Item | Value |
---|---|
geneid | 92689 |
ensemblid | ENSG00000197712.12 |
hgncid | 25087 |
symbol | FAM114A1 |
name | family with sequence similarity 114 member A1 |
refseq_nuc | NM_138389.4 |
refseq_prot | NP_612398.2 |
ensembl_nuc | ENST00000358869.5 |
ensembl_prot | ENSP00000351740.2 |
mane_status | MANE Select |
chr | chr4 |
start | 38867806 |
end | 38945739 |
strand | + |
ver | v1.2 |
region | chr4:38867806-38945739 |
region5000 | chr4:38862806-38950739 |
regionname0 | FAM114A1_chr4_38867806_38945739 |
regionname5000 | FAM114A1_chr4_38862806_38950739 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 563 | 268 | 49 | 48 | 130 | 7 | 32 | 97 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | MSDDA others(558): Show |
chr4 | 38862806 | 38950739 |
a0002 | 0/0 | 563 | 54 | 27 | 9 | 13 | 2 | 3 | 10 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | MSDDA others(558): Show |
chr4 | 38862806 | 38950739 |
a0003 | 0/0 | 563 | 9 | 0 | 6 | 1 | 1 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | MSDDA others(558): Show |
chr4 | 38862806 | 38950739 |
a0004 | 0/0 | 563 | 9 | 3 | 2 | 2 | 0 | 2 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | MSDDA others(558): Show |
chr4 | 38862806 | 38950739 |
a0005 | 0/0 | 563 | 8 | 5 | 0 | 0 | 0 | 3 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | MSDDA others(558): Show |
chr4 | 38862806 | 38950739 |
a0006 | 0/0 | 563 | 5 | 0 | 4 | 1 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | MSDDA others(558): Show |
chr4 | 38862806 | 38950739 |
a0007 | 0/0 | 563 | 4 | 0 | 0 | 2 | 0 | 2 | 2 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | MSDDA others(558): Show |
chr4 | 38862806 | 38950739 |
a0008 | 0/0 | 563 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | MSDDA others(558): Show |
chr4 | 38862806 | 38950739 |
a0009 | 0/0 | 563 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | MSDDA others(558): Show |
chr4 | 38862806 | 38950739 |
a0010 | 0/0 | 563 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | MSDDA others(558): Show |
chr4 | 38862806 | 38950739 |
a0011 | 0/0 | 563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | MSDDA others(558): Show |
chr4 | 38862806 | 38950739 |
a0012 | 0/0 | 563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | MSDDA others(558): Show |
chr4 | 38862806 | 38950739 |
a0013 | 0/0 | 563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | MSDDA others(558): Show |
chr4 | 38862806 | 38950739 |
a0014 | 0/0 | 563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | MSDDA others(558): Show |
chr4 | 38862806 | 38950739 |
a0015 | 0/0 | 563 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | MSDDA others(558): Show |
chr4 | 38862806 | 38950739 |
a0016 | 0/0 | 563 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | MSDDA others(558): Show |
chr4 | 38862806 | 38950739 |
a0017 | 0/0 | 563 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | MSDDA others(558): Show |
chr4 | 38862806 | 38950739 |
a0018 | 0/0 | 563 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | MSDDA others(558): Show |
chr4 | 38862806 | 38950739 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1689 | 142 | 31 | 25 | 60 | 4 | 21 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0001c0002 | 1/0 | 1689 | 68 | 4 | 21 | 32 | 2 | 8 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0001c0004 | 0/0 | 1689 | 26 | 8 | 0 | 18 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0001c0005 | 0/0 | 1689 | 10 | 1 | 0 | 8 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0001c0008 | 0/0 | 1689 | 6 | 0 | 0 | 6 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0001c0009 | 0/0 | 1689 | 6 | 1 | 1 | 1 | 1 | 2 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0001c0013 | 0/0 | 1689 | 3 | 0 | 0 | 3 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0001c0023 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0001c0037 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0001c0038 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0001c0039 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0001c0043 | 0/0 | 1689 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0001c0044 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0001c0046 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0002c0003 | 0/0 | 1689 | 32 | 17 | 4 | 10 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0002c0006 | 0/0 | 1689 | 7 | 1 | 3 | 0 | 1 | 2 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0002c0016 | 0/0 | 1689 | 2 | 1 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0002c0022 | 0/0 | 1689 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0002c0025 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0002c0026 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0002c0027 | 0/0 | 1689 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0002c0028 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0002c0029 | 0/0 | 1689 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0002c0032 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0002c0034 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0002c0053 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0002c0054 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0002c0056 | 0/0 | 1689 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0002c0057 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0003c0007 | 0/0 | 1689 | 6 | 0 | 4 | 0 | 1 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0003c0018 | 0/0 | 1689 | 2 | 0 | 2 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0003c0024 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0004c0011 | 0/0 | 1689 | 4 | 2 | 1 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0004c0020 | 0/0 | 1689 | 2 | 1 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0004c0036 | 0/0 | 1689 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0004c0041 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0004c0042 | 0/0 | 1689 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0005c0012 | 0/0 | 1689 | 3 | 1 | 0 | 0 | 0 | 2 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0005c0015 | 0/0 | 1689 | 3 | 3 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0005c0030 | 0/0 | 1689 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0005c0055 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0006c0010 | 0/0 | 1689 | 4 | 0 | 4 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0006c0035 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0007c0021 | 0/0 | 1689 | 2 | 0 | 0 | 1 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0007c0048 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0007c0049 | 0/0 | 1689 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0008c0014 | 0/0 | 1689 | 3 | 3 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0009c0017 | 0/0 | 1689 | 2 | 0 | 1 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0010c0019 | 0/0 | 1689 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0011c0033 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0012c0040 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0013c0052 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0014c0051 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0015c0050 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0016c0047 | 0/0 | 1689 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0017c0031 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 | ||
a0018c0045 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ATGTC others(1684): Show |
chr4 | 38862806 | 38950739 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4060 | 18 | 3 | 5 | 6 | 0 | 3 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0002 | 0/0 | 4064 | 55 | 6 | 11 | 25 | 1 | 12 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0004 | 0/0 | 4059 | 14 | 2 | 3 | 4 | 2 | 3 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0005 | 0/0 | 4064 | 8 | 8 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0006 | 0/0 | 4059 | 8 | 0 | 0 | 8 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0007 | 0/0 | 4060 | 6 | 3 | 0 | 3 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0008 | 0/0 | 4059 | 5 | 0 | 0 | 5 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0009 | 0/0 | 4058 | 2 | 0 | 1 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4053): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0010 | 0/0 | 4059 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0011 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4053): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0012 | 0/0 | 4065 | 4 | 1 | 1 | 1 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4060): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0013 | 0/0 | 4061 | 2 | 0 | 0 | 1 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4056): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0014 | 0/0 | 4064 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0015 | 0/0 | 4058 | 2 | 0 | 2 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4053): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0016 | 0/0 | 4060 | 2 | 1 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0017 | 0/0 | 4060 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0021 | 0/0 | 4060 | 2 | 0 | 1 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0026 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0027 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0031 | 0/0 | 4064 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0035 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0038 | 0/0 | 4064 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0041 | 0/0 | 4060 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0001c0001t0042 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0001c0002t0001 | 1/0 | 4060 | 44 | 2 | 14 | 21 | 2 | 4 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0001c0002t0002 | 0/0 | 4064 | 7 | 0 | 1 | 4 | 0 | 2 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0001c0002t0006 | 0/0 | 4059 | 4 | 0 | 4 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0001c0002t0007 | 0/0 | 4060 | 4 | 0 | 0 | 3 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0001c0002t0008 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0001c0002t0011 | 0/0 | 4058 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4053): Show |
chr4 | 38862806 | 38950739 |
a0001c0002t0013 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4056): Show |
chr4 | 38862806 | 38950739 |
a0001c0002t0014 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0001c0002t0019 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0001c0002t0020 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0001c0002t0028 | 0/0 | 4060 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0001c0002t0037 | 0/0 | 4064 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0001c0002t0040 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4060): Show |
chr4 | 38862806 | 38950739 |
a0001c0004t0001 | 0/0 | 4060 | 2 | 1 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0001c0004t0002 | 0/0 | 4064 | 9 | 2 | 0 | 7 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0001c0004t0004 | 0/0 | 4059 | 4 | 0 | 0 | 4 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0001c0004t0006 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0001c0004t0007 | 0/0 | 4060 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0001c0004t0008 | 0/0 | 4059 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0001c0004t0011 | 0/0 | 4058 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4053): Show |
chr4 | 38862806 | 38950739 |
a0001c0004t0022 | 0/0 | 4064 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0001c0004t0029 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0001c0004t0039 | 0/0 | 4064 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0001c0005t0003 | 0/0 | 4059 | 10 | 1 | 0 | 8 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0001c0008t0006 | 0/0 | 4059 | 6 | 0 | 0 | 6 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0001c0009t0003 | 0/0 | 4059 | 5 | 1 | 1 | 1 | 1 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0001c0009t0010 | 0/0 | 4059 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0001c0013t0001 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0001c0013t0002 | 0/0 | 4064 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0001c0013t0006 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0001c0023t0002 | 0/0 | 4064 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0001c0037t0003 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0001c0038t0005 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0001c0039t0024 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4060): Show |
chr4 | 38862806 | 38950739 |
a0001c0043t0001 | 0/0 | 4060 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0001c0044t0024 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4060): Show |
chr4 | 38862806 | 38950739 |
a0001c0046t0002 | 0/0 | 4064 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0002c0003t0001 | 0/0 | 4060 | 6 | 1 | 2 | 3 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0002c0003t0002 | 0/0 | 4064 | 5 | 4 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0002c0003t0004 | 0/0 | 4059 | 4 | 1 | 0 | 2 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0002c0003t0005 | 0/0 | 4064 | 7 | 7 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0002c0003t0006 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0002c0003t0007 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0002c0003t0010 | 0/0 | 4059 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0002c0003t0012 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4060): Show |
chr4 | 38862806 | 38950739 |
a0002c0003t0016 | 0/0 | 4060 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0002c0003t0017 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0002c0003t0018 | 0/0 | 4059 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0002c0003t0032 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0002c0006t0001 | 0/0 | 4060 | 5 | 0 | 3 | 0 | 0 | 2 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0002c0006t0010 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0002c0006t0011 | 0/0 | 4058 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4053): Show |
chr4 | 38862806 | 38950739 |
a0002c0016t0001 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0002c0016t0007 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0002c0022t0005 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0002c0022t0010 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0002c0025t0003 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0002c0026t0005 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0002c0027t0003 | 0/0 | 4059 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0002c0028t0030 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0002c0029t0043 | 0/0 | 4060 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0002c0032t0044 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4060): Show |
chr4 | 38862806 | 38950739 |
a0002c0034t0020 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0002c0053t0001 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0002c0054t0036 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0002c0056t0005 | 0/0 | 4064 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0002c0057t0005 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0003c0007t0009 | 0/0 | 4058 | 4 | 0 | 3 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4053): Show |
chr4 | 38862806 | 38950739 |
a0003c0007t0015 | 0/0 | 4058 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4053): Show |
chr4 | 38862806 | 38950739 |
a0003c0007t0025 | 0/0 | 4059 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0003c0018t0003 | 0/0 | 4059 | 2 | 0 | 2 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0003c0024t0001 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0004c0011t0001 | 0/0 | 4060 | 2 | 0 | 1 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0004c0011t0002 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0004c0011t0014 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0004c0020t0003 | 0/0 | 4059 | 2 | 1 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0004c0036t0004 | 0/0 | 4059 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0004c0041t0003 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0004c0042t0003 | 0/0 | 4059 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0005c0012t0001 | 0/0 | 4060 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0005c0012t0033 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0005c0012t0034 | 0/0 | 4060 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0005c0015t0002 | 0/0 | 4064 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0005c0015t0005 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0005c0030t0003 | 0/0 | 4059 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0005c0055t0012 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4060): Show |
chr4 | 38862806 | 38950739 |
a0006c0010t0003 | 0/0 | 4059 | 3 | 0 | 3 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0006c0010t0007 | 0/0 | 4060 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0006c0035t0003 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0007c0021t0004 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0007c0021t0013 | 0/0 | 4061 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4056): Show |
chr4 | 38862806 | 38950739 |
a0007c0048t0008 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0007c0049t0002 | 0/0 | 4064 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0008c0014t0001 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0008c0014t0005 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0008c0014t0023 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0009c0017t0003 | 0/0 | 4059 | 2 | 0 | 1 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0010c0019t0001 | 0/0 | 4060 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0011c0033t0011 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4053): Show |
chr4 | 38862806 | 38950739 |
a0012c0040t0023 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0013c0052t0005 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0014c0051t0005 | 0/0 | 4064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4059): Show |
chr4 | 38862806 | 38950739 |
a0015c0050t0003 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
a0016c0047t0009 | 0/0 | 4058 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4053): Show |
chr4 | 38862806 | 38950739 |
a0017c0031t0019 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4055): Show |
chr4 | 38862806 | 38950739 |
a0018c0045t0004 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | ACTCC others(4054): Show |
chr4 | 38862806 | 38950739 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0001g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0006g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0006g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0006g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0006g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0007g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0007g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0007g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0007g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0007g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0008g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0008g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0008g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0008g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0008g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0009g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0009g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0010g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0010g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0011g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0012g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0012g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0012g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0012g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0013g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0013g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0014g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0014g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0015g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0015g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0016g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0016g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0017g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0017g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0021g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0021g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0026g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0027g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0031g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0035g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0038g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0041g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0001t0042g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0207 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0006g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0006g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0006g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0006g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0007g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0007g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0007g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0007g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0008g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0011g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0013g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0014g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0019g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0020g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0028g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0037g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0002t0040g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0007g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0007g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0008g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0008g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0011g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0011g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0022g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0029g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0004t0039g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0005t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0005t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0005t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0005t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0005t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0005t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0005t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0005t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0005t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0005t0003g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0008t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0008t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0008t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0008t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0008t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0008t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0009t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0009t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0009t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0009t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0009t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0009t0010g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0013t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0013t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0013t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0023t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0037t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0038t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0039t0024g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0043t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0044t0024g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0001c0046t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0004g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0005g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0005g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0005g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0005g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0005g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0007g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0010g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0010g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0012g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0016g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0017g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0018g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0018g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0003t0032g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0006t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0006t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0006t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0006t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0006t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0006t0010g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0006t0011g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0016t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0016t0007g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0022t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0022t0010g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0025t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0026t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0027t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0028t0030g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0029t0043g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0032t0044g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0034t0020g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0053t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0054t0036g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0056t0005g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0002c0057t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0003c0007t0009g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0003c0007t0009g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0003c0007t0009g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0003c0007t0009g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0003c0007t0015g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0003c0007t0025g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0003c0018t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0003c0018t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0003c0024t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0004c0011t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0004c0011t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0004c0011t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0004c0011t0014g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0004c0020t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0004c0020t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0004c0036t0004g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0004c0041t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0004c0042t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0005c0012t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0005c0012t0033g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0005c0012t0034g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0005c0015t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0005c0015t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0005c0015t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0005c0030t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0005c0055t0012g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0006c0010t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0006c0010t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0006c0010t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0006c0010t0007g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0006c0035t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0007c0021t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0007c0021t0013g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0007c0048t0008g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0007c0049t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0008c0014t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0008c0014t0005g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0008c0014t0023g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0009c0017t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0009c0017t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0010c0019t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0010c0019t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0011c0033t0011g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0012c0040t0023g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0013c0052t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0014c0051t0005g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0015c0050t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0016c0047t0009g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0017c0031t0019g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
a0018c0045t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0209 | EUR | GBR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0049 | EUR | GBR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00140 | hp1 | a0001 | c0001 | t0013 | g0238 | EUR | GBR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00140 | hp2 | a0002 | c0003 | t0004 | g0022 | EUR | GBR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0350 | EUR | FIN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00323 | hp2 | a0003 | c0007 | t0015 | g0031 | EUR | FIN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00408 | hp2 | a0001 | c0002 | t0002 | g0141 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00438 | hp2 | a0001 | c0013 | t0001 | g0290 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00544 | hp1 | a0001 | c0008 | t0006 | g0061 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00544 | hp2 | a0002 | c0003 | t0006 | g0036 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00558 | hp2 | a0001 | c0008 | t0006 | g0066 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00597 | hp1 | a0001 | c0004 | t0007 | g0136 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00597 | hp2 | a0001 | c0008 | t0006 | g0085 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00609 | hp2 | a0001 | c0002 | t0020 | g0237 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00621 | hp1 | a0002 | c0016 | t0007 | g0125 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00621 | hp2 | a0001 | c0008 | t0006 | g0065 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00639 | hp1 | a0002 | c0003 | t0016 | g0034 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0223 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00642 | hp2 | a0001 | c0002 | t0006 | g0327 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00673 | hp1 | a0001 | c0001 | t0006 | g0304 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | CHS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0182 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00735 | hp2 | a0001 | c0009 | t0003 | g0090 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00741 | hp1 | a0001 | c0002 | t0028 | g0351 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG00741 | hp2 | a0003 | c0007 | t0009 | g0032 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01069 | hp1 | a0003 | c0018 | t0003 | g0037 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0268 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01070 | hp2 | a0003 | c0007 | t0025 | g0035 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01071 | hp2 | a0003 | c0018 | t0003 | g0024 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01074 | hp1 | a0001 | c0002 | t0006 | g0329 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01074 | hp2 | a0001 | c0001 | t0015 | g0221 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0199 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0206 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01099 | hp1 | a0002 | c0006 | t0001 | g0033 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01106 | hp2 | a0004 | c0020 | t0003 | g0101 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01109 | hp1 | a0001 | c0001 | t0009 | g0149 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01109 | hp2 | a0002 | c0056 | t0005 | g0252 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01167 | hp2 | a0001 | c0043 | t0001 | g0006 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0236 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01175 | hp2 | a0001 | c0001 | t0015 | g0232 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01192 | hp2 | a0003 | c0007 | t0009 | g0025 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01243 | hp1 | a0002 | c0029 | t0043 | g0115 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0220 | AMR | PUR | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0201 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01255 | hp2 | a0002 | c0006 | t0001 | g0354 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0183 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01256 | hp2 | a0003 | c0007 | t0009 | g0030 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01257 | hp1 | a0001 | c0002 | t0011 | g0219 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01257 | hp2 | a0002 | c0003 | t0001 | g0128 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0253 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0137 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0088 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0205 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01361 | hp2 | a0001 | c0001 | t0021 | g0054 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01433 | hp1 | a0006 | c0010 | t0003 | g0172 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0166 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01516 | hp1 | a0001 | c0009 | t0003 | g0056 | EUR | IBS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0203 | EUR | IBS | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0231 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01884 | hp2 | a0004 | c0011 | t0014 | g0269 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01891 | hp1 | a0001 | c0044 | t0024 | g0226 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01891 | hp2 | a0002 | c0003 | t0005 | g0364 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01943 | hp2 | a0004 | c0011 | t0001 | g0302 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01952 | hp2 | a0001 | c0002 | t0002 | g0146 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01975 | hp2 | a0009 | c0017 | t0003 | g0126 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01978 | hp1 | a0002 | c0003 | t0002 | g0121 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01978 | hp2 | a0001 | c0002 | t0006 | g0188 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0200 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01993 | hp2 | a0006 | c0010 | t0007 | g0175 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02004 | hp1 | a0006 | c0010 | t0003 | g0189 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0314 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02027 | hp2 | a0003 | c0024 | t0001 | g0116 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02040 | hp2 | a0004 | c0041 | t0003 | g0158 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0181 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02074 | hp1 | a0001 | c0001 | t0007 | g0230 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02132 | hp1 | a0001 | c0005 | t0003 | g0283 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02135 | hp2 | a0001 | c0001 | t0038 | g0298 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02145 | hp1 | a0002 | c0057 | t0005 | g0251 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02145 | hp2 | a0002 | c0032 | t0044 | g0352 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02148 | hp1 | a0001 | c0001 | t0012 | g0334 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02148 | hp2 | a0002 | c0006 | t0001 | g0122 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02165 | hp1 | a0001 | c0005 | t0003 | g0222 | EAS | CDX | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02165 | hp2 | a0002 | c0003 | t0007 | g0117 | EAS | CDX | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02257 | hp1 | a0012 | c0040 | t0023 | g0235 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02257 | hp2 | a0001 | c0001 | t0007 | g0227 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02258 | hp1 | a0004 | c0020 | t0003 | g0046 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0301 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02273 | hp1 | a0002 | c0003 | t0001 | g0127 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02273 | hp2 | a0001 | c0002 | t0006 | g0174 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02280 | hp1 | a0002 | c0003 | t0005 | g0339 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02280 | hp2 | a0002 | c0003 | t0004 | g0342 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0204 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02300 | hp2 | a0006 | c0010 | t0003 | g0318 | AMR | PEL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0276 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02451 | hp2 | a0002 | c0003 | t0002 | g0043 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02523 | hp2 | a0001 | c0001 | t0013 | g0225 | EAS | KHV | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02602 | hp1 | a0001 | c0001 | t0009 | g0148 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02602 | hp2 | a0001 | c0005 | t0003 | g0323 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02615 | hp1 | a0002 | c0003 | t0005 | g0353 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0277 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02622 | hp1 | a0005 | c0012 | t0033 | g0341 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02622 | hp2 | a0008 | c0014 | t0001 | g0012 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02630 | hp1 | a0001 | c0004 | t0002 | g0286 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0195 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02647 | hp1 | a0005 | c0015 | t0002 | g0244 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02647 | hp2 | a0001 | c0004 | t0029 | g0015 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02698 | hp1 | a0005 | c0030 | t0003 | g0113 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0319 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02717 | hp1 | a0002 | c0053 | t0001 | g0245 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02717 | hp2 | a0001 | c0001 | t0035 | g0312 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02723 | hp1 | a0002 | c0003 | t0002 | g0045 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0069 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02738 | hp1 | a0001 | c0001 | t0012 | g0333 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02738 | hp2 | a0004 | c0042 | t0003 | g0167 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02809 | hp1 | a0002 | c0003 | t0010 | g0362 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02809 | hp2 | a0014 | c0051 | t0005 | g0344 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02818 | hp1 | a0002 | c0003 | t0032 | g0357 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02818 | hp2 | a0002 | c0054 | t0036 | g0243 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02886 | hp1 | a0001 | c0001 | t0014 | g0295 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02886 | hp2 | a0002 | c0003 | t0001 | g0359 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02896 | hp1 | a0001 | c0037 | t0003 | g0009 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02896 | hp2 | a0001 | c0004 | t0022 | g0003 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02897 | hp1 | a0005 | c0015 | t0002 | g0250 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02897 | hp2 | a0001 | c0004 | t0022 | g0003 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02922 | hp1 | a0005 | c0055 | t0012 | g0356 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02922 | hp2 | a0001 | c0039 | t0024 | g0261 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02965 | hp1 | a0001 | c0001 | t0012 | g0170 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02965 | hp2 | a0002 | c0003 | t0005 | g0343 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02970 | hp2 | a0001 | c0001 | t0010 | g0299 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0216 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02976 | hp2 | a0005 | c0015 | t0005 | g0246 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03041 | hp1 | a0008 | c0014 | t0005 | g0311 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03041 | hp2 | a0002 | c0003 | t0005 | g0042 | AFR | GWD | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03098 | hp1 | a0001 | c0001 | t0007 | g0256 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03098 | hp2 | a0002 | c0003 | t0012 | g0112 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03130 | hp1 | a0001 | c0001 | t0011 | g0010 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03130 | hp2 | a0002 | c0003 | t0005 | g0360 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03139 | hp1 | a0010 | c0019 | t0001 | g0282 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03139 | hp2 | a0001 | c0001 | t0042 | g0214 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03195 | hp2 | a0002 | c0026 | t0005 | g0039 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03225 | hp1 | a0001 | c0004 | t0001 | g0260 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03225 | hp2 | a0004 | c0011 | t0002 | g0313 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03239 | hp1 | a0001 | c0002 | t0037 | g0202 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0309 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03453 | hp1 | a0002 | c0003 | t0002 | g0358 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03486 | hp1 | a0001 | c0004 | t0002 | g0004 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03486 | hp2 | a0002 | c0022 | t0005 | g0249 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0163 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03490 | hp2 | a0002 | c0006 | t0001 | g0020 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03491 | hp2 | a0003 | c0007 | t0009 | g0023 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0233 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03516 | hp1 | a0001 | c0001 | t0014 | g0196 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0297 | AFR | ESN | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03579 | hp2 | a0015 | c0050 | t0003 | g0345 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03654 | hp2 | a0004 | c0036 | t0004 | g0008 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03688 | hp1 | a0002 | c0006 | t0001 | g0038 | SAS | STU | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0194 | SAS | STU | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03704 | hp1 | a0007 | c0049 | t0002 | g0348 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0215 | SAS | PJL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03831 | hp1 | a0001 | c0002 | t0007 | g0168 | SAS | BEB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0234 | SAS | BEB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03834 | hp1 | a0007 | c0021 | t0013 | g0340 | SAS | BEB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03834 | hp2 | a0002 | c0027 | t0003 | g0029 | SAS | BEB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0179 | SAS | BEB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03927 | hp2 | a0005 | c0012 | t0001 | g0027 | SAS | BEB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0257 | SAS | STU | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG04115 | hp2 | a0016 | c0047 | t0009 | g0150 | SAS | STU | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0139 | SAS | BEB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0330 | SAS | BEB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG04199 | hp1 | a0001 | c0009 | t0010 | g0332 | SAS | STU | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG04199 | hp2 | a0005 | c0012 | t0034 | g0021 | SAS | STU | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | STU | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | STU | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG04228 | hp2 | a0001 | c0001 | t0016 | g0322 | SAS | STU | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18522 | hp1 | a0002 | c0022 | t0010 | g0248 | AFR | YRI | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18522 | hp2 | a0001 | c0038 | t0005 | g0011 | AFR | YRI | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18612 | hp1 | a0001 | c0001 | t0008 | g0078 | EAS | CHB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | CHB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18906 | hp1 | a0002 | c0003 | t0005 | g0044 | AFR | YRI | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18906 | hp2 | a0001 | c0005 | t0003 | g0274 | AFR | YRI | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18940 | hp1 | a0001 | c0002 | t0008 | g0060 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18941 | hp1 | a0001 | c0046 | t0002 | g0095 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18941 | hp2 | a0001 | c0001 | t0017 | g0138 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18942 | hp2 | a0001 | c0004 | t0006 | g0258 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18945 | hp2 | a0001 | c0001 | t0006 | g0142 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18950 | hp1 | a0001 | c0004 | t0008 | g0098 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18950 | hp2 | a0007 | c0021 | t0004 | g0347 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18951 | hp2 | a0001 | c0005 | t0003 | g0154 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18952 | hp1 | a0001 | c0004 | t0002 | g0349 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18953 | hp1 | a0001 | c0004 | t0002 | g0082 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18953 | hp2 | a0017 | c0031 | t0019 | g0028 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18954 | hp1 | a0001 | c0001 | t0006 | g0081 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18956 | hp1 | a0007 | c0048 | t0008 | g0346 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18956 | hp2 | a0001 | c0004 | t0007 | g0331 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18960 | hp1 | a0001 | c0004 | t0004 | g0059 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0308 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18962 | hp2 | a0001 | c0002 | t0007 | g0366 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18963 | hp1 | a0001 | c0013 | t0006 | g0171 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18970 | hp1 | a0001 | c0009 | t0003 | g0155 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18970 | hp2 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18971 | hp2 | a0001 | c0002 | t0007 | g0303 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18974 | hp1 | a0001 | c0001 | t0008 | g0110 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18974 | hp2 | a0001 | c0001 | t0012 | g0184 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18978 | hp1 | a0002 | c0003 | t0004 | g0130 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18978 | hp2 | a0018 | c0045 | t0004 | g0185 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18979 | hp1 | a0002 | c0003 | t0001 | g0131 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18979 | hp2 | a0001 | c0008 | t0006 | g0084 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18980 | hp1 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18981 | hp1 | a0001 | c0001 | t0006 | g0068 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18983 | hp2 | a0001 | c0001 | t0007 | g0273 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18987 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18987 | hp2 | a0001 | c0004 | t0001 | g0058 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18988 | hp1 | a0001 | c0001 | t0027 | g0070 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18988 | hp2 | a0009 | c0017 | t0003 | g0134 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18992 | hp1 | a0001 | c0001 | t0006 | g0080 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18992 | hp2 | a0001 | c0001 | t0008 | g0224 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18993 | hp1 | a0001 | c0004 | t0004 | g0106 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18993 | hp2 | a0001 | c0004 | t0039 | g0310 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18999 | hp1 | a0002 | c0003 | t0018 | g0119 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19000 | hp2 | a0001 | c0002 | t0013 | g0160 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19002 | hp1 | a0002 | c0003 | t0001 | g0123 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19002 | hp2 | a0001 | c0004 | t0004 | g0104 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19004 | hp1 | a0001 | c0013 | t0002 | g0076 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19004 | hp2 | a0002 | c0003 | t0001 | g0120 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19005 | hp1 | a0001 | c0001 | t0008 | g0240 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19007 | hp1 | a0001 | c0005 | t0003 | g0091 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19007 | hp2 | a0002 | c0025 | t0003 | g0124 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19009 | hp2 | a0001 | c0001 | t0007 | g0162 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19030 | hp1 | a0001 | c0009 | t0003 | g0335 | AFR | LWK | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19030 | hp2 | a0001 | c0004 | t0011 | g0255 | AFR | LWK | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0320 | AFR | LWK | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19043 | hp2 | a0001 | c0004 | t0011 | g0190 | AFR | LWK | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19054 | hp2 | a0001 | c0001 | t0008 | g0109 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19057 | hp1 | a0001 | c0004 | t0002 | g0099 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19060 | hp1 | a0001 | c0008 | t0006 | g0111 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19060 | hp2 | a0002 | c0034 | t0020 | g0133 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19062 | hp1 | a0001 | c0001 | t0026 | g0317 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19062 | hp2 | a0001 | c0002 | t0007 | g0365 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19063 | hp1 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19066 | hp1 | a0002 | c0003 | t0018 | g0129 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19066 | hp2 | a0001 | c0005 | t0003 | g0285 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19068 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19068 | hp2 | a0002 | c0003 | t0004 | g0118 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19070 | hp2 | a0001 | c0001 | t0031 | g0289 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19078 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19078 | hp2 | a0001 | c0023 | t0002 | g0108 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19079 | hp1 | a0001 | c0004 | t0004 | g0064 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19079 | hp2 | a0001 | c0001 | t0006 | g0294 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19083 | hp1 | a0001 | c0005 | t0003 | g0067 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19084 | hp1 | a0004 | c0011 | t0001 | g0075 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19085 | hp1 | a0001 | c0002 | t0019 | g0288 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19085 | hp2 | a0001 | c0004 | t0008 | g0048 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19086 | hp1 | a0001 | c0001 | t0021 | g0169 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19086 | hp2 | a0001 | c0001 | t0006 | g0087 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19088 | hp1 | a0002 | c0003 | t0017 | g0132 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19088 | hp2 | a0006 | c0035 | t0003 | g0210 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19090 | hp1 | a0001 | c0001 | t0017 | g0300 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19090 | hp2 | a0001 | c0001 | t0006 | g0143 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19091 | hp1 | a0001 | c0004 | t0002 | g0001 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19091 | hp2 | a0001 | c0005 | t0003 | g0140 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19240 | hp1 | a0001 | c0001 | t0010 | g0259 | AFR | YRI | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA19240 | hp2 | a0010 | c0019 | t0001 | g0321 | AFR | YRI | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0292 | AFR | ASW | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0144 | AFR | ASW | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0254 | EUR | TSI | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA20805 | hp2 | a0002 | c0006 | t0011 | g0026 | EUR | TSI | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | GIH | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA20905 | hp2 | a0001 | c0009 | t0003 | g0270 | SAS | GIH | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0103 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG01123 | hp2 | a0001 | c0001 | t0041 | g0328 | AMR | CLM | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02109 | hp1 | a0002 | c0006 | t0010 | g0337 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02109 | hp2 | a0011 | c0033 | t0011 | g0355 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02486 | hp1 | a0002 | c0028 | t0030 | g0363 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02559 | hp1 | a0001 | c0002 | t0040 | g0307 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG02559 | hp2 | a0013 | c0052 | t0005 | g0247 | AFR | ACB | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03471 | hp1 | a0002 | c0016 | t0001 | g0361 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG03471 | hp2 | a0002 | c0003 | t0010 | g0338 | AFR | MSL | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG06807 | hp1 | a0001 | c0002 | t0014 | g0151 | AFR | USA | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | USA | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18955 | hp1 | a0001 | c0005 | t0003 | g0153 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA20300 | hp1 | a0008 | c0014 | t0023 | g0306 | AFR | USA | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA20300 | hp2 | a0002 | c0003 | t0002 | g0114 | AFR | USA | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0281 | AFR | LWK | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
NA21309 | hp2 | a0001 | c0001 | t0016 | g0208 | AFR | LWK | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0100 | REF | REF | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0207 | REF | REF | FAM114A1_chr4_38862806_38950739 | FAM114A1 | chr4 | 38862806 | 38950739 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:38878197 | C | T | 3 | a0007 a0014 a0015 |
6 | HG02809.hp2 HG03579.hp2 HG03704.hp1 others(3): Show |
missense_variant | MODERATE | c.119C>T | p.Ser40Leu | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/15 | 305/4060 | 119/1692 | 40/563 | chr4 | 38878197 | |||
chr4:38878328 | G | A | 7 | a0002 a0003 a0005 others(4): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
missense_variant | MODERATE | c.250G>A | p.Gly84Arg | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/15 | 436/4060 | 250/1692 | 84/563 | chr4 | 38878328 | |||
chr4:38878425 | T | C | 7 | a0002 a0003 a0005 others(4): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
missense_variant&splice_region_variant | MODERATE | c.347T>C | p.Leu116Pro | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/15 | 533/4060 | 347/1692 | 116/563 | chr4 | 38878425 | |||
chr4:38891810 | C | T | 1 | a0011 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.416C>T | p.Ser139Leu | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/15 | 602/4060 | 416/1692 | 139/563 | chr4 | 38891810 | |||
chr4:38905522 | G | T | 1 | a0016 | 1 | HG04115.hp2 | missense_variant&splice_region_variant | MODERATE | c.437G>T | p.Gly146Val | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 5/15 | 623/4060 | 437/1692 | 146/563 | chr4 | 38905522 | |||
chr4:38905784 | G | A | 1 | a0013 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.580G>A | p.Ala194Thr | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/15 | 766/4060 | 580/1692 | 194/563 | chr4 | 38905784 | |||
chr4:38908695 | C | T | 1 | a0017 | 1 | NA18953.hp2 | missense_variant | MODERATE | c.761C>T | p.Thr254Met | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/15 | 947/4060 | 761/1692 | 254/563 | chr4 | 38908695 | |||
chr4:38922788 | T | C | 1 | a0012 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.964T>C | p.Ser322Pro | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/15 | 1150/4060 | 964/1692 | 322/563 | chr4 | 38922788 | |||
chr4:38929271 | C | T | 1 | a0018 | 1 | NA18978.hp2 | missense_variant | MODERATE | c.1099C>T | p.Arg367Cys | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/15 | 1285/4060 | 1099/1692 | 367/563 | chr4 | 38929271 | |||
chr4:38929272 | G | A | 2 | a0006 a0009 |
7 | HG01433.hp1 HG01975.hp2 HG01993.hp2 others(4): Show |
missense_variant | MODERATE | c.1100G>A | p.Arg367His | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/15 | 1286/4060 | 1100/1692 | 367/563 | chr4 | 38929272 | |||
chr4:38931493 | G | A | 1 | a0010 | 2 | HG03139.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.1204G>A | p.Val402Met | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 11/15 | 1390/4060 | 1204/1692 | 402/563 | chr4 | 38931493 | |||
chr4:38932238 | G | A | 5 | a0003 a0004 a0006 others(2): Show |
26 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(23): Show |
missense_variant | MODERATE | c.1327G>A | p.Val443Ile | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/15 | 1513/4060 | 1327/1692 | 443/563 | chr4 | 38932238 | |||
chr4:38932248 | C | T | 3 | a0005 a0008 a0014 |
12 | HG02622.hp1 HG02622.hp2 HG02647.hp1 others(9): Show |
missense_variant | MODERATE | c.1337C>T | p.Ser446Leu | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/15 | 1523/4060 | 1337/1692 | 446/563 | chr4 | 38932248 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:38878099 | C | T | 8 | a0002c0022 a0002c0053 a0002c0054 others(5): Show |
11 | HG01109.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
synonymous_variant | LOW | c.21C>T | p.Asp7Asp | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/15 | 207/4060 | 21/1692 | 7/563 | chr4 | 38878099 | |||
chr4:38878315 | G | A | 1 | a0001c0023 | 1 | NA19078.hp2 | synonymous_variant | LOW | c.237G>A | p.Glu79Glu | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/15 | 423/4060 | 237/1692 | 79/563 | chr4 | 38878315 | |||
chr4:38891769 | A | G | 1 | a0002c0034 | 1 | NA19060.hp2 | synonymous_variant | LOW | c.375A>G | p.Gly125Gly | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/15 | 561/4060 | 375/1692 | 125/563 | chr4 | 38891769 | |||
chr4:38905535 | G | A | 5 | a0002c0022 a0002c0053 a0002c0054 others(2): Show |
8 | HG02559.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
synonymous_variant | LOW | c.450G>A | p.Thr150Thr | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 5/15 | 636/4060 | 450/1692 | 150/563 | chr4 | 38905535 | |||
chr4:38905601 | A | G | 2 | a0002c0032 a0002c0057 |
2 | HG02145.hp1 HG02145.hp2 |
synonymous_variant | LOW | c.516A>G | p.Gly172Gly | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 5/15 | 702/4060 | 516/1692 | 172/563 | chr4 | 38905601 | |||
chr4:38914989 | G | A | 2 | a0001c0008 a0001c0023 |
7 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(4): Show |
synonymous_variant | LOW | c.861G>A | p.Ala287Ala | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/15 | 1047/4060 | 861/1692 | 287/563 | chr4 | 38914989 | |||
chr4:38915010 | T | C | 17 | a0001c0004 a0001c0013 a0001c0037 others(14): Show |
48 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(45): Show |
synonymous_variant | LOW | c.882T>C | p.Asp294Asp | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/15 | 1068/4060 | 882/1692 | 294/563 | chr4 | 38915010 | |||
chr4:38915064 | C | T | 1 | a0001c0046 | 1 | NA18941.hp1 | synonymous_variant | LOW | c.936C>T | p.Ser312Ser | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/15 | 1122/4060 | 936/1692 | 312/563 | chr4 | 38915064 | |||
chr4:38929300 | A | G | 4 | a0003c0007 a0003c0018 a0004c0020 others(1): Show |
11 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(8): Show |
synonymous_variant | LOW | c.1128A>G | p.Leu376Leu | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/15 | 1314/4060 | 1128/1692 | 376/563 | chr4 | 38929300 | |||
chr4:38932279 | G | T | 8 | a0001c0038 a0001c0039 a0001c0043 others(5): Show |
8 | HG01167.hp2 HG01243.hp1 HG01891.hp1 others(5): Show |
synonymous_variant | LOW | c.1368G>T | p.Ala456Ala | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/15 | 1554/4060 | 1368/1692 | 456/563 | chr4 | 38932279 | |||
chr4:38935751 | T | C | 45 | a0001c0001 a0001c0004 a0001c0008 others(42): Show |
275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
synonymous_variant | LOW | c.1497T>C | p.Ser499Ser | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/15 | 1683/4060 | 1497/1692 | 499/563 | chr4 | 38935751 | |||
chr4:38943548 | A | G | 15 | a0001c0005 a0001c0009 a0001c0037 others(12): Show |
35 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(32): Show |
synonymous_variant | LOW | c.1683A>G | p.Ala561Ala | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1869/4060 | 1683/1692 | 561/563 | chr4 | 38943548 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:38943596 | C | T | 13 | a0001c0001t0005 a0001c0038t0005 a0002c0003t0005 others(10): Show |
26 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*39C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 39 | chr4 | 38943596 | ||||||
chr4:38943655 | T | C | 1 | a0002c0003t0018 | 2 | NA18999.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*98T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 98 | chr4 | 38943655 | ||||||
chr4:38943658 | A | G | 1 | a0001c0001t0042 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 101 | chr4 | 38943658 | ||||||
chr4:38943842 | G | C | 77 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(74): Show |
165 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*285G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 285 | chr4 | 38943842 | ||||||
chr4:38943883 | A | C | 1 | a0001c0001t0041 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*326A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 326 | chr4 | 38943883 | ||||||
chr4:38943949 | T | C | 1 | a0005c0012t0033 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*392T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 392 | chr4 | 38943949 | ||||||
chr4:38944001 | G | A | 1 | a0001c0001t0042 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*444G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 444 | chr4 | 38944001 | ||||||
chr4:38944068 | C | CT | 6 | a0001c0001t0013 a0001c0002t0013 a0001c0002t0028 others(3): Show |
7 | HG00140.hp1 HG00741.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*530dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 531 | INFO_REALIGN_3_PRIME | chr4 | 38944068 | |||||
chr4:38944068 | C | CTTTT | 35 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0014 others(32): Show |
123 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*527_*530dupTTTT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 531 | INFO_REALIGN_3_PRIME | chr4 | 38944068 | |||||
chr4:38944068 | C | CTTTTT | 7 | a0001c0001t0012 a0001c0002t0040 a0001c0039t0024 others(4): Show |
10 | HG01891.hp1 HG02145.hp2 HG02148.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*526_*530dupTTTTT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 531 | INFO_REALIGN_3_PRIME | chr4 | 38944068 | |||||
chr4:38944154 | C | T | 1 | a0001c0001t0042 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*597C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 597 | chr4 | 38944154 | ||||||
chr4:38944213 | T | C | 46 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0012 others(43): Show |
138 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*656T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 656 | chr4 | 38944213 | ||||||
chr4:38944225 | C | T | 1 | a0001c0004t0039 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*668C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 668 | chr4 | 38944225 | ||||||
chr4:38944317 | G | A | 2 | a0001c0001t0016 a0002c0003t0016 |
3 | HG00639.hp1 HG04228.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*760G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 760 | chr4 | 38944317 | ||||||
chr4:38944350 | T | G | 2 | a0001c0002t0019 a0017c0031t0019 |
2 | NA18953.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*793T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 793 | chr4 | 38944350 | ||||||
chr4:38944359 | C | T | 54 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0008 others(51): Show |
120 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*802C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 802 | chr4 | 38944359 | ||||||
chr4:38944366 | G | A | 2 | a0001c0001t0042 a0001c0004t0022 |
3 | HG02896.hp2 HG02897.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*809G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 809 | chr4 | 38944366 | ||||||
chr4:38944398 | T | C | 45 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0012 others(42): Show |
137 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*841T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 841 | chr4 | 38944398 | ||||||
chr4:38944410 | T | C | 1 | a0005c0012t0034 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*853T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 853 | chr4 | 38944410 | ||||||
chr4:38944432 | G | A | 24 | a0001c0001t0005 a0001c0001t0014 a0001c0001t0042 others(21): Show |
39 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*875G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 875 | chr4 | 38944432 | ||||||
chr4:38944520 | C | T | 1 | a0002c0054t0036 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*963C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 963 | chr4 | 38944520 | ||||||
chr4:38944533 | G | A | 44 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0012 others(41): Show |
136 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*976G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 976 | chr4 | 38944533 | ||||||
chr4:38944536 | G | A | 2 | a0001c0001t0017 a0002c0003t0017 |
3 | NA18941.hp2 NA19088.hp1 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*979G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 979 | chr4 | 38944536 | ||||||
chr4:38944647 | G | A | 54 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0008 others(51): Show |
120 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1090G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1090 | chr4 | 38944647 | ||||||
chr4:38944651 | C | T | 1 | a0001c0001t0027 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1094C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1094 | chr4 | 38944651 | ||||||
chr4:38944654 | G | A | 7 | a0001c0001t0006 a0001c0001t0027 a0001c0002t0006 others(4): Show |
22 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1097G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1097 | chr4 | 38944654 | ||||||
chr4:38944709 | G | A | 2 | a0008c0014t0023 a0012c0040t0023 |
2 | HG02257.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1152G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1152 | chr4 | 38944709 | ||||||
chr4:38944803 | C | T | 1 | a0001c0001t0038 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1246C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1246 | chr4 | 38944803 | ||||||
chr4:38944804 | G | A | 11 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0027 others(8): Show |
31 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1247G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1247 | chr4 | 38944804 | ||||||
chr4:38944827 | C | T | 15 | a0001c0005t0003 a0001c0009t0003 a0001c0037t0003 others(12): Show |
33 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1270C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1270 | chr4 | 38944827 | ||||||
chr4:38944844 | GA | G | 54 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0008 others(51): Show |
120 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1293delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1293 | INFO_REALIGN_3_PRIME | chr4 | 38944844 | |||||
chr4:38944860 | A | G | 54 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0008 others(51): Show |
120 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1303A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1303 | chr4 | 38944860 | ||||||
chr4:38944865 | A | G | 45 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0012 others(42): Show |
137 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1308A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1308 | chr4 | 38944865 | ||||||
chr4:38945070 | A | T | 2 | a0001c0002t0020 a0002c0034t0020 |
2 | HG00609.hp2 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1513A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1513 | chr4 | 38945070 | ||||||
chr4:38945107 | G | A | 1 | a0001c0001t0042 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1550G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1550 | chr4 | 38945107 | ||||||
chr4:38945116 | G | A | 2 | a0001c0001t0042 a0005c0012t0034 |
2 | HG03139.hp2 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1559G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1559 | chr4 | 38945116 | ||||||
chr4:38945137 | G | A | 4 | a0001c0001t0009 a0003c0007t0009 a0003c0007t0025 others(1): Show |
8 | HG00741.hp2 HG01070.hp2 HG01109.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1580G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1580 | chr4 | 38945137 | ||||||
chr4:38945156 | T | C | 1 | a0001c0001t0042 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1599T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1599 | chr4 | 38945156 | ||||||
chr4:38945173 | C | T | 16 | a0001c0001t0026 a0001c0005t0003 a0001c0009t0003 others(13): Show |
34 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1616C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1616 | chr4 | 38945173 | ||||||
chr4:38945175 | G | C | 2 | a0001c0001t0015 a0003c0007t0015 |
3 | HG00323.hp2 HG01074.hp2 HG01175.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1618G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1618 | chr4 | 38945175 | ||||||
chr4:38945203 | C | T | 54 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0008 others(51): Show |
120 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1646C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1646 | chr4 | 38945203 | ||||||
chr4:38945243 | C | T | 1 | a0001c0001t0042 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1686C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1686 | chr4 | 38945243 | ||||||
chr4:38945267 | G | C | 1 | a0001c0002t0037 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1710G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1710 | chr4 | 38945267 | ||||||
chr4:38945327 | GC | G | 10 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0015 others(7): Show |
16 | HG00323.hp2 HG00741.hp2 HG01074.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1772delC | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1772 | INFO_REALIGN_3_PRIME | chr4 | 38945327 | |||||
chr4:38945393 | G | A | 10 | a0001c0001t0004 a0001c0002t0020 a0001c0002t0028 others(7): Show |
30 | HG00140.hp2 HG00609.hp2 HG00741.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1836G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 1836 | chr4 | 38945393 | ||||||
chr4:38945615 | A | G | 2 | a0001c0039t0024 a0001c0044t0024 |
2 | HG01891.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2058A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 15/15 | 2058 | chr4 | 38945615 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:38867901 | C | A | 12 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0005g0005 others(9): Show |
12 | HG01167.hp2 HG02486.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-158+67C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 1/14 | chr4 | 38867901 | |||||||
chr4:38867926 | C | A | 4 | a0001c0001t0001g0019 a0001c0001t0002g0016 a0001c0001t0002g0017 others(1): Show |
4 | HG02080.hp1 HG02135.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.-158+92C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 1/14 | chr4 | 38867926 | |||||||
chr4:38867941 | G | A | 19 | a0002c0003t0004g0022 a0002c0003t0006g0036 a0002c0003t0016g0034 others(16): Show |
19 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.-158+107G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 1/14 | chr4 | 38867941 | |||||||
chr4:38868144 | TGCGTGAA others(35): Show |
T | 1 | a0002c0026t0005g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-157-253_-157-212d others(44): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 1/14 | chr4 | 38868144 | |||||||
chr4:38868288 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0002g0040 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-157-110G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 1/14 | chr4 | 38868288 | |||||||
chr4:38868667 | C | T | 2 | a0001c0002t0007g0365 a0001c0002t0007g0366 |
2 | NA18962.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-9+121C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38868667 | |||||||
chr4:38868764 | G | A | 5 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0005g0042 others(2): Show |
5 | HG02451.hp2 HG02723.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+218G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38868764 | |||||||
chr4:38868850 | C | T | 31 | a0002c0003t0001g0359 a0002c0003t0002g0358 a0002c0003t0004g0022 others(28): Show |
31 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.-9+304C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38868850 | |||||||
chr4:38868991 | G | A | 1 | a0002c0006t0001g0020 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-9+445G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38868991 | |||||||
chr4:38869209 | G | A | 1 | a0004c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-9+663G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869209 | |||||||
chr4:38869241 | A | G | 1 | a0002c0032t0044g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-9+695A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869241 | |||||||
chr4:38869352 | A | G | 1 | a0001c0002t0028g0351 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-9+806A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869352 | |||||||
chr4:38869420 | A | T | 1 | a0002c0026t0005g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-9+874A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869420 | |||||||
chr4:38869596 | C | T | 1 | a0001c0002t0001g0350 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-9+1050C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869596 | |||||||
chr4:38869695 | C | T | 1 | a0001c0004t0002g0349 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-9+1149C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869695 | |||||||
chr4:38869713 | G | GT | 5 | a0007c0021t0004g0347 a0007c0048t0008g0346 a0007c0049t0002g0348 others(2): Show |
5 | HG02809.hp2 HG03579.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+1172dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38869713 | ||||||
chr4:38869719 | G | T | 11 | a0002c0003t0004g0342 a0002c0003t0005g0339 a0002c0003t0005g0343 others(8): Show |
11 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-9+1173G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869719 | |||||||
chr4:38869725 | T | G | 1 | a0001c0001t0002g0047 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-9+1179T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869725 | |||||||
chr4:38869764 | T | C | 71 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(68): Show |
76 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-9+1218T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869764 | |||||||
chr4:38869798 | A | T | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-9+1252A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869798 | |||||||
chr4:38869805 | T | A | 5 | a0002c0003t0002g0114 a0002c0003t0012g0112 a0002c0029t0043g0115 others(2): Show |
5 | HG01243.hp1 HG02027.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+1259T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869805 | |||||||
chr4:38869806 | T | A | 62 | a0001c0002t0007g0365 a0001c0002t0007g0366 a0002c0003t0001g0120 others(59): Show |
62 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.-9+1260T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869806 | |||||||
chr4:38869901 | C | T | 1 | a0004c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-9+1355C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869901 | |||||||
chr4:38869904 | T | C | 2 | a0002c0003t0005g0339 a0002c0003t0010g0338 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-9+1358T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38869904 | |||||||
chr4:38870015 | C | A | 1 | a0002c0003t0007g0117 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-9+1469C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870015 | |||||||
chr4:38870047 | G | A | 36 | a0002c0003t0001g0359 a0002c0003t0002g0114 a0002c0003t0002g0358 others(33): Show |
36 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.-9+1501G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870047 | |||||||
chr4:38870086 | A | T | 2 | a0002c0003t0005g0364 a0002c0028t0030g0363 |
2 | HG01891.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-9+1540A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870086 | |||||||
chr4:38870162 | C | T | 87 | a0001c0001t0001g0041 a0001c0001t0001g0264 a0001c0001t0001g0275 others(84): Show |
88 | HG00438.hp2 HG00642.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.-9+1616C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870162 | |||||||
chr4:38870276 | C | T | 23 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(20): Show |
23 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.-9+1730C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870276 | |||||||
chr4:38870498 | C | G | 2 | a0001c0001t0004g0253 a0001c0001t0004g0254 |
2 | HG01261.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-9+1952C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870498 | |||||||
chr4:38870514 | G | A | 2 | a0001c0001t0007g0256 a0001c0004t0011g0255 |
2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-9+1968G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870514 | |||||||
chr4:38870546 | G | A | 2 | a0001c0001t0004g0257 a0002c0026t0005g0039 |
2 | HG03195.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-9+2000G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870546 | |||||||
chr4:38870562 | C | T | 1 | a0001c0001t0002g0336 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-9+2016C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870562 | |||||||
chr4:38870592 | C | T | 53 | a0002c0003t0001g0359 a0002c0003t0002g0114 a0002c0003t0002g0358 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-9+2046C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870592 | |||||||
chr4:38870648 | T | G | 1 | a0001c0004t0006g0258 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-9+2102T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870648 | |||||||
chr4:38870744 | A | G | 36 | a0002c0003t0001g0359 a0002c0003t0002g0114 a0002c0003t0002g0358 others(33): Show |
36 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.-9+2198A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870744 | |||||||
chr4:38870758 | C | T | 1 | a0001c0002t0001g0242 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-9+2212C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870758 | |||||||
chr4:38870926 | G | A | 2 | a0001c0001t0010g0259 a0001c0004t0001g0260 |
2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-9+2380G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870926 | |||||||
chr4:38870971 | G | A | 47 | a0002c0003t0001g0359 a0002c0003t0002g0114 a0002c0003t0002g0358 others(44): Show |
47 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.-9+2425G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870971 | |||||||
chr4:38870991 | A | C | 5 | a0002c0003t0004g0342 a0002c0003t0005g0339 a0002c0003t0005g0343 others(2): Show |
5 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+2445A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38870991 | |||||||
chr4:38871086 | C | CT | 12 | a0001c0001t0002g0239 a0001c0001t0002g0241 a0001c0001t0005g0231 others(9): Show |
12 | HG00140.hp1 HG00609.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.-9+2561dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38871086 | ||||||
chr4:38871086 | CT | C | 50 | a0001c0001t0001g0019 a0001c0001t0002g0105 a0001c0001t0002g0325 others(47): Show |
50 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-9+2561delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38871086 | ||||||
chr4:38871086 | CTT | C | 190 | a0001c0001t0001g0041 a0001c0001t0001g0050 a0001c0001t0001g0062 others(187): Show |
196 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.-9+2560_-9+2561del others(2): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38871086 | ||||||
chr4:38871086 | CTTT | C | 10 | a0001c0001t0004g0262 a0001c0039t0024g0261 a0002c0003t0004g0342 others(7): Show |
10 | HG01255.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9+2559_-9+2561del others(3): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38871086 | ||||||
chr4:38871092 | T | C | 1 | a0001c0004t0008g0048 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-9+2546T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38871092 | |||||||
chr4:38871168 | T | C | 23 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(20): Show |
23 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.-9+2622T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38871168 | |||||||
chr4:38871194 | A | G | 2 | a0001c0001t0007g0256 a0001c0004t0011g0255 |
2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-9+2648A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38871194 | |||||||
chr4:38871535 | A | G | 1 | a0001c0001t0012g0334 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-9+2989A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38871535 | |||||||
chr4:38871604 | G | A | 1 | a0002c0028t0030g0363 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-9+3058G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38871604 | |||||||
chr4:38871711 | C | T | 67 | a0001c0001t0001g0050 a0001c0001t0001g0062 a0001c0001t0002g0049 others(64): Show |
72 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.-9+3165C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38871711 | |||||||
chr4:38871870 | G | A | 5 | a0002c0003t0002g0114 a0002c0003t0012g0112 a0002c0029t0043g0115 others(2): Show |
5 | HG01243.hp1 HG02027.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+3324G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38871870 | |||||||
chr4:38871878 | G | T | 1 | a0002c0006t0001g0038 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-9+3332G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38871878 | |||||||
chr4:38872096 | T | C | 14 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0004g0253 others(11): Show |
14 | HG01167.hp2 HG01261.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-9+3550T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38872096 | |||||||
chr4:38872175 | T | A | 67 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0004g0253 others(64): Show |
67 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.-9+3629T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38872175 | |||||||
chr4:38872190 | T | C | 87 | a0001c0001t0001g0041 a0001c0001t0001g0264 a0001c0001t0001g0275 others(84): Show |
88 | HG00438.hp2 HG00642.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.-9+3644T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38872190 | |||||||
chr4:38872272 | C | G | 1 | a0002c0003t0005g0343 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-9+3726C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38872272 | |||||||
chr4:38872377 | T | C | 67 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0004g0253 others(64): Show |
67 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.-9+3831T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38872377 | |||||||
chr4:38872558 | G | A | 1 | a0001c0001t0002g0263 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-9+4012G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38872558 | |||||||
chr4:38872677 | T | C | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-9+4131T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38872677 | |||||||
chr4:38872683 | A | G | 3 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0002g0241 |
3 | HG00558.hp1 HG00673.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.-9+4137A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38872683 | |||||||
chr4:38872746 | T | C | 1 | a0001c0001t0002g0049 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-9+4200T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38872746 | |||||||
chr4:38872866 | T | A | 30 | a0002c0003t0001g0359 a0002c0003t0002g0358 a0002c0003t0004g0022 others(27): Show |
30 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.-9+4320T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38872866 | |||||||
chr4:38873005 | A | G | 1 | a0009c0017t0003g0134 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-9+4459A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873005 | |||||||
chr4:38873014 | T | A | 1 | a0002c0003t0018g0119 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-9+4468T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873014 | |||||||
chr4:38873016 | A | G | 53 | a0002c0003t0001g0359 a0002c0003t0002g0114 a0002c0003t0002g0358 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-9+4470A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873016 | |||||||
chr4:38873024 | C | T | 53 | a0002c0003t0001g0359 a0002c0003t0002g0114 a0002c0003t0002g0358 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-9+4478C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873024 | |||||||
chr4:38873181 | A | G | 67 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0004g0253 others(64): Show |
67 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.-9+4635A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873181 | |||||||
chr4:38873275 | A | G | 1 | a0001c0001t0012g0333 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-9+4729A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873275 | |||||||
chr4:38873307 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-9+4761T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873307 | |||||||
chr4:38873344 | C | T | 23 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(20): Show |
23 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8-4727C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873344 | |||||||
chr4:38873440 | C | A | 1 | a0002c0003t0012g0112 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-8-4631C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873440 | |||||||
chr4:38873471 | T | C | 1 | a0004c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-8-4600T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873471 | |||||||
chr4:38873518 | A | G | 90 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0004g0253 others(87): Show |
90 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.-8-4553A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873518 | |||||||
chr4:38873646 | G | C | 1 | a0001c0002t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-8-4425G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873646 | |||||||
chr4:38873694 | T | C | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-4377T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873694 | |||||||
chr4:38873772 | G | T | 24 | a0002c0003t0001g0359 a0002c0003t0002g0358 a0002c0003t0004g0022 others(21): Show |
24 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.-8-4299G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873772 | |||||||
chr4:38873912 | C | T | 1 | a0004c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-8-4159C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38873912 | |||||||
chr4:38874075 | T | G | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-3996T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874075 | |||||||
chr4:38874076 | G | A | 11 | a0002c0022t0005g0249 a0002c0022t0010g0248 a0002c0053t0001g0245 others(8): Show |
11 | HG01109.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-3995G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874076 | |||||||
chr4:38874092 | G | T | 2 | a0001c0001t0016g0322 a0001c0005t0003g0323 |
2 | HG02602.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-8-3979G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874092 | |||||||
chr4:38874116 | C | T | 53 | a0002c0003t0001g0359 a0002c0003t0002g0114 a0002c0003t0002g0358 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-8-3955C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874116 | |||||||
chr4:38874176 | A | G | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-3895A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874176 | |||||||
chr4:38874247 | A | G | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-3824A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874247 | |||||||
chr4:38874276 | G | A | 1 | a0014c0051t0005g0344 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-8-3795G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874276 | |||||||
chr4:38874288 | T | C | 6 | a0002c0003t0004g0342 a0002c0003t0005g0339 a0002c0003t0005g0343 others(3): Show |
6 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-3783T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874288 | |||||||
chr4:38874290 | A | T | 1 | a0010c0019t0001g0321 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-8-3781A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874290 | |||||||
chr4:38874329 | G | A | 6 | a0002c0003t0004g0342 a0002c0003t0005g0339 a0002c0003t0005g0343 others(3): Show |
6 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-3742G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874329 | |||||||
chr4:38874438 | A | G | 1 | a0003c0024t0001g0116 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-8-3633A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874438 | |||||||
chr4:38874514 | T | C | 1 | a0001c0002t0001g0265 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-8-3557T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874514 | |||||||
chr4:38874612 | A | G | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-3459A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874612 | |||||||
chr4:38874646 | C | A | 47 | a0002c0003t0001g0359 a0002c0003t0002g0114 a0002c0003t0002g0358 others(44): Show |
47 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.-8-3425C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874646 | |||||||
chr4:38874715 | G | T | 1 | a0001c0001t0007g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-8-3356G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874715 | |||||||
chr4:38874745 | C | T | 1 | a0002c0032t0044g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-8-3326C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874745 | |||||||
chr4:38874746 | G | T | 1 | a0001c0002t0001g0103 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-8-3325G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874746 | |||||||
chr4:38874769 | T | G | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-3302T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874769 | |||||||
chr4:38874771 | T | C | 46 | a0002c0003t0001g0359 a0002c0003t0002g0114 a0002c0003t0002g0358 others(43): Show |
46 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.-8-3300T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874771 | |||||||
chr4:38874839 | T | C | 3 | a0002c0003t0004g0342 a0002c0003t0005g0343 a0005c0012t0033g0341 |
3 | HG02280.hp2 HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-8-3232T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874839 | |||||||
chr4:38874988 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-8-3083T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38874988 | |||||||
chr4:38875186 | A | C | 14 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0004g0253 others(11): Show |
14 | HG01167.hp2 HG01261.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-2885A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875186 | |||||||
chr4:38875188 | TA | T | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-2882delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875188 | |||||||
chr4:38875202 | T | G | 46 | a0002c0003t0001g0359 a0002c0003t0002g0114 a0002c0003t0002g0358 others(43): Show |
46 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.-8-2869T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875202 | |||||||
chr4:38875205 | A | G | 14 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0004g0253 others(11): Show |
14 | HG01167.hp2 HG01261.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-2866A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875205 | |||||||
chr4:38875218 | T | C | 4 | a0001c0001t0017g0138 a0001c0002t0002g0139 a0001c0002t0002g0141 others(1): Show |
4 | HG00408.hp2 HG04184.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-2853T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875218 | |||||||
chr4:38875319 | T | C | 1 | a0001c0001t0004g0257 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-8-2752T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875319 | |||||||
chr4:38875376 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0002g0016 a0001c0001t0002g0017 others(1): Show |
4 | HG02080.hp1 HG02135.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-2695G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875376 | |||||||
chr4:38875432 | A | G | 5 | a0002c0003t0004g0342 a0002c0003t0005g0339 a0002c0003t0005g0343 others(2): Show |
5 | HG02280.hp1 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-2639A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875432 | |||||||
chr4:38875463 | C | T | 1 | a0001c0044t0024g0226 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-8-2608C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875463 | |||||||
chr4:38875464 | G | C | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-2607G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875464 | |||||||
chr4:38875635 | C | T | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-2436C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875635 | |||||||
chr4:38875651 | G | T | 1 | a0001c0001t0002g0102 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-8-2420G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875651 | |||||||
chr4:38875724 | C | T | 1 | a0001c0009t0010g0332 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-8-2347C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875724 | |||||||
chr4:38875836 | T | C | 53 | a0002c0003t0001g0359 a0002c0003t0002g0114 a0002c0003t0002g0358 others(50): Show |
53 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-8-2235T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875836 | |||||||
chr4:38875850 | A | G | 1 | a0004c0020t0003g0101 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-8-2221A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875850 | |||||||
chr4:38875874 | G | A | 6 | a0002c0003t0002g0114 a0002c0003t0012g0112 a0002c0006t0010g0337 others(3): Show |
6 | HG01243.hp1 HG02027.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-2197G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875874 | |||||||
chr4:38875881 | C | G | 1 | a0001c0001t0013g0225 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-8-2190C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38875881 | |||||||
chr4:38876061 | G | A | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-2010G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876061 | |||||||
chr4:38876099 | T | C | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1972T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876099 | |||||||
chr4:38876103 | A | G | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1968A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876103 | |||||||
chr4:38876122 | AT | A | 168 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(165): Show |
173 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.-8-1941delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38876122 | ||||||
chr4:38876156 | CT | C | 23 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(20): Show |
23 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8-1913delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38876156 | ||||||
chr4:38876159 | ATTCTTTT | A | 43 | a0001c0001t0001g0041 a0001c0001t0001g0296 a0001c0001t0001g0315 others(40): Show |
43 | HG00673.hp1 HG01943.hp1 HG01943.hp2 others(40): Show |
intron_variant | MODIFIER | c.-8-1902_-8-1896del others(7): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38876159 | ||||||
chr4:38876166 | TTTC | T | 26 | a0002c0003t0001g0120 a0002c0003t0001g0359 a0002c0003t0002g0358 others(23): Show |
26 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-8-1902_-8-1900del others(3): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38876166 | ||||||
chr4:38876167 | TTC | T | 34 | a0002c0003t0001g0123 a0002c0003t0001g0127 a0002c0003t0001g0128 others(31): Show |
34 | HG00621.hp1 HG01109.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.-8-1902_-8-1901del others(2): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38876167 | ||||||
chr4:38876168 | TC | T | 7 | a0002c0003t0002g0114 a0002c0003t0002g0121 a0002c0003t0004g0118 others(4): Show |
7 | HG01243.hp1 HG01978.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-1902delC | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876168 | |||||||
chr4:38876169 | C | CT | 21 | a0001c0001t0001g0019 a0001c0001t0001g0062 a0001c0001t0001g0211 others(18): Show |
21 | HG00438.hp1 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-8-1882dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38876169 | ||||||
chr4:38876169 | C | T | 7 | a0002c0003t0004g0342 a0002c0003t0005g0339 a0002c0003t0005g0343 others(4): Show |
7 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-1902C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876169 | |||||||
chr4:38876169 | CT | C | 24 | a0001c0001t0002g0092 a0001c0001t0002g0097 a0001c0001t0002g0197 others(21): Show |
24 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.-8-1882delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38876169 | ||||||
chr4:38876173 | T | C | 3 | a0001c0001t0005g0005 a0001c0004t0002g0004 a0001c0043t0001g0006 |
3 | HG01167.hp2 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-8-1898T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876173 | |||||||
chr4:38876195 | G | A | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1876G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876195 | |||||||
chr4:38876208 | C | T | 10 | a0001c0001t0002g0013 a0001c0001t0005g0005 a0001c0001t0005g0014 others(7): Show |
10 | HG01167.hp2 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-1863C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876208 | |||||||
chr4:38876257 | C | T | 4 | a0002c0003t0001g0359 a0002c0003t0005g0360 a0002c0003t0010g0362 others(1): Show |
4 | HG02809.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1814C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876257 | |||||||
chr4:38876450 | T | C | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1621T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876450 | |||||||
chr4:38876451 | G | A | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1620G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876451 | |||||||
chr4:38876459 | T | C | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1612T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876459 | |||||||
chr4:38876460 | T | C | 84 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0053 others(81): Show |
84 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.-8-1611T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876460 | |||||||
chr4:38876461 | G | A | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1610G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876461 | |||||||
chr4:38876462 | C | T | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1609C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876462 | |||||||
chr4:38876463 | A | G | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1608A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876463 | |||||||
chr4:38876466 | C | A | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1605C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876466 | |||||||
chr4:38876467 | T | G | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1604T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876467 | |||||||
chr4:38876473 | C | A | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1598C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876473 | |||||||
chr4:38876531 | T | C | 2 | a0001c0001t0006g0142 a0001c0001t0006g0143 |
2 | NA18945.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-8-1540T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876531 | |||||||
chr4:38876573 | T | C | 168 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(165): Show |
173 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.-8-1498T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876573 | |||||||
chr4:38876591 | C | T | 1 | a0001c0001t0005g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-8-1480C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876591 | |||||||
chr4:38876598 | A | C | 1 | a0001c0002t0028g0351 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-8-1473A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876598 | |||||||
chr4:38876671 | G | A | 1 | a0001c0037t0003g0009 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-8-1400G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876671 | |||||||
chr4:38876766 | A | G | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1305A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876766 | |||||||
chr4:38876859 | T | C | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-1212T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876859 | |||||||
chr4:38876873 | G | A | 23 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(20): Show |
23 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8-1198G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38876873 | |||||||
chr4:38877076 | C | T | 23 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(20): Show |
23 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8-995C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877076 | |||||||
chr4:38877101 | G | A | 1 | a0002c0003t0005g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-8-970G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877101 | |||||||
chr4:38877132 | C | A | 10 | a0001c0001t0002g0013 a0001c0001t0005g0005 a0001c0001t0005g0014 others(7): Show |
10 | HG01167.hp2 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-939C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877132 | |||||||
chr4:38877189 | A | G | 1 | a0001c0001t0002g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-8-882A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877189 | |||||||
chr4:38877263 | G | A | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-808G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877263 | |||||||
chr4:38877362 | A | C | 47 | a0002c0003t0001g0359 a0002c0003t0002g0114 a0002c0003t0002g0358 others(44): Show |
47 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.-8-709A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877362 | |||||||
chr4:38877382 | A | C | 4 | a0001c0001t0001g0019 a0001c0001t0002g0016 a0001c0001t0002g0017 others(1): Show |
4 | HG02080.hp1 HG02135.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-689A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877382 | |||||||
chr4:38877457 | A | T | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-8-614A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877457 | |||||||
chr4:38877487 | A | G | 4 | a0007c0021t0004g0347 a0007c0021t0013g0340 a0007c0048t0008g0346 others(1): Show |
4 | HG03704.hp1 HG03834.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-584A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877487 | |||||||
chr4:38877531 | G | A | 1 | a0001c0009t0010g0332 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-8-540G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877531 | |||||||
chr4:38877665 | TA | T | 47 | a0002c0003t0001g0359 a0002c0003t0002g0114 a0002c0003t0002g0358 others(44): Show |
47 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.-8-398delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38877665 | ||||||
chr4:38877691 | G | A | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-380G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877691 | |||||||
chr4:38877763 | G | A | 2 | a0007c0021t0004g0347 a0007c0048t0008g0346 |
2 | NA18950.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.-8-308G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877763 | |||||||
chr4:38877827 | C | G | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-244C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877827 | |||||||
chr4:38877878 | C | T | 6 | a0007c0021t0004g0347 a0007c0021t0013g0340 a0007c0048t0008g0346 others(3): Show |
6 | HG02809.hp2 HG03579.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-193C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877878 | |||||||
chr4:38877879 | G | A | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-192G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877879 | |||||||
chr4:38877896 | G | A | 2 | a0002c0003t0005g0339 a0002c0003t0010g0338 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-8-175G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877896 | |||||||
chr4:38877919 | A | G | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-152A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877919 | |||||||
chr4:38877960 | G | A | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-111G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877960 | |||||||
chr4:38877964 | C | CA | 131 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(128): Show |
136 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.-8-92dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38877964 | ||||||
chr4:38877964 | C | CAA | 12 | a0001c0001t0002g0016 a0001c0004t0001g0058 a0002c0003t0004g0342 others(9): Show |
12 | HG01069.hp1 HG01255.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.-8-93_-8-92dupAA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38877964 | ||||||
chr4:38877964 | C | CAAA | 60 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(57): Show |
60 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.-8-94_-8-92dupAAA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38877964 | ||||||
chr4:38877964 | C | CAAAA | 6 | a0002c0003t0001g0359 a0002c0003t0005g0360 a0002c0003t0010g0338 others(3): Show |
6 | HG02145.hp2 HG02148.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-95_-8-92dupAAAA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr4 | 38877964 | ||||||
chr4:38877978 | AAG | A | 6 | a0007c0021t0004g0347 a0007c0021t0013g0340 a0007c0048t0008g0346 others(3): Show |
6 | HG02809.hp2 HG03579.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-92_-8-91delAG | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38877978 | |||||||
chr4:38878034 | C | T | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-8-37C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 2/14 | chr4 | 38878034 | |||||||
chr4:38878468 | C | T | 1 | a0001c0004t0008g0098 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.348+42C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38878468 | |||||||
chr4:38878507 | G | A | 1 | a0001c0039t0024g0261 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.348+81G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38878507 | |||||||
chr4:38878515 | A | T | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.348+89A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38878515 | |||||||
chr4:38878546 | C | T | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.348+120C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38878546 | |||||||
chr4:38878560 | A | ATGTGT | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.348+135_348+139dup others(5): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38878560 | ||||||
chr4:38878692 | C | A | 168 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(165): Show |
173 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.348+266C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38878692 | |||||||
chr4:38878763 | A | G | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.348+337A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38878763 | |||||||
chr4:38878879 | C | A | 1 | a0001c0001t0002g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.348+453C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38878879 | |||||||
chr4:38878957 | G | C | 2 | a0001c0004t0001g0058 a0001c0004t0004g0059 |
2 | NA18960.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.348+531G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38878957 | |||||||
chr4:38878977 | C | T | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.348+551C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38878977 | |||||||
chr4:38879172 | T | G | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.348+746T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879172 | |||||||
chr4:38879274 | C | A | 6 | a0007c0021t0004g0347 a0007c0021t0013g0340 a0007c0048t0008g0346 others(3): Show |
6 | HG02809.hp2 HG03579.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+848C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879274 | |||||||
chr4:38879365 | C | T | 1 | a0002c0003t0007g0117 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.348+939C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879365 | |||||||
chr4:38879541 | A | T | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.348+1115A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879541 | |||||||
chr4:38879561 | C | T | 1 | a0002c0003t0002g0358 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.348+1135C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879561 | |||||||
chr4:38879567 | G | A | 76 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(73): Show |
76 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.348+1141G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879567 | |||||||
chr4:38879590 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0002g0016 a0001c0001t0002g0017 others(1): Show |
4 | HG02080.hp1 HG02135.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+1164G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879590 | |||||||
chr4:38879607 | G | T | 1 | a0001c0004t0007g0331 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.348+1181G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879607 | |||||||
chr4:38879608 | C | T | 1 | a0001c0004t0007g0331 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.348+1182C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879608 | |||||||
chr4:38879623 | C | T | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+1197C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879623 | |||||||
chr4:38879644 | A | AGCCC | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+1220_348+1221i others(6): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38879644 | ||||||
chr4:38879723 | TA | T | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+1299delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38879723 | ||||||
chr4:38879742 | T | G | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+1316T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879742 | |||||||
chr4:38879758 | G | C | 4 | a0007c0021t0004g0347 a0007c0021t0013g0340 a0007c0048t0008g0346 others(1): Show |
4 | HG03704.hp1 HG03834.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+1332G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879758 | |||||||
chr4:38879793 | T | C | 67 | a0001c0001t0001g0050 a0001c0001t0001g0062 a0001c0001t0002g0049 others(64): Show |
72 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.348+1367T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879793 | |||||||
chr4:38879801 | G | A | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+1375G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879801 | |||||||
chr4:38879884 | T | C | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+1458T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879884 | |||||||
chr4:38879904 | C | T | 1 | a0002c0032t0044g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.348+1478C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879904 | |||||||
chr4:38879921 | T | G | 3 | a0001c0001t0009g0148 a0001c0001t0009g0149 a0016c0047t0009g0150 |
3 | HG01109.hp1 HG02602.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.348+1495T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38879921 | |||||||
chr4:38880074 | TAAATA | T | 10 | a0002c0003t0001g0359 a0002c0006t0001g0354 a0002c0006t0011g0026 others(7): Show |
10 | HG01255.hp2 HG02698.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+1674_348+1678d others(7): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880074 | ||||||
chr4:38880074 | TAAATAAA others(3): Show |
T | 79 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(76): Show |
84 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.348+1669_348+1678d others(12): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880074 | ||||||
chr4:38880085 | A | AAATAGAG others(3): Show |
2 | a0003c0007t0025g0035 a0013c0052t0005g0247 |
2 | HG01070.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.348+1663_348+1664i others(12): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880085 | ||||||
chr4:38880085 | A | AAATAGAG others(13): Show |
3 | a0002c0003t0012g0112 a0002c0003t0032g0357 a0005c0055t0012g0356 |
3 | HG02818.hp1 HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.348+1663_348+1664i others(22): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880085 | ||||||
chr4:38880085 | AAATAAAA others(18): Show |
A | 1 | a0002c0028t0030g0363 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.348+1664_348+1688d others(27): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880085 | ||||||
chr4:38880087 | A | ATAGAG | 13 | a0002c0003t0005g0360 a0002c0003t0016g0034 a0002c0006t0001g0033 others(10): Show |
13 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.348+1663_348+1664i others(7): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880087 | ||||||
chr4:38880087 | A | ATAGAGTA others(8): Show |
5 | a0002c0003t0006g0036 a0002c0003t0010g0362 a0002c0006t0010g0337 others(2): Show |
5 | HG00544.hp2 HG01109.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+1663_348+1664i others(17): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880087 | ||||||
chr4:38880087 | ATAAAATA others(13): Show |
A | 2 | a0002c0003t0004g0022 a0002c0003t0005g0364 |
2 | HG00140.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.348+1664_348+1683d others(22): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880087 | ||||||
chr4:38880090 | A | G | 32 | a0002c0003t0002g0114 a0002c0003t0005g0353 a0002c0003t0005g0360 others(29): Show |
32 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.348+1664A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880090 | |||||||
chr4:38880092 | A | G | 12 | a0002c0003t0002g0114 a0002c0003t0005g0353 a0002c0022t0005g0249 others(9): Show |
12 | HG01070.hp2 HG01243.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.348+1666A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880092 | |||||||
chr4:38880095 | A | AAATAGAG others(13): Show |
4 | a0002c0003t0001g0128 a0002c0003t0002g0121 a0002c0003t0007g0117 others(1): Show |
4 | HG01257.hp2 HG01978.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+1673_348+1674i others(22): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880095 | ||||||
chr4:38880095 | A | AAATAGAG others(18): Show |
1 | a0002c0003t0004g0118 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.348+1673_348+1674i others(27): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880095 | ||||||
chr4:38880095 | A | AAATAGAG others(23): Show |
1 | a0002c0003t0005g0339 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.348+1673_348+1674i others(32): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880095 | ||||||
chr4:38880095 | A | AAATAGAG others(33): Show |
3 | a0002c0003t0004g0130 a0002c0003t0018g0119 a0002c0003t0018g0129 |
3 | NA18978.hp1 NA18999.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.348+1673_348+1674i others(42): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880095 | ||||||
chr4:38880095 | A | AAATAGAG others(58): Show |
3 | a0002c0003t0002g0043 a0002c0003t0005g0042 a0002c0003t0005g0044 |
3 | HG02451.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.348+1673_348+1674i others(67): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880095 | ||||||
chr4:38880095 | A | AAATAGAG others(68): Show |
1 | a0002c0026t0005g0039 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.348+1673_348+1674i others(77): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880095 | ||||||
chr4:38880095 | A | AAATAGAG others(68): Show |
1 | a0002c0003t0002g0045 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.348+1673_348+1674i others(77): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880095 | ||||||
chr4:38880095 | A | G | 35 | a0002c0003t0001g0359 a0002c0003t0002g0114 a0002c0003t0005g0353 others(32): Show |
35 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.348+1669A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880095 | |||||||
chr4:38880097 | A | ATAGAG | 6 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0131 others(3): Show |
6 | HG00621.hp1 HG02148.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+1673_348+1674i others(7): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880097 | ||||||
chr4:38880097 | A | ATAGAGTA others(8): Show |
5 | a0002c0003t0001g0127 a0002c0003t0017g0132 a0002c0034t0020g0133 others(2): Show |
5 | HG01975.hp2 HG02273.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+1673_348+1674i others(17): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880097 | ||||||
chr4:38880097 | A | ATAGAGTA others(3): Show |
1 | a0002c0022t0010g0248 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.348+1673_348+1674i others(12): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880097 | ||||||
chr4:38880097 | A | G | 17 | a0002c0003t0001g0359 a0002c0003t0005g0360 a0002c0003t0016g0034 others(14): Show |
17 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.348+1671A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880097 | |||||||
chr4:38880097 | ATAAAATA others(3): Show |
A | 4 | a0002c0003t0004g0342 a0002c0003t0005g0343 a0002c0032t0044g0352 others(1): Show |
4 | HG02145.hp2 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+1674_348+1683d others(12): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880097 | ||||||
chr4:38880100 | A | G | 69 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(66): Show |
69 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.348+1674A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880100 | |||||||
chr4:38880102 | A | G | 19 | a0002c0003t0002g0114 a0002c0003t0002g0358 a0002c0003t0005g0042 others(16): Show |
19 | HG01069.hp1 HG01071.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.348+1676A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880102 | |||||||
chr4:38880107 | G | A | 57 | a0002c0003t0001g0127 a0002c0003t0001g0128 a0002c0003t0002g0045 others(54): Show |
57 | HG00323.hp2 HG00544.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.348+1681G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880107 | |||||||
chr4:38880107 | G | GTAGAA | 29 | a0001c0001t0001g0211 a0001c0001t0001g0217 a0001c0001t0001g0218 others(26): Show |
29 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.348+1747_348+1751d others(7): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | ||||||
chr4:38880107 | G | GTAGAATA others(3): Show |
17 | a0001c0001t0001g0315 a0001c0001t0002g0287 a0001c0001t0002g0314 others(14): Show |
17 | HG00438.hp2 HG00642.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.348+1742_348+1751d others(12): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | ||||||
chr4:38880107 | G | GTAGAATA others(8): Show |
3 | a0001c0001t0026g0317 a0001c0002t0001g0223 a0001c0005t0003g0222 |
3 | HG00639.hp2 HG02165.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.348+1737_348+1751d others(17): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | ||||||
chr4:38880107 | G | GTAGAATA others(13): Show |
3 | a0001c0001t0002g0291 a0001c0001t0004g0319 a0006c0010t0003g0318 |
3 | HG02083.hp1 HG02300.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.348+1732_348+1751d others(22): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | ||||||
chr4:38880107 | G | GTAGAATA others(53): Show |
1 | a0001c0001t0008g0224 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.348+1692_348+1751d others(62): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | ||||||
chr4:38880107 | G | GTAGAATA others(18): Show |
1 | a0007c0049t0002g0348 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.348+1690_348+1691i others(27): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | ||||||
chr4:38880107 | G | GTAGAATA others(23): Show |
2 | a0007c0021t0013g0340 a0014c0051t0005g0344 |
2 | HG02809.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.348+1690_348+1691i others(32): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | ||||||
chr4:38880107 | G | GTAGAATA others(28): Show |
1 | a0007c0048t0008g0346 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.348+1690_348+1691i others(37): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | ||||||
chr4:38880107 | G | GTAGAATA others(113): Show |
1 | a0007c0021t0004g0347 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.348+1690_348+1691i others(122): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | ||||||
chr4:38880107 | GTAGAA | G | 37 | a0001c0001t0001g0173 a0001c0001t0001g0275 a0001c0001t0001g0296 others(34): Show |
38 | HG00673.hp2 HG00735.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.348+1747_348+1751d others(7): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | ||||||
chr4:38880107 | GTAGAATA others(3): Show |
G | 17 | a0001c0001t0001g0161 a0001c0001t0002g0165 a0001c0001t0004g0268 others(14): Show |
17 | HG00597.hp1 HG01069.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.348+1742_348+1751d others(12): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | ||||||
chr4:38880107 | GTAGAATA others(8): Show |
G | 14 | a0001c0001t0001g0159 a0001c0001t0002g0292 a0001c0001t0004g0262 others(11): Show |
14 | HG00741.hp1 HG02040.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.348+1737_348+1751d others(17): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | ||||||
chr4:38880107 | GTAGAATA others(13): Show |
G | 4 | a0001c0001t0005g0014 a0001c0001t0005g0231 a0001c0001t0007g0227 others(1): Show |
4 | HG01884.hp1 HG02257.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+1732_348+1751d others(22): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | ||||||
chr4:38880107 | GTAGAATA others(18): Show |
G | 8 | a0001c0001t0005g0005 a0001c0001t0007g0230 a0001c0002t0014g0151 others(5): Show |
8 | HG01167.hp2 HG02074.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+1727_348+1751d others(27): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | ||||||
chr4:38880107 | GTAGAATA others(23): Show |
G | 6 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0004g0253 others(3): Show |
6 | HG01261.hp1 HG02486.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+1722_348+1751d others(32): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | ||||||
chr4:38880107 | GTAGAATA others(38): Show |
G | 70 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(67): Show |
75 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.348+1707_348+1751d others(47): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880107 | ||||||
chr4:38880111 | AATAGAAT others(37): Show |
A | 1 | a0001c0004t0001g0058 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.348+1687_348+1730d others(46): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38880111 | ||||||
chr4:38880112 | A | G | 14 | a0002c0003t0002g0358 a0002c0003t0004g0022 a0002c0003t0004g0342 others(11): Show |
14 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.348+1686A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880112 | |||||||
chr4:38880117 | A | G | 1 | a0002c0028t0030g0363 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.348+1691A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880117 | |||||||
chr4:38880122 | A | G | 2 | a0002c0003t0004g0022 a0002c0003t0005g0364 |
2 | HG00140.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.348+1696A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880122 | |||||||
chr4:38880127 | A | G | 1 | a0002c0028t0030g0363 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.348+1701A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880127 | |||||||
chr4:38880156 | A | C | 1 | a0001c0004t0001g0058 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.348+1730A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880156 | |||||||
chr4:38880177 | A | ATAGAATA others(16): Show |
2 | a0001c0002t0001g0147 a0001c0002t0001g0305 |
2 | NA18973.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.348+1751_348+1752i others(25): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880177 | |||||||
chr4:38880200 | G | C | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+1774G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880200 | |||||||
chr4:38880267 | G | C | 341 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(338): Show |
347 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.348+1841G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880267 | |||||||
chr4:38880274 | T | G | 2 | a0002c0003t0004g0342 a0005c0012t0033g0341 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.348+1848T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880274 | |||||||
chr4:38880278 | C | T | 1 | a0001c0002t0002g0141 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.348+1852C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880278 | |||||||
chr4:38880290 | A | G | 1 | a0002c0032t0044g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.348+1864A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880290 | |||||||
chr4:38880319 | A | G | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+1893A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880319 | |||||||
chr4:38880352 | T | G | 7 | a0001c0002t0001g0135 a0001c0002t0001g0152 a0001c0002t0001g0156 others(4): Show |
7 | NA18951.hp2 NA18955.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.348+1926T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880352 | |||||||
chr4:38880408 | C | T | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+1982C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880408 | |||||||
chr4:38880611 | T | A | 1 | a0001c0005t0003g0285 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.348+2185T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880611 | |||||||
chr4:38880685 | A | G | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+2259A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880685 | |||||||
chr4:38880713 | T | G | 1 | a0004c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.348+2287T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880713 | |||||||
chr4:38880716 | G | A | 24 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(21): Show |
24 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.348+2290G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880716 | |||||||
chr4:38880847 | T | C | 1 | a0001c0002t0008g0060 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.348+2421T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880847 | |||||||
chr4:38880886 | T | C | 1 | a0004c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.348+2460T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880886 | |||||||
chr4:38880913 | G | A | 1 | a0002c0057t0005g0251 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.348+2487G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880913 | |||||||
chr4:38880951 | G | A | 7 | a0001c0002t0001g0135 a0001c0002t0001g0152 a0001c0002t0001g0156 others(4): Show |
7 | NA18951.hp2 NA18955.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.348+2525G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880951 | |||||||
chr4:38880978 | A | G | 16 | a0002c0003t0002g0114 a0002c0003t0012g0112 a0002c0022t0005g0249 others(13): Show |
16 | HG01109.hp2 HG01243.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.348+2552A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38880978 | |||||||
chr4:38881138 | T | C | 12 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0004g0253 others(9): Show |
13 | HG01069.hp2 HG01261.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.348+2712T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38881138 | |||||||
chr4:38881201 | C | CA | 61 | a0001c0001t0002g0007 a0001c0001t0002g0145 a0001c0001t0005g0005 others(58): Show |
61 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.348+2789dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38881201 | ||||||
chr4:38881201 | C | CAA | 37 | a0001c0001t0002g0013 a0001c0001t0011g0010 a0001c0002t0014g0151 others(34): Show |
37 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(34): Show |
intron_variant | MODIFIER | c.348+2788_348+2789d others(4): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38881201 | ||||||
chr4:38881352 | C | G | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.348+2926C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38881352 | |||||||
chr4:38881458 | C | T | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+3032C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38881458 | |||||||
chr4:38881624 | A | G | 18 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(15): Show |
18 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.348+3198A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38881624 | |||||||
chr4:38881630 | C | T | 24 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(21): Show |
24 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.348+3204C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38881630 | |||||||
chr4:38881684 | G | C | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+3258G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38881684 | |||||||
chr4:38881773 | T | C | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+3347T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38881773 | |||||||
chr4:38881846 | A | T | 1 | a0001c0001t0002g0097 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.348+3420A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38881846 | |||||||
chr4:38881880 | A | G | 1 | a0001c0004t0007g0136 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.348+3454A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38881880 | |||||||
chr4:38882041 | G | A | 2 | a0002c0003t0005g0364 a0002c0028t0030g0363 |
2 | HG01891.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.348+3615G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882041 | |||||||
chr4:38882070 | T | C | 5 | a0001c0001t0001g0296 a0001c0001t0010g0299 a0001c0001t0014g0295 others(2): Show |
5 | HG02723.hp2 HG02886.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+3644T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882070 | |||||||
chr4:38882108 | C | T | 13 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0005g0005 others(10): Show |
13 | HG01167.hp2 HG02486.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.348+3682C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882108 | |||||||
chr4:38882166 | G | C | 1 | a0002c0006t0001g0020 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.348+3740G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882166 | |||||||
chr4:38882168 | C | T | 47 | a0002c0003t0001g0359 a0002c0003t0002g0114 a0002c0003t0002g0358 others(44): Show |
47 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.348+3742C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882168 | |||||||
chr4:38882173 | G | A | 5 | a0002c0003t0017g0132 a0007c0021t0004g0347 a0007c0021t0013g0340 others(2): Show |
5 | HG03704.hp1 HG03834.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+3747G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882173 | |||||||
chr4:38882174 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.348+3748C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882174 | |||||||
chr4:38882178 | G | C | 1 | a0001c0001t0002g0278 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.348+3752G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882178 | |||||||
chr4:38882180 | T | C | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+3754T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882180 | |||||||
chr4:38882185 | G | A | 1 | a0002c0003t0005g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.348+3759G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882185 | |||||||
chr4:38882269 | A | G | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+3843A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882269 | |||||||
chr4:38882278 | G | C | 64 | a0002c0003t0001g0359 a0002c0003t0002g0043 a0002c0003t0002g0045 others(61): Show |
64 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.348+3852G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882278 | |||||||
chr4:38882282 | G | A | 19 | a0001c0008t0006g0061 a0002c0003t0001g0120 a0002c0003t0001g0123 others(16): Show |
19 | HG00544.hp1 HG00621.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.348+3856G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882282 | |||||||
chr4:38882318 | C | CA | 152 | a0001c0001t0001g0050 a0001c0001t0001g0161 a0001c0001t0001g0211 others(149): Show |
157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.348+3915dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38882318 | ||||||
chr4:38882318 | C | CAA | 25 | a0001c0001t0001g0019 a0001c0001t0001g0062 a0001c0001t0002g0007 others(22): Show |
25 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.348+3914_348+3915d others(4): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38882318 | ||||||
chr4:38882318 | CA | C | 7 | a0001c0001t0001g0284 a0001c0001t0002g0013 a0001c0001t0002g0271 others(4): Show |
7 | HG01074.hp1 HG01123.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.348+3915delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38882318 | ||||||
chr4:38882318 | CAAAAAAA others(3): Show |
C | 2 | a0002c0003t0005g0339 a0002c0003t0010g0338 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.348+3906_348+3915d others(12): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38882318 | ||||||
chr4:38882414 | G | T | 4 | a0001c0001t0001g0019 a0001c0001t0002g0016 a0001c0001t0002g0017 others(1): Show |
4 | HG02080.hp1 HG02135.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+3988G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882414 | |||||||
chr4:38882428 | G | A | 8 | a0001c0001t0002g0287 a0001c0001t0002g0291 a0001c0001t0002g0336 others(5): Show |
8 | HG02027.hp1 HG02083.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+4002G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882428 | |||||||
chr4:38882432 | C | A | 6 | a0007c0021t0004g0347 a0007c0021t0013g0340 a0007c0048t0008g0346 others(3): Show |
6 | HG02809.hp2 HG03579.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.348+4006C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882432 | |||||||
chr4:38882445 | T | C | 1 | a0004c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.348+4019T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882445 | |||||||
chr4:38882614 | A | T | 1 | a0005c0030t0003g0113 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.348+4188A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882614 | |||||||
chr4:38882670 | A | G | 10 | a0001c0001t0002g0007 a0001c0001t0005g0005 a0001c0001t0005g0014 others(7): Show |
10 | HG01167.hp2 HG02486.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+4244A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882670 | |||||||
chr4:38882679 | C | T | 1 | a0001c0002t0001g0199 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.348+4253C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882679 | |||||||
chr4:38882752 | TG | T | 161 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(158): Show |
164 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.348+4328delG | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38882752 | ||||||
chr4:38882798 | A | G | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+4372A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882798 | |||||||
chr4:38882893 | A | G | 46 | a0002c0003t0001g0359 a0002c0003t0002g0114 a0002c0003t0002g0358 others(43): Show |
46 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.348+4467A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38882893 | |||||||
chr4:38883005 | CT | C | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+4582delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38883005 | ||||||
chr4:38883041 | G | C | 1 | a0001c0009t0003g0335 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.348+4615G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883041 | |||||||
chr4:38883267 | C | T | 2 | a0001c0002t0006g0327 a0001c0002t0006g0329 |
2 | HG00642.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.348+4841C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883267 | |||||||
chr4:38883298 | C | T | 2 | a0001c0001t0007g0256 a0001c0004t0011g0255 |
2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.348+4872C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883298 | |||||||
chr4:38883338 | G | T | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.348+4912G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883338 | |||||||
chr4:38883410 | G | A | 2 | a0001c0001t0006g0142 a0001c0001t0006g0143 |
2 | NA18945.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.348+4984G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883410 | |||||||
chr4:38883416 | C | G | 16 | a0002c0003t0002g0114 a0002c0003t0012g0112 a0002c0022t0005g0249 others(13): Show |
16 | HG01109.hp2 HG01243.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.348+4990C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883416 | |||||||
chr4:38883423 | T | TAAAAGAC others(293): Show |
1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.348+5012_348+5013i others(302): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38883423 | ||||||
chr4:38883635 | G | A | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+5209G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883635 | |||||||
chr4:38883774 | T | C | 1 | a0004c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.348+5348T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883774 | |||||||
chr4:38883814 | G | A | 1 | a0001c0001t0002g0053 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.348+5388G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883814 | |||||||
chr4:38883844 | C | T | 1 | a0001c0004t0008g0098 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.348+5418C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883844 | |||||||
chr4:38883890 | G | A | 1 | a0004c0011t0014g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.348+5464G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38883890 | |||||||
chr4:38884180 | G | A | 1 | a0017c0031t0019g0028 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.348+5754G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884180 | |||||||
chr4:38884180 | G | T | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.348+5754G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884180 | |||||||
chr4:38884224 | A | G | 5 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0005g0042 others(2): Show |
5 | HG02451.hp2 HG02723.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+5798A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884224 | |||||||
chr4:38884269 | G | A | 1 | a0002c0034t0020g0133 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.348+5843G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884269 | |||||||
chr4:38884341 | C | T | 1 | a0001c0001t0012g0184 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.348+5915C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884341 | |||||||
chr4:38884378 | G | A | 2 | a0001c0001t0002g0051 a0001c0001t0002g0102 |
2 | HG01981.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.348+5952G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884378 | |||||||
chr4:38884399 | G | A | 11 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(8): Show |
11 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.348+5973G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884399 | |||||||
chr4:38884522 | A | G | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+6096A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884522 | |||||||
chr4:38884659 | G | A | 1 | a0007c0021t0004g0347 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.348+6233G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884659 | |||||||
chr4:38884672 | G | A | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+6246G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884672 | |||||||
chr4:38884772 | G | C | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+6346G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884772 | |||||||
chr4:38884773 | G | T | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+6347G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884773 | |||||||
chr4:38884799 | G | A | 68 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(65): Show |
71 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.348+6373G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884799 | |||||||
chr4:38884829 | C | T | 10 | a0001c0001t0002g0007 a0001c0001t0005g0005 a0001c0001t0005g0014 others(7): Show |
10 | HG01167.hp2 HG02486.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+6403C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38884829 | |||||||
chr4:38885031 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.348+6605G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38885031 | |||||||
chr4:38885044 | G | A | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.348+6618G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38885044 | |||||||
chr4:38885116 | C | T | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.349-6627C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38885116 | |||||||
chr4:38885161 | G | A | 82 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(79): Show |
82 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.349-6582G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38885161 | |||||||
chr4:38885607 | A | G | 6 | a0001c0001t0002g0316 a0001c0001t0002g0325 a0001c0002t0001g0279 others(3): Show |
6 | HG02132.hp1 NA18951.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-6136A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38885607 | |||||||
chr4:38885681 | G | T | 18 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0127 others(15): Show |
18 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.349-6062G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38885681 | |||||||
chr4:38885730 | C | T | 164 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(161): Show |
167 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.349-6013C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38885730 | |||||||
chr4:38885919 | T | C | 6 | a0001c0001t0005g0297 a0001c0001t0005g0301 a0001c0001t0007g0320 others(3): Show |
6 | HG02258.hp2 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-5824T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38885919 | |||||||
chr4:38886172 | CT | C | 24 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0005g0014 others(21): Show |
24 | HG01257.hp1 HG02145.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.349-5554delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38886172 | ||||||
chr4:38886273 | G | A | 1 | a0004c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.349-5470G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38886273 | |||||||
chr4:38886296 | C | T | 1 | a0001c0004t0008g0048 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.349-5447C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38886296 | |||||||
chr4:38886312 | C | T | 84 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(81): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.349-5431C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38886312 | |||||||
chr4:38886316 | A | G | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.349-5427A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38886316 | |||||||
chr4:38886373 | T | G | 84 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(81): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.349-5370T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38886373 | |||||||
chr4:38886421 | T | G | 1 | a0001c0001t0002g0241 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.349-5322T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38886421 | |||||||
chr4:38886547 | G | T | 1 | a0002c0003t0005g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.349-5196G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38886547 | |||||||
chr4:38886550 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.349-5193C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38886550 | |||||||
chr4:38886922 | C | T | 47 | a0002c0003t0001g0359 a0002c0003t0002g0114 a0002c0003t0002g0358 others(44): Show |
47 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.349-4821C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38886922 | |||||||
chr4:38886927 | C | CA | 16 | a0001c0001t0001g0062 a0001c0001t0002g0013 a0001c0001t0002g0063 others(13): Show |
16 | HG00438.hp1 HG01257.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.349-4798dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38886927 | ||||||
chr4:38886927 | CA | C | 14 | a0001c0002t0001g0242 a0001c0002t0002g0018 a0002c0003t0002g0043 others(11): Show |
14 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.349-4798delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38886927 | ||||||
chr4:38886989 | C | T | 167 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(164): Show |
170 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.349-4754C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38886989 | |||||||
chr4:38887080 | A | T | 1 | a0001c0001t0005g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.349-4663A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38887080 | |||||||
chr4:38887121 | G | A | 1 | a0001c0001t0002g0071 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.349-4622G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38887121 | |||||||
chr4:38887175 | T | C | 1 | a0001c0001t0002g0287 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.349-4568T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38887175 | |||||||
chr4:38887195 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0002g0040 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.349-4548A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38887195 | |||||||
chr4:38887220 | C | T | 11 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(8): Show |
11 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.349-4523C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38887220 | |||||||
chr4:38887272 | C | T | 5 | a0002c0003t0002g0114 a0002c0003t0012g0112 a0002c0029t0043g0115 others(2): Show |
5 | HG01243.hp1 HG02027.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-4471C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38887272 | |||||||
chr4:38887776 | G | A | 1 | a0004c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.349-3967G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38887776 | |||||||
chr4:38887953 | T | C | 1 | a0001c0001t0007g0273 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.349-3790T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38887953 | |||||||
chr4:38888014 | A | G | 1 | a0001c0001t0004g0268 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.349-3729A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38888014 | |||||||
chr4:38888020 | A | G | 4 | a0007c0021t0004g0347 a0007c0021t0013g0340 a0007c0048t0008g0346 others(1): Show |
4 | HG03704.hp1 HG03834.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-3723A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38888020 | |||||||
chr4:38888105 | A | T | 1 | a0001c0004t0001g0058 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.349-3638A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38888105 | |||||||
chr4:38888190 | A | G | 84 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(81): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.349-3553A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38888190 | |||||||
chr4:38888651 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.349-3092T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38888651 | |||||||
chr4:38888717 | T | C | 1 | a0001c0001t0002g0278 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.349-3026T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38888717 | |||||||
chr4:38888723 | A | G | 11 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(8): Show |
11 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.349-3020A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38888723 | |||||||
chr4:38888841 | G | C | 3 | a0001c0001t0035g0312 a0001c0002t0040g0307 a0004c0011t0002g0313 |
3 | HG02559.hp1 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.349-2902G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38888841 | |||||||
chr4:38888849 | A | G | 1 | a0001c0002t0001g0209 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.349-2894A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38888849 | |||||||
chr4:38888930 | AT | A | 6 | a0007c0021t0004g0347 a0007c0021t0013g0340 a0007c0048t0008g0346 others(3): Show |
6 | HG02809.hp2 HG03579.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-2807delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38888930 | ||||||
chr4:38888951 | T | C | 2 | a0001c0001t0010g0259 a0001c0004t0001g0260 |
2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.349-2792T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38888951 | |||||||
chr4:38889170 | C | T | 1 | a0004c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.349-2573C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38889170 | |||||||
chr4:38889328 | G | A | 1 | a0001c0013t0006g0171 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.349-2415G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38889328 | |||||||
chr4:38889335 | G | T | 1 | a0002c0003t0005g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.349-2408G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38889335 | |||||||
chr4:38889406 | A | G | 11 | a0002c0022t0005g0249 a0002c0022t0010g0248 a0002c0053t0001g0245 others(8): Show |
11 | HG01109.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.349-2337A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38889406 | |||||||
chr4:38889528 | A | G | 1 | a0001c0001t0001g0275 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.349-2215A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38889528 | |||||||
chr4:38889552 | C | T | 74 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(71): Show |
77 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.349-2191C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38889552 | |||||||
chr4:38889558 | G | A | 1 | a0005c0055t0012g0356 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.349-2185G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38889558 | |||||||
chr4:38889813 | G | A | 43 | a0002c0003t0001g0359 a0002c0003t0002g0358 a0002c0003t0004g0022 others(40): Show |
43 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.349-1930G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38889813 | |||||||
chr4:38889885 | G | A | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.349-1858G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38889885 | |||||||
chr4:38890064 | T | C | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.349-1679T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890064 | |||||||
chr4:38890116 | A | G | 107 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(104): Show |
111 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.349-1627A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890116 | |||||||
chr4:38890180 | G | T | 1 | a0001c0001t0010g0259 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.349-1563G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890180 | |||||||
chr4:38890273 | C | T | 14 | a0002c0003t0004g0022 a0002c0003t0016g0034 a0002c0006t0001g0033 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.349-1470C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890273 | |||||||
chr4:38890319 | C | T | 3 | a0002c0003t0004g0342 a0002c0003t0005g0343 a0005c0012t0033g0341 |
3 | HG02280.hp2 HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.349-1424C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890319 | |||||||
chr4:38890320 | G | A | 11 | a0002c0022t0005g0249 a0002c0022t0010g0248 a0002c0053t0001g0245 others(8): Show |
11 | HG01109.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.349-1423G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890320 | |||||||
chr4:38890327 | C | T | 17 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0004g0253 others(14): Show |
18 | HG01069.hp2 HG01261.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.349-1416C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890327 | |||||||
chr4:38890380 | T | C | 143 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(140): Show |
147 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.349-1363T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890380 | |||||||
chr4:38890381 | G | A | 15 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0004g0268 others(12): Show |
16 | HG01069.hp2 HG01884.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.349-1362G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890381 | |||||||
chr4:38890397 | G | A | 3 | a0001c0001t0004g0253 a0001c0001t0007g0256 a0001c0004t0011g0255 |
3 | HG01261.hp1 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.349-1346G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890397 | |||||||
chr4:38890401 | C | CA | 29 | a0001c0001t0002g0013 a0001c0001t0002g0271 a0001c0001t0002g0272 others(26): Show |
30 | HG00140.hp2 HG01069.hp2 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.349-1331dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38890401 | ||||||
chr4:38890401 | C | CAA | 99 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(96): Show |
102 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.349-1332_349-1331d others(4): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38890401 | ||||||
chr4:38890401 | CA | C | 11 | a0002c0022t0005g0249 a0002c0022t0010g0248 a0002c0053t0001g0245 others(8): Show |
11 | HG01109.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.349-1331delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38890401 | ||||||
chr4:38890413 | C | A | 75 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0271 others(72): Show |
76 | HG00621.hp1 HG01069.hp2 HG01167.hp2 others(73): Show |
intron_variant | MODIFIER | c.349-1330C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890413 | |||||||
chr4:38890589 | G | T | 5 | a0002c0003t0002g0114 a0002c0003t0012g0112 a0002c0029t0043g0115 others(2): Show |
5 | HG01243.hp1 HG02027.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-1154G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890589 | |||||||
chr4:38890600 | C | T | 75 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0271 others(72): Show |
76 | HG00621.hp1 HG01069.hp2 HG01167.hp2 others(73): Show |
intron_variant | MODIFIER | c.349-1143C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890600 | |||||||
chr4:38890703 | G | T | 1 | a0001c0001t0002g0180 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.349-1040G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38890703 | |||||||
chr4:38891023 | G | C | 1 | a0001c0001t0017g0138 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.349-720G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891023 | |||||||
chr4:38891028 | T | C | 68 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(65): Show |
71 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.349-715T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891028 | |||||||
chr4:38891119 | C | T | 2 | a0001c0002t0001g0179 a0001c0002t0001g0234 |
2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.349-624C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891119 | |||||||
chr4:38891180 | G | A | 1 | a0001c0001t0027g0070 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.349-563G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891180 | |||||||
chr4:38891189 | G | C | 6 | a0001c0001t0002g0013 a0001c0001t0007g0256 a0001c0001t0011g0010 others(3): Show |
6 | HG02109.hp1 HG02896.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-554G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891189 | |||||||
chr4:38891274 | C | T | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.349-469C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891274 | |||||||
chr4:38891285 | T | C | 6 | a0007c0021t0004g0347 a0007c0021t0013g0340 a0007c0048t0008g0346 others(3): Show |
6 | HG02809.hp2 HG03579.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-458T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891285 | |||||||
chr4:38891309 | A | G | 6 | a0007c0021t0004g0347 a0007c0021t0013g0340 a0007c0048t0008g0346 others(3): Show |
6 | HG02809.hp2 HG03579.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-434A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891309 | |||||||
chr4:38891357 | T | TA | 154 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(151): Show |
158 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.349-384dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | 38891357 | ||||||
chr4:38891412 | C | G | 1 | a0012c0040t0023g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.349-331C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891412 | |||||||
chr4:38891465 | A | G | 3 | a0002c0003t0004g0342 a0002c0003t0005g0343 a0005c0012t0033g0341 |
3 | HG02280.hp2 HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.349-278A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891465 | |||||||
chr4:38891472 | G | C | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.349-271G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891472 | |||||||
chr4:38891622 | C | T | 1 | a0001c0001t0004g0277 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.349-121C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891622 | |||||||
chr4:38891674 | A | T | 12 | a0001c0001t0002g0013 a0001c0001t0007g0256 a0001c0001t0011g0010 others(9): Show |
12 | HG02258.hp1 HG02809.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.349-69A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | chr4 | 38891674 | |||||||
chr4:38891850 | T | C | 1 | a0002c0006t0001g0020 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.436+20T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38891850 | |||||||
chr4:38892115 | G | A | 27 | a0001c0001t0002g0007 a0001c0001t0002g0271 a0001c0001t0002g0272 others(24): Show |
28 | HG01069.hp2 HG01167.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.436+285G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38892115 | |||||||
chr4:38892221 | C | A | 41 | a0001c0001t0002g0013 a0001c0001t0004g0257 a0001c0001t0007g0256 others(38): Show |
41 | HG00621.hp1 HG01243.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.436+391C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38892221 | |||||||
chr4:38892222 | G | T | 91 | a0001c0001t0001g0050 a0001c0001t0001g0062 a0001c0001t0002g0007 others(88): Show |
95 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.436+392G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38892222 | |||||||
chr4:38892387 | T | C | 2 | a0002c0006t0010g0337 a0004c0020t0003g0046 |
2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.436+557T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38892387 | |||||||
chr4:38892552 | A | G | 27 | a0001c0001t0002g0007 a0001c0001t0002g0271 a0001c0001t0002g0272 others(24): Show |
28 | HG01069.hp2 HG01167.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.436+722A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38892552 | |||||||
chr4:38892577 | T | C | 1 | a0004c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.436+747T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38892577 | |||||||
chr4:38892605 | G | A | 10 | a0001c0001t0001g0173 a0001c0001t0001g0187 a0001c0001t0002g0186 others(7): Show |
10 | HG01346.hp2 HG01433.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.436+775G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38892605 | |||||||
chr4:38892759 | A | G | 143 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(140): Show |
147 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.436+929A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38892759 | |||||||
chr4:38892857 | C | T | 1 | a0001c0037t0003g0009 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.436+1027C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38892857 | |||||||
chr4:38892958 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0002g0016 a0001c0001t0002g0017 others(1): Show |
4 | HG02080.hp1 HG02135.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+1128C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38892958 | |||||||
chr4:38893067 | A | G | 4 | a0001c0001t0002g0007 a0001c0001t0004g0253 a0001c0001t0004g0254 others(1): Show |
4 | HG01261.hp1 HG02486.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+1237A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38893067 | |||||||
chr4:38893206 | A | G | 1 | a0001c0001t0006g0143 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.436+1376A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38893206 | |||||||
chr4:38893284 | G | T | 3 | a0001c0001t0002g0013 a0001c0001t0011g0010 a0001c0037t0003g0009 |
3 | HG02896.hp1 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.436+1454G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38893284 | |||||||
chr4:38893408 | T | G | 25 | a0001c0001t0002g0007 a0001c0001t0002g0271 a0001c0001t0002g0272 others(22): Show |
26 | HG01069.hp2 HG01167.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.436+1578T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38893408 | |||||||
chr4:38893550 | G | A | 1 | a0001c0001t0002g0053 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.436+1720G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38893550 | |||||||
chr4:38893887 | G | A | 1 | a0004c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.436+2057G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38893887 | |||||||
chr4:38894119 | C | T | 5 | a0001c0001t0001g0019 a0001c0001t0002g0016 a0001c0001t0002g0017 others(2): Show |
5 | HG02080.hp1 HG02135.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+2289C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38894119 | |||||||
chr4:38894162 | C | CA | 23 | a0001c0001t0002g0047 a0001c0001t0002g0191 a0001c0001t0002g0314 others(20): Show |
23 | HG00609.hp2 HG01109.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.436+2358dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38894162 | ||||||
chr4:38894162 | CAAAAAA | C | 75 | a0001c0001t0001g0050 a0001c0001t0001g0062 a0001c0001t0002g0049 others(72): Show |
78 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.436+2353_436+2358d others(8): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38894162 | ||||||
chr4:38894162 | CAAAAAAA | C | 87 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0271 others(84): Show |
88 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.436+2352_436+2358d others(9): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38894162 | ||||||
chr4:38894347 | A | T | 5 | a0001c0001t0012g0170 a0002c0003t0002g0114 a0002c0029t0043g0115 others(2): Show |
5 | HG01243.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+2517A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38894347 | |||||||
chr4:38894508 | C | A | 4 | a0001c0001t0002g0013 a0001c0001t0011g0010 a0001c0037t0003g0009 others(1): Show |
4 | HG02109.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+2678C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38894508 | |||||||
chr4:38894531 | A | G | 7 | a0001c0001t0002g0287 a0001c0001t0002g0291 a0001c0001t0002g0336 others(4): Show |
7 | HG02027.hp1 HG02083.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.436+2701A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38894531 | |||||||
chr4:38894642 | A | G | 1 | a0002c0003t0006g0036 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.436+2812A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38894642 | |||||||
chr4:38894648 | G | A | 5 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0005g0042 others(2): Show |
5 | HG02451.hp2 HG02723.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+2818G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38894648 | |||||||
chr4:38894653 | G | T | 2 | a0002c0003t0001g0359 a0002c0003t0005g0360 |
2 | HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.436+2823G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38894653 | |||||||
chr4:38894661 | G | A | 1 | a0001c0001t0002g0292 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.436+2831G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38894661 | |||||||
chr4:38894775 | C | T | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.436+2945C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38894775 | |||||||
chr4:38894862 | G | A | 36 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0004g0257 others(33): Show |
37 | HG00621.hp1 HG01069.hp2 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.436+3032G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38894862 | |||||||
chr4:38895205 | G | A | 1 | a0002c0003t0005g0360 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.436+3375G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895205 | |||||||
chr4:38895345 | C | T | 1 | a0002c0029t0043g0115 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.436+3515C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895345 | |||||||
chr4:38895386 | G | A | 3 | a0002c0003t0004g0342 a0002c0003t0005g0343 a0005c0012t0033g0341 |
3 | HG02280.hp2 HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.436+3556G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895386 | |||||||
chr4:38895410 | C | T | 25 | a0001c0001t0004g0257 a0002c0003t0001g0120 a0002c0003t0001g0123 others(22): Show |
25 | HG00621.hp1 HG01255.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.436+3580C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895410 | |||||||
chr4:38895442 | A | G | 8 | a0001c0001t0001g0173 a0001c0001t0001g0187 a0001c0001t0002g0186 others(5): Show |
8 | HG01346.hp2 HG01433.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.436+3612A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895442 | |||||||
chr4:38895505 | C | T | 1 | a0001c0002t0007g0168 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.436+3675C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895505 | |||||||
chr4:38895633 | G | A | 161 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(158): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.436+3803G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895633 | |||||||
chr4:38895669 | A | G | 42 | a0001c0001t0001g0041 a0001c0001t0002g0040 a0001c0001t0002g0271 others(39): Show |
43 | HG00621.hp1 HG01069.hp2 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.436+3839A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895669 | |||||||
chr4:38895686 | G | A | 1 | a0014c0051t0005g0344 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.436+3856G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895686 | |||||||
chr4:38895690 | C | T | 9 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0005g0042 others(6): Show |
9 | HG02280.hp1 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.436+3860C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895690 | |||||||
chr4:38895691 | G | A | 1 | a0001c0001t0021g0054 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.436+3861G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895691 | |||||||
chr4:38895774 | G | A | 42 | a0001c0001t0001g0041 a0001c0001t0002g0040 a0001c0001t0002g0271 others(39): Show |
43 | HG00621.hp1 HG01069.hp2 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.436+3944G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895774 | |||||||
chr4:38895779 | T | G | 1 | a0001c0004t0002g0349 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.436+3949T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895779 | |||||||
chr4:38895781 | C | A | 2 | a0001c0001t0007g0256 a0001c0004t0011g0255 |
2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.436+3951C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895781 | |||||||
chr4:38895850 | T | C | 1 | a0001c0005t0003g0285 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.436+4020T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38895850 | |||||||
chr4:38896133 | A | G | 17 | a0001c0001t0001g0041 a0001c0001t0002g0040 a0001c0001t0002g0271 others(14): Show |
18 | HG01069.hp2 HG01884.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.436+4303A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38896133 | |||||||
chr4:38896557 | A | G | 1 | a0001c0001t0002g0102 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.436+4727A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38896557 | |||||||
chr4:38896585 | G | A | 1 | a0002c0003t0005g0364 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.436+4755G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38896585 | |||||||
chr4:38896626 | GT | G | 163 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(160): Show |
167 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.436+4798delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38896626 | ||||||
chr4:38896848 | G | C | 169 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(166): Show |
173 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.436+5018G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38896848 | |||||||
chr4:38897113 | T | C | 5 | a0002c0003t0005g0353 a0002c0003t0032g0357 a0002c0006t0001g0354 others(2): Show |
5 | HG01255.hp2 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+5283T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38897113 | |||||||
chr4:38897348 | C | A | 1 | a0001c0001t0001g0159 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.436+5518C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38897348 | |||||||
chr4:38897389 | T | C | 1 | a0001c0039t0024g0261 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.436+5559T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38897389 | |||||||
chr4:38897487 | C | T | 25 | a0001c0001t0004g0257 a0002c0003t0001g0120 a0002c0003t0001g0123 others(22): Show |
25 | HG00621.hp1 HG01255.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.436+5657C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38897487 | |||||||
chr4:38897682 | A | G | 6 | a0001c0001t0002g0094 a0001c0001t0008g0109 a0001c0001t0008g0110 others(3): Show |
6 | HG02080.hp2 NA18940.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.436+5852A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38897682 | |||||||
chr4:38897718 | CA | C | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.436+5890delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38897718 | ||||||
chr4:38897777 | TA | T | 12 | a0002c0003t0016g0034 a0002c0006t0001g0033 a0002c0006t0011g0026 others(9): Show |
12 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+5959delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38897777 | ||||||
chr4:38897848 | C | T | 5 | a0001c0002t0001g0093 a0007c0021t0004g0347 a0007c0021t0013g0340 others(2): Show |
5 | HG02132.hp2 HG03704.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+6018C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38897848 | |||||||
chr4:38897853 | G | A | 45 | a0001c0001t0001g0041 a0001c0001t0002g0007 a0001c0001t0002g0040 others(42): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.436+6023G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38897853 | |||||||
chr4:38897938 | T | C | 45 | a0001c0001t0001g0041 a0001c0001t0002g0007 a0001c0001t0002g0040 others(42): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.436+6108T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38897938 | |||||||
chr4:38897945 | C | CA | 35 | a0001c0001t0001g0062 a0001c0001t0002g0063 a0001c0001t0002g0071 others(32): Show |
38 | HG00438.hp1 HG00609.hp1 HG02080.hp2 others(35): Show |
intron_variant | MODIFIER | c.436+6128dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38897945 | ||||||
chr4:38898027 | C | T | 12 | a0001c0001t0007g0256 a0001c0004t0011g0255 a0002c0003t0002g0043 others(9): Show |
12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+6197C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898027 | |||||||
chr4:38898086 | A | G | 12 | a0001c0001t0007g0256 a0001c0004t0011g0255 a0002c0003t0002g0043 others(9): Show |
12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+6256A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898086 | |||||||
chr4:38898099 | G | A | 12 | a0001c0001t0007g0256 a0001c0004t0011g0255 a0002c0003t0002g0043 others(9): Show |
12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+6269G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898099 | |||||||
chr4:38898126 | A | G | 2 | a0002c0032t0044g0352 a0002c0057t0005g0251 |
2 | HG02145.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.436+6296A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898126 | |||||||
chr4:38898232 | A | C | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.436+6402A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898232 | |||||||
chr4:38898243 | G | C | 1 | a0001c0001t0002g0292 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.436+6413G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898243 | |||||||
chr4:38898257 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.436+6427C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898257 | |||||||
chr4:38898258 | G | A | 7 | a0001c0002t0001g0093 a0007c0021t0004g0347 a0007c0021t0013g0340 others(4): Show |
7 | HG02132.hp2 HG02809.hp2 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.436+6428G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898258 | |||||||
chr4:38898313 | C | T | 2 | a0001c0002t0001g0147 a0001c0002t0001g0305 |
2 | NA18973.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.436+6483C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898313 | |||||||
chr4:38898379 | C | T | 1 | a0008c0014t0023g0306 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.436+6549C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898379 | |||||||
chr4:38898436 | C | G | 110 | a0001c0001t0001g0041 a0001c0001t0001g0050 a0001c0001t0001g0062 others(107): Show |
113 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.436+6606C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898436 | |||||||
chr4:38898469 | G | A | 2 | a0001c0001t0007g0256 a0001c0004t0011g0255 |
2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.436+6639G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898469 | |||||||
chr4:38898512 | A | C | 123 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(120): Show |
126 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.436+6682A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898512 | |||||||
chr4:38898764 | C | A | 20 | a0001c0001t0004g0257 a0002c0003t0001g0120 a0002c0003t0001g0123 others(17): Show |
20 | HG00621.hp1 HG01257.hp2 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.437-6758C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898764 | |||||||
chr4:38898776 | A | G | 345 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(342): Show |
351 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.437-6746A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898776 | |||||||
chr4:38898843 | A | G | 1 | a0001c0001t0009g0149 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.437-6679A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898843 | |||||||
chr4:38898910 | A | T | 12 | a0001c0001t0007g0256 a0001c0004t0011g0255 a0002c0003t0002g0043 others(9): Show |
12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.437-6612A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38898910 | |||||||
chr4:38898946 | A | ATG | 12 | a0001c0001t0007g0256 a0001c0004t0011g0255 a0002c0003t0002g0043 others(9): Show |
12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.437-6574_437-6573d others(4): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38898946 | ||||||
chr4:38898968 | TATATATG others(11): Show |
T | 69 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(66): Show |
72 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.437-6535_437-6518d others(20): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38898968 | ||||||
chr4:38898973 | A | ATGTTATA others(14): Show |
12 | a0001c0001t0007g0256 a0001c0004t0011g0255 a0002c0003t0002g0043 others(9): Show |
12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.437-6530_437-6529i others(23): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38898973 | ||||||
chr4:38899001 | T | C | 4 | a0001c0001t0017g0138 a0001c0002t0002g0139 a0001c0002t0002g0141 others(1): Show |
4 | HG00408.hp2 HG04184.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-6521T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899001 | |||||||
chr4:38899038 | T | TAGAC | 22 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0004g0268 others(19): Show |
23 | HG01069.hp2 HG01884.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.437-6483_437-6482i others(6): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38899038 | ||||||
chr4:38899040 | T | G | 22 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0004g0268 others(19): Show |
23 | HG01069.hp2 HG01884.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.437-6482T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899040 | |||||||
chr4:38899040 | T | TATAGACA others(1): Show |
23 | a0002c0003t0004g0022 a0002c0003t0006g0036 a0002c0003t0016g0034 others(20): Show |
23 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.437-6481_437-6480i others(10): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38899040 | ||||||
chr4:38899042 | G | GACAGAT | 137 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(134): Show |
140 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.437-6478_437-6473d others(8): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38899042 | ||||||
chr4:38899042 | G | T | 45 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0004g0268 others(42): Show |
46 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.437-6480G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899042 | |||||||
chr4:38899085 | T | C | 2 | a0001c0001t0002g0097 a0001c0001t0004g0077 |
2 | HG02074.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.437-6437T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899085 | |||||||
chr4:38899242 | G | A | 1 | a0001c0009t0003g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.437-6280G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899242 | |||||||
chr4:38899254 | C | T | 3 | a0001c0001t0007g0256 a0001c0004t0011g0255 a0002c0003t0002g0358 |
3 | HG03098.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.437-6268C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899254 | |||||||
chr4:38899255 | G | A | 1 | a0003c0007t0009g0023 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.437-6267G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899255 | |||||||
chr4:38899274 | C | T | 1 | a0001c0001t0002g0016 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.437-6248C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899274 | |||||||
chr4:38899381 | A | G | 12 | a0001c0001t0007g0256 a0001c0004t0011g0255 a0002c0003t0002g0043 others(9): Show |
12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.437-6141A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899381 | |||||||
chr4:38899454 | G | A | 1 | a0001c0001t0009g0149 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.437-6068G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899454 | |||||||
chr4:38899651 | C | T | 12 | a0001c0001t0007g0256 a0001c0004t0011g0255 a0002c0003t0002g0043 others(9): Show |
12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.437-5871C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899651 | |||||||
chr4:38899855 | T | G | 1 | a0001c0001t0002g0292 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.437-5667T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899855 | |||||||
chr4:38899908 | T | A | 174 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(171): Show |
178 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.437-5614T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899908 | |||||||
chr4:38899954 | A | G | 12 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0004g0268 others(9): Show |
13 | HG01069.hp2 HG01884.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.437-5568A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38899954 | |||||||
chr4:38900011 | C | T | 8 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(5): Show |
8 | HG02280.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-5511C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38900011 | |||||||
chr4:38900148 | A | C | 182 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(179): Show |
186 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.437-5374A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38900148 | |||||||
chr4:38900225 | T | A | 14 | a0001c0001t0007g0256 a0001c0002t0002g0308 a0001c0002t0028g0351 others(11): Show |
14 | HG00741.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.437-5297T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38900225 | |||||||
chr4:38900225 | T | TA | 8 | a0001c0001t0021g0169 a0001c0001t0035g0312 a0001c0002t0001g0147 others(5): Show |
8 | HG00597.hp1 HG01243.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.437-5285dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38900225 | ||||||
chr4:38900225 | TA | T | 171 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(168): Show |
175 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.437-5285delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38900225 | ||||||
chr4:38900234 | A | C | 12 | a0001c0001t0007g0256 a0001c0004t0011g0255 a0002c0003t0002g0043 others(9): Show |
12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.437-5288A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38900234 | |||||||
chr4:38900264 | G | A | 6 | a0001c0001t0012g0334 a0001c0001t0041g0328 a0001c0002t0001g0324 others(3): Show |
6 | HG00642.hp2 HG01074.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-5258G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38900264 | |||||||
chr4:38900334 | A | G | 12 | a0001c0001t0007g0256 a0001c0004t0011g0255 a0002c0003t0002g0043 others(9): Show |
12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.437-5188A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38900334 | |||||||
chr4:38900512 | C | T | 182 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(179): Show |
186 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.437-5010C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38900512 | |||||||
chr4:38900810 | T | C | 12 | a0001c0001t0007g0256 a0001c0004t0011g0255 a0002c0003t0002g0043 others(9): Show |
12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.437-4712T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38900810 | |||||||
chr4:38900851 | G | A | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-4671G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38900851 | |||||||
chr4:38900947 | C | CA | 8 | a0002c0022t0005g0249 a0002c0022t0010g0248 a0002c0053t0001g0245 others(5): Show |
8 | HG02559.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-4565dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38900947 | ||||||
chr4:38900947 | CA | C | 145 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(142): Show |
149 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.437-4565delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38900947 | ||||||
chr4:38900991 | A | G | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-4531A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38900991 | |||||||
chr4:38901092 | C | T | 3 | a0001c0001t0002g0007 a0001c0002t0014g0151 a0008c0014t0001g0012 |
3 | HG02486.hp2 HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.437-4430C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901092 | |||||||
chr4:38901204 | A | T | 1 | a0001c0008t0006g0066 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.437-4318A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901204 | |||||||
chr4:38901287 | GT | G | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-4225delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38901287 | ||||||
chr4:38901321 | TGTC | T | 170 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(167): Show |
174 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.437-4197_437-4195d others(5): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38901321 | ||||||
chr4:38901440 | G | A | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-4082G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901440 | |||||||
chr4:38901477 | A | G | 1 | a0001c0001t0002g0097 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.437-4045A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901477 | |||||||
chr4:38901530 | G | A | 2 | a0001c0001t0007g0256 a0001c0004t0011g0255 |
2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.437-3992G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901530 | |||||||
chr4:38901572 | A | G | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-3950A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901572 | |||||||
chr4:38901594 | T | G | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-3928T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901594 | |||||||
chr4:38901705 | G | A | 8 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(5): Show |
8 | HG02280.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-3817G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901705 | |||||||
chr4:38901715 | G | A | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-3807G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901715 | |||||||
chr4:38901716 | A | G | 1 | a0001c0009t0003g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.437-3806A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901716 | |||||||
chr4:38901748 | G | A | 2 | a0001c0001t0009g0148 a0001c0001t0009g0149 |
2 | HG01109.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.437-3774G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901748 | |||||||
chr4:38901791 | G | A | 8 | a0002c0022t0005g0249 a0002c0022t0010g0248 a0002c0053t0001g0245 others(5): Show |
8 | HG02559.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-3731G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901791 | |||||||
chr4:38901989 | C | T | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-3533C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38901989 | |||||||
chr4:38902027 | G | A | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-3495G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902027 | |||||||
chr4:38902126 | T | C | 1 | a0001c0001t0002g0213 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.437-3396T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902126 | |||||||
chr4:38902154 | C | T | 2 | a0001c0001t0007g0256 a0001c0004t0011g0255 |
2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.437-3368C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902154 | |||||||
chr4:38902220 | T | C | 1 | a0001c0001t0002g0079 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.437-3302T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902220 | |||||||
chr4:38902330 | G | A | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-3192G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902330 | |||||||
chr4:38902370 | C | T | 3 | a0001c0001t0007g0256 a0001c0004t0002g0099 a0001c0004t0011g0255 |
3 | HG03098.hp1 NA19030.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.437-3152C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902370 | |||||||
chr4:38902371 | G | A | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-3151G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902371 | |||||||
chr4:38902414 | C | T | 14 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0004g0268 others(11): Show |
15 | HG01069.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.437-3108C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902414 | |||||||
chr4:38902560 | A | G | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-2962A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902560 | |||||||
chr4:38902601 | G | C | 8 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(5): Show |
8 | HG02280.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-2921G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902601 | |||||||
chr4:38902669 | C | T | 1 | a0001c0001t0004g0262 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.437-2853C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902669 | |||||||
chr4:38902688 | G | A | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-2834G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902688 | |||||||
chr4:38902714 | A | T | 8 | a0002c0022t0005g0249 a0002c0022t0010g0248 a0002c0053t0001g0245 others(5): Show |
8 | HG02559.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-2808A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902714 | |||||||
chr4:38902760 | G | C | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-2762G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902760 | |||||||
chr4:38902899 | T | G | 2 | a0002c0003t0005g0339 a0002c0003t0010g0338 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.437-2623T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902899 | |||||||
chr4:38902960 | T | C | 183 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(180): Show |
187 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.437-2562T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38902960 | |||||||
chr4:38903043 | C | G | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-2479C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903043 | |||||||
chr4:38903112 | T | G | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-2410T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903112 | |||||||
chr4:38903158 | T | C | 1 | a0004c0020t0003g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.437-2364T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903158 | |||||||
chr4:38903185 | G | A | 3 | a0001c0001t0006g0080 a0001c0001t0006g0081 a0001c0004t0002g0082 |
3 | NA18953.hp1 NA18954.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.437-2337G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903185 | |||||||
chr4:38903205 | T | A | 1 | a0008c0014t0023g0306 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.437-2317T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903205 | |||||||
chr4:38903279 | G | A | 1 | a0002c0003t0002g0045 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.437-2243G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903279 | |||||||
chr4:38903511 | C | T | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-2011C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903511 | |||||||
chr4:38903573 | A | T | 172 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(169): Show |
176 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.437-1949A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903573 | |||||||
chr4:38903664 | C | G | 4 | a0001c0001t0001g0019 a0001c0001t0002g0016 a0001c0001t0002g0017 others(1): Show |
4 | HG02080.hp1 HG02135.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-1858C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903664 | |||||||
chr4:38903723 | C | T | 1 | a0001c0001t0002g0165 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.437-1799C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903723 | |||||||
chr4:38903842 | A | G | 174 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(171): Show |
178 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.437-1680A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903842 | |||||||
chr4:38903863 | T | C | 3 | a0001c0001t0002g0013 a0001c0001t0011g0010 a0001c0037t0003g0009 |
3 | HG02896.hp1 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.437-1659T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903863 | |||||||
chr4:38903873 | C | G | 1 | a0001c0023t0002g0108 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.437-1649C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903873 | |||||||
chr4:38903917 | A | G | 1 | a0001c0023t0002g0108 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.437-1605A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903917 | |||||||
chr4:38903931 | A | T | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-1591A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903931 | |||||||
chr4:38903966 | T | C | 1 | a0001c0001t0008g0078 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.437-1556T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38903966 | |||||||
chr4:38904105 | G | A | 11 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0004g0268 others(8): Show |
12 | HG01069.hp2 HG01884.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.437-1417G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904105 | |||||||
chr4:38904110 | T | G | 69 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(66): Show |
72 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.437-1412T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904110 | |||||||
chr4:38904144 | C | T | 8 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(5): Show |
8 | HG02280.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-1378C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904144 | |||||||
chr4:38904152 | C | T | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-1370C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904152 | |||||||
chr4:38904164 | G | A | 1 | a0001c0001t0008g0224 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.437-1358G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904164 | |||||||
chr4:38904173 | C | T | 3 | a0001c0001t0001g0211 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG00642.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.437-1349C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904173 | |||||||
chr4:38904298 | A | G | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-1224A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904298 | |||||||
chr4:38904323 | G | T | 2 | a0002c0056t0005g0252 a0005c0055t0012g0356 |
2 | HG01109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.437-1199G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904323 | |||||||
chr4:38904370 | T | C | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-1152T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904370 | |||||||
chr4:38904389 | G | A | 1 | a0002c0016t0001g0361 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.437-1133G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904389 | |||||||
chr4:38904416 | C | T | 1 | a0002c0003t0032g0357 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.437-1106C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904416 | |||||||
chr4:38904417 | C | A | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-1105C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904417 | |||||||
chr4:38904467 | C | T | 4 | a0001c0001t0006g0068 a0001c0001t0006g0294 a0001c0001t0006g0304 others(1): Show |
4 | HG00673.hp1 NA18981.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-1055C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904467 | |||||||
chr4:38904599 | G | A | 1 | a0001c0001t0038g0298 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.437-923G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904599 | |||||||
chr4:38904673 | A | G | 7 | a0001c0002t0001g0093 a0007c0021t0004g0347 a0007c0021t0013g0340 others(4): Show |
7 | HG02132.hp2 HG02809.hp2 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.437-849A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904673 | |||||||
chr4:38904935 | T | G | 4 | a0002c0003t0001g0359 a0002c0003t0005g0360 a0002c0003t0010g0362 others(1): Show |
4 | HG02809.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-587T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904935 | |||||||
chr4:38904960 | G | A | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-562G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38904960 | |||||||
chr4:38905096 | A | G | 129 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(126): Show |
132 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.437-426A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905096 | |||||||
chr4:38905125 | G | A | 2 | a0002c0003t0005g0339 a0002c0003t0010g0338 |
2 | HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.437-397G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905125 | |||||||
chr4:38905218 | G | A | 1 | a0001c0001t0042g0214 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.437-304G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905218 | |||||||
chr4:38905255 | C | T | 7 | a0001c0001t0002g0197 a0001c0001t0002g0239 a0001c0001t0006g0142 others(4): Show |
7 | HG01106.hp1 NA18945.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.437-267C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905255 | |||||||
chr4:38905256 | G | A | 1 | a0002c0003t0002g0358 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.437-266G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905256 | |||||||
chr4:38905330 | C | T | 64 | a0001c0001t0001g0050 a0001c0001t0001g0062 a0001c0001t0002g0049 others(61): Show |
67 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.437-192C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905330 | |||||||
chr4:38905400 | T | A | 19 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(16): Show |
19 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.437-122T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905400 | |||||||
chr4:38905400 | T | TA | 8 | a0001c0001t0035g0312 a0001c0002t0040g0307 a0002c0003t0005g0353 others(5): Show |
8 | HG01255.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-107dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38905400 | ||||||
chr4:38905400 | TA | T | 7 | a0001c0001t0001g0218 a0001c0001t0002g0092 a0001c0001t0017g0138 others(4): Show |
7 | HG00323.hp1 HG01070.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.437-107delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr4 | 38905400 | ||||||
chr4:38905401 | A | T | 44 | a0001c0001t0001g0041 a0001c0001t0002g0007 a0001c0001t0002g0040 others(41): Show |
44 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.437-121A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905401 | |||||||
chr4:38905402 | A | T | 3 | a0001c0001t0001g0041 a0001c0043t0001g0006 a0002c0027t0003g0029 |
3 | HG01167.hp2 HG03579.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.437-120A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905402 | |||||||
chr4:38905412 | A | G | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-110A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905412 | |||||||
chr4:38905457 | T | C | 10 | a0002c0003t0002g0043 a0002c0003t0002g0045 a0002c0003t0004g0342 others(7): Show |
10 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-65T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905457 | |||||||
chr4:38905476 | C | T | 1 | a0001c0001t0009g0148 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.437-46C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 4/14 | chr4 | 38905476 | |||||||
chr4:38905721 | G | A | 2 | a0002c0032t0044g0352 a0002c0057t0005g0251 |
2 | HG02145.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.551-34G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 5/14 | chr4 | 38905721 | |||||||
chr4:38905986 | G | T | 8 | a0001c0001t0012g0170 a0002c0003t0006g0036 a0002c0006t0001g0020 others(5): Show |
8 | HG00544.hp2 HG01243.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.657+125G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38905986 | |||||||
chr4:38906020 | C | T | 1 | a0002c0006t0001g0038 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.657+159C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906020 | |||||||
chr4:38906269 | G | A | 2 | a0002c0032t0044g0352 a0002c0057t0005g0251 |
2 | HG02145.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.657+408G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906269 | |||||||
chr4:38906336 | C | G | 1 | a0002c0003t0005g0364 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.657+475C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906336 | |||||||
chr4:38906338 | T | TC | 4 | a0001c0001t0001g0041 a0001c0004t0011g0255 a0001c0038t0005g0011 others(1): Show |
4 | HG03471.hp2 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.657+480dupC | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr4 | 38906338 | ||||||
chr4:38906367 | C | T | 76 | a0001c0001t0001g0161 a0001c0001t0001g0264 a0001c0001t0001g0284 others(73): Show |
79 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.657+506C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906367 | |||||||
chr4:38906390 | TC | T | 48 | a0001c0001t0002g0047 a0001c0001t0002g0097 a0001c0001t0002g0292 others(45): Show |
50 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.657+534delC | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr4 | 38906390 | ||||||
chr4:38906417 | G | A | 133 | a0001c0001t0002g0047 a0001c0001t0002g0055 a0001c0001t0002g0083 others(130): Show |
135 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.657+556G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906417 | |||||||
chr4:38906465 | G | T | 2 | a0001c0001t0002g0017 a0001c0002t0002g0018 |
2 | NA18966.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.657+604G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906465 | |||||||
chr4:38906484 | A | G | 1 | a0001c0002t0001g0103 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.657+623A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906484 | |||||||
chr4:38906544 | G | GT | 4 | a0001c0004t0002g0349 a0001c0004t0007g0331 a0005c0012t0001g0027 others(1): Show |
4 | HG02698.hp1 HG03927.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.657+690dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr4 | 38906544 | ||||||
chr4:38906604 | G | A | 4 | a0001c0043t0001g0006 a0002c0003t0002g0043 a0002c0003t0002g0045 others(1): Show |
4 | HG01167.hp2 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.657+743G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906604 | |||||||
chr4:38906787 | G | A | 2 | a0002c0003t0018g0119 a0002c0003t0018g0129 |
2 | NA18999.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.657+926G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906787 | |||||||
chr4:38906969 | T | A | 9 | a0001c0001t0002g0176 a0001c0001t0002g0180 a0001c0001t0002g0215 others(6): Show |
9 | HG01081.hp2 HG02145.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.657+1108T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906969 | |||||||
chr4:38906995 | G | C | 142 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(139): Show |
142 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.657+1134G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38906995 | |||||||
chr4:38907016 | T | G | 5 | a0001c0001t0009g0149 a0001c0004t0002g0349 a0001c0004t0007g0331 others(2): Show |
5 | HG01109.hp1 HG02698.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.657+1155T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38907016 | |||||||
chr4:38907022 | G | A | 195 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(192): Show |
198 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.657+1161G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38907022 | |||||||
chr4:38907577 | G | A | 1 | a0001c0002t0001g0223 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.658-1015G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38907577 | |||||||
chr4:38907655 | A | G | 11 | a0002c0006t0011g0026 a0003c0007t0009g0023 a0003c0007t0009g0025 others(8): Show |
11 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.658-937A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38907655 | |||||||
chr4:38907706 | A | G | 7 | a0001c0001t0005g0195 a0001c0002t0014g0151 a0008c0014t0001g0012 others(4): Show |
7 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.658-886A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38907706 | |||||||
chr4:38907833 | A | T | 7 | a0001c0001t0005g0195 a0001c0002t0014g0151 a0008c0014t0001g0012 others(4): Show |
7 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.658-759A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38907833 | |||||||
chr4:38907853 | A | G | 4 | a0001c0004t0002g0349 a0001c0004t0007g0331 a0005c0012t0001g0027 others(1): Show |
4 | HG02698.hp1 HG03927.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.658-739A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38907853 | |||||||
chr4:38908297 | C | G | 9 | a0001c0001t0001g0198 a0001c0001t0001g0296 a0001c0001t0002g0191 others(6): Show |
9 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.658-295C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38908297 | |||||||
chr4:38908413 | A | G | 1 | a0013c0052t0005g0247 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.658-179A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 6/14 | chr4 | 38908413 | |||||||
chr4:38908741 | G | T | 48 | a0001c0001t0001g0161 a0001c0001t0002g0040 a0001c0001t0002g0271 others(45): Show |
52 | HG00735.hp2 HG01069.hp2 HG01516.hp1 others(49): Show |
intron_variant | MODIFIER | c.792+15G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38908741 | |||||||
chr4:38908872 | C | T | 17 | a0001c0001t0001g0198 a0001c0001t0001g0296 a0001c0001t0002g0176 others(14): Show |
17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.792+146C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38908872 | |||||||
chr4:38908925 | C | T | 48 | a0001c0001t0001g0161 a0001c0001t0002g0040 a0001c0001t0002g0271 others(45): Show |
52 | HG00735.hp2 HG01069.hp2 HG01516.hp1 others(49): Show |
intron_variant | MODIFIER | c.792+199C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38908925 | |||||||
chr4:38908938 | A | G | 1 | a0001c0001t0005g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.792+212A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38908938 | |||||||
chr4:38908948 | G | A | 1 | a0013c0052t0005g0247 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.792+222G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38908948 | |||||||
chr4:38909109 | A | G | 123 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(120): Show |
123 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.792+383A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38909109 | |||||||
chr4:38909170 | C | T | 165 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(162): Show |
165 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.792+444C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38909170 | |||||||
chr4:38909332 | T | C | 6 | a0001c0001t0005g0195 a0001c0002t0014g0151 a0008c0014t0001g0012 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+606T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38909332 | |||||||
chr4:38909452 | A | G | 1 | a0001c0001t0002g0197 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.792+726A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38909452 | |||||||
chr4:38909547 | A | T | 219 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(216): Show |
223 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.792+821A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38909547 | |||||||
chr4:38909550 | CTT | C | 61 | a0001c0001t0001g0041 a0001c0001t0001g0198 a0001c0001t0001g0296 others(58): Show |
61 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.792+825_792+826del others(2): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38909550 | |||||||
chr4:38909584 | A | G | 60 | a0001c0001t0001g0161 a0001c0001t0002g0040 a0001c0001t0002g0049 others(57): Show |
64 | HG00099.hp2 HG00735.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.792+858A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38909584 | |||||||
chr4:38909694 | A | G | 58 | a0001c0001t0001g0161 a0001c0001t0002g0040 a0001c0001t0002g0049 others(55): Show |
62 | HG00099.hp2 HG00735.hp2 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.792+968A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38909694 | |||||||
chr4:38909724 | C | T | 61 | a0001c0001t0001g0041 a0001c0001t0001g0198 a0001c0001t0001g0296 others(58): Show |
61 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.792+998C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38909724 | |||||||
chr4:38909974 | G | A | 50 | a0001c0001t0001g0161 a0001c0001t0002g0040 a0001c0001t0002g0049 others(47): Show |
54 | HG00099.hp2 HG01255.hp1 HG01255.hp2 others(51): Show |
intron_variant | MODIFIER | c.792+1248G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38909974 | |||||||
chr4:38910095 | C | T | 1 | a0001c0001t0002g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.792+1369C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38910095 | |||||||
chr4:38910116 | G | A | 2 | a0005c0012t0001g0027 a0005c0030t0003g0113 |
2 | HG02698.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.792+1390G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38910116 | |||||||
chr4:38910142 | G | A | 50 | a0001c0001t0001g0161 a0001c0001t0002g0040 a0001c0001t0002g0049 others(47): Show |
54 | HG00099.hp2 HG01255.hp1 HG01255.hp2 others(51): Show |
intron_variant | MODIFIER | c.792+1416G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38910142 | |||||||
chr4:38910168 | G | A | 13 | a0001c0001t0001g0161 a0001c0004t0001g0058 a0001c0004t0002g0001 others(10): Show |
16 | HG04228.hp1 NA18942.hp2 NA18950.hp1 others(13): Show |
intron_variant | MODIFIER | c.792+1442G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38910168 | |||||||
chr4:38910220 | T | C | 219 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(216): Show |
223 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.792+1494T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38910220 | |||||||
chr4:38910261 | G | A | 1 | a0001c0008t0006g0084 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.792+1535G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38910261 | |||||||
chr4:38910587 | G | C | 219 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(216): Show |
223 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.792+1861G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38910587 | |||||||
chr4:38910602 | T | G | 1 | a0005c0030t0003g0113 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.792+1876T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38910602 | |||||||
chr4:38910749 | C | T | 1 | a0001c0001t0006g0087 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.792+2023C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38910749 | |||||||
chr4:38910863 | A | G | 94 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(91): Show |
94 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.792+2137A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38910863 | |||||||
chr4:38911000 | G | A | 219 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(216): Show |
223 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.792+2274G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911000 | |||||||
chr4:38911023 | G | A | 1 | a0001c0001t0001g0275 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.792+2297G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911023 | |||||||
chr4:38911195 | C | T | 213 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(210): Show |
217 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.792+2469C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911195 | |||||||
chr4:38911259 | C | T | 3 | a0001c0001t0042g0214 a0002c0003t0002g0043 a0002c0003t0010g0338 |
3 | HG02451.hp2 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.792+2533C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911259 | |||||||
chr4:38911263 | A | C | 219 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(216): Show |
223 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.792+2537A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911263 | |||||||
chr4:38911337 | G | A | 3 | a0001c0001t0042g0214 a0002c0003t0002g0043 a0002c0003t0010g0338 |
3 | HG02451.hp2 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.792+2611G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911337 | |||||||
chr4:38911377 | A | G | 219 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(216): Show |
223 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.792+2651A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911377 | |||||||
chr4:38911503 | T | G | 1 | a0013c0052t0005g0247 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.792+2777T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911503 | |||||||
chr4:38911750 | G | A | 12 | a0001c0001t0002g0007 a0001c0001t0011g0010 a0001c0001t0035g0312 others(9): Show |
12 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.792+3024G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911750 | |||||||
chr4:38911786 | T | TTATCCTA | 12 | a0001c0001t0017g0138 a0001c0004t0002g0099 a0001c0004t0002g0349 others(9): Show |
12 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.792+3061_792+3067d others(9): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 38911786 | ||||||
chr4:38911804 | G | A | 1 | a0001c0001t0002g0072 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.792+3078G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911804 | |||||||
chr4:38911806 | A | G | 1 | a0007c0021t0004g0347 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.792+3080A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911806 | |||||||
chr4:38911833 | TTTTTTTT others(4): Show |
T | 1 | a0001c0046t0002g0095 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.793-3078_793-3068d others(13): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 38911833 | ||||||
chr4:38911834 | TTTTTTTT others(3): Show |
T | 1 | a0001c0001t0002g0165 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.793-3070_793-3061d others(12): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 38911834 | ||||||
chr4:38911844 | C | CT | 45 | a0001c0001t0001g0173 a0001c0001t0001g0264 a0001c0001t0002g0040 others(42): Show |
45 | HG00558.hp2 HG00609.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.793-3068dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 38911844 | ||||||
chr4:38911844 | C | T | 1 | a0002c0003t0004g0130 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.793-3077C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911844 | |||||||
chr4:38911850 | TTTTCTTT others(4): Show |
T | 111 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(108): Show |
111 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.793-3067_793-3057d others(13): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 38911850 | ||||||
chr4:38911851 | T | C | 10 | a0001c0001t0002g0049 a0001c0001t0002g0089 a0001c0001t0002g0309 others(7): Show |
10 | HG00099.hp2 HG01255.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.793-3070T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911851 | |||||||
chr4:38911861 | C | CT | 18 | a0001c0001t0002g0013 a0001c0001t0007g0227 a0001c0001t0013g0238 others(15): Show |
18 | HG00140.hp1 HG01361.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.793-3043dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 38911861 | ||||||
chr4:38911861 | CT | C | 53 | a0001c0001t0001g0041 a0001c0001t0002g0007 a0001c0001t0002g0049 others(50): Show |
53 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.793-3043delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 38911861 | ||||||
chr4:38911861 | CTTTTTTT others(4): Show |
C | 1 | a0001c0002t0001g0166 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.793-3053_793-3043d others(13): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 38911861 | ||||||
chr4:38911862 | T | C | 111 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(108): Show |
111 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.793-3059T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38911862 | |||||||
chr4:38912007 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.793-2914T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912007 | |||||||
chr4:38912165 | G | A | 1 | a0016c0047t0009g0150 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.793-2756G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912165 | |||||||
chr4:38912280 | T | C | 17 | a0001c0001t0001g0198 a0001c0001t0001g0296 a0001c0001t0002g0176 others(14): Show |
17 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.793-2641T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912280 | |||||||
chr4:38912330 | G | C | 221 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(218): Show |
225 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.793-2591G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912330 | |||||||
chr4:38912369 | C | T | 1 | a0002c0057t0005g0251 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.793-2552C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912369 | |||||||
chr4:38912450 | T | G | 1 | a0001c0001t0002g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.793-2471T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912450 | |||||||
chr4:38912485 | A | T | 1 | a0001c0001t0002g0089 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.793-2436A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912485 | |||||||
chr4:38912500 | T | C | 8 | a0001c0001t0004g0281 a0001c0001t0007g0256 a0001c0002t0040g0307 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.793-2421T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912500 | |||||||
chr4:38912612 | G | C | 1 | a0001c0001t0007g0227 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.793-2309G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912612 | |||||||
chr4:38912674 | G | A | 6 | a0001c0001t0001g0211 a0001c0001t0001g0217 a0001c0001t0001g0218 others(3): Show |
6 | HG00140.hp1 HG00642.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.793-2247G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912674 | |||||||
chr4:38912677 | T | C | 6 | a0001c0001t0005g0195 a0001c0002t0014g0151 a0008c0014t0001g0012 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.793-2244T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912677 | |||||||
chr4:38912724 | C | A | 4 | a0001c0001t0002g0007 a0001c0001t0011g0010 a0001c0009t0003g0335 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-2197C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912724 | |||||||
chr4:38912767 | C | T | 2 | a0002c0053t0001g0245 a0002c0054t0036g0243 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.793-2154C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912767 | |||||||
chr4:38912819 | G | C | 13 | a0001c0001t0017g0138 a0001c0004t0002g0099 a0001c0004t0002g0349 others(10): Show |
13 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.793-2102G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38912819 | |||||||
chr4:38913000 | C | T | 1 | a0008c0014t0023g0306 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.793-1921C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38913000 | |||||||
chr4:38913160 | TA | T | 19 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0004g0268 others(16): Show |
19 | HG00323.hp2 HG00735.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.793-1758delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr4 | 38913160 | ||||||
chr4:38913234 | G | C | 1 | a0002c0003t0002g0358 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.793-1687G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38913234 | |||||||
chr4:38913680 | G | A | 8 | a0001c0001t0002g0049 a0001c0001t0002g0089 a0001c0001t0002g0309 others(5): Show |
8 | HG00099.hp2 HG01255.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.793-1241G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38913680 | |||||||
chr4:38913699 | T | C | 51 | a0001c0001t0002g0071 a0001c0001t0002g0292 a0001c0001t0005g0301 others(48): Show |
55 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.793-1222T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38913699 | |||||||
chr4:38913866 | G | A | 3 | a0001c0001t0001g0211 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG00642.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.793-1055G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38913866 | |||||||
chr4:38914055 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.793-866G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38914055 | |||||||
chr4:38914065 | A | G | 1 | a0008c0014t0023g0306 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.793-856A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38914065 | |||||||
chr4:38914244 | A | G | 2 | a0002c0053t0001g0245 a0002c0054t0036g0243 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.793-677A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38914244 | |||||||
chr4:38914424 | G | A | 1 | a0002c0054t0036g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.793-497G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38914424 | |||||||
chr4:38914514 | C | A | 47 | a0001c0001t0002g0071 a0001c0001t0002g0292 a0001c0001t0005g0301 others(44): Show |
51 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.793-407C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38914514 | |||||||
chr4:38914844 | A | C | 342 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(339): Show |
348 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.793-77A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 7/14 | chr4 | 38914844 | |||||||
chr4:38915293 | T | G | 219 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(216): Show |
223 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.945+220T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38915293 | |||||||
chr4:38915323 | C | T | 3 | a0001c0001t0010g0259 a0001c0005t0003g0274 a0002c0028t0030g0363 |
3 | HG02486.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.945+250C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38915323 | |||||||
chr4:38915445 | A | G | 3 | a0001c0001t0005g0231 a0002c0003t0002g0045 a0002c0003t0005g0364 |
3 | HG01884.hp1 HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.945+372A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38915445 | |||||||
chr4:38915606 | C | T | 1 | a0013c0052t0005g0247 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.945+533C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38915606 | |||||||
chr4:38915712 | T | C | 3 | a0001c0001t0010g0259 a0001c0005t0003g0274 a0002c0028t0030g0363 |
3 | HG02486.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.945+639T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38915712 | |||||||
chr4:38915717 | A | AT | 49 | a0001c0001t0001g0041 a0001c0001t0001g0198 a0001c0001t0001g0296 others(46): Show |
49 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.945+651dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915717 | ||||||
chr4:38915744 | G | GGT | 51 | a0001c0001t0002g0176 a0001c0001t0002g0314 a0001c0001t0004g0086 others(48): Show |
51 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.945+720_945+721dup others(2): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915744 | ||||||
chr4:38915744 | G | GGTGT | 8 | a0001c0001t0005g0297 a0001c0002t0001g0088 a0001c0002t0001g0236 others(5): Show |
8 | HG00597.hp2 HG01175.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.945+718_945+721dup others(4): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915744 | ||||||
chr4:38915744 | GGT | G | 51 | a0001c0001t0001g0062 a0001c0001t0001g0284 a0001c0001t0001g0315 others(48): Show |
51 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.945+720_945+721del others(2): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915744 | ||||||
chr4:38915744 | GGTGT | G | 39 | a0001c0001t0001g0198 a0001c0001t0001g0211 a0001c0001t0001g0217 others(36): Show |
39 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.945+718_945+721del others(4): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915744 | ||||||
chr4:38915744 | GGTGTGT | G | 29 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0051 others(26): Show |
29 | HG00408.hp1 HG01891.hp1 HG01981.hp1 others(26): Show |
intron_variant | MODIFIER | c.945+716_945+721del others(6): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915744 | ||||||
chr4:38915744 | GGTGTGTG others(1): Show |
G | 52 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0161 others(49): Show |
52 | HG00609.hp1 HG00673.hp2 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.945+714_945+721del others(8): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915744 | ||||||
chr4:38915744 | GGTGTGTG others(3): Show |
G | 4 | a0001c0001t0002g0055 a0001c0001t0002g0229 a0002c0006t0001g0354 others(1): Show |
4 | HG00558.hp1 HG01255.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.945+712_945+721del others(10): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915744 | ||||||
chr4:38915744 | GGTGTGTG others(5): Show |
G | 21 | a0001c0001t0001g0159 a0001c0001t0001g0173 a0001c0001t0002g0083 others(18): Show |
21 | HG00408.hp2 HG00544.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.945+710_945+721del others(12): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915744 | ||||||
chr4:38915744 | GGTGTGTG others(11): Show |
G | 2 | a0001c0001t0042g0214 a0002c0003t0002g0043 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.945+704_945+721del others(18): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915744 | ||||||
chr4:38915744 | GGTGTGTG others(15): Show |
G | 1 | a0001c0008t0006g0111 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.945+700_945+721del others(22): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915744 | ||||||
chr4:38915771 | G | GTC | 43 | a0001c0004t0001g0058 a0001c0004t0001g0260 a0001c0004t0002g0001 others(40): Show |
47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+699_945+700ins others(2): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915771 | ||||||
chr4:38915783 | GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0002g0073 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.945+712_945+723del others(12): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915783 | ||||||
chr4:38915787 | GTGTGTGT | G | 4 | a0001c0001t0002g0057 a0001c0001t0002g0165 a0001c0001t0002g0228 others(1): Show |
4 | HG01192.hp1 HG02523.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.945+716_945+722del others(7): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915787 | ||||||
chr4:38915793 | GT | G | 4 | a0001c0001t0001g0187 a0001c0001t0002g0316 a0001c0002t0001g0279 others(1): Show |
4 | HG00642.hp2 HG01346.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.945+723delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915793 | ||||||
chr4:38915805 | AGCACTTA others(93): Show |
A | 3 | a0001c0001t0001g0211 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG00642.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.945+734_945+833del others(100): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38915805 | ||||||
chr4:38915862 | T | C | 1 | a0001c0001t0042g0214 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.945+789T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38915862 | |||||||
chr4:38916073 | C | T | 37 | a0001c0001t0002g0049 a0001c0001t0002g0089 a0001c0001t0002g0271 others(34): Show |
37 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.945+1000C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916073 | |||||||
chr4:38916082 | G | C | 43 | a0001c0004t0001g0058 a0001c0004t0001g0260 a0001c0004t0002g0001 others(40): Show |
47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+1009G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916082 | |||||||
chr4:38916209 | A | G | 87 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(84): Show |
87 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.945+1136A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916209 | |||||||
chr4:38916253 | C | T | 43 | a0001c0004t0001g0058 a0001c0004t0001g0260 a0001c0004t0002g0001 others(40): Show |
47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+1180C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916253 | |||||||
chr4:38916362 | A | G | 43 | a0001c0004t0001g0058 a0001c0004t0001g0260 a0001c0004t0002g0001 others(40): Show |
47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+1289A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916362 | |||||||
chr4:38916472 | T | A | 19 | a0001c0001t0001g0198 a0001c0001t0001g0296 a0001c0001t0002g0176 others(16): Show |
19 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.945+1399T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916472 | |||||||
chr4:38916551 | C | T | 128 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(125): Show |
132 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.945+1478C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916551 | |||||||
chr4:38916563 | G | A | 1 | a0001c0005t0003g0323 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.945+1490G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916563 | |||||||
chr4:38916608 | A | G | 1 | a0006c0035t0003g0210 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.945+1535A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916608 | |||||||
chr4:38916658 | G | A | 43 | a0001c0004t0001g0058 a0001c0004t0001g0260 a0001c0004t0002g0001 others(40): Show |
47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+1585G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916658 | |||||||
chr4:38916829 | G | T | 43 | a0001c0004t0001g0058 a0001c0004t0001g0260 a0001c0004t0002g0001 others(40): Show |
47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+1756G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916829 | |||||||
chr4:38916897 | A | G | 49 | a0001c0001t0001g0041 a0001c0001t0001g0198 a0001c0001t0001g0296 others(46): Show |
49 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.945+1824A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916897 | |||||||
chr4:38916968 | G | A | 11 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0004g0268 others(8): Show |
11 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.945+1895G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916968 | |||||||
chr4:38916991 | C | A | 43 | a0001c0004t0001g0058 a0001c0004t0001g0260 a0001c0004t0002g0001 others(40): Show |
47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+1918C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38916991 | |||||||
chr4:38917069 | C | T | 85 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(82): Show |
85 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.945+1996C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917069 | |||||||
chr4:38917120 | A | G | 3 | a0001c0001t0002g0047 a0004c0011t0001g0302 a0006c0010t0003g0172 |
3 | HG01433.hp1 HG01943.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.945+2047A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917120 | |||||||
chr4:38917149 | C | CAAAT | 38 | a0001c0001t0001g0041 a0001c0001t0002g0089 a0001c0001t0002g0271 others(35): Show |
38 | HG01069.hp2 HG01255.hp1 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.945+2112_945+2115d others(6): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917149 | ||||||
chr4:38917149 | C | CAAATAAA others(1): Show |
37 | a0001c0001t0001g0198 a0001c0001t0001g0211 a0001c0001t0001g0217 others(34): Show |
37 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.945+2108_945+2115d others(10): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917149 | ||||||
chr4:38917149 | C | CAAATAAA others(5): Show |
82 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(79): Show |
82 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.945+2104_945+2115d others(14): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917149 | ||||||
chr4:38917149 | C | CAAATAAA others(9): Show |
13 | a0001c0001t0001g0159 a0001c0001t0001g0173 a0001c0001t0002g0016 others(10): Show |
13 | HG01099.hp2 HG01123.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.945+2100_945+2115d others(18): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917149 | ||||||
chr4:38917149 | C | CAAATAAA others(13): Show |
1 | a0001c0001t0035g0312 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.945+2096_945+2115d others(22): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917149 | ||||||
chr4:38917149 | CAAAT | C | 3 | a0001c0001t0005g0014 a0002c0003t0005g0044 a0004c0011t0014g0269 |
3 | HG01884.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.945+2112_945+2115d others(6): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917149 | ||||||
chr4:38917149 | CAAATAAA others(5): Show |
C | 1 | a0001c0001t0002g0263 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.945+2104_945+2115d others(14): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917149 | ||||||
chr4:38917149 | CAAATAAA others(9): Show |
C | 43 | a0001c0004t0001g0058 a0001c0004t0001g0260 a0001c0004t0002g0001 others(40): Show |
47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+2100_945+2115d others(18): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917149 | ||||||
chr4:38917185 | T | TAAATAAA others(5): Show |
1 | a0005c0012t0034g0021 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.945+2115_945+2116i others(14): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917185 | ||||||
chr4:38917185 | T | TAAATAAA others(9): Show |
1 | a0001c0001t0011g0010 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.945+2115_945+2116i others(18): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917185 | ||||||
chr4:38917185 | T | TAAATAAA others(9): Show |
1 | a0001c0001t0002g0007 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.945+2115_945+2116i others(18): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917185 | ||||||
chr4:38917185 | T | TAAATAAA others(13): Show |
1 | a0001c0009t0003g0335 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.945+2115_945+2116i others(22): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917185 | ||||||
chr4:38917218 | A | T | 11 | a0002c0006t0011g0026 a0003c0007t0009g0023 a0003c0007t0009g0025 others(8): Show |
11 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.945+2145A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917218 | |||||||
chr4:38917235 | G | A | 6 | a0001c0001t0005g0195 a0001c0002t0014g0151 a0008c0014t0001g0012 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.945+2162G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917235 | |||||||
chr4:38917337 | C | CA | 43 | a0001c0004t0001g0058 a0001c0004t0001g0260 a0001c0004t0002g0001 others(40): Show |
47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+2275dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917337 | ||||||
chr4:38917499 | T | C | 220 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(217): Show |
224 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.945+2426T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917499 | |||||||
chr4:38917545 | A | C | 7 | a0001c0001t0001g0187 a0001c0001t0001g0284 a0001c0002t0001g0144 others(4): Show |
7 | HG00642.hp2 HG01074.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.945+2472A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917545 | |||||||
chr4:38917600 | T | TTTG | 43 | a0001c0004t0001g0058 a0001c0004t0001g0260 a0001c0004t0002g0001 others(40): Show |
47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+2533_945+2535d others(5): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38917600 | ||||||
chr4:38917748 | C | T | 10 | a0001c0001t0001g0041 a0001c0001t0004g0281 a0001c0001t0007g0256 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.945+2675C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917748 | |||||||
chr4:38917795 | A | C | 43 | a0001c0004t0001g0058 a0001c0004t0001g0260 a0001c0004t0002g0001 others(40): Show |
47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.945+2722A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917795 | |||||||
chr4:38917943 | G | A | 90 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(87): Show |
90 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.945+2870G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917943 | |||||||
chr4:38917944 | C | T | 39 | a0001c0001t0002g0049 a0001c0001t0002g0089 a0001c0001t0002g0271 others(36): Show |
39 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.945+2871C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917944 | |||||||
chr4:38917949 | A | G | 220 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(217): Show |
224 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.945+2876A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38917949 | |||||||
chr4:38918014 | C | T | 90 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(87): Show |
90 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.945+2941C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38918014 | |||||||
chr4:38918093 | G | A | 1 | a0001c0001t0010g0299 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.945+3020G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38918093 | |||||||
chr4:38918220 | G | A | 2 | a0001c0001t0002g0278 a0001c0001t0007g0230 |
2 | HG02074.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.945+3147G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38918220 | |||||||
chr4:38918376 | G | A | 41 | a0001c0004t0001g0058 a0001c0004t0001g0260 a0001c0004t0002g0001 others(38): Show |
45 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.945+3303G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38918376 | |||||||
chr4:38918707 | C | G | 4 | a0001c0001t0002g0013 a0001c0001t0007g0227 a0002c0003t0005g0353 others(1): Show |
4 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.945+3634C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38918707 | |||||||
chr4:38918788 | G | A | 41 | a0001c0004t0001g0058 a0001c0004t0001g0260 a0001c0004t0002g0001 others(38): Show |
45 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.945+3715G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38918788 | |||||||
chr4:38918820 | G | A | 1 | a0002c0003t0010g0338 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.945+3747G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38918820 | |||||||
chr4:38918862 | G | A | 2 | a0001c0001t0042g0214 a0002c0003t0002g0043 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.945+3789G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38918862 | |||||||
chr4:38918917 | C | T | 7 | a0001c0001t0002g0049 a0001c0001t0002g0089 a0001c0001t0002g0309 others(4): Show |
7 | HG00099.hp2 HG01255.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.945+3844C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38918917 | |||||||
chr4:38918970 | A | T | 48 | a0001c0001t0002g0049 a0001c0001t0002g0089 a0001c0001t0002g0309 others(45): Show |
52 | HG00099.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.946-3800A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38918970 | |||||||
chr4:38919048 | G | C | 1 | a0002c0003t0004g0022 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.946-3722G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38919048 | |||||||
chr4:38919084 | C | T | 14 | a0001c0001t0002g0083 a0001c0001t0002g0145 a0001c0001t0002g0177 others(11): Show |
14 | HG00408.hp2 HG00544.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.946-3686C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38919084 | |||||||
chr4:38919421 | C | T | 58 | a0001c0001t0001g0198 a0001c0001t0001g0296 a0001c0001t0002g0094 others(55): Show |
61 | HG00597.hp1 HG00621.hp1 HG02027.hp2 others(58): Show |
intron_variant | MODIFIER | c.946-3349C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38919421 | |||||||
chr4:38919670 | T | A | 1 | a0002c0003t0005g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.946-3100T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38919670 | |||||||
chr4:38919909 | A | G | 2 | a0001c0001t0007g0273 a0017c0031t0019g0028 |
2 | NA18953.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.946-2861A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38919909 | |||||||
chr4:38919933 | G | T | 5 | a0001c0002t0001g0135 a0001c0002t0001g0156 a0001c0002t0001g0157 others(2): Show |
5 | NA18951.hp1 NA18955.hp2 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.946-2837G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38919933 | |||||||
chr4:38919938 | C | T | 1 | a0001c0001t0002g0309 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.946-2832C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38919938 | |||||||
chr4:38920436 | A | T | 3 | a0002c0003t0001g0359 a0002c0053t0001g0245 a0002c0054t0036g0243 |
3 | HG02717.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.946-2334A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38920436 | |||||||
chr4:38920512 | A | G | 9 | a0001c0001t0014g0295 a0001c0001t0035g0312 a0001c0004t0011g0190 others(6): Show |
9 | HG01109.hp2 HG02109.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.946-2258A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38920512 | |||||||
chr4:38920701 | T | C | 3 | a0002c0003t0001g0359 a0002c0053t0001g0245 a0002c0054t0036g0243 |
3 | HG02717.hp1 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.946-2069T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38920701 | |||||||
chr4:38920711 | T | G | 78 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(75): Show |
78 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.946-2059T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38920711 | |||||||
chr4:38920737 | T | C | 92 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0062 others(89): Show |
93 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.946-2033T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38920737 | |||||||
chr4:38920946 | T | C | 211 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(208): Show |
215 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.946-1824T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38920946 | |||||||
chr4:38920973 | A | T | 210 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(207): Show |
214 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.946-1797A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38920973 | |||||||
chr4:38921012 | C | A | 12 | a0001c0001t0005g0014 a0001c0001t0014g0295 a0001c0001t0035g0312 others(9): Show |
12 | HG01109.hp2 HG02109.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.946-1758C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921012 | |||||||
chr4:38921036 | G | C | 12 | a0001c0001t0005g0014 a0001c0001t0014g0295 a0001c0001t0035g0312 others(9): Show |
12 | HG01109.hp2 HG02109.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.946-1734G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921036 | |||||||
chr4:38921116 | T | C | 23 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0213 others(20): Show |
23 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.946-1654T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921116 | |||||||
chr4:38921171 | T | C | 16 | a0001c0001t0001g0041 a0001c0001t0005g0231 a0001c0001t0007g0256 others(13): Show |
16 | HG01255.hp2 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.946-1599T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921171 | |||||||
chr4:38921338 | GCCTCAAA others(132): Show |
G | 2 | a0001c0001t0014g0295 a0001c0009t0003g0335 |
2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.946-1410_946-1272d others(2): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38921338 | ||||||
chr4:38921358 | A | G | 1 | a0001c0001t0005g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.946-1412A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921358 | |||||||
chr4:38921597 | T | G | 1 | a0002c0003t0010g0362 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.946-1173T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921597 | |||||||
chr4:38921621 | A | G | 1 | a0001c0002t0020g0237 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.946-1149A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921621 | |||||||
chr4:38921740 | A | C | 2 | a0002c0028t0030g0363 a0015c0050t0003g0345 |
2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.946-1030A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921740 | |||||||
chr4:38921782 | G | A | 1 | a0002c0003t0002g0358 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.946-988G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921782 | |||||||
chr4:38921822 | T | C | 1 | a0001c0001t0042g0214 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.946-948T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921822 | |||||||
chr4:38921891 | G | GA | 203 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0062 others(200): Show |
208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.946-878dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr4 | 38921891 | ||||||
chr4:38921973 | C | T | 6 | a0002c0003t0002g0043 a0002c0003t0005g0343 a0002c0006t0001g0354 others(3): Show |
6 | HG01109.hp2 HG01255.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.946-797C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38921973 | |||||||
chr4:38922000 | G | A | 1 | a0005c0030t0003g0113 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.946-770G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922000 | |||||||
chr4:38922005 | G | A | 2 | a0001c0001t0005g0014 a0002c0003t0005g0044 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.946-765G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922005 | |||||||
chr4:38922210 | G | A | 15 | a0001c0001t0001g0050 a0001c0001t0004g0319 a0001c0001t0005g0297 others(12): Show |
15 | HG01891.hp1 HG01943.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.946-560G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922210 | |||||||
chr4:38922306 | C | T | 10 | a0002c0006t0011g0026 a0003c0007t0009g0023 a0003c0007t0009g0025 others(7): Show |
10 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.946-464C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922306 | |||||||
chr4:38922400 | A | G | 49 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(46): Show |
49 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.946-370A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922400 | |||||||
chr4:38922484 | C | T | 1 | a0001c0001t0042g0214 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.946-286C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922484 | |||||||
chr4:38922490 | T | C | 1 | a0002c0003t0010g0362 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.946-280T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922490 | |||||||
chr4:38922501 | C | T | 6 | a0001c0002t0002g0139 a0001c0002t0002g0141 a0001c0013t0002g0076 others(3): Show |
6 | HG00408.hp2 HG00544.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.946-269C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922501 | |||||||
chr4:38922502 | T | C | 1 | a0001c0001t0014g0295 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.946-268T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922502 | |||||||
chr4:38922609 | A | C | 38 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(35): Show |
38 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.946-161A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922609 | |||||||
chr4:38922614 | G | T | 1 | a0001c0001t0006g0143 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.946-156G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922614 | |||||||
chr4:38922619 | A | G | 3 | a0001c0039t0024g0261 a0001c0044t0024g0226 a0002c0026t0005g0039 |
3 | HG01891.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.946-151A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922619 | |||||||
chr4:38922641 | A | G | 2 | a0001c0001t0005g0014 a0002c0003t0005g0044 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.946-129A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922641 | |||||||
chr4:38922654 | C | T | 30 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(27): Show |
30 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.946-116C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922654 | |||||||
chr4:38922709 | G | A | 38 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(35): Show |
38 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.946-61G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922709 | |||||||
chr4:38922737 | A | G | 35 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(32): Show |
35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.946-33A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 8/14 | chr4 | 38922737 | |||||||
chr4:38922990 | G | C | 2 | a0001c0001t0005g0014 a0002c0003t0005g0044 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1069+97G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38922990 | |||||||
chr4:38923035 | G | C | 1 | a0001c0001t0002g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1069+142G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923035 | |||||||
chr4:38923142 | G | A | 37 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(34): Show |
37 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1069+249G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923142 | |||||||
chr4:38923149 | T | C | 35 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(32): Show |
35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069+256T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923149 | |||||||
chr4:38923156 | A | G | 35 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(32): Show |
35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069+263A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923156 | |||||||
chr4:38923198 | C | T | 2 | a0004c0020t0003g0046 a0015c0050t0003g0345 |
2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1069+305C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923198 | |||||||
chr4:38923224 | C | CT | 169 | a0001c0001t0001g0041 a0001c0001t0001g0050 a0001c0001t0001g0062 others(166): Show |
175 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.1069+349dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 38923224 | ||||||
chr4:38923224 | C | CTT | 10 | a0001c0001t0001g0019 a0001c0001t0002g0071 a0001c0001t0002g0165 others(7): Show |
10 | HG02055.hp1 HG02135.hp1 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.1069+348_1069+349d others(4): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 38923224 | ||||||
chr4:38923224 | C | CTTT | 18 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(15): Show |
18 | HG00597.hp1 HG00621.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1069+347_1069+349d others(5): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 38923224 | ||||||
chr4:38923224 | C | CTTTT | 11 | a0001c0002t0001g0199 a0001c0002t0040g0307 a0002c0006t0011g0026 others(8): Show |
11 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.1069+346_1069+349d others(6): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 38923224 | ||||||
chr4:38923250 | A | C | 35 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(32): Show |
35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069+357A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923250 | |||||||
chr4:38923255 | C | T | 1 | a0003c0007t0009g0023 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1069+362C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923255 | |||||||
chr4:38923380 | G | A | 3 | a0001c0001t0002g0013 a0001c0004t0022g0003 a0004c0011t0014g0269 |
4 | HG01884.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1069+487G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923380 | |||||||
chr4:38923463 | T | C | 35 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(32): Show |
35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069+570T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923463 | |||||||
chr4:38923472 | C | T | 2 | a0001c0001t0005g0014 a0002c0003t0005g0044 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1069+579C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923472 | |||||||
chr4:38923508 | G | A | 36 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(33): Show |
36 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.1069+615G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923508 | |||||||
chr4:38923516 | T | C | 43 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(40): Show |
43 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.1069+623T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923516 | |||||||
chr4:38923596 | T | C | 1 | a0004c0042t0003g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1069+703T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923596 | |||||||
chr4:38923596 | T | G | 35 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(32): Show |
35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069+703T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923596 | |||||||
chr4:38923689 | A | C | 1 | a0002c0032t0044g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1069+796A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923689 | |||||||
chr4:38923708 | T | G | 37 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(34): Show |
37 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1069+815T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923708 | |||||||
chr4:38923738 | C | A | 2 | a0001c0001t0005g0014 a0002c0003t0005g0044 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1069+845C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923738 | |||||||
chr4:38923745 | C | T | 2 | a0001c0001t0005g0014 a0002c0003t0005g0044 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1069+852C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923745 | |||||||
chr4:38923746 | A | G | 37 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(34): Show |
37 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1069+853A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923746 | |||||||
chr4:38923750 | G | A | 2 | a0001c0001t0005g0014 a0002c0003t0005g0044 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1069+857G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923750 | |||||||
chr4:38923799 | C | G | 2 | a0001c0001t0005g0014 a0002c0003t0005g0044 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1069+906C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923799 | |||||||
chr4:38923801 | T | C | 37 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(34): Show |
37 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1069+908T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923801 | |||||||
chr4:38923804 | A | G | 29 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(26): Show |
29 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1069+911A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923804 | |||||||
chr4:38923811 | T | G | 35 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(32): Show |
35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069+918T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923811 | |||||||
chr4:38923882 | A | G | 2 | a0004c0020t0003g0046 a0015c0050t0003g0345 |
2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1069+989A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38923882 | |||||||
chr4:38924048 | A | G | 35 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(32): Show |
35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069+1155A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924048 | |||||||
chr4:38924097 | T | C | 6 | a0001c0002t0002g0139 a0001c0002t0002g0141 a0001c0013t0002g0076 others(3): Show |
6 | HG00408.hp2 HG00544.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1069+1204T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924097 | |||||||
chr4:38924101 | G | A | 36 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(33): Show |
36 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.1069+1208G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924101 | |||||||
chr4:38924162 | GAT | G | 35 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(32): Show |
35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069+1278_1069+127 others(6): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 38924162 | ||||||
chr4:38924181 | A | G | 3 | a0001c0001t0001g0211 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG00642.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1069+1288A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924181 | |||||||
chr4:38924203 | T | A | 35 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(32): Show |
35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069+1310T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924203 | |||||||
chr4:38924212 | A | G | 35 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(32): Show |
35 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1069+1319A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924212 | |||||||
chr4:38924226 | A | G | 37 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(34): Show |
37 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1069+1333A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924226 | |||||||
chr4:38924290 | G | T | 37 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(34): Show |
37 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1069+1397G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924290 | |||||||
chr4:38924292 | A | G | 37 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(34): Show |
37 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1069+1399A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924292 | |||||||
chr4:38924297 | A | G | 37 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(34): Show |
37 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1069+1404A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924297 | |||||||
chr4:38924316 | G | T | 2 | a0001c0001t0005g0014 a0002c0003t0005g0044 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1069+1423G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924316 | |||||||
chr4:38924352 | C | T | 29 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(26): Show |
29 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1069+1459C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924352 | |||||||
chr4:38924367 | G | C | 1 | a0001c0002t0001g0103 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1069+1474G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924367 | |||||||
chr4:38924387 | G | A | 3 | a0001c0001t0002g0013 a0001c0001t0042g0214 a0004c0011t0014g0269 |
3 | HG01884.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1069+1494G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924387 | |||||||
chr4:38924627 | A | G | 1 | a0001c0001t0012g0334 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1069+1734A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924627 | |||||||
chr4:38924642 | C | G | 2 | a0001c0002t0001g0179 a0001c0002t0001g0234 |
2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1069+1749C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924642 | |||||||
chr4:38924651 | G | T | 34 | a0001c0001t0002g0013 a0001c0001t0005g0297 a0001c0001t0042g0214 others(31): Show |
34 | HG01433.hp1 HG01884.hp2 HG01943.hp2 others(31): Show |
intron_variant | MODIFIER | c.1069+1758G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924651 | |||||||
chr4:38924675 | G | A | 1 | a0007c0021t0004g0347 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1069+1782G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924675 | |||||||
chr4:38924694 | G | A | 31 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(28): Show |
31 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.1069+1801G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924694 | |||||||
chr4:38924855 | C | A | 29 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(26): Show |
29 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1069+1962C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38924855 | |||||||
chr4:38925061 | T | C | 1 | a0001c0001t0017g0300 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1069+2168T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925061 | |||||||
chr4:38925079 | C | T | 2 | a0001c0001t0011g0010 a0002c0003t0010g0362 |
2 | HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1069+2186C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925079 | |||||||
chr4:38925239 | C | T | 10 | a0002c0006t0011g0026 a0003c0007t0009g0023 a0003c0007t0009g0025 others(7): Show |
10 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.1069+2346C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925239 | |||||||
chr4:38925364 | G | T | 1 | a0001c0002t0002g0141 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1069+2471G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925364 | |||||||
chr4:38925392 | A | C | 6 | a0001c0002t0002g0139 a0001c0002t0002g0141 a0001c0013t0002g0076 others(3): Show |
6 | HG00408.hp2 HG00544.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1069+2499A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925392 | |||||||
chr4:38925393 | T | C | 2 | a0001c0001t0011g0010 a0002c0003t0010g0362 |
2 | HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1069+2500T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925393 | |||||||
chr4:38925411 | G | T | 1 | a0002c0003t0005g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1069+2518G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925411 | |||||||
chr4:38925531 | C | G | 5 | a0001c0002t0040g0307 a0001c0004t0011g0190 a0001c0038t0005g0011 others(2): Show |
5 | HG02257.hp1 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1069+2638C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925531 | |||||||
chr4:38925609 | A | G | 243 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(240): Show |
248 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.1069+2716A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925609 | |||||||
chr4:38925760 | C | T | 1 | a0001c0009t0003g0056 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1069+2867C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925760 | |||||||
chr4:38925775 | T | C | 238 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(235): Show |
242 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.1069+2882T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38925775 | |||||||
chr4:38925870 | A | AT | 116 | a0001c0001t0001g0198 a0001c0001t0001g0264 a0001c0001t0001g0296 others(113): Show |
119 | HG00140.hp2 HG00408.hp1 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.1069+2987dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 38925870 | ||||||
chr4:38925870 | AT | A | 29 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(26): Show |
29 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1069+2987delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 38925870 | ||||||
chr4:38926057 | T | C | 3 | a0005c0012t0001g0027 a0005c0012t0034g0021 a0005c0030t0003g0113 |
3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1069+3164T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926057 | |||||||
chr4:38926273 | G | A | 1 | a0001c0001t0012g0184 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1070-2969G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926273 | |||||||
chr4:38926340 | G | A | 29 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(26): Show |
29 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1070-2902G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926340 | |||||||
chr4:38926360 | C | A | 1 | a0001c0001t0001g0264 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1070-2882C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926360 | |||||||
chr4:38926422 | A | G | 1 | a0001c0001t0011g0010 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1070-2820A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926422 | |||||||
chr4:38926430 | C | G | 2 | a0001c0001t0005g0216 a0002c0057t0005g0251 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1070-2812C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926430 | |||||||
chr4:38926457 | C | CT | 7 | a0001c0001t0002g0145 a0001c0001t0026g0317 a0001c0004t0004g0106 others(4): Show |
7 | HG01099.hp1 HG02738.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.1070-2771dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 38926457 | ||||||
chr4:38926458 | T | C | 2 | a0001c0002t0001g0156 a0004c0011t0014g0269 |
2 | HG01884.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1070-2784T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926458 | |||||||
chr4:38926477 | T | TA | 3 | a0001c0001t0005g0231 a0002c0003t0005g0364 a0013c0052t0005g0247 |
3 | HG01884.hp1 HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1070-2764dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 38926477 | ||||||
chr4:38926563 | C | T | 2 | a0004c0020t0003g0046 a0015c0050t0003g0345 |
2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1070-2679C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926563 | |||||||
chr4:38926658 | G | A | 29 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(26): Show |
29 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1070-2584G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926658 | |||||||
chr4:38926705 | G | A | 8 | a0001c0001t0004g0281 a0001c0001t0010g0259 a0001c0001t0010g0299 others(5): Show |
8 | HG02280.hp1 HG02818.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1070-2537G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926705 | |||||||
chr4:38926735 | C | T | 1 | a0001c0004t0007g0136 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1070-2507C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926735 | |||||||
chr4:38926752 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1070-2490G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926752 | |||||||
chr4:38926929 | CCTTAGAG others(2): Show |
C | 29 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(26): Show |
29 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1070-2308_1070-230 others(13): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr4 | 38926929 | ||||||
chr4:38926944 | C | G | 1 | a0001c0013t0006g0171 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1070-2298C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38926944 | |||||||
chr4:38927020 | A | G | 233 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(230): Show |
236 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.1070-2222A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927020 | |||||||
chr4:38927047 | G | A | 1 | a0001c0002t0020g0237 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1070-2195G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927047 | |||||||
chr4:38927049 | T | G | 34 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(31): Show |
34 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.1070-2193T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927049 | |||||||
chr4:38927054 | T | C | 34 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(31): Show |
34 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.1070-2188T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927054 | |||||||
chr4:38927111 | A | G | 34 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(31): Show |
34 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.1070-2131A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927111 | |||||||
chr4:38927133 | C | A | 2 | a0001c0002t0002g0139 a0001c0002t0002g0141 |
2 | HG00408.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1070-2109C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927133 | |||||||
chr4:38927189 | T | A | 34 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(31): Show |
34 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.1070-2053T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927189 | |||||||
chr4:38927354 | T | G | 65 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(62): Show |
66 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1070-1888T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927354 | |||||||
chr4:38927457 | G | A | 4 | a0001c0038t0005g0011 a0001c0043t0001g0006 a0002c0029t0043g0115 others(1): Show |
4 | HG01167.hp2 HG01243.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1070-1785G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927457 | |||||||
chr4:38927464 | G | T | 3 | a0005c0012t0001g0027 a0005c0012t0034g0021 a0005c0030t0003g0113 |
3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1070-1778G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927464 | |||||||
chr4:38927480 | C | T | 4 | a0001c0001t0002g0239 a0001c0001t0002g0241 a0001c0001t0002g0280 others(1): Show |
4 | HG00673.hp2 HG01106.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1070-1762C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927480 | |||||||
chr4:38927696 | T | C | 1 | a0002c0006t0001g0020 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1070-1546T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927696 | |||||||
chr4:38927718 | C | G | 3 | a0001c0039t0024g0261 a0001c0044t0024g0226 a0002c0026t0005g0039 |
3 | HG01891.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1070-1524C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927718 | |||||||
chr4:38927811 | G | C | 2 | a0001c0001t0012g0170 a0004c0011t0014g0269 |
2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1070-1431G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927811 | |||||||
chr4:38927826 | G | A | 6 | a0001c0038t0005g0011 a0001c0043t0001g0006 a0002c0003t0032g0357 others(3): Show |
6 | HG01167.hp2 HG01243.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1070-1416G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927826 | |||||||
chr4:38927828 | C | T | 149 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(146): Show |
152 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.1070-1414C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927828 | |||||||
chr4:38927833 | G | A | 149 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(146): Show |
152 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.1070-1409G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927833 | |||||||
chr4:38927880 | C | T | 1 | a0004c0011t0014g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1070-1362C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927880 | |||||||
chr4:38927943 | A | G | 6 | a0001c0002t0002g0139 a0001c0002t0002g0141 a0001c0013t0002g0076 others(3): Show |
6 | HG00408.hp2 HG00544.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1070-1299A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927943 | |||||||
chr4:38927951 | G | T | 14 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(11): Show |
14 | HG00597.hp1 HG00621.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.1070-1291G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927951 | |||||||
chr4:38927969 | A | G | 14 | a0001c0001t0002g0053 a0001c0001t0002g0271 a0001c0001t0002g0272 others(11): Show |
14 | HG00597.hp1 HG00621.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.1070-1273A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927969 | |||||||
chr4:38927971 | C | T | 1 | a0001c0001t0042g0214 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1070-1271C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927971 | |||||||
chr4:38927981 | C | G | 8 | a0005c0012t0033g0341 a0005c0015t0002g0244 a0005c0015t0002g0250 others(5): Show |
8 | HG02622.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1070-1261C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38927981 | |||||||
chr4:38928093 | C | T | 29 | a0001c0038t0005g0011 a0001c0043t0001g0006 a0002c0003t0032g0357 others(26): Show |
29 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.1070-1149C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38928093 | |||||||
chr4:38928138 | C | T | 1 | a0001c0002t0001g0178 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1070-1104C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38928138 | |||||||
chr4:38928151 | CT | C | 50 | a0001c0001t0002g0013 a0001c0001t0012g0170 a0001c0001t0042g0214 others(47): Show |
50 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.1070-1090delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38928151 | |||||||
chr4:38928163 | G | A | 2 | a0001c0001t0005g0014 a0002c0003t0005g0044 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1070-1079G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38928163 | |||||||
chr4:38928196 | C | G | 1 | a0001c0001t0002g0096 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1070-1046C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38928196 | |||||||
chr4:38928636 | C | G | 9 | a0004c0011t0002g0313 a0005c0012t0033g0341 a0005c0015t0002g0244 others(6): Show |
9 | HG02622.hp1 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1070-606C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38928636 | |||||||
chr4:38928681 | G | C | 4 | a0001c0001t0007g0162 a0001c0001t0007g0273 a0001c0004t0007g0331 others(1): Show |
4 | NA18953.hp2 NA18956.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1070-561G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38928681 | |||||||
chr4:38928812 | G | A | 31 | a0001c0001t0002g0013 a0001c0001t0012g0170 a0001c0013t0006g0171 others(28): Show |
31 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.1070-430G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38928812 | |||||||
chr4:38928848 | A | G | 212 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(209): Show |
215 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.1070-394A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38928848 | |||||||
chr4:38929058 | G | A | 15 | a0001c0013t0006g0171 a0002c0025t0003g0124 a0003c0024t0001g0116 others(12): Show |
15 | HG01433.hp1 HG01943.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.1070-184G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38929058 | |||||||
chr4:38929065 | C | T | 7 | a0001c0001t0007g0227 a0001c0001t0007g0256 a0001c0001t0007g0320 others(4): Show |
7 | HG02257.hp2 HG02717.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1070-177C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38929065 | |||||||
chr4:38929098 | T | C | 9 | a0004c0011t0002g0313 a0005c0012t0033g0341 a0005c0015t0002g0244 others(6): Show |
9 | HG02622.hp1 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1070-144T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38929098 | |||||||
chr4:38929115 | G | T | 1 | a0001c0001t0002g0239 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1070-127G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38929115 | |||||||
chr4:38929171 | T | C | 1 | a0001c0001t0002g0013 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1070-71T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38929171 | |||||||
chr4:38929222 | C | A | 2 | a0001c0001t0005g0014 a0002c0003t0005g0044 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1070-20C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 9/14 | chr4 | 38929222 | |||||||
chr4:38929342 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1161+9T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38929342 | |||||||
chr4:38929364 | T | TA | 5 | a0001c0001t0042g0214 a0005c0012t0001g0027 a0005c0012t0034g0021 others(2): Show |
5 | HG02698.hp1 HG02976.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1161+40dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr4 | 38929364 | ||||||
chr4:38929364 | T | TAA | 166 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(163): Show |
169 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.1161+39_1161+40dup others(2): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr4 | 38929364 | ||||||
chr4:38929374 | C | A | 172 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(169): Show |
175 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.1161+41C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38929374 | |||||||
chr4:38929476 | A | C | 167 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(164): Show |
170 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.1161+143A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38929476 | |||||||
chr4:38929639 | C | T | 167 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(164): Show |
170 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.1161+306C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38929639 | |||||||
chr4:38929784 | A | T | 167 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(164): Show |
170 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.1161+451A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38929784 | |||||||
chr4:38929956 | G | A | 2 | a0004c0020t0003g0046 a0015c0050t0003g0345 |
2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1161+623G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38929956 | |||||||
chr4:38929977 | T | A | 11 | a0001c0002t0001g0002 a0001c0002t0001g0135 a0001c0002t0001g0152 others(8): Show |
13 | NA18945.hp1 NA18951.hp1 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1161+644T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38929977 | |||||||
chr4:38930025 | T | C | 10 | a0001c0009t0003g0335 a0005c0012t0033g0341 a0005c0015t0002g0244 others(7): Show |
10 | HG02622.hp1 HG02622.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1161+692T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38930025 | |||||||
chr4:38930475 | T | C | 174 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(171): Show |
177 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.1162-976T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38930475 | |||||||
chr4:38930544 | C | A | 26 | a0002c0025t0003g0124 a0003c0007t0009g0023 a0003c0007t0009g0025 others(23): Show |
26 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.1162-907C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38930544 | |||||||
chr4:38930581 | G | T | 1 | a0001c0046t0002g0095 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1162-870G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38930581 | |||||||
chr4:38930904 | G | A | 1 | a0001c0001t0042g0214 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1162-547G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38930904 | |||||||
chr4:38930990 | G | A | 3 | a0005c0012t0001g0027 a0005c0012t0034g0021 a0005c0030t0003g0113 |
3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1162-461G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38930990 | |||||||
chr4:38931061 | A | T | 1 | a0001c0001t0002g0176 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1162-390A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931061 | |||||||
chr4:38931087 | T | A | 1 | a0001c0001t0007g0230 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1162-364T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931087 | |||||||
chr4:38931094 | A | G | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1162-357A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931094 | |||||||
chr4:38931138 | C | T | 3 | a0005c0012t0001g0027 a0005c0012t0034g0021 a0005c0030t0003g0113 |
3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1162-313C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931138 | |||||||
chr4:38931208 | T | C | 3 | a0001c0039t0024g0261 a0001c0044t0024g0226 a0002c0026t0005g0039 |
3 | HG01891.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1162-243T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931208 | |||||||
chr4:38931217 | T | C | 3 | a0005c0012t0001g0027 a0005c0012t0034g0021 a0005c0030t0003g0113 |
3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1162-234T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931217 | |||||||
chr4:38931301 | C | A | 282 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(279): Show |
286 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.1162-150C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931301 | |||||||
chr4:38931322 | G | A | 2 | a0001c0001t0004g0203 a0001c0002t0001g0166 |
2 | HG01496.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1162-129G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931322 | |||||||
chr4:38931400 | A | C | 1 | a0013c0052t0005g0247 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1162-51A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931400 | |||||||
chr4:38931414 | C | T | 1 | a0002c0003t0002g0045 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1162-37C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931414 | |||||||
chr4:38931415 | G | T | 2 | a0001c0001t0005g0014 a0002c0003t0005g0044 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1162-36G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931415 | |||||||
chr4:38931443 | C | T | 1 | a0008c0014t0023g0306 | 1 | NA20300.hp1 | splice_region_variant&intron_variant | LOW | c.1162-8C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 10/14 | chr4 | 38931443 | |||||||
chr4:38931824 | G | A | 1 | a0006c0035t0003g0210 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1323+212G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 11/14 | chr4 | 38931824 | |||||||
chr4:38931970 | A | G | 147 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(144): Show |
150 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1324-265A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 11/14 | chr4 | 38931970 | |||||||
chr4:38931989 | C | G | 1 | a0001c0001t0042g0214 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1324-246C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 11/14 | chr4 | 38931989 | |||||||
chr4:38932069 | A | C | 144 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(141): Show |
147 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1324-166A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 11/14 | chr4 | 38932069 | |||||||
chr4:38932105 | A | G | 144 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(141): Show |
147 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1324-130A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 11/14 | chr4 | 38932105 | |||||||
chr4:38932135 | G | C | 9 | a0005c0012t0033g0341 a0005c0015t0002g0244 a0005c0015t0002g0250 others(6): Show |
9 | HG02622.hp1 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1324-100G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 11/14 | chr4 | 38932135 | |||||||
chr4:38932182 | T | C | 1 | a0001c0001t0012g0170 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1324-53T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 11/14 | chr4 | 38932182 | |||||||
chr4:38932379 | G | A | 12 | a0005c0012t0001g0027 a0005c0012t0033g0341 a0005c0012t0034g0021 others(9): Show |
12 | HG02622.hp1 HG02622.hp2 HG02647.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.1463+5G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38932379 | |||||||
chr4:38932447 | C | T | 1 | a0007c0049t0002g0348 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1463+73C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38932447 | |||||||
chr4:38932628 | T | C | 166 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(163): Show |
169 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1463+254T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38932628 | |||||||
chr4:38932697 | A | G | 3 | a0005c0012t0001g0027 a0005c0012t0034g0021 a0005c0030t0003g0113 |
3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1463+323A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38932697 | |||||||
chr4:38932841 | A | T | 9 | a0005c0012t0033g0341 a0005c0015t0002g0244 a0005c0015t0002g0250 others(6): Show |
9 | HG02622.hp1 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1463+467A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38932841 | |||||||
chr4:38932857 | A | AT | 151 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(148): Show |
155 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1463+498dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr4 | 38932857 | ||||||
chr4:38932857 | A | ATTT | 6 | a0005c0015t0002g0244 a0005c0015t0002g0250 a0005c0015t0005g0246 others(3): Show |
6 | HG02647.hp1 HG02809.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1463+496_1463+498d others(5): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr4 | 38932857 | ||||||
chr4:38932968 | C | T | 2 | a0001c0001t0012g0170 a0002c0003t0010g0362 |
2 | HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1463+594C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38932968 | |||||||
chr4:38933001 | G | A | 2 | a0001c0001t0002g0336 a0002c0006t0001g0033 |
2 | HG01099.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1463+627G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38933001 | |||||||
chr4:38933176 | T | A | 2 | a0001c0001t0005g0014 a0002c0003t0005g0044 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1463+802T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38933176 | |||||||
chr4:38933443 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1463+1069C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38933443 | |||||||
chr4:38933522 | T | A | 1 | a0004c0036t0004g0008 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1463+1148T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38933522 | |||||||
chr4:38933546 | T | C | 1 | a0001c0001t0002g0316 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1463+1172T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38933546 | |||||||
chr4:38933842 | T | C | 4 | a0001c0001t0005g0231 a0002c0003t0005g0364 a0012c0040t0023g0235 others(1): Show |
4 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1463+1468T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38933842 | |||||||
chr4:38933922 | G | A | 1 | a0004c0011t0002g0313 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1463+1548G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38933922 | |||||||
chr4:38934015 | G | A | 1 | a0001c0001t0015g0232 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1463+1641G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934015 | |||||||
chr4:38934138 | C | G | 68 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0292 others(65): Show |
68 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.1464-1580C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934138 | |||||||
chr4:38934245 | A | G | 1 | a0001c0001t0004g0281 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1464-1473A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934245 | |||||||
chr4:38934262 | C | T | 1 | a0005c0015t0005g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1464-1456C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934262 | |||||||
chr4:38934333 | A | G | 18 | a0001c0001t0001g0296 a0001c0001t0002g0191 a0001c0001t0002g0213 others(15): Show |
18 | HG01109.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1464-1385A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934333 | |||||||
chr4:38934337 | A | G | 9 | a0001c0001t0007g0162 a0001c0001t0007g0273 a0001c0002t0001g0093 others(6): Show |
9 | HG00597.hp1 HG00621.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.1464-1381A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934337 | |||||||
chr4:38934458 | A | G | 2 | a0001c0001t0002g0007 a0002c0003t0002g0114 |
2 | HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1464-1260A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934458 | |||||||
chr4:38934527 | T | C | 1 | a0001c0001t0002g0280 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1464-1191T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934527 | |||||||
chr4:38934588 | A | C | 1 | a0002c0054t0036g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1464-1130A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934588 | |||||||
chr4:38934806 | C | T | 2 | a0001c0001t0007g0230 a0002c0003t0007g0117 |
2 | HG02074.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1464-912C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934806 | |||||||
chr4:38934918 | CT | C | 20 | a0001c0001t0005g0014 a0001c0001t0006g0087 a0001c0002t0001g0350 others(17): Show |
20 | HG00323.hp1 HG02109.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1464-787delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr4 | 38934918 | ||||||
chr4:38934919 | T | C | 3 | a0001c0002t0040g0307 a0001c0005t0003g0274 a0002c0028t0030g0363 |
3 | HG02486.hp1 HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1464-799T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38934919 | |||||||
chr4:38935152 | G | A | 1 | a0001c0008t0006g0111 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1464-566G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935152 | |||||||
chr4:38935212 | G | A | 199 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(196): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1464-506G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935212 | |||||||
chr4:38935236 | C | T | 1 | a0001c0023t0002g0108 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1464-482C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935236 | |||||||
chr4:38935393 | G | C | 5 | a0001c0001t0005g0014 a0002c0003t0005g0044 a0005c0012t0001g0027 others(2): Show |
5 | HG02698.hp1 HG03453.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1464-325G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935393 | |||||||
chr4:38935396 | A | G | 5 | a0001c0001t0005g0014 a0002c0003t0005g0044 a0005c0012t0001g0027 others(2): Show |
5 | HG02698.hp1 HG03453.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1464-322A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935396 | |||||||
chr4:38935398 | A | G | 5 | a0001c0001t0005g0014 a0002c0003t0005g0044 a0005c0012t0001g0027 others(2): Show |
5 | HG02698.hp1 HG03453.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1464-320A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935398 | |||||||
chr4:38935434 | A | G | 39 | a0001c0001t0001g0264 a0001c0001t0004g0277 a0001c0001t0005g0005 others(36): Show |
39 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.1464-284A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935434 | |||||||
chr4:38935462 | A | G | 1 | a0001c0001t0035g0312 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1464-256A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935462 | |||||||
chr4:38935580 | A | T | 10 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0292 others(7): Show |
10 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1464-138A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935580 | |||||||
chr4:38935600 | C | T | 1 | a0001c0001t0035g0312 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1464-118C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935600 | |||||||
chr4:38935655 | G | A | 2 | a0001c0001t0005g0014 a0002c0003t0005g0044 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1464-63G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 12/14 | chr4 | 38935655 | |||||||
chr4:38936088 | TG | T | 3 | a0001c0001t0014g0295 a0001c0009t0003g0335 a0001c0037t0003g0009 |
3 | HG02886.hp1 HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1536+299delG | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936088 | |||||||
chr4:38936098 | G | GT | 10 | a0001c0001t0005g0005 a0001c0001t0005g0195 a0001c0001t0005g0216 others(7): Show |
10 | HG01109.hp2 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1536+320dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 38936098 | ||||||
chr4:38936098 | G | T | 6 | a0001c0001t0005g0014 a0001c0001t0042g0214 a0002c0003t0005g0044 others(3): Show |
6 | HG02698.hp1 HG03139.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1536+308G>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936098 | |||||||
chr4:38936100 | T | G | 6 | a0001c0001t0005g0014 a0001c0001t0042g0214 a0002c0003t0005g0044 others(3): Show |
6 | HG02698.hp1 HG03139.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1536+310T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936100 | |||||||
chr4:38936102 | T | TG | 17 | a0001c0001t0002g0191 a0001c0001t0002g0213 a0002c0003t0001g0359 others(14): Show |
17 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1536+312_1536+313i others(3): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936102 | |||||||
chr4:38936143 | G | A | 2 | a0001c0001t0035g0312 a0004c0011t0014g0269 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1536+353G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936143 | |||||||
chr4:38936153 | C | T | 11 | a0001c0001t0005g0005 a0001c0001t0005g0195 a0001c0001t0005g0216 others(8): Show |
11 | HG00735.hp2 HG01109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1536+363C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936153 | |||||||
chr4:38936155 | C | G | 23 | a0001c0001t0001g0264 a0001c0001t0009g0148 a0001c0004t0001g0058 others(20): Show |
23 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.1536+365C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936155 | |||||||
chr4:38936178 | T | C | 6 | a0001c0001t0005g0014 a0001c0001t0042g0214 a0002c0003t0005g0044 others(3): Show |
6 | HG02698.hp1 HG03139.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1536+388T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936178 | |||||||
chr4:38936197 | G | A | 198 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(195): Show |
202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1536+407G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936197 | |||||||
chr4:38936259 | AT | A | 4 | a0001c0001t0042g0214 a0005c0012t0001g0027 a0005c0012t0034g0021 others(1): Show |
4 | HG02698.hp1 HG03139.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1536+477delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 38936259 | ||||||
chr4:38936315 | C | T | 3 | a0005c0012t0001g0027 a0005c0012t0034g0021 a0005c0030t0003g0113 |
3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1536+525C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936315 | |||||||
chr4:38936316 | G | A | 1 | a0001c0001t0008g0224 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1536+526G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936316 | |||||||
chr4:38936329 | C | T | 1 | a0001c0004t0029g0015 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1536+539C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936329 | |||||||
chr4:38936354 | A | G | 3 | a0005c0012t0001g0027 a0005c0012t0034g0021 a0005c0030t0003g0113 |
3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1536+564A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936354 | |||||||
chr4:38936374 | G | A | 3 | a0001c0001t0002g0191 a0001c0001t0002g0213 a0002c0003t0012g0112 |
3 | HG02055.hp1 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1536+584G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936374 | |||||||
chr4:38936548 | A | AT | 17 | a0001c0001t0001g0284 a0001c0001t0002g0191 a0001c0001t0002g0193 others(14): Show |
17 | HG00408.hp2 HG00438.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1536+780dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 38936548 | ||||||
chr4:38936548 | AT | A | 38 | a0001c0001t0002g0180 a0001c0001t0004g0183 a0001c0001t0004g0277 others(35): Show |
38 | HG01109.hp2 HG01256.hp1 HG01993.hp2 others(35): Show |
intron_variant | MODIFIER | c.1536+780delT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 38936548 | ||||||
chr4:38936577 | G | C | 2 | a0001c0001t0004g0183 a0003c0007t0009g0025 |
2 | HG01192.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.1536+787G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936577 | |||||||
chr4:38936656 | G | A | 1 | a0001c0001t0035g0312 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1536+866G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936656 | |||||||
chr4:38936701 | C | T | 16 | a0001c0001t0004g0277 a0001c0001t0005g0005 a0001c0001t0005g0195 others(13): Show |
16 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1536+911C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936701 | |||||||
chr4:38936702 | G | A | 7 | a0001c0001t0007g0227 a0001c0001t0007g0256 a0001c0001t0007g0320 others(4): Show |
7 | HG01255.hp2 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1536+912G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936702 | |||||||
chr4:38936720 | C | G | 3 | a0005c0012t0001g0027 a0005c0012t0034g0021 a0005c0030t0003g0113 |
3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1536+930C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936720 | |||||||
chr4:38936741 | C | T | 22 | a0001c0001t0001g0264 a0001c0001t0009g0148 a0001c0004t0001g0058 others(19): Show |
22 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1536+951C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936741 | |||||||
chr4:38936776 | C | A | 1 | a0001c0004t0002g0082 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1536+986C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936776 | |||||||
chr4:38936868 | G | C | 1 | a0001c0001t0005g0005 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1536+1078G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936868 | |||||||
chr4:38936937 | A | T | 261 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(258): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1536+1147A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38936937 | |||||||
chr4:38937262 | G | C | 1 | a0002c0003t0001g0359 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1536+1472G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937262 | |||||||
chr4:38937495 | G | A | 39 | a0001c0001t0001g0050 a0001c0001t0001g0161 a0001c0001t0001g0315 others(36): Show |
39 | HG00544.hp2 HG00639.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.1536+1705G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937495 | |||||||
chr4:38937534 | A | G | 104 | a0001c0001t0001g0041 a0001c0001t0001g0062 a0001c0001t0001g0159 others(101): Show |
107 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.1536+1744A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937534 | |||||||
chr4:38937602 | C | T | 2 | a0001c0001t0005g0014 a0002c0003t0005g0044 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1536+1812C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937602 | |||||||
chr4:38937636 | T | C | 24 | a0001c0001t0002g0191 a0001c0001t0002g0213 a0001c0001t0004g0277 others(21): Show |
24 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.1536+1846T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937636 | |||||||
chr4:38937702 | C | T | 1 | a0004c0011t0014g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1536+1912C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937702 | |||||||
chr4:38937797 | C | T | 1 | a0004c0011t0014g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1536+2007C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937797 | |||||||
chr4:38937808 | C | T | 1 | a0001c0013t0001g0290 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1536+2018C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937808 | |||||||
chr4:38937882 | G | A | 3 | a0005c0012t0001g0027 a0005c0012t0034g0021 a0005c0030t0003g0113 |
3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1536+2092G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937882 | |||||||
chr4:38937895 | C | T | 1 | a0001c0001t0031g0289 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1536+2105C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937895 | |||||||
chr4:38937933 | C | T | 75 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0211 others(72): Show |
76 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1536+2143C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38937933 | |||||||
chr4:38938213 | T | A | 64 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0211 others(61): Show |
65 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.1536+2423T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38938213 | |||||||
chr4:38938495 | A | T | 3 | a0005c0012t0001g0027 a0005c0012t0034g0021 a0005c0030t0003g0113 |
3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1537-2473A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38938495 | |||||||
chr4:38938516 | G | A | 1 | a0001c0001t0042g0214 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1537-2452G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38938516 | |||||||
chr4:38938595 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1537-2373C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38938595 | |||||||
chr4:38938628 | C | T | 1 | a0005c0015t0005g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1537-2340C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38938628 | |||||||
chr4:38939009 | A | G | 121 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(118): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1537-1959A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38939009 | |||||||
chr4:38939193 | T | C | 149 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(146): Show |
150 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.1537-1775T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38939193 | |||||||
chr4:38939212 | A | G | 45 | a0001c0001t0001g0050 a0001c0001t0001g0161 a0001c0001t0001g0315 others(42): Show |
45 | HG00544.hp2 HG00639.hp1 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.1537-1756A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38939212 | |||||||
chr4:38939524 | G | A | 1 | a0011c0033t0011g0355 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1537-1444G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38939524 | |||||||
chr4:38939836 | C | T | 6 | a0001c0001t0010g0259 a0001c0001t0010g0299 a0001c0004t0029g0015 others(3): Show |
6 | HG02280.hp1 HG02647.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1537-1132C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38939836 | |||||||
chr4:38939844 | T | C | 45 | a0001c0001t0001g0050 a0001c0001t0001g0161 a0001c0001t0001g0315 others(42): Show |
45 | HG00544.hp2 HG00639.hp1 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.1537-1124T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38939844 | |||||||
chr4:38939886 | C | CT | 129 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(126): Show |
130 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.1537-1064dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 38939886 | ||||||
chr4:38939886 | CTTT | C | 23 | a0001c0001t0001g0264 a0001c0001t0009g0148 a0001c0004t0001g0058 others(20): Show |
23 | HG00735.hp2 HG00741.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.1537-1066_1537-106 others(7): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 38939886 | ||||||
chr4:38939962 | C | A | 6 | a0001c0001t0004g0277 a0001c0001t0005g0014 a0001c0038t0005g0011 others(3): Show |
6 | HG02145.hp2 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1537-1006C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38939962 | |||||||
chr4:38940047 | C | G | 1 | a0001c0001t0002g0309 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1537-921C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940047 | |||||||
chr4:38940053 | T | G | 1 | a0005c0012t0033g0341 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1537-915T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940053 | |||||||
chr4:38940074 | G | A | 64 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0211 others(61): Show |
65 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.1537-894G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940074 | |||||||
chr4:38940087 | C | T | 3 | a0001c0001t0002g0228 a0001c0046t0002g0095 a0004c0011t0002g0313 |
3 | HG02523.hp1 HG03225.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.1537-881C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940087 | |||||||
chr4:38940382 | GA | G | 257 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0050 others(254): Show |
258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.1537-577delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr4 | 38940382 | ||||||
chr4:38940383 | A | G | 1 | a0001c0004t0002g0001 | 4 | NA18970.hp2 NA18980.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.1537-585A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940383 | |||||||
chr4:38940394 | G | A | 77 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0211 others(74): Show |
78 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1537-574G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940394 | |||||||
chr4:38940598 | C | T | 1 | a0002c0006t0010g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1537-370C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940598 | |||||||
chr4:38940668 | C | T | 3 | a0001c0001t0004g0266 a0002c0003t0004g0118 a0002c0003t0004g0130 |
3 | NA18959.hp1 NA18978.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1537-300C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940668 | |||||||
chr4:38940669 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1537-299G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940669 | |||||||
chr4:38940680 | C | A | 1 | a0001c0004t0029g0015 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1537-288C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940680 | |||||||
chr4:38940781 | C | T | 1 | a0001c0001t0004g0262 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1537-187C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 13/14 | chr4 | 38940781 | |||||||
chr4:38941076 | C | CT | 243 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0062 others(240): Show |
247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1590+69dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr4 | 38941076 | ||||||
chr4:38941076 | C | CTT | 16 | a0001c0001t0001g0173 a0001c0001t0001g0187 a0001c0001t0001g0284 others(13): Show |
16 | HG01123.hp2 HG01257.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.1590+68_1590+69dup others(2): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr4 | 38941076 | ||||||
chr4:38941168 | C | T | 1 | a0001c0001t0035g0312 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1590+147C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941168 | |||||||
chr4:38941227 | T | C | 7 | a0006c0010t0003g0172 a0006c0010t0003g0189 a0006c0010t0003g0318 others(4): Show |
7 | HG01433.hp1 HG01975.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.1590+206T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941227 | |||||||
chr4:38941443 | A | G | 3 | a0005c0012t0001g0027 a0005c0012t0034g0021 a0005c0030t0003g0113 |
3 | HG02698.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1590+422A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941443 | |||||||
chr4:38941469 | C | T | 2 | a0001c0001t0005g0014 a0002c0003t0005g0044 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1590+448C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941469 | |||||||
chr4:38941523 | C | T | 2 | a0001c0002t0007g0365 a0001c0002t0007g0366 |
2 | NA18962.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1590+502C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941523 | |||||||
chr4:38941561 | T | C | 1 | a0001c0002t0006g0188 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1590+540T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941561 | |||||||
chr4:38941657 | A | T | 4 | a0001c0002t0001g0002 a0001c0002t0001g0152 a0001c0002t0001g0212 others(1): Show |
6 | NA18945.hp1 NA18952.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1590+636A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941657 | |||||||
chr4:38941739 | C | T | 1 | a0002c0003t0004g0130 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1590+718C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941739 | |||||||
chr4:38941778 | A | G | 2 | a0001c0001t0014g0196 a0001c0004t0001g0260 |
2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1590+757A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941778 | |||||||
chr4:38941835 | A | G | 2 | a0001c0001t0002g0228 a0001c0046t0002g0095 |
2 | HG02523.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.1590+814A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941835 | |||||||
chr4:38941878 | A | G | 1 | a0007c0049t0002g0348 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1590+857A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941878 | |||||||
chr4:38941924 | C | A | 10 | a0001c0001t0002g0191 a0001c0001t0002g0213 a0001c0001t0009g0148 others(7): Show |
10 | HG00741.hp2 HG01070.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1590+903C>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941924 | |||||||
chr4:38941941 | A | T | 1 | a0001c0001t0002g0097 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1590+920A>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38941941 | |||||||
chr4:38942010 | A | G | 154 | a0001c0001t0001g0173 a0001c0001t0001g0187 a0001c0001t0001g0284 others(151): Show |
157 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1590+989A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942010 | |||||||
chr4:38942077 | A | C | 1 | a0002c0003t0010g0362 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1590+1056A>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942077 | |||||||
chr4:38942113 | C | T | 1 | a0001c0001t0005g0297 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1590+1092C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942113 | |||||||
chr4:38942187 | T | C | 60 | a0001c0001t0001g0050 a0001c0001t0004g0266 a0001c0001t0006g0068 others(57): Show |
62 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1590+1166T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942187 | |||||||
chr4:38942213 | T | A | 31 | a0001c0001t0001g0019 a0001c0001t0001g0275 a0001c0001t0004g0077 others(28): Show |
31 | HG00140.hp2 HG00609.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.1590+1192T>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942213 | |||||||
chr4:38942426 | G | GAA | 6 | a0001c0001t0008g0109 a0001c0001t0008g0110 a0001c0001t0008g0224 others(3): Show |
6 | NA18956.hp1 NA18974.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.1591-1027_1591-102 others(6): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr4 | 38942426 | ||||||
chr4:38942447 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1591-1009C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942447 | |||||||
chr4:38942480 | C | T | 124 | a0001c0001t0001g0019 a0001c0001t0001g0275 a0001c0001t0004g0077 others(121): Show |
124 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.1591-976C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942480 | |||||||
chr4:38942562 | T | C | 1 | a0001c0001t0004g0268 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1591-894T>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942562 | |||||||
chr4:38942589 | C | G | 1 | a0004c0041t0003g0158 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1591-867C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942589 | |||||||
chr4:38942597 | T | G | 2 | a0001c0004t0002g0286 a0002c0003t0002g0045 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1591-859T>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942597 | |||||||
chr4:38942704 | C | G | 11 | a0001c0001t0002g0013 a0001c0001t0002g0040 a0001c0001t0002g0292 others(8): Show |
11 | HG02257.hp1 HG02451.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.1591-752C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942704 | |||||||
chr4:38942729 | A | G | 2 | a0001c0001t0014g0196 a0001c0002t0014g0151 |
2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1591-727A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942729 | |||||||
chr4:38942817 | G | A | 2 | a0002c0003t0010g0362 a0002c0006t0010g0337 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1591-639G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942817 | |||||||
chr4:38942865 | C | G | 3 | a0001c0002t0001g0163 a0001c0002t0001g0233 a0001c0002t0019g0288 |
3 | HG03490.hp1 HG03492.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1591-591C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942865 | |||||||
chr4:38942872 | TACCCTGG others(17): Show |
T | 94 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0016 others(91): Show |
97 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.1591-581_1591-558d others(26): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr4 | 38942872 | ||||||
chr4:38942961 | G | A | 2 | a0001c0039t0024g0261 a0001c0044t0024g0226 |
2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1591-495G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942961 | |||||||
chr4:38942970 | A | G | 257 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0016 others(254): Show |
261 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.1591-486A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38942970 | |||||||
chr4:38943019 | C | T | 35 | a0001c0001t0005g0005 a0001c0001t0005g0014 a0001c0001t0005g0195 others(32): Show |
35 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.1591-437C>T | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38943019 | |||||||
chr4:38943070 | G | C | 1 | a0001c0001t0007g0320 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1591-386G>C | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38943070 | |||||||
chr4:38943125 | G | A | 8 | a0001c0001t0004g0203 a0001c0001t0004g0253 a0001c0001t0004g0254 others(5): Show |
8 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1591-331G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38943125 | |||||||
chr4:38943142 | A | G | 3 | a0001c0002t0001g0163 a0001c0002t0001g0233 a0001c0002t0019g0288 |
3 | HG03490.hp1 HG03492.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1591-314A>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38943142 | |||||||
chr4:38943171 | G | A | 2 | a0002c0003t0010g0362 a0002c0006t0010g0337 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1591-285G>A | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38943171 | |||||||
chr4:38943191 | C | CA | 104 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0016 others(101): Show |
107 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.1591-244dupA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr4 | 38943191 | ||||||
chr4:38943191 | C | CAA | 10 | a0001c0001t0002g0017 a0001c0001t0002g0057 a0001c0001t0002g0165 others(7): Show |
10 | HG01106.hp1 HG01192.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.1591-245_1591-244d others(4): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr4 | 38943191 | ||||||
chr4:38943191 | CA | C | 46 | a0001c0001t0004g0077 a0001c0001t0004g0086 a0001c0001t0004g0194 others(43): Show |
46 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1591-244delA | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr4 | 38943191 | ||||||
chr4:38943254 | C | G | 1 | a0001c0001t0005g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1591-202C>G | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | chr4 | 38943254 | |||||||
chr4:38943355 | A | AT | 259 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0016 others(256): Show |
263 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.1591-100dupT | FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr4 | 38943355 |