Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6396 |
| ensemblid | ENSG00000157020.18 |
| hgncid | 10697 |
| symbol | SEC13 |
| name | SEC13 homolog, nuclear pore and COPII coat complex component |
| refseq_nuc | NM_183352.3 |
| refseq_prot | NP_899195.1 |
| ensembl_nuc | ENST00000350697.8 |
| ensembl_prot | ENSP00000312122.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 10300931 |
| end | 10321112 |
| strand | - |
| ver | v1.2 |
| region | chr3:10300931-10321112 |
| region5000 | chr3:10295931-10326112 |
| regionname0 | SEC13_chr3_10300931_10321112 |
| regionname5000 | SEC13_chr3_10295931_10326112 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 322 | 378 | 96 | 61 | 159 | 10 | 50 | 111 | SEC13_chr3_10295931_10326112 | SEC13 | MVSVI others(317): Show |
chr3 | 10295931 | 10326112 |
| a0002 | 0/0 | 322 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | MVSVI others(317): Show |
chr3 | 10295931 | 10326112 |
| a0003 | 0/0 | 322 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | MVSVI others(317): Show |
chr3 | 10295931 | 10326112 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 966 | 370 | 89 | 60 | 159 | 10 | 50 | SEC13_chr3_10295931_10326112 | SEC13 | ATGGT others(961): Show |
chr3 | 10295931 | 10326112 | ||
| a0001c0002 | 0/0 | 966 | 7 | 7 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | ATGGT others(961): Show |
chr3 | 10295931 | 10326112 | ||
| a0001c0004 | 0/0 | 966 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | ATGGT others(961): Show |
chr3 | 10295931 | 10326112 | ||
| a0002c0003 | 0/0 | 966 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | ATGGT others(961): Show |
chr3 | 10295931 | 10326112 | ||
| a0003c0005 | 0/0 | 966 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | ATGGT others(961): Show |
chr3 | 10295931 | 10326112 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1359 | 316 | 71 | 45 | 155 | 7 | 37 | SEC13_chr3_10295931_10326112 | SEC13 | GTTCC others(1354): Show |
chr3 | 10295931 | 10326112 |
| a0001c0001t0002 | 1/0 | 1359 | 51 | 16 | 15 | 3 | 3 | 13 | SEC13_chr3_10295931_10326112 | SEC13 | GTTCC others(1354): Show |
chr3 | 10295931 | 10326112 |
| a0001c0001t0003 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | GTTCC others(1354): Show |
chr3 | 10295931 | 10326112 |
| a0001c0001t0004 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | GTTCC others(1354): Show |
chr3 | 10295931 | 10326112 |
| a0001c0001t0005 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | GTTCC others(1354): Show |
chr3 | 10295931 | 10326112 |
| a0001c0002t0002 | 0/0 | 1359 | 7 | 7 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | GTTCC others(1354): Show |
chr3 | 10295931 | 10326112 |
| a0001c0004t0002 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | GTTCC others(1354): Show |
chr3 | 10295931 | 10326112 |
| a0002c0003t0002 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | GTTCC others(1354): Show |
chr3 | 10295931 | 10326112 |
| a0003c0005t0001 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | GTTCC others(1354): Show |
chr3 | 10295931 | 10326112 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 22 | 0 | 11 | 8 | 1 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0002 | 0/0 | 17 | 0 | 3 | 11 | 2 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0003 | 0/0 | 14 | 0 | 1 | 12 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0004 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 2 | 2 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0011 | 0/0 | 4 | 2 | 0 | 0 | 1 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0223 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0012 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0019 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0001c0004t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0002c0003t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| a0003c0005t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0018 | EUR | GBR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | GBR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0018 | EUR | FIN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01106 | hp1 | a0002 | c0003 | t0002 | g0232 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0018 | EUR | IBS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01981 | hp1 | a0001 | c0004 | t0002 | g0050 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0062 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CDX | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CDX | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0095 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0122 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0238 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0116 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0117 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0121 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | STU | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | STU | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | BEB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | BEB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | STU | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | STU | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | STU | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | STU | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | STU | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0098 | AFR | YRI | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | YRI | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18984 | hp1 | a0003 | c0005 | t0001 | g0144 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0209 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | LWK | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | YRI | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ASW | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | ASW | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | GIH | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | GIH | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0115 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | USA | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | USA | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | USA | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | USA | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0223 | REF | REF | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0079 | REF | REF | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:10305050 | T | C | 1 | a0003 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.691A>G | p.Ile231Val | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/9 | 751/1359 | 691/969 | 231/322 | chr3 | 10305050 | |||
| chr3:10312066 | C | T | 1 | a0002 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.349G>A | p.Gly117Ser | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/9 | 409/1359 | 349/969 | 117/322 | chr3 | 10312066 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:10301303 | G | A | 1 | a0001c0004 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.927C>T | p.Ser309Ser | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 9/9 | 987/1359 | 927/969 | 309/322 | chr3 | 10301303 | |||
| chr3:10312595 | C | T | 1 | a0001c0002 | 7 | HG02630.hp1 HG02630.hp2 HG02809.hp1 others(4): Show |
synonymous_variant | LOW | c.300G>A | p.Ala100Ala | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 4/9 | 360/1359 | 300/969 | 100/322 | chr3 | 10312595 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:10301061 | A | C | 1 | a0001c0001t0005 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*200T>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 9/9 | 200 | chr3 | 10301061 | ||||||
| chr3:10301192 | C | T | 5 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(2): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*69G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 9/9 | 69 | chr3 | 10301192 | ||||||
| chr3:10301206 | C | G | 1 | a0001c0001t0004 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*55G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 9/9 | 55 | chr3 | 10301206 | ||||||
| chr3:10321104 | C | T | 1 | a0001c0001t0003 | 1 | HG03516.hp1 | 5_prime_UTR_variant | MODIFIER | c.-52G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/9 | 52 | chr3 | 10321104 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:10301409 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.856-35G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10301409 | |||||||
| chr3:10301520 | C | A | 3 | a0001c0001t0001g0091 a0001c0001t0001g0099 a0001c0001t0001g0126 |
3 | NA18979.hp2 NA18985.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.856-146G>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10301520 | |||||||
| chr3:10301560 | G | A | 40 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(37): Show |
57 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.856-186C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10301560 | |||||||
| chr3:10301588 | T | C | 2 | a0001c0001t0002g0038 a0001c0002t0002g0117 |
3 | HG02622.hp1 HG02723.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.856-214A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10301588 | |||||||
| chr3:10301638 | G | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(2): Show |
5 | HG00673.hp2 HG02071.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.856-264C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10301638 | |||||||
| chr3:10301728 | T | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0084 a0001c0001t0001g0152 others(2): Show |
9 | HG00438.hp1 HG02015.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.856-354A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10301728 | |||||||
| chr3:10301926 | A | AAATT | 11 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0037 others(8): Show |
14 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.856-556_856-553dup others(4): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10301926 | |||||||
| chr3:10301943 | T | TA | 10 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0047 others(7): Show |
27 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.856-570dupT | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10301943 | |||||||
| chr3:10301992 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.856-618T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10301992 | |||||||
| chr3:10302035 | A | G | 15 | a0001c0001t0002g0025 a0001c0001t0002g0072 a0001c0001t0002g0078 others(12): Show |
16 | HG01891.hp2 HG02572.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.856-661T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302035 | |||||||
| chr3:10302153 | G | A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0047 others(7): Show |
27 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.856-779C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302153 | |||||||
| chr3:10302173 | G | A | 3 | a0001c0001t0001g0210 a0001c0001t0001g0214 a0001c0001t0001g0216 |
3 | HG02055.hp1 HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.856-799C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302173 | |||||||
| chr3:10302193 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0067 a0001c0001t0001g0073 |
4 | HG01891.hp1 HG02258.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-819C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302193 | |||||||
| chr3:10302427 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
243 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.856-1053C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302427 | |||||||
| chr3:10302495 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.856-1121C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302495 | |||||||
| chr3:10302646 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.856-1272C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302646 | |||||||
| chr3:10302743 | A | G | 18 | a0001c0001t0001g0221 a0001c0001t0002g0025 a0001c0001t0002g0038 others(15): Show |
20 | HG01891.hp2 HG02572.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.855+1283T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302743 | |||||||
| chr3:10302824 | G | A | 1 | a0001c0001t0002g0229 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.855+1202C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302824 | |||||||
| chr3:10302900 | G | A | 15 | a0001c0001t0002g0025 a0001c0001t0002g0072 a0001c0001t0002g0078 others(12): Show |
16 | HG01891.hp2 HG02572.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.855+1126C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302900 | |||||||
| chr3:10302962 | T | TTAGA | 15 | a0001c0001t0002g0025 a0001c0001t0002g0072 a0001c0001t0002g0078 others(12): Show |
16 | HG01891.hp2 HG02572.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.855+1060_855+1063d others(6): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302962 | |||||||
| chr3:10303005 | G | A | 48 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(45): Show |
72 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.855+1021C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303005 | |||||||
| chr3:10303038 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.855+988T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303038 | |||||||
| chr3:10303159 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0143 |
3 | HG01070.hp1 HG01071.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.855+867C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303159 | |||||||
| chr3:10303173 | C | T | 11 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0243 others(8): Show |
13 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.855+853G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303173 | |||||||
| chr3:10303267 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.855+759G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303267 | |||||||
| chr3:10303324 | C | T | 8 | a0001c0001t0001g0028 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
9 | HG01070.hp1 HG01071.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.855+702G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303324 | |||||||
| chr3:10303447 | G | GACCTTGG others(29): Show |
1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.855+543_855+578dup others(36): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303447 | |||||||
| chr3:10303496 | G | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
304 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.855+530C>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303496 | |||||||
| chr3:10303843 | G | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(50): Show |
79 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.855+183C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303843 | |||||||
| chr3:10303972 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.855+54G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303972 | |||||||
| chr3:10303973 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.855+53C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303973 | |||||||
| chr3:10304184 | C | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0215 others(1): Show |
6 | HG01884.hp1 HG02145.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.709-12G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/8 | chr3 | 10304184 | |||||||
| chr3:10304237 | C | T | 38 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(35): Show |
55 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.709-65G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/8 | chr3 | 10304237 | |||||||
| chr3:10304379 | C | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(9): Show |
18 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.709-207G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/8 | chr3 | 10304379 | |||||||
| chr3:10304386 | C | T | 8 | a0001c0001t0001g0028 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
9 | HG01070.hp1 HG01071.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.709-214G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/8 | chr3 | 10304386 | |||||||
| chr3:10304387 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.709-215C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/8 | chr3 | 10304387 | |||||||
| chr3:10304737 | G | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(50): Show |
79 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.708+296C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/8 | chr3 | 10304737 | |||||||
| chr3:10304786 | T | A | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.708+247A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/8 | chr3 | 10304786 | |||||||
| chr3:10304889 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.708+144T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/8 | chr3 | 10304889 | |||||||
| chr3:10304993 | G | A | 1 | a0001c0001t0002g0227 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.708+40C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/8 | chr3 | 10304993 | |||||||
| chr3:10305030 | G | C | 1 | a0001c0001t0001g0133 | 1 | HG01358.hp1 | splice_region_variant&intron_variant | LOW | c.708+3C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/8 | chr3 | 10305030 | |||||||
| chr3:10305193 | C | T | 13 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0089 others(10): Show |
15 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.585-37G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 6/8 | chr3 | 10305193 | |||||||
| chr3:10305311 | G | GT | 16 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(13): Show |
21 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.585-156dupA | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 6/8 | chr3 | 10305311 | |||||||
| chr3:10305312 | T | A | 1 | a0001c0001t0001g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.585-156A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 6/8 | chr3 | 10305312 | |||||||
| chr3:10305312 | T | TA | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
232 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.585-157dupT | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 6/8 | chr3 | 10305312 | |||||||
| chr3:10305312 | T | TAA | 8 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(5): Show |
8 | HG00673.hp2 HG01993.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.585-158_585-157dup others(2): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 6/8 | chr3 | 10305312 | |||||||
| chr3:10305321 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.585-165G>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 6/8 | chr3 | 10305321 | |||||||
| chr3:10305459 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.584+100C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 6/8 | chr3 | 10305459 | |||||||
| chr3:10305460 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.584+99T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 6/8 | chr3 | 10305460 | |||||||
| chr3:10305829 | G | A | 1 | a0001c0001t0004g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.451-137C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10305829 | |||||||
| chr3:10305862 | CAACAGT | C | 52 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(49): Show |
78 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.451-176_451-171del others(6): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10305862 | |||||||
| chr3:10305892 | G | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(2): Show |
5 | HG00673.hp2 HG02071.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-200C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10305892 | |||||||
| chr3:10306001 | A | G | 2 | a0001c0001t0002g0096 a0001c0001t0002g0118 |
2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.451-309T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306001 | |||||||
| chr3:10306023 | G | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.451-331C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306023 | |||||||
| chr3:10306038 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.451-346G>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306038 | |||||||
| chr3:10306126 | C | T | 11 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0243 others(8): Show |
13 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.451-434G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306126 | |||||||
| chr3:10306159 | A | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(50): Show |
79 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.451-467T>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306159 | |||||||
| chr3:10306196 | G | T | 8 | a0001c0001t0001g0028 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
9 | HG01070.hp1 HG01071.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.451-504C>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306196 | |||||||
| chr3:10306286 | T | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0084 a0001c0001t0001g0152 others(2): Show |
9 | HG00438.hp1 HG02015.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.451-594A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306286 | |||||||
| chr3:10306393 | T | G | 1 | a0001c0001t0001g0029 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.451-701A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306393 | |||||||
| chr3:10306432 | T | G | 15 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(12): Show |
20 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.451-740A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306432 | |||||||
| chr3:10306435 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.451-743G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306435 | |||||||
| chr3:10306437 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0156 |
2 | HG01071.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.451-745G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306437 | |||||||
| chr3:10306501 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.451-809A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306501 | |||||||
| chr3:10306535 | C | T | 8 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0213 others(5): Show |
10 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.451-843G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306535 | |||||||
| chr3:10306551 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.451-859A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306551 | |||||||
| chr3:10306682 | T | TA | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0215 |
5 | HG01884.hp1 HG02145.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-991dupT | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306682 | |||||||
| chr3:10306746 | C | T | 11 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0243 others(8): Show |
13 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.451-1054G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306746 | |||||||
| chr3:10306781 | T | C | 1 | a0001c0001t0001g0016 | 3 | HG00741.hp2 HG03654.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.451-1089A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306781 | |||||||
| chr3:10306824 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.451-1132A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306824 | |||||||
| chr3:10306849 | G | A | 15 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(12): Show |
20 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.451-1157C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306849 | |||||||
| chr3:10306934 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.451-1242G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306934 | |||||||
| chr3:10307053 | A | AT | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(70): Show |
143 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.451-1362dupA | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307053 | |||||||
| chr3:10307065 | A | T | 45 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(42): Show |
64 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.451-1373T>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307065 | |||||||
| chr3:10307066 | A | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0211 others(1): Show |
6 | HG01884.hp1 HG02145.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-1374T>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307066 | |||||||
| chr3:10307090 | C | G | 1 | a0001c0001t0004g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.451-1398G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307090 | |||||||
| chr3:10307146 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.451-1454C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307146 | |||||||
| chr3:10307212 | CT | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.451-1521delA | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307212 | |||||||
| chr3:10307310 | GTGATTC | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(70): Show |
143 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.451-1624_451-1619d others(8): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307310 | |||||||
| chr3:10307322 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.451-1630G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307322 | |||||||
| chr3:10307331 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.451-1639G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307331 | |||||||
| chr3:10307333 | C | T | 38 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(35): Show |
55 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.451-1641G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307333 | |||||||
| chr3:10307366 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.451-1674C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307366 | |||||||
| chr3:10307478 | T | G | 1 | a0001c0001t0001g0174 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.451-1786A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307478 | |||||||
| chr3:10307493 | A | G | 16 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0084 others(13): Show |
27 | HG00438.hp1 HG02015.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.451-1801T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307493 | |||||||
| chr3:10307494 | T | G | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | HG01071.hp1 HG01175.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-1802A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307494 | |||||||
| chr3:10307531 | AG | A | 39 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(36): Show |
56 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.451-1840delC | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307531 | |||||||
| chr3:10307613 | C | T | 1 | a0001c0001t0001g0017 | 3 | HG02615.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.451-1921G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307613 | |||||||
| chr3:10307631 | T | G | 1 | a0001c0001t0001g0180 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.451-1939A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307631 | |||||||
| chr3:10307688 | C | T | 1 | a0001c0001t0002g0226 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.451-1996G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307688 | |||||||
| chr3:10307690 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(65): Show |
131 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.451-1998C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307690 | |||||||
| chr3:10307762 | C | T | 38 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(35): Show |
55 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.451-2070G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307762 | |||||||
| chr3:10307822 | G | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0201 |
2 | NA18947.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.451-2130C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307822 | |||||||
| chr3:10307873 | C | G | 1 | a0001c0001t0002g0235 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.451-2181G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307873 | |||||||
| chr3:10307972 | C | G | 9 | a0001c0001t0001g0028 a0001c0001t0001g0141 a0001c0001t0001g0142 others(6): Show |
10 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.451-2280G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307972 | |||||||
| chr3:10308085 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.451-2393A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308085 | |||||||
| chr3:10308219 | C | G | 1 | a0001c0001t0001g0212 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.451-2527G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308219 | |||||||
| chr3:10308480 | A | AGTC | 3 | a0001c0001t0001g0107 a0001c0001t0001g0130 a0001c0001t0001g0134 |
3 | HG00642.hp1 HG02451.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.451-2789_451-2788i others(5): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308480 | |||||||
| chr3:10308562 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0005g0209 |
2 | NA18998.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.451-2870T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308562 | |||||||
| chr3:10308566 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.451-2874A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308566 | |||||||
| chr3:10308653 | T | C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0214 a0001c0001t0001g0216 |
3 | HG02055.hp1 HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.451-2961A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308653 | |||||||
| chr3:10308653 | TTGAAGAG others(6): Show |
T | 1 | a0001c0001t0001g0022 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.451-2974_451-2962d others(15): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308653 | |||||||
| chr3:10308673 | C | CTAAT | 11 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0243 others(8): Show |
13 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.451-2985_451-2982d others(6): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308673 | |||||||
| chr3:10308718 | ACCC | A | 16 | a0001c0001t0002g0025 a0001c0001t0002g0072 a0001c0001t0002g0078 others(13): Show |
17 | HG01891.hp2 HG02572.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.451-3029_451-3027d others(5): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308718 | |||||||
| chr3:10308739 | A | T | 9 | a0001c0001t0001g0028 a0001c0001t0001g0141 a0001c0001t0001g0142 others(6): Show |
10 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.451-3047T>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308739 | |||||||
| chr3:10308783 | TGAGTTGA | T | 11 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0243 others(8): Show |
13 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.451-3098_451-3092d others(9): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308783 | |||||||
| chr3:10308789 | G | A | 9 | a0001c0001t0001g0028 a0001c0001t0001g0141 a0001c0001t0001g0142 others(6): Show |
10 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.451-3097C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308789 | |||||||
| chr3:10308791 | A | AT | 10 | a0001c0001t0001g0028 a0001c0001t0001g0060 a0001c0001t0001g0141 others(7): Show |
11 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.451-3100dupA | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308791 | |||||||
| chr3:10308791 | AT | A | 92 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(89): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.451-3100delA | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308791 | |||||||
| chr3:10308791 | ATT | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(108): Show |
202 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.451-3101_451-3100d others(4): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308791 | |||||||
| chr3:10308791 | ATTT | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0183 others(1): Show |
6 | HG01256.hp2 HG02015.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-3102_451-3100d others(5): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308791 | |||||||
| chr3:10308792 | T | A | 11 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0243 others(8): Show |
13 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.451-3100A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308792 | |||||||
| chr3:10308812 | T | C | 16 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(13): Show |
21 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.451-3120A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308812 | |||||||
| chr3:10308814 | T | A | 6 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(3): Show |
6 | HG00673.hp2 HG01993.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-3122A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308814 | |||||||
| chr3:10308865 | C | T | 4 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0246 others(1): Show |
4 | HG00639.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+3100G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308865 | |||||||
| chr3:10308933 | A | AT | 35 | a0001c0001t0001g0043 a0001c0001t0001g0210 a0001c0001t0001g0214 others(32): Show |
40 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.450+3031dupA | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308933 | |||||||
| chr3:10308933 | A | ATT | 13 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(10): Show |
17 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.450+3030_450+3031d others(4): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308933 | |||||||
| chr3:10308933 | AT | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(90): Show |
167 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.450+3031delA | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308933 | |||||||
| chr3:10308933 | ATT | A | 30 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(27): Show |
47 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.450+3030_450+3031d others(4): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308933 | |||||||
| chr3:10308933 | ATTTTTTT | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(46): Show |
75 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.450+3025_450+3031d others(9): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308933 | |||||||
| chr3:10309117 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(72): Show |
147 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.450+2848A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309117 | |||||||
| chr3:10309126 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.450+2839G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309126 | |||||||
| chr3:10309198 | A | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(73): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.450+2767T>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309198 | |||||||
| chr3:10309284 | C | CTT | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(73): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.450+2679_450+2680d others(4): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309284 | |||||||
| chr3:10309490 | C | T | 1 | a0001c0001t0003g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.450+2475G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309490 | |||||||
| chr3:10309497 | TG | T | 11 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0243 others(8): Show |
13 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.450+2467delC | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309497 | |||||||
| chr3:10309546 | A | C | 11 | a0001c0001t0001g0028 a0001c0001t0001g0141 a0001c0001t0001g0142 others(8): Show |
12 | HG01070.hp1 HG01071.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.450+2419T>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309546 | |||||||
| chr3:10309552 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(83): Show |
160 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.450+2413A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309552 | |||||||
| chr3:10309590 | T | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(83): Show |
160 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.450+2375A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309590 | |||||||
| chr3:10309602 | A | G | 1 | a0001c0001t0002g0038 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.450+2363T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309602 | |||||||
| chr3:10309799 | A | G | 16 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(13): Show |
21 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.450+2166T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309799 | |||||||
| chr3:10310009 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0198 |
3 | HG01358.hp2 HG01952.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.450+1956C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310009 | |||||||
| chr3:10310010 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.450+1955C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310010 | |||||||
| chr3:10310039 | ATCACAGA others(2): Show |
A | 8 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0213 others(5): Show |
10 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.450+1917_450+1925d others(11): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310039 | |||||||
| chr3:10310146 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(172): Show |
273 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.450+1819C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310146 | |||||||
| chr3:10310245 | C | T | 1 | a0001c0001t0001g0030 | 2 | HG02602.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.450+1720G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310245 | |||||||
| chr3:10310264 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.450+1701C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310264 | |||||||
| chr3:10310265 | C | G | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.450+1700G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310265 | |||||||
| chr3:10310265 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.450+1700G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310265 | |||||||
| chr3:10310348 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.450+1617C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310348 | |||||||
| chr3:10310351 | T | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(78): Show |
153 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.450+1614A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310351 | |||||||
| chr3:10310423 | G | A | 1 | a0001c0001t0001g0032 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.450+1542C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310423 | |||||||
| chr3:10310504 | A | AAAAC | 2 | a0001c0001t0001g0027 a0001c0001t0001g0088 |
3 | NA18968.hp1 NA19057.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.450+1457_450+1460d others(6): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310504 | |||||||
| chr3:10310559 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0129 |
2 | NA19003.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.450+1406C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310559 | |||||||
| chr3:10310581 | G | A | 1 | a0001c0001t0002g0235 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.450+1384C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310581 | |||||||
| chr3:10310669 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.450+1296T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310669 | |||||||
| chr3:10310670 | T | A | 1 | a0001c0001t0001g0184 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.450+1295A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310670 | |||||||
| chr3:10310698 | C | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(72): Show |
147 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.450+1267G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310698 | |||||||
| chr3:10310796 | T | C | 16 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(13): Show |
21 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.450+1169A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310796 | |||||||
| chr3:10310848 | A | G | 5 | a0001c0001t0001g0036 a0001c0001t0001g0213 a0001c0001t0001g0217 others(2): Show |
6 | HG01099.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+1117T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310848 | |||||||
| chr3:10310886 | T | G | 1 | a0001c0001t0001g0204 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.450+1079A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310886 | |||||||
| chr3:10310904 | T | G | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.450+1061A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310904 | |||||||
| chr3:10311019 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(72): Show |
147 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.450+946G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311019 | |||||||
| chr3:10311029 | TA | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
187 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.450+935delT | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311029 | |||||||
| chr3:10311059 | C | A | 1 | a0001c0001t0001g0141 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.450+906G>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311059 | |||||||
| chr3:10311081 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.450+884C>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311081 | |||||||
| chr3:10311162 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.450+803T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311162 | |||||||
| chr3:10311168 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0083 others(5): Show |
25 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.450+797G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311168 | |||||||
| chr3:10311197 | G | T | 39 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(36): Show |
56 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.450+768C>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311197 | |||||||
| chr3:10311327 | A | C | 1 | a0001c0001t0002g0236 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.450+638T>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311327 | |||||||
| chr3:10311383 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.450+582C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311383 | |||||||
| chr3:10311384 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.450+581G>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311384 | |||||||
| chr3:10311428 | T | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0159 a0001c0001t0001g0169 others(2): Show |
9 | HG00408.hp1 HG00673.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.450+537A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311428 | |||||||
| chr3:10311458 | T | G | 27 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0243 others(24): Show |
30 | HG00639.hp2 HG01109.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.450+507A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311458 | |||||||
| chr3:10311594 | A | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(69): Show |
103 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.450+371T>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311594 | |||||||
| chr3:10311646 | T | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(72): Show |
147 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.450+319A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311646 | |||||||
| chr3:10311866 | T | C | 39 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(36): Show |
56 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.450+99A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311866 | |||||||
| chr3:10311942 | C | T | 45 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(42): Show |
62 | HG00099.hp2 HG00673.hp2 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.450+23G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311942 | |||||||
| chr3:10312260 | T | TC | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0211 others(1): Show |
6 | HG01884.hp1 HG02145.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.317-163dupG | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 4/8 | chr3 | 10312260 | |||||||
| chr3:10312484 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.316+95G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 4/8 | chr3 | 10312484 | |||||||
| chr3:10312517 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0002g0038 |
3 | HG02622.hp1 HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.316+62C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 4/8 | chr3 | 10312517 | |||||||
| chr3:10312746 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.165-16A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10312746 | |||||||
| chr3:10312786 | T | C | 2 | a0001c0001t0001g0059 a0001c0001t0001g0074 |
2 | HG01192.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.165-56A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10312786 | |||||||
| chr3:10312995 | G | C | 1 | a0001c0001t0001g0093 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.165-265C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10312995 | |||||||
| chr3:10313009 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.165-279G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313009 | |||||||
| chr3:10313011 | G | C | 1 | a0001c0001t0001g0210 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.165-281C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313011 | |||||||
| chr3:10313087 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.165-357A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313087 | |||||||
| chr3:10313156 | T | C | 26 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0243 others(23): Show |
29 | HG00639.hp2 HG01109.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.165-426A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313156 | |||||||
| chr3:10313187 | T | C | 15 | a0001c0001t0002g0025 a0001c0001t0002g0078 a0001c0001t0002g0081 others(12): Show |
16 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.165-457A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313187 | |||||||
| chr3:10313290 | C | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0076 |
3 | HG01070.hp2 HG03017.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.165-560G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313290 | |||||||
| chr3:10313291 | G | A | 11 | a0001c0001t0001g0026 a0001c0001t0001g0097 a0001c0001t0001g0101 others(8): Show |
12 | HG02027.hp2 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.165-561C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313291 | |||||||
| chr3:10313486 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.165-756A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313486 | |||||||
| chr3:10313570 | C | T | 1 | a0001c0002t0002g0115 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.165-840G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313570 | |||||||
| chr3:10313581 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.165-851C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313581 | |||||||
| chr3:10313603 | G | A | 15 | a0001c0001t0002g0025 a0001c0001t0002g0078 a0001c0001t0002g0081 others(12): Show |
16 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.165-873C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313603 | |||||||
| chr3:10313641 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.165-911T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313641 | |||||||
| chr3:10313791 | A | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0051 |
3 | HG03834.hp2 HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.165-1061T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313791 | |||||||
| chr3:10313841 | G | C | 1 | a0001c0001t0001g0125 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.165-1111C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313841 | |||||||
| chr3:10313900 | C | G | 48 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(45): Show |
65 | HG00099.hp2 HG00673.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.165-1170G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313900 | |||||||
| chr3:10313984 | C | G | 13 | a0001c0001t0002g0025 a0001c0001t0002g0096 a0001c0001t0002g0102 others(10): Show |
14 | HG01891.hp2 HG02630.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.165-1254G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313984 | |||||||
| chr3:10314100 | T | G | 1 | a0001c0001t0001g0112 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.164+1221A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10314100 | |||||||
| chr3:10314122 | CT | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(71): Show |
147 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.164+1198delA | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10314122 | |||||||
| chr3:10314405 | A | G | 11 | a0001c0001t0001g0028 a0001c0001t0001g0141 a0001c0001t0001g0142 others(8): Show |
12 | HG01070.hp1 HG01071.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.164+916T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10314405 | |||||||
| chr3:10314462 | A | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.164+859T>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10314462 | |||||||
| chr3:10314565 | AT | A | 8 | a0001c0001t0001g0028 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
9 | HG01070.hp1 HG01071.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.164+755delA | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10314565 | |||||||
| chr3:10314630 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.164+691G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10314630 | |||||||
| chr3:10314884 | T | A | 1 | a0001c0001t0001g0189 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.164+437A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10314884 | |||||||
| chr3:10314930 | G | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0068 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.164+391C>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10314930 | |||||||
| chr3:10315056 | T | A | 42 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(39): Show |
59 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.164+265A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10315056 | |||||||
| chr3:10315076 | G | A | 56 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(53): Show |
74 | HG00099.hp2 HG00673.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164+245C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10315076 | |||||||
| chr3:10315694 | C | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0215 |
5 | HG01884.hp1 HG02145.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.49-258G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10315694 | |||||||
| chr3:10315701 | T | G | 1 | a0001c0001t0002g0061 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.49-265A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10315701 | |||||||
| chr3:10315709 | C | T | 5 | a0001c0001t0001g0047 a0001c0001t0001g0231 a0001c0001t0002g0020 others(2): Show |
6 | HG01928.hp1 HG01975.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-273G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10315709 | |||||||
| chr3:10315725 | G | A | 1 | a0001c0001t0004g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.49-289C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10315725 | |||||||
| chr3:10316016 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.49-580G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316016 | |||||||
| chr3:10316174 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.49-738G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316174 | |||||||
| chr3:10316180 | G | A | 1 | a0001c0002t0002g0121 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.49-744C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316180 | |||||||
| chr3:10316268 | C | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(139): Show |
245 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.49-832G>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316268 | |||||||
| chr3:10316404 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(54): Show |
85 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.49-968T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316404 | |||||||
| chr3:10316412 | C | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(72): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.49-976G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316412 | |||||||
| chr3:10316432 | C | A | 5 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(2): Show |
5 | HG00639.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-996G>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316432 | |||||||
| chr3:10316645 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.49-1209C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316645 | |||||||
| chr3:10316740 | G | A | 67 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(64): Show |
97 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.49-1304C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316740 | |||||||
| chr3:10316776 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.48+1274G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316776 | |||||||
| chr3:10316853 | T | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(55): Show |
86 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.48+1197A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316853 | |||||||
| chr3:10316941 | C | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(71): Show |
146 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.48+1109G>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316941 | |||||||
| chr3:10316985 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.48+1065C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316985 | |||||||
| chr3:10317001 | C | CA | 15 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0037 others(12): Show |
20 | HG01099.hp2 HG01106.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.48+1048dupT | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317001 | |||||||
| chr3:10317001 | CA | C | 101 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
140 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.48+1048delT | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317001 | |||||||
| chr3:10317001 | CAA | C | 12 | a0001c0001t0001g0066 a0001c0001t0001g0087 a0001c0001t0001g0097 others(9): Show |
12 | HG01071.hp1 HG01175.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.48+1047_48+1048del others(2): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317001 | |||||||
| chr3:10317018 | A | G | 25 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0243 others(22): Show |
28 | HG00639.hp2 HG01109.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.48+1032T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317018 | |||||||
| chr3:10317038 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(72): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.48+1012A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317038 | |||||||
| chr3:10317453 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.48+597C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317453 | |||||||
| chr3:10317511 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.48+539A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317511 | |||||||
| chr3:10317566 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.48+484G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317566 | |||||||
| chr3:10317654 | C | T | 1 | a0003c0005t0001g0144 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.48+396G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317654 | |||||||
| chr3:10317674 | C | G | 1 | a0001c0001t0001g0153 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.48+376G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317674 | |||||||
| chr3:10317740 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.48+310G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317740 | |||||||
| chr3:10317753 | C | G | 1 | a0001c0001t0001g0016 | 3 | HG00741.hp2 HG03654.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.48+297G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317753 | |||||||
| chr3:10317778 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
342 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.48+272T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317778 | |||||||
| chr3:10317779 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.48+271A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317779 | |||||||
| chr3:10317944 | T | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(50): Show |
79 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.48+106A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317944 | |||||||
| chr3:10317948 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.48+102A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317948 | |||||||
| chr3:10318145 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.4-51T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10318145 | |||||||
| chr3:10318184 | C | CTCAT | 8 | a0001c0001t0001g0028 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
9 | HG01070.hp1 HG01071.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.4-94_4-91dupATGA | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10318184 | |||||||
| chr3:10318188 | T | C | 26 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0243 others(23): Show |
29 | HG00639.hp2 HG01109.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.4-94A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10318188 | |||||||
| chr3:10318190 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4-96G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10318190 | |||||||
| chr3:10318325 | G | A | 47 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(44): Show |
64 | HG00099.hp2 HG00673.hp2 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.4-231C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10318325 | |||||||
| chr3:10318385 | A | C | 1 | a0001c0001t0001g0009 | 5 | NA18944.hp2 NA18962.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.4-291T>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10318385 | |||||||
| chr3:10318520 | C | T | 1 | a0001c0001t0002g0014 | 3 | HG01175.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.4-426G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10318520 | |||||||
| chr3:10318696 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0211 others(1): Show |
6 | HG01884.hp1 HG02145.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-602C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10318696 | |||||||
| chr3:10318753 | T | C | 1 | a0001c0002t0002g0122 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4-659A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10318753 | |||||||
| chr3:10318970 | C | G | 5 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(2): Show |
5 | HG00673.hp2 HG02071.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.4-876G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10318970 | |||||||
| chr3:10319047 | T | G | 1 | a0001c0001t0001g0197 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.4-953A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319047 | |||||||
| chr3:10319127 | G | C | 1 | a0001c0001t0001g0073 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4-1033C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319127 | |||||||
| chr3:10319241 | T | C | 6 | a0001c0001t0001g0097 a0001c0001t0001g0103 a0001c0001t0001g0123 others(3): Show |
6 | NA18951.hp1 NA18953.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.4-1147A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319241 | |||||||
| chr3:10319369 | T | C | 1 | a0001c0001t0001g0126 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.4-1275A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319369 | |||||||
| chr3:10319587 | G | C | 5 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(2): Show |
5 | HG00673.hp2 HG02071.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+1463C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319587 | |||||||
| chr3:10319761 | T | TGA | 3 | a0001c0001t0001g0210 a0001c0001t0002g0061 a0001c0001t0002g0229 |
3 | HG02559.hp2 HG04115.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3+1287_3+1288dupTC | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319761 | |||||||
| chr3:10319761 | TGA | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0066 others(3): Show |
11 | HG02559.hp1 HG02818.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.3+1287_3+1288delTC | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319761 | |||||||
| chr3:10319761 | TGAGA | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(69): Show |
101 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.3+1285_3+1288delTC others(2): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319761 | |||||||
| chr3:10319761 | TGAGAGAG others(1): Show |
T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(67): Show |
143 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.3+1281_3+1288delTC others(6): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319761 | |||||||
| chr3:10319761 | TGAGAGAG others(3): Show |
T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA19085.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.3+1279_3+1288delTC others(8): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319761 | |||||||
| chr3:10319761 | TGAGAGAG others(11): Show |
T | 12 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0046 others(9): Show |
14 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.3+1271_3+1288delTC others(16): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319761 | |||||||
| chr3:10319777 | AGAGAGAG others(8): Show |
A | 1 | a0001c0001t0001g0148 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3+1258_3+1272delCT others(13): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319777 | |||||||
| chr3:10319790 | G | A | 1 | a0001c0001t0004g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3+1260C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319790 | |||||||
| chr3:10319791 | A | G | 1 | a0001c0001t0004g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3+1259T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319791 | |||||||
| chr3:10319791 | AG | A | 10 | a0001c0001t0001g0024 a0001c0001t0001g0045 a0001c0001t0001g0068 others(7): Show |
11 | HG00735.hp2 HG01891.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3+1258delC | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319791 | |||||||
| chr3:10319792 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3+1258C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319792 | |||||||
| chr3:10319792 | G | C | 1 | a0001c0001t0001g0042 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3+1258C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319792 | |||||||
| chr3:10319793 | A | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0004g0062 |
3 | HG00673.hp2 HG02055.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.3+1257T>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319793 | |||||||
| chr3:10319793 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0067 |
2 | HG02071.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3+1257T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319793 | |||||||
| chr3:10319794 | GA | G | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0002g0038 others(1): Show |
5 | HG01934.hp2 HG02622.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+1255delT | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319794 | |||||||
| chr3:10319795 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3+1255T>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319795 | |||||||
| chr3:10319795 | A | G | 15 | a0001c0001t0001g0024 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
16 | HG00673.hp2 HG00735.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.3+1255T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319795 | |||||||
| chr3:10319795 | AAG | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0146 a0001c0001t0001g0214 others(3): Show |
7 | HG01070.hp1 HG01071.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.3+1253_3+1254delCT | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319795 | |||||||
| chr3:10319796 | A | C | 11 | a0001c0001t0001g0024 a0001c0001t0001g0045 a0001c0001t0001g0068 others(8): Show |
12 | HG00735.hp2 HG01891.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.3+1254T>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319796 | |||||||
| chr3:10319796 | A | G | 11 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(8): Show |
12 | HG00673.hp2 HG01099.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.3+1254T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319796 | |||||||
| chr3:10319797 | G | A | 6 | a0001c0001t0001g0036 a0001c0001t0001g0212 a0001c0001t0001g0213 others(3): Show |
7 | HG01099.hp2 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3+1253C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319797 | |||||||
| chr3:10319798 | G | A | 7 | a0001c0001t0001g0037 a0001c0001t0001g0142 a0001c0001t0001g0143 others(4): Show |
9 | HG00621.hp1 HG01106.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.3+1252C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319798 | |||||||
| chr3:10319799 | C | A | 13 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0146 others(10): Show |
16 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.3+1251G>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319799 | |||||||
| chr3:10319799 | C | G | 22 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0042 others(19): Show |
24 | HG00621.hp1 HG00673.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.3+1251G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319799 | |||||||
| chr3:10319799 | CG | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(85): Show |
161 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.3+1250delC | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319799 | |||||||
| chr3:10319799 | CGGG | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0026 others(34): Show |
56 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.3+1248_3+1250delCC others(1): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319799 | |||||||
| chr3:10319799 | CGGGG | C | 27 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0035 others(24): Show |
34 | HG01081.hp1 HG01255.hp2 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.3+1247_3+1250delCC others(2): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319799 | |||||||
| chr3:10319800 | G | A | 10 | a0001c0001t0001g0037 a0001c0001t0001g0141 a0001c0001t0001g0142 others(7): Show |
11 | HG00621.hp1 HG01106.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.3+1250C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319800 | |||||||
| chr3:10319800 | G | GAGAGAA | 2 | a0001c0001t0001g0036 a0001c0001t0001g0217 |
3 | HG01099.hp2 HG02109.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3+1249_3+1250insTT others(4): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319800 | |||||||
| chr3:10319801 | G | A | 10 | a0001c0001t0001g0028 a0001c0001t0001g0145 a0001c0001t0001g0146 others(7): Show |
11 | HG00621.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.3+1249C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319801 | |||||||
| chr3:10319802 | G | A | 8 | a0001c0001t0001g0037 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
9 | HG01167.hp2 HG01169.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.3+1248C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319802 | |||||||
| chr3:10319802 | G | C | 1 | a0001c0001t0002g0038 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.3+1248C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319802 | |||||||
| chr3:10319803 | G | A | 8 | a0001c0001t0001g0028 a0001c0001t0001g0037 a0001c0001t0001g0141 others(5): Show |
10 | HG01070.hp1 HG01071.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.3+1247C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319803 | |||||||
| chr3:10319803 | G | C | 8 | a0001c0001t0001g0036 a0001c0001t0001g0067 a0001c0001t0001g0212 others(5): Show |
9 | HG01099.hp2 HG02109.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.3+1247C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319803 | |||||||
| chr3:10319804 | G | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
6 | HG01070.hp1 HG01071.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+1246C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319804 | |||||||
| chr3:10319804 | G | C | 11 | a0001c0001t0001g0024 a0001c0001t0001g0068 a0001c0001t0001g0069 others(8): Show |
12 | HG00621.hp1 HG00735.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.3+1246C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319804 | |||||||
| chr3:10319804 | G | T | 1 | a0001c0001t0001g0201 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3+1246C>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319804 | |||||||
| chr3:10319805 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3+1245C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319805 | |||||||
| chr3:10319805 | G | C | 4 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+1245C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319805 | |||||||
| chr3:10319805 | G | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(69): Show |
145 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.3+1245C>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319805 | |||||||
| chr3:10319806 | G | C | 1 | a0001c0001t0001g0037 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3+1244C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319806 | |||||||
| chr3:10319811 | G | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(70): Show |
146 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.3+1239C>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319811 | |||||||
| chr3:10319817 | A | G | 2 | a0001c0001t0001g0082 a0001c0001t0001g0148 |
2 | HG01993.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.3+1233T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319817 | |||||||
| chr3:10319853 | AGGAG | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(2): Show |
5 | HG00673.hp2 HG02071.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+1193_3+1196delCT others(2): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319853 | |||||||
| chr3:10319864 | C | CGAGAGAG others(1): Show |
202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.3+1185_3+1186insTC others(6): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319864 | |||||||
| chr3:10319864 | C | CGGGAGAG others(1): Show |
16 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(13): Show |
22 | HG00735.hp2 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.3+1178_3+1185dupTC others(6): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319864 | |||||||
| chr3:10319873 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3+1177T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319873 | |||||||
| chr3:10319912 | G | T | 1 | a0001c0001t0002g0224 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3+1138C>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319912 | |||||||
| chr3:10319919 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3+1131C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319919 | |||||||
| chr3:10320006 | G | GGA | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(74): Show |
150 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.3+1042_3+1043dupTC | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320006 | |||||||
| chr3:10320006 | GGAGAGA | G | 40 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0021 others(37): Show |
57 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.3+1038_3+1043delTC others(4): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320006 | |||||||
| chr3:10320032 | T | A | 1 | a0001c0001t0001g0208 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3+1018A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320032 | |||||||
| chr3:10320269 | G | C | 1 | a0001c0001t0005g0209 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3+781C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320269 | |||||||
| chr3:10320319 | T | C | 17 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(14): Show |
21 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.3+731A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320319 | |||||||
| chr3:10320608 | T | C | 23 | a0001c0001t0001g0231 a0001c0001t0001g0242 a0001c0001t0002g0018 others(20): Show |
28 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.3+442A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320608 | |||||||
| chr3:10320685 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3+365A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320685 | |||||||
| chr3:10320788 | T | C | 1 | a0001c0001t0003g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3+262A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320788 | |||||||
| chr3:10320865 | C | T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(2): Show |
5 | HG00673.hp2 HG02071.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+185G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320865 | |||||||
| chr3:10320886 | G | A | 11 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0243 others(8): Show |
13 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.3+164C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320886 | |||||||
| chr3:10320938 | G | A | 1 | a0001c0001t0003g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3+112C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320938 |