:113140073 | CT | C | 83 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(80): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.370+621delT | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr13 | 113140073 | ||||||
| chr13:113140073 | CTTTTTTT others(2): Show |
C | 6 | a0001c0004t0001g0288 a0001c0004t0001g0289 a0001c0004t0001g0290 others(3): Show |
7 | HG01070.hp2 HG01071.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.370+613_370+621del others(9): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr13 | 113140073 | ||||||
| chr13:113140108 | C | T | 1 | a0001c0002t0001g0363 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.370+638C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 4/7 | chr13 | 113140108 | |||||||
| chr13:113140175 | G | A | 1 | a0001c0002t0001g0238 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.370+705G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 4/7 | chr13 | 113140175 | |||||||
| chr13:113140235 | G | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0314 a0001c0001t0001g0315 others(1): Show |
5 | NA18944.hp1 NA18949.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.371-684G>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 4/7 | chr13 | 113140235 | |||||||
| chr13:113140283 | G | A | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0185 others(1): Show |
4 | NA18940.hp1 NA18967.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.371-636G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 4/7 | chr13 | 113140283 | |||||||
| chr13:113140509 | T | C | 1 | a0003c0005t0001g0034 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.371-410T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 4/7 | chr13 | 113140509 | |||||||
| chr13:113140629 | G | A | 3 | a0001c0004t0001g0288 a0001c0006t0001g0025 a0001c0006t0001g0287 |
4 | HG01070.hp2 HG01071.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.371-290G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 4/7 | chr13 | 113140629 | |||||||
| chr13:113140655 | A | AG | 27 | a0001c0001t0001g0045 a0001c0001t0001g0065 a0001c0001t0001g0095 others(24): Show |
27 | HG00423.hp2 HG00438.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.371-259dupG | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr13 | 113140655 | ||||||
| chr13:113140828 | G | A | 3 | a0001c0002t0001g0161 a0001c0002t0001g0296 a0001c0002t0001g0363 |
3 | HG01884.hp1 HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.371-91G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 4/7 | chr13 | 113140828 | |||||||
| chr13:113140838 | T | G | 1 | a0001c0001t0001g0269 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.371-81T>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 4/7 | chr13 | 113140838 | |||||||
| chr13:113140853 | C | T | 2 | a0001c0002t0001g0161 a0001c0002t0001g0296 |
2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.371-66C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 4/7 | chr13 | 113140853 | |||||||
| chr13:113140901 | C | T | 2 | a0001c0007t0001g0051 a0001c0007t0001g0164 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.371-18C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 4/7 | chr13 | 113140901 | |||||||
| chr13:113141105 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.502+55G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113141105 | |||||||
| chr13:113141114 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.502+64G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113141114 | |||||||
| chr13:113141273 | G | A | 9 | a0001c0001t0001g0028 a0001c0001t0001g0126 a0001c0001t0001g0128 others(6): Show |
10 | NA18959.hp2 NA18964.hp1 NA18967.hp2 others(7): Show |
intron_variant | MODIFIER | c.502+223G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113141273 | |||||||
| chr13:113141303 | A | G | 10 | a0001c0004t0001g0288 a0001c0004t0001g0289 a0001c0004t0001g0290 others(7): Show |
11 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.502+253A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113141303 | |||||||
| chr13:113141338 | A | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0045 a0001c0001t0001g0046 others(5): Show |
9 | HG00639.hp2 HG00741.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.502+288A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113141338 | |||||||
| chr13:113141357 | T | C | 307 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(304): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.502+307T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113141357 | |||||||
| chr13:113141373 | G | A | 2 | a0001c0004t0001g0294 a0001c0004t0001g0365 |
2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.502+323G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113141373 | |||||||
| chr13:113141482 | G | A | 27 | a0001c0001t0001g0163 a0001c0001t0001g0166 a0001c0001t0001g0167 others(24): Show |
28 | HG00438.hp1 HG00673.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.502+432G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113141482 | |||||||
| chr13:113141550 | G | A | 10 | a0001c0004t0001g0288 a0001c0004t0001g0289 a0001c0004t0001g0290 others(7): Show |
11 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.502+500G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113141550 | |||||||
| chr13:113141653 | C | T | 1 | a0001c0002t0001g0362 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.502+603C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113141653 | |||||||
| chr13:113141660 | C | T | 3 | a0001c0002t0001g0161 a0001c0002t0001g0296 a0001c0002t0001g0363 |
3 | HG01884.hp1 HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.502+610C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113141660 | |||||||
| chr13:113141824 | G | A | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 |
3 | HG01255.hp1 HG01261.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.502+774G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113141824 | |||||||
| chr13:113141824 | G | C | 1 | a0001c0002t0001g0096 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.502+774G>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113141824 | |||||||
| chr13:113141832 | C | T | 1 | a0001c0002t0001g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.502+782C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113141832 | |||||||
| chr13:113141902 | G | C | 1 | a0001c0001t0001g0197 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.502+852G>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113141902 | |||||||
| chr13:113141949 | C | T | 3 | a0001c0002t0001g0161 a0001c0002t0001g0296 a0001c0002t0001g0363 |
3 | HG01884.hp1 HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.502+899C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113141949 | |||||||
| chr13:113141970 | C | A | 1 | a0001c0002t0001g0362 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.502+920C>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113141970 | |||||||
| chr13:113141973 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.502+923G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113141973 | |||||||
| chr13:113142141 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.502+1091G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142141 | |||||||
| chr13:113142266 | G | A | 1 | a0001c0002t0001g0362 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.502+1216G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142266 | |||||||
| chr13:113142267 | T | C | 5 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0308 others(2): Show |
5 | HG00741.hp1 HG02040.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.502+1217T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142267 | |||||||
| chr13:113142270 | A | G | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG00741.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.502+1220A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142270 | |||||||
| chr13:113142273 | A | G | 11 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(8): Show |
11 | HG00099.hp2 HG00733.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.502+1223A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142273 | |||||||
| chr13:113142277 | C | T | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.502+1227C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142277 | |||||||
| chr13:113142279 | T | C | 14 | a0001c0001t0001g0066 a0001c0001t0001g0120 a0001c0001t0001g0121 others(11): Show |
14 | HG00099.hp2 HG00733.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.502+1229T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142279 | |||||||
| chr13:113142296 | T | C | 4 | a0001c0001t0001g0199 a0001c0001t0001g0254 a0001c0006t0001g0025 others(1): Show |
5 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+1246T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142296 | |||||||
| chr13:113142312 | C | T | 2 | a0001c0006t0001g0025 a0001c0006t0001g0287 |
3 | HG01070.hp2 HG01071.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.502+1262C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142312 | |||||||
| chr13:113142337 | C | A | 1 | a0001c0004t0001g0295 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.502+1287C>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142337 | |||||||
| chr13:113142337 | C | T | 2 | a0001c0001t0001g0266 a0001c0002t0001g0267 |
2 | NA18960.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.502+1287C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142337 | |||||||
| chr13:113142352 | C | T | 78 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0016 others(75): Show |
88 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.502+1302C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142352 | |||||||
| chr13:113142358 | A | G | 12 | a0001c0001t0001g0076 a0001c0001t0001g0266 a0001c0002t0001g0075 others(9): Show |
13 | HG01070.hp2 HG01071.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.502+1308A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142358 | |||||||
| chr13:113142376 | G | C | 42 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0018 others(39): Show |
50 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.502+1326G>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142376 | |||||||
| chr13:113142385 | CA | C | 282 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(279): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.502+1350delA | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr13 | 113142385 | ||||||
| chr13:113142386 | A | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0045 others(4): Show |
9 | HG00639.hp2 HG01109.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.502+1336A>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142386 | |||||||
| chr13:113142387 | A | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
201 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.502+1337A>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142387 | |||||||
| chr13:113142388 | A | C | 2 | a0001c0002t0001g0226 a0001c0002t0001g0229 |
2 | NA18957.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.502+1338A>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142388 | |||||||
| chr13:113142394 | AAAAAAAT others(375): Show |
A | 5 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0221 others(2): Show |
5 | HG00741.hp1 HG01358.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+1350_503-1070d others(2): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr13 | 113142394 | ||||||
| chr13:113142395 | AAAAAATT others(374): Show |
A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
6 | HG00639.hp2 HG01109.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.502+1351_503-1070d others(2): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr13 | 113142395 | ||||||
| chr13:113142400 | A | C | 1 | a0001c0001t0001g0311 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.502+1350A>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142400 | |||||||
| chr13:113142411 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.502+1361A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142411 | |||||||
| chr13:113142423 | G | A | 42 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0018 others(39): Show |
51 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.502+1373G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142423 | |||||||
| chr13:113142430 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.502+1380G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142430 | |||||||
| chr13:113142439 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.502+1389G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142439 | |||||||
| chr13:113142443 | A | G | 1 | a0001c0001t0001g0311 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.502+1393A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142443 | |||||||
| chr13:113142462 | A | G | 4 | a0001c0002t0001g0362 a0001c0004t0001g0288 a0001c0006t0001g0025 others(1): Show |
5 | HG01070.hp2 HG01071.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-1389A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142462 | |||||||
| chr13:113142481 | C | T | 2 | a0001c0002t0001g0317 a0001c0002t0001g0333 |
2 | HG02080.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.503-1370C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142481 | |||||||
| chr13:113142556 | C | CA | 31 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0022 others(28): Show |
32 | HG00738.hp1 HG00741.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.503-1273dupA | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr13 | 113142556 | ||||||
| chr13:113142556 | C | CAA | 6 | a0001c0001t0001g0041 a0001c0002t0001g0035 a0002c0003t0001g0279 others(3): Show |
6 | HG01891.hp1 HG01891.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.503-1274_503-1273d others(4): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr13 | 113142556 | ||||||
| chr13:113142556 | CA | C | 48 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0052 others(45): Show |
49 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.503-1273delA | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr13 | 113142556 | ||||||
| chr13:113142694 | G | C | 11 | a0001c0001t0001g0076 a0001c0001t0001g0159 a0001c0002t0001g0075 others(8): Show |
11 | HG02145.hp2 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.503-1157G>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142694 | |||||||
| chr13:113142737 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.503-1114C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142737 | |||||||
| chr13:113142762 | TA | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(213): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.503-1078delA | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr13 | 113142762 | ||||||
| chr13:113142792 | C | T | 2 | a0001c0002t0001g0362 a0001c0002t0001g0363 |
2 | HG01496.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.503-1059C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142792 | |||||||
| chr13:113142793 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.503-1058G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142793 | |||||||
| chr13:113142800 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.503-1051C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142800 | |||||||
| chr13:113142804 | C | T | 3 | a0001c0004t0001g0289 a0001c0004t0001g0290 a0001c0004t0001g0295 |
3 | HG02145.hp2 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.503-1047C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142804 | |||||||
| chr13:113142846 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.503-1005C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142846 | |||||||
| chr13:113142848 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.503-1003C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142848 | |||||||
| chr13:113142861 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0039 |
2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.503-990G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142861 | |||||||
| chr13:113142867 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.503-984G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113142867 | |||||||
| chr13:113142872 | CA | C | 4 | a0001c0002t0001g0053 a0001c0002t0001g0243 a0001c0002t0001g0304 others(1): Show |
4 | HG00597.hp2 HG02080.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.503-977delA | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr13 | 113142872 | ||||||
| chr13:113143020 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.503-831C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113143020 | |||||||
| chr13:113143032 | G | A | 33 | a0001c0001t0001g0041 a0001c0001t0001g0113 a0001c0001t0001g0141 others(30): Show |
34 | HG00438.hp1 HG00673.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.503-819G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113143032 | |||||||
| chr13:113143283 | G | A | 1 | a0001c0004t0001g0292 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.503-568G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113143283 | |||||||
| chr13:113143354 | T | G | 2 | a0001c0001t0001g0239 a0006c0011t0001g0184 |
2 | NA19056.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.503-497T>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113143354 | |||||||
| chr13:113143375 | C | A | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.503-476C>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113143375 | |||||||
| chr13:113143464 | T | C | 1 | a0001c0001t0001g0011 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.503-387T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113143464 | |||||||
| chr13:113143487 | A | G | 7 | a0001c0001t0001g0209 a0001c0001t0001g0236 a0001c0002t0001g0194 others(4): Show |
7 | HG00099.hp1 HG00639.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.503-364A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113143487 | |||||||
| chr13:113143579 | G | A | 4 | a0001c0002t0001g0035 a0003c0005t0001g0034 a0003c0005t0001g0361 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.503-272G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113143579 | |||||||
| chr13:113143659 | G | A | 5 | a0001c0001t0001g0041 a0001c0002t0001g0038 a0001c0002t0001g0042 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.503-192G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113143659 | |||||||
| chr13:113143684 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG01928.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.503-167C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113143684 | |||||||
| chr13:113143794 | C | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG01255.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.503-57C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113143794 | |||||||
| chr13:113143831 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG01175.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.503-20G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 5/7 | chr13 | 113143831 | |||||||
| chr13:113144287 | A | C | 9 | a0002c0003t0001g0003 a0002c0003t0001g0023 a0002c0003t0001g0277 others(6): Show |
13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.747+192A>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113144287 | |||||||
| chr13:113144301 | G | A | 2 | a0001c0001t0001g0091 a0001c0002t0001g0211 |
2 | NA18993.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.747+206G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113144301 | |||||||
| chr13:113144314 | A | C | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.747+219A>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113144314 | |||||||
| chr13:113144374 | C | T | 1 | a0001c0002t0001g0363 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.747+279C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113144374 | |||||||
| chr13:113144430 | G | C | 3 | a0001c0001t0001g0159 a0001c0007t0001g0051 a0001c0007t0001g0164 |
3 | HG02615.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.747+335G>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113144430 | |||||||
| chr13:113144437 | G | A | 1 | a0001c0002t0001g0201 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.747+342G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113144437 | |||||||
| chr13:113144488 | G | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0073 a0001c0001t0001g0116 others(6): Show |
10 | HG00733.hp2 HG01070.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.747+393G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113144488 | |||||||
| chr13:113144516 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.747+421C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113144516 | |||||||
| chr13:113144518 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.747+423G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113144518 | |||||||
| chr13:113144528 | C | T | 4 | a0001c0002t0001g0035 a0002c0003t0001g0280 a0003c0005t0001g0034 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+433C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113144528 | |||||||
| chr13:113144568 | G | A | 1 | a0001c0002t0001g0322 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.747+473G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113144568 | |||||||
| chr13:113144570 | C | T | 52 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0018 others(49): Show |
59 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.747+475C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113144570 | |||||||
| chr13:113144596 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.747+501C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113144596 | |||||||
| chr13:113144776 | C | T | 1 | a0001c0002t0001g0270 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.747+681C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113144776 | |||||||
| chr13:113144846 | T | C | 1 | a0001c0002t0001g0367 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.747+751T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113144846 | |||||||
| chr13:113144848 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0039 |
3 | HG02451.hp2 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.747+753G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113144848 | |||||||
| chr13:113144854 | C | T | 1 | a0001c0002t0001g0363 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.747+759C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113144854 | |||||||
| chr13:113144863 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.747+768G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113144863 | |||||||
| chr13:113144881 | A | AT | 19 | a0001c0001t0001g0056 a0001c0001t0001g0159 a0001c0001t0001g0166 others(16): Show |
23 | HG00423.hp2 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.747+801dupT | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr13 | 113144881 | ||||||
| chr13:113145003 | C | T | 1 | a0001c0002t0001g0362 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.747+908C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145003 | |||||||
| chr13:113145004 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.747+909G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145004 | |||||||
| chr13:113145023 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.747+928C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145023 | |||||||
| chr13:113145027 | T | C | 4 | a0001c0001t0001g0022 a0001c0002t0001g0150 a0001c0002t0001g0304 others(1): Show |
5 | HG00597.hp2 HG03041.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.747+932T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145027 | |||||||
| chr13:113145035 | C | T | 1 | a0001c0002t0001g0172 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.747+940C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145035 | |||||||
| chr13:113145071 | G | A | 126 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(123): Show |
135 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.747+976G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145071 | |||||||
| chr13:113145082 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.747+987G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145082 | |||||||
| chr13:113145127 | A | G | 1 | a0001c0002t0001g0247 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.747+1032A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145127 | |||||||
| chr13:113145132 | A | G | 1 | a0001c0002t0001g0247 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.747+1037A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145132 | |||||||
| chr13:113145165 | A | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(218): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.747+1070A>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145165 | |||||||
| chr13:113145176 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.747+1081G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145176 | |||||||
| chr13:113145265 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.747+1170A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145265 | |||||||
| chr13:113145278 | A | G | 12 | a0001c0004t0001g0289 a0001c0004t0001g0290 a0001c0004t0001g0295 others(9): Show |
16 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.747+1183A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145278 | |||||||
| chr13:113145307 | T | G | 1 | a0001c0004t0001g0292 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.747+1212T>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145307 | |||||||
| chr13:113145373 | T | TAAAAGCA others(51): Show |
4 | a0001c0001t0001g0041 a0001c0002t0001g0038 a0001c0002t0001g0042 others(1): Show |
4 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+1330_747+1387d others(60): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr13 | 113145373 | ||||||
| chr13:113145373 | TAAAAGCA others(51): Show |
T | 1 | a0001c0002t0001g0094 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.747+1330_747+1387d others(60): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr13 | 113145373 | ||||||
| chr13:113145510 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.747+1415G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145510 | |||||||
| chr13:113145513 | T | C | 6 | a0001c0004t0001g0288 a0001c0004t0001g0289 a0001c0004t0001g0290 others(3): Show |
7 | HG01070.hp2 HG01071.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.747+1418T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145513 | |||||||
| chr13:113145526 | T | C | 2 | a0001c0001t0002g0138 a0001c0001t0002g0155 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.747+1431T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145526 | |||||||
| chr13:113145529 | G | A | 1 | a0001c0001t0001g0314 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.747+1434G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145529 | |||||||
| chr13:113145565 | C | T | 1 | a0001c0002t0001g0161 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.747+1470C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145565 | |||||||
| chr13:113145580 | A | G | 2 | a0001c0001t0001g0072 a0001c0002t0001g0362 |
2 | HG01496.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.747+1485A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145580 | |||||||
| chr13:113145647 | A | G | 209 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(206): Show |
235 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.747+1552A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145647 | |||||||
| chr13:113145656 | T | C | 2 | a0001c0001t0001g0268 a0001c0002t0001g0363 |
2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.747+1561T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145656 | |||||||
| chr13:113145661 | C | T | 1 | a0001c0002t0001g0363 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.747+1566C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145661 | |||||||
| chr13:113145662 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0170 |
2 | HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.747+1567G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145662 | |||||||
| chr13:113145695 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.747+1600G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145695 | |||||||
| chr13:113145698 | C | T | 19 | a0001c0001t0001g0036 a0001c0001t0001g0039 a0001c0001t0001g0063 others(16): Show |
22 | HG00639.hp1 HG01243.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.747+1603C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145698 | |||||||
| chr13:113145705 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.747+1610C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145705 | |||||||
| chr13:113145718 | G | A | 27 | a0001c0001t0001g0041 a0001c0001t0001g0067 a0001c0001t0001g0088 others(24): Show |
30 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.747+1623G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145718 | |||||||
| chr13:113145823 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.748-1556C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145823 | |||||||
| chr13:113145894 | G | C | 7 | a0001c0004t0001g0294 a0002c0003t0001g0003 a0002c0003t0001g0277 others(4): Show |
10 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.748-1485G>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145894 | |||||||
| chr13:113145986 | G | A | 4 | a0001c0001t0001g0231 a0001c0001t0001g0239 a0001c0001t0001g0258 others(1): Show |
4 | HG02074.hp2 NA19011.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.748-1393G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113145986 | |||||||
| chr13:113146192 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0183 |
2 | HG00733.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.748-1187G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113146192 | |||||||
| chr13:113146308 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
221 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.748-1071T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113146308 | |||||||
| chr13:113146341 | C | T | 6 | a0001c0001t0001g0020 a0001c0001t0001g0099 a0001c0001t0001g0111 others(3): Show |
7 | HG00280.hp2 HG01255.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.748-1038C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113146341 | |||||||
| chr13:113146403 | G | A | 2 | a0001c0001t0001g0117 a0001c0002t0001g0363 |
2 | HG01074.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.748-976G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113146403 | |||||||
| chr13:113146443 | G | A | 7 | a0001c0004t0001g0294 a0002c0003t0001g0003 a0002c0003t0001g0277 others(4): Show |
10 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.748-936G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113146443 | |||||||
| chr13:113146448 | G | A | 2 | a0001c0002t0001g0171 a0001c0004t0001g0293 |
2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.748-931G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113146448 | |||||||
| chr13:113146493 | G | A | 1 | a0001c0001t0001g0324 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.748-886G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113146493 | |||||||
| chr13:113146730 | C | T | 2 | a0001c0002t0001g0002 a0001c0004t0001g0292 |
5 | HG01243.hp1 HG01243.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-649C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113146730 | |||||||
| chr13:113146875 | A | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.748-504A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113146875 | |||||||
| chr13:113146944 | G | T | 5 | a0001c0001t0001g0093 a0001c0001t0001g0113 a0001c0001t0001g0141 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.748-435G>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113146944 | |||||||
| chr13:113147064 | A | C | 1 | a0001c0002t0001g0362 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.748-315A>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113147064 | |||||||
| chr13:113147291 | G | A | 2 | a0001c0002t0001g0084 a0001c0002t0001g0281 |
2 | HG01109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.748-88G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 6/7 | chr13 | 113147291 | |||||||
| chr13:113147529 | A | G | 347 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(344): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.865+33A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113147529 | |||||||
| chr13:113147586 | G | C | 7 | a0001c0004t0001g0294 a0002c0003t0001g0003 a0002c0003t0001g0277 others(4): Show |
10 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.865+90G>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113147586 | |||||||
| chr13:113147632 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.865+136A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113147632 | |||||||
| chr13:113147728 | G | A | 1 | a0001c0002t0001g0161 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.865+232G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113147728 | |||||||
| chr13:113147728 | G | C | 1 | a0001c0001t0001g0251 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.865+232G>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113147728 | |||||||
| chr13:113147839 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.865+343T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113147839 | |||||||
| chr13:113148009 | T | C | 1 | a0001c0002t0001g0161 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.865+513T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148009 | |||||||
| chr13:113148030 | T | G | 7 | a0001c0004t0001g0294 a0002c0003t0001g0003 a0002c0003t0001g0277 others(4): Show |
10 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.865+534T>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148030 | |||||||
| chr13:113148111 | C | T | 1 | a0001c0002t0001g0317 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.865+615C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148111 | |||||||
| chr13:113148330 | CA | C | 10 | a0001c0001t0001g0080 a0001c0001t0001g0116 a0001c0001t0001g0117 others(7): Show |
10 | HG00140.hp1 HG00733.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.866-570delA | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148330 | ||||||
| chr13:113148341 | A | AATATATA others(17): Show |
1 | a0001c0002t0001g0217 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.866-574_866-573ins others(24): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148341 | ||||||
| chr13:113148343 | A | AATATATA others(11): Show |
3 | a0001c0002t0001g0107 a0001c0002t0001g0260 a0001c0002t0001g0333 |
3 | HG02155.hp1 NA18990.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.866-572_866-571ins others(18): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148343 | ||||||
| chr13:113148343 | A | AATATATA others(13): Show |
1 | a0001c0002t0001g0317 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.866-572_866-571ins others(20): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148343 | ||||||
| chr13:113148343 | A | AATATATA others(15): Show |
1 | a0001c0002t0001g0103 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.866-572_866-571ins others(22): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148343 | ||||||
| chr13:113148343 | A | ATATATAT others(12): Show |
1 | a0001c0002t0001g0267 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.866-573_866-572ins others(19): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148343 | |||||||
| chr13:113148343 | A | ATATATAT others(16): Show |
1 | a0001c0002t0001g0369 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.866-573_866-572ins others(23): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148343 | |||||||
| chr13:113148343 | A | T | 14 | a0001c0001t0001g0124 a0001c0001t0001g0135 a0001c0001t0001g0175 others(11): Show |
16 | HG00438.hp2 HG02970.hp1 HG02976.hp1 others(13): Show |
intron_variant | MODIFIER | c.866-573A>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148343 | |||||||
| chr13:113148345 | A | AAAAAATA others(3): Show |
1 | a0001c0002t0001g0358 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.866-570_866-569ins others(10): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148345 | ||||||
| chr13:113148345 | A | AAAAATAT | 8 | a0001c0002t0001g0100 a0001c0002t0001g0225 a0001c0002t0001g0247 others(5): Show |
8 | HG00597.hp2 HG00639.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.866-570_866-569ins others(7): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148345 | ||||||
| chr13:113148345 | A | AAAATATA others(3): Show |
1 | a0001c0002t0001g0367 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.866-570_866-569ins others(10): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148345 | ||||||
| chr13:113148345 | A | AAAATATA others(5): Show |
4 | a0001c0004t0001g0294 a0002c0003t0001g0003 a0002c0003t0001g0279 others(1): Show |
7 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.866-570_866-569ins others(12): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148345 | ||||||
| chr13:113148345 | A | AAAATATA others(7): Show |
1 | a0002c0003t0001g0280 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.866-570_866-569ins others(14): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148345 | ||||||
| chr13:113148345 | A | AAAATATA others(15): Show |
2 | a0001c0002t0001g0017 a0001c0002t0001g0216 |
3 | NA18944.hp2 NA19056.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.866-570_866-569ins others(22): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148345 | ||||||
| chr13:113148345 | A | AAATATAT | 31 | a0001c0002t0001g0031 a0001c0002t0001g0048 a0001c0002t0001g0057 others(28): Show |
31 | HG00423.hp2 HG00558.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.866-570_866-569ins others(7): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148345 | ||||||
| chr13:113148345 | A | AAATATAT others(2): Show |
8 | a0001c0002t0001g0044 a0001c0002t0001g0110 a0001c0002t0001g0144 others(5): Show |
8 | HG00099.hp1 HG00741.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.866-570_866-569ins others(9): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148345 | ||||||
| chr13:113148345 | A | AAATATAT others(4): Show |
2 | a0002c0003t0001g0277 a0002c0003t0001g0360 |
2 | HG02109.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.866-570_866-569ins others(11): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148345 | ||||||
| chr13:113148345 | A | AAATATAT others(10): Show |
1 | a0001c0002t0001g0032 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.866-570_866-569ins others(17): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148345 | ||||||
| chr13:113148345 | A | AAATATAT others(12): Show |
1 | a0001c0002t0001g0101 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.866-570_866-569ins others(19): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148345 | ||||||
| chr13:113148345 | A | AAT | 7 | a0001c0001t0001g0043 a0001c0001t0001g0088 a0001c0001t0001g0089 others(4): Show |
7 | HG01496.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.866-554_866-553dup others(2): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148345 | ||||||
| chr13:113148345 | A | AATATATA others(9): Show |
1 | a0001c0002t0001g0351 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.866-568_866-553dup others(16): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148345 | ||||||
| chr13:113148345 | A | AATATATA others(11): Show |
8 | a0001c0002t0001g0053 a0001c0002t0001g0062 a0001c0002t0001g0096 others(5): Show |
8 | HG00558.hp1 HG02080.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.866-570_866-553dup others(18): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148345 | ||||||
| chr13:113148345 | A | AATATATA others(13): Show |
2 | a0001c0002t0001g0127 a0001c0002t0001g0329 |
2 | NA18947.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.866-553_866-552ins others(20): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148345 | ||||||
| chr13:113148345 | A | AATATATA others(15): Show |
1 | a0001c0002t0001g0205 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.866-553_866-552ins others(22): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148345 | ||||||
| chr13:113148345 | A | AATATATA others(17): Show |
1 | a0001c0002t0001g0229 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.866-553_866-552ins others(24): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148345 | ||||||
| chr13:113148345 | A | AATATATA others(23): Show |
1 | a0001c0002t0001g0328 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.866-553_866-552ins others(30): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148345 | ||||||
| chr13:113148345 | A | AATATATA others(25): Show |
1 | a0001c0002t0001g0327 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.866-553_866-552ins others(32): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148345 | ||||||
| chr13:113148345 | A | AATTATAT others(10): Show |
1 | a0001c0002t0001g0253 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.866-569_866-568ins others(17): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148345 | ||||||
| chr13:113148345 | A | AT | 5 | a0001c0001t0001g0054 a0001c0001t0001g0190 a0001c0001t0001g0193 others(2): Show |
5 | HG02486.hp1 HG03540.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.866-571_866-570ins others(1): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148345 | |||||||
| chr13:113148345 | A | ATATATAT | 3 | a0001c0002t0001g0102 a0001c0002t0001g0211 a0001c0002t0001g0368 |
3 | HG02004.hp1 NA18954.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.866-571_866-570ins others(7): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148345 | |||||||
| chr13:113148345 | A | ATATATAT others(10): Show |
1 | a0001c0002t0001g0330 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.866-571_866-570ins others(17): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148345 | |||||||
| chr13:113148345 | A | ATATATAT others(12): Show |
3 | a0001c0002t0001g0014 a0001c0002t0001g0130 a0004c0010t0001g0014 |
3 | HG01346.hp1 HG02273.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.866-571_866-570ins others(19): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148345 | |||||||
| chr13:113148345 | A | T | 99 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(96): Show |
114 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.866-571A>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148345 | |||||||
| chr13:113148346 | AT | A | 7 | a0001c0001t0001g0065 a0001c0002t0001g0075 a0001c0002t0001g0195 others(4): Show |
7 | HG02280.hp1 HG02809.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.866-569delT | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148346 | |||||||
| chr13:113148347 | T | A | 13 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0039 others(10): Show |
18 | HG00323.hp1 HG00408.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.866-569T>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148347 | |||||||
| chr13:113148349 | T | A | 1 | a0001c0002t0001g0195 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.866-567T>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148349 | |||||||
| chr13:113148354 | ATATATAT others(17): Show |
A | 4 | a0001c0002t0001g0195 a0001c0002t0001g0235 a0001c0002t0001g0240 others(1): Show |
4 | NA18947.hp1 NA18959.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.866-552_866-529del others(24): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148354 | ||||||
| chr13:113148362 | A | ATATATAT others(3): Show |
1 | a0001c0002t0001g0363 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.866-553_866-552ins others(10): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148362 | ||||||
| chr13:113148363 | T | C | 60 | a0001c0001t0001g0011 a0001c0002t0001g0031 a0001c0002t0001g0044 others(57): Show |
61 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.866-553T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148363 | |||||||
| chr13:113148363 | T | TATATATA others(1): Show |
5 | a0001c0002t0001g0145 a0001c0002t0001g0160 a0001c0002t0001g0162 others(2): Show |
5 | HG02132.hp1 HG03017.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.866-553_866-552ins others(8): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148363 | |||||||
| chr13:113148364 | G | A | 3 | a0001c0001t0001g0257 a0001c0002t0001g0161 a0001c0002t0001g0363 |
3 | HG01884.hp1 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.866-552G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148364 | |||||||
| chr13:113148377 | T | C | 2 | a0001c0002t0001g0002 a0001c0004t0001g0292 |
5 | HG01243.hp1 HG01243.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.866-539T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148377 | |||||||
| chr13:113148391 | C | CAT | 5 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(2): Show |
6 | HG00140.hp1 HG00323.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.866-517_866-516dup others(2): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148391 | ||||||
| chr13:113148391 | C | CGT | 3 | a0001c0001t0001g0072 a0001c0001t0001g0086 a0001c0001t0001g0275 |
3 | HG01884.hp2 HG06807.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.866-525_866-524ins others(2): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148391 | |||||||
| chr13:113148391 | C | T | 4 | a0001c0002t0001g0195 a0001c0002t0001g0235 a0001c0002t0001g0240 others(1): Show |
4 | NA18947.hp1 NA18959.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.866-525C>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148391 | |||||||
| chr13:113148392 | A | G | 2 | a0001c0002t0001g0165 a0001c0002t0001g0172 |
2 | HG01952.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.866-524A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148392 | |||||||
| chr13:113148395 | T | C | 4 | a0001c0002t0001g0195 a0001c0002t0001g0235 a0001c0002t0001g0240 others(1): Show |
4 | NA18947.hp1 NA18959.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.866-521T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148395 | |||||||
| chr13:113148397 | T | C | 4 | a0001c0002t0001g0195 a0001c0002t0001g0235 a0001c0002t0001g0240 others(1): Show |
4 | NA18947.hp1 NA18959.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.866-519T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148397 | |||||||
| chr13:113148397 | T | TAC | 2 | a0001c0001t0001g0007 a0001c0001t0001g0052 |
4 | HG02015.hp1 HG02165.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.866-518_866-517ins others(2): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148397 | ||||||
| chr13:113148399 | T | C | 9 | a0001c0001t0001g0007 a0001c0001t0001g0052 a0001c0001t0001g0072 others(6): Show |
11 | HG01884.hp2 HG02015.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.866-517T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148399 | |||||||
| chr13:113148399 | T | TAC | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
282 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.866-503_866-502dup others(2): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148399 | ||||||
| chr13:113148399 | T | TACAC | 19 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0027 others(16): Show |
25 | HG01192.hp1 HG01243.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.866-505_866-502dup others(4): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148399 | ||||||
| chr13:113148399 | T | TACACAC | 4 | a0001c0002t0001g0044 a0001c0002t0001g0144 a0001c0002t0001g0307 others(1): Show |
4 | HG00741.hp2 HG01346.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.866-507_866-502dup others(6): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148399 | ||||||
| chr13:113148399 | T | TACACACA others(1): Show |
3 | a0001c0002t0001g0100 a0001c0002t0001g0206 a0001c0002t0001g0298 |
3 | HG00738.hp1 HG02155.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.866-509_866-502dup others(8): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148399 | ||||||
| chr13:113148399 | T | TATACACA others(1): Show |
56 | a0001c0002t0001g0031 a0001c0002t0001g0048 a0001c0002t0001g0057 others(53): Show |
56 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.866-516_866-515ins others(8): Show |
F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113148399 | ||||||
| chr13:113148469 | T | C | 1 | a0001c0002t0001g0362 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.866-447T>C | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148469 | |||||||
| chr13:113148483 | A | G | 31 | a0001c0002t0001g0014 a0001c0002t0001g0017 a0001c0002t0001g0032 others(28): Show |
32 | HG00423.hp1 HG00558.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.866-433A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148483 | |||||||
| chr13:113148539 | T | G | 1 | a0001c0001t0001g0190 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.866-377T>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148539 | |||||||
| chr13:113148615 | G | A | 5 | a0001c0001t0001g0091 a0001c0001t0001g0231 a0001c0001t0001g0332 others(2): Show |
5 | HG02040.hp2 HG02074.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.866-301G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148615 | |||||||
| chr13:113148809 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0060 |
3 | NA18957.hp2 NA18971.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.866-107G>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148809 | |||||||
| chr13:113148814 | A | G | 32 | a0001c0002t0001g0014 a0001c0002t0001g0017 a0001c0002t0001g0032 others(29): Show |
33 | HG00423.hp1 HG00558.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.866-102A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148814 | |||||||
| chr13:113148814 | A | T | 1 | a0001c0002t0001g0253 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.866-102A>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148814 | |||||||
| chr13:113148825 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.866-91A>G | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148825 | |||||||
| chr13:113148830 | A | T | 1 | a0001c0004t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.866-86A>T | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148830 | |||||||
| chr13:113148832 | T | A | 3 | a0001c0002t0001g0127 a0001c0002t0001g0130 a0001c0002t0001g0329 |
3 | NA18612.hp2 NA18947.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.866-84T>A | F10 | ENSG00000126218.12 | transcript | ENST00000375559.8 | protein_coding | 7/7 | chr13 | 113148832 |