Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 130074 |
| ensemblid | ENSG00000152102.18 |
| hgncid | 27016 |
| symbol | FAM168B |
| name | family with sequence similarity 168 member B |
| refseq_nuc | NM_001009993.4 |
| refseq_prot | NP_001009993.2 |
| ensembl_nuc | ENST00000389915.4 |
| ensembl_prot | ENSP00000374565.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 131047876 |
| end | 131093460 |
| strand | - |
| ver | v1.2 |
| region | chr2:131047876-131093460 |
| region5000 | chr2:131042876-131098460 |
| regionname0 | FAM168B_chr2_131047876_131093460 |
| regionname5000 | FAM168B_chr2_131042876_131098460 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 585 | 260 | 94 | 58 | 68 | 10 | 28 | FAM168B_chr2_131042876_131098460 | FAM168B | ATGAA others(580): Show |
chr2 | 131042876 | 131098460 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5435 | 140 | 34 | 38 | 42 | 5 | 20 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5430): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0002 | 0/0 | 5434 | 32 | 1 | 6 | 19 | 3 | 3 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5429): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0003 | 0/0 | 5434 | 15 | 12 | 0 | 1 | 0 | 2 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5429): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0004 | 0/0 | 5435 | 9 | 9 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5430): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0005 | 0/0 | 5434 | 7 | 6 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5429): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0006 | 0/0 | 5435 | 6 | 4 | 2 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5430): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0007 | 0/0 | 5434 | 5 | 4 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5429): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0008 | 0/0 | 5434 | 5 | 4 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5429): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0009 | 0/0 | 5434 | 3 | 1 | 2 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5429): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0010 | 0/0 | 5434 | 3 | 3 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5429): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0011 | 0/1 | 5434 | 3 | 0 | 1 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5429): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0012 | 0/0 | 5435 | 3 | 3 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5430): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0013 | 0/0 | 5434 | 3 | 3 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5429): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0014 | 0/0 | 5434 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5429): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0015 | 0/0 | 5434 | 2 | 0 | 1 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5429): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0016 | 0/0 | 5435 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5430): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0017 | 0/0 | 5435 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5430): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0018 | 0/0 | 5434 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5429): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0019 | 0/0 | 5434 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5429): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0020 | 0/0 | 5434 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5429): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0021 | 0/0 | 5435 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5430): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0022 | 0/0 | 5435 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5430): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0023 | 0/0 | 5434 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5429): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0024 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5429): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0025 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5429): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0026 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5429): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0027 | 0/0 | 5434 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5429): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0028 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5430): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0029 | 0/0 | 5435 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5430): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0030 | 0/0 | 5435 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5430): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0031 | 0/0 | 5435 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5430): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0032 | 0/0 | 5435 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5430): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0033 | 0/0 | 5435 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5430): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0034 | 0/0 | 5435 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5430): Show |
chr2 | 131042876 | 131098460 |
| a0001c0001t0035 | 0/0 | 5434 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | GTCGG others(5429): Show |
chr2 | 131042876 | 131098460 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 0 | 2 | 7 | 2 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0002 | 0/0 | 9 | 2 | 4 | 3 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0011 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0003g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0004g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0005g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0006g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0006g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0007g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0007g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0008g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0009g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0009g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0010g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0011g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0011g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0012g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0012g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0013g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0013g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0013g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0014g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0014g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0015g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0015g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0016g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0016g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0017g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0018g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0019g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0020g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0021g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0022g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0023g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0024g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0025g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0026g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0027g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0028g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0029g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0030g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0031g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0032g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0033g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0034g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| a0001c0001t0035g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0011 | g0020 | EUR | GBR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0021 | EUR | FIN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | FIN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00639 | hp1 | a0001 | c0001 | t0032 | g0085 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00642 | hp1 | a0001 | c0001 | t0011 | g0020 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG00741 | hp2 | a0001 | c0001 | t0015 | g0165 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01099 | hp1 | a0001 | c0001 | t0030 | g0096 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01106 | hp2 | a0001 | c0001 | t0034 | g0067 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01109 | hp2 | a0001 | c0001 | t0031 | g0047 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01175 | hp2 | a0001 | c0001 | t0009 | g0188 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0164 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0143 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0194 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0024 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01261 | hp2 | a0001 | c0001 | t0009 | g0022 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0132 | EUR | IBS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0131 | EUR | IBS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0028 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0154 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01943 | hp1 | a0001 | c0001 | t0023 | g0162 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01943 | hp2 | a0001 | c0001 | t0008 | g0122 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02055 | hp1 | a0001 | c0001 | t0013 | g0026 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | KHV | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | CDX | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | CDX | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02257 | hp2 | a0001 | c0001 | t0014 | g0190 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0053 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0202 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02451 | hp1 | a0001 | c0001 | t0013 | g0167 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0201 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0205 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02615 | hp1 | a0001 | c0001 | t0010 | g0009 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02615 | hp2 | a0001 | c0001 | t0028 | g0197 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02622 | hp2 | a0001 | c0001 | t0012 | g0189 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02647 | hp1 | a0001 | c0001 | t0009 | g0022 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0198 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0148 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02738 | hp1 | a0001 | c0001 | t0020 | g0186 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02818 | hp1 | a0001 | c0001 | t0012 | g0023 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0018 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02886 | hp2 | a0001 | c0001 | t0012 | g0023 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02896 | hp1 | a0001 | c0001 | t0016 | g0046 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02897 | hp2 | a0001 | c0001 | t0016 | g0036 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02922 | hp2 | a0001 | c0001 | t0026 | g0187 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0200 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0166 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0142 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0156 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0147 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0196 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0195 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03130 | hp1 | a0001 | c0001 | t0014 | g0191 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03139 | hp1 | a0001 | c0001 | t0017 | g0025 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0203 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03239 | hp1 | a0001 | c0001 | t0027 | g0160 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0054 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03704 | hp2 | a0001 | c0001 | t0019 | g0146 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | BEB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0185 | SAS | STU | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | STU | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | STU | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18522 | hp1 | a0001 | c0001 | t0017 | g0025 | AFR | YRI | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | CHB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18968 | hp1 | a0001 | c0001 | t0021 | g0179 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18992 | hp1 | a0001 | c0001 | t0018 | g0169 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18993 | hp2 | a0001 | c0001 | t0033 | g0111 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18995 | hp1 | a0001 | c0001 | t0029 | g0108 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19030 | hp1 | a0001 | c0001 | t0025 | g0129 | AFR | LWK | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | LWK | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | LWK | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0155 | AFR | LWK | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19060 | hp2 | a0001 | c0001 | t0035 | g0152 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19085 | hp1 | a0001 | c0001 | t0022 | g0063 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0055 | AFR | YRI | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | ASW | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0141 | AFR | ASW | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA20805 | hp2 | a0001 | c0001 | t0015 | g0158 | EUR | TSI | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | GIH | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | GIH | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02109 | hp2 | a0001 | c0001 | t0013 | g0168 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0204 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG06807 | hp1 | a0001 | c0001 | t0024 | g0199 | AFR | USA | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | USA | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | USA | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | USA | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | LWK | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0011 | g0161 | REF | REF | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0011 | REF | REF | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
| 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 |
|---|
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:131047985 | G | A | 1 | a0001c0001t0027 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4480C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 4918 | chr2 | 131047985 | ||||||
| chr2:131048004 | T | C | 1 | a0001c0001t0015 | 2 | HG00741.hp2 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4461A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 4899 | chr2 | 131048004 | ||||||
| chr2:131048052 | T | A | 1 | a0001c0001t0023 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4413A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 4851 | chr2 | 131048052 | ||||||
| chr2:131048185 | C | A | 1 | a0001c0001t0019 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4280G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 4718 | chr2 | 131048185 | ||||||
| chr2:131048325 | A | G | 1 | a0001c0001t0013 | 3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4140T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 4578 | chr2 | 131048325 | ||||||
| chr2:131048411 | G | T | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(10): Show |
66 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*4054C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 4492 | chr2 | 131048411 | ||||||
| chr2:131048432 | G | A | 1 | a0001c0001t0026 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4033C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 4471 | chr2 | 131048432 | ||||||
| chr2:131048540 | G | A | 1 | a0001c0001t0017 | 2 | HG03139.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3925C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 4363 | chr2 | 131048540 | ||||||
| chr2:131048840 | A | G | 1 | a0001c0001t0025 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3625T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 4063 | chr2 | 131048840 | ||||||
| chr2:131048878 | T | G | 1 | a0001c0001t0033 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3587A>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 4025 | chr2 | 131048878 | ||||||
| chr2:131049004 | G | C | 2 | a0001c0001t0012 a0001c0001t0014 |
5 | HG02257.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3461C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 3899 | chr2 | 131049004 | ||||||
| chr2:131049240 | C | T | 1 | a0001c0001t0005 | 7 | HG01243.hp1 HG01891.hp1 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3225G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 3663 | chr2 | 131049240 | ||||||
| chr2:131049259 | C | T | 1 | a0001c0001t0025 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3206G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 3644 | chr2 | 131049259 | ||||||
| chr2:131049332 | T | C | 2 | a0001c0001t0004 a0001c0001t0017 |
11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3133A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 3571 | chr2 | 131049332 | ||||||
| chr2:131049526 | C | T | 1 | a0001c0001t0032 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2939G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 3377 | chr2 | 131049526 | ||||||
| chr2:131049555 | A | G | 2 | a0001c0001t0004 a0001c0001t0017 |
11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2910T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 3348 | chr2 | 131049555 | ||||||
| chr2:131049673 | AT | A | 1 | a0001c0001t0013 | 3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2791delA | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 3229 | chr2 | 131049673 | ||||||
| chr2:131049788 | C | T | 1 | a0001c0001t0018 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2677G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 3115 | chr2 | 131049788 | ||||||
| chr2:131049887 | C | T | 1 | a0001c0001t0011 | 2 | HG00099.hp1 HG00642.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2578G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 3016 | chr2 | 131049887 | ||||||
| chr2:131049982 | C | T | 1 | a0001c0001t0025 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2483G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 2921 | chr2 | 131049982 | ||||||
| chr2:131050265 | T | C | 1 | a0001c0001t0016 | 2 | HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2200A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 2638 | chr2 | 131050265 | ||||||
| chr2:131050409 | C | A | 4 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0014 others(1): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2056G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 2494 | chr2 | 131050409 | ||||||
| chr2:131050666 | A | G | 1 | a0001c0001t0025 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1799T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 2237 | chr2 | 131050666 | ||||||
| chr2:131050826 | C | G | 1 | a0001c0001t0031 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1639G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 2077 | chr2 | 131050826 | ||||||
| chr2:131050870 | C | T | 1 | a0001c0001t0007 | 5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1595G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 2033 | chr2 | 131050870 | ||||||
| chr2:131050877 | T | C | 1 | a0001c0001t0020 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1588A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 2026 | chr2 | 131050877 | ||||||
| chr2:131050896 | G | C | 1 | a0001c0001t0013 | 3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1569C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 2007 | chr2 | 131050896 | ||||||
| chr2:131050951 | G | A | 1 | a0001c0001t0034 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1514C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1952 | chr2 | 131050951 | ||||||
| chr2:131050976 | C | T | 2 | a0001c0001t0010 a0001c0001t0030 |
4 | HG01099.hp1 HG02615.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1489G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1927 | chr2 | 131050976 | ||||||
| chr2:131050983 | A | AT | 2 | a0001c0001t0004 a0001c0001t0017 |
11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1481dupA | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1919 | chr2 | 131050983 | ||||||
| chr2:131051082 | C | T | 10 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0009 others(7): Show |
29 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1383G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1821 | chr2 | 131051082 | ||||||
| chr2:131051205 | A | T | 1 | a0001c0001t0025 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1260T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1698 | chr2 | 131051205 | ||||||
| chr2:131051473 | A | G | 1 | a0001c0001t0029 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*992T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1430 | chr2 | 131051473 | ||||||
| chr2:131051483 | GA | G | 21 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(18): Show |
96 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*981delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1419 | chr2 | 131051483 | ||||||
| chr2:131051486 | A | T | 1 | a0001c0001t0024 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*979T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1417 | chr2 | 131051486 | ||||||
| chr2:131051552 | G | T | 1 | a0001c0001t0023 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*913C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1351 | chr2 | 131051552 | ||||||
| chr2:131051624 | C | T | 24 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(21): Show |
102 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*841G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1279 | chr2 | 131051624 | ||||||
| chr2:131051739 | C | T | 1 | a0001c0001t0022 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*726G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1164 | chr2 | 131051739 | ||||||
| chr2:131051825 | T | C | 1 | a0001c0001t0013 | 3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*640A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1078 | chr2 | 131051825 | ||||||
| chr2:131051863 | A | T | 5 | a0001c0001t0002 a0001c0001t0018 a0001c0001t0019 others(2): Show |
36 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*602T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1040 | chr2 | 131051863 | ||||||
| chr2:131052152 | T | G | 1 | a0001c0001t0035 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*313A>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 751 | chr2 | 131052152 | ||||||
| chr2:131093249 | C | A | 2 | a0001c0001t0004 a0001c0001t0017 |
11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-47G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/7 | 10603 | chr2 | 131093249 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:131052474 | C | G | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.*13-22G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 6/6 | chr2 | 131052474 | |||||||
| chr2:131052475 | T | A | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.*13-23A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 6/6 | chr2 | 131052475 | |||||||
| chr2:131052543 | G | A | 7 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.*13-91C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 6/6 | chr2 | 131052543 | |||||||
| chr2:131052694 | T | G | 51 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(48): Show |
65 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.*12+197A>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 6/6 | chr2 | 131052694 | |||||||
| chr2:131052776 | G | C | 1 | a0001c0001t0024g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*12+115C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 6/6 | chr2 | 131052776 | |||||||
| chr2:131052807 | T | C | 8 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(5): Show |
11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.*12+84A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 6/6 | chr2 | 131052807 | |||||||
| chr2:131053174 | C | T | 4 | a0001c0001t0007g0018 a0001c0001t0007g0141 a0001c0001t0007g0142 others(1): Show |
5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.476-159G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131053174 | |||||||
| chr2:131053187 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0039 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.476-172A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131053187 | |||||||
| chr2:131053189 | G | A | 1 | a0001c0001t0025g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.476-174C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131053189 | |||||||
| chr2:131053655 | T | C | 1 | a0001c0001t0010g0009 | 3 | HG02615.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.476-640A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131053655 | |||||||
| chr2:131053670 | A | T | 1 | a0001c0001t0006g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.476-655T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131053670 | |||||||
| chr2:131053747 | T | C | 82 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(79): Show |
105 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.476-732A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131053747 | |||||||
| chr2:131053960 | C | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0069 |
2 | HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.476-945G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131053960 | |||||||
| chr2:131054070 | A | G | 23 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(20): Show |
29 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.476-1055T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054070 | |||||||
| chr2:131054095 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0107 |
3 | HG00735.hp1 HG01928.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.476-1080C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054095 | |||||||
| chr2:131054134 | A | C | 1 | a0001c0001t0001g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.476-1119T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054134 | |||||||
| chr2:131054236 | T | TA | 4 | a0001c0001t0007g0018 a0001c0001t0007g0141 a0001c0001t0007g0142 others(1): Show |
5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.475+1035dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054236 | |||||||
| chr2:131054236 | TA | T | 12 | a0001c0001t0001g0093 a0001c0001t0001g0138 a0001c0001t0002g0176 others(9): Show |
14 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.475+1035delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054236 | |||||||
| chr2:131054322 | A | C | 1 | a0001c0001t0001g0052 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.475+950T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054322 | |||||||
| chr2:131054525 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.475+747A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054525 | |||||||
| chr2:131054806 | T | C | 1 | a0001c0001t0003g0151 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.475+466A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054806 | |||||||
| chr2:131054811 | G | C | 3 | a0001c0001t0001g0068 a0001c0001t0001g0106 a0001c0001t0001g0125 |
3 | HG02723.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.475+461C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054811 | |||||||
| chr2:131054854 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.475+418C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054854 | |||||||
| chr2:131054989 | A | G | 3 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 |
3 | HG02258.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.475+283T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054989 | |||||||
| chr2:131054999 | G | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
12 | HG01109.hp2 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.475+273C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054999 | |||||||
| chr2:131055119 | T | C | 3 | a0001c0001t0013g0026 a0001c0001t0013g0167 a0001c0001t0013g0168 |
3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.475+153A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131055119 | |||||||
| chr2:131055165 | C | T | 52 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(49): Show |
68 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.475+107G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131055165 | |||||||
| chr2:131055204 | C | T | 2 | a0001c0001t0003g0157 a0001c0001t0035g0152 |
2 | NA18953.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.475+68G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131055204 | |||||||
| chr2:131055219 | C | T | 2 | a0001c0001t0014g0190 a0001c0001t0014g0191 |
2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.475+53G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131055219 | |||||||
| chr2:131055744 | G | A | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.155-49C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131055744 | |||||||
| chr2:131055869 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.155-174T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131055869 | |||||||
| chr2:131055959 | A | C | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.155-264T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131055959 | |||||||
| chr2:131056199 | T | C | 52 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(49): Show |
68 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.155-504A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131056199 | |||||||
| chr2:131056503 | A | C | 1 | a0001c0001t0025g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.155-808T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131056503 | |||||||
| chr2:131056557 | G | A | 8 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(5): Show |
11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-862C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131056557 | |||||||
| chr2:131056659 | A | G | 4 | a0001c0001t0001g0124 a0001c0001t0008g0053 a0001c0001t0008g0054 others(1): Show |
4 | HG02258.hp1 HG03209.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-964T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131056659 | |||||||
| chr2:131056685 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.155-990G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131056685 | |||||||
| chr2:131056692 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.155-997G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131056692 | |||||||
| chr2:131056847 | CAGA | C | 8 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(5): Show |
11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-1155_155-1153d others(5): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131056847 | |||||||
| chr2:131056891 | C | G | 1 | a0001c0001t0002g0175 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.155-1196G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131056891 | |||||||
| chr2:131056891 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.155-1196G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131056891 | |||||||
| chr2:131056981 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.155-1286A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131056981 | |||||||
| chr2:131057011 | C | T | 1 | a0001c0001t0025g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.155-1316G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131057011 | |||||||
| chr2:131057275 | A | G | 5 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(2): Show |
6 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.155-1580T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131057275 | |||||||
| chr2:131057572 | C | T | 1 | a0001c0001t0031g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.155-1877G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131057572 | |||||||
| chr2:131057817 | G | A | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.155-2122C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131057817 | |||||||
| chr2:131057883 | T | C | 4 | a0001c0001t0007g0018 a0001c0001t0007g0141 a0001c0001t0007g0142 others(1): Show |
5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-2188A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131057883 | |||||||
| chr2:131058120 | GTA | G | 75 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(72): Show |
97 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.155-2427_155-2426d others(4): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131058120 | |||||||
| chr2:131058297 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0073 |
5 | HG01255.hp1 HG01934.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-2602G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131058297 | |||||||
| chr2:131058329 | A | G | 1 | a0001c0001t0002g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.155-2634T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131058329 | |||||||
| chr2:131058405 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.155-2710G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131058405 | |||||||
| chr2:131058709 | A | T | 1 | a0001c0001t0001g0105 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.155-3014T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131058709 | |||||||
| chr2:131058826 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02895.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.155-3131G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131058826 | |||||||
| chr2:131058900 | T | A | 1 | a0001c0001t0007g0142 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.155-3205A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131058900 | |||||||
| chr2:131058915 | A | C | 1 | a0001c0001t0012g0023 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.155-3220T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131058915 | |||||||
| chr2:131058943 | T | C | 11 | a0001c0001t0003g0006 a0001c0001t0003g0149 a0001c0001t0003g0150 others(8): Show |
15 | HG01243.hp1 HG01891.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.155-3248A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131058943 | |||||||
| chr2:131059479 | T | C | 1 | a0001c0001t0010g0009 | 3 | HG02615.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.155-3784A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131059479 | |||||||
| chr2:131059517 | A | G | 4 | a0001c0001t0007g0018 a0001c0001t0007g0141 a0001c0001t0007g0142 others(1): Show |
5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-3822T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131059517 | |||||||
| chr2:131059615 | C | A | 50 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(47): Show |
64 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.155-3920G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131059615 | |||||||
| chr2:131059615 | CCCTCTGT others(6): Show |
C | 1 | a0001c0001t0001g0117 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.155-3933_155-3921d others(15): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131059615 | |||||||
| chr2:131059797 | A | T | 99 | a0001c0001t0001g0008 a0001c0001t0001g0045 a0001c0001t0001g0104 others(96): Show |
124 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.155-4102T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131059797 | |||||||
| chr2:131059807 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.155-4112C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131059807 | |||||||
| chr2:131059879 | T | C | 3 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0026g0187 |
4 | HG01175.hp2 HG01261.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-4184A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131059879 | |||||||
| chr2:131059896 | C | G | 1 | a0001c0001t0001g0128 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.155-4201G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131059896 | |||||||
| chr2:131060198 | G | A | 8 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(5): Show |
11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-4503C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131060198 | |||||||
| chr2:131060267 | G | A | 1 | a0001c0001t0008g0053 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.155-4572C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131060267 | |||||||
| chr2:131060284 | A | G | 52 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(49): Show |
68 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.155-4589T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131060284 | |||||||
| chr2:131060487 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.155-4792T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131060487 | |||||||
| chr2:131060913 | G | A | 4 | a0001c0001t0007g0018 a0001c0001t0007g0141 a0001c0001t0007g0142 others(1): Show |
5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-5218C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131060913 | |||||||
| chr2:131061063 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.155-5368C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131061063 | |||||||
| chr2:131061149 | C | A | 52 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(49): Show |
68 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.155-5454G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131061149 | |||||||
| chr2:131061177 | G | A | 52 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(49): Show |
68 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.155-5482C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131061177 | |||||||
| chr2:131061247 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.155-5552C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131061247 | |||||||
| chr2:131061292 | AT | A | 6 | a0001c0001t0006g0024 a0001c0001t0006g0195 a0001c0001t0006g0196 others(3): Show |
7 | HG01258.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.155-5598delA | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131061292 | |||||||
| chr2:131061295 | T | TA | 6 | a0001c0001t0001g0092 a0001c0001t0007g0018 a0001c0001t0007g0141 others(3): Show |
7 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.155-5601dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131061295 | |||||||
| chr2:131061295 | TA | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0093 a0001c0001t0001g0123 others(2): Show |
5 | HG01943.hp2 HG02895.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-5601delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131061295 | |||||||
| chr2:131061482 | C | G | 1 | a0001c0001t0003g0148 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.155-5787G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131061482 | |||||||
| chr2:131061782 | GA | G | 63 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(60): Show |
82 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.155-6088delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131061782 | |||||||
| chr2:131062078 | C | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(177): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.155-6383G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062078 | |||||||
| chr2:131062180 | A | T | 3 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 |
3 | HG02258.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.155-6485T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062180 | |||||||
| chr2:131062270 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.155-6575A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062270 | |||||||
| chr2:131062292 | T | C | 1 | a0001c0001t0031g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.155-6597A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062292 | |||||||
| chr2:131062464 | T | C | 3 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0109 |
3 | HG01934.hp1 HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.155-6769A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062464 | |||||||
| chr2:131062479 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.155-6784C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062479 | |||||||
| chr2:131062524 | T | C | 6 | a0001c0001t0002g0007 a0001c0001t0002g0171 a0001c0001t0002g0172 others(3): Show |
9 | HG00544.hp2 HG00673.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.155-6829A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062524 | |||||||
| chr2:131062636 | C | A | 1 | a0001c0001t0010g0009 | 3 | HG02615.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.155-6941G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062636 | |||||||
| chr2:131062663 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.155-6968C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062663 | |||||||
| chr2:131062744 | G | A | 1 | a0001c0001t0025g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.155-7049C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062744 | |||||||
| chr2:131062869 | G | A | 52 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(49): Show |
68 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.155-7174C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062869 | |||||||
| chr2:131062926 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.155-7231T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062926 | |||||||
| chr2:131062941 | C | G | 1 | a0001c0001t0001g0048 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.155-7246G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062941 | |||||||
| chr2:131063242 | C | A | 1 | a0001c0001t0001g0086 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.155-7547G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131063242 | |||||||
| chr2:131063304 | C | CAACAATG others(220): Show |
1 | a0001c0001t0002g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.155-7610_155-7609i others(229): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131063304 | |||||||
| chr2:131063405 | T | C | 52 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(49): Show |
68 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.155-7710A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131063405 | |||||||
| chr2:131063639 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.155-7944C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131063639 | |||||||
| chr2:131063725 | G | A | 1 | a0001c0001t0014g0191 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.155-8030C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131063725 | |||||||
| chr2:131064156 | G | A | 1 | a0001c0001t0006g0198 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.154+7699C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131064156 | |||||||
| chr2:131064204 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.154+7651C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131064204 | |||||||
| chr2:131064486 | G | A | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+7369C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131064486 | |||||||
| chr2:131064565 | A | G | 1 | a0001c0001t0004g0200 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.154+7290T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131064565 | |||||||
| chr2:131064749 | T | C | 4 | a0001c0001t0007g0018 a0001c0001t0007g0141 a0001c0001t0007g0142 others(1): Show |
5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.154+7106A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131064749 | |||||||
| chr2:131064879 | T | A | 28 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(25): Show |
36 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.154+6976A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131064879 | |||||||
| chr2:131064935 | T | G | 1 | a0001c0001t0024g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.154+6920A>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131064935 | |||||||
| chr2:131064976 | C | T | 1 | a0001c0001t0002g0174 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.154+6879G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131064976 | |||||||
| chr2:131064993 | A | G | 3 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0026g0187 |
4 | HG01175.hp2 HG01261.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+6862T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131064993 | |||||||
| chr2:131065034 | A | G | 79 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(76): Show |
102 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.154+6821T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065034 | |||||||
| chr2:131065055 | T | C | 1 | a0001c0001t0002g0178 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.154+6800A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065055 | |||||||
| chr2:131065085 | G | A | 2 | a0001c0001t0002g0131 a0001c0001t0002g0132 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.154+6770C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065085 | |||||||
| chr2:131065295 | A | AT | 8 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(5): Show |
11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.154+6559dupA | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065295 | |||||||
| chr2:131065420 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0090 |
2 | HG00741.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.154+6435G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065420 | |||||||
| chr2:131065511 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0088 |
2 | HG00642.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.154+6344C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065511 | |||||||
| chr2:131065563 | C | T | 9 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(6): Show |
12 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.154+6292G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065563 | |||||||
| chr2:131065564 | G | A | 2 | a0001c0001t0005g0019 a0001c0001t0005g0155 |
3 | HG02630.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.154+6291C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065564 | |||||||
| chr2:131065619 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.154+6236C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065619 | |||||||
| chr2:131065650 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.154+6205C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065650 | |||||||
| chr2:131065703 | C | T | 1 | a0001c0001t0001g0015 | 2 | HG00738.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.154+6152G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065703 | |||||||
| chr2:131065759 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.154+6096T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065759 | |||||||
| chr2:131065807 | G | GA | 7 | a0001c0001t0001g0074 a0001c0001t0003g0157 a0001c0001t0007g0018 others(4): Show |
8 | HG01243.hp2 HG01258.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+6047dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065807 | |||||||
| chr2:131065878 | C | G | 6 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(3): Show |
7 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.154+5977G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065878 | |||||||
| chr2:131065955 | C | T | 1 | a0001c0001t0005g0147 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.154+5900G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065955 | |||||||
| chr2:131066017 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.154+5838C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066017 | |||||||
| chr2:131066050 | T | C | 52 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(49): Show |
68 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.154+5805A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066050 | |||||||
| chr2:131066161 | C | CT | 70 | a0001c0001t0001g0061 a0001c0001t0001g0124 a0001c0001t0001g0125 others(67): Show |
85 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.154+5693dupA | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066161 | |||||||
| chr2:131066161 | CT | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0060 a0001c0001t0001g0069 others(2): Show |
6 | HG02717.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.154+5693delA | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066161 | |||||||
| chr2:131066205 | G | A | 1 | a0001c0001t0005g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.154+5650C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066205 | |||||||
| chr2:131066337 | G | A | 7 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+5518C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066337 | |||||||
| chr2:131066471 | G | A | 4 | a0001c0001t0001g0089 a0001c0001t0001g0123 a0001c0001t0008g0054 others(1): Show |
4 | HG02080.hp2 HG03516.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+5384C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066471 | |||||||
| chr2:131066520 | A | C | 1 | a0001c0001t0001g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.154+5335T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066520 | |||||||
| chr2:131066567 | C | G | 1 | a0001c0001t0031g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.154+5288G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066567 | |||||||
| chr2:131066661 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.154+5194A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066661 | |||||||
| chr2:131066712 | G | T | 1 | a0001c0001t0006g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.154+5143C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066712 | |||||||
| chr2:131066917 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0090 |
2 | HG00741.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.154+4938A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066917 | |||||||
| chr2:131067285 | C | T | 3 | a0001c0001t0013g0026 a0001c0001t0013g0167 a0001c0001t0013g0168 |
3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.154+4570G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131067285 | |||||||
| chr2:131067315 | T | A | 1 | a0001c0001t0001g0042 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.154+4540A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131067315 | |||||||
| chr2:131067346 | C | T | 1 | a0001c0001t0010g0009 | 3 | HG02615.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.154+4509G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131067346 | |||||||
| chr2:131067358 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.154+4497T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131067358 | |||||||
| chr2:131067523 | T | C | 5 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0092 others(2): Show |
5 | HG01934.hp1 HG01975.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+4332A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131067523 | |||||||
| chr2:131067723 | T | TCA | 3 | a0001c0001t0002g0180 a0001c0001t0007g0018 a0001c0001t0021g0179 |
4 | HG02818.hp2 HG03486.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+4130_154+4131d others(4): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131067723 | |||||||
| chr2:131067770 | G | A | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+4085C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131067770 | |||||||
| chr2:131067947 | G | T | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+3908C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131067947 | |||||||
| chr2:131067988 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.154+3867C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131067988 | |||||||
| chr2:131068080 | C | G | 6 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(3): Show |
7 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.154+3775G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131068080 | |||||||
| chr2:131068305 | T | A | 1 | a0001c0001t0001g0134 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.154+3550A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131068305 | |||||||
| chr2:131068457 | G | A | 1 | a0001c0001t0025g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.154+3398C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131068457 | |||||||
| chr2:131068522 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.154+3333A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131068522 | |||||||
| chr2:131068742 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.154+3113T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131068742 | |||||||
| chr2:131068825 | A | G | 8 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(5): Show |
11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.154+3030T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131068825 | |||||||
| chr2:131068886 | T | C | 5 | a0001c0001t0007g0018 a0001c0001t0007g0141 a0001c0001t0007g0142 others(2): Show |
6 | HG01243.hp2 HG02258.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.154+2969A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131068886 | |||||||
| chr2:131068983 | T | C | 9 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(6): Show |
12 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.154+2872A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131068983 | |||||||
| chr2:131068999 | G | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
7 | HG01884.hp2 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.154+2856C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131068999 | |||||||
| chr2:131069307 | G | A | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+2548C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131069307 | |||||||
| chr2:131069320 | C | T | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+2535G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131069320 | |||||||
| chr2:131069510 | T | G | 52 | a0001c0001t0001g0051 a0001c0001t0002g0003 a0001c0001t0002g0007 others(49): Show |
68 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.154+2345A>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131069510 | |||||||
| chr2:131069511 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.154+2344C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131069511 | |||||||
| chr2:131069524 | T | C | 79 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(76): Show |
102 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.154+2331A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131069524 | |||||||
| chr2:131069555 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.154+2300C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131069555 | |||||||
| chr2:131069784 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.154+2071G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131069784 | |||||||
| chr2:131069903 | G | C | 1 | a0001c0001t0001g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.154+1952C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131069903 | |||||||
| chr2:131070000 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0064 |
2 | HG03831.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.154+1855G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131070000 | |||||||
| chr2:131070041 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.154+1814A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131070041 | |||||||
| chr2:131071023 | A | G | 1 | a0001c0001t0008g0053 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.154+832T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071023 | |||||||
| chr2:131071065 | C | T | 13 | a0001c0001t0003g0006 a0001c0001t0003g0017 a0001c0001t0003g0149 others(10): Show |
18 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.154+790G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071065 | |||||||
| chr2:131071337 | G | A | 1 | a0001c0001t0005g0155 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.154+518C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071337 | |||||||
| chr2:131071379 | G | A | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+476C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071379 | |||||||
| chr2:131071469 | C | T | 5 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0092 others(2): Show |
5 | HG01934.hp1 HG01975.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+386G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071469 | |||||||
| chr2:131071476 | A | T | 4 | a0001c0001t0007g0018 a0001c0001t0007g0141 a0001c0001t0007g0142 others(1): Show |
5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.154+379T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071476 | |||||||
| chr2:131071522 | C | G | 2 | a0001c0001t0001g0050 a0001c0001t0029g0108 |
2 | NA18995.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.154+333G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071522 | |||||||
| chr2:131071576 | T | C | 1 | a0001c0001t0002g0185 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.154+279A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071576 | |||||||
| chr2:131071579 | C | G | 1 | a0001c0001t0001g0069 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.154+276G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071579 | |||||||
| chr2:131071815 | C | A | 4 | a0001c0001t0001g0074 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
4 | HG01258.hp1 HG03492.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+40G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071815 | |||||||
| chr2:131071841 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.154+14G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071841 | |||||||
| chr2:131071984 | G | GACAC | 24 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(21): Show |
32 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.71-47_71-46insGTGT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131071984 | |||||||
| chr2:131071987 | A | ACACC | 51 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(48): Show |
65 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.71-50_71-49insGGTG | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131071987 | |||||||
| chr2:131072267 | G | A | 1 | a0001c0001t0015g0158 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.71-329C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131072267 | |||||||
| chr2:131072307 | A | G | 4 | a0001c0001t0012g0023 a0001c0001t0012g0189 a0001c0001t0014g0190 others(1): Show |
5 | HG02257.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-369T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131072307 | |||||||
| chr2:131072346 | A | C | 6 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(3): Show |
7 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-408T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131072346 | |||||||
| chr2:131072393 | G | C | 7 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-455C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131072393 | |||||||
| chr2:131072464 | T | A | 7 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-526A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131072464 | |||||||
| chr2:131072601 | G | C | 7 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-663C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131072601 | |||||||
| chr2:131072626 | T | A | 4 | a0001c0001t0007g0018 a0001c0001t0007g0141 a0001c0001t0007g0142 others(1): Show |
5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-688A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131072626 | |||||||
| chr2:131072741 | G | A | 52 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(49): Show |
68 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.71-803C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131072741 | |||||||
| chr2:131072749 | G | A | 3 | a0001c0001t0013g0026 a0001c0001t0013g0167 a0001c0001t0013g0168 |
3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.71-811C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131072749 | |||||||
| chr2:131073086 | C | T | 23 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(20): Show |
29 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.71-1148G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131073086 | |||||||
| chr2:131073137 | C | T | 1 | a0001c0001t0025g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.71-1199G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131073137 | |||||||
| chr2:131073431 | C | T | 9 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(6): Show |
12 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.71-1493G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131073431 | |||||||
| chr2:131073585 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.71-1647C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131073585 | |||||||
| chr2:131073661 | T | C | 1 | a0001c0001t0006g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.71-1723A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131073661 | |||||||
| chr2:131073802 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.71-1864A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131073802 | |||||||
| chr2:131073966 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.71-2028T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131073966 | |||||||
| chr2:131073974 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.71-2036A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131073974 | |||||||
| chr2:131074005 | G | A | 2 | a0001c0001t0008g0054 a0001c0001t0008g0055 |
2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.71-2067C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074005 | |||||||
| chr2:131074030 | G | A | 1 | a0001c0001t0031g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.71-2092C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074030 | |||||||
| chr2:131074094 | G | A | 3 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0026g0187 |
4 | HG01175.hp2 HG01261.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-2156C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074094 | |||||||
| chr2:131074138 | C | CT | 8 | a0001c0001t0001g0045 a0001c0001t0001g0104 a0001c0001t0007g0018 others(5): Show |
9 | HG01243.hp2 HG01891.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.71-2201dupA | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074138 | |||||||
| chr2:131074178 | G | C | 2 | a0001c0001t0008g0054 a0001c0001t0008g0055 |
2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.71-2240C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074178 | |||||||
| chr2:131074246 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.71-2308T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074246 | |||||||
| chr2:131074270 | G | A | 1 | a0001c0001t0015g0158 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.71-2332C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074270 | |||||||
| chr2:131074379 | G | A | 6 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(3): Show |
7 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-2441C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074379 | |||||||
| chr2:131074410 | A | G | 52 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(49): Show |
68 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.71-2472T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074410 | |||||||
| chr2:131074433 | C | T | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.71-2495G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074433 | |||||||
| chr2:131074434 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.71-2496C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074434 | |||||||
| chr2:131074596 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.71-2658C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074596 | |||||||
| chr2:131074647 | A | C | 4 | a0001c0001t0004g0010 a0001c0001t0004g0203 a0001c0001t0004g0204 others(1): Show |
6 | HG02109.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-2709T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074647 | |||||||
| chr2:131074686 | A | G | 1 | a0001c0001t0031g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.71-2748T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074686 | |||||||
| chr2:131074812 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.71-2874G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074812 | |||||||
| chr2:131074813 | G | C | 3 | a0001c0001t0013g0026 a0001c0001t0013g0167 a0001c0001t0013g0168 |
3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.71-2875C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074813 | |||||||
| chr2:131074826 | T | A | 1 | a0001c0001t0024g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.71-2888A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074826 | |||||||
| chr2:131075015 | C | T | 4 | a0001c0001t0007g0018 a0001c0001t0007g0141 a0001c0001t0007g0142 others(1): Show |
5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-3077G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075015 | |||||||
| chr2:131075076 | G | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
8 | HG01884.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-3138C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075076 | |||||||
| chr2:131075213 | TG | T | 8 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(5): Show |
11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-3276delC | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075213 | |||||||
| chr2:131075275 | T | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0034 others(26): Show |
42 | HG00558.hp1 HG00639.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.71-3337A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075275 | |||||||
| chr2:131075275 | T | TA | 51 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(48): Show |
67 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.71-3338dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075275 | |||||||
| chr2:131075275 | TA | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0060 others(3): Show |
7 | HG01069.hp1 HG01884.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-3338delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075275 | |||||||
| chr2:131075499 | C | CT | 14 | a0001c0001t0001g0104 a0001c0001t0004g0010 a0001c0001t0004g0200 others(11): Show |
18 | HG01257.hp1 HG01258.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.71-3562dupA | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075499 | |||||||
| chr2:131075499 | CT | C | 7 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0040 others(4): Show |
7 | HG02055.hp2 HG02895.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-3562delA | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075499 | |||||||
| chr2:131075536 | CCA | C | 8 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(5): Show |
11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-3600_71-3599del others(2): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075536 | |||||||
| chr2:131075627 | T | C | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.71-3689A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075627 | |||||||
| chr2:131075644 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.71-3706C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075644 | |||||||
| chr2:131075706 | T | G | 1 | a0001c0001t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.71-3768A>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075706 | |||||||
| chr2:131075731 | G | A | 7 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-3793C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075731 | |||||||
| chr2:131075783 | C | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG00735.hp2 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.71-3845G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075783 | |||||||
| chr2:131075816 | T | C | 1 | a0001c0001t0001g0016 | 2 | HG03017.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.71-3878A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075816 | |||||||
| chr2:131075843 | G | A | 1 | a0001c0001t0004g0202 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.71-3905C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075843 | |||||||
| chr2:131075967 | C | T | 1 | a0001c0001t0024g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.71-4029G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075967 | |||||||
| chr2:131076050 | G | A | 9 | a0001c0001t0003g0148 a0001c0001t0003g0156 a0001c0001t0003g0157 others(6): Show |
10 | HG00099.hp1 HG00642.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.71-4112C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076050 | |||||||
| chr2:131076130 | C | T | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.71-4192G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076130 | |||||||
| chr2:131076185 | T | C | 93 | a0001c0001t0001g0008 a0001c0001t0001g0124 a0001c0001t0001g0133 others(90): Show |
118 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.71-4247A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076185 | |||||||
| chr2:131076249 | C | T | 5 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(2): Show |
6 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-4311G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076249 | |||||||
| chr2:131076319 | CCTACATC others(4): Show |
C | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.71-4392_71-4382del others(11): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076319 | |||||||
| chr2:131076457 | T | C | 79 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(76): Show |
102 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.71-4519A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076457 | |||||||
| chr2:131076563 | G | A | 1 | a0001c0001t0024g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.71-4625C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076563 | |||||||
| chr2:131076652 | T | TA | 30 | a0001c0001t0001g0008 a0001c0001t0001g0136 a0001c0001t0001g0137 others(27): Show |
38 | HG01257.hp1 HG01258.hp2 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.71-4715dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076652 | |||||||
| chr2:131076652 | TA | T | 7 | a0001c0001t0001g0081 a0001c0001t0001g0193 a0001c0001t0002g0172 others(4): Show |
8 | HG01975.hp1 HG02040.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-4715delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076652 | |||||||
| chr2:131076690 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.71-4752T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076690 | |||||||
| chr2:131076707 | A | T | 1 | a0001c0001t0022g0063 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.71-4769T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076707 | |||||||
| chr2:131076716 | T | A | 7 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-4778A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076716 | |||||||
| chr2:131076834 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.71-4896G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076834 | |||||||
| chr2:131076956 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0033g0111 |
2 | NA18951.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.71-5018C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076956 | |||||||
| chr2:131077003 | C | A | 1 | a0001c0001t0002g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.71-5065G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077003 | |||||||
| chr2:131077045 | G | A | 52 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(49): Show |
68 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.71-5107C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077045 | |||||||
| chr2:131077058 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | NA18992.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.71-5120C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077058 | |||||||
| chr2:131077175 | A | C | 5 | a0001c0001t0001g0124 a0001c0001t0008g0053 a0001c0001t0008g0054 others(2): Show |
5 | HG01109.hp2 HG02258.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-5237T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077175 | |||||||
| chr2:131077212 | T | TA | 9 | a0001c0001t0001g0072 a0001c0001t0001g0095 a0001c0001t0001g0112 others(6): Show |
12 | HG01243.hp2 HG02055.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.71-5275dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077212 | |||||||
| chr2:131077212 | TA | T | 67 | a0001c0001t0001g0035 a0001c0001t0001g0062 a0001c0001t0001g0070 others(64): Show |
84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.71-5275delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077212 | |||||||
| chr2:131077212 | TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0001g0039 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.71-5284_71-5275del others(10): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077212 | |||||||
| chr2:131077213 | A | G | 6 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(3): Show |
7 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-5275T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077213 | |||||||
| chr2:131077333 | G | A | 1 | a0001c0001t0024g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.70+5244C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077333 | |||||||
| chr2:131077346 | T | G | 1 | a0001c0001t0002g0145 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.70+5231A>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077346 | |||||||
| chr2:131077555 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.70+5022G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077555 | |||||||
| chr2:131077741 | A | T | 2 | a0001c0001t0014g0190 a0001c0001t0014g0191 |
2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.70+4836T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077741 | |||||||
| chr2:131077853 | T | C | 4 | a0001c0001t0007g0018 a0001c0001t0007g0141 a0001c0001t0007g0142 others(1): Show |
5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+4724A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077853 | |||||||
| chr2:131077981 | A | G | 7 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.70+4596T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077981 | |||||||
| chr2:131078023 | T | C | 1 | a0001c0001t0031g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.70+4554A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078023 | |||||||
| chr2:131078082 | A | T | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.70+4495T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078082 | |||||||
| chr2:131078202 | G | A | 1 | a0001c0001t0003g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.70+4375C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078202 | |||||||
| chr2:131078236 | G | C | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.70+4341C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078236 | |||||||
| chr2:131078320 | T | C | 9 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(6): Show |
12 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.70+4257A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078320 | |||||||
| chr2:131078543 | C | G | 5 | a0001c0001t0001g0124 a0001c0001t0008g0053 a0001c0001t0008g0054 others(2): Show |
5 | HG01109.hp2 HG02258.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+4034G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078543 | |||||||
| chr2:131078700 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.70+3877A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078700 | |||||||
| chr2:131078706 | A | G | 96 | a0001c0001t0001g0008 a0001c0001t0001g0124 a0001c0001t0001g0133 others(93): Show |
121 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.70+3871T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078706 | |||||||
| chr2:131078787 | C | G | 1 | a0001c0001t0003g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.70+3790G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078787 | |||||||
| chr2:131078841 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.70+3736A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078841 | |||||||
| chr2:131078925 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.70+3652A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078925 | |||||||
| chr2:131078988 | A | C | 1 | a0001c0001t0025g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.70+3589T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078988 | |||||||
| chr2:131079022 | G | A | 3 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0026g0187 |
4 | HG01175.hp2 HG01261.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+3555C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131079022 | |||||||
| chr2:131079036 | T | A | 1 | a0001c0001t0001g0074 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.70+3541A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131079036 | |||||||
| chr2:131079222 | A | C | 1 | a0001c0001t0001g0102 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.70+3355T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131079222 | |||||||
| chr2:131079251 | T | C | 1 | a0001c0001t0005g0166 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.70+3326A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131079251 | |||||||
| chr2:131079339 | G | A | 1 | a0001c0001t0024g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.70+3238C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131079339 | |||||||
| chr2:131079346 | A | G | 82 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(79): Show |
105 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.70+3231T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131079346 | |||||||
| chr2:131079507 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.70+3070C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131079507 | |||||||
| chr2:131079657 | G | A | 1 | a0001c0001t0003g0159 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.70+2920C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131079657 | |||||||
| chr2:131079669 | C | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(177): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.70+2908G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131079669 | |||||||
| chr2:131079990 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.70+2587C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131079990 | |||||||
| chr2:131080327 | C | T | 4 | a0001c0001t0007g0018 a0001c0001t0007g0141 a0001c0001t0007g0142 others(1): Show |
5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+2250G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131080327 | |||||||
| chr2:131080543 | G | A | 1 | a0001c0001t0019g0146 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.70+2034C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131080543 | |||||||
| chr2:131080762 | C | T | 7 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0040 others(4): Show |
7 | HG02055.hp2 HG02895.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.70+1815G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131080762 | |||||||
| chr2:131080800 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.70+1777C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131080800 | |||||||
| chr2:131080801 | C | G | 1 | a0001c0001t0008g0055 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.70+1776G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131080801 | |||||||
| chr2:131080879 | C | A | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.70+1698G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131080879 | |||||||
| chr2:131080934 | T | C | 4 | a0001c0001t0007g0018 a0001c0001t0007g0141 a0001c0001t0007g0142 others(1): Show |
5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+1643A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131080934 | |||||||
| chr2:131081005 | C | G | 1 | a0001c0001t0001g0061 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.70+1572G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131081005 | |||||||
| chr2:131081338 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.70+1239A>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131081338 | |||||||
| chr2:131081417 | C | T | 50 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(47): Show |
64 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.70+1160G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131081417 | |||||||
| chr2:131081889 | A | T | 1 | a0001c0001t0002g0185 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.70+688T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131081889 | |||||||
| chr2:131082027 | C | T | 2 | a0001c0001t0012g0023 a0001c0001t0012g0189 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.70+550G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131082027 | |||||||
| chr2:131082254 | T | C | 1 | a0001c0001t0025g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.70+323A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131082254 | |||||||
| chr2:131082257 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.70+320A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131082257 | |||||||
| chr2:131082347 | G | A | 1 | a0001c0001t0002g0183 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.70+230C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131082347 | |||||||
| chr2:131082389 | A | G | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.70+188T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131082389 | |||||||
| chr2:131082489 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02895.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.70+88G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131082489 | |||||||
| chr2:131082490 | G | A | 1 | a0001c0001t0027g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.70+87C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131082490 | |||||||
| chr2:131082820 | G | A | 1 | a0001c0001t0020g0186 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-11-163C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131082820 | |||||||
| chr2:131082835 | G | A | 1 | a0001c0001t0006g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-11-178C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131082835 | |||||||
| chr2:131083183 | G | A | 9 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(6): Show |
12 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11-526C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083183 | |||||||
| chr2:131083197 | T | C | 1 | a0001c0001t0031g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-11-540A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083197 | |||||||
| chr2:131083348 | G | A | 4 | a0001c0001t0007g0018 a0001c0001t0007g0141 a0001c0001t0007g0142 others(1): Show |
5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-691C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083348 | |||||||
| chr2:131083358 | A | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0069 |
2 | HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-11-701T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083358 | |||||||
| chr2:131083486 | AGCCAAGC others(4): Show |
A | 1 | a0001c0001t0001g0115 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-11-840_-11-830del others(11): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083486 | |||||||
| chr2:131083539 | G | A | 3 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0026g0187 |
4 | HG01175.hp2 HG01261.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-882C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083539 | |||||||
| chr2:131083654 | A | T | 1 | a0001c0001t0001g0077 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-11-997T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083654 | |||||||
| chr2:131083845 | T | A | 1 | a0001c0001t0001g0133 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-11-1188A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083845 | |||||||
| chr2:131083874 | G | GTATT | 7 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0058 others(4): Show |
7 | HG01261.hp1 HG01517.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11-1221_-11-1218d others(6): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083874 | |||||||
| chr2:131083874 | GTATT | G | 37 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0037 others(34): Show |
44 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.-11-1221_-11-1218d others(6): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083874 | |||||||
| chr2:131083874 | GTATTTAT others(1): Show |
G | 62 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0043 others(59): Show |
77 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.-11-1225_-11-1218d others(10): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083874 | |||||||
| chr2:131083874 | GTATTTAT others(5): Show |
G | 6 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(3): Show |
7 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-1229_-11-1218d others(14): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083874 | |||||||
| chr2:131083874 | GTATTTAT others(9): Show |
G | 8 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(5): Show |
10 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11-1233_-11-1218d others(18): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083874 | |||||||
| chr2:131083930 | A | C | 4 | a0001c0001t0001g0124 a0001c0001t0008g0053 a0001c0001t0008g0054 others(1): Show |
4 | HG02258.hp1 HG03209.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-1273T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083930 | |||||||
| chr2:131083998 | G | C | 1 | a0001c0001t0024g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-11-1341C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083998 | |||||||
| chr2:131084052 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-11-1395C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084052 | |||||||
| chr2:131084127 | C | T | 1 | a0001c0001t0025g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-11-1470G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084127 | |||||||
| chr2:131084143 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0120 |
2 | HG01258.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-11-1486C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084143 | |||||||
| chr2:131084191 | C | G | 1 | a0001c0001t0001g0037 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-11-1534G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084191 | |||||||
| chr2:131084197 | C | A | 9 | a0001c0001t0001g0073 a0001c0001t0003g0151 a0001c0001t0006g0024 others(6): Show |
10 | HG01257.hp1 HG01258.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11-1540G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084197 | |||||||
| chr2:131084198 | A | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | NA18971.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-11-1541T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084198 | |||||||
| chr2:131084235 | G | A | 1 | a0001c0001t0008g0055 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-11-1578C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084235 | |||||||
| chr2:131084239 | G | A | 1 | a0001c0001t0005g0166 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-11-1582C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084239 | |||||||
| chr2:131084378 | T | A | 7 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11-1721A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084378 | |||||||
| chr2:131084448 | C | A | 54 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(51): Show |
70 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.-11-1791G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084448 | |||||||
| chr2:131084500 | A | G | 1 | a0001c0001t0003g0017 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-11-1843T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084500 | |||||||
| chr2:131084581 | A | G | 8 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(5): Show |
11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11-1924T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084581 | |||||||
| chr2:131084606 | G | T | 5 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(2): Show |
6 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-1949C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084606 | |||||||
| chr2:131084880 | G | T | 2 | a0001c0001t0002g0021 a0001c0001t0002g0170 |
3 | HG00280.hp1 HG01192.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-11-2223C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084880 | |||||||
| chr2:131085297 | A | G | 4 | a0001c0001t0001g0074 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
4 | HG01258.hp1 HG03492.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-2640T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131085297 | |||||||
| chr2:131085408 | A | G | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG00735.hp2 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-11-2751T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131085408 | |||||||
| chr2:131085522 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-11-2865G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131085522 | |||||||
| chr2:131085585 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-11-2928G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131085585 | |||||||
| chr2:131085686 | C | T | 1 | a0001c0001t0025g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-11-3029G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131085686 | |||||||
| chr2:131085706 | ACTGT | A | 9 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(6): Show |
12 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11-3053_-11-3050d others(6): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131085706 | |||||||
| chr2:131086038 | T | C | 7 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11-3381A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086038 | |||||||
| chr2:131086312 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0073 |
5 | HG01255.hp1 HG01934.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-3655T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086312 | |||||||
| chr2:131086551 | G | A | 1 | a0001c0001t0025g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-11-3894C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086551 | |||||||
| chr2:131086578 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-11-3921A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086578 | |||||||
| chr2:131086644 | A | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | NA18971.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-11-3987T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086644 | |||||||
| chr2:131086647 | T | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(64): Show |
84 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-11-3990A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086647 | |||||||
| chr2:131086721 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-11-4064A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086721 | |||||||
| chr2:131086766 | TAAGAGTC others(310): Show |
T | 27 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(24): Show |
34 | HG01175.hp2 HG01243.hp2 HG01257.hp1 others(31): Show |
intron_variant | MODIFIER | c.-11-4426_-11-4110d others(2): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086766 | |||||||
| chr2:131086781 | AAAGGCCG others(312): Show |
A | 55 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(52): Show |
71 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-11-4443_-11-4125d others(2): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086781 | |||||||
| chr2:131086838 | G | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG00735.hp2 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-11-4181C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086838 | |||||||
| chr2:131086858 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-11-4201C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086858 | |||||||
| chr2:131086981 | T | C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0045 a0001c0001t0001g0104 others(14): Show |
19 | HG00735.hp2 HG01109.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-11-4324A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086981 | |||||||
| chr2:131087030 | C | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0106 |
2 | HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-11-4373G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087030 | |||||||
| chr2:131087044 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-11-4387G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087044 | |||||||
| chr2:131087045 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-11-4388C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087045 | |||||||
| chr2:131087063 | C | CA | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(89): Show |
117 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-11-4407dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087063 | |||||||
| chr2:131087063 | C | CAA | 18 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(15): Show |
18 | HG01261.hp1 HG01884.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-11-4408_-11-4407d others(4): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087063 | |||||||
| chr2:131087063 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0140 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-11-4419_-11-4407d others(15): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087063 | |||||||
| chr2:131087063 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0008g0053 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-11-4423_-11-4407d others(19): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087063 | |||||||
| chr2:131087063 | C | CAAAAAAA others(11): Show |
3 | a0001c0001t0001g0137 a0001c0001t0008g0054 a0001c0001t0008g0055 |
3 | HG01884.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-11-4424_-11-4407d others(20): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087063 | |||||||
| chr2:131087063 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0008 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-11-4425_-11-4407d others(21): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087063 | |||||||
| chr2:131087063 | C | CAAAAAAA others(15): Show |
2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-11-4428_-11-4407d others(24): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087063 | |||||||
| chr2:131087063 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0136 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-11-4407_-11-4406i others(25): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087063 | |||||||
| chr2:131087063 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-11-4407_-11-4406i others(26): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087063 | |||||||
| chr2:131087102 | A | T | 55 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(52): Show |
71 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-11-4445T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087102 | |||||||
| chr2:131087177 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-11-4520C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087177 | |||||||
| chr2:131087183 | G | A | 1 | a0001c0001t0004g0205 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-11-4526C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087183 | |||||||
| chr2:131087199 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-11-4542G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087199 | |||||||
| chr2:131087367 | G | A | 1 | a0001c0001t0025g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-11-4710C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087367 | |||||||
| chr2:131087467 | G | A | 4 | a0001c0001t0007g0018 a0001c0001t0007g0141 a0001c0001t0007g0142 others(1): Show |
5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-4810C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087467 | |||||||
| chr2:131087697 | A | C | 1 | a0001c0001t0008g0053 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-11-5040T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087697 | |||||||
| chr2:131087814 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-11-5157G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087814 | |||||||
| chr2:131087982 | A | C | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12+5232T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087982 | |||||||
| chr2:131088020 | C | T | 7 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12+5194G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088020 | |||||||
| chr2:131088118 | C | T | 4 | a0001c0001t0012g0023 a0001c0001t0012g0189 a0001c0001t0014g0190 others(1): Show |
5 | HG02257.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+5096G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088118 | |||||||
| chr2:131088199 | T | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-12+5015A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088199 | |||||||
| chr2:131088226 | A | G | 1 | a0001c0001t0024g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-12+4988T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088226 | |||||||
| chr2:131088250 | GA | G | 95 | a0001c0001t0001g0008 a0001c0001t0001g0125 a0001c0001t0001g0133 others(92): Show |
120 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.-12+4963delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088250 | |||||||
| chr2:131088328 | T | C | 9 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(6): Show |
12 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12+4886A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088328 | |||||||
| chr2:131088605 | G | A | 1 | a0001c0001t0007g0018 | 2 | HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-12+4609C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088605 | |||||||
| chr2:131088629 | G | A | 82 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(79): Show |
105 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.-12+4585C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088629 | |||||||
| chr2:131088802 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0104 a0001c0001t0016g0036 others(1): Show |
4 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+4412C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088802 | |||||||
| chr2:131088802 | G | C | 51 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(48): Show |
65 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.-12+4412C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088802 | |||||||
| chr2:131088959 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12+4255C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088959 | |||||||
| chr2:131088965 | C | CT | 85 | a0001c0001t0001g0037 a0001c0001t0001g0051 a0001c0001t0001g0052 others(82): Show |
108 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.-12+4248dupA | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088965 | |||||||
| chr2:131089029 | C | T | 1 | a0001c0001t0003g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-12+4185G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131089029 | |||||||
| chr2:131089030 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-12+4184C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131089030 | |||||||
| chr2:131089154 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-12+4060G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131089154 | |||||||
| chr2:131089471 | G | A | 1 | a0001c0001t0007g0141 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-12+3743C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131089471 | |||||||
| chr2:131089701 | G | C | 1 | a0001c0001t0001g0034 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-12+3513C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131089701 | |||||||
| chr2:131089704 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-12+3510G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131089704 | |||||||
| chr2:131089847 | C | T | 9 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(6): Show |
12 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12+3367G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131089847 | |||||||
| chr2:131089892 | G | A | 50 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(47): Show |
64 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-12+3322C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131089892 | |||||||
| chr2:131089933 | G | A | 1 | a0001c0001t0003g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-12+3281C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131089933 | |||||||
| chr2:131090086 | G | A | 55 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(52): Show |
71 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-12+3128C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090086 | |||||||
| chr2:131090088 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0049 |
3 | HG03710.hp1 NA18971.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-12+3126G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090088 | |||||||
| chr2:131090112 | G | C | 1 | a0001c0001t0007g0018 | 2 | HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-12+3102C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090112 | |||||||
| chr2:131090135 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0117 |
2 | HG00735.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-12+3079C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090135 | |||||||
| chr2:131090151 | C | CA | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(156): Show |
203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.-12+3062dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090151 | |||||||
| chr2:131090151 | C | CAA | 25 | a0001c0001t0001g0005 a0001c0001t0001g0109 a0001c0001t0001g0110 others(22): Show |
30 | HG00544.hp1 HG00741.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.-12+3061_-12+3062d others(4): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090151 | |||||||
| chr2:131090319 | C | CA | 12 | a0001c0001t0001g0008 a0001c0001t0001g0118 a0001c0001t0001g0119 others(9): Show |
15 | HG00733.hp2 HG01258.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12+2894dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090319 | |||||||
| chr2:131090319 | CA | C | 81 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0038 others(78): Show |
102 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.-12+2894delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090319 | |||||||
| chr2:131090319 | CAA | C | 5 | a0001c0001t0003g0017 a0001c0001t0003g0148 a0001c0001t0007g0141 others(2): Show |
6 | HG02257.hp1 HG02698.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+2893_-12+2894d others(4): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090319 | |||||||
| chr2:131090418 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-12+2796G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090418 | |||||||
| chr2:131090486 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
8 | HG01884.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12+2728A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090486 | |||||||
| chr2:131090713 | A | C | 1 | a0001c0001t0001g0035 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-12+2501T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090713 | |||||||
| chr2:131090736 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-12+2478T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090736 | |||||||
| chr2:131090890 | C | T | 1 | a0001c0001t0005g0147 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-12+2324G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090890 | |||||||
| chr2:131090974 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-12+2240G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090974 | |||||||
| chr2:131091059 | T | C | 82 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(79): Show |
105 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.-12+2155A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131091059 | |||||||
| chr2:131091318 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0008g0122 |
2 | HG01069.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.-12+1896C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131091318 | |||||||
| chr2:131091318 | G | C | 1 | a0001c0001t0025g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-12+1896C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131091318 | |||||||
| chr2:131091516 | G | C | 4 | a0001c0001t0010g0009 a0001c0001t0013g0026 a0001c0001t0013g0167 others(1): Show |
6 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+1698C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131091516 | |||||||
| chr2:131091591 | G | C | 28 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(25): Show |
36 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.-12+1623C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131091591 | |||||||
| chr2:131091595 | C | G | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12+1619G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131091595 | |||||||
| chr2:131091686 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0032 |
2 | NA18971.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-12+1528G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131091686 | |||||||
| chr2:131091861 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-12+1353C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131091861 | |||||||
| chr2:131091965 | T | TAA | 51 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0021 others(48): Show |
66 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.-12+1247_-12+1248d others(4): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131091965 | |||||||
| chr2:131091965 | TA | T | 7 | a0001c0001t0009g0022 a0001c0001t0009g0188 a0001c0001t0012g0023 others(4): Show |
9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12+1248delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131091965 | |||||||
| chr2:131092004 | C | A | 8 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(5): Show |
11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12+1210G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092004 | |||||||
| chr2:131092036 | T | C | 4 | a0001c0001t0012g0023 a0001c0001t0012g0189 a0001c0001t0014g0190 others(1): Show |
5 | HG02257.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+1178A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092036 | |||||||
| chr2:131092062 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-12+1152A>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092062 | |||||||
| chr2:131092143 | C | CA | 5 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0004g0203 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+1070dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092143 | |||||||
| chr2:131092143 | CA | C | 5 | a0001c0001t0001g0030 a0001c0001t0002g0130 a0001c0001t0002g0131 others(2): Show |
6 | HG01433.hp1 HG01515.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+1070delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092143 | |||||||
| chr2:131092210 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-12+1004A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092210 | |||||||
| chr2:131092285 | T | A | 1 | a0001c0001t0001g0127 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-12+929A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092285 | |||||||
| chr2:131092366 | C | CTTT | 23 | a0001c0001t0004g0010 a0001c0001t0004g0200 a0001c0001t0004g0201 others(20): Show |
29 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.-12+847_-12+848ins others(3): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092366 | |||||||
| chr2:131092555 | C | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0008g0028 |
3 | HG01517.hp2 HG01884.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-12+659G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092555 | |||||||
| chr2:131092680 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-12+534A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092680 | |||||||
| chr2:131092806 | C | CA | 8 | a0001c0001t0002g0192 a0001c0001t0009g0022 a0001c0001t0009g0188 others(5): Show |
10 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12+407dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092806 | |||||||
| chr2:131092814 | T | A | 91 | a0001c0001t0001g0008 a0001c0001t0001g0133 a0001c0001t0001g0134 others(88): Show |
116 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.-12+400A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092814 | |||||||
| chr2:131092821 | A | G | 1 | a0001c0001t0013g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-12+393T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092821 | |||||||
| chr2:131092863 | C | A | 1 | a0001c0001t0001g0193 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-12+351G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092863 | |||||||
| chr2:131092867 | T | C | 1 | a0001c0001t0024g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-12+347A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092867 | |||||||
| chr2:131092962 | G | A | 7 | a0001c0001t0006g0024 a0001c0001t0006g0194 a0001c0001t0006g0195 others(4): Show |
8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12+252C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092962 |