Item | Value |
---|---|
geneid | 338 |
ensemblid | ENSG00000084674.15 |
hgncid | 603 |
symbol | APOB |
name | apolipoprotein B |
refseq_nuc | NM_000384.3 |
refseq_prot | NP_000375.3 |
ensembl_nuc | ENST00000233242.5 |
ensembl_prot | ENSP00000233242.1 |
mane_status | MANE Select |
chr | chr2 |
start | 21001429 |
end | 21044073 |
strand | - |
ver | v1.2 |
region | chr2:21001429-21044073 |
region5000 | chr2:20996429-21049073 |
regionname0 | APOB_chr2_21001429_21044073 |
regionname5000 | APOB_chr2_20996429_21049073 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 4563 | 71 | 4 | 4 | 47 | 1 | 15 | 35 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0002 | 0/0 | 4560 | 57 | 12 | 19 | 16 | 3 | 7 | 14 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4555): Show |
chr2 | 20996429 | 21049073 |
a0003 | 0/0 | 4563 | 37 | 16 | 11 | 1 | 2 | 7 | 1 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0004 | 0/0 | 4563 | 24 | 0 | 0 | 23 | 0 | 1 | 18 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0005 | 0/0 | 4563 | 20 | 7 | 8 | 5 | 0 | 0 | 4 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0006 | 0/0 | 4563 | 16 | 0 | 2 | 11 | 2 | 1 | 7 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0007 | 0/0 | 4560 | 13 | 1 | 1 | 11 | 0 | 0 | 8 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4555): Show |
chr2 | 20996429 | 21049073 |
a0008 | 0/0 | 4563 | 12 | 2 | 3 | 3 | 2 | 2 | 2 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0009 | 0/0 | 4560 | 7 | 3 | 2 | 2 | 0 | 0 | 2 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4555): Show |
chr2 | 20996429 | 21049073 |
a0010 | 0/0 | 4563 | 7 | 5 | 1 | 0 | 0 | 1 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0011 | 0/0 | 4563 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0012 | 0/0 | 4563 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0013 | 0/0 | 4560 | 6 | 1 | 0 | 4 | 0 | 1 | 3 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4555): Show |
chr2 | 20996429 | 21049073 |
a0014 | 0/0 | 4563 | 5 | 0 | 0 | 5 | 0 | 0 | 3 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0015 | 0/0 | 4563 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0016 | 0/0 | 4563 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0017 | 0/0 | 4563 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0018 | 0/0 | 4563 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0019 | 0/0 | 4563 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0020 | 0/0 | 4563 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0021 | 0/0 | 4563 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0022 | 0/0 | 4563 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0023 | 0/0 | 4563 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0024 | 0/0 | 4563 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0025 | 0/0 | 4563 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0026 | 0/1 | 4563 | 2 | 0 | 0 | 0 | 0 | 1 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0027 | 1/0 | 4563 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0028 | 0/0 | 4563 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0029 | 0/0 | 4563 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0030 | 0/0 | 4563 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0031 | 0/0 | 4563 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0032 | 0/0 | 4563 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0033 | 0/0 | 4563 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0034 | 0/0 | 4563 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0035 | 0/0 | 4563 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0036 | 0/0 | 4563 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0037 | 0/0 | 4563 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0038 | 0/0 | 4563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0039 | 0/0 | 4563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0040 | 0/0 | 4563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0041 | 0/0 | 4563 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0042 | 0/0 | 4563 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0043 | 0/0 | 4563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0044 | 0/0 | 4560 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4555): Show |
chr2 | 20996429 | 21049073 |
a0045 | 0/0 | 4563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0046 | 0/0 | 4563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0047 | 0/0 | 4563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0048 | 0/0 | 4563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0049 | 0/0 | 4563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0050 | 0/0 | 4563 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0051 | 0/0 | 4563 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0052 | 0/0 | 4563 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0053 | 0/0 | 4563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0054 | 0/0 | 4563 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0055 | 0/0 | 4563 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
a0056 | 0/0 | 4563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | MDPPR others(4558): Show |
chr2 | 20996429 | 21049073 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 13689 | 57 | 3 | 3 | 38 | 1 | 12 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0001c0014 | 0/0 | 13689 | 5 | 0 | 0 | 5 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0001c0036 | 0/0 | 13689 | 2 | 0 | 0 | 2 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0001c0040 | 0/0 | 13689 | 2 | 1 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0001c0085 | 0/0 | 13689 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0001c0086 | 0/0 | 13689 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0001c0088 | 0/0 | 13689 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0001c0090 | 0/0 | 13689 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0001c0101 | 0/0 | 13689 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0002c0002 | 0/0 | 13680 | 25 | 2 | 6 | 10 | 2 | 5 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0002c0012 | 0/0 | 13680 | 6 | 0 | 6 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0002c0016 | 0/0 | 13680 | 4 | 4 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0002c0024 | 0/0 | 13680 | 2 | 0 | 0 | 2 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0002c0025 | 0/0 | 13680 | 2 | 1 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0002c0028 | 0/0 | 13680 | 2 | 0 | 1 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0002c0029 | 0/0 | 13680 | 2 | 0 | 0 | 0 | 0 | 2 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0002c0030 | 0/0 | 13680 | 2 | 0 | 2 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0002c0043 | 0/0 | 13680 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0002c0044 | 0/0 | 13680 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0002c0050 | 0/0 | 13680 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0002c0051 | 0/0 | 13680 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0002c0052 | 0/0 | 13680 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0002c0053 | 0/0 | 13680 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0002c0054 | 0/0 | 13680 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0002c0055 | 0/0 | 13680 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0002c0056 | 0/0 | 13680 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0002c0057 | 0/0 | 13680 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0002c0058 | 0/0 | 13680 | 1 | 0 | 0 | 0 | 1 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0002c0062 | 0/0 | 13680 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0003c0005 | 0/0 | 13689 | 15 | 13 | 2 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0003c0007 | 0/0 | 13689 | 12 | 2 | 5 | 1 | 0 | 4 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0003c0008 | 0/0 | 13689 | 10 | 1 | 4 | 0 | 2 | 3 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0004c0003 | 0/0 | 13689 | 22 | 0 | 0 | 21 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0004c0097 | 0/0 | 13689 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0004c0098 | 0/0 | 13689 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0005c0004 | 0/0 | 13689 | 19 | 7 | 7 | 5 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0005c0072 | 0/0 | 13689 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0006c0006 | 0/0 | 13689 | 13 | 0 | 2 | 10 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0006c0076 | 0/0 | 13689 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0006c0083 | 0/0 | 13689 | 1 | 0 | 0 | 0 | 1 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0006c0095 | 0/0 | 13689 | 1 | 0 | 0 | 0 | 1 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0007c0010 | 0/0 | 13680 | 8 | 0 | 0 | 8 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0007c0021 | 0/0 | 13680 | 3 | 1 | 1 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0007c0027 | 0/0 | 13680 | 2 | 0 | 0 | 2 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0008c0009 | 0/0 | 13689 | 10 | 1 | 3 | 2 | 2 | 2 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0008c0034 | 0/0 | 13689 | 2 | 1 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0009c0046 | 0/0 | 13680 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0009c0047 | 0/0 | 13680 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0009c0048 | 0/0 | 13680 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0009c0049 | 0/0 | 13680 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0009c0059 | 0/0 | 13680 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0009c0060 | 0/0 | 13680 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0009c0061 | 0/0 | 13680 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0010c0019 | 0/0 | 13689 | 4 | 3 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0010c0031 | 0/0 | 13689 | 2 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0010c0075 | 0/0 | 13689 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0011c0011 | 0/0 | 13689 | 7 | 7 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0012c0013 | 0/0 | 13689 | 6 | 5 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0013c0017 | 0/0 | 13680 | 4 | 1 | 0 | 3 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0013c0026 | 0/0 | 13680 | 2 | 0 | 0 | 1 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0014c0015 | 0/0 | 13689 | 5 | 0 | 0 | 5 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0015c0020 | 0/0 | 13689 | 4 | 1 | 3 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0016c0022 | 0/0 | 13689 | 3 | 2 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0016c0069 | 0/0 | 13689 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0017c0018 | 0/0 | 13689 | 4 | 4 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0018c0023 | 0/0 | 13689 | 3 | 2 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0019c0041 | 0/0 | 13689 | 2 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0019c0104 | 0/0 | 13689 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0020c0039 | 0/0 | 13689 | 2 | 0 | 2 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0021c0038 | 0/0 | 13689 | 2 | 0 | 2 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0022c0032 | 0/0 | 13689 | 2 | 0 | 2 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0023c0042 | 0/0 | 13689 | 2 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0024c0035 | 0/0 | 13689 | 2 | 0 | 0 | 2 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0025c0033 | 0/0 | 13689 | 2 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0026c0037 | 0/1 | 13689 | 2 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0027c0068 | 1/0 | 13689 | 1 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0028c0081 | 0/0 | 13689 | 1 | 0 | 0 | 0 | 1 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0029c0084 | 0/0 | 13689 | 1 | 0 | 0 | 0 | 1 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0030c0080 | 0/0 | 13689 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0031c0087 | 0/0 | 13689 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0032c0092 | 0/0 | 13689 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0033c0096 | 0/0 | 13689 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0034c0082 | 0/0 | 13689 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0035c0089 | 0/0 | 13689 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0036c0077 | 0/0 | 13689 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0037c0070 | 0/0 | 13689 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0038c0099 | 0/0 | 13689 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0039c0071 | 0/0 | 13689 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0040c0102 | 0/0 | 13689 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0041c0105 | 0/0 | 13689 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0042c0079 | 0/0 | 13689 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0043c0103 | 0/0 | 13689 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0044c0045 | 0/0 | 13680 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13675): Show |
chr2 | 20996429 | 21049073 | ||
a0045c0074 | 0/0 | 13689 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0046c0066 | 0/0 | 13689 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0047c0067 | 0/0 | 13689 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0048c0064 | 0/0 | 13689 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0049c0100 | 0/0 | 13689 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0050c0063 | 0/0 | 13689 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0051c0093 | 0/0 | 13689 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0052c0094 | 0/0 | 13689 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0053c0065 | 0/0 | 13689 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0054c0078 | 0/0 | 13689 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0055c0091 | 0/0 | 13689 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 | ||
a0056c0073 | 0/0 | 13689 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATGGA others(13684): Show |
chr2 | 20996429 | 21049073 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 14121 | 57 | 3 | 3 | 38 | 1 | 12 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0001c0014t0001 | 0/0 | 14121 | 5 | 0 | 0 | 5 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0001c0036t0001 | 0/0 | 14121 | 2 | 0 | 0 | 2 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0001c0040t0001 | 0/0 | 14121 | 2 | 1 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0001c0085t0001 | 0/0 | 14121 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0001c0086t0001 | 0/0 | 14121 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0001c0088t0001 | 0/0 | 14121 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0001c0090t0001 | 0/0 | 14121 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0001c0101t0001 | 0/0 | 14121 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0002c0002t0001 | 0/0 | 14112 | 25 | 2 | 6 | 10 | 2 | 5 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0002c0012t0001 | 0/0 | 14112 | 4 | 0 | 4 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0002c0012t0003 | 0/0 | 14112 | 2 | 0 | 2 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0002c0016t0001 | 0/0 | 14112 | 4 | 4 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0002c0024t0001 | 0/0 | 14112 | 2 | 0 | 0 | 2 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0002c0025t0001 | 0/0 | 14112 | 2 | 1 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0002c0028t0001 | 0/0 | 14112 | 2 | 0 | 1 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0002c0029t0001 | 0/0 | 14112 | 2 | 0 | 0 | 0 | 0 | 2 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0002c0030t0001 | 0/0 | 14112 | 2 | 0 | 2 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0002c0043t0001 | 0/0 | 14112 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0002c0044t0001 | 0/0 | 14112 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0002c0050t0001 | 0/0 | 14112 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0002c0051t0001 | 0/0 | 14112 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0002c0052t0002 | 0/0 | 14112 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0002c0053t0001 | 0/0 | 14112 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0002c0054t0001 | 0/0 | 14112 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0002c0055t0001 | 0/0 | 14112 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0002c0056t0001 | 0/0 | 14112 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0002c0057t0001 | 0/0 | 14112 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0002c0058t0001 | 0/0 | 14112 | 1 | 0 | 0 | 0 | 1 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0002c0062t0001 | 0/0 | 14112 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0003c0005t0001 | 0/0 | 14121 | 15 | 13 | 2 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0003c0007t0001 | 0/0 | 14121 | 11 | 2 | 4 | 1 | 0 | 4 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0003c0007t0006 | 0/0 | 14121 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0003c0008t0001 | 0/0 | 14121 | 10 | 1 | 4 | 0 | 2 | 3 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0004c0003t0001 | 0/0 | 14121 | 21 | 0 | 0 | 20 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0004c0003t0005 | 0/0 | 14121 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0004c0097t0001 | 0/0 | 14121 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0004c0098t0001 | 0/0 | 14121 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0005c0004t0001 | 0/0 | 14121 | 19 | 7 | 7 | 5 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0005c0072t0001 | 0/0 | 14121 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0006c0006t0001 | 0/0 | 14121 | 13 | 0 | 2 | 10 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0006c0076t0001 | 0/0 | 14121 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0006c0083t0001 | 0/0 | 14121 | 1 | 0 | 0 | 0 | 1 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0006c0095t0001 | 0/0 | 14121 | 1 | 0 | 0 | 0 | 1 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0007c0010t0001 | 0/0 | 14112 | 8 | 0 | 0 | 8 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0007c0021t0001 | 0/0 | 14112 | 3 | 1 | 1 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0007c0027t0001 | 0/0 | 14112 | 2 | 0 | 0 | 2 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0008c0009t0001 | 0/0 | 14121 | 10 | 1 | 3 | 2 | 2 | 2 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0008c0034t0001 | 0/0 | 14121 | 2 | 1 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0009c0046t0002 | 0/0 | 14112 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0009c0047t0001 | 0/0 | 14112 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0009c0048t0001 | 0/0 | 14112 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0009c0049t0001 | 0/0 | 14112 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0009c0059t0001 | 0/0 | 14112 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0009c0060t0001 | 0/0 | 14112 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0009c0061t0001 | 0/0 | 14112 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0010c0019t0001 | 0/0 | 14121 | 3 | 2 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0010c0019t0004 | 0/0 | 14121 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0010c0031t0001 | 0/0 | 14121 | 2 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0010c0075t0001 | 0/0 | 14121 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0011c0011t0001 | 0/0 | 14121 | 7 | 7 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0012c0013t0001 | 0/0 | 14121 | 6 | 5 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0013c0017t0001 | 0/0 | 14112 | 4 | 1 | 0 | 3 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0013c0026t0001 | 0/0 | 14112 | 2 | 0 | 0 | 1 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0014c0015t0001 | 0/0 | 14121 | 5 | 0 | 0 | 5 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0015c0020t0001 | 0/0 | 14121 | 4 | 1 | 3 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0016c0022t0001 | 0/0 | 14121 | 3 | 2 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0016c0069t0001 | 0/0 | 14121 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0017c0018t0001 | 0/0 | 14121 | 4 | 4 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0018c0023t0001 | 0/0 | 14121 | 3 | 2 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0019c0041t0001 | 0/0 | 14121 | 2 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0019c0104t0001 | 0/0 | 14121 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0020c0039t0001 | 0/0 | 14121 | 2 | 0 | 2 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0021c0038t0001 | 0/0 | 14121 | 2 | 0 | 2 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0022c0032t0001 | 0/0 | 14121 | 2 | 0 | 2 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0023c0042t0001 | 0/0 | 14121 | 2 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0024c0035t0001 | 0/0 | 14121 | 2 | 0 | 0 | 2 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0025c0033t0001 | 0/0 | 14121 | 2 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0026c0037t0001 | 0/1 | 14121 | 2 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0027c0068t0001 | 1/0 | 14121 | 1 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0028c0081t0001 | 0/0 | 14121 | 1 | 0 | 0 | 0 | 1 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0029c0084t0001 | 0/0 | 14121 | 1 | 0 | 0 | 0 | 1 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0030c0080t0001 | 0/0 | 14121 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0031c0087t0001 | 0/0 | 14121 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0032c0092t0003 | 0/0 | 14121 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0033c0096t0001 | 0/0 | 14121 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0034c0082t0001 | 0/0 | 14121 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0035c0089t0001 | 0/0 | 14121 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0036c0077t0001 | 0/0 | 14121 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0037c0070t0001 | 0/0 | 14121 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0038c0099t0002 | 0/0 | 14121 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0039c0071t0001 | 0/0 | 14121 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0040c0102t0001 | 0/0 | 14121 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0041c0105t0001 | 0/0 | 14121 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0042c0079t0001 | 0/0 | 14121 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0043c0103t0004 | 0/0 | 14121 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0044c0045t0001 | 0/0 | 14112 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14107): Show |
chr2 | 20996429 | 21049073 |
a0045c0074t0001 | 0/0 | 14121 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0046c0066t0001 | 0/0 | 14121 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0047c0067t0002 | 0/0 | 14121 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0048c0064t0001 | 0/0 | 14121 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0049c0100t0001 | 0/0 | 14121 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0050c0063t0001 | 0/0 | 14121 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0051c0093t0001 | 0/0 | 14121 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0052c0094t0001 | 0/0 | 14121 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0053c0065t0004 | 0/0 | 14121 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0054c0078t0001 | 0/0 | 14121 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0055c0091t0001 | 0/0 | 14121 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
a0056c0073t0001 | 0/0 | 14121 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | ATTCC others(14116): Show |
chr2 | 20996429 | 21049073 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 22 | 1 | 1 | 16 | 1 | 3 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0011 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0014t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0036t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0036t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0040t0001g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0085t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0086t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0088t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0090t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0001c0101t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0002t0001g0004 | 0/0 | 7 | 0 | 3 | 0 | 2 | 2 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0002t0001g0009 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0002t0001g0014 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0012t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0012t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0012t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0012t0003g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0016t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0016t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0016t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0016t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0024t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0024t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0025t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0028t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0028t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0029t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0029t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0030t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0043t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0044t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0050t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0051t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0052t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0053t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0054t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0055t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0056t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0057t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0058t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0002c0062t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0005t0001g0003 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0005t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0005t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0005t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0005t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0005t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0005t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0007t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0007t0001g0048 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0007t0001g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0007t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0007t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0007t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0007t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0007t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0007t0006g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0008t0001g0010 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0008t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0008t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0008t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0008t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0003c0008t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0004c0003t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0004c0003t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0004c0003t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0004c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0004c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0004c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0004c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0004c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0004c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0004c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0004c0003t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0004c0097t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0004c0098t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0005c0004t0001g0002 | 0/0 | 9 | 0 | 6 | 3 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0005c0004t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0005c0004t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0005c0004t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0005c0004t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0005c0004t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0005c0004t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0005c0004t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0005c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0005c0004t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0005c0072t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0006c0006t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0006c0006t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0006c0006t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0006c0006t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0006c0006t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0006c0006t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0006c0006t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0006c0006t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0006c0006t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0006c0006t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0006c0006t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0006c0076t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0006c0083t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0006c0095t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0007c0010t0001g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0007c0010t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0007c0010t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0007c0021t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0007c0021t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0007c0021t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0007c0027t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0008c0009t0001g0016 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0008c0009t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0008c0009t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0008c0009t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0008c0009t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0008c0009t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0008c0009t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0008c0034t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0008c0034t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0009c0046t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0009c0047t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0009c0048t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0009c0049t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0009c0059t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0009c0060t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0009c0061t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0010c0019t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0010c0019t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0010c0019t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0010c0031t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0010c0075t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0011c0011t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0011c0011t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0011c0011t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0012c0013t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0012c0013t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0012c0013t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0012c0013t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0013c0017t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0013c0017t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0013c0017t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0013c0026t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0013c0026t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0014c0015t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0014c0015t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0014c0015t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0015c0020t0001g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0015c0020t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0015c0020t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0016c0022t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0016c0022t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0016c0069t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0017c0018t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0017c0018t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0018c0023t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0018c0023t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0018c0023t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0019c0041t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0019c0041t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0019c0104t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0020c0039t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0021c0038t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0022c0032t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0023c0042t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0023c0042t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0024c0035t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0025c0033t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0025c0033t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0026c0037t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0026c0037t0001g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0027c0068t0001g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0028c0081t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0029c0084t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0030c0080t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0031c0087t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0032c0092t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0033c0096t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0034c0082t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0035c0089t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0036c0077t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0037c0070t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0038c0099t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0039c0071t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0040c0102t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0041c0105t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0042c0079t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0043c0103t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0044c0045t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0045c0074t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0046c0066t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0047c0067t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0048c0064t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0049c0100t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0050c0063t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0051c0093t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0052c0094t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0053c0065t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0054c0078t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0055c0091t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
a0056c0073t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0008 | t0001 | g0151 | EUR | GBR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00099 | hp2 | a0006 | c0083 | t0001 | g0110 | EUR | GBR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0004 | EUR | FIN | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00280 | hp2 | a0028 | c0081 | t0001 | g0165 | EUR | FIN | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00323 | hp1 | a0029 | c0084 | t0001 | g0175 | EUR | FIN | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0004 | EUR | FIN | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00408 | hp1 | a0001 | c0014 | t0001 | g0008 | EAS | CHS | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00408 | hp2 | a0030 | c0080 | t0001 | g0183 | EAS | CHS | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00544 | hp1 | a0031 | c0087 | t0001 | g0160 | EAS | CHS | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00544 | hp2 | a0004 | c0003 | t0005 | g0052 | EAS | CHS | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00558 | hp1 | a0006 | c0006 | t0001 | g0035 | EAS | CHS | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00558 | hp2 | a0004 | c0003 | t0001 | g0007 | EAS | CHS | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00621 | hp2 | a0004 | c0003 | t0001 | g0200 | EAS | CHS | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00642 | hp1 | a0003 | c0008 | t0001 | g0150 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00642 | hp2 | a0008 | c0009 | t0001 | g0016 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00673 | hp1 | a0001 | c0036 | t0001 | g0187 | EAS | CHS | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00673 | hp2 | a0006 | c0006 | t0001 | g0168 | EAS | CHS | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00733 | hp2 | a0003 | c0007 | t0001 | g0048 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00735 | hp1 | a0008 | c0009 | t0001 | g0164 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00735 | hp2 | a0002 | c0012 | t0001 | g0089 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00738 | hp1 | a0032 | c0092 | t0003 | g0179 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00738 | hp2 | a0033 | c0096 | t0001 | g0172 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00741 | hp1 | a0009 | c0060 | t0001 | g0093 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG00741 | hp2 | a0007 | c0021 | t0001 | g0099 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01069 | hp1 | a0002 | c0012 | t0003 | g0021 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01069 | hp2 | a0003 | c0007 | t0001 | g0049 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01070 | hp1 | a0003 | c0008 | t0001 | g0010 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01070 | hp2 | a0003 | c0007 | t0001 | g0027 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01071 | hp1 | a0003 | c0007 | t0001 | g0027 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01071 | hp2 | a0002 | c0012 | t0003 | g0021 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01081 | hp2 | a0005 | c0004 | t0001 | g0002 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01099 | hp1 | a0015 | c0020 | t0001 | g0044 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01106 | hp1 | a0003 | c0008 | t0001 | g0033 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01106 | hp2 | a0020 | c0039 | t0001 | g0036 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01109 | hp1 | a0009 | c0059 | t0001 | g0092 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01109 | hp2 | a0034 | c0082 | t0001 | g0167 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01167 | hp1 | a0006 | c0006 | t0001 | g0109 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01167 | hp2 | a0010 | c0019 | t0001 | g0120 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01168 | hp1 | a0002 | c0028 | t0001 | g0075 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01168 | hp2 | a0015 | c0020 | t0001 | g0177 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01175 | hp1 | a0015 | c0020 | t0001 | g0204 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01175 | hp2 | a0005 | c0072 | t0001 | g0118 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01192 | hp1 | a0003 | c0008 | t0001 | g0010 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01192 | hp2 | a0020 | c0039 | t0001 | g0036 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0097 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01243 | hp2 | a0003 | c0005 | t0001 | g0113 | AMR | PUR | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01255 | hp1 | a0016 | c0022 | t0001 | g0103 | AMR | CLM | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | CLM | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01256 | hp1 | a0002 | c0055 | t0001 | g0081 | AMR | CLM | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01256 | hp2 | a0021 | c0038 | t0001 | g0040 | AMR | CLM | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01258 | hp1 | a0002 | c0057 | t0001 | g0079 | AMR | CLM | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01258 | hp2 | a0021 | c0038 | t0001 | g0040 | AMR | CLM | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01261 | hp1 | a0003 | c0005 | t0001 | g0116 | AMR | CLM | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01261 | hp2 | a0022 | c0032 | t0001 | g0028 | AMR | CLM | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01346 | hp1 | a0005 | c0004 | t0001 | g0127 | AMR | CLM | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | CLM | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01358 | hp1 | a0005 | c0004 | t0001 | g0002 | AMR | CLM | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01358 | hp2 | a0002 | c0012 | t0001 | g0024 | AMR | CLM | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01361 | hp1 | a0002 | c0030 | t0001 | g0022 | AMR | CLM | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01361 | hp2 | a0005 | c0004 | t0001 | g0002 | AMR | CLM | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01433 | hp1 | a0018 | c0023 | t0001 | g0144 | AMR | CLM | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01433 | hp2 | a0022 | c0032 | t0001 | g0028 | AMR | CLM | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01496 | hp2 | a0012 | c0013 | t0001 | g0025 | AMR | CLM | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01515 | hp2 | a0003 | c0008 | t0001 | g0010 | EUR | IBS | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01884 | hp1 | a0003 | c0005 | t0001 | g0003 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01884 | hp2 | a0019 | c0041 | t0001 | g0224 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01891 | hp1 | a0016 | c0022 | t0001 | g0029 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01891 | hp2 | a0023 | c0042 | t0001 | g0225 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01934 | hp1 | a0002 | c0025 | t0001 | g0019 | AMR | PEL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01934 | hp2 | a0035 | c0089 | t0001 | g0207 | AMR | PEL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01952 | hp1 | a0008 | c0009 | t0001 | g0208 | AMR | PEL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01952 | hp2 | a0005 | c0004 | t0001 | g0002 | AMR | PEL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01975 | hp1 | a0002 | c0030 | t0001 | g0022 | AMR | PEL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01978 | hp1 | a0036 | c0077 | t0001 | g0157 | AMR | PEL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01978 | hp2 | a0037 | c0070 | t0001 | g0146 | AMR | PEL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01981 | hp1 | a0002 | c0056 | t0001 | g0082 | AMR | PEL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01981 | hp2 | a0002 | c0012 | t0001 | g0086 | AMR | PEL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02004 | hp1 | a0002 | c0012 | t0001 | g0024 | AMR | PEL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02004 | hp2 | a0005 | c0004 | t0001 | g0002 | AMR | PEL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02027 | hp2 | a0006 | c0076 | t0001 | g0135 | EAS | KHV | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02055 | hp1 | a0008 | c0009 | t0001 | g0016 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02055 | hp2 | a0038 | c0099 | t0002 | g0230 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02056 | hp2 | a0002 | c0028 | t0001 | g0076 | EAS | KHV | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02074 | hp1 | a0013 | c0017 | t0001 | g0084 | EAS | KHV | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02074 | hp2 | a0006 | c0006 | t0001 | g0166 | EAS | KHV | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02080 | hp1 | a0007 | c0021 | t0001 | g0065 | EAS | KHV | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02080 | hp2 | a0002 | c0024 | t0001 | g0070 | EAS | KHV | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02083 | hp1 | a0007 | c0010 | t0001 | g0006 | EAS | KHV | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02083 | hp2 | a0008 | c0034 | t0001 | g0191 | EAS | KHV | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02129 | hp1 | a0014 | c0015 | t0001 | g0015 | EAS | KHV | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02132 | hp1 | a0004 | c0003 | t0001 | g0042 | EAS | KHV | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02132 | hp2 | a0024 | c0035 | t0001 | g0038 | EAS | KHV | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02135 | hp1 | a0014 | c0015 | t0001 | g0154 | EAS | KHV | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02135 | hp2 | a0024 | c0035 | t0001 | g0038 | EAS | KHV | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02145 | hp1 | a0003 | c0008 | t0001 | g0033 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02145 | hp2 | a0040 | c0102 | t0001 | g0223 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02148 | hp1 | a0005 | c0004 | t0001 | g0002 | AMR | PEL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02148 | hp2 | a0001 | c0040 | t0001 | g0041 | AMR | PEL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02165 | hp1 | a0004 | c0098 | t0001 | g0149 | EAS | CDX | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CDX | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02257 | hp1 | a0019 | c0104 | t0001 | g0148 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02257 | hp2 | a0002 | c0016 | t0001 | g0053 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02258 | hp1 | a0015 | c0020 | t0001 | g0044 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02258 | hp2 | a0009 | c0047 | t0001 | g0062 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02280 | hp1 | a0011 | c0011 | t0001 | g0017 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02280 | hp2 | a0002 | c0050 | t0001 | g0061 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02300 | hp1 | a0006 | c0006 | t0001 | g0130 | AMR | PEL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02300 | hp2 | a0041 | c0105 | t0001 | g0219 | AMR | PEL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02451 | hp1 | a0010 | c0019 | t0001 | g0030 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02451 | hp2 | a0012 | c0013 | t0001 | g0026 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02523 | hp2 | a0042 | c0079 | t0001 | g0195 | EAS | KHV | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02572 | hp1 | a0003 | c0005 | t0001 | g0003 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02572 | hp2 | a0025 | c0033 | t0001 | g0173 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02602 | hp1 | a0004 | c0003 | t0001 | g0042 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02602 | hp2 | a0003 | c0007 | t0001 | g0048 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02615 | hp1 | a0017 | c0018 | t0001 | g0050 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02615 | hp2 | a0003 | c0005 | t0001 | g0114 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02622 | hp1 | a0003 | c0005 | t0001 | g0003 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02622 | hp2 | a0008 | c0034 | t0001 | g0198 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02630 | hp1 | a0018 | c0023 | t0001 | g0106 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02630 | hp2 | a0010 | c0019 | t0004 | g0231 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02647 | hp1 | a0043 | c0103 | t0004 | g0233 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02647 | hp2 | a0002 | c0025 | t0001 | g0019 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02698 | hp1 | a0010 | c0075 | t0001 | g0102 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02698 | hp2 | a0001 | c0090 | t0001 | g0170 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02717 | hp1 | a0002 | c0016 | t0001 | g0054 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02717 | hp2 | a0003 | c0005 | t0001 | g0003 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02723 | hp2 | a0002 | c0043 | t0001 | g0071 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02735 | hp2 | a0002 | c0029 | t0001 | g0074 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02809 | hp1 | a0025 | c0033 | t0001 | g0134 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02809 | hp2 | a0002 | c0016 | t0001 | g0055 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02886 | hp1 | a0019 | c0041 | t0001 | g0222 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0091 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02895 | hp1 | a0011 | c0011 | t0001 | g0047 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02895 | hp2 | a0012 | c0013 | t0001 | g0025 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02897 | hp1 | a0011 | c0011 | t0001 | g0047 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02897 | hp2 | a0003 | c0005 | t0001 | g0031 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02922 | hp1 | a0005 | c0004 | t0001 | g0128 | AFR | ESN | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02922 | hp2 | a0003 | c0007 | t0001 | g0105 | AFR | ESN | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02965 | hp1 | a0005 | c0004 | t0001 | g0032 | AFR | ESN | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02965 | hp2 | a0011 | c0011 | t0001 | g0017 | AFR | ESN | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02970 | hp1 | a0003 | c0005 | t0001 | g0003 | AFR | ESN | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02970 | hp2 | a0012 | c0013 | t0001 | g0203 | AFR | ESN | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02976 | hp1 | a0010 | c0019 | t0001 | g0030 | AFR | ESN | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02976 | hp2 | a0005 | c0004 | t0001 | g0032 | AFR | ESN | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03017 | hp1 | a0003 | c0007 | t0001 | g0049 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03041 | hp1 | a0009 | c0046 | t0002 | g0066 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03041 | hp2 | a0044 | c0045 | t0001 | g0067 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03098 | hp1 | a0017 | c0018 | t0001 | g0050 | AFR | MSL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03098 | hp2 | a0011 | c0011 | t0001 | g0046 | AFR | MSL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03130 | hp1 | a0012 | c0013 | t0001 | g0100 | AFR | ESN | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03130 | hp2 | a0003 | c0007 | t0001 | g0104 | AFR | ESN | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03139 | hp1 | a0005 | c0004 | t0001 | g0125 | AFR | ESN | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03139 | hp2 | a0017 | c0018 | t0001 | g0051 | AFR | ESN | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03195 | hp2 | a0005 | c0004 | t0001 | g0126 | AFR | ESN | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0095 | AFR | MSL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03209 | hp2 | a0045 | c0074 | t0001 | g0129 | AFR | MSL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03225 | hp1 | a0046 | c0066 | t0001 | g0122 | AFR | MSL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03225 | hp2 | a0003 | c0005 | t0001 | g0003 | AFR | MSL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03239 | hp1 | a0003 | c0008 | t0001 | g0010 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03239 | hp2 | a0003 | c0007 | t0001 | g0228 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03453 | hp1 | a0003 | c0005 | t0001 | g0117 | AFR | MSL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03453 | hp2 | a0013 | c0017 | t0001 | g0090 | AFR | MSL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03486 | hp1 | a0003 | c0005 | t0001 | g0031 | AFR | MSL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03486 | hp2 | a0002 | c0052 | t0002 | g0077 | AFR | MSL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03540 | hp1 | a0003 | c0005 | t0001 | g0003 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03540 | hp2 | a0002 | c0016 | t0001 | g0056 | AFR | GWD | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03579 | hp1 | a0048 | c0064 | t0001 | g0221 | AFR | MSL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03654 | hp1 | a0008 | c0009 | t0001 | g0039 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0087 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03669 | hp1 | a0002 | c0029 | t0001 | g0085 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03669 | hp2 | a0006 | c0006 | t0001 | g0180 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03688 | hp1 | a0001 | c0085 | t0001 | g0184 | SAS | STU | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03704 | hp2 | a0008 | c0009 | t0001 | g0182 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03710 | hp2 | a0003 | c0008 | t0001 | g0153 | SAS | PJL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0009 | SAS | BEB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG04115 | hp1 | a0001 | c0086 | t0001 | g0185 | SAS | STU | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG04115 | hp2 | a0003 | c0007 | t0001 | g0107 | SAS | STU | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG04184 | hp2 | a0003 | c0008 | t0001 | g0152 | SAS | BEB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | STU | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG04204 | hp2 | a0013 | c0026 | t0001 | g0060 | SAS | STU | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | STU | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG04228 | hp2 | a0026 | c0037 | t0001 | g0111 | SAS | STU | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18522 | hp1 | a0002 | c0053 | t0001 | g0072 | AFR | YRI | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18522 | hp2 | a0023 | c0042 | t0001 | g0226 | AFR | YRI | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18612 | hp2 | a0007 | c0010 | t0001 | g0006 | EAS | CHB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18747 | hp1 | a0005 | c0004 | t0001 | g0216 | EAS | CHB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18906 | hp1 | a0009 | c0048 | t0001 | g0063 | AFR | YRI | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18906 | hp2 | a0003 | c0005 | t0001 | g0112 | AFR | YRI | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18939 | hp2 | a0001 | c0014 | t0001 | g0008 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18941 | hp1 | a0004 | c0003 | t0001 | g0202 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18942 | hp1 | a0007 | c0010 | t0001 | g0064 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18945 | hp1 | a0006 | c0006 | t0001 | g0138 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18945 | hp2 | a0003 | c0007 | t0001 | g0145 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18946 | hp1 | a0001 | c0088 | t0001 | g0188 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18948 | hp1 | a0004 | c0003 | t0001 | g0005 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18948 | hp2 | a0050 | c0063 | t0001 | g0133 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18949 | hp2 | a0004 | c0003 | t0001 | g0140 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18950 | hp1 | a0004 | c0003 | t0001 | g0007 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18950 | hp2 | a0006 | c0006 | t0001 | g0037 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18959 | hp1 | a0007 | c0027 | t0001 | g0018 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18960 | hp1 | a0004 | c0003 | t0001 | g0007 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18960 | hp2 | a0006 | c0006 | t0001 | g0035 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18961 | hp1 | a0008 | c0009 | t0001 | g0212 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18962 | hp2 | a0009 | c0049 | t0001 | g0068 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18963 | hp2 | a0004 | c0003 | t0001 | g0007 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18965 | hp1 | a0002 | c0024 | t0001 | g0059 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18968 | hp1 | a0005 | c0004 | t0001 | g0002 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18968 | hp2 | a0013 | c0017 | t0001 | g0020 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18969 | hp1 | a0051 | c0093 | t0001 | g0159 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18971 | hp1 | a0002 | c0051 | t0001 | g0080 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18971 | hp2 | a0001 | c0036 | t0001 | g0218 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18973 | hp1 | a0013 | c0026 | t0001 | g0058 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18973 | hp2 | a0004 | c0003 | t0001 | g0005 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18974 | hp2 | a0004 | c0003 | t0001 | g0101 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18980 | hp1 | a0004 | c0003 | t0001 | g0227 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18980 | hp2 | a0007 | c0010 | t0001 | g0006 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18982 | hp2 | a0007 | c0010 | t0001 | g0069 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18986 | hp2 | a0001 | c0014 | t0001 | g0008 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18994 | hp2 | a0001 | c0101 | t0001 | g0213 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18995 | hp1 | a0004 | c0003 | t0001 | g0007 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18995 | hp2 | a0007 | c0010 | t0001 | g0006 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18999 | hp2 | a0004 | c0097 | t0001 | g0201 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19000 | hp1 | a0052 | c0094 | t0001 | g0210 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19003 | hp1 | a0007 | c0010 | t0001 | g0006 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19005 | hp1 | a0009 | c0061 | t0001 | g0094 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19007 | hp1 | a0004 | c0003 | t0001 | g0005 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19009 | hp1 | a0002 | c0044 | t0001 | g0057 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19010 | hp2 | a0007 | c0010 | t0001 | g0006 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19011 | hp2 | a0014 | c0015 | t0001 | g0155 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19012 | hp2 | a0004 | c0003 | t0001 | g0005 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19030 | hp1 | a0005 | c0004 | t0001 | g0229 | AFR | LWK | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19030 | hp2 | a0005 | c0004 | t0001 | g0124 | AFR | LWK | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19043 | hp1 | a0053 | c0065 | t0004 | g0232 | AFR | LWK | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19043 | hp2 | a0016 | c0022 | t0001 | g0029 | AFR | LWK | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19054 | hp1 | a0005 | c0004 | t0001 | g0002 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19060 | hp2 | a0005 | c0004 | t0001 | g0147 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19063 | hp2 | a0004 | c0003 | t0001 | g0005 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19064 | hp1 | a0004 | c0003 | t0001 | g0005 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19064 | hp2 | a0014 | c0015 | t0001 | g0015 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19065 | hp1 | a0013 | c0017 | t0001 | g0020 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19066 | hp1 | a0014 | c0015 | t0001 | g0015 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19066 | hp2 | a0002 | c0062 | t0001 | g0096 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19074 | hp1 | a0008 | c0009 | t0001 | g0205 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19074 | hp2 | a0054 | c0078 | t0001 | g0181 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19082 | hp1 | a0004 | c0003 | t0001 | g0005 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19082 | hp2 | a0006 | c0006 | t0001 | g0137 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19083 | hp1 | a0001 | c0014 | t0001 | g0008 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19083 | hp2 | a0005 | c0004 | t0001 | g0002 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19084 | hp1 | a0055 | c0091 | t0001 | g0217 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19085 | hp1 | a0006 | c0006 | t0001 | g0161 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19090 | hp1 | a0001 | c0014 | t0001 | g0008 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19090 | hp2 | a0004 | c0003 | t0001 | g0199 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19091 | hp1 | a0007 | c0027 | t0001 | g0018 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19091 | hp2 | a0006 | c0006 | t0001 | g0136 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19240 | hp1 | a0056 | c0073 | t0001 | g0115 | AFR | YRI | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA19240 | hp2 | a0012 | c0013 | t0001 | g0026 | AFR | YRI | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA20752 | hp1 | a0008 | c0009 | t0001 | g0039 | EUR | TSI | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA20752 | hp2 | a0006 | c0095 | t0001 | g0169 | EUR | TSI | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA20805 | hp1 | a0002 | c0058 | t0001 | g0073 | EUR | TSI | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA20805 | hp2 | a0008 | c0009 | t0001 | g0016 | EUR | TSI | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0009 | SAS | GIH | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG01123 | hp2 | a0003 | c0007 | t0006 | g0108 | AMR | CLM | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02109 | hp1 | a0011 | c0011 | t0001 | g0017 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02109 | hp2 | a0039 | c0071 | t0001 | g0119 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02486 | hp1 | a0003 | c0005 | t0001 | g0003 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02486 | hp2 | a0016 | c0069 | t0001 | g0131 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02559 | hp1 | a0011 | c0011 | t0001 | g0046 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG02559 | hp2 | a0010 | c0031 | t0001 | g0045 | AFR | ACB | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03471 | hp1 | a0047 | c0067 | t0002 | g0123 | AFR | MSL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG03471 | hp2 | a0010 | c0031 | t0001 | g0045 | AFR | MSL | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG06807 | hp1 | a0017 | c0018 | t0001 | g0051 | AFR | USA | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
HG06807 | hp2 | a0049 | c0100 | t0001 | g0209 | AFR | USA | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18955 | hp1 | a0006 | c0006 | t0001 | g0037 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA18955 | hp2 | a0004 | c0003 | t0001 | g0220 | EAS | JPT | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA20300 | hp1 | a0001 | c0040 | t0001 | g0041 | AFR | USA | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA20300 | hp2 | a0002 | c0054 | t0001 | g0078 | AFR | USA | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA21309 | hp1 | a0007 | c0021 | t0001 | g0098 | AFR | LWK | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
NA21309 | hp2 | a0018 | c0023 | t0001 | g0143 | AFR | LWK | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
homoSapiens | chm13v2 | a0026 | c0037 | t0001 | g0141 | REF | REF | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
homoSapiens | grch38p0 | a0027 | c0068 | t0001 | g0121 | REF | REF | APOB_chr2_20996429_21049073 | APOB | chr2 | 20996429 | 21049073 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:21001971 | G | A | 4 | a0002 a0017 a0018 others(1): Show |
13 | HG01433.hp1 HG01934.hp1 HG01934.hp2 others(10): Show |
missense_variant | MODERATE | c.13451C>T | p.Thr4484Met | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 29/29 | 13579/14121 | 13451/13692 | 4484/4563 | chr2 | 21001971 | |||
chr2:21001981 | C | T | 1 | a0015 | 4 | HG01099.hp1 HG01168.hp2 HG01175.hp1 others(1): Show |
missense_variant | MODERATE | c.13441G>A | p.Ala4481Thr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 29/29 | 13569/14121 | 13441/13692 | 4481/4563 | chr2 | 21001981 | |||
chr2:21002053 | C | T | 1 | a0002 | 1 | HG01256.hp1 | missense_variant | MODERATE | c.13369G>A | p.Asp4457Asn | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 29/29 | 13497/14121 | 13369/13692 | 4457/4563 | chr2 | 21002053 | |||
chr2:21002239 | C | T | 1 | a0039 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.13183G>A | p.Gly4395Ser | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 29/29 | 13311/14121 | 13183/13692 | 4395/4563 | chr2 | 21002239 | |||
chr2:21002250 | G | A | 1 | a0002 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.13172C>T | p.Pro4391Leu | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 29/29 | 13300/14121 | 13172/13692 | 4391/4563 | chr2 | 21002250 | |||
chr2:21002409 | C | T | 36 | a0002 a0003 a0004 others(33): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
missense_variant | MODERATE | c.13013G>A | p.Ser4338Asn | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 29/29 | 13141/14121 | 13013/13692 | 4338/4563 | chr2 | 21002409 | |||
chr2:21002613 | C | G | 4 | a0002 a0005 a0037 others(1): Show |
27 | HG01081.hp2 HG01168.hp1 HG01175.hp2 others(24): Show |
missense_variant | MODERATE | c.12809G>C | p.Arg4270Thr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 29/29 | 12937/14121 | 12809/13692 | 4270/4563 | chr2 | 21002613 | |||
chr2:21002619 | A | G | 2 | a0045 a0053 |
2 | HG03209.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.12803T>C | p.Met4268Thr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 29/29 | 12931/14121 | 12803/13692 | 4268/4563 | chr2 | 21002619 | |||
chr2:21002725 | A | T | 3 | a0009 a0012 a0016 |
11 | HG01255.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
missense_variant | MODERATE | c.12697T>A | p.Ser4233Thr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 29/29 | 12825/14121 | 12697/13692 | 4233/4563 | chr2 | 21002725 | |||
chr2:21002881 | C | T | 12 | a0006 a0009 a0011 others(9): Show |
45 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(42): Show |
missense_variant | MODERATE | c.12541G>A | p.Glu4181Lys | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 29/29 | 12669/14121 | 12541/13692 | 4181/4563 | chr2 | 21002881 | |||
chr2:21004340 | C | T | 1 | a0031 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.12016G>A | p.Val4006Ile | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 28/29 | 12144/14121 | 12016/13692 | 4006/4563 | chr2 | 21004340 | |||
chr2:21005107 | C | T | 1 | a0024 | 2 | HG02132.hp2 HG02135.hp2 |
missense_variant | MODERATE | c.11761G>A | p.Val3921Ile | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 11889/14121 | 11761/13692 | 3921/4563 | chr2 | 21005107 | |||
chr2:21005955 | C | T | 2 | a0002 a0032 |
9 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(6): Show |
missense_variant | MODERATE | c.10913G>A | p.Arg3638Gln | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 11041/14121 | 10913/13692 | 3638/4563 | chr2 | 21005955 | |||
chr2:21006574 | G | C | 1 | a0002 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.10294C>G | p.Gln3432Glu | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 10422/14121 | 10294/13692 | 3432/4563 | chr2 | 21006574 | |||
chr2:21006931 | G | T | 1 | a0034 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.9937C>A | p.Leu3313Ile | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 10065/14121 | 9937/13692 | 3313/4563 | chr2 | 21006931 | |||
chr2:21006988 | A | G | 3 | a0009 a0012 a0016 |
11 | HG01255.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
missense_variant | MODERATE | c.9880T>C | p.Ser3294Pro | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 10008/14121 | 9880/13692 | 3294/4563 | chr2 | 21006988 | |||
chr2:21007033 | T | C | 2 | a0002 a0018 |
4 | HG01433.hp1 HG02630.hp1 NA18522.hp1 others(1): Show |
missense_variant | MODERATE | c.9835A>G | p.Ser3279Gly | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 9963/14121 | 9835/13692 | 3279/4563 | chr2 | 21007033 | |||
chr2:21007377 | G | A | 1 | a0055 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.9491C>T | p.Thr3164Met | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 9619/14121 | 9491/13692 | 3164/4563 | chr2 | 21007377 | |||
chr2:21007728 | G | C | 1 | a0002 | 2 | HG01934.hp1 HG02647.hp2 |
missense_variant | MODERATE | c.9140C>G | p.Thr3047Arg | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 9268/14121 | 9140/13692 | 3047/4563 | chr2 | 21007728 | |||
chr2:21008406 | G | A | 2 | a0009 a0029 |
2 | HG00323.hp1 HG00741.hp1 |
missense_variant | MODERATE | c.8462C>T | p.Pro2821Leu | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 8590/14121 | 8462/13692 | 2821/4563 | chr2 | 21008406 | |||
chr2:21008515 | T | G | 2 | a0007 a0055 |
11 | HG02083.hp1 NA18612.hp2 NA18942.hp1 others(8): Show |
missense_variant | MODERATE | c.8353A>C | p.Asn2785His | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 8481/14121 | 8353/13692 | 2785/4563 | chr2 | 21008515 | |||
chr2:21008652 | G | A | 19 | a0001 a0007 a0010 others(16): Show |
120 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(117): Show |
missense_variant | MODERATE | c.8216C>T | p.Pro2739Leu | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 8344/14121 | 8216/13692 | 2739/4563 | chr2 | 21008652 | |||
chr2:21009172 | C | T | 1 | a0020 | 2 | HG01106.hp2 HG01192.hp2 |
missense_variant | MODERATE | c.7696G>A | p.Glu2566Lys | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7824/14121 | 7696/13692 | 2566/4563 | chr2 | 21009172 | |||
chr2:21009253 | C | T | 1 | a0028 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.7615G>A | p.Val2539Ile | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7743/14121 | 7615/13692 | 2539/4563 | chr2 | 21009253 | |||
chr2:21009291 | A | G | 1 | a0040 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.7577T>C | p.Met2526Thr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7705/14121 | 7577/13692 | 2526/4563 | chr2 | 21009291 | |||
chr2:21009396 | A | G | 1 | a0037 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.7472T>C | p.Leu2491Ser | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7600/14121 | 7472/13692 | 2491/4563 | chr2 | 21009396 | |||
chr2:21009501 | G | T | 3 | a0009 a0012 a0016 |
11 | HG01255.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
missense_variant | MODERATE | c.7367C>A | p.Ala2456Asp | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7495/14121 | 7367/13692 | 2456/4563 | chr2 | 21009501 | |||
chr2:21009626 | T | G | 2 | a0045 a0053 |
2 | HG03209.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.7242A>C | p.Glu2414Asp | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7370/14121 | 7242/13692 | 2414/4563 | chr2 | 21009626 | |||
chr2:21009828 | C | T | 1 | a0030 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.7040G>A | p.Arg2347Lys | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7168/14121 | 7040/13692 | 2347/4563 | chr2 | 21009828 | |||
chr2:21009927 | A | G | 1 | a0009 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.6941T>C | p.Leu2314Pro | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7069/14121 | 6941/13692 | 2314/4563 | chr2 | 21009927 | |||
chr2:21009931 | T | C | 52 | a0001 a0002 a0003 others(49): Show |
345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
missense_variant | MODERATE | c.6937A>G | p.Ile2313Val | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7065/14121 | 6937/13692 | 2313/4563 | chr2 | 21009931 | |||
chr2:21009973 | C | G | 4 | a0002 a0009 a0038 others(1): Show |
4 | HG02055.hp2 HG03041.hp1 HG03471.hp1 others(1): Show |
missense_variant | MODERATE | c.6895G>C | p.Asp2299His | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7023/14121 | 6895/13692 | 2299/4563 | chr2 | 21009973 | |||
chr2:21011100 | T | C | 1 | a0026 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.5768A>G | p.His1923Arg | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 5896/14121 | 5768/13692 | 1923/4563 | chr2 | 21011100 | |||
chr2:21011127 | T | C | 1 | a0002 | 2 | HG01361.hp1 HG01975.hp1 |
missense_variant | MODERATE | c.5741A>G | p.Asn1914Ser | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 5869/14121 | 5741/13692 | 1914/4563 | chr2 | 21011127 | |||
chr2:21011409 | T | G | 1 | a0021 | 2 | HG01256.hp2 HG01258.hp2 |
missense_variant | MODERATE | c.5459A>C | p.Lys1820Thr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 5587/14121 | 5459/13692 | 1820/4563 | chr2 | 21011409 | |||
chr2:21012493 | T | C | 1 | a0025 | 2 | HG02572.hp2 HG02809.hp1 |
missense_variant | MODERATE | c.4375A>G | p.Ser1459Gly | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 4503/14121 | 4375/13692 | 1459/4563 | chr2 | 21012493 | |||
chr2:21013213 | C | T | 1 | a0042 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.4163G>A | p.Arg1388His | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 25/29 | 4291/14121 | 4163/13692 | 1388/4563 | chr2 | 21013213 | |||
chr2:21014578 | G | T | 1 | a0043 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.3712C>A | p.Leu1238Ile | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 24/29 | 3840/14121 | 3712/13692 | 1238/4563 | chr2 | 21014578 | |||
chr2:21015135 | G | T | 7 | a0019 a0023 a0025 others(4): Show |
11 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
missense_variant | MODERATE | c.3634C>A | p.Leu1212Met | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 23/29 | 3762/14121 | 3634/13692 | 1212/4563 | chr2 | 21015135 | |||
chr2:21015451 | G | A | 1 | a0033 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.3427C>T | p.Pro1143Ser | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 22/29 | 3555/14121 | 3427/13692 | 1143/4563 | chr2 | 21015451 | |||
chr2:21015453 | G | A | 1 | a0051 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.3425C>T | p.Ser1142Leu | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 22/29 | 3553/14121 | 3425/13692 | 1142/4563 | chr2 | 21015453 | |||
chr2:21015496 | G | A | 1 | a0056 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.3382C>T | p.Arg1128Cys | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 22/29 | 3510/14121 | 3382/13692 | 1128/4563 | chr2 | 21015496 | |||
chr2:21019061 | C | T | 1 | a0054 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.3052G>A | p.Ala1018Thr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/29 | 3180/14121 | 3052/13692 | 1018/4563 | chr2 | 21019061 | |||
chr2:21019859 | G | A | 1 | a0052 | 1 | NA19000.hp1 | missense_variant | MODERATE | c.2863C>T | p.Pro955Ser | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 19/29 | 2991/14121 | 2863/13692 | 955/4563 | chr2 | 21019859 | |||
chr2:21024971 | G | T | 1 | a0002 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.2398C>A | p.Leu800Met | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 16/29 | 2526/14121 | 2398/13692 | 800/4563 | chr2 | 21024971 | |||
chr2:21026810 | G | T | 4 | a0011 a0019 a0040 others(1): Show |
12 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
missense_variant | MODERATE | c.2222C>A | p.Thr741Asn | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 15/29 | 2350/14121 | 2222/13692 | 741/4563 | chr2 | 21026810 | |||
chr2:21026844 | C | T | 1 | a0022 | 2 | HG01261.hp2 HG01433.hp2 |
missense_variant | MODERATE | c.2188G>A | p.Val730Ile | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 15/29 | 2316/14121 | 2188/13692 | 730/4563 | chr2 | 21026844 | |||
chr2:21027842 | C | G | 1 | a0036 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.2053G>C | p.Ala685Pro | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 14/29 | 2181/14121 | 2053/13692 | 685/4563 | chr2 | 21027842 | |||
chr2:21028042 | G | A | 32 | a0001 a0004 a0006 others(29): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
missense_variant | MODERATE | c.1853C>T | p.Ala618Val | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 14/29 | 1981/14121 | 1853/13692 | 618/4563 | chr2 | 21028042 | |||
chr2:21029662 | G | A | 2 | a0004 a0009 |
26 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(23): Show |
missense_variant | MODERATE | c.1594C>T | p.Arg532Trp | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 12/29 | 1722/14121 | 1594/13692 | 532/4563 | chr2 | 21029662 | |||
chr2:21032483 | A | G | 1 | a0053 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1223T>C | p.Ile408Thr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 10/29 | 1351/14121 | 1223/13692 | 408/4563 | chr2 | 21032483 | |||
chr2:21037186 | T | C | 1 | a0038 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.607A>G | p.Ile203Val | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 6/29 | 735/14121 | 607/13692 | 203/4563 | chr2 | 21037186 | |||
chr2:21037187 | T | A | 1 | a0049 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.606A>T | p.Glu202Asp | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 6/29 | 734/14121 | 606/13692 | 202/4563 | chr2 | 21037187 | |||
chr2:21037212 | G | A | 1 | a0014 | 5 | HG02129.hp1 HG02135.hp1 NA19011.hp2 others(2): Show |
missense_variant | MODERATE | c.581C>T | p.Thr194Met | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 6/29 | 709/14121 | 581/13692 | 194/4563 | chr2 | 21037212 | |||
chr2:21038061 | G | A | 1 | a0019 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.434C>T | p.Pro145Leu | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 5/29 | 562/14121 | 434/13692 | 145/4563 | chr2 | 21038061 | |||
chr2:21038062 | G | A | 7 | a0002 a0011 a0019 others(4): Show |
16 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
missense_variant | MODERATE | c.433C>T | p.Pro145Ser | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 5/29 | 561/14121 | 433/13692 | 145/4563 | chr2 | 21038062 | |||
chr2:21041014 | A | G | 1 | a0048 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.307T>C | p.Tyr103His | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/29 | 435/14121 | 307/13692 | 103/4563 | chr2 | 21041014 | |||
chr2:21041028 | G | A | 3 | a0002 a0009 a0013 |
53 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(50): Show |
missense_variant | MODERATE | c.293C>T | p.Thr98Ile | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/29 | 421/14121 | 293/13692 | 98/4563 | chr2 | 21041028 | |||
chr2:21041038 | T | C | 1 | a0002 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.283A>G | p.Ser95Gly | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/29 | 411/14121 | 283/13692 | 95/4563 | chr2 | 21041038 | |||
chr2:21041083 | C | G | 1 | a0050 | 1 | NA18948.hp2 | missense_variant&splice_region_variant | MODERATE | c.238G>C | p.Val80Leu | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/29 | 366/14121 | 238/13692 | 80/4563 | chr2 | 21041083 | |||
chr2:21042384 | T | C | 1 | a0041 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.214A>G | p.Ser72Gly | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 3/29 | 342/14121 | 214/13692 | 72/4563 | chr2 | 21042384 | |||
chr2:21043902 | GGCAGCGC others(2): Show |
G | 5 | a0002 a0007 a0009 others(2): Show |
84 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(81): Show |
disruptive_inframe_deletion | MODERATE | c.35_43delTGGCGCTGC | p.Leu12_Leu14del | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 1/29 | 171/14121 | 35/13692 | 12/4563 | chr2 | 21043902 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:21001970 | C | T | 1 | a0004c0097 | 1 | NA18999.hp2 | synonymous_variant | LOW | c.13452G>A | p.Thr4484Thr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 29/29 | 13580/14121 | 13452/13692 | 4484/4563 | chr2 | 21001970 | |||
chr2:21001973 | C | T | 2 | a0001c0088 a0045c0074 |
2 | HG03209.hp2 NA18946.hp1 |
synonymous_variant | LOW | c.13449G>A | p.Ala4483Ala | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 29/29 | 13577/14121 | 13449/13692 | 4483/4563 | chr2 | 21001973 | |||
chr2:21002576 | C | T | 1 | a0001c0085 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.12846G>A | p.Glu4282Glu | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 29/29 | 12974/14121 | 12846/13692 | 4282/4563 | chr2 | 21002576 | |||
chr2:21002723 | C | T | 1 | a0010c0031 | 2 | HG02559.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.12699G>A | p.Ser4233Ser | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 29/29 | 12827/14121 | 12699/13692 | 4233/4563 | chr2 | 21002723 | |||
chr2:21003074 | A | G | 1 | a0002c0054 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.12348T>C | p.Tyr4116Tyr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 29/29 | 12476/14121 | 12348/13692 | 4116/4563 | chr2 | 21003074 | |||
chr2:21003170 | A | G | 1 | a0001c0036 | 2 | HG00673.hp1 NA18971.hp2 |
synonymous_variant | LOW | c.12252T>C | p.Tyr4084Tyr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 29/29 | 12380/14121 | 12252/13692 | 4084/4563 | chr2 | 21003170 | |||
chr2:21004422 | G | A | 1 | a0004c0098 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.11934C>T | p.Ile3978Ile | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 28/29 | 12062/14121 | 11934/13692 | 3978/4563 | chr2 | 21004422 | |||
chr2:21004656 | G | A | 4 | a0009c0047 a0012c0013 a0016c0022 others(1): Show |
11 | HG01255.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
synonymous_variant | LOW | c.11808C>T | p.Ile3936Ile | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 27/29 | 11936/14121 | 11808/13692 | 3936/4563 | chr2 | 21004656 | |||
chr2:21005426 | G | A | 1 | a0002c0057 | 1 | HG01258.hp1 | synonymous_variant | LOW | c.11442C>T | p.Thr3814Thr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 11570/14121 | 11442/13692 | 3814/4563 | chr2 | 21005426 | |||
chr2:21005903 | T | C | 1 | a0001c0090 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.10965A>G | p.Glu3655Glu | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 11093/14121 | 10965/13692 | 3655/4563 | chr2 | 21005903 | |||
chr2:21006131 | G | A | 2 | a0003c0005 a0056c0073 |
16 | HG01243.hp2 HG01261.hp1 HG01884.hp1 others(13): Show |
synonymous_variant | LOW | c.10737C>T | p.Thr3579Thr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 10865/14121 | 10737/13692 | 3579/4563 | chr2 | 21006131 | |||
chr2:21006167 | C | A | 1 | a0004c0098 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.10701G>T | p.Thr3567Thr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 10829/14121 | 10701/13692 | 3567/4563 | chr2 | 21006167 | |||
chr2:21006167 | C | T | 7 | a0019c0041 a0019c0104 a0023c0042 others(4): Show |
10 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(7): Show |
synonymous_variant | LOW | c.10701G>A | p.Thr3567Thr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 10829/14121 | 10701/13692 | 3567/4563 | chr2 | 21006167 | |||
chr2:21007058 | G | A | 1 | a0002c0044 | 1 | NA19009.hp1 | synonymous_variant | LOW | c.9810C>T | p.Phe3270Phe | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 9938/14121 | 9810/13692 | 3270/4563 | chr2 | 21007058 | |||
chr2:21007190 | T | A | 1 | a0001c0090 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.9678A>T | p.Thr3226Thr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 9806/14121 | 9678/13692 | 3226/4563 | chr2 | 21007190 | |||
chr2:21007391 | C | T | 2 | a0001c0014 a0050c0063 |
6 | HG00408.hp1 NA18939.hp2 NA18948.hp2 others(3): Show |
synonymous_variant | LOW | c.9477G>A | p.Lys3159Lys | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 9605/14121 | 9477/13692 | 3159/4563 | chr2 | 21007391 | |||
chr2:21007574 | G | A | 1 | a0006c0083 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.9294C>T | p.Tyr3098Tyr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 9422/14121 | 9294/13692 | 3098/4563 | chr2 | 21007574 | |||
chr2:21007864 | G | A | 1 | a0011c0011 | 7 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(4): Show |
synonymous_variant | LOW | c.9004C>T | p.Leu3002Leu | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 9132/14121 | 9004/13692 | 3002/4563 | chr2 | 21007864 | |||
chr2:21007979 | G | A | 2 | a0045c0074 a0053c0065 |
2 | HG03209.hp2 NA19043.hp1 |
synonymous_variant | LOW | c.8889C>T | p.Ile2963Ile | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 9017/14121 | 8889/13692 | 2963/4563 | chr2 | 21007979 | |||
chr2:21008399 | A | G | 2 | a0001c0085 a0001c0086 |
2 | HG03688.hp1 HG04115.hp1 |
synonymous_variant | LOW | c.8469T>C | p.Ala2823Ala | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 8597/14121 | 8469/13692 | 2823/4563 | chr2 | 21008399 | |||
chr2:21008720 | G | A | 1 | a0005c0072 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.8148C>T | p.Ile2716Ile | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 8276/14121 | 8148/13692 | 2716/4563 | chr2 | 21008720 | |||
chr2:21009323 | G | A | 16 | a0002c0002 a0002c0012 a0002c0030 others(13): Show |
79 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(76): Show |
synonymous_variant | LOW | c.7545C>T | p.Thr2515Thr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7673/14121 | 7545/13692 | 2515/4563 | chr2 | 21009323 | |||
chr2:21009932 | G | A | 16 | a0002c0002 a0002c0012 a0002c0030 others(13): Show |
79 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(76): Show |
synonymous_variant | LOW | c.6936C>T | p.Asp2312Asp | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 7064/14121 | 6936/13692 | 2312/4563 | chr2 | 21009932 | |||
chr2:21010607 | G | T | 1 | a0046c0066 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.6261C>A | p.Thr2087Thr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 6389/14121 | 6261/13692 | 2087/4563 | chr2 | 21010607 | |||
chr2:21011546 | G | A | 1 | a0007c0027 | 2 | NA18959.hp1 NA19091.hp1 |
synonymous_variant | LOW | c.5322C>T | p.Tyr1774Tyr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 5450/14121 | 5322/13692 | 1774/4563 | chr2 | 21011546 | |||
chr2:21012503 | G | A | 7 | a0019c0041 a0019c0104 a0023c0042 others(4): Show |
10 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(7): Show |
synonymous_variant | LOW | c.4365C>T | p.Phe1455Phe | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/29 | 4493/14121 | 4365/13692 | 1455/4563 | chr2 | 21012503 | |||
chr2:21016621 | T | C | 2 | a0045c0074 a0053c0065 |
2 | HG03209.hp2 NA19043.hp1 |
synonymous_variant | LOW | c.3150A>G | p.Thr1050Thr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 21/29 | 3278/14121 | 3150/13692 | 1050/4563 | chr2 | 21016621 | |||
chr2:21019899 | T | C | 1 | a0010c0075 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.2823A>G | p.Thr941Thr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 19/29 | 2951/14121 | 2823/13692 | 941/4563 | chr2 | 21019899 | |||
chr2:21022941 | G | A | 3 | a0006c0095 a0020c0039 a0033c0096 |
4 | HG00738.hp2 HG01106.hp2 HG01192.hp2 others(1): Show |
synonymous_variant | LOW | c.2706C>T | p.Asn902Asn | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/29 | 2834/14121 | 2706/13692 | 902/4563 | chr2 | 21022941 | |||
chr2:21027992 | G | T | 1 | a0006c0076 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.1903C>A | p.Arg635Arg | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 14/29 | 2031/14121 | 1903/13692 | 635/4563 | chr2 | 21027992 | |||
chr2:21028371 | G | C | 1 | a0001c0040 | 2 | HG02148.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.1785C>G | p.Ser595Ser | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 13/29 | 1913/14121 | 1785/13692 | 595/4563 | chr2 | 21028371 | |||
chr2:21037220 | G | A | 1 | a0001c0101 | 1 | NA18994.hp2 | synonymous_variant | LOW | c.573C>T | p.Thr191Thr | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 6/29 | 701/14121 | 573/13692 | 191/4563 | chr2 | 21037220 | |||
chr2:21042469 | C | G | 1 | a0016c0022 | 3 | HG01255.hp1 HG01891.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.129G>C | p.Ala43Ala | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 3/29 | 257/14121 | 129/13692 | 43/4563 | chr2 | 21042469 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:21001501 | T | C | 2 | a0002c0012t0003 a0032c0092t0003 |
3 | HG00738.hp1 HG01069.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*229A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 29/29 | 229 | chr2 | 21001501 | ||||||
chr2:21001550 | C | A | 4 | a0002c0052t0002 a0009c0046t0002 a0038c0099t0002 others(1): Show |
4 | HG02055.hp2 HG03041.hp1 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*180G>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 29/29 | 180 | chr2 | 21001550 | ||||||
chr2:21001551 | G | A | 1 | a0003c0007t0006 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*179C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 29/29 | 179 | chr2 | 21001551 | ||||||
chr2:21001719 | C | A | 4 | a0002c0052t0002 a0009c0046t0002 a0038c0099t0002 others(1): Show |
4 | HG02055.hp2 HG03041.hp1 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*11G>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 29/29 | 11 | chr2 | 21001719 | ||||||
chr2:21044024 | A | G | 1 | a0004c0003t0005 | 1 | HG00544.hp2 | 5_prime_UTR_variant | MODIFIER | c.-79T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 1/29 | 79 | chr2 | 21044024 | ||||||
chr2:21044060 | G | C | 3 | a0010c0019t0004 a0043c0103t0004 a0053c0065t0004 |
3 | HG02630.hp2 HG02647.hp1 NA19043.hp1 |
5_prime_UTR_variant | MODIFIER | c.-115C>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 1/29 | 115 | chr2 | 21044060 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:21003380 | A | G | 18 | a0002c0024t0001g0059 a0002c0024t0001g0070 a0002c0028t0001g0075 others(15): Show |
27 | HG01081.hp2 HG01168.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.12088-46T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 28/28 | chr2 | 21003380 | |||||||
chr2:21003688 | A | G | 153 | a0001c0001t0001g0186 a0002c0002t0001g0004 a0002c0002t0001g0009 others(150): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.12088-354T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 28/28 | chr2 | 21003688 | |||||||
chr2:21003722 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.12088-388G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 28/28 | chr2 | 21003722 | |||||||
chr2:21003904 | A | C | 8 | a0009c0047t0001g0062 a0012c0013t0001g0025 a0012c0013t0001g0026 others(5): Show |
11 | HG01255.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.12087+365T>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 28/28 | chr2 | 21003904 | |||||||
chr2:21003966 | C | A | 1 | a0003c0005t0001g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.12087+303G>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 28/28 | chr2 | 21003966 | |||||||
chr2:21004459 | G | A | 9 | a0002c0025t0001g0019 a0002c0043t0001g0071 a0002c0050t0001g0061 others(6): Show |
12 | HG01433.hp1 HG01934.hp1 HG02280.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.11904-7C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 27/28 | chr2 | 21004459 | |||||||
chr2:21004473 | G | A | 1 | a0034c0082t0001g0167 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.11904-21C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 27/28 | chr2 | 21004473 | |||||||
chr2:21004511 | C | G | 31 | a0002c0025t0001g0019 a0002c0029t0001g0085 a0002c0043t0001g0071 others(28): Show |
38 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.11903+50G>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 27/28 | chr2 | 21004511 | |||||||
chr2:21004905 | A | G | 1 | a0004c0097t0001g0201 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.11788+175T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/28 | chr2 | 21004905 | |||||||
chr2:21004979 | G | C | 2 | a0002c0025t0001g0019 a0002c0043t0001g0071 |
3 | HG01934.hp1 HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.11788+101C>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 26/28 | chr2 | 21004979 | |||||||
chr2:21012747 | T | C | 2 | a0045c0074t0001g0129 a0053c0065t0004g0232 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4217-96A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 25/28 | chr2 | 21012747 | |||||||
chr2:21012881 | C | A | 1 | a0004c0097t0001g0201 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.4217-230G>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 25/28 | chr2 | 21012881 | |||||||
chr2:21012956 | C | T | 1 | a0007c0010t0001g0069 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.4216+204G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 25/28 | chr2 | 21012956 | |||||||
chr2:21012976 | G | T | 4 | a0002c0052t0002g0077 a0009c0046t0002g0066 a0038c0099t0002g0230 others(1): Show |
4 | HG02055.hp2 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.4216+184C>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 25/28 | chr2 | 21012976 | |||||||
chr2:21012990 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4216+170G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 25/28 | chr2 | 21012990 | |||||||
chr2:21013610 | A | G | 229 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(226): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.3843-77T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 24/28 | chr2 | 21013610 | |||||||
chr2:21013720 | A | G | 1 | a0005c0004t0001g0147 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3843-187T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 24/28 | chr2 | 21013720 | |||||||
chr2:21013861 | C | A | 1 | a0004c0003t0001g0042 | 2 | HG02132.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.3843-328G>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 24/28 | chr2 | 21013861 | |||||||
chr2:21013960 | A | G | 1 | a0046c0066t0001g0122 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3843-427T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 24/28 | chr2 | 21013960 | |||||||
chr2:21014158 | T | C | 6 | a0002c0025t0001g0019 a0002c0043t0001g0071 a0002c0053t0001g0072 others(3): Show |
7 | HG01433.hp1 HG01934.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.3842+290A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 24/28 | chr2 | 21014158 | |||||||
chr2:21014235 | C | T | 8 | a0009c0047t0001g0062 a0012c0013t0001g0025 a0012c0013t0001g0026 others(5): Show |
11 | HG01255.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.3842+213G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 24/28 | chr2 | 21014235 | |||||||
chr2:21014274 | G | A | 1 | a0044c0045t0001g0067 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3842+174C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 24/28 | chr2 | 21014274 | |||||||
chr2:21014365 | T | A | 1 | a0001c0001t0001g0189 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3842+83A>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 24/28 | chr2 | 21014365 | |||||||
chr2:21014366 | A | T | 22 | a0002c0029t0001g0085 a0006c0006t0001g0035 a0006c0006t0001g0037 others(19): Show |
26 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.3842+82T>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 24/28 | chr2 | 21014366 | |||||||
chr2:21014370 | A | C | 8 | a0009c0047t0001g0062 a0012c0013t0001g0025 a0012c0013t0001g0026 others(5): Show |
11 | HG01255.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.3842+78T>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 24/28 | chr2 | 21014370 | |||||||
chr2:21014672 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(75): Show |
124 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.3697-79C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 23/28 | chr2 | 21014672 | |||||||
chr2:21014747 | G | A | 1 | a0008c0009t0001g0164 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3697-154C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 23/28 | chr2 | 21014747 | |||||||
chr2:21014803 | C | A | 1 | a0001c0001t0001g0190 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3697-210G>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 23/28 | chr2 | 21014803 | |||||||
chr2:21014914 | T | G | 26 | a0002c0029t0001g0074 a0003c0007t0001g0048 a0003c0007t0001g0049 others(23): Show |
39 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.3696+159A>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 23/28 | chr2 | 21014914 | |||||||
chr2:21014926 | A | G | 1 | a0045c0074t0001g0129 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3696+147T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 23/28 | chr2 | 21014926 | |||||||
chr2:21014980 | C | T | 1 | a0012c0013t0001g0203 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3696+93G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 23/28 | chr2 | 21014980 | |||||||
chr2:21015270 | C | T | 8 | a0009c0047t0001g0062 a0012c0013t0001g0025 a0012c0013t0001g0026 others(5): Show |
11 | HG01255.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.3509-10G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 22/28 | chr2 | 21015270 | |||||||
chr2:21015644 | T | C | 1 | a0015c0020t0001g0044 | 2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.3333-99A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 21/28 | chr2 | 21015644 | |||||||
chr2:21015892 | C | T | 1 | a0002c0024t0001g0059 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3333-347G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 21/28 | chr2 | 21015892 | |||||||
chr2:21015926 | T | A | 2 | a0023c0042t0001g0225 a0023c0042t0001g0226 |
2 | HG01891.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3333-381A>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 21/28 | chr2 | 21015926 | |||||||
chr2:21016025 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(205): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.3332+414A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 21/28 | chr2 | 21016025 | |||||||
chr2:21016112 | A | G | 2 | a0009c0060t0001g0093 a0029c0084t0001g0175 |
2 | HG00323.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.3332+327T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 21/28 | chr2 | 21016112 | |||||||
chr2:21016121 | C | A | 3 | a0003c0008t0001g0150 a0003c0008t0001g0152 a0003c0008t0001g0153 |
3 | HG00642.hp1 HG03710.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.3332+318G>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 21/28 | chr2 | 21016121 | |||||||
chr2:21016211 | T | A | 1 | a0010c0019t0001g0030 | 2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3332+228A>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 21/28 | chr2 | 21016211 | |||||||
chr2:21016286 | C | CA | 5 | a0012c0013t0001g0026 a0012c0013t0001g0100 a0044c0045t0001g0067 others(2): Show |
6 | HG02451.hp2 HG03041.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.3332+152dupT | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 21/28 | chr2 | 21016286 | |||||||
chr2:21016712 | C | T | 4 | a0002c0028t0001g0075 a0002c0029t0001g0085 a0006c0006t0001g0035 others(1): Show |
5 | HG00558.hp1 HG00673.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.3122-63G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016712 | |||||||
chr2:21016713 | G | A | 2 | a0002c0052t0002g0077 a0038c0099t0002g0230 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3122-64C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016713 | |||||||
chr2:21016718 | C | A | 1 | a0009c0059t0001g0092 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3122-69G>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016718 | |||||||
chr2:21016723 | A | G | 2 | a0008c0009t0001g0016 a0009c0059t0001g0092 |
4 | HG00642.hp2 HG01109.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.3122-74T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016723 | |||||||
chr2:21016739 | C | G | 1 | a0008c0009t0001g0016 | 3 | HG00642.hp2 HG02055.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.3122-90G>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016739 | |||||||
chr2:21016751 | A | G | 3 | a0006c0006t0001g0136 a0006c0006t0001g0137 a0010c0019t0004g0231 |
3 | HG02630.hp2 NA19082.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3122-102T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016751 | |||||||
chr2:21016755 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3122-106G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016755 | |||||||
chr2:21016789 | T | C | 35 | a0001c0001t0001g0192 a0001c0036t0001g0218 a0002c0024t0001g0059 others(32): Show |
54 | HG00733.hp2 HG01069.hp2 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.3122-140A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016789 | |||||||
chr2:21016793 | G | A | 1 | a0002c0062t0001g0096 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3122-144C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016793 | |||||||
chr2:21016795 | T | C | 18 | a0001c0001t0001g0178 a0002c0002t0001g0004 a0002c0002t0001g0009 others(15): Show |
33 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.3122-146A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016795 | |||||||
chr2:21016799 | A | G | 1 | a0002c0062t0001g0096 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3122-150T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016799 | |||||||
chr2:21016800 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3122-151A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016800 | |||||||
chr2:21016840 | C | T | 2 | a0001c0001t0001g0197 a0023c0042t0001g0225 |
2 | HG01891.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.3122-191G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016840 | |||||||
chr2:21016847 | G | A | 2 | a0003c0007t0001g0104 a0003c0007t0001g0105 |
2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3122-198C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016847 | |||||||
chr2:21016856 | T | C | 2 | a0032c0092t0003g0179 a0049c0100t0001g0209 |
2 | HG00738.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3122-207A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016856 | |||||||
chr2:21016900 | C | T | 1 | a0005c0072t0001g0118 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3122-251G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016900 | |||||||
chr2:21016901 | A | G | 3 | a0002c0002t0001g0013 a0005c0004t0001g0032 a0005c0072t0001g0118 |
6 | HG01175.hp2 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.3122-252T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016901 | |||||||
chr2:21016946 | T | A | 1 | a0049c0100t0001g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3122-297A>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016946 | |||||||
chr2:21016983 | C | CAAA | 21 | a0003c0007t0001g0027 a0005c0004t0001g0229 a0006c0006t0001g0035 others(18): Show |
25 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.3122-337_3122-335d others(5): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016983 | |||||||
chr2:21016983 | C | CAAAA | 5 | a0005c0004t0001g0032 a0005c0004t0001g0124 a0005c0004t0001g0125 others(2): Show |
6 | HG01346.hp1 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3122-338_3122-335d others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016983 | |||||||
chr2:21016986 | AAAAT | A | 6 | a0001c0001t0001g0194 a0001c0014t0001g0008 a0017c0018t0001g0050 others(3): Show |
12 | HG00408.hp1 HG02615.hp1 HG03098.hp1 others(9): Show |
intron_variant | MODIFIER | c.3122-341_3122-338d others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016986 | |||||||
chr2:21016988 | AAT | A | 3 | a0016c0022t0001g0029 a0016c0022t0001g0103 a0016c0069t0001g0131 |
4 | HG01255.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3122-341_3122-340d others(4): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016988 | |||||||
chr2:21016989 | AT | A | 15 | a0002c0002t0001g0023 a0002c0002t0001g0088 a0004c0003t0001g0007 others(12): Show |
16 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.3122-341delA | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016989 | |||||||
chr2:21016990 | T | A | 104 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0013 others(101): Show |
157 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.3122-341A>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016990 | |||||||
chr2:21016994 | T | A | 74 | a0002c0002t0001g0023 a0002c0002t0001g0088 a0002c0012t0001g0024 others(71): Show |
105 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.3122-345A>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016994 | |||||||
chr2:21016995 | A | AAAAAT | 8 | a0002c0024t0001g0059 a0002c0024t0001g0070 a0002c0028t0001g0075 others(5): Show |
16 | HG01081.hp2 HG01168.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.3122-347_3122-346i others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016995 | |||||||
chr2:21016995 | A | AAAAT | 11 | a0002c0029t0001g0074 a0002c0052t0002g0077 a0003c0007t0001g0048 others(8): Show |
13 | HG00733.hp2 HG01069.hp2 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.3122-347_3122-346i others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016995 | |||||||
chr2:21016995 | A | AAT | 8 | a0002c0025t0001g0019 a0002c0043t0001g0071 a0002c0053t0001g0072 others(5): Show |
9 | HG01433.hp1 HG01934.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3122-347_3122-346i others(4): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016995 | |||||||
chr2:21016998 | T | A | 15 | a0003c0007t0001g0145 a0004c0003t0001g0007 a0004c0003t0001g0199 others(12): Show |
20 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.3122-349A>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016998 | |||||||
chr2:21016998 | TA | T | 10 | a0019c0041t0001g0222 a0019c0041t0001g0224 a0019c0104t0001g0148 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.3122-350delT | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21016998 | |||||||
chr2:21017010 | T | C | 1 | a0020c0039t0001g0036 | 2 | HG01106.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.3122-361A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017010 | |||||||
chr2:21017010 | TAAATAAA others(29): Show |
T | 2 | a0002c0002t0001g0091 a0002c0002t0001g0095 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3122-397_3122-362d others(38): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017010 | |||||||
chr2:21017012 | A | T | 38 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0013 others(35): Show |
65 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.3122-363T>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017012 | |||||||
chr2:21017014 | T | C | 23 | a0001c0001t0001g0158 a0003c0007t0001g0027 a0006c0006t0001g0035 others(20): Show |
27 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.3122-365A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017014 | |||||||
chr2:21017018 | C | T | 11 | a0018c0023t0001g0143 a0019c0041t0001g0222 a0019c0041t0001g0224 others(8): Show |
11 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.3122-369G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017018 | |||||||
chr2:21017022 | CAAAT | C | 2 | a0016c0022t0001g0029 a0016c0022t0001g0103 |
3 | HG01255.hp1 HG01891.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3122-377_3122-374d others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017022 | |||||||
chr2:21017026 | T | C | 12 | a0009c0046t0002g0066 a0019c0041t0001g0222 a0019c0041t0001g0224 others(9): Show |
12 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.3122-377A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017026 | |||||||
chr2:21017042 | TAAAG | T | 38 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0013 others(35): Show |
65 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.3122-397_3122-394d others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017042 | |||||||
chr2:21017046 | G | T | 1 | a0053c0065t0004g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3122-397C>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017046 | |||||||
chr2:21017106 | C | T | 1 | a0010c0075t0001g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3122-457G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017106 | |||||||
chr2:21017139 | A | AT | 44 | a0003c0007t0001g0027 a0003c0007t0001g0145 a0004c0003t0001g0005 others(41): Show |
61 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.3122-491dupA | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017139 | |||||||
chr2:21017149 | T | C | 1 | a0005c0004t0001g0216 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3122-500A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017149 | |||||||
chr2:21017159 | A | C | 148 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0013 others(145): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.3122-510T>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017159 | |||||||
chr2:21017173 | C | T | 2 | a0045c0074t0001g0129 a0053c0065t0004g0232 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3122-524G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017173 | |||||||
chr2:21017239 | T | A | 1 | a0046c0066t0001g0122 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3122-590A>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017239 | |||||||
chr2:21017251 | G | A | 3 | a0011c0011t0001g0017 a0011c0011t0001g0046 a0011c0011t0001g0047 |
7 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.3122-602C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017251 | |||||||
chr2:21017254 | C | T | 1 | a0046c0066t0001g0122 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3122-605G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017254 | |||||||
chr2:21017269 | G | T | 14 | a0005c0004t0001g0229 a0009c0046t0002g0066 a0019c0041t0001g0222 others(11): Show |
14 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.3122-620C>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017269 | |||||||
chr2:21017276 | G | A | 1 | a0042c0079t0001g0195 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3122-627C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017276 | |||||||
chr2:21017492 | A | G | 150 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0013 others(147): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.3122-843T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017492 | |||||||
chr2:21017504 | C | T | 3 | a0010c0019t0001g0120 a0013c0017t0001g0090 a0039c0071t0001g0119 |
3 | HG01167.hp2 HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3122-855G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017504 | |||||||
chr2:21017536 | G | A | 1 | a0010c0075t0001g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3122-887C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017536 | |||||||
chr2:21017631 | C | T | 6 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0001g0097 others(3): Show |
10 | HG01243.hp1 HG01255.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.3122-982G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017631 | |||||||
chr2:21017690 | C | T | 4 | a0005c0004t0001g0229 a0009c0046t0002g0066 a0044c0045t0001g0067 others(1): Show |
4 | HG03041.hp1 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3122-1041G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017690 | |||||||
chr2:21017842 | C | T | 3 | a0016c0022t0001g0029 a0016c0022t0001g0103 a0016c0069t0001g0131 |
4 | HG01255.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3121+1150G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21017842 | |||||||
chr2:21018016 | C | A | 1 | a0002c0016t0001g0056 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3121+976G>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21018016 | |||||||
chr2:21018066 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3121+926G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21018066 | |||||||
chr2:21018087 | G | T | 1 | a0038c0099t0002g0230 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3121+905C>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21018087 | |||||||
chr2:21018124 | C | T | 3 | a0011c0011t0001g0017 a0011c0011t0001g0046 a0011c0011t0001g0047 |
7 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.3121+868G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21018124 | |||||||
chr2:21018283 | T | G | 3 | a0016c0022t0001g0029 a0016c0022t0001g0103 a0016c0069t0001g0131 |
4 | HG01255.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3121+709A>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21018283 | |||||||
chr2:21018298 | A | C | 11 | a0010c0075t0001g0102 a0019c0041t0001g0222 a0019c0041t0001g0224 others(8): Show |
11 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.3121+694T>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21018298 | |||||||
chr2:21018339 | G | A | 3 | a0025c0033t0001g0134 a0025c0033t0001g0173 a0043c0103t0004g0233 |
3 | HG02572.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3121+653C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21018339 | |||||||
chr2:21018418 | C | T | 1 | a0005c0004t0001g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3121+574G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21018418 | |||||||
chr2:21018633 | A | G | 39 | a0002c0016t0001g0054 a0002c0024t0001g0059 a0002c0024t0001g0070 others(36): Show |
50 | HG00733.hp2 HG01069.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.3121+359T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21018633 | |||||||
chr2:21018770 | T | C | 1 | a0003c0007t0001g0048 | 2 | HG00733.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3121+222A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21018770 | |||||||
chr2:21018872 | C | T | 19 | a0006c0006t0001g0035 a0006c0006t0001g0109 a0006c0006t0001g0130 others(16): Show |
22 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.3121+120G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 20/28 | chr2 | 21018872 | |||||||
chr2:21019364 | G | A | 1 | a0010c0075t0001g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3000-251C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 19/28 | chr2 | 21019364 | |||||||
chr2:21019457 | C | A | 1 | a0049c0100t0001g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2999+266G>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 19/28 | chr2 | 21019457 | |||||||
chr2:21019457 | C | T | 1 | a0004c0003t0001g0200 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2999+266G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 19/28 | chr2 | 21019457 | |||||||
chr2:21019458 | G | A | 1 | a0003c0008t0001g0153 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2999+265C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 19/28 | chr2 | 21019458 | |||||||
chr2:21019531 | A | G | 1 | a0012c0013t0001g0100 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2999+192T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 19/28 | chr2 | 21019531 | |||||||
chr2:21019628 | G | C | 1 | a0002c0016t0001g0053 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2999+95C>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 19/28 | chr2 | 21019628 | |||||||
chr2:21019917 | C | T | 1 | a0007c0010t0001g0064 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2817-12G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21019917 | |||||||
chr2:21019924 | A | C | 1 | a0006c0006t0001g0180 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2817-19T>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21019924 | |||||||
chr2:21019976 | G | A | 1 | a0007c0010t0001g0069 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2817-71C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21019976 | |||||||
chr2:21020172 | C | G | 1 | a0015c0020t0001g0204 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2817-267G>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21020172 | |||||||
chr2:21020213 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2817-308C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21020213 | |||||||
chr2:21020310 | C | T | 1 | a0006c0006t0001g0130 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2817-405G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21020310 | |||||||
chr2:21020463 | C | T | 1 | a0018c0023t0001g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2817-558G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21020463 | |||||||
chr2:21020572 | G | A | 3 | a0016c0022t0001g0029 a0016c0022t0001g0103 a0016c0069t0001g0131 |
4 | HG01255.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2817-667C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21020572 | |||||||
chr2:21020740 | G | A | 3 | a0016c0022t0001g0029 a0016c0022t0001g0103 a0016c0069t0001g0131 |
4 | HG01255.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2817-835C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21020740 | |||||||
chr2:21020782 | T | C | 3 | a0016c0022t0001g0029 a0016c0022t0001g0103 a0016c0069t0001g0131 |
4 | HG01255.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2817-877A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21020782 | |||||||
chr2:21020783 | G | A | 3 | a0011c0011t0001g0017 a0011c0011t0001g0046 a0011c0011t0001g0047 |
7 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2817-878C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21020783 | |||||||
chr2:21021120 | C | T | 1 | a0002c0016t0001g0053 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2817-1215G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21021120 | |||||||
chr2:21021128 | G | T | 40 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0013 others(37): Show |
69 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.2817-1223C>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21021128 | |||||||
chr2:21021152 | A | G | 1 | a0014c0015t0001g0155 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2817-1247T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21021152 | |||||||
chr2:21021218 | G | A | 1 | a0002c0029t0001g0085 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2817-1313C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21021218 | |||||||
chr2:21021371 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2816+1460G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21021371 | |||||||
chr2:21021388 | G | C | 1 | a0001c0040t0001g0041 | 2 | HG02148.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2816+1443C>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21021388 | |||||||
chr2:21021447 | G | A | 4 | a0011c0011t0001g0017 a0011c0011t0001g0046 a0011c0011t0001g0047 others(1): Show |
8 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2816+1384C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21021447 | |||||||
chr2:21021486 | T | G | 37 | a0001c0001t0001g0001 a0001c0001t0001g0158 a0001c0001t0001g0162 others(34): Show |
64 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.2816+1345A>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21021486 | |||||||
chr2:21021559 | A | C | 3 | a0016c0022t0001g0029 a0016c0022t0001g0103 a0016c0069t0001g0131 |
4 | HG01255.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2816+1272T>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21021559 | |||||||
chr2:21021559 | A | T | 1 | a0001c0001t0001g0214 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2816+1272T>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21021559 | |||||||
chr2:21021784 | C | T | 1 | a0003c0008t0001g0150 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2816+1047G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21021784 | |||||||
chr2:21021925 | A | G | 10 | a0019c0041t0001g0222 a0019c0041t0001g0224 a0019c0104t0001g0148 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2816+906T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21021925 | |||||||
chr2:21022052 | C | T | 1 | a0013c0026t0001g0058 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2816+779G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21022052 | |||||||
chr2:21022110 | C | A | 1 | a0001c0001t0001g0171 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2816+721G>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21022110 | |||||||
chr2:21022112 | C | T | 2 | a0005c0004t0001g0229 a0046c0066t0001g0122 |
2 | HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2816+719G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21022112 | |||||||
chr2:21022140 | T | A | 1 | a0010c0075t0001g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2816+691A>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21022140 | |||||||
chr2:21022206 | G | A | 1 | a0006c0006t0001g0168 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2816+625C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21022206 | |||||||
chr2:21022332 | A | G | 1 | a0038c0099t0002g0230 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2816+499T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21022332 | |||||||
chr2:21022434 | C | G | 1 | a0009c0046t0002g0066 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2816+397G>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21022434 | |||||||
chr2:21022457 | G | T | 142 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0013 others(139): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.2816+374C>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21022457 | |||||||
chr2:21022495 | A | G | 57 | a0002c0024t0001g0059 a0002c0024t0001g0070 a0002c0025t0001g0019 others(54): Show |
74 | HG00733.hp2 HG01069.hp2 HG01081.hp2 others(71): Show |
intron_variant | MODIFIER | c.2816+336T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 18/28 | chr2 | 21022495 | |||||||
chr2:21023265 | A | T | 6 | a0002c0025t0001g0019 a0002c0043t0001g0071 a0002c0053t0001g0072 others(3): Show |
7 | HG01433.hp1 HG01934.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2605-223T>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 17/28 | chr2 | 21023265 | |||||||
chr2:21023335 | A | G | 14 | a0016c0022t0001g0029 a0016c0022t0001g0103 a0016c0069t0001g0131 others(11): Show |
15 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.2604+190T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 17/28 | chr2 | 21023335 | |||||||
chr2:21023434 | G | C | 56 | a0002c0024t0001g0059 a0002c0024t0001g0070 a0002c0025t0001g0019 others(53): Show |
73 | HG00733.hp2 HG01069.hp2 HG01081.hp2 others(70): Show |
intron_variant | MODIFIER | c.2604+91C>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 17/28 | chr2 | 21023434 | |||||||
chr2:21023441 | C | T | 1 | a0015c0020t0001g0204 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2604+84G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 17/28 | chr2 | 21023441 | |||||||
chr2:21023510 | C | G | 1 | a0003c0007t0001g0048 | 2 | HG00733.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.2604+15G>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 17/28 | chr2 | 21023510 | |||||||
chr2:21023947 | A | G | 1 | a0005c0004t0001g0124 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2437-255T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 16/28 | chr2 | 21023947 | |||||||
chr2:21024089 | G | A | 1 | a0046c0066t0001g0122 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2437-397C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 16/28 | chr2 | 21024089 | |||||||
chr2:21024151 | T | C | 1 | a0010c0075t0001g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2437-459A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 16/28 | chr2 | 21024151 | |||||||
chr2:21024193 | T | A | 16 | a0003c0007t0001g0145 a0004c0003t0001g0005 a0004c0003t0001g0007 others(13): Show |
27 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.2437-501A>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 16/28 | chr2 | 21024193 | |||||||
chr2:21024303 | C | T | 2 | a0009c0046t0002g0066 a0044c0045t0001g0067 |
2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2437-611G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 16/28 | chr2 | 21024303 | |||||||
chr2:21024339 | C | T | 40 | a0003c0007t0001g0145 a0004c0003t0001g0005 a0004c0003t0001g0007 others(37): Show |
56 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.2436+594G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 16/28 | chr2 | 21024339 | |||||||
chr2:21024415 | C | T | 1 | a0002c0016t0001g0053 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2436+518G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 16/28 | chr2 | 21024415 | |||||||
chr2:21024857 | C | T | 3 | a0003c0005t0001g0031 a0003c0005t0001g0112 a0003c0005t0001g0113 |
4 | HG01243.hp2 HG02897.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2436+76G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 16/28 | chr2 | 21024857 | |||||||
chr2:21024893 | G | A | 2 | a0045c0074t0001g0129 a0053c0065t0004g0232 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2436+40C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 16/28 | chr2 | 21024893 | |||||||
chr2:21025383 | G | A | 1 | a0002c0012t0001g0086 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2245-259C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 15/28 | chr2 | 21025383 | |||||||
chr2:21025613 | A | G | 1 | a0047c0067t0002g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2245-489T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 15/28 | chr2 | 21025613 | |||||||
chr2:21025790 | C | T | 6 | a0002c0025t0001g0019 a0002c0043t0001g0071 a0002c0053t0001g0072 others(3): Show |
7 | HG01433.hp1 HG01934.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2245-666G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 15/28 | chr2 | 21025790 | |||||||
chr2:21025850 | A | G | 1 | a0009c0059t0001g0092 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2245-726T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 15/28 | chr2 | 21025850 | |||||||
chr2:21025965 | A | G | 6 | a0002c0025t0001g0019 a0002c0043t0001g0071 a0002c0053t0001g0072 others(3): Show |
7 | HG01433.hp1 HG01934.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2244+823T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 15/28 | chr2 | 21025965 | |||||||
chr2:21026026 | C | T | 1 | a0014c0015t0001g0154 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2244+762G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 15/28 | chr2 | 21026026 | |||||||
chr2:21026282 | CT | C | 5 | a0009c0046t0002g0066 a0016c0022t0001g0029 a0016c0022t0001g0103 others(2): Show |
6 | HG01255.hp1 HG01891.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2244+505delA | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 15/28 | chr2 | 21026282 | |||||||
chr2:21026308 | C | T | 1 | a0049c0100t0001g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2244+480G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 15/28 | chr2 | 21026308 | |||||||
chr2:21026309 | G | A | 1 | a0002c0058t0001g0073 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2244+479C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 15/28 | chr2 | 21026309 | |||||||
chr2:21026532 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2244+256T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 15/28 | chr2 | 21026532 | |||||||
chr2:21026544 | A | G | 1 | a0010c0075t0001g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2244+244T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 15/28 | chr2 | 21026544 | |||||||
chr2:21026574 | A | G | 1 | a0049c0100t0001g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2244+214T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 15/28 | chr2 | 21026574 | |||||||
chr2:21026785 | C | T | 3 | a0016c0022t0001g0029 a0016c0022t0001g0103 a0016c0069t0001g0131 |
4 | HG01255.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.2244+3G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 15/28 | chr2 | 21026785 | |||||||
chr2:21026995 | A | G | 1 | a0004c0003t0001g0140 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2068-31T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 14/28 | chr2 | 21026995 | |||||||
chr2:21026999 | G | T | 1 | a0053c0065t0004g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2068-35C>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 14/28 | chr2 | 21026999 | |||||||
chr2:21027306 | A | AT | 20 | a0002c0044t0001g0057 a0003c0007t0001g0104 a0003c0007t0001g0145 others(17): Show |
23 | HG01346.hp1 HG01496.hp2 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.2068-343dupA | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 14/28 | chr2 | 21027306 | |||||||
chr2:21027306 | A | ATTT | 37 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0013 others(34): Show |
64 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.2068-345_2068-343d others(5): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 14/28 | chr2 | 21027306 | |||||||
chr2:21027306 | A | ATTTT | 4 | a0002c0062t0001g0096 a0003c0005t0001g0112 a0003c0008t0001g0010 others(1): Show |
8 | HG01070.hp1 HG01106.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.2068-346_2068-343d others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 14/28 | chr2 | 21027306 | |||||||
chr2:21027306 | AT | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(73): Show |
125 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.2068-343delA | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 14/28 | chr2 | 21027306 | |||||||
chr2:21027306 | ATT | A | 6 | a0009c0046t0002g0066 a0016c0022t0001g0029 a0016c0022t0001g0103 others(3): Show |
7 | HG01255.hp1 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2068-344_2068-343d others(4): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 14/28 | chr2 | 21027306 | |||||||
chr2:21027351 | G | A | 43 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0013 others(40): Show |
74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.2068-387C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 14/28 | chr2 | 21027351 | |||||||
chr2:21027367 | A | T | 11 | a0011c0011t0001g0017 a0011c0011t0001g0046 a0011c0011t0001g0047 others(8): Show |
15 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2068-403T>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 14/28 | chr2 | 21027367 | |||||||
chr2:21027383 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2068-419C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 14/28 | chr2 | 21027383 | |||||||
chr2:21027415 | G | A | 1 | a0004c0003t0001g0140 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2067+413C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 14/28 | chr2 | 21027415 | |||||||
chr2:21027564 | C | A | 4 | a0002c0025t0001g0019 a0002c0043t0001g0071 a0005c0004t0001g0229 others(1): Show |
5 | HG01934.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2067+264G>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 14/28 | chr2 | 21027564 | |||||||
chr2:21027593 | G | A | 4 | a0002c0025t0001g0019 a0002c0043t0001g0071 a0005c0004t0001g0229 others(1): Show |
5 | HG01934.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2067+235C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 14/28 | chr2 | 21027593 | |||||||
chr2:21027741 | C | T | 1 | a0047c0067t0002g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2067+87G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 14/28 | chr2 | 21027741 | |||||||
chr2:21028168 | T | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(199): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1830-103A>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 13/28 | chr2 | 21028168 | |||||||
chr2:21028841 | G | A | 8 | a0003c0005t0001g0003 a0003c0005t0001g0031 a0003c0005t0001g0112 others(5): Show |
16 | HG01243.hp2 HG01261.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1618-303C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 12/28 | chr2 | 21028841 | |||||||
chr2:21028928 | T | C | 8 | a0002c0016t0001g0053 a0002c0016t0001g0054 a0002c0016t0001g0055 others(5): Show |
9 | HG02257.hp2 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1618-390A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 12/28 | chr2 | 21028928 | |||||||
chr2:21028946 | G | A | 1 | a0008c0034t0001g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1618-408C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 12/28 | chr2 | 21028946 | |||||||
chr2:21029224 | C | T | 1 | a0002c0050t0001g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1617+415G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 12/28 | chr2 | 21029224 | |||||||
chr2:21029225 | G | A | 1 | a0010c0075t0001g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1617+414C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 12/28 | chr2 | 21029225 | |||||||
chr2:21029231 | C | T | 1 | a0008c0009t0001g0164 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1617+408G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 12/28 | chr2 | 21029231 | |||||||
chr2:21029312 | G | A | 1 | a0016c0069t0001g0131 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1617+327C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 12/28 | chr2 | 21029312 | |||||||
chr2:21029432 | A | G | 2 | a0010c0019t0004g0231 a0010c0031t0001g0045 |
3 | HG02559.hp2 HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1617+207T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 12/28 | chr2 | 21029432 | |||||||
chr2:21029493 | G | GAGGA | 4 | a0003c0007t0001g0104 a0003c0007t0001g0105 a0003c0007t0006g0108 others(1): Show |
4 | HG01123.hp2 HG02922.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1617+142_1617+145d others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 12/28 | chr2 | 21029493 | |||||||
chr2:21029493 | GAGGA | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(129): Show |
199 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1617+142_1617+145d others(6): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 12/28 | chr2 | 21029493 | |||||||
chr2:21029493 | GAGGAAGG others(5): Show |
G | 2 | a0010c0019t0004g0231 a0010c0031t0001g0045 |
3 | HG02559.hp2 HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1617+134_1617+145d others(14): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 12/28 | chr2 | 21029493 | |||||||
chr2:21029844 | G | A | 1 | a0053c0065t0004g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1470+54C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 11/28 | chr2 | 21029844 | |||||||
chr2:21030027 | G | A | 4 | a0002c0025t0001g0019 a0002c0043t0001g0071 a0005c0004t0001g0229 others(1): Show |
5 | HG01934.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1353-12C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 10/28 | chr2 | 21030027 | |||||||
chr2:21030325 | A | G | 1 | a0010c0075t0001g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1353-310T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 10/28 | chr2 | 21030325 | |||||||
chr2:21030368 | A | G | 8 | a0003c0005t0001g0003 a0003c0005t0001g0031 a0003c0005t0001g0112 others(5): Show |
16 | HG01243.hp2 HG01261.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1353-353T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 10/28 | chr2 | 21030368 | |||||||
chr2:21030749 | CA | C | 7 | a0002c0002t0001g0004 a0002c0057t0001g0079 a0003c0008t0001g0033 others(4): Show |
14 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.1353-735delT | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 10/28 | chr2 | 21030749 | |||||||
chr2:21030756 | A | T | 7 | a0002c0002t0001g0004 a0002c0057t0001g0079 a0003c0008t0001g0033 others(4): Show |
14 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.1353-741T>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 10/28 | chr2 | 21030756 | |||||||
chr2:21031084 | C | A | 1 | a0012c0013t0001g0203 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1353-1069G>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 10/28 | chr2 | 21031084 | |||||||
chr2:21031220 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1352+1134G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 10/28 | chr2 | 21031220 | |||||||
chr2:21031245 | A | G | 1 | a0010c0075t0001g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1352+1109T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 10/28 | chr2 | 21031245 | |||||||
chr2:21031297 | C | A | 1 | a0015c0020t0001g0204 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1352+1057G>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 10/28 | chr2 | 21031297 | |||||||
chr2:21031692 | T | C | 2 | a0003c0008t0001g0152 a0003c0008t0001g0153 |
2 | HG03710.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1352+662A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 10/28 | chr2 | 21031692 | |||||||
chr2:21031831 | C | T | 1 | a0005c0004t0001g0229 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1352+523G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 10/28 | chr2 | 21031831 | |||||||
chr2:21031852 | A | C | 12 | a0001c0001t0001g0162 a0011c0011t0001g0017 a0011c0011t0001g0046 others(9): Show |
16 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1352+502T>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 10/28 | chr2 | 21031852 | |||||||
chr2:21031858 | C | T | 10 | a0011c0011t0001g0017 a0011c0011t0001g0046 a0011c0011t0001g0047 others(7): Show |
14 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1352+496G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 10/28 | chr2 | 21031858 | |||||||
chr2:21031864 | C | A | 1 | a0007c0021t0001g0099 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1352+490G>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 10/28 | chr2 | 21031864 | |||||||
chr2:21031864 | C | CA | 5 | a0002c0053t0001g0072 a0018c0023t0001g0106 a0018c0023t0001g0143 others(2): Show |
5 | HG01433.hp1 HG02630.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1352+489dupT | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 10/28 | chr2 | 21031864 | |||||||
chr2:21031867 | A | C | 2 | a0005c0004t0001g0229 a0006c0006t0001g0161 |
2 | NA19030.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1352+487T>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 10/28 | chr2 | 21031867 | |||||||
chr2:21032125 | T | C | 8 | a0002c0016t0001g0053 a0002c0016t0001g0054 a0002c0016t0001g0055 others(5): Show |
9 | HG02257.hp2 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1352+229A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 10/28 | chr2 | 21032125 | |||||||
chr2:21032294 | G | T | 4 | a0002c0053t0001g0072 a0018c0023t0001g0106 a0018c0023t0001g0143 others(1): Show |
4 | HG01433.hp1 HG02630.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1352+60C>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 10/28 | chr2 | 21032294 | |||||||
chr2:21032701 | C | CCATCT | 202 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(199): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1125-121_1125-120i others(7): Show |
APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 9/28 | chr2 | 21032701 | |||||||
chr2:21032860 | G | A | 5 | a0001c0001t0001g0206 a0008c0009t0001g0205 a0008c0009t0001g0208 others(2): Show |
5 | HG01934.hp2 HG01952.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1125-279C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 9/28 | chr2 | 21032860 | |||||||
chr2:21032861 | G | A | 5 | a0001c0001t0001g0206 a0008c0009t0001g0205 a0008c0009t0001g0208 others(2): Show |
5 | HG01934.hp2 HG01952.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1125-280C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 9/28 | chr2 | 21032861 | |||||||
chr2:21033131 | C | T | 1 | a0010c0075t0001g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1124+168G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 9/28 | chr2 | 21033131 | |||||||
chr2:21033541 | G | A | 1 | a0017c0018t0001g0051 | 2 | HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.905-23C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 8/28 | chr2 | 21033541 | |||||||
chr2:21033617 | A | T | 1 | a0005c0072t0001g0118 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.905-99T>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 8/28 | chr2 | 21033617 | |||||||
chr2:21033993 | T | A | 12 | a0002c0050t0001g0061 a0011c0011t0001g0017 a0011c0011t0001g0046 others(9): Show |
16 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.905-475A>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 8/28 | chr2 | 21033993 | |||||||
chr2:21034342 | A | G | 1 | a0031c0087t0001g0160 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.904+474T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 8/28 | chr2 | 21034342 | |||||||
chr2:21034386 | C | T | 1 | a0003c0008t0001g0150 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.904+430G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 8/28 | chr2 | 21034386 | |||||||
chr2:21034542 | G | C | 2 | a0002c0025t0001g0019 a0002c0043t0001g0071 |
3 | HG01934.hp1 HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.904+274C>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 8/28 | chr2 | 21034542 | |||||||
chr2:21034637 | A | T | 1 | a0018c0023t0001g0143 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.904+179T>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 8/28 | chr2 | 21034637 | |||||||
chr2:21034756 | A | G | 1 | a0002c0054t0001g0078 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.904+60T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 8/28 | chr2 | 21034756 | |||||||
chr2:21034805 | G | C | 3 | a0002c0002t0001g0091 a0002c0002t0001g0095 a0013c0017t0001g0090 |
3 | HG02886.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.904+11C>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 8/28 | chr2 | 21034805 | |||||||
chr2:21035012 | A | G | 2 | a0001c0001t0001g0158 a0051c0093t0001g0159 |
2 | HG00621.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.819-111T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 7/28 | chr2 | 21035012 | |||||||
chr2:21035039 | C | T | 3 | a0002c0002t0001g0091 a0002c0002t0001g0095 a0013c0017t0001g0090 |
3 | HG02886.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.819-138G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 7/28 | chr2 | 21035039 | |||||||
chr2:21035055 | T | C | 1 | a0002c0012t0001g0089 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.819-154A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 7/28 | chr2 | 21035055 | |||||||
chr2:21035103 | C | T | 1 | a0036c0077t0001g0157 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.819-202G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 7/28 | chr2 | 21035103 | |||||||
chr2:21035104 | G | A | 3 | a0002c0002t0001g0091 a0002c0002t0001g0095 a0013c0017t0001g0090 |
3 | HG02886.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.819-203C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 7/28 | chr2 | 21035104 | |||||||
chr2:21035442 | A | G | 1 | a0013c0017t0001g0020 | 2 | NA18968.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.818+142T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 7/28 | chr2 | 21035442 | |||||||
chr2:21035729 | G | A | 1 | a0023c0042t0001g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.694-21C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 6/28 | chr2 | 21035729 | |||||||
chr2:21036222 | C | T | 1 | a0004c0003t0005g0052 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.694-514G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 6/28 | chr2 | 21036222 | |||||||
chr2:21036457 | T | C | 1 | a0053c0065t0004g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.693+643A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 6/28 | chr2 | 21036457 | |||||||
chr2:21036690 | T | C | 43 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0013 others(40): Show |
73 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.693+410A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 6/28 | chr2 | 21036690 | |||||||
chr2:21036740 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(120): Show |
189 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.693+360T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 6/28 | chr2 | 21036740 | |||||||
chr2:21037264 | G | A | 8 | a0002c0016t0001g0053 a0002c0016t0001g0054 a0002c0016t0001g0055 others(5): Show |
9 | HG02257.hp2 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.538-9C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 5/28 | chr2 | 21037264 | |||||||
chr2:21037318 | A | G | 1 | a0053c0065t0004g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.538-63T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 5/28 | chr2 | 21037318 | |||||||
chr2:21037427 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0156 |
3 | HG00597.hp2 HG02056.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.538-172T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 5/28 | chr2 | 21037427 | |||||||
chr2:21037489 | G | A | 1 | a0005c0004t0001g0229 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.538-234C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 5/28 | chr2 | 21037489 | |||||||
chr2:21037530 | C | T | 1 | a0002c0044t0001g0057 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.538-275G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 5/28 | chr2 | 21037530 | |||||||
chr2:21037729 | G | A | 201 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(198): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.537+229C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 5/28 | chr2 | 21037729 | |||||||
chr2:21038261 | C | T | 12 | a0002c0050t0001g0061 a0011c0011t0001g0017 a0011c0011t0001g0046 others(9): Show |
16 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.384-150G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21038261 | |||||||
chr2:21038340 | T | C | 1 | a0010c0075t0001g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.384-229A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21038340 | |||||||
chr2:21038371 | C | T | 1 | a0053c0065t0004g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.384-260G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21038371 | |||||||
chr2:21038398 | G | A | 2 | a0002c0002t0001g0091 a0002c0002t0001g0095 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.384-287C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21038398 | |||||||
chr2:21038402 | C | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0043 a0001c0001t0001g0211 others(3): Show |
10 | HG02165.hp2 NA18946.hp2 NA18961.hp1 others(7): Show |
intron_variant | MODIFIER | c.384-291G>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21038402 | |||||||
chr2:21038410 | C | T | 1 | a0002c0062t0001g0096 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.384-299G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21038410 | |||||||
chr2:21038475 | T | C | 1 | a0007c0010t0001g0069 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.384-364A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21038475 | |||||||
chr2:21038618 | G | T | 1 | a0010c0019t0004g0231 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.384-507C>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21038618 | |||||||
chr2:21038635 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(200): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.384-524A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21038635 | |||||||
chr2:21038974 | A | G | 1 | a0002c0029t0001g0074 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.384-863T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21038974 | |||||||
chr2:21039126 | A | C | 1 | a0002c0058t0001g0073 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.384-1015T>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21039126 | |||||||
chr2:21039163 | T | C | 1 | a0038c0099t0002g0230 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.384-1052A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21039163 | |||||||
chr2:21039254 | A | T | 3 | a0014c0015t0001g0015 a0014c0015t0001g0154 a0014c0015t0001g0155 |
5 | HG02129.hp1 HG02135.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-1143T>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21039254 | |||||||
chr2:21039318 | C | T | 12 | a0002c0053t0001g0072 a0003c0005t0001g0003 a0003c0005t0001g0031 others(9): Show |
20 | HG01243.hp2 HG01261.hp1 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.384-1207G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21039318 | |||||||
chr2:21039319 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.384-1208C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21039319 | |||||||
chr2:21039443 | G | T | 1 | a0053c0065t0004g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.384-1332C>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21039443 | |||||||
chr2:21039471 | C | T | 6 | a0002c0016t0001g0053 a0002c0016t0001g0054 a0002c0016t0001g0055 others(3): Show |
7 | HG02257.hp2 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.384-1360G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21039471 | |||||||
chr2:21039503 | G | T | 1 | a0053c0065t0004g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.384-1392C>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21039503 | |||||||
chr2:21039555 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(117): Show |
185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.383+1383C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21039555 | |||||||
chr2:21039667 | G | A | 1 | a0007c0021t0001g0099 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.383+1271C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21039667 | |||||||
chr2:21039674 | A | C | 5 | a0001c0001t0001g0142 a0002c0025t0001g0019 a0002c0043t0001g0071 others(2): Show |
6 | HG01934.hp1 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.383+1264T>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21039674 | |||||||
chr2:21039853 | T | C | 1 | a0004c0003t0001g0140 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.383+1085A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21039853 | |||||||
chr2:21039987 | G | A | 3 | a0002c0025t0001g0019 a0002c0043t0001g0071 a0046c0066t0001g0122 |
4 | HG01934.hp1 HG02647.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+951C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21039987 | |||||||
chr2:21039987 | G | C | 1 | a0053c0065t0004g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.383+951C>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21039987 | |||||||
chr2:21040045 | T | C | 1 | a0016c0069t0001g0131 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.383+893A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21040045 | |||||||
chr2:21040062 | C | T | 1 | a0004c0003t0001g0140 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.383+876G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21040062 | |||||||
chr2:21040362 | C | T | 1 | a0010c0019t0004g0231 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.383+576G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21040362 | |||||||
chr2:21040524 | G | A | 1 | a0002c0002t0001g0095 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.383+414C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21040524 | |||||||
chr2:21040699 | G | A | 1 | a0002c0024t0001g0070 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.383+239C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21040699 | |||||||
chr2:21040765 | G | A | 1 | a0010c0075t0001g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.383+173C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21040765 | |||||||
chr2:21040767 | T | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(203): Show |
311 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.383+171A>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21040767 | |||||||
chr2:21040895 | C | T | 4 | a0006c0006t0001g0136 a0006c0006t0001g0137 a0006c0006t0001g0138 others(1): Show |
4 | HG02027.hp2 NA18945.hp1 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+43G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21040895 | |||||||
chr2:21040899 | C | T | 1 | a0025c0033t0001g0134 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.383+39G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 4/28 | chr2 | 21040899 | |||||||
chr2:21041089 | A | G | 2 | a0001c0001t0001g0132 a0001c0001t0001g0215 |
2 | HG03688.hp2 HG03942.hp1 |
splice_region_variant&intron_variant | LOW | c.238-6T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 3/28 | chr2 | 21041089 | |||||||
chr2:21041206 | T | G | 1 | a0010c0075t0001g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.238-123A>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 3/28 | chr2 | 21041206 | |||||||
chr2:21041269 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.238-186A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 3/28 | chr2 | 21041269 | |||||||
chr2:21041408 | G | A | 1 | a0011c0011t0001g0047 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.238-325C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 3/28 | chr2 | 21041408 | |||||||
chr2:21041552 | G | A | 1 | a0015c0020t0001g0044 | 2 | HG01099.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.238-469C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 3/28 | chr2 | 21041552 | |||||||
chr2:21041655 | G | A | 1 | a0002c0002t0001g0097 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.238-572C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 3/28 | chr2 | 21041655 | |||||||
chr2:21041862 | T | C | 21 | a0002c0016t0001g0053 a0002c0016t0001g0054 a0002c0016t0001g0055 others(18): Show |
27 | HG02080.hp1 HG02080.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.237+499A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 3/28 | chr2 | 21041862 | |||||||
chr2:21042065 | T | C | 2 | a0001c0014t0001g0008 a0055c0091t0001g0217 |
6 | HG00408.hp1 NA18939.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.237+296A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 3/28 | chr2 | 21042065 | |||||||
chr2:21042065 | T | G | 21 | a0002c0016t0001g0053 a0002c0016t0001g0054 a0002c0016t0001g0055 others(18): Show |
27 | HG02080.hp1 HG02080.hp2 HG02083.hp1 others(24): Show |
intron_variant | MODIFIER | c.237+296A>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 3/28 | chr2 | 21042065 | |||||||
chr2:21042123 | T | C | 1 | a0001c0036t0001g0218 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.237+238A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 3/28 | chr2 | 21042123 | |||||||
chr2:21042127 | G | A | 1 | a0010c0075t0001g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.237+234C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 3/28 | chr2 | 21042127 | |||||||
chr2:21042269 | C | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(140): Show |
219 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.237+92G>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 3/28 | chr2 | 21042269 | |||||||
chr2:21042620 | T | A | 1 | a0004c0003t0001g0220 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.122-144A>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 2/28 | chr2 | 21042620 | |||||||
chr2:21042646 | A | T | 10 | a0003c0007t0001g0027 a0003c0007t0001g0048 a0003c0007t0001g0049 others(7): Show |
14 | HG00099.hp2 HG00733.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.122-170T>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 2/28 | chr2 | 21042646 | |||||||
chr2:21042649 | A | T | 1 | a0018c0023t0001g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.122-173T>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 2/28 | chr2 | 21042649 | |||||||
chr2:21042823 | T | C | 10 | a0010c0031t0001g0045 a0011c0011t0001g0017 a0011c0011t0001g0046 others(7): Show |
15 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.122-347A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 2/28 | chr2 | 21042823 | |||||||
chr2:21042973 | C | A | 1 | a0043c0103t0004g0233 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.122-497G>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 2/28 | chr2 | 21042973 | |||||||
chr2:21043026 | C | T | 2 | a0003c0007t0001g0104 a0003c0007t0001g0105 |
2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.121+487G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 2/28 | chr2 | 21043026 | |||||||
chr2:21043063 | G | C | 1 | a0011c0011t0001g0017 | 3 | HG02109.hp1 HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.121+450C>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 2/28 | chr2 | 21043063 | |||||||
chr2:21043120 | G | A | 1 | a0004c0003t0001g0227 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.121+393C>T | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 2/28 | chr2 | 21043120 | |||||||
chr2:21043292 | C | T | 20 | a0002c0016t0001g0053 a0002c0016t0001g0054 a0002c0016t0001g0055 others(17): Show |
26 | HG02080.hp1 HG02080.hp2 HG02083.hp1 others(23): Show |
intron_variant | MODIFIER | c.121+221G>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 2/28 | chr2 | 21043292 | |||||||
chr2:21043351 | T | C | 3 | a0003c0007t0001g0048 a0003c0007t0001g0049 a0003c0007t0001g0228 |
5 | HG00733.hp2 HG01069.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+162A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 2/28 | chr2 | 21043351 | |||||||
chr2:21043490 | C | G | 1 | a0016c0022t0001g0103 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.121+23G>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 2/28 | chr2 | 21043490 | |||||||
chr2:21043491 | G | T | 1 | a0010c0075t0001g0102 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.121+22C>A | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 2/28 | chr2 | 21043491 | |||||||
chr2:21043668 | A | G | 1 | a0004c0003t0001g0101 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.83-117T>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 1/28 | chr2 | 21043668 | |||||||
chr2:21043733 | T | C | 4 | a0005c0004t0001g0229 a0017c0018t0001g0050 a0017c0018t0001g0051 others(1): Show |
6 | HG02055.hp2 HG02615.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.82+131A>G | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 1/28 | chr2 | 21043733 | |||||||
chr2:21043787 | C | G | 3 | a0012c0013t0001g0025 a0012c0013t0001g0026 a0012c0013t0001g0100 |
5 | HG01496.hp2 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+77G>C | APOB | ENSG00000084674.15 | transcript | ENST00000233242.5 | protein_coding | 1/28 | chr2 | 21043787 |