Item | Value |
---|---|
geneid | 85462 |
ensemblid | ENSG00000137460.10 |
hgncid | 29363 |
symbol | FHDC1 |
name | FH2 domain containing 1 |
refseq_nuc | NM_001371116.1 |
refseq_prot | NP_001358045.1 |
ensembl_nuc | ENST00000511601.6 |
ensembl_prot | ENSP00000427567.1 |
mane_status | MANE Select |
chr | chr4 |
start | 152936323 |
end | 152979671 |
strand | + |
ver | v1.2 |
region | chr4:152936323-152979671 |
region5000 | chr4:152931323-152984671 |
regionname0 | FHDC1_chr4_152936323_152979671 |
regionname5000 | FHDC1_chr4_152931323_152984671 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1143 | 170 | 57 | 30 | 57 | 1 | 23 | 41 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0002 | 0/0 | 1143 | 156 | 8 | 38 | 75 | 16 | 19 | 53 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0003 | 0/0 | 1143 | 30 | 8 | 2 | 19 | 0 | 1 | 16 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0004 | 0/0 | 1143 | 26 | 0 | 2 | 24 | 0 | 0 | 21 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0005 | 0/0 | 1143 | 9 | 0 | 0 | 9 | 0 | 0 | 9 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0006 | 0/0 | 1143 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0007 | 0/0 | 1143 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0008 | 0/0 | 1143 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0009 | 0/0 | 1143 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0010 | 0/0 | 1143 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0011 | 0/0 | 1143 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0012 | 0/0 | 1143 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0013 | 0/0 | 1143 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0014 | 0/0 | 1143 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0015 | 0/0 | 1143 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0016 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0017 | 0/0 | 1143 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0018 | 0/0 | 1143 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0019 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0020 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0021 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0022 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0023 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0024 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0025 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0026 | 0/0 | 1147 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1142): Show |
chr4 | 152931323 | 152984671 |
a0027 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0028 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0029 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0030 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0031 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0032 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0033 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0034 | 0/0 | 1143 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
a0035 | 0/0 | 1143 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | MHVMN others(1138): Show |
chr4 | 152931323 | 152984671 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 1/0 | 3429 | 135 | 39 | 25 | 51 | 0 | 19 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0001c0005 | 0/1 | 3429 | 20 | 4 | 5 | 6 | 1 | 3 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0001c0007 | 0/0 | 3429 | 6 | 6 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0001c0010 | 0/0 | 3429 | 4 | 4 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0001c0013 | 0/0 | 3429 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0001c0040 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0001c0051 | 0/0 | 3429 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0002c0001 | 0/0 | 3429 | 145 | 7 | 35 | 74 | 13 | 16 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0002c0008 | 0/0 | 3429 | 5 | 0 | 2 | 0 | 3 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0002c0018 | 0/0 | 3429 | 2 | 0 | 0 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0002c0030 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0002c0042 | 0/0 | 3429 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0002c0044 | 0/0 | 3429 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0002c0052 | 0/0 | 3429 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0003c0004 | 0/0 | 3429 | 24 | 2 | 2 | 19 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0003c0011 | 0/0 | 3429 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0003c0023 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0003c0025 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0003c0027 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0004c0003 | 0/0 | 3429 | 25 | 0 | 2 | 23 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0004c0028 | 0/0 | 3429 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0005c0006 | 0/0 | 3429 | 9 | 0 | 0 | 9 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0006c0016 | 0/0 | 3429 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0006c0039 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0007c0009 | 0/0 | 3429 | 4 | 4 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0008c0012 | 0/0 | 3429 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0008c0033 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0009c0015 | 0/0 | 3429 | 3 | 0 | 0 | 3 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0010c0014 | 0/0 | 3429 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0011c0017 | 0/0 | 3429 | 2 | 0 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0012c0046 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0012c0047 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0013c0019 | 0/0 | 3429 | 2 | 0 | 0 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0014c0020 | 0/0 | 3429 | 2 | 0 | 0 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0015c0032 | 0/0 | 3429 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0016c0036 | 0/0 | 3429 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0017c0041 | 0/0 | 3429 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0018c0022 | 0/0 | 3429 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0019c0038 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0020c0049 | 0/0 | 3429 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0021c0034 | 0/0 | 3429 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0022c0035 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0023c0055 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0024c0050 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0025c0045 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0026c0054 | 0/0 | 3441 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3436): Show |
chr4 | 152931323 | 152984671 | ||
a0027c0026 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0028c0048 | 0/0 | 3429 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0029c0024 | 0/0 | 3429 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0030c0043 | 0/0 | 3429 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0031c0037 | 0/0 | 3429 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0032c0021 | 0/0 | 3429 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0033c0029 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0034c0053 | 0/0 | 3429 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 | ||
a0035c0031 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | ATGCA others(3424): Show |
chr4 | 152931323 | 152984671 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 6596 | 8 | 5 | 1 | 1 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0002t0002 | 0/0 | 6596 | 66 | 0 | 17 | 38 | 0 | 11 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0002t0003 | 0/0 | 6596 | 20 | 15 | 1 | 4 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0002t0004 | 0/0 | 6596 | 8 | 0 | 0 | 3 | 0 | 5 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0002t0005 | 1/0 | 6597 | 7 | 6 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6592): Show |
chr4 | 152931323 | 152984671 |
a0001c0002t0006 | 0/0 | 6597 | 5 | 5 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6592): Show |
chr4 | 152931323 | 152984671 |
a0001c0002t0013 | 0/0 | 6596 | 2 | 0 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0002t0014 | 0/0 | 6597 | 3 | 1 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6592): Show |
chr4 | 152931323 | 152984671 |
a0001c0002t0017 | 0/0 | 6596 | 2 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0002t0019 | 0/0 | 6596 | 2 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0002t0024 | 0/0 | 6596 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0002t0025 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0002t0028 | 0/0 | 6597 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6592): Show |
chr4 | 152931323 | 152984671 |
a0001c0002t0031 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0002t0042 | 0/0 | 6595 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6590): Show |
chr4 | 152931323 | 152984671 |
a0001c0002t0043 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0002t0047 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0002t0048 | 0/0 | 6597 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6592): Show |
chr4 | 152931323 | 152984671 |
a0001c0002t0051 | 0/0 | 6596 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0002t0052 | 0/0 | 6581 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6576): Show |
chr4 | 152931323 | 152984671 |
a0001c0002t0053 | 0/0 | 6596 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0005t0001 | 0/0 | 6596 | 4 | 0 | 3 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0005t0002 | 0/1 | 6596 | 14 | 2 | 2 | 6 | 0 | 3 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0005t0020 | 0/0 | 6596 | 2 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0007t0007 | 0/0 | 6596 | 5 | 5 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0007t0027 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0010t0003 | 0/0 | 6596 | 2 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0010t0022 | 0/0 | 6596 | 2 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0013t0003 | 0/0 | 6596 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0040t0003 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0001c0051t0002 | 0/0 | 6596 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0002c0001t0001 | 0/0 | 6596 | 128 | 6 | 34 | 65 | 11 | 12 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0002c0001t0010 | 0/0 | 6596 | 4 | 0 | 0 | 4 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0002c0001t0011 | 0/0 | 6596 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0002c0001t0013 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0002c0001t0016 | 0/0 | 6596 | 3 | 0 | 0 | 1 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0002c0001t0021 | 0/0 | 6596 | 2 | 0 | 0 | 0 | 1 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0002c0001t0034 | 0/0 | 6595 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6590): Show |
chr4 | 152931323 | 152984671 |
a0002c0001t0036 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6590): Show |
chr4 | 152931323 | 152984671 |
a0002c0001t0037 | 0/0 | 6596 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0002c0001t0038 | 0/0 | 6596 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0002c0001t0040 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0002c0008t0008 | 0/0 | 6596 | 5 | 0 | 2 | 0 | 3 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0002c0018t0001 | 0/0 | 6596 | 2 | 0 | 0 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0002c0030t0001 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0002c0042t0001 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0002c0044t0039 | 0/0 | 6596 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0002c0052t0001 | 0/0 | 6596 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0003c0004t0001 | 0/0 | 6596 | 7 | 1 | 0 | 6 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0003c0004t0002 | 0/0 | 6596 | 12 | 0 | 1 | 10 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0003c0004t0003 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0003c0004t0005 | 0/0 | 6597 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6592): Show |
chr4 | 152931323 | 152984671 |
a0003c0004t0006 | 0/0 | 6597 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6592): Show |
chr4 | 152931323 | 152984671 |
a0003c0004t0025 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0003c0004t0030 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0003c0011t0003 | 0/0 | 6596 | 2 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0003c0011t0046 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0003c0023t0004 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0003c0025t0045 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0003c0027t0041 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0004c0003t0001 | 0/0 | 6596 | 23 | 0 | 2 | 21 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0004c0003t0011 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0004c0003t0033 | 0/0 | 6595 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6590): Show |
chr4 | 152931323 | 152984671 |
a0004c0028t0001 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0005c0006t0001 | 0/0 | 6596 | 9 | 0 | 0 | 9 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0006c0016t0009 | 0/0 | 6596 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0006c0039t0044 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0007c0009t0015 | 0/0 | 6597 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6592): Show |
chr4 | 152931323 | 152984671 |
a0007c0009t0029 | 0/0 | 6597 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6592): Show |
chr4 | 152931323 | 152984671 |
a0008c0012t0001 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0008c0012t0018 | 0/0 | 6596 | 2 | 2 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0008c0033t0001 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0009c0015t0003 | 0/0 | 6596 | 3 | 0 | 0 | 3 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0010c0014t0012 | 0/0 | 6597 | 3 | 3 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6592): Show |
chr4 | 152931323 | 152984671 |
a0011c0017t0002 | 0/0 | 6596 | 2 | 0 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0012c0046t0023 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6590): Show |
chr4 | 152931323 | 152984671 |
a0012c0047t0023 | 0/0 | 6595 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6590): Show |
chr4 | 152931323 | 152984671 |
a0013c0019t0026 | 0/0 | 6596 | 2 | 0 | 0 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0014c0020t0002 | 0/0 | 6596 | 2 | 0 | 0 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0015c0032t0001 | 0/0 | 6596 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0016c0036t0002 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0017c0041t0001 | 0/0 | 6596 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0018c0022t0049 | 0/0 | 6597 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6592): Show |
chr4 | 152931323 | 152984671 |
a0019c0038t0006 | 0/0 | 6597 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6592): Show |
chr4 | 152931323 | 152984671 |
a0020c0049t0001 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0021c0034t0003 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0022c0035t0001 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0023c0055t0035 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0024c0050t0032 | 0/0 | 6597 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6592): Show |
chr4 | 152931323 | 152984671 |
a0025c0045t0003 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0026c0054t0001 | 0/0 | 6608 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6603): Show |
chr4 | 152931323 | 152984671 |
a0027c0026t0050 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0028c0048t0001 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0029c0024t0003 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0030c0043t0011 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0031c0037t0003 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0032c0021t0001 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0033c0029t0009 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0034c0053t0001 | 0/0 | 6596 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
a0035c0031t0001 | 0/0 | 6596 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | AGTGA others(6591): Show |
chr4 | 152931323 | 152984671 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0402 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0002g0403 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0004g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0004g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0005g0142 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0005g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0006g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0006g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0006g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0013g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0014g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0014g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0017g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0017g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0019g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0019g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0024g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0024g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0025g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0028g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0031g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0042g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0043g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0047g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0048g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0051g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0052g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0002t0053g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0020g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0005t0020g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0007t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0007t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0007t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0007t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0007t0007g0396 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0007t0027g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0010t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0010t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0010t0022g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0010t0022g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0013t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0013t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0013t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0040t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0001c0051t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0001 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0001g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0010g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0010g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0010g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0010g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0011g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0011g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0013g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0016g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0016g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0016g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0021g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0021g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0034g0404 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0036g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0037g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0038g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0001t0040g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0008t0008g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0008t0008g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0008t0008g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0008t0008g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0018t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0030t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0042t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0044t0039g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0002c0052t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0001g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0001g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0001g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0002g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0003g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0006g0391 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0025g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0004t0030g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0011t0003g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0011t0003g0398 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0011t0046g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0023t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0025t0045g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0003c0027t0041g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0001g0401 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0011g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0003t0033g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0004c0028t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0005c0006t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0005c0006t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0005c0006t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0005c0006t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0005c0006t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0005c0006t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0005c0006t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0005c0006t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0005c0006t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0006c0016t0009g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0006c0016t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0006c0016t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0006c0039t0044g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0007c0009t0015g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0007c0009t0015g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0007c0009t0015g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0007c0009t0029g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0008c0012t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0008c0012t0018g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0008c0012t0018g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0008c0033t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0009c0015t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0009c0015t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0009c0015t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0010c0014t0012g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0010c0014t0012g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0010c0014t0012g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0011c0017t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0012c0046t0023g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0012c0047t0023g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0013c0019t0026g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0013c0019t0026g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0014c0020t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0014c0020t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0015c0032t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0016c0036t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0017c0041t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0018c0022t0049g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0019c0038t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0020c0049t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0021c0034t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0022c0035t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0023c0055t0035g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0024c0050t0032g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0025c0045t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0026c0054t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0027c0026t0050g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0028c0048t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0029c0024t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0030c0043t0011g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0031c0037t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0032c0021t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0033c0029t0009g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0034c0053t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
a0035c0031t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0001 | t0001 | g0323 | EUR | GBR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00099 | hp2 | a0002 | c0001 | t0021 | g0101 | EUR | GBR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00140 | hp1 | a0001 | c0005 | t0001 | g0131 | EUR | GBR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00140 | hp2 | a0015 | c0032 | t0001 | g0117 | EUR | GBR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00280 | hp1 | a0002 | c0001 | t0001 | g0320 | EUR | FIN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00280 | hp2 | a0002 | c0008 | t0008 | g0009 | EUR | FIN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00323 | hp1 | a0002 | c0001 | t0001 | g0016 | EUR | FIN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00323 | hp2 | a0002 | c0008 | t0008 | g0303 | EUR | FIN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0199 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00408 | hp2 | a0002 | c0001 | t0001 | g0013 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00423 | hp1 | a0002 | c0042 | t0001 | g0342 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00423 | hp2 | a0002 | c0001 | t0001 | g0369 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0285 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00438 | hp2 | a0002 | c0001 | t0001 | g0376 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00544 | hp1 | a0002 | c0001 | t0001 | g0287 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00544 | hp2 | a0002 | c0001 | t0001 | g0221 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00558 | hp1 | a0016 | c0036 | t0002 | g0266 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00558 | hp2 | a0004 | c0003 | t0001 | g0394 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00597 | hp1 | a0001 | c0002 | t0025 | g0399 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00597 | hp2 | a0002 | c0001 | t0001 | g0400 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00609 | hp1 | a0002 | c0001 | t0001 | g0107 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00609 | hp2 | a0002 | c0001 | t0001 | g0281 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00621 | hp1 | a0002 | c0001 | t0001 | g0284 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | CHS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00639 | hp1 | a0002 | c0001 | t0001 | g0016 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00639 | hp2 | a0002 | c0001 | t0001 | g0014 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00642 | hp1 | a0002 | c0001 | t0001 | g0315 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00642 | hp2 | a0017 | c0041 | t0001 | g0261 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00735 | hp1 | a0002 | c0001 | t0001 | g0091 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00735 | hp2 | a0002 | c0001 | t0001 | g0210 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00741 | hp1 | a0002 | c0001 | t0001 | g0291 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG00741 | hp2 | a0002 | c0001 | t0001 | g0316 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01069 | hp1 | a0001 | c0005 | t0001 | g0029 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0279 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01070 | hp1 | a0001 | c0002 | t0014 | g0012 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01070 | hp2 | a0004 | c0003 | t0001 | g0390 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01071 | hp1 | a0001 | c0005 | t0001 | g0030 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01071 | hp2 | a0001 | c0002 | t0014 | g0012 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0023 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01074 | hp2 | a0002 | c0001 | t0001 | g0112 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01081 | hp1 | a0001 | c0002 | t0003 | g0132 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0278 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01099 | hp1 | a0002 | c0001 | t0001 | g0213 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01099 | hp2 | a0002 | c0001 | t0001 | g0304 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01106 | hp1 | a0002 | c0001 | t0001 | g0192 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01106 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01109 | hp1 | a0002 | c0044 | t0039 | g0113 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01109 | hp2 | a0002 | c0008 | t0008 | g0095 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01167 | hp1 | a0002 | c0001 | t0001 | g0011 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01167 | hp2 | a0001 | c0002 | t0013 | g0025 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01168 | hp2 | a0001 | c0005 | t0002 | g0314 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01169 | hp1 | a0001 | c0002 | t0013 | g0025 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01169 | hp2 | a0001 | c0005 | t0002 | g0313 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01175 | hp1 | a0002 | c0001 | t0001 | g0269 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01175 | hp2 | a0003 | c0004 | t0006 | g0391 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01192 | hp1 | a0001 | c0005 | t0001 | g0318 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01192 | hp2 | a0002 | c0001 | t0001 | g0011 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01243 | hp1 | a0002 | c0001 | t0001 | g0069 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01243 | hp2 | a0018 | c0022 | t0049 | g0035 | AMR | PUR | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01256 | hp1 | a0011 | c0017 | t0002 | g0010 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01256 | hp2 | a0002 | c0001 | t0001 | g0074 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01258 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01258 | hp2 | a0011 | c0017 | t0002 | g0010 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01261 | hp1 | a0002 | c0001 | t0001 | g0312 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01261 | hp2 | a0001 | c0002 | t0002 | g0065 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01346 | hp1 | a0002 | c0001 | t0001 | g0227 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01346 | hp2 | a0002 | c0001 | t0001 | g0319 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0214 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01358 | hp2 | a0002 | c0001 | t0001 | g0060 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0280 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01361 | hp2 | a0002 | c0001 | t0001 | g0071 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01433 | hp1 | a0002 | c0001 | t0001 | g0306 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01496 | hp2 | a0002 | c0001 | t0001 | g0194 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01515 | hp1 | a0002 | c0001 | t0034 | g0404 | EUR | IBS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01515 | hp2 | a0002 | c0001 | t0001 | g0001 | EUR | IBS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01516 | hp1 | a0002 | c0001 | t0001 | g0110 | EUR | IBS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01516 | hp2 | a0002 | c0001 | t0001 | g0007 | EUR | IBS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01517 | hp1 | a0002 | c0001 | t0001 | g0001 | EUR | IBS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01517 | hp2 | a0002 | c0001 | t0001 | g0007 | EUR | IBS | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01884 | hp1 | a0002 | c0001 | t0001 | g0169 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01884 | hp2 | a0001 | c0002 | t0005 | g0325 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01891 | hp1 | a0001 | c0002 | t0003 | g0246 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01891 | hp2 | a0001 | c0007 | t0007 | g0396 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0232 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01934 | hp1 | a0002 | c0001 | t0001 | g0274 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0402 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01975 | hp1 | a0002 | c0001 | t0001 | g0015 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0220 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01978 | hp1 | a0002 | c0001 | t0001 | g0053 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01978 | hp2 | a0001 | c0002 | t0042 | g0224 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01981 | hp1 | a0001 | c0002 | t0053 | g0003 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0219 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0290 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01993 | hp2 | a0002 | c0001 | t0001 | g0072 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02004 | hp1 | a0002 | c0001 | t0001 | g0248 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0238 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02015 | hp1 | a0002 | c0001 | t0001 | g0239 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02027 | hp1 | a0001 | c0005 | t0002 | g0204 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0267 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02040 | hp1 | a0002 | c0001 | t0001 | g0068 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02040 | hp2 | a0002 | c0001 | t0001 | g0293 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02055 | hp1 | a0001 | c0005 | t0002 | g0167 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02055 | hp2 | a0019 | c0038 | t0006 | g0056 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02056 | hp1 | a0002 | c0001 | t0001 | g0087 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02056 | hp2 | a0002 | c0001 | t0001 | g0216 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02071 | hp1 | a0009 | c0015 | t0003 | g0066 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02071 | hp2 | a0004 | c0003 | t0001 | g0006 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02074 | hp1 | a0002 | c0001 | t0001 | g0116 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02074 | hp2 | a0002 | c0001 | t0001 | g0273 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02080 | hp1 | a0020 | c0049 | t0001 | g0286 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02080 | hp2 | a0021 | c0034 | t0003 | g0109 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02083 | hp1 | a0001 | c0002 | t0003 | g0082 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02083 | hp2 | a0003 | c0004 | t0025 | g0307 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02129 | hp1 | a0002 | c0001 | t0001 | g0208 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02129 | hp2 | a0002 | c0001 | t0001 | g0081 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0283 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02132 | hp2 | a0002 | c0001 | t0001 | g0157 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0295 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02145 | hp1 | a0001 | c0013 | t0003 | g0137 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02145 | hp2 | a0006 | c0016 | t0009 | g0171 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0234 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02148 | hp2 | a0002 | c0001 | t0001 | g0127 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02155 | hp1 | a0001 | c0005 | t0002 | g0294 | EAS | CDX | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02155 | hp2 | a0003 | c0004 | t0002 | g0054 | EAS | CDX | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02165 | hp1 | a0002 | c0001 | t0001 | g0085 | EAS | CDX | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0064 | EAS | CDX | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0189 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02257 | hp2 | a0002 | c0001 | t0001 | g0070 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02258 | hp1 | a0007 | c0009 | t0015 | g0173 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02258 | hp2 | a0022 | c0035 | t0001 | g0329 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02273 | hp1 | a0002 | c0001 | t0001 | g0017 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02273 | hp2 | a0004 | c0003 | t0001 | g0381 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02280 | hp1 | a0023 | c0055 | t0035 | g0241 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02280 | hp2 | a0001 | c0002 | t0003 | g0326 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02293 | hp1 | a0003 | c0004 | t0002 | g0389 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02300 | hp1 | a0002 | c0001 | t0001 | g0086 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02300 | hp2 | a0002 | c0001 | t0001 | g0015 | AMR | PEL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02523 | hp1 | a0001 | c0002 | t0004 | g0045 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0297 | EAS | KHV | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02572 | hp1 | a0001 | c0005 | t0002 | g0166 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0255 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02602 | hp1 | a0002 | c0001 | t0001 | g0061 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02602 | hp2 | a0001 | c0002 | t0002 | g0019 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02615 | hp1 | a0001 | c0007 | t0007 | g0168 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02615 | hp2 | a0010 | c0014 | t0012 | g0361 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02622 | hp1 | a0001 | c0002 | t0003 | g0328 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02622 | hp2 | a0001 | c0040 | t0003 | g0190 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02630 | hp1 | a0007 | c0009 | t0015 | g0139 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02630 | hp2 | a0001 | c0010 | t0022 | g0143 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02647 | hp1 | a0001 | c0002 | t0003 | g0250 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02647 | hp2 | a0001 | c0010 | t0022 | g0185 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02683 | hp1 | a0002 | c0001 | t0001 | g0196 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0403 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0183 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02698 | hp2 | a0002 | c0001 | t0001 | g0134 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02717 | hp1 | a0001 | c0002 | t0003 | g0254 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02717 | hp2 | a0001 | c0002 | t0017 | g0363 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02723 | hp1 | a0001 | c0010 | t0003 | g0251 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02723 | hp2 | a0001 | c0002 | t0003 | g0141 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02735 | hp1 | a0002 | c0001 | t0016 | g0032 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02735 | hp2 | a0002 | c0001 | t0001 | g0013 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0301 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0321 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02809 | hp1 | a0001 | c0002 | t0005 | g0259 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02809 | hp2 | a0003 | c0027 | t0041 | g0191 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02818 | hp1 | a0001 | c0007 | t0007 | g0172 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0145 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02886 | hp1 | a0003 | c0023 | t0004 | g0037 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02886 | hp2 | a0002 | c0001 | t0001 | g0252 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02895 | hp1 | a0008 | c0012 | t0018 | g0149 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02895 | hp2 | a0001 | c0002 | t0006 | g0209 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02896 | hp1 | a0001 | c0002 | t0003 | g0258 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02896 | hp2 | a0010 | c0014 | t0012 | g0211 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02897 | hp1 | a0001 | c0002 | t0003 | g0257 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02897 | hp2 | a0008 | c0012 | t0018 | g0150 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02922 | hp1 | a0006 | c0039 | t0044 | g0144 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02922 | hp2 | a0008 | c0012 | t0001 | g0181 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02965 | hp1 | a0012 | c0047 | t0023 | g0153 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02965 | hp2 | a0001 | c0013 | t0003 | g0136 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02970 | hp1 | a0001 | c0002 | t0019 | g0200 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02970 | hp2 | a0001 | c0002 | t0006 | g0395 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02976 | hp1 | a0003 | c0011 | t0046 | g0039 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02976 | hp2 | a0002 | c0001 | t0001 | g0177 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03017 | hp1 | a0002 | c0052 | t0001 | g0156 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0197 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03041 | hp1 | a0001 | c0002 | t0006 | g0330 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03041 | hp2 | a0012 | c0046 | t0023 | g0123 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03098 | hp1 | a0001 | c0010 | t0003 | g0253 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03098 | hp2 | a0003 | c0004 | t0005 | g0202 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03130 | hp1 | a0001 | c0002 | t0003 | g0151 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03130 | hp2 | a0003 | c0025 | t0045 | g0036 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03139 | hp1 | a0006 | c0016 | t0009 | g0170 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03139 | hp2 | a0003 | c0004 | t0001 | g0388 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03195 | hp1 | a0001 | c0002 | t0003 | g0327 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03195 | hp2 | a0001 | c0007 | t0007 | g0154 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03209 | hp1 | a0001 | c0002 | t0003 | g0147 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03209 | hp2 | a0001 | c0002 | t0003 | g0311 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03225 | hp1 | a0024 | c0050 | t0032 | g0148 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03225 | hp2 | a0025 | c0045 | t0003 | g0161 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0245 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03239 | hp2 | a0001 | c0002 | t0051 | g0049 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03453 | hp1 | a0001 | c0002 | t0006 | g0159 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03453 | hp2 | a0001 | c0007 | t0007 | g0058 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0187 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03486 | hp2 | a0001 | c0007 | t0027 | g0365 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03490 | hp1 | a0026 | c0054 | t0001 | g0001 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03490 | hp2 | a0002 | c0018 | t0001 | g0004 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03491 | hp1 | a0001 | c0002 | t0004 | g0033 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03491 | hp2 | a0001 | c0002 | t0004 | g0048 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03492 | hp1 | a0001 | c0002 | t0004 | g0034 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03492 | hp2 | a0002 | c0018 | t0001 | g0004 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03516 | hp1 | a0001 | c0002 | t0047 | g0040 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03516 | hp2 | a0007 | c0009 | t0029 | g0366 | AFR | ESN | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03540 | hp1 | a0001 | c0002 | t0003 | g0152 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03540 | hp2 | a0001 | c0002 | t0005 | g0146 | AFR | GWD | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03579 | hp1 | a0001 | c0002 | t0005 | g0260 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03579 | hp2 | a0003 | c0011 | t0003 | g0398 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03654 | hp1 | a0002 | c0001 | t0021 | g0201 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03654 | hp2 | a0001 | c0002 | t0004 | g0047 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03669 | hp1 | a0001 | c0005 | t0002 | g0193 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0292 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03688 | hp1 | a0002 | c0001 | t0001 | g0128 | SAS | STU | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03688 | hp2 | a0001 | c0005 | t0002 | g0186 | SAS | STU | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03704 | hp1 | a0013 | c0019 | t0026 | g0046 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03704 | hp2 | a0001 | c0051 | t0002 | g0155 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03710 | hp1 | a0002 | c0001 | t0001 | g0062 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03710 | hp2 | a0013 | c0019 | t0026 | g0052 | SAS | PJL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03831 | hp1 | a0002 | c0001 | t0001 | g0249 | SAS | BEB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03831 | hp2 | a0003 | c0004 | t0002 | g0121 | SAS | BEB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03834 | hp1 | a0002 | c0001 | t0001 | g0111 | SAS | BEB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03834 | hp2 | a0002 | c0001 | t0001 | g0126 | SAS | BEB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03927 | hp1 | a0002 | c0001 | t0001 | g0133 | SAS | BEB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0305 | SAS | BEB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03942 | hp1 | a0001 | c0002 | t0028 | g0368 | SAS | BEB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0275 | SAS | BEB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0198 | SAS | STU | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG04115 | hp2 | a0001 | c0005 | t0002 | g0300 | SAS | STU | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG04184 | hp1 | a0002 | c0001 | t0038 | g0160 | SAS | BEB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG04184 | hp2 | a0001 | c0002 | t0004 | g0051 | SAS | BEB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG04199 | hp1 | a0002 | c0001 | t0016 | g0050 | SAS | STU | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG04199 | hp2 | a0002 | c0001 | t0001 | g0387 | SAS | STU | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG04204 | hp1 | a0014 | c0020 | t0002 | g0097 | SAS | STU | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0063 | SAS | STU | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG04228 | hp1 | a0002 | c0001 | t0001 | g0256 | SAS | STU | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG04228 | hp2 | a0014 | c0020 | t0002 | g0322 | SAS | STU | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18522 | hp1 | a0027 | c0026 | t0050 | g0038 | AFR | YRI | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18522 | hp2 | a0001 | c0002 | t0003 | g0174 | AFR | YRI | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18612 | hp1 | a0003 | c0004 | t0030 | g0028 | EAS | CHB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18612 | hp2 | a0004 | c0003 | t0011 | g0393 | EAS | CHB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18747 | hp1 | a0002 | c0001 | t0001 | g0018 | EAS | CHB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0114 | EAS | CHB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0164 | AFR | YRI | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18906 | hp2 | a0001 | c0002 | t0005 | g0055 | AFR | YRI | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18939 | hp1 | a0003 | c0004 | t0002 | g0385 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18939 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18940 | hp1 | a0005 | c0006 | t0001 | g0088 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18940 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18941 | hp1 | a0003 | c0004 | t0001 | g0384 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18941 | hp2 | a0004 | c0003 | t0001 | g0308 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18942 | hp1 | a0002 | c0001 | t0001 | g0242 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0370 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18943 | hp1 | a0002 | c0001 | t0001 | g0223 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18943 | hp2 | a0003 | c0004 | t0002 | g0122 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0372 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18944 | hp2 | a0003 | c0004 | t0002 | g0027 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18945 | hp1 | a0004 | c0003 | t0001 | g0338 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18945 | hp2 | a0005 | c0006 | t0001 | g0129 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18946 | hp1 | a0002 | c0001 | t0001 | g0182 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18946 | hp2 | a0002 | c0001 | t0001 | g0184 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18947 | hp1 | a0005 | c0006 | t0001 | g0017 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18947 | hp2 | a0002 | c0001 | t0016 | g0042 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18948 | hp1 | a0005 | c0006 | t0001 | g0264 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18948 | hp2 | a0002 | c0001 | t0001 | g0377 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18949 | hp1 | a0005 | c0006 | t0001 | g0357 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18949 | hp2 | a0002 | c0001 | t0001 | g0079 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18950 | hp1 | a0003 | c0004 | t0001 | g0021 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18950 | hp2 | a0002 | c0001 | t0011 | g0108 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18952 | hp1 | a0002 | c0001 | t0001 | g0233 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18952 | hp2 | a0002 | c0001 | t0001 | g0099 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18953 | hp1 | a0002 | c0001 | t0001 | g0094 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0302 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18954 | hp1 | a0001 | c0002 | t0043 | g0026 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18954 | hp2 | a0002 | c0001 | t0036 | g0203 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18956 | hp1 | a0003 | c0004 | t0001 | g0331 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18956 | hp2 | a0003 | c0004 | t0002 | g0005 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18960 | hp2 | a0009 | c0015 | t0003 | g0119 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18961 | hp1 | a0001 | c0002 | t0004 | g0043 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18961 | hp2 | a0002 | c0001 | t0001 | g0178 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18962 | hp1 | a0001 | c0002 | t0024 | g0026 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18962 | hp2 | a0004 | c0003 | t0001 | g0020 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18964 | hp1 | a0003 | c0004 | t0003 | g0392 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18964 | hp2 | a0003 | c0004 | t0002 | g0005 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18966 | hp1 | a0002 | c0001 | t0001 | g0371 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18966 | hp2 | a0002 | c0001 | t0001 | g0244 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18967 | hp1 | a0002 | c0001 | t0001 | g0092 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18968 | hp1 | a0003 | c0004 | t0002 | g0027 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0374 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18969 | hp2 | a0002 | c0001 | t0001 | g0353 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18970 | hp1 | a0002 | c0001 | t0010 | g0022 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18970 | hp2 | a0002 | c0001 | t0001 | g0358 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18971 | hp1 | a0001 | c0002 | t0003 | g0229 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18971 | hp2 | a0004 | c0003 | t0001 | g0333 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18973 | hp1 | a0004 | c0003 | t0001 | g0332 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18973 | hp2 | a0004 | c0003 | t0001 | g0006 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18974 | hp1 | a0002 | c0001 | t0011 | g0077 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18974 | hp2 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18975 | hp1 | a0004 | c0003 | t0001 | g0378 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18975 | hp2 | a0002 | c0001 | t0001 | g0205 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18977 | hp1 | a0005 | c0006 | t0001 | g0236 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18977 | hp2 | a0002 | c0001 | t0001 | g0237 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0355 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18979 | hp2 | a0002 | c0001 | t0001 | g0265 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18980 | hp1 | a0002 | c0001 | t0001 | g0352 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18980 | hp2 | a0001 | c0002 | t0003 | g0106 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18981 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18981 | hp2 | a0002 | c0001 | t0040 | g0298 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18982 | hp1 | a0028 | c0048 | t0001 | g0288 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0373 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18983 | hp1 | a0002 | c0001 | t0001 | g0243 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18983 | hp2 | a0002 | c0001 | t0001 | g0247 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18984 | hp1 | a0002 | c0001 | t0001 | g0350 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18984 | hp2 | a0004 | c0003 | t0001 | g0337 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18985 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18985 | hp2 | a0002 | c0001 | t0010 | g0347 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18987 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18987 | hp2 | a0001 | c0005 | t0002 | g0075 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18990 | hp1 | a0029 | c0024 | t0003 | g0120 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18990 | hp2 | a0002 | c0001 | t0001 | g0235 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18991 | hp1 | a0002 | c0001 | t0001 | g0180 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18991 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18993 | hp1 | a0002 | c0001 | t0001 | g0073 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18993 | hp2 | a0030 | c0043 | t0011 | g0383 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18997 | hp1 | a0031 | c0037 | t0003 | g0225 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA18997 | hp2 | a0005 | c0006 | t0001 | g0118 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19000 | hp1 | a0004 | c0003 | t0001 | g0309 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19000 | hp2 | a0002 | c0001 | t0001 | g0299 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19001 | hp1 | a0032 | c0021 | t0001 | g0356 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19001 | hp2 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19002 | hp1 | a0004 | c0003 | t0033 | g0272 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0379 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19003 | hp1 | a0002 | c0001 | t0001 | g0078 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19003 | hp2 | a0004 | c0028 | t0001 | g0339 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19004 | hp1 | a0003 | c0004 | t0001 | g0334 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19005 | hp1 | a0002 | c0001 | t0001 | g0282 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19005 | hp2 | a0004 | c0003 | t0001 | g0020 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19007 | hp1 | a0001 | c0005 | t0002 | g0348 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19007 | hp2 | a0004 | c0003 | t0001 | g0268 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19009 | hp1 | a0002 | c0001 | t0001 | g0104 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19009 | hp2 | a0002 | c0001 | t0001 | g0158 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19010 | hp1 | a0004 | c0003 | t0001 | g0340 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19010 | hp2 | a0002 | c0001 | t0001 | g0351 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19011 | hp1 | a0003 | c0004 | t0001 | g0380 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19030 | hp1 | a0001 | c0002 | t0006 | g0324 | AFR | LWK | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19030 | hp2 | a0033 | c0029 | t0009 | g0176 | AFR | LWK | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19043 | hp1 | a0001 | c0005 | t0020 | g0057 | AFR | LWK | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19043 | hp2 | a0001 | c0002 | t0005 | g0096 | AFR | LWK | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19054 | hp1 | a0002 | c0001 | t0001 | g0080 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19054 | hp2 | a0004 | c0003 | t0001 | g0341 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19056 | hp1 | a0001 | c0002 | t0024 | g0270 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19056 | hp2 | a0002 | c0001 | t0001 | g0022 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19062 | hp1 | a0004 | c0003 | t0001 | g0317 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19062 | hp2 | a0009 | c0015 | t0003 | g0222 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19063 | hp1 | a0001 | c0002 | t0052 | g0041 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0349 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19064 | hp2 | a0004 | c0003 | t0001 | g0382 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19065 | hp1 | a0002 | c0001 | t0001 | g0125 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19065 | hp2 | a0003 | c0004 | t0002 | g0310 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19066 | hp1 | a0004 | c0003 | t0001 | g0336 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19066 | hp2 | a0003 | c0004 | t0001 | g0021 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19068 | hp2 | a0004 | c0003 | t0001 | g0335 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19070 | hp1 | a0004 | c0003 | t0001 | g0401 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19070 | hp2 | a0002 | c0001 | t0001 | g0375 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19074 | hp1 | a0002 | c0001 | t0010 | g0344 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19074 | hp2 | a0002 | c0001 | t0001 | g0093 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19076 | hp1 | a0002 | c0001 | t0001 | g0207 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19076 | hp2 | a0003 | c0004 | t0002 | g0059 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19077 | hp1 | a0002 | c0001 | t0001 | g0090 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0296 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19078 | hp1 | a0002 | c0001 | t0001 | g0346 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19078 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19079 | hp1 | a0005 | c0006 | t0001 | g0179 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19079 | hp2 | a0002 | c0001 | t0001 | g0089 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19080 | hp1 | a0001 | c0005 | t0002 | g0276 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19080 | hp2 | a0003 | c0004 | t0002 | g0115 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19081 | hp1 | a0001 | c0002 | t0004 | g0044 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19081 | hp2 | a0002 | c0001 | t0001 | g0354 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19082 | hp1 | a0004 | c0003 | t0001 | g0386 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19082 | hp2 | a0002 | c0001 | t0001 | g0231 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19085 | hp1 | a0001 | c0002 | t0003 | g0345 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19085 | hp2 | a0002 | c0001 | t0010 | g0228 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19086 | hp1 | a0002 | c0001 | t0001 | g0124 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19086 | hp2 | a0034 | c0053 | t0001 | g0215 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19087 | hp1 | a0005 | c0006 | t0001 | g0343 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0271 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19088 | hp1 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19088 | hp2 | a0001 | c0005 | t0002 | g0277 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19240 | hp1 | a0001 | c0013 | t0003 | g0138 | AFR | YRI | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA19240 | hp2 | a0002 | c0001 | t0013 | g0367 | AFR | YRI | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA20129 | hp1 | a0001 | c0002 | t0017 | g0362 | AFR | ASW | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA20129 | hp2 | a0035 | c0031 | t0001 | g0163 | AFR | ASW | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA20752 | hp1 | a0002 | c0001 | t0001 | g0004 | EUR | TSI | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA20752 | hp2 | a0002 | c0001 | t0001 | g0014 | EUR | TSI | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA20805 | hp1 | a0002 | c0008 | t0008 | g0130 | EUR | TSI | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA20805 | hp2 | a0002 | c0001 | t0001 | g0360 | EUR | TSI | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01123 | hp1 | a0002 | c0008 | t0008 | g0009 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG01123 | hp2 | a0002 | c0001 | t0037 | g0206 | AMR | CLM | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02109 | hp1 | a0003 | c0011 | t0003 | g0397 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02109 | hp2 | a0001 | c0005 | t0020 | g0162 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02486 | hp1 | a0001 | c0002 | t0031 | g0175 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02486 | hp2 | a0001 | c0002 | t0048 | g0031 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02559 | hp1 | a0002 | c0001 | t0001 | g0289 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG02559 | hp2 | a0008 | c0033 | t0001 | g0263 | AFR | ACB | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03471 | hp1 | a0010 | c0014 | t0012 | g0364 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG03471 | hp2 | a0007 | c0009 | t0015 | g0165 | AFR | MSL | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG06807 | hp1 | a0002 | c0030 | t0001 | g0188 | AFR | USA | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
HG06807 | hp2 | a0006 | c0016 | t0009 | g0212 | AFR | USA | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA20300 | hp1 | a0001 | c0002 | t0014 | g0240 | AFR | USA | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA20300 | hp2 | a0001 | c0002 | t0003 | g0140 | AFR | USA | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA21309 | hp1 | a0001 | c0002 | t0019 | g0135 | AFR | LWK | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
NA21309 | hp2 | a0002 | c0001 | t0001 | g0359 | AFR | LWK | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
homoSapiens | chm13v2 | a0001 | c0005 | t0002 | g0067 | REF | REF | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
homoSapiens | grch38p0 | a0001 | c0002 | t0005 | g0142 | REF | REF | FHDC1_chr4_152931323_152984671 | FHDC1 | chr4 | 152931323 | 152984671 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:152943167 | C | T | 1 | a0023 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.110C>T | p.Pro37Leu | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/12 | 327/6597 | 110/3432 | 37/1143 | chr4 | 152943167 | |||
chr4:152943168 | T | TCCTCCTC others(5): Show |
1 | a0026 | 1 | HG03490.hp1 | disruptive_inframe_insertion | MODERATE | c.117_128dupTCCACCCC others(4): Show |
p.Pro40_Pro43dup | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/12 | 346/6597 | 129/3432 | 43/1143 | INFO_REALIGN_3_PRIME | chr4 | 152943168 | ||
chr4:152943271 | A | G | 1 | a0034 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.214A>G | p.Ile72Val | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/12 | 431/6597 | 214/3432 | 72/1143 | chr4 | 152943271 | |||
chr4:152943325 | C | A | 1 | a0032 | 1 | NA19001.hp1 | missense_variant | MODERATE | c.268C>A | p.His90Asn | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/12 | 485/6597 | 268/3432 | 90/1143 | chr4 | 152943325 | |||
chr4:152953514 | G | A | 5 | a0003 a0004 a0018 others(2): Show |
59 | HG00558.hp2 HG01070.hp2 HG01175.hp2 others(56): Show |
missense_variant | MODERATE | c.514G>A | p.Ala172Thr | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 3/12 | 731/6597 | 514/3432 | 172/1143 | chr4 | 152953514 | |||
chr4:152954224 | C | G | 1 | a0024 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.568C>G | p.Arg190Gly | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/12 | 785/6597 | 568/3432 | 190/1143 | chr4 | 152954224 | |||
chr4:152954225 | G | A | 1 | a0033 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.569G>A | p.Arg190Gln | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/12 | 786/6597 | 569/3432 | 190/1143 | chr4 | 152954225 | |||
chr4:152960754 | C | T | 1 | a0020 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.760C>T | p.Arg254Trp | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/12 | 977/6597 | 760/3432 | 254/1143 | chr4 | 152960754 | |||
chr4:152974687 | C | T | 2 | a0014 a0028 |
3 | HG04204.hp1 HG04228.hp2 NA18982.hp1 |
missense_variant | MODERATE | c.1396C>T | p.Arg466Trp | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1613/6597 | 1396/3432 | 466/1143 | chr4 | 152974687 | |||
chr4:152974745 | G | A | 1 | a0035 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.1454G>A | p.Arg485His | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1671/6597 | 1454/3432 | 485/1143 | chr4 | 152974745 | |||
chr4:152974760 | G | A | 1 | a0015 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.1469G>A | p.Gly490Glu | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1686/6597 | 1469/3432 | 490/1143 | chr4 | 152974760 | |||
chr4:152974834 | C | A | 1 | a0008 | 4 | HG02559.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
missense_variant | MODERATE | c.1543C>A | p.Leu515Met | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1760/6597 | 1543/3432 | 515/1143 | chr4 | 152974834 | |||
chr4:152974901 | G | A | 1 | a0011 | 2 | HG01256.hp1 HG01258.hp2 |
missense_variant | MODERATE | c.1610G>A | p.Arg537His | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1827/6597 | 1610/3432 | 537/1143 | chr4 | 152974901 | |||
chr4:152975008 | C | T | 2 | a0005 a0028 |
10 | NA18940.hp1 NA18945.hp2 NA18947.hp1 others(7): Show |
missense_variant | MODERATE | c.1717C>T | p.Arg573Trp | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1934/6597 | 1717/3432 | 573/1143 | chr4 | 152975008 | |||
chr4:152975020 | C | T | 1 | a0012 | 2 | HG02965.hp1 HG03041.hp2 |
missense_variant | MODERATE | c.1729C>T | p.Arg577Trp | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1946/6597 | 1729/3432 | 577/1143 | chr4 | 152975020 | |||
chr4:152975105 | C | T | 3 | a0013 a0023 a0027 |
4 | HG02280.hp1 HG03704.hp1 HG03710.hp2 others(1): Show |
missense_variant | MODERATE | c.1814C>T | p.Ser605Leu | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2031/6597 | 1814/3432 | 605/1143 | chr4 | 152975105 | |||
chr4:152975144 | A | T | 1 | a0025 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.1853A>T | p.Gln618Leu | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2070/6597 | 1853/3432 | 618/1143 | chr4 | 152975144 | |||
chr4:152975147 | C | A | 2 | a0007 a0018 |
5 | HG01243.hp2 HG02258.hp1 HG02630.hp1 others(2): Show |
missense_variant | MODERATE | c.1856C>A | p.Ala619Glu | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2073/6597 | 1856/3432 | 619/1143 | chr4 | 152975147 | |||
chr4:152975206 | C | T | 11 | a0002 a0004 a0005 others(8): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
missense_variant | MODERATE | c.1915C>T | p.Arg639Cys | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2132/6597 | 1915/3432 | 639/1143 | chr4 | 152975206 | |||
chr4:152975215 | G | A | 1 | a0023 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.1924G>A | p.Val642Ile | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2141/6597 | 1924/3432 | 642/1143 | chr4 | 152975215 | |||
chr4:152975228 | G | A | 1 | a0021 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.1937G>A | p.Arg646Gln | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2154/6597 | 1937/3432 | 646/1143 | chr4 | 152975228 | |||
chr4:152975294 | T | C | 1 | a0022 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.2003T>C | p.Leu668Pro | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2220/6597 | 2003/3432 | 668/1143 | chr4 | 152975294 | |||
chr4:152975491 | A | T | 3 | a0007 a0018 a0024 |
6 | HG01243.hp2 HG02258.hp1 HG02630.hp1 others(3): Show |
missense_variant | MODERATE | c.2200A>T | p.Ser734Cys | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2417/6597 | 2200/3432 | 734/1143 | chr4 | 152975491 | |||
chr4:152975539 | G | A | 1 | a0024 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.2248G>A | p.Gly750Arg | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2465/6597 | 2248/3432 | 750/1143 | chr4 | 152975539 | |||
chr4:152975830 | G | A | 1 | a0010 | 3 | HG02615.hp2 HG02896.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.2539G>A | p.Gly847Ser | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2756/6597 | 2539/3432 | 847/1143 | chr4 | 152975830 | |||
chr4:152975965 | C | T | 1 | a0030 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.2674C>T | p.Arg892Trp | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2891/6597 | 2674/3432 | 892/1143 | chr4 | 152975965 | |||
chr4:152976009 | G | A | 1 | a0016 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.2718G>A | p.Met906Ile | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2935/6597 | 2718/3432 | 906/1143 | chr4 | 152976009 | |||
chr4:152976160 | C | A | 1 | a0031 | 1 | NA18997.hp1 | missense_variant | MODERATE | c.2869C>A | p.Leu957Met | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 3086/6597 | 2869/3432 | 957/1143 | chr4 | 152976160 | |||
chr4:152976373 | G | C | 1 | a0019 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.3082G>C | p.Glu1028Gln | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 3299/6597 | 3082/3432 | 1028/1143 | chr4 | 152976373 | |||
chr4:152976538 | A | G | 2 | a0006 a0033 |
5 | HG02145.hp2 HG02922.hp1 HG03139.hp1 others(2): Show |
missense_variant | MODERATE | c.3247A>G | p.Ser1083Gly | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 3464/6597 | 3247/3432 | 1083/1143 | chr4 | 152976538 | |||
chr4:152976608 | G | A | 2 | a0009 a0029 |
4 | HG02071.hp1 NA18960.hp2 NA18990.hp1 others(1): Show |
missense_variant | MODERATE | c.3317G>A | p.Ser1106Asn | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 3534/6597 | 3317/3432 | 1106/1143 | chr4 | 152976608 | |||
chr4:152976623 | C | A | 1 | a0017 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.3332C>A | p.Ala1111Asp | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 3549/6597 | 3332/3432 | 1111/1143 | chr4 | 152976623 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:152943300 | A | C | 2 | a0001c0051 a0002c0052 |
2 | HG03017.hp1 HG03704.hp2 |
synonymous_variant | LOW | c.243A>C | p.Pro81Pro | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/12 | 460/6597 | 243/3432 | 81/1143 | chr4 | 152943300 | |||
chr4:152964952 | G | A | 1 | a0002c0030 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.1077G>A | p.Leu359Leu | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/12 | 1294/6597 | 1077/3432 | 359/1143 | chr4 | 152964952 | |||
chr4:152972475 | C | G | 1 | a0004c0028 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.1317C>G | p.Thr439Thr | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/12 | 1534/6597 | 1317/3432 | 439/1143 | chr4 | 152972475 | |||
chr4:152974683 | C | T | 1 | a0003c0027 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.1392C>T | p.His464His | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1609/6597 | 1392/3432 | 464/1143 | chr4 | 152974683 | |||
chr4:152974893 | G | A | 2 | a0001c0013 a0003c0011 |
6 | HG02109.hp1 HG02145.hp1 HG02965.hp2 others(3): Show |
synonymous_variant | LOW | c.1602G>A | p.Pro534Pro | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1819/6597 | 1602/3432 | 534/1143 | chr4 | 152974893 | |||
chr4:152975163 | C | T | 3 | a0001c0010 a0006c0016 a0033c0029 |
8 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(5): Show |
synonymous_variant | LOW | c.1872C>T | p.Ala624Ala | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2089/6597 | 1872/3432 | 624/1143 | chr4 | 152975163 | |||
chr4:152975214 | C | T | 1 | a0033c0029 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1923C>T | p.Gly641Gly | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2140/6597 | 1923/3432 | 641/1143 | chr4 | 152975214 | |||
chr4:152975286 | A | C | 1 | a0001c0040 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1995A>C | p.Pro665Pro | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2212/6597 | 1995/3432 | 665/1143 | chr4 | 152975286 | |||
chr4:152975286 | A | G | 1 | a0002c0044 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.1995A>G | p.Pro665Pro | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2212/6597 | 1995/3432 | 665/1143 | chr4 | 152975286 | |||
chr4:152975286 | A | T | 2 | a0001c0007 a0003c0025 |
7 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(4): Show |
synonymous_variant | LOW | c.1995A>T | p.Pro665Pro | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2212/6597 | 1995/3432 | 665/1143 | chr4 | 152975286 | |||
chr4:152975505 | G | A | 2 | a0012c0046 a0012c0047 |
2 | HG02965.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.2214G>A | p.Ala738Ala | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2431/6597 | 2214/3432 | 738/1143 | chr4 | 152975505 | |||
chr4:152975529 | C | G | 1 | a0002c0018 | 2 | HG03490.hp2 HG03492.hp2 |
synonymous_variant | LOW | c.2238C>G | p.Pro746Pro | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2455/6597 | 2238/3432 | 746/1143 | chr4 | 152975529 | |||
chr4:152975613 | G | C | 2 | a0001c0005 a0003c0023 |
20 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
synonymous_variant | LOW | c.2322G>C | p.Ser774Ser | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2539/6597 | 2322/3432 | 774/1143 | chr4 | 152975613 | |||
chr4:152976018 | C | G | 1 | a0002c0042 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.2727C>G | p.Thr909Thr | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2944/6597 | 2727/3432 | 909/1143 | chr4 | 152976018 | |||
chr4:152976525 | C | T | 1 | a0008c0033 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.3234C>T | p.Ala1078Ala | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 3451/6597 | 3234/3432 | 1078/1143 | chr4 | 152976525 | |||
chr4:152976618 | G | A | 17 | a0002c0001 a0002c0018 a0002c0030 others(14): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
synonymous_variant | LOW | c.3327G>A | p.Thr1109Thr | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 3544/6597 | 3327/3432 | 1109/1143 | chr4 | 152976618 | |||
chr4:152976720 | G | A | 1 | a0012c0046 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.3429G>A | p.Lys1143Lys | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 3646/6597 | 3429/3432 | 1143/1143 | chr4 | 152976720 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:152936340 | G | T | 1 | a0001c0002t0053 | 1 | HG01981.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-200G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/12 | chr4 | 152936340 | |||||||
chr4:152936344 | A | G | 12 | a0001c0002t0004 a0001c0002t0047 a0001c0002t0048 others(9): Show |
22 | HG01243.hp2 HG02486.hp2 HG02523.hp1 others(19): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-196A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/12 | chr4 | 152936344 | |||||||
chr4:152936385 | G | C | 7 | a0001c0002t0013 a0001c0002t0017 a0001c0002t0028 others(4): Show |
11 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-155G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/12 | 6673 | chr4 | 152936385 | ||||||
chr4:152943022 | G | A | 12 | a0001c0002t0004 a0001c0002t0047 a0001c0002t0048 others(9): Show |
22 | HG01243.hp2 HG02486.hp2 HG02523.hp1 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-36G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/12 | 36 | chr4 | 152943022 | ||||||
chr4:152976732 | T | C | 3 | a0001c0007t0007 a0001c0007t0027 a0003c0025t0045 |
7 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*9T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 9 | chr4 | 152976732 | ||||||
chr4:152976772 | A | G | 2 | a0001c0002t0025 a0003c0004t0025 |
2 | HG00597.hp1 HG02083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*49A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 49 | chr4 | 152976772 | ||||||
chr4:152976841 | T | C | 1 | a0008c0012t0018 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*118T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 118 | chr4 | 152976841 | ||||||
chr4:152976867 | A | G | 1 | a0006c0039t0044 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*144A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 144 | chr4 | 152976867 | ||||||
chr4:152976980 | CCT | C | 55 | a0001c0002t0001 a0001c0002t0003 a0001c0002t0013 others(52): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*259_*260delTC | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 259 | INFO_REALIGN_3_PRIME | chr4 | 152976980 | |||||
chr4:152977014 | G | A | 18 | a0001c0002t0003 a0001c0002t0017 a0001c0002t0019 others(15): Show |
45 | HG00597.hp1 HG01081.hp1 HG01891.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*291G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 291 | chr4 | 152977014 | ||||||
chr4:152977026 | A | G | 86 | a0001c0002t0001 a0001c0002t0002 a0001c0002t0003 others(83): Show |
407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
3_prime_UTR_variant | MODIFIER | c.*303A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 303 | chr4 | 152977026 | ||||||
chr4:152977053 | A | G | 1 | a0001c0002t0043 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*330A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 330 | chr4 | 152977053 | ||||||
chr4:152977110 | T | G | 1 | a0001c0005t0020 | 2 | HG02109.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*387T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 387 | chr4 | 152977110 | ||||||
chr4:152977157 | T | C | 2 | a0006c0016t0009 a0033c0029t0009 |
4 | HG02145.hp2 HG03139.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*434T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 434 | chr4 | 152977157 | ||||||
chr4:152977182 | A | G | 16 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0024 others(13): Show |
115 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*459A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 459 | chr4 | 152977182 | ||||||
chr4:152977187 | T | C | 1 | a0006c0039t0044 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*464T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 464 | chr4 | 152977187 | ||||||
chr4:152977290 | G | T | 18 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0024 others(15): Show |
118 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*567G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 567 | chr4 | 152977290 | ||||||
chr4:152977404 | G | T | 1 | a0006c0039t0044 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*681G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 681 | chr4 | 152977404 | ||||||
chr4:152977449 | T | C | 1 | a0002c0008t0008 | 5 | HG00280.hp2 HG00323.hp2 HG01109.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*726T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 726 | chr4 | 152977449 | ||||||
chr4:152977540 | C | T | 4 | a0007c0009t0015 a0007c0009t0029 a0018c0022t0049 others(1): Show |
6 | HG01243.hp2 HG02258.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*817C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 817 | chr4 | 152977540 | ||||||
chr4:152977673 | G | A | 1 | a0001c0002t0051 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*950G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 950 | chr4 | 152977673 | ||||||
chr4:152977685 | T | A | 2 | a0002c0001t0010 a0004c0003t0033 |
5 | NA18970.hp1 NA18985.hp2 NA19002.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*962T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 962 | chr4 | 152977685 | ||||||
chr4:152977876 | T | C | 1 | a0001c0002t0024 | 2 | NA18962.hp1 NA19056.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1153T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1153 | chr4 | 152977876 | ||||||
chr4:152977912 | A | G | 3 | a0008c0012t0018 a0012c0046t0023 a0012c0047t0023 |
4 | HG02895.hp1 HG02897.hp2 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1189A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1189 | chr4 | 152977912 | ||||||
chr4:152977920 | G | A | 4 | a0002c0001t0021 a0002c0001t0034 a0012c0046t0023 others(1): Show |
5 | HG00099.hp2 HG01515.hp1 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1197G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1197 | chr4 | 152977920 | ||||||
chr4:152977949 | G | A | 1 | a0024c0050t0032 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1226G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1226 | chr4 | 152977949 | ||||||
chr4:152978029 | T | C | 2 | a0023c0055t0035 a0027c0026t0050 |
2 | HG02280.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1306T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1306 | chr4 | 152978029 | ||||||
chr4:152978166 | C | T | 1 | a0001c0002t0048 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1443C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1443 | chr4 | 152978166 | ||||||
chr4:152978352 | C | G | 1 | a0002c0001t0040 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1629C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1629 | chr4 | 152978352 | ||||||
chr4:152978421 | A | C | 85 | a0001c0002t0001 a0001c0002t0002 a0001c0002t0003 others(82): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
3_prime_UTR_variant | MODIFIER | c.*1698A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1698 | chr4 | 152978421 | ||||||
chr4:152978506 | C | T | 87 | a0001c0002t0001 a0001c0002t0002 a0001c0002t0003 others(84): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
3_prime_UTR_variant | MODIFIER | c.*1783C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1783 | chr4 | 152978506 | ||||||
chr4:152978519 | G | T | 1 | a0002c0044t0039 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1796G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1796 | chr4 | 152978519 | ||||||
chr4:152978558 | TG | T | 87 | a0001c0002t0001 a0001c0002t0002 a0001c0002t0003 others(84): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
3_prime_UTR_variant | MODIFIER | c.*1838delG | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1838 | INFO_REALIGN_3_PRIME | chr4 | 152978558 | |||||
chr4:152978630 | AT | A | 6 | a0001c0002t0042 a0002c0001t0034 a0002c0001t0036 others(3): Show |
6 | HG01515.hp1 HG01978.hp2 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1917delT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 1917 | INFO_REALIGN_3_PRIME | chr4 | 152978630 | |||||
chr4:152978759 | C | T | 1 | a0002c0001t0038 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2036C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2036 | chr4 | 152978759 | ||||||
chr4:152978769 | G | A | 1 | a0002c0001t0037 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2046G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2046 | chr4 | 152978769 | ||||||
chr4:152978788 | A | C | 3 | a0013c0019t0026 a0023c0055t0035 a0027c0026t0050 |
4 | HG02280.hp1 HG03704.hp1 HG03710.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2065A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2065 | chr4 | 152978788 | ||||||
chr4:152978843 | T | C | 3 | a0002c0001t0011 a0004c0003t0011 a0030c0043t0011 |
4 | NA18612.hp2 NA18950.hp2 NA18974.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2120T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2120 | chr4 | 152978843 | ||||||
chr4:152978873 | A | G | 98 | a0001c0002t0001 a0001c0002t0002 a0001c0002t0003 others(95): Show |
429 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(426): Show |
3_prime_UTR_variant | MODIFIER | c.*2150A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2150 | chr4 | 152978873 | ||||||
chr4:152979096 | C | G | 1 | a0008c0012t0018 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2373C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2373 | chr4 | 152979096 | ||||||
chr4:152979122 | A | G | 2 | a0001c0002t0019 a0001c0002t0047 |
3 | HG02970.hp1 HG03516.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2399A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2399 | chr4 | 152979122 | ||||||
chr4:152979249 | C | G | 1 | a0006c0039t0044 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2526C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2526 | chr4 | 152979249 | ||||||
chr4:152979342 | ATCTCTAA others(8): Show |
A | 1 | a0001c0002t0052 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2620_*2634delTCTC others(11): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2620 | chr4 | 152979342 | ||||||
chr4:152979438 | G | A | 2 | a0001c0002t0014 a0001c0002t0028 |
4 | HG01070.hp1 HG01071.hp2 HG03942.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2715G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2715 | chr4 | 152979438 | ||||||
chr4:152979522 | G | A | 1 | a0003c0004t0030 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2799G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2799 | chr4 | 152979522 | ||||||
chr4:152979666 | A | G | 1 | a0006c0039t0044 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2943A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 12/12 | 2943 | chr4 | 152979666 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:152936487 | G | A | 2 | a0003c0004t0002g0005 a0003c0004t0030g0028 |
3 | NA18612.hp1 NA18956.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.-131+78G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152936487 | |||||||
chr4:152936525 | G | A | 2 | a0001c0005t0001g0029 a0001c0005t0001g0030 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-131+116G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152936525 | |||||||
chr4:152936606 | T | C | 22 | a0001c0002t0004g0033 a0001c0002t0004g0034 a0001c0002t0004g0043 others(19): Show |
22 | HG01243.hp2 HG02486.hp2 HG02523.hp1 others(19): Show |
intron_variant | MODIFIER | c.-131+197T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152936606 | |||||||
chr4:152936852 | A | T | 1 | a0002c0001t0034g0404 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-131+443A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152936852 | |||||||
chr4:152936881 | C | T | 21 | a0001c0002t0004g0033 a0001c0002t0004g0034 a0001c0002t0004g0043 others(18): Show |
21 | HG01243.hp2 HG02523.hp1 HG02735.hp1 others(18): Show |
intron_variant | MODIFIER | c.-131+472C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152936881 | |||||||
chr4:152936949 | G | T | 1 | a0001c0002t0002g0403 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-131+540G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152936949 | |||||||
chr4:152937048 | G | C | 1 | a0002c0001t0001g0053 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-131+639G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152937048 | |||||||
chr4:152937222 | G | A | 3 | a0001c0002t0004g0033 a0001c0002t0004g0034 a0002c0001t0016g0032 |
3 | HG02735.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-131+813G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152937222 | |||||||
chr4:152937330 | C | A | 1 | a0003c0004t0002g0054 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-131+921C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152937330 | |||||||
chr4:152937447 | A | G | 280 | a0001c0002t0001g0187 a0001c0002t0001g0189 a0001c0002t0001g0195 others(277): Show |
300 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.-131+1038A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152937447 | |||||||
chr4:152937496 | A | G | 1 | a0001c0002t0002g0402 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-131+1087A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152937496 | |||||||
chr4:152937590 | G | A | 1 | a0001c0002t0005g0055 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-131+1181G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152937590 | |||||||
chr4:152937713 | G | T | 1 | a0004c0003t0001g0401 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-131+1304G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152937713 | |||||||
chr4:152937945 | G | T | 1 | a0001c0002t0048g0031 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-131+1536G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152937945 | |||||||
chr4:152938070 | G | A | 3 | a0001c0005t0020g0057 a0001c0007t0007g0058 a0019c0038t0006g0056 |
3 | HG02055.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-131+1661G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938070 | |||||||
chr4:152938109 | A | T | 300 | a0001c0002t0001g0164 a0001c0002t0001g0187 a0001c0002t0001g0189 others(297): Show |
320 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.-131+1700A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938109 | |||||||
chr4:152938135 | A | G | 36 | a0001c0002t0002g0370 a0001c0002t0002g0372 a0001c0002t0002g0373 others(33): Show |
38 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.-131+1726A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938135 | |||||||
chr4:152938137 | G | T | 1 | a0002c0001t0001g0369 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-131+1728G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938137 | |||||||
chr4:152938183 | G | C | 1 | a0001c0002t0048g0031 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-131+1774G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938183 | |||||||
chr4:152938190 | C | CT | 176 | a0001c0002t0001g0255 a0001c0002t0001g0301 a0001c0002t0002g0002 others(173): Show |
191 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.-131+1797dupT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 152938190 | ||||||
chr4:152938190 | C | CTT | 9 | a0001c0002t0017g0362 a0001c0002t0017g0363 a0001c0002t0052g0041 others(6): Show |
9 | HG02615.hp2 HG02717.hp2 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.-131+1796_-131+179 others(6): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 152938190 | ||||||
chr4:152938190 | C | CTTT | 19 | a0001c0002t0004g0033 a0001c0002t0004g0034 a0001c0002t0004g0043 others(16): Show |
20 | HG01167.hp2 HG01169.hp1 HG02523.hp1 others(17): Show |
intron_variant | MODIFIER | c.-131+1795_-131+179 others(7): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 152938190 | ||||||
chr4:152938190 | CT | C | 6 | a0001c0002t0001g0164 a0001c0002t0002g0370 a0001c0002t0048g0031 others(3): Show |
6 | HG02109.hp2 HG02486.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-131+1797delT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 152938190 | ||||||
chr4:152938302 | A | T | 37 | a0001c0002t0001g0187 a0001c0002t0001g0189 a0001c0002t0001g0195 others(34): Show |
39 | HG00408.hp1 HG00735.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.-131+1893A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938302 | |||||||
chr4:152938313 | G | A | 1 | a0010c0014t0012g0211 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-131+1904G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938313 | |||||||
chr4:152938319 | G | T | 3 | a0001c0005t0020g0057 a0001c0007t0007g0058 a0019c0038t0006g0056 |
3 | HG02055.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-131+1910G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938319 | |||||||
chr4:152938409 | G | A | 2 | a0001c0002t0004g0043 a0002c0001t0016g0042 |
2 | NA18947.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.-131+2000G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938409 | |||||||
chr4:152938437 | G | C | 1 | a0003c0004t0002g0059 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-131+2028G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938437 | |||||||
chr4:152938503 | C | G | 3 | a0001c0005t0020g0057 a0001c0007t0007g0058 a0019c0038t0006g0056 |
3 | HG02055.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-131+2094C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938503 | |||||||
chr4:152938744 | G | A | 1 | a0003c0004t0002g0054 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-131+2335G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938744 | |||||||
chr4:152938766 | A | G | 3 | a0001c0002t0001g0164 a0001c0005t0020g0162 a0035c0031t0001g0163 |
3 | HG02109.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-131+2357A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938766 | |||||||
chr4:152938778 | C | G | 18 | a0001c0002t0002g0023 a0001c0002t0002g0024 a0001c0002t0002g0349 others(15): Show |
20 | HG01074.hp1 NA18939.hp2 NA18940.hp2 others(17): Show |
intron_variant | MODIFIER | c.-131+2369C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938778 | |||||||
chr4:152938951 | G | A | 1 | a0006c0016t0009g0212 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-131+2542G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938951 | |||||||
chr4:152938954 | C | G | 6 | a0001c0002t0047g0040 a0003c0011t0046g0039 a0003c0023t0004g0037 others(3): Show |
6 | HG01243.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-131+2545C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938954 | |||||||
chr4:152938982 | G | T | 278 | a0001c0002t0001g0187 a0001c0002t0001g0189 a0001c0002t0001g0195 others(275): Show |
298 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.-131+2573G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152938982 | |||||||
chr4:152939020 | G | A | 174 | a0001c0002t0001g0255 a0001c0002t0001g0301 a0001c0002t0002g0002 others(171): Show |
189 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.-131+2611G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939020 | |||||||
chr4:152939113 | C | T | 1 | a0002c0001t0001g0400 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-131+2704C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939113 | |||||||
chr4:152939152 | T | C | 15 | a0001c0002t0004g0033 a0001c0002t0004g0034 a0001c0002t0004g0043 others(12): Show |
15 | HG02523.hp1 HG02735.hp1 HG03239.hp2 others(12): Show |
intron_variant | MODIFIER | c.-131+2743T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939152 | |||||||
chr4:152939210 | G | T | 1 | a0001c0002t0006g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-131+2801G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939210 | |||||||
chr4:152939261 | AGT | A | 12 | a0003c0004t0001g0021 a0003c0004t0001g0331 a0003c0004t0001g0334 others(9): Show |
13 | NA18945.hp1 NA18950.hp1 NA18956.hp1 others(10): Show |
intron_variant | MODIFIER | c.-131+2861_-131+286 others(6): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 152939261 | ||||||
chr4:152939274 | C | G | 1 | a0002c0042t0001g0342 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-131+2865C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939274 | |||||||
chr4:152939313 | T | C | 31 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0214 others(28): Show |
35 | HG00544.hp2 HG01099.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.-131+2904T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939313 | |||||||
chr4:152939497 | G | A | 22 | a0001c0002t0004g0033 a0001c0002t0004g0034 a0001c0002t0004g0043 others(19): Show |
22 | HG01243.hp2 HG02486.hp2 HG02523.hp1 others(19): Show |
intron_variant | MODIFIER | c.-131+3088G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939497 | |||||||
chr4:152939510 | G | A | 3 | a0002c0001t0001g0178 a0002c0001t0001g0180 a0005c0006t0001g0179 |
3 | NA18961.hp2 NA18991.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-131+3101G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939510 | |||||||
chr4:152939521 | G | A | 3 | a0001c0002t0013g0025 a0001c0007t0027g0365 a0010c0014t0012g0361 |
4 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-131+3112G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939521 | |||||||
chr4:152939550 | T | C | 3 | a0001c0002t0001g0164 a0001c0005t0020g0162 a0035c0031t0001g0163 |
3 | HG02109.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-131+3141T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939550 | |||||||
chr4:152939605 | C | T | 296 | a0001c0002t0001g0164 a0001c0002t0001g0187 a0001c0002t0001g0189 others(293): Show |
316 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.-131+3196C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939605 | |||||||
chr4:152939607 | T | C | 12 | a0001c0002t0002g0370 a0001c0002t0002g0372 a0001c0002t0002g0373 others(9): Show |
12 | HG00438.hp2 HG00597.hp2 NA18942.hp2 others(9): Show |
intron_variant | MODIFIER | c.-131+3198T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939607 | |||||||
chr4:152939740 | G | A | 1 | a0008c0012t0001g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-130-3188G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939740 | |||||||
chr4:152939915 | G | A | 5 | a0001c0002t0004g0043 a0001c0002t0004g0044 a0001c0002t0004g0045 others(2): Show |
5 | HG02523.hp1 NA18947.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.-130-3013G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152939915 | |||||||
chr4:152940042 | A | G | 174 | a0001c0002t0001g0255 a0001c0002t0001g0301 a0001c0002t0002g0002 others(171): Show |
189 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.-130-2886A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940042 | |||||||
chr4:152940046 | C | T | 8 | a0001c0002t0003g0326 a0001c0002t0003g0327 a0001c0002t0003g0328 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-130-2882C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940046 | |||||||
chr4:152940049 | G | A | 1 | a0001c0002t0031g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-130-2879G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940049 | |||||||
chr4:152940071 | G | A | 3 | a0001c0002t0001g0164 a0001c0005t0020g0162 a0035c0031t0001g0163 |
3 | HG02109.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-130-2857G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940071 | |||||||
chr4:152940142 | C | G | 1 | a0001c0002t0048g0031 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-130-2786C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940142 | |||||||
chr4:152940167 | G | A | 1 | a0002c0001t0001g0213 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-130-2761G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940167 | |||||||
chr4:152940278 | G | A | 5 | a0001c0002t0002g0063 a0002c0001t0001g0060 a0002c0001t0001g0061 others(2): Show |
5 | HG01358.hp2 HG02602.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.-130-2650G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940278 | |||||||
chr4:152940752 | A | G | 2 | a0001c0002t0004g0043 a0002c0001t0016g0042 |
2 | NA18947.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.-130-2176A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940752 | |||||||
chr4:152940816 | C | T | 3 | a0001c0005t0020g0057 a0001c0007t0007g0058 a0019c0038t0006g0056 |
3 | HG02055.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-130-2112C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940816 | |||||||
chr4:152940941 | CT | C | 3 | a0001c0002t0004g0033 a0001c0002t0004g0034 a0002c0001t0016g0032 |
3 | HG02735.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-130-1986delT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940941 | |||||||
chr4:152940944 | T | C | 3 | a0001c0002t0004g0033 a0001c0002t0004g0034 a0002c0001t0016g0032 |
3 | HG02735.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-130-1984T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940944 | |||||||
chr4:152940970 | T | G | 1 | a0002c0001t0001g0178 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-130-1958T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940970 | |||||||
chr4:152940978 | A | G | 2 | a0002c0001t0001g0157 a0002c0001t0001g0158 |
2 | HG02132.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-130-1950A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152940978 | |||||||
chr4:152941101 | T | C | 1 | a0002c0001t0001g0239 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-130-1827T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152941101 | |||||||
chr4:152941198 | T | C | 3 | a0001c0005t0020g0057 a0001c0007t0007g0058 a0019c0038t0006g0056 |
3 | HG02055.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-130-1730T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152941198 | |||||||
chr4:152941721 | G | A | 1 | a0002c0001t0001g0182 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-130-1207G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152941721 | |||||||
chr4:152941801 | A | T | 22 | a0001c0002t0004g0033 a0001c0002t0004g0034 a0001c0002t0004g0043 others(19): Show |
22 | HG01243.hp2 HG02486.hp2 HG02523.hp1 others(19): Show |
intron_variant | MODIFIER | c.-130-1127A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152941801 | |||||||
chr4:152941813 | G | A | 22 | a0001c0002t0004g0033 a0001c0002t0004g0034 a0001c0002t0004g0043 others(19): Show |
22 | HG01243.hp2 HG02486.hp2 HG02523.hp1 others(19): Show |
intron_variant | MODIFIER | c.-130-1115G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152941813 | |||||||
chr4:152941903 | A | G | 1 | a0001c0002t0025g0399 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-130-1025A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152941903 | |||||||
chr4:152941922 | G | A | 1 | a0001c0002t0002g0214 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-130-1006G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152941922 | |||||||
chr4:152942062 | T | G | 37 | a0001c0002t0001g0187 a0001c0002t0001g0189 a0001c0002t0001g0195 others(34): Show |
39 | HG00408.hp1 HG00423.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.-130-866T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152942062 | |||||||
chr4:152942094 | T | A | 1 | a0001c0002t0002g0064 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-130-834T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152942094 | |||||||
chr4:152942278 | C | T | 36 | a0001c0002t0002g0370 a0001c0002t0002g0372 a0001c0002t0002g0373 others(33): Show |
38 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.-130-650C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152942278 | |||||||
chr4:152942600 | C | T | 1 | a0002c0001t0001g0323 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-130-328C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152942600 | |||||||
chr4:152942673 | A | G | 12 | a0001c0002t0002g0370 a0001c0002t0002g0372 a0001c0002t0002g0373 others(9): Show |
12 | HG00438.hp2 HG00597.hp2 NA18942.hp2 others(9): Show |
intron_variant | MODIFIER | c.-130-255A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152942673 | |||||||
chr4:152942708 | A | G | 2 | a0001c0051t0002g0155 a0002c0052t0001g0156 |
2 | HG03017.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-130-220A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 1/11 | chr4 | 152942708 | |||||||
chr4:152943747 | C | T | 2 | a0001c0002t0002g0063 a0001c0002t0002g0238 |
2 | HG02004.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.498+192C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152943747 | |||||||
chr4:152943875 | C | CA | 94 | a0001c0002t0001g0187 a0001c0002t0001g0189 a0001c0002t0001g0195 others(91): Show |
99 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.498+320_498+321ins others(1): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152943875 | |||||||
chr4:152943903 | A | C | 1 | a0032c0021t0001g0356 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.498+348A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152943903 | |||||||
chr4:152944047 | T | G | 387 | a0001c0002t0001g0103 a0001c0002t0001g0164 a0001c0002t0001g0187 others(384): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.498+492T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152944047 | |||||||
chr4:152944160 | T | G | 1 | a0025c0045t0003g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.498+605T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152944160 | |||||||
chr4:152944187 | A | T | 256 | a0001c0002t0001g0187 a0001c0002t0001g0189 a0001c0002t0001g0195 others(253): Show |
277 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.498+632A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152944187 | |||||||
chr4:152944336 | G | GA | 182 | a0001c0002t0001g0255 a0001c0002t0001g0301 a0001c0002t0002g0002 others(179): Show |
198 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.498+787dupA | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152944336 | ||||||
chr4:152944383 | T | C | 296 | a0001c0002t0001g0164 a0001c0002t0001g0187 a0001c0002t0001g0189 others(293): Show |
317 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.498+828T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152944383 | |||||||
chr4:152944396 | CACA | C | 6 | a0001c0002t0047g0040 a0003c0011t0046g0039 a0003c0023t0004g0037 others(3): Show |
6 | HG01243.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.498+861_498+863del others(3): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152944396 | ||||||
chr4:152944429 | G | A | 1 | a0008c0012t0001g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.498+874G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152944429 | |||||||
chr4:152944778 | G | A | 172 | a0001c0002t0001g0255 a0001c0002t0001g0301 a0001c0002t0002g0002 others(169): Show |
187 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.498+1223G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152944778 | |||||||
chr4:152944873 | C | A | 1 | a0001c0002t0002g0065 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.498+1318C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152944873 | |||||||
chr4:152944946 | C | G | 1 | a0014c0020t0002g0322 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.498+1391C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152944946 | |||||||
chr4:152945000 | GGTGGACC others(3): Show |
G | 3 | a0002c0001t0001g0242 a0002c0001t0001g0243 a0002c0001t0001g0244 |
3 | NA18942.hp1 NA18966.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.498+1451_498+1460d others(12): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152945000 | ||||||
chr4:152945194 | CAG | C | 9 | a0001c0002t0003g0174 a0001c0002t0005g0055 a0001c0005t0020g0057 others(6): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.498+1652_498+1653d others(4): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152945194 | ||||||
chr4:152945194 | CAGAG | C | 4 | a0001c0002t0001g0164 a0001c0005t0020g0162 a0025c0045t0003g0161 others(1): Show |
4 | HG02109.hp2 HG03225.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+1650_498+1653d others(6): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152945194 | ||||||
chr4:152945367 | T | A | 4 | a0001c0002t0019g0135 a0001c0013t0003g0136 a0001c0013t0003g0137 others(1): Show |
4 | HG02145.hp1 HG02965.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+1812T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152945367 | |||||||
chr4:152945411 | A | G | 1 | a0002c0001t0001g0210 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.498+1856A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152945411 | |||||||
chr4:152945520 | A | G | 3 | a0001c0005t0020g0057 a0001c0007t0007g0058 a0019c0038t0006g0056 |
3 | HG02055.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.498+1965A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152945520 | |||||||
chr4:152945602 | G | C | 257 | a0001c0002t0001g0187 a0001c0002t0001g0189 a0001c0002t0001g0195 others(254): Show |
278 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.498+2047G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152945602 | |||||||
chr4:152945675 | T | C | 1 | a0003c0004t0002g0054 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.498+2120T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152945675 | |||||||
chr4:152946097 | T | C | 1 | a0002c0042t0001g0342 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.498+2542T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152946097 | |||||||
chr4:152946179 | G | A | 1 | a0007c0009t0015g0139 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.498+2624G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152946179 | |||||||
chr4:152946421 | G | A | 1 | a0001c0002t0002g0245 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.498+2866G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152946421 | |||||||
chr4:152946529 | C | T | 1 | a0001c0002t0006g0330 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.498+2974C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152946529 | |||||||
chr4:152946703 | G | A | 1 | a0001c0002t0003g0246 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.498+3148G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152946703 | |||||||
chr4:152946955 | G | A | 5 | a0001c0002t0003g0326 a0001c0002t0003g0327 a0001c0002t0005g0325 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.498+3400G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152946955 | |||||||
chr4:152947177 | C | T | 1 | a0001c0002t0028g0368 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.498+3622C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152947177 | |||||||
chr4:152947216 | C | CA | 9 | a0001c0002t0002g0183 a0001c0002t0006g0330 a0001c0002t0013g0025 others(6): Show |
10 | HG01167.hp2 HG01169.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.498+3676dupA | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152947216 | ||||||
chr4:152947216 | CA | C | 6 | a0001c0002t0002g0355 a0001c0002t0006g0209 a0002c0001t0001g0134 others(3): Show |
6 | HG02698.hp2 HG02895.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.498+3676delA | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152947216 | ||||||
chr4:152947293 | T | A | 1 | a0001c0002t0002g0379 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.498+3738T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152947293 | |||||||
chr4:152947465 | T | G | 1 | a0001c0002t0002g0379 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.498+3910T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152947465 | |||||||
chr4:152947660 | T | G | 1 | a0002c0001t0001g0184 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.498+4105T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152947660 | |||||||
chr4:152947810 | AAGAG | A | 275 | a0001c0002t0001g0187 a0001c0002t0001g0189 a0001c0002t0001g0195 others(272): Show |
296 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.498+4277_498+4280d others(6): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152947810 | ||||||
chr4:152948157 | T | C | 29 | a0001c0002t0001g0187 a0001c0002t0001g0189 a0001c0002t0001g0195 others(26): Show |
31 | HG00408.hp1 HG00423.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.498+4602T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152948157 | |||||||
chr4:152948357 | C | A | 15 | a0001c0002t0004g0033 a0001c0002t0004g0034 a0001c0002t0004g0043 others(12): Show |
15 | HG02523.hp1 HG02735.hp1 HG03239.hp2 others(12): Show |
intron_variant | MODIFIER | c.498+4802C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152948357 | |||||||
chr4:152948371 | A | AC | 15 | a0001c0002t0004g0033 a0001c0002t0004g0034 a0001c0002t0004g0043 others(12): Show |
15 | HG02523.hp1 HG02735.hp1 HG03239.hp2 others(12): Show |
intron_variant | MODIFIER | c.498+4817dupC | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152948371 | ||||||
chr4:152948374 | T | A | 15 | a0001c0002t0004g0033 a0001c0002t0004g0034 a0001c0002t0004g0043 others(12): Show |
15 | HG02523.hp1 HG02735.hp1 HG03239.hp2 others(12): Show |
intron_variant | MODIFIER | c.498+4819T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152948374 | |||||||
chr4:152948439 | G | A | 10 | a0001c0002t0013g0025 a0001c0002t0017g0362 a0001c0002t0017g0363 others(7): Show |
11 | HG01167.hp2 HG01169.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.498+4884G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152948439 | |||||||
chr4:152948523 | A | G | 1 | a0001c0002t0002g0321 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.498+4968A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152948523 | |||||||
chr4:152948630 | T | A | 1 | a0001c0002t0002g0379 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.499-4869T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152948630 | |||||||
chr4:152948717 | A | G | 1 | a0002c0001t0001g0133 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.499-4782A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152948717 | |||||||
chr4:152948842 | A | G | 6 | a0001c0005t0002g0167 a0001c0005t0020g0057 a0001c0007t0007g0058 others(3): Show |
6 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.499-4657A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152948842 | |||||||
chr4:152948950 | A | T | 1 | a0002c0001t0001g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.499-4549A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152948950 | |||||||
chr4:152949090 | G | GTAA | 7 | a0001c0005t0001g0131 a0002c0001t0001g0128 a0002c0001t0001g0360 others(4): Show |
8 | HG00140.hp1 HG01256.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.499-4375_499-4373d others(5): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949090 | ||||||
chr4:152949090 | G | GTAATAA | 3 | a0001c0002t0002g0065 a0001c0002t0003g0132 a0001c0002t0003g0152 |
3 | HG01081.hp1 HG01261.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.499-4378_499-4373d others(8): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949090 | ||||||
chr4:152949090 | G | GTAATAAT others(2): Show |
3 | a0001c0007t0007g0154 a0002c0001t0037g0206 a0012c0047t0023g0153 |
3 | HG01123.hp2 HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.499-4381_499-4373d others(11): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949090 | ||||||
chr4:152949090 | GTAA | G | 12 | a0001c0002t0001g0187 a0001c0002t0001g0189 a0001c0002t0006g0159 others(9): Show |
12 | HG02109.hp2 HG02257.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.499-4375_499-4373d others(5): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949090 | ||||||
chr4:152949090 | GTAATAA | G | 4 | a0001c0002t0006g0209 a0001c0002t0017g0362 a0001c0005t0002g0186 others(1): Show |
4 | HG02647.hp2 HG02895.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-4378_499-4373d others(8): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949090 | ||||||
chr4:152949090 | GTAATAAT others(2): Show |
G | 3 | a0001c0002t0002g0183 a0006c0016t0009g0170 a0006c0016t0009g0171 |
3 | HG02145.hp2 HG02698.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.499-4381_499-4373d others(11): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949090 | ||||||
chr4:152949090 | GTAATAAT others(8): Show |
G | 1 | a0002c0001t0001g0375 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.499-4387_499-4373d others(17): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949090 | ||||||
chr4:152949090 | GTAATAAT others(11): Show |
G | 8 | a0001c0002t0002g0370 a0001c0002t0002g0372 a0001c0002t0002g0373 others(5): Show |
8 | NA18942.hp2 NA18944.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.499-4390_499-4373d others(20): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949090 | ||||||
chr4:152949090 | GTAATAAT others(14): Show |
G | 2 | a0003c0004t0001g0380 a0004c0003t0001g0381 |
2 | HG02273.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.499-4393_499-4373d others(23): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949090 | ||||||
chr4:152949106 | TAATAATA others(14): Show |
T | 1 | a0001c0002t0002g0379 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.499-4390_499-4370d others(23): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949106 | ||||||
chr4:152949106 | TAATAATA others(17): Show |
T | 1 | a0002c0001t0001g0247 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.499-4390_499-4367d others(26): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949106 | ||||||
chr4:152949106 | TAATAATA others(32): Show |
T | 1 | a0025c0045t0003g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.499-4390_499-4352d others(41): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949106 | ||||||
chr4:152949109 | TAATAATA others(11): Show |
T | 4 | a0002c0001t0001g0376 a0002c0001t0001g0400 a0004c0003t0001g0378 others(1): Show |
4 | HG00438.hp2 HG00597.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-4387_499-4370d others(20): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949109 | ||||||
chr4:152949109 | TAATAATA others(14): Show |
T | 7 | a0001c0002t0002g0232 a0001c0002t0006g0395 a0001c0007t0007g0396 others(4): Show |
7 | HG01891.hp2 HG01928.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.499-4387_499-4367d others(23): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949109 | ||||||
chr4:152949109 | TAATAATA others(17): Show |
T | 4 | a0001c0002t0002g0302 a0002c0001t0001g0208 a0002c0001t0001g0350 others(1): Show |
4 | HG02129.hp1 NA18953.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-4387_499-4364d others(26): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949109 | ||||||
chr4:152949110 | A | G | 1 | a0001c0002t0031g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.499-4389A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949110 | |||||||
chr4:152949112 | T | G | 2 | a0001c0002t0003g0082 a0002c0001t0001g0001 |
2 | HG01258.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.499-4387T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949112 | |||||||
chr4:152949112 | TAATAATA others(8): Show |
T | 1 | a0004c0003t0001g0394 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.499-4384_499-4370d others(17): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949112 | ||||||
chr4:152949112 | TAATAATA others(11): Show |
T | 4 | a0001c0002t0028g0368 a0001c0007t0007g0172 a0002c0001t0001g0256 others(1): Show |
4 | HG02818.hp1 HG03942.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.499-4384_499-4367d others(20): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949112 | ||||||
chr4:152949112 | TAATAATA others(14): Show |
T | 9 | a0001c0002t0002g0238 a0001c0005t0001g0029 a0001c0005t0001g0030 others(6): Show |
10 | HG00323.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.499-4384_499-4364d others(23): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949112 | ||||||
chr4:152949112 | TAATAATA others(17): Show |
T | 31 | a0001c0002t0002g0002 a0001c0002t0002g0023 a0001c0002t0002g0024 others(28): Show |
33 | HG00423.hp2 HG00544.hp1 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.499-4384_499-4361d others(26): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949112 | ||||||
chr4:152949112 | TAATAATA others(20): Show |
T | 1 | a0017c0041t0001g0261 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.499-4384_499-4358d others(29): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949112 | ||||||
chr4:152949113 | A | G | 1 | a0001c0002t0031g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.499-4386A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949113 | |||||||
chr4:152949115 | T | G | 7 | a0001c0002t0001g0187 a0001c0002t0003g0082 a0002c0001t0001g0001 others(4): Show |
7 | HG00140.hp2 HG01258.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.499-4384T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949115 | |||||||
chr4:152949115 | T | TAAGAAGA others(5): Show |
2 | a0002c0001t0001g0111 a0029c0024t0003g0120 |
2 | HG03834.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.499-4382_499-4381i others(14): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949115 | ||||||
chr4:152949115 | T | TAAGAAGA others(8): Show |
1 | a0002c0001t0001g0099 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.499-4382_499-4381i others(17): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949115 | ||||||
chr4:152949115 | TAATAATA others(8): Show |
T | 1 | a0001c0007t0007g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.499-4381_499-4367d others(17): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949115 | ||||||
chr4:152949115 | TAATAATA others(11): Show |
T | 3 | a0001c0002t0048g0031 a0003c0004t0006g0391 a0007c0009t0015g0173 |
3 | HG01175.hp2 HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.499-4381_499-4364d others(20): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949115 | ||||||
chr4:152949115 | TAATAATA others(14): Show |
T | 7 | a0001c0002t0013g0025 a0001c0005t0002g0276 a0002c0001t0001g0016 others(4): Show |
8 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.499-4381_499-4361d others(23): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949115 | ||||||
chr4:152949115 | TAATAATA others(17): Show |
T | 40 | a0001c0002t0001g0255 a0001c0002t0001g0301 a0001c0002t0002g0002 others(37): Show |
42 | HG00323.hp2 HG00609.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.499-4381_499-4358d others(26): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949115 | ||||||
chr4:152949115 | TAATAATA others(20): Show |
T | 3 | a0002c0001t0001g0184 a0003c0004t0002g0005 a0004c0003t0001g0006 |
4 | HG02071.hp2 NA18946.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-4381_499-4355d others(29): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949115 | ||||||
chr4:152949116 | A | G | 1 | a0001c0002t0031g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.499-4383A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949116 | |||||||
chr4:152949118 | T | G | 15 | a0001c0002t0001g0187 a0001c0002t0003g0082 a0001c0002t0019g0200 others(12): Show |
15 | HG00140.hp2 HG01258.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.499-4381T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949118 | |||||||
chr4:152949118 | T | TAAGAAG | 3 | a0001c0002t0001g0103 a0005c0006t0001g0118 a0009c0015t0003g0119 |
3 | HG00621.hp2 NA18960.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.499-4379_499-4378i others(8): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949118 | ||||||
chr4:152949118 | T | TAAGAAGA others(2): Show |
4 | a0001c0002t0005g0096 a0002c0001t0001g0078 a0002c0001t0001g0080 others(1): Show |
4 | NA19003.hp1 NA19043.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.499-4379_499-4378i others(11): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949118 | ||||||
chr4:152949118 | T | TAAGAAGA others(58): Show |
1 | a0007c0009t0015g0165 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.499-4379_499-4378i others(67): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949118 | ||||||
chr4:152949118 | T | TAAGAAGA others(67): Show |
1 | a0001c0005t0002g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.499-4379_499-4378i others(76): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949118 | ||||||
chr4:152949118 | TAATAATA others(8): Show |
T | 1 | a0001c0007t0027g0365 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.499-4378_499-4364d others(17): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949118 | ||||||
chr4:152949118 | TAATAATA others(11): Show |
T | 5 | a0001c0002t0003g0174 a0001c0002t0025g0399 a0001c0005t0002g0167 others(2): Show |
5 | HG00597.hp1 HG01070.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.499-4378_499-4361d others(20): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949118 | ||||||
chr4:152949118 | TAATAATA others(14): Show |
T | 7 | a0002c0001t0001g0273 a0002c0018t0001g0004 a0003c0004t0001g0021 others(4): Show |
8 | HG02074.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.499-4378_499-4358d others(23): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949118 | ||||||
chr4:152949118 | TAATAATA others(17): Show |
T | 53 | a0001c0002t0002g0003 a0001c0002t0002g0219 a0001c0002t0002g0226 others(50): Show |
53 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.499-4378_499-4355d others(26): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949118 | ||||||
chr4:152949119 | A | G | 1 | a0001c0002t0031g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.499-4380A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949119 | |||||||
chr4:152949121 | T | G | 29 | a0001c0002t0001g0103 a0001c0002t0001g0187 a0001c0002t0003g0082 others(26): Show |
29 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.499-4378T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949121 | |||||||
chr4:152949121 | T | TAAG | 5 | a0001c0002t0002g0403 a0002c0001t0001g0069 a0002c0001t0001g0071 others(2): Show |
5 | HG01243.hp1 HG01361.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.499-4376_499-4375i others(5): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949121 | ||||||
chr4:152949121 | T | TAAGAAG | 3 | a0001c0002t0001g0145 a0001c0002t0002g0083 a0001c0002t0002g0084 |
3 | HG02818.hp2 NA18981.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.499-4376_499-4375i others(8): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949121 | ||||||
chr4:152949121 | T | TAAGAAGA others(5): Show |
5 | a0001c0002t0002g0114 a0001c0010t0022g0143 a0002c0001t0001g0133 others(2): Show |
5 | HG02071.hp1 HG02630.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.499-4376_499-4375i others(14): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949121 | ||||||
chr4:152949121 | T | TAAGAAGA others(14): Show |
1 | a0001c0002t0003g0106 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.499-4376_499-4375i others(23): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949121 | ||||||
chr4:152949121 | T | TAAGAAGA others(17): Show |
1 | a0001c0002t0002g0100 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.499-4376_499-4375i others(26): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949121 | ||||||
chr4:152949121 | TAATAAGA others(11): Show |
T | 2 | a0001c0005t0020g0057 a0001c0007t0007g0058 |
2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.499-4375_499-4358d others(20): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949121 | ||||||
chr4:152949121 | TAATAAGA others(14): Show |
T | 4 | a0001c0002t0002g0292 a0001c0005t0002g0277 a0002c0001t0001g0291 others(1): Show |
4 | HG00741.hp1 HG01099.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-4375_499-4355d others(23): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949121 | ||||||
chr4:152949121 | TAATAAGA others(17): Show |
T | 23 | a0001c0002t0002g0218 a0001c0002t0002g0296 a0001c0002t0002g0321 others(20): Show |
24 | HG00408.hp2 HG00741.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.499-4375_499-4352d others(26): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949121 | ||||||
chr4:152949122 | A | G | 1 | a0001c0002t0031g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.499-4377A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949122 | |||||||
chr4:152949124 | T | G | 65 | a0001c0002t0001g0103 a0001c0002t0001g0145 a0001c0002t0001g0164 others(62): Show |
66 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.499-4375T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949124 | |||||||
chr4:152949124 | T | TAAGAAG | 7 | a0001c0002t0002g0105 a0001c0002t0003g0151 a0002c0001t0001g0001 others(4): Show |
9 | HG01074.hp2 HG01106.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.499-4332_499-4327d others(8): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949124 | T | TAAGAAGA others(2): Show |
7 | a0001c0002t0002g0076 a0001c0002t0002g0098 a0001c0005t0002g0193 others(4): Show |
7 | HG03041.hp2 HG03669.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.499-4335_499-4327d others(11): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949124 | T | TAAGAAGA others(5): Show |
10 | a0001c0002t0005g0146 a0002c0001t0001g0061 a0002c0001t0001g0074 others(7): Show |
10 | HG00609.hp1 HG01256.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.499-4338_499-4327d others(14): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949124 | T | TAAGAAGA others(8): Show |
2 | a0001c0002t0003g0140 a0003c0004t0002g0121 |
2 | HG03831.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.499-4341_499-4327d others(17): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949124 | T | TAATAAG | 4 | a0001c0002t0002g0063 a0001c0005t0002g0075 a0002c0001t0001g0091 others(1): Show |
4 | HG00735.hp1 HG01109.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-4373_499-4372i others(8): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949124 | T | TAATAAGA others(2): Show |
11 | a0001c0051t0002g0155 a0002c0001t0001g0089 a0002c0001t0001g0090 others(8): Show |
11 | HG00735.hp2 HG01496.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.499-4373_499-4372i others(11): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949124 | T | TAATAAGA others(5): Show |
2 | a0001c0002t0002g0008 a0002c0001t0001g0068 |
2 | HG02040.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.499-4373_499-4372i others(14): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949124 | T | TAATAAGA others(8): Show |
2 | a0001c0002t0002g0064 a0001c0002t0002g0102 |
2 | HG02165.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.499-4373_499-4372i others(17): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949124 | T | TAATAAGA others(20): Show |
1 | a0001c0002t0002g0008 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.499-4373_499-4372i others(29): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949124 | T | TAATAATA others(2): Show |
5 | a0001c0002t0003g0147 a0002c0001t0001g0110 a0002c0001t0001g0116 others(2): Show |
5 | HG01516.hp1 HG02074.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.499-4373_499-4372i others(11): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949124 | T | TAATAATA others(5): Show |
2 | a0002c0001t0001g0072 a0003c0004t0002g0059 |
2 | HG01993.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.499-4373_499-4372i others(14): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949124 | T | TAATAATA others(8): Show |
2 | a0002c0001t0001g0073 a0005c0006t0001g0088 |
2 | NA18940.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.499-4373_499-4372i others(17): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949124 | T | TAATAATA others(14): Show |
2 | a0001c0002t0003g0141 a0002c0001t0001g0124 |
2 | HG02723.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.499-4373_499-4372i others(23): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949124 | T | TAATAATA others(11): Show |
2 | a0002c0001t0001g0125 a0007c0009t0015g0139 |
2 | HG02630.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.499-4373_499-4372i others(20): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949124 | T | TGATGATG others(6): Show |
1 | a0001c0002t0031g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.499-4375_499-4374i others(15): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949124 | |||||||
chr4:152949124 | TAAG | T | 13 | a0001c0002t0001g0195 a0001c0002t0004g0033 a0001c0002t0004g0034 others(10): Show |
14 | HG00423.hp1 HG01167.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.499-4329_499-4327d others(5): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949124 | TAAGAAG | T | 4 | a0001c0002t0047g0040 a0002c0001t0001g0182 a0002c0001t0001g0205 others(1): Show |
4 | HG03516.hp1 NA18946.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-4332_499-4327d others(8): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949124 | TAAGAAGA others(2): Show |
T | 6 | a0001c0002t0002g0197 a0001c0002t0002g0198 a0001c0002t0002g0199 others(3): Show |
6 | HG00408.hp1 HG02976.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.499-4335_499-4327d others(11): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949124 | TAAGAAGA others(5): Show |
T | 1 | a0013c0019t0026g0052 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.499-4338_499-4327d others(14): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949124 | TAAGAAGA others(11): Show |
T | 4 | a0001c0002t0005g0055 a0002c0001t0001g0319 a0002c0001t0001g0320 others(1): Show |
4 | HG00280.hp1 HG01346.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-4344_499-4327d others(20): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949124 | TAAGAAGA others(14): Show |
T | 1 | a0004c0003t0001g0341 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.499-4347_499-4327d others(23): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949124 | TAAGAAGA others(17): Show |
T | 14 | a0001c0002t0002g0003 a0001c0002t0002g0230 a0001c0002t0002g0271 others(11): Show |
14 | HG00099.hp1 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.499-4350_499-4327d others(26): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949124 | ||||||
chr4:152949127 | G | T | 11 | a0001c0002t0019g0135 a0001c0005t0001g0131 a0001c0007t0007g0154 others(8): Show |
12 | HG00140.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.499-4372G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949127 | |||||||
chr4:152949130 | G | T | 14 | a0001c0002t0001g0195 a0001c0002t0004g0047 a0001c0002t0019g0135 others(11): Show |
15 | HG00423.hp1 HG01167.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.499-4369G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949130 | |||||||
chr4:152949133 | G | T | 14 | a0001c0002t0001g0195 a0001c0002t0004g0047 a0001c0002t0019g0135 others(11): Show |
14 | HG00423.hp1 HG01167.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.499-4366G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949133 | |||||||
chr4:152949136 | G | T | 9 | a0001c0002t0002g0197 a0001c0002t0002g0198 a0001c0002t0004g0047 others(6): Show |
9 | HG02976.hp1 HG03017.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.499-4363G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949136 | |||||||
chr4:152949139 | G | T | 6 | a0001c0002t0002g0198 a0002c0001t0021g0201 a0002c0001t0036g0203 others(3): Show |
6 | HG02976.hp1 HG03654.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.499-4360G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949139 | |||||||
chr4:152949140 | A | T | 1 | a0001c0002t0002g0379 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.499-4359A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949140 | |||||||
chr4:152949142 | G | T | 2 | a0003c0011t0046g0039 a0013c0019t0026g0052 |
2 | HG02976.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.499-4357G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949142 | |||||||
chr4:152949145 | G | T | 3 | a0002c0001t0001g0319 a0002c0001t0001g0320 a0013c0019t0026g0052 |
3 | HG00280.hp1 HG01346.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.499-4354G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949145 | |||||||
chr4:152949148 | G | T | 3 | a0002c0001t0001g0319 a0002c0001t0001g0320 a0004c0003t0001g0341 |
3 | HG00280.hp1 HG01346.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.499-4351G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949148 | |||||||
chr4:152949151 | G | T | 3 | a0001c0005t0001g0318 a0002c0001t0001g0320 a0004c0003t0001g0317 |
3 | HG00280.hp1 HG01192.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.499-4348G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949151 | |||||||
chr4:152949154 | G | T | 1 | a0001c0005t0001g0318 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.499-4345G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949154 | |||||||
chr4:152949157 | G | GAAGAAGA others(26): Show |
1 | a0001c0002t0031g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.499-4334_499-4333i others(35): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949157 | ||||||
chr4:152949157 | G | T | 1 | a0001c0005t0001g0318 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.499-4342G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949157 | |||||||
chr4:152949167 | A | C | 1 | a0002c0001t0037g0206 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.499-4332A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949167 | |||||||
chr4:152949170 | A | AAGAAGAA others(8): Show |
1 | a0002c0001t0038g0160 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.499-4327_499-4326i others(17): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949170 | ||||||
chr4:152949170 | A | AAGAAGAA others(5): Show |
1 | a0002c0001t0001g0060 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.499-4327_499-4326i others(14): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949170 | ||||||
chr4:152949170 | A | C | 29 | a0001c0002t0001g0187 a0001c0002t0001g0189 a0001c0002t0001g0195 others(26): Show |
31 | HG00408.hp1 HG00423.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.499-4329A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949170 | |||||||
chr4:152949173 | C | A | 4 | a0001c0002t0031g0175 a0001c0005t0002g0166 a0002c0001t0001g0068 others(1): Show |
4 | HG02040.hp1 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.499-4326C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949173 | |||||||
chr4:152949203 | T | C | 272 | a0001c0002t0001g0187 a0001c0002t0001g0189 a0001c0002t0001g0195 others(269): Show |
293 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.499-4296T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949203 | |||||||
chr4:152949204 | G | A | 1 | a0001c0010t0022g0185 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.499-4295G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949204 | |||||||
chr4:152949351 | G | A | 1 | a0002c0001t0001g0248 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.499-4148G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949351 | |||||||
chr4:152949493 | AAATAAAA others(7): Show |
A | 1 | a0001c0002t0031g0175 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.499-4004_499-3991d others(16): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949493 | ||||||
chr4:152949502 | G | A | 187 | a0001c0002t0001g0255 a0001c0002t0001g0301 a0001c0002t0002g0002 others(184): Show |
203 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.499-3997G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949502 | |||||||
chr4:152949643 | G | A | 2 | a0001c0002t0003g0140 a0001c0002t0003g0141 |
2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.499-3856G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949643 | |||||||
chr4:152949657 | G | A | 2 | a0008c0012t0001g0181 a0023c0055t0035g0241 |
2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.499-3842G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949657 | |||||||
chr4:152949693 | C | G | 11 | a0001c0005t0001g0318 a0001c0005t0002g0313 a0001c0005t0002g0314 others(8): Show |
11 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.499-3806C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949693 | |||||||
chr4:152949695 | G | A | 1 | a0002c0001t0001g0249 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.499-3804G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949695 | |||||||
chr4:152949755 | G | A | 5 | a0002c0001t0001g0007 a0002c0001t0001g0192 a0002c0001t0001g0194 others(2): Show |
6 | HG00735.hp2 HG01106.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.499-3744G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949755 | |||||||
chr4:152949836 | G | GCGTTAAT others(9): Show |
1 | a0001c0002t0002g0379 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.499-3662_499-3647d others(18): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152949836 | ||||||
chr4:152949837 | C | T | 1 | a0002c0001t0001g0205 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.499-3662C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949837 | |||||||
chr4:152949963 | G | A | 34 | a0001c0002t0002g0370 a0001c0002t0002g0372 a0001c0002t0002g0373 others(31): Show |
37 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.499-3536G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152949963 | |||||||
chr4:152950147 | A | G | 2 | a0001c0002t0003g0311 a0025c0045t0003g0161 |
2 | HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.499-3352A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152950147 | |||||||
chr4:152950188 | C | T | 155 | a0001c0002t0001g0301 a0001c0002t0002g0002 a0001c0002t0002g0003 others(152): Show |
171 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.499-3311C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152950188 | |||||||
chr4:152950232 | C | T | 1 | a0004c0003t0001g0340 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.499-3267C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152950232 | |||||||
chr4:152950252 | C | G | 2 | a0002c0001t0001g0205 a0002c0001t0036g0203 |
2 | NA18954.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.499-3247C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152950252 | |||||||
chr4:152950726 | C | T | 3 | a0002c0001t0001g0124 a0002c0001t0001g0125 a0002c0001t0001g0126 |
3 | HG03834.hp2 NA19065.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.499-2773C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152950726 | |||||||
chr4:152950785 | T | G | 1 | a0001c0002t0013g0025 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.499-2714T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152950785 | |||||||
chr4:152950798 | C | T | 4 | a0001c0002t0006g0395 a0001c0007t0007g0396 a0003c0011t0003g0397 others(1): Show |
4 | HG01891.hp2 HG02109.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-2701C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152950798 | |||||||
chr4:152950807 | C | T | 5 | a0001c0005t0002g0167 a0001c0005t0020g0057 a0001c0007t0007g0058 others(2): Show |
5 | HG02055.hp1 HG02055.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.499-2692C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152950807 | |||||||
chr4:152950876 | AG | A | 6 | a0001c0002t0003g0174 a0001c0002t0005g0055 a0001c0007t0007g0172 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.499-2621delG | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152950876 | ||||||
chr4:152951007 | C | T | 1 | a0001c0002t0002g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.499-2492C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152951007 | |||||||
chr4:152951200 | C | T | 1 | a0012c0046t0023g0123 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.499-2299C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152951200 | |||||||
chr4:152951291 | C | T | 227 | a0001c0002t0001g0164 a0001c0002t0001g0255 a0001c0002t0001g0301 others(224): Show |
245 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.499-2208C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152951291 | |||||||
chr4:152951388 | C | G | 1 | a0002c0001t0001g0269 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.499-2111C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152951388 | |||||||
chr4:152951555 | T | C | 1 | a0025c0045t0003g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.499-1944T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152951555 | |||||||
chr4:152951561 | A | G | 4 | a0001c0005t0020g0057 a0001c0007t0007g0058 a0002c0001t0001g0011 others(1): Show |
5 | HG01167.hp1 HG01192.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.499-1938A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152951561 | |||||||
chr4:152951602 | AAC | A | 8 | a0001c0002t0004g0033 a0001c0002t0004g0034 a0001c0002t0004g0044 others(5): Show |
8 | HG02523.hp1 HG02735.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.499-1895_499-1894d others(4): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 152951602 | ||||||
chr4:152951696 | T | C | 2 | a0001c0002t0006g0159 a0001c0002t0047g0040 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.499-1803T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152951696 | |||||||
chr4:152951699 | A | G | 2 | a0008c0012t0018g0149 a0008c0012t0018g0150 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.499-1800A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152951699 | |||||||
chr4:152951814 | G | A | 7 | a0001c0002t0004g0047 a0001c0002t0004g0048 a0001c0002t0004g0051 others(4): Show |
7 | HG03239.hp2 HG03491.hp2 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.499-1685G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152951814 | |||||||
chr4:152951962 | A | G | 1 | a0002c0001t0001g0134 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.499-1537A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152951962 | |||||||
chr4:152952119 | C | T | 249 | a0001c0002t0001g0189 a0001c0002t0001g0255 a0001c0002t0001g0301 others(246): Show |
268 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.499-1380C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152952119 | |||||||
chr4:152952288 | T | C | 2 | a0001c0010t0022g0185 a0008c0033t0001g0263 |
2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.499-1211T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152952288 | |||||||
chr4:152952297 | AGTTGTTT others(144): Show |
A | 2 | a0004c0003t0001g0386 a0004c0003t0033g0272 |
2 | NA19002.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.499-1201_499-1051d others(2): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152952297 | |||||||
chr4:152952703 | G | A | 1 | a0024c0050t0032g0148 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.499-796G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152952703 | |||||||
chr4:152952731 | G | C | 1 | a0012c0046t0023g0123 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.499-768G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152952731 | |||||||
chr4:152952989 | G | A | 2 | a0001c0005t0002g0167 a0001c0007t0007g0168 |
2 | HG02055.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.499-510G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152952989 | |||||||
chr4:152953003 | A | T | 1 | a0002c0001t0001g0116 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.499-496A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953003 | |||||||
chr4:152953027 | G | A | 1 | a0001c0002t0002g0403 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.499-472G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953027 | |||||||
chr4:152953038 | G | A | 3 | a0002c0001t0001g0184 a0002c0001t0001g0208 a0002c0001t0001g0273 |
3 | HG02074.hp2 HG02129.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.499-461G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953038 | |||||||
chr4:152953070 | G | A | 9 | a0001c0002t0004g0033 a0001c0002t0004g0034 a0001c0002t0004g0044 others(6): Show |
9 | HG02486.hp2 HG02523.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.499-429G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953070 | |||||||
chr4:152953086 | A | G | 3 | a0001c0005t0020g0057 a0001c0007t0007g0058 a0019c0038t0006g0056 |
3 | HG02055.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.499-413A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953086 | |||||||
chr4:152953121 | G | A | 3 | a0001c0002t0004g0051 a0002c0001t0001g0128 a0002c0001t0016g0050 |
3 | HG03688.hp1 HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.499-378G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953121 | |||||||
chr4:152953157 | C | T | 54 | a0003c0004t0001g0021 a0003c0004t0001g0331 a0003c0004t0001g0334 others(51): Show |
59 | HG00558.hp2 HG01070.hp2 HG01175.hp2 others(56): Show |
intron_variant | MODIFIER | c.499-342C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953157 | |||||||
chr4:152953181 | A | G | 1 | a0012c0046t0023g0123 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.499-318A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953181 | |||||||
chr4:152953420 | A | C | 1 | a0002c0001t0001g0068 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.499-79A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953420 | |||||||
chr4:152953424 | G | T | 2 | a0002c0001t0013g0367 a0007c0009t0029g0366 |
2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.499-75G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953424 | |||||||
chr4:152953487 | T | G | 1 | a0002c0001t0001g0274 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.499-12T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 2/11 | chr4 | 152953487 | |||||||
chr4:152953618 | C | A | 5 | a0001c0007t0027g0365 a0002c0001t0013g0367 a0007c0009t0029g0366 others(2): Show |
5 | HG02615.hp2 HG03486.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.560+58C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 3/11 | chr4 | 152953618 | |||||||
chr4:152953964 | A | C | 58 | a0001c0007t0007g0154 a0001c0010t0022g0185 a0003c0004t0001g0021 others(55): Show |
63 | HG00558.hp2 HG01070.hp2 HG01175.hp2 others(60): Show |
intron_variant | MODIFIER | c.561-253A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 3/11 | chr4 | 152953964 | |||||||
chr4:152954669 | AGAGT | A | 54 | a0003c0004t0001g0021 a0003c0004t0001g0331 a0003c0004t0001g0334 others(51): Show |
59 | HG00558.hp2 HG01070.hp2 HG01175.hp2 others(56): Show |
intron_variant | MODIFIER | c.663+354_663+357del others(4): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 152954669 | ||||||
chr4:152954694 | A | G | 180 | a0001c0002t0001g0189 a0001c0002t0001g0255 a0001c0002t0001g0301 others(177): Show |
194 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.663+375A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152954694 | |||||||
chr4:152954705 | A | G | 7 | a0001c0002t0003g0326 a0001c0002t0003g0327 a0001c0002t0005g0325 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.663+386A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152954705 | |||||||
chr4:152954861 | A | T | 1 | a0001c0002t0003g0311 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.663+542A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152954861 | |||||||
chr4:152954919 | A | G | 21 | a0001c0002t0003g0174 a0001c0002t0003g0326 a0001c0002t0003g0327 others(18): Show |
22 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.663+600A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152954919 | |||||||
chr4:152954977 | A | C | 1 | a0001c0007t0007g0154 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.663+658A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152954977 | |||||||
chr4:152955025 | C | A | 239 | a0001c0002t0001g0189 a0001c0002t0001g0255 a0001c0002t0001g0301 others(236): Show |
258 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.663+706C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955025 | |||||||
chr4:152955050 | C | G | 399 | a0001c0002t0001g0103 a0001c0002t0001g0164 a0001c0002t0001g0187 others(396): Show |
427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.663+731C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955050 | |||||||
chr4:152955051 | A | T | 1 | a0004c0003t0001g0268 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.663+732A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955051 | |||||||
chr4:152955104 | T | A | 56 | a0001c0002t0002g0275 a0001c0007t0007g0154 a0003c0004t0001g0021 others(53): Show |
61 | HG01070.hp2 HG01175.hp2 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.663+785T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955104 | |||||||
chr4:152955104 | T | TA | 6 | a0001c0002t0004g0047 a0001c0002t0004g0048 a0001c0002t0004g0051 others(3): Show |
6 | HG03239.hp2 HG03491.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.663+794dupA | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 152955104 | ||||||
chr4:152955105 | A | T | 1 | a0002c0001t0001g0306 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.663+786A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955105 | |||||||
chr4:152955141 | A | C | 1 | a0001c0002t0002g0114 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.663+822A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955141 | |||||||
chr4:152955321 | A | C | 7 | a0001c0002t0004g0047 a0001c0002t0004g0048 a0001c0002t0051g0049 others(4): Show |
7 | HG02071.hp1 HG02080.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.663+1002A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955321 | |||||||
chr4:152955587 | C | T | 1 | a0025c0045t0003g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.663+1268C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955587 | |||||||
chr4:152955760 | G | A | 1 | a0019c0038t0006g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.663+1441G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955760 | |||||||
chr4:152955798 | A | G | 1 | a0001c0002t0002g0305 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.663+1479A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955798 | |||||||
chr4:152955821 | C | G | 1 | a0002c0008t0008g0130 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.663+1502C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955821 | |||||||
chr4:152955850 | T | G | 63 | a0001c0002t0003g0152 a0001c0002t0004g0051 a0001c0010t0022g0185 others(60): Show |
68 | HG00558.hp2 HG01070.hp2 HG01175.hp2 others(65): Show |
intron_variant | MODIFIER | c.663+1531T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955850 | |||||||
chr4:152955868 | T | C | 4 | a0001c0002t0019g0135 a0001c0007t0007g0172 a0007c0009t0015g0173 others(1): Show |
4 | HG02258.hp1 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.663+1549T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955868 | |||||||
chr4:152955947 | C | T | 1 | a0002c0001t0001g0249 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.663+1628C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152955947 | |||||||
chr4:152956131 | A | C | 7 | a0001c0002t0003g0152 a0001c0002t0004g0047 a0001c0002t0004g0048 others(4): Show |
7 | HG02145.hp2 HG03139.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.663+1812A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152956131 | |||||||
chr4:152956391 | C | A | 2 | a0003c0004t0025g0307 a0004c0003t0001g0268 |
2 | HG02083.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.663+2072C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152956391 | |||||||
chr4:152956416 | C | A | 1 | a0002c0001t0001g0011 | 2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.663+2097C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152956416 | |||||||
chr4:152956869 | C | T | 2 | a0001c0005t0001g0131 a0001c0005t0001g0318 |
2 | HG00140.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.663+2550C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152956869 | |||||||
chr4:152956884 | C | T | 1 | a0001c0002t0006g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.663+2565C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152956884 | |||||||
chr4:152957236 | T | C | 4 | a0001c0002t0004g0047 a0001c0002t0004g0048 a0001c0002t0051g0049 others(1): Show |
4 | HG03239.hp2 HG03491.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.663+2917T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152957236 | |||||||
chr4:152957328 | A | G | 189 | a0001c0002t0001g0189 a0001c0002t0001g0255 a0001c0002t0001g0301 others(186): Show |
204 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.663+3009A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152957328 | |||||||
chr4:152957463 | G | A | 3 | a0001c0002t0002g0278 a0001c0002t0002g0279 a0001c0002t0002g0280 |
3 | HG01069.hp2 HG01081.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.664-3102G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152957463 | |||||||
chr4:152957876 | G | A | 1 | a0003c0004t0001g0388 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.664-2689G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152957876 | |||||||
chr4:152957918 | A | AC | 10 | a0001c0002t0003g0140 a0001c0002t0003g0141 a0001c0002t0003g0250 others(7): Show |
10 | HG02055.hp2 HG02630.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.664-2646dupC | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 152957918 | ||||||
chr4:152957920 | A | C | 286 | a0001c0002t0001g0164 a0001c0002t0001g0189 a0001c0002t0001g0255 others(283): Show |
307 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(304): Show |
intron_variant | MODIFIER | c.664-2645A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152957920 | |||||||
chr4:152957929 | A | G | 210 | a0001c0002t0001g0189 a0001c0002t0001g0255 a0001c0002t0001g0301 others(207): Show |
225 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.664-2636A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152957929 | |||||||
chr4:152958002 | T | C | 211 | a0001c0002t0001g0189 a0001c0002t0001g0255 a0001c0002t0001g0301 others(208): Show |
226 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.664-2563T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958002 | |||||||
chr4:152958027 | G | A | 1 | a0004c0003t0001g0332 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.664-2538G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958027 | |||||||
chr4:152958030 | G | A | 1 | a0012c0046t0023g0123 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.664-2535G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958030 | |||||||
chr4:152958048 | C | T | 1 | a0001c0002t0002g0355 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.664-2517C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958048 | |||||||
chr4:152958113 | T | C | 1 | a0002c0001t0001g0312 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.664-2452T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958113 | |||||||
chr4:152958222 | G | C | 10 | a0001c0002t0003g0140 a0001c0002t0003g0141 a0001c0002t0003g0250 others(7): Show |
10 | HG02055.hp2 HG02630.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.664-2343G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958222 | |||||||
chr4:152958370 | C | T | 4 | a0003c0004t0002g0005 a0003c0004t0003g0392 a0003c0004t0030g0028 others(1): Show |
6 | HG02071.hp2 NA18612.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-2195C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958370 | |||||||
chr4:152958466 | G | A | 10 | a0001c0002t0003g0140 a0001c0002t0003g0141 a0001c0002t0003g0250 others(7): Show |
10 | HG02055.hp2 HG02630.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.664-2099G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958466 | |||||||
chr4:152958500 | A | AT | 206 | a0001c0002t0001g0189 a0001c0002t0001g0255 a0001c0002t0001g0301 others(203): Show |
221 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.664-2057dupT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 152958500 | ||||||
chr4:152958556 | T | C | 10 | a0001c0002t0003g0140 a0001c0002t0003g0141 a0001c0002t0003g0250 others(7): Show |
10 | HG02055.hp2 HG02630.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.664-2009T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958556 | |||||||
chr4:152958607 | C | G | 2 | a0001c0007t0027g0365 a0010c0014t0012g0361 |
2 | HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.664-1958C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958607 | |||||||
chr4:152958726 | C | T | 207 | a0001c0002t0001g0189 a0001c0002t0001g0255 a0001c0002t0001g0301 others(204): Show |
222 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.664-1839C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958726 | |||||||
chr4:152958728 | C | G | 190 | a0001c0002t0001g0189 a0001c0002t0001g0255 a0001c0002t0001g0301 others(187): Show |
205 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.664-1837C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958728 | |||||||
chr4:152958886 | A | C | 4 | a0001c0007t0007g0154 a0001c0010t0022g0185 a0008c0033t0001g0263 others(1): Show |
4 | HG02559.hp2 HG02647.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.664-1679A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958886 | |||||||
chr4:152958945 | T | G | 5 | a0001c0002t0002g0403 a0001c0002t0004g0047 a0001c0002t0004g0048 others(2): Show |
5 | HG02683.hp2 HG03239.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.664-1620T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958945 | |||||||
chr4:152958959 | G | A | 2 | a0001c0002t0001g0164 a0001c0005t0020g0162 |
2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.664-1606G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958959 | |||||||
chr4:152958997 | A | T | 187 | a0001c0002t0001g0189 a0001c0002t0001g0255 a0001c0002t0001g0301 others(184): Show |
202 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.664-1568A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958997 | |||||||
chr4:152958999 | G | C | 10 | a0001c0002t0003g0140 a0001c0002t0003g0141 a0001c0002t0003g0250 others(7): Show |
10 | HG02055.hp2 HG02630.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.664-1566G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152958999 | |||||||
chr4:152959037 | A | G | 3 | a0001c0002t0003g0152 a0006c0016t0009g0170 a0006c0016t0009g0171 |
3 | HG02145.hp2 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.664-1528A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959037 | |||||||
chr4:152959405 | T | C | 4 | a0001c0007t0007g0154 a0001c0010t0022g0185 a0008c0033t0001g0263 others(1): Show |
4 | HG02559.hp2 HG02647.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.664-1160T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959405 | |||||||
chr4:152959439 | T | C | 2 | a0001c0005t0002g0166 a0007c0009t0015g0165 |
2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.664-1126T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959439 | |||||||
chr4:152959503 | T | C | 195 | a0001c0002t0001g0189 a0001c0002t0001g0255 a0001c0002t0001g0301 others(192): Show |
210 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.664-1062T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959503 | |||||||
chr4:152959585 | G | C | 1 | a0001c0002t0001g0164 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.664-980G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959585 | |||||||
chr4:152959594 | C | T | 195 | a0001c0002t0001g0189 a0001c0002t0001g0255 a0001c0002t0001g0301 others(192): Show |
210 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.664-971C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959594 | |||||||
chr4:152959619 | T | G | 206 | a0001c0002t0001g0189 a0001c0002t0001g0255 a0001c0002t0001g0301 others(203): Show |
221 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.664-946T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959619 | |||||||
chr4:152959627 | C | T | 3 | a0001c0002t0003g0152 a0006c0016t0009g0170 a0006c0016t0009g0171 |
3 | HG02145.hp2 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.664-938C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959627 | |||||||
chr4:152959679 | G | A | 1 | a0004c0003t0001g0308 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.664-886G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959679 | |||||||
chr4:152959723 | C | T | 262 | a0001c0002t0001g0189 a0001c0002t0001g0255 a0001c0002t0001g0301 others(259): Show |
282 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.664-842C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959723 | |||||||
chr4:152959780 | A | C | 2 | a0001c0002t0017g0362 a0025c0045t0003g0161 |
2 | HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.664-785A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959780 | |||||||
chr4:152959800 | C | T | 248 | a0001c0002t0001g0189 a0001c0002t0001g0255 a0001c0002t0001g0301 others(245): Show |
268 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.664-765C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959800 | |||||||
chr4:152959941 | A | ACATCGGT | 264 | a0001c0002t0001g0189 a0001c0002t0001g0255 a0001c0002t0001g0301 others(261): Show |
284 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.664-623_664-622ins others(7): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 152959941 | ||||||
chr4:152959947 | C | T | 1 | a0001c0002t0005g0325 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.664-618C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959947 | |||||||
chr4:152959948 | G | A | 67 | a0001c0002t0002g0217 a0001c0002t0002g0278 a0001c0002t0003g0140 others(64): Show |
70 | HG00558.hp2 HG00609.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.664-617G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152959948 | |||||||
chr4:152960036 | A | G | 1 | a0002c0001t0001g0359 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.664-529A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152960036 | |||||||
chr4:152960139 | G | A | 1 | a0001c0002t0002g0218 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.664-426G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152960139 | |||||||
chr4:152960151 | A | T | 3 | a0001c0002t0003g0152 a0006c0016t0009g0170 a0006c0016t0009g0171 |
3 | HG02145.hp2 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.664-414A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152960151 | |||||||
chr4:152960318 | C | T | 1 | a0001c0002t0006g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.664-247C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152960318 | |||||||
chr4:152960319 | G | A | 1 | a0001c0007t0007g0154 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.664-246G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 4/11 | chr4 | 152960319 | |||||||
chr4:152960683 | C | T | 141 | a0001c0002t0001g0103 a0001c0002t0001g0145 a0001c0002t0001g0301 others(138): Show |
155 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.749+33C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 5/11 | chr4 | 152960683 | |||||||
chr4:152960719 | A | G | 1 | a0002c0001t0001g0011 | 2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.750-25A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 5/11 | chr4 | 152960719 | |||||||
chr4:152960728 | C | CT | 4 | a0001c0002t0001g0145 a0001c0002t0005g0325 a0003c0011t0003g0398 others(1): Show |
4 | HG01884.hp2 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.750-10dupT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 152960728 | ||||||
chr4:152960850 | T | C | 4 | a0002c0001t0001g0070 a0002c0001t0001g0071 a0002c0001t0001g0072 others(1): Show |
4 | HG01361.hp2 HG01993.hp2 HG02257.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.850+6T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152960850 | |||||||
chr4:152960867 | G | A | 2 | a0001c0010t0022g0185 a0008c0033t0001g0263 |
2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.850+23G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152960867 | |||||||
chr4:152960905 | A | T | 278 | a0001c0002t0001g0103 a0001c0002t0001g0145 a0001c0002t0001g0164 others(275): Show |
297 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(294): Show |
intron_variant | MODIFIER | c.850+61A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152960905 | |||||||
chr4:152960906 | A | T | 1 | a0002c0001t0001g0304 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.850+62A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152960906 | |||||||
chr4:152960995 | G | C | 1 | a0001c0002t0002g0219 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.850+151G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152960995 | |||||||
chr4:152961028 | G | T | 3 | a0001c0002t0003g0106 a0005c0006t0001g0264 a0005c0006t0001g0357 |
3 | NA18948.hp1 NA18949.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.850+184G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961028 | |||||||
chr4:152961130 | G | A | 13 | a0001c0002t0004g0044 a0001c0002t0004g0045 a0001c0002t0052g0041 others(10): Show |
15 | HG00639.hp2 HG01243.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.850+286G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961130 | |||||||
chr4:152961191 | G | A | 1 | a0002c0001t0001g0249 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.850+347G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961191 | |||||||
chr4:152961246 | C | CTG | 380 | a0001c0002t0001g0103 a0001c0002t0001g0145 a0001c0002t0001g0164 others(377): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.850+403_850+404ins others(2): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 152961246 | ||||||
chr4:152961301 | C | G | 12 | a0001c0002t0004g0044 a0001c0002t0004g0045 a0001c0002t0052g0041 others(9): Show |
14 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.850+457C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961301 | |||||||
chr4:152961315 | G | C | 1 | a0001c0002t0002g0275 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.850+471G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961315 | |||||||
chr4:152961413 | C | T | 2 | a0005c0006t0001g0264 a0005c0006t0001g0357 |
2 | NA18948.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.850+569C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961413 | |||||||
chr4:152961431 | A | G | 64 | a0001c0002t0001g0145 a0001c0002t0002g0098 a0001c0002t0002g0217 others(61): Show |
67 | HG00544.hp2 HG00597.hp2 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.850+587A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961431 | |||||||
chr4:152961459 | T | C | 188 | a0001c0002t0001g0103 a0001c0002t0001g0187 a0001c0002t0001g0189 others(185): Show |
204 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.850+615T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961459 | |||||||
chr4:152961466 | G | A | 1 | a0028c0048t0001g0288 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.850+622G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961466 | |||||||
chr4:152961490 | G | A | 2 | a0001c0010t0022g0185 a0008c0033t0001g0263 |
2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.850+646G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961490 | |||||||
chr4:152961717 | T | C | 5 | a0004c0003t0001g0332 a0004c0003t0001g0336 a0004c0003t0001g0337 others(2): Show |
5 | NA18945.hp1 NA18973.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.850+873T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961717 | |||||||
chr4:152961855 | A | G | 2 | a0003c0011t0003g0398 a0008c0012t0001g0181 |
2 | HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.851-959A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961855 | |||||||
chr4:152961967 | C | T | 1 | a0003c0011t0003g0398 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.851-847C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152961967 | |||||||
chr4:152962306 | G | T | 177 | a0001c0002t0001g0103 a0001c0002t0001g0187 a0001c0002t0002g0002 others(174): Show |
192 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.851-508G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152962306 | |||||||
chr4:152962427 | G | T | 1 | a0003c0011t0003g0398 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.851-387G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152962427 | |||||||
chr4:152962498 | A | G | 2 | a0003c0011t0003g0398 a0008c0012t0001g0181 |
2 | HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.851-316A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152962498 | |||||||
chr4:152962710 | C | T | 1 | a0002c0001t0001g0216 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.851-104C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 6/11 | chr4 | 152962710 | |||||||
chr4:152962940 | G | GGT | 211 | a0001c0002t0001g0103 a0001c0002t0001g0187 a0001c0002t0001g0189 others(208): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.922-42_922-41dupGT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | ||||||
chr4:152962940 | G | GGTGT | 56 | a0001c0002t0002g0063 a0001c0002t0002g0064 a0001c0002t0002g0098 others(53): Show |
61 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.922-44_922-41dupGT others(2): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | ||||||
chr4:152962940 | G | GGTGTGT | 18 | a0001c0002t0002g0370 a0001c0002t0002g0374 a0001c0002t0005g0325 others(15): Show |
19 | HG00544.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.922-46_922-41dupGT others(4): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | ||||||
chr4:152962940 | G | GGTGTGTG others(1): Show |
12 | a0001c0002t0001g0145 a0001c0002t0001g0255 a0001c0002t0002g0105 others(9): Show |
12 | HG02572.hp1 HG02572.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.922-48_922-41dupGT others(6): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | ||||||
chr4:152962940 | G | GGTGTGTG others(3): Show |
1 | a0002c0001t0001g0126 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.922-50_922-41dupGT others(8): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | ||||||
chr4:152962940 | GGT | G | 29 | a0001c0002t0001g0164 a0001c0002t0002g0065 a0001c0002t0002g0218 others(26): Show |
30 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.922-42_922-41delGT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | ||||||
chr4:152962940 | GGTGT | G | 3 | a0001c0002t0002g0305 a0003c0027t0041g0191 a0014c0020t0002g0322 |
3 | HG02809.hp2 HG03927.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.922-44_922-41delGT others(2): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | ||||||
chr4:152962940 | GGTGTGT | G | 3 | a0002c0001t0001g0128 a0012c0046t0023g0123 a0012c0047t0023g0153 |
3 | HG02965.hp1 HG03041.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.922-46_922-41delGT others(4): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | ||||||
chr4:152962940 | GGTGTGTG others(1): Show |
G | 12 | a0001c0002t0004g0044 a0001c0002t0004g0045 a0001c0002t0052g0041 others(9): Show |
14 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.922-48_922-41delGT others(6): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | ||||||
chr4:152962940 | GGTGTGTG others(3): Show |
G | 4 | a0001c0002t0002g0114 a0001c0002t0003g0152 a0006c0016t0009g0170 others(1): Show |
4 | HG02145.hp2 HG03139.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.922-50_922-41delGT others(8): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | ||||||
chr4:152962940 | GGTGTGTG others(11): Show |
G | 1 | a0002c0001t0001g0239 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.922-58_922-41delGT others(16): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962940 | ||||||
chr4:152962947 | G | T | 2 | a0001c0002t0001g0164 a0001c0002t0003g0246 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.921+63G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | chr4 | 152962947 | |||||||
chr4:152962951 | G | T | 1 | a0002c0001t0001g0128 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.921+67G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | chr4 | 152962951 | |||||||
chr4:152962953 | G | T | 11 | a0001c0002t0004g0044 a0001c0002t0004g0045 a0001c0002t0052g0041 others(8): Show |
13 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.921+69G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | chr4 | 152962953 | |||||||
chr4:152962967 | GTGTGTGT others(9): Show |
G | 2 | a0001c0010t0022g0185 a0008c0033t0001g0263 |
2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.922-52_922-37delGT others(14): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 152962967 | ||||||
chr4:152962983 | A | G | 1 | a0002c0001t0001g0013 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.922-40A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | chr4 | 152962983 | |||||||
chr4:152963012 | G | C | 2 | a0003c0011t0003g0398 a0008c0012t0001g0181 |
2 | HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.922-11G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 7/11 | chr4 | 152963012 | |||||||
chr4:152963479 | T | C | 5 | a0001c0002t0003g0326 a0003c0011t0003g0398 a0008c0012t0001g0181 others(2): Show |
5 | HG02280.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1029+349T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963479 | |||||||
chr4:152963489 | A | G | 1 | a0004c0003t0001g0268 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1029+359A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963489 | |||||||
chr4:152963582 | AGG | A | 17 | a0001c0002t0001g0164 a0001c0002t0003g0246 a0001c0002t0004g0044 others(14): Show |
19 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1029+456_1029+457d others(4): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963582 | ||||||
chr4:152963589 | G | GGGTAATG others(69): Show |
1 | a0001c0002t0013g0025 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1029+460_1029+535d others(78): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963589 | ||||||
chr4:152963634 | T | TA | 17 | a0001c0002t0001g0164 a0001c0002t0003g0246 a0001c0002t0004g0044 others(14): Show |
19 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1029+504_1029+505i others(3): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963634 | |||||||
chr4:152963675 | G | A | 6 | a0001c0002t0002g0292 a0002c0001t0001g0004 a0002c0001t0001g0062 others(3): Show |
7 | HG00741.hp1 HG01099.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.1029+545G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963675 | |||||||
chr4:152963742 | T | A | 5 | a0001c0002t0001g0164 a0001c0002t0003g0246 a0003c0027t0041g0191 others(2): Show |
5 | HG01891.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1029+612T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963742 | |||||||
chr4:152963745 | G | T | 1 | a0004c0003t0001g0338 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1029+615G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963745 | |||||||
chr4:152963769 | G | GT | 39 | a0001c0002t0002g0008 a0001c0002t0002g0064 a0001c0002t0002g0076 others(36): Show |
41 | HG00438.hp2 HG00735.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1029+673dupT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | ||||||
chr4:152963769 | G | GTT | 15 | a0001c0002t0002g0198 a0001c0002t0005g0146 a0001c0002t0005g0259 others(12): Show |
15 | HG01109.hp2 HG02027.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.1029+672_1029+673d others(4): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | ||||||
chr4:152963769 | G | GTTT | 9 | a0001c0002t0017g0363 a0001c0005t0002g0166 a0001c0005t0002g0277 others(6): Show |
9 | HG00423.hp2 HG01074.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1029+671_1029+673d others(5): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | ||||||
chr4:152963769 | G | GTTTTTTT others(9): Show |
2 | a0001c0002t0003g0328 a0022c0035t0001g0329 |
2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1029+658_1029+673d others(18): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | ||||||
chr4:152963769 | GT | G | 18 | a0001c0002t0002g0302 a0001c0002t0003g0132 a0001c0002t0003g0152 others(15): Show |
19 | HG01081.hp1 HG01123.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1029+673delT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | ||||||
chr4:152963769 | GTT | G | 10 | a0001c0002t0019g0135 a0001c0005t0001g0029 a0001c0007t0007g0058 others(7): Show |
10 | HG01069.hp1 HG02258.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1029+672_1029+673d others(4): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | ||||||
chr4:152963769 | GTTTTT | G | 20 | a0001c0002t0001g0103 a0001c0002t0002g0105 a0001c0002t0002g0234 others(17): Show |
20 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.1029+669_1029+673d others(7): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | ||||||
chr4:152963769 | GTTTTTT | G | 147 | a0001c0002t0001g0164 a0001c0002t0001g0187 a0001c0002t0002g0002 others(144): Show |
162 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1029+668_1029+673d others(8): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | ||||||
chr4:152963769 | GTTTTTTT | G | 18 | a0001c0002t0002g0100 a0001c0002t0002g0279 a0001c0002t0004g0044 others(15): Show |
20 | HG00323.hp2 HG00639.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.1029+667_1029+673d others(9): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | ||||||
chr4:152963769 | GTTTTTTT others(5): Show |
G | 13 | a0001c0002t0001g0189 a0001c0002t0001g0255 a0001c0002t0002g0373 others(10): Show |
14 | HG00597.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1029+662_1029+673d others(14): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | ||||||
chr4:152963769 | GTTTTTTT others(6): Show |
G | 54 | a0001c0002t0002g0098 a0001c0002t0002g0217 a0001c0002t0002g0218 others(51): Show |
57 | HG00544.hp2 HG01243.hp2 HG01433.hp1 others(54): Show |
intron_variant | MODIFIER | c.1029+661_1029+673d others(15): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | ||||||
chr4:152963769 | GTTTTTTT others(7): Show |
G | 3 | a0001c0002t0001g0145 a0001c0002t0005g0325 a0006c0039t0044g0144 |
3 | HG01884.hp2 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1029+660_1029+673d others(16): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | ||||||
chr4:152963769 | GTTTTTTT others(12): Show |
G | 2 | a0001c0005t0020g0162 a0002c0001t0001g0216 |
2 | HG02056.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1029+655_1029+673d others(21): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | ||||||
chr4:152963769 | GTTTTTTT others(15): Show |
G | 1 | a0006c0016t0009g0170 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1029+652_1029+673d others(24): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 152963769 | ||||||
chr4:152963780 | T | G | 1 | a0005c0006t0001g0179 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1029+650T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963780 | |||||||
chr4:152963783 | T | G | 2 | a0001c0005t0002g0075 a0001c0010t0022g0143 |
2 | HG02630.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1029+653T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963783 | |||||||
chr4:152963784 | T | G | 4 | a0001c0002t0019g0135 a0001c0007t0007g0058 a0001c0007t0007g0154 others(1): Show |
4 | HG02258.hp1 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1029+654T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963784 | |||||||
chr4:152963785 | T | G | 1 | a0001c0002t0002g0372 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1029+655T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963785 | |||||||
chr4:152963786 | T | G | 1 | a0024c0050t0032g0148 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1029+656T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963786 | |||||||
chr4:152963787 | T | G | 1 | a0004c0003t0001g0333 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1029+657T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963787 | |||||||
chr4:152963788 | T | G | 2 | a0001c0005t0002g0075 a0003c0004t0025g0307 |
2 | HG02083.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1029+658T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963788 | |||||||
chr4:152963913 | C | T | 12 | a0001c0002t0004g0044 a0001c0002t0004g0045 a0001c0002t0052g0041 others(9): Show |
14 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1029+783C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963913 | |||||||
chr4:152963986 | A | C | 24 | a0001c0002t0002g0098 a0001c0002t0002g0218 a0001c0002t0002g0372 others(21): Show |
24 | HG00597.hp2 HG01433.hp1 HG01978.hp2 others(21): Show |
intron_variant | MODIFIER | c.1029+856A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963986 | |||||||
chr4:152963999 | A | T | 3 | a0003c0027t0041g0191 a0012c0046t0023g0123 a0012c0047t0023g0153 |
3 | HG02809.hp2 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1029+869A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152963999 | |||||||
chr4:152964066 | G | A | 1 | a0002c0001t0001g0061 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1030-839G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152964066 | |||||||
chr4:152964089 | C | T | 1 | a0004c0003t0001g0317 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1030-816C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152964089 | |||||||
chr4:152964203 | G | A | 1 | a0002c0001t0001g0196 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1030-702G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152964203 | |||||||
chr4:152964240 | C | T | 14 | a0001c0002t0001g0164 a0001c0002t0003g0246 a0001c0002t0004g0044 others(11): Show |
16 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1030-665C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152964240 | |||||||
chr4:152964506 | ATGGCTCC others(1): Show |
A | 3 | a0002c0001t0001g0072 a0002c0001t0001g0111 a0002c0001t0001g0134 |
3 | HG01993.hp2 HG02698.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1030-398_1030-391d others(10): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152964506 | |||||||
chr4:152964647 | T | G | 2 | a0001c0002t0001g0164 a0001c0002t0003g0246 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1030-258T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 8/11 | chr4 | 152964647 | |||||||
chr4:152965236 | T | G | 310 | a0001c0002t0001g0103 a0001c0002t0001g0145 a0001c0002t0001g0164 others(307): Show |
332 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.1100+261T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965236 | |||||||
chr4:152965254 | C | T | 4 | a0002c0001t0013g0367 a0006c0016t0009g0212 a0007c0009t0029g0366 others(1): Show |
4 | HG03516.hp2 HG06807.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1100+279C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965254 | |||||||
chr4:152965397 | T | G | 17 | a0001c0002t0001g0164 a0001c0002t0003g0246 a0001c0002t0004g0044 others(14): Show |
19 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1100+422T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965397 | |||||||
chr4:152965402 | G | A | 2 | a0002c0001t0001g0007 a0002c0001t0016g0032 |
3 | HG01516.hp2 HG01517.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1100+427G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965402 | |||||||
chr4:152965414 | G | T | 1 | a0002c0001t0001g0351 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1100+439G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965414 | |||||||
chr4:152965546 | T | C | 1 | a0010c0014t0012g0364 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1100+571T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965546 | |||||||
chr4:152965587 | A | G | 2 | a0001c0010t0022g0185 a0008c0033t0001g0263 |
2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1100+612A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965587 | |||||||
chr4:152965767 | A | G | 18 | a0001c0002t0001g0164 a0001c0002t0001g0255 a0001c0002t0003g0246 others(15): Show |
20 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1100+792A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965767 | |||||||
chr4:152965799 | G | A | 1 | a0001c0002t0002g0199 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1100+824G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965799 | |||||||
chr4:152965893 | C | T | 1 | a0001c0005t0020g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1100+918C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965893 | |||||||
chr4:152965918 | C | T | 3 | a0001c0002t0042g0224 a0002c0001t0001g0306 a0004c0003t0001g0382 |
3 | HG01433.hp1 HG01978.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1100+943C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965918 | |||||||
chr4:152965936 | C | A | 3 | a0003c0027t0041g0191 a0012c0046t0023g0123 a0012c0047t0023g0153 |
3 | HG02809.hp2 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1100+961C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152965936 | |||||||
chr4:152966324 | G | A | 1 | a0002c0001t0001g0128 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1100+1349G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152966324 | |||||||
chr4:152966536 | T | A | 2 | a0001c0002t0003g0151 a0001c0040t0003g0190 |
2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1101-1444T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152966536 | |||||||
chr4:152966576 | C | T | 1 | a0003c0004t0030g0028 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1101-1404C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152966576 | |||||||
chr4:152966665 | C | T | 17 | a0001c0002t0001g0164 a0001c0002t0003g0246 a0001c0002t0004g0044 others(14): Show |
19 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1101-1315C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152966665 | |||||||
chr4:152966989 | G | A | 1 | a0034c0053t0001g0215 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1101-991G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152966989 | |||||||
chr4:152967007 | T | C | 296 | a0001c0002t0001g0103 a0001c0002t0001g0145 a0001c0002t0001g0187 others(293): Show |
316 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1101-973T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967007 | |||||||
chr4:152967054 | G | T | 1 | a0002c0001t0040g0298 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1101-926G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967054 | |||||||
chr4:152967069 | A | G | 1 | a0002c0001t0001g0128 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1101-911A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967069 | |||||||
chr4:152967104 | A | G | 2 | a0002c0001t0001g0014 a0002c0008t0008g0303 |
3 | HG00323.hp2 HG00639.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1101-876A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967104 | |||||||
chr4:152967155 | G | A | 12 | a0001c0002t0004g0044 a0001c0002t0004g0045 a0001c0002t0052g0041 others(9): Show |
14 | HG00323.hp2 HG00639.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1101-825G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967155 | |||||||
chr4:152967254 | C | T | 28 | a0001c0002t0001g0301 a0001c0002t0002g0065 a0001c0002t0002g0379 others(25): Show |
29 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.1101-726C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967254 | |||||||
chr4:152967426 | C | CA | 14 | a0001c0002t0004g0044 a0001c0002t0004g0045 a0001c0002t0052g0041 others(11): Show |
16 | HG00639.hp2 HG01243.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.1101-542dupA | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 152967426 | ||||||
chr4:152967488 | C | T | 293 | a0001c0002t0001g0103 a0001c0002t0001g0145 a0001c0002t0001g0187 others(290): Show |
314 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(311): Show |
intron_variant | MODIFIER | c.1101-492C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967488 | |||||||
chr4:152967697 | C | G | 2 | a0001c0002t0003g0328 a0022c0035t0001g0329 |
2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1101-283C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967697 | |||||||
chr4:152967711 | C | A | 3 | a0001c0005t0002g0166 a0010c0014t0012g0211 a0010c0014t0012g0364 |
3 | HG02572.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1101-269C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967711 | |||||||
chr4:152967711 | C | T | 1 | a0002c0001t0001g0306 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1101-269C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967711 | |||||||
chr4:152967734 | T | A | 101 | a0001c0002t0001g0145 a0001c0002t0001g0189 a0001c0002t0001g0255 others(98): Show |
106 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.1101-246T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967734 | |||||||
chr4:152967734 | T | C | 1 | a0001c0007t0007g0396 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1101-246T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967734 | |||||||
chr4:152967755 | C | G | 1 | a0002c0001t0001g0061 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1101-225C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967755 | |||||||
chr4:152967827 | A | G | 3 | a0001c0002t0003g0152 a0006c0016t0009g0170 a0006c0016t0009g0171 |
3 | HG02145.hp2 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1101-153A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967827 | |||||||
chr4:152967943 | T | C | 41 | a0001c0002t0001g0103 a0001c0002t0002g0008 a0001c0002t0002g0302 others(38): Show |
43 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1101-37T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 9/11 | chr4 | 152967943 | |||||||
chr4:152968113 | A | G | 56 | a0001c0002t0001g0145 a0001c0002t0001g0255 a0001c0002t0002g0063 others(53): Show |
59 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.1218+16A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968113 | |||||||
chr4:152968158 | G | C | 3 | a0001c0007t0027g0365 a0008c0033t0001g0263 a0035c0031t0001g0163 |
3 | HG02559.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1218+61G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968158 | |||||||
chr4:152968259 | G | A | 1 | a0003c0004t0001g0388 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1218+162G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968259 | |||||||
chr4:152968293 | A | AT | 14 | a0001c0002t0001g0301 a0001c0002t0014g0012 a0001c0002t0014g0240 others(11): Show |
16 | HG01070.hp1 HG01071.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1218+208dupT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 152968293 | ||||||
chr4:152968295 | T | A | 2 | a0013c0019t0026g0046 a0013c0019t0026g0052 |
2 | HG03704.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1218+198T>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968295 | |||||||
chr4:152968310 | C | T | 301 | a0001c0002t0001g0103 a0001c0002t0001g0195 a0001c0002t0001g0255 others(298): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.1218+213C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968310 | |||||||
chr4:152968388 | C | T | 19 | a0001c0002t0002g0065 a0001c0002t0002g0183 a0001c0002t0003g0106 others(16): Show |
19 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1218+291C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968388 | |||||||
chr4:152968454 | T | G | 232 | a0001c0002t0001g0103 a0001c0002t0001g0145 a0001c0002t0001g0164 others(229): Show |
244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1218+357T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968454 | |||||||
chr4:152968517 | C | T | 1 | a0021c0034t0003g0109 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1218+420C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968517 | |||||||
chr4:152968519 | C | T | 1 | a0023c0055t0035g0241 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1218+422C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968519 | |||||||
chr4:152968520 | G | A | 379 | a0001c0002t0001g0103 a0001c0002t0001g0145 a0001c0002t0001g0164 others(376): Show |
407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.1218+423G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968520 | |||||||
chr4:152968622 | G | A | 1 | a0001c0002t0002g0226 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1218+525G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968622 | |||||||
chr4:152968741 | G | T | 2 | a0002c0001t0001g0093 a0004c0003t0001g0337 |
2 | NA18984.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1218+644G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968741 | |||||||
chr4:152968794 | T | C | 1 | a0002c0001t0001g0194 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1218+697T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968794 | |||||||
chr4:152968796 | G | A | 7 | a0003c0025t0045g0036 a0007c0009t0015g0139 a0007c0009t0015g0165 others(4): Show |
7 | HG01243.hp2 HG02258.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218+699G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968796 | |||||||
chr4:152968954 | G | A | 258 | a0001c0002t0001g0103 a0001c0002t0001g0145 a0001c0002t0001g0164 others(255): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1218+857G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968954 | |||||||
chr4:152968975 | G | A | 53 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0008 others(50): Show |
62 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1218+878G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152968975 | |||||||
chr4:152969039 | T | C | 2 | a0002c0001t0001g0079 a0002c0001t0016g0042 |
2 | NA18947.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1218+942T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969039 | |||||||
chr4:152969051 | C | T | 1 | a0001c0002t0002g0379 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1218+954C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969051 | |||||||
chr4:152969052 | G | A | 1 | a0002c0001t0034g0404 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1218+955G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969052 | |||||||
chr4:152969066 | A | G | 1 | a0003c0004t0002g0122 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1218+969A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969066 | |||||||
chr4:152969086 | TA | T | 30 | a0001c0002t0001g0164 a0001c0002t0001g0187 a0001c0002t0001g0255 others(27): Show |
31 | HG01167.hp2 HG01168.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.1218+1004delA | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 152969086 | ||||||
chr4:152969120 | T | G | 1 | a0001c0005t0002g0294 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1218+1023T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969120 | |||||||
chr4:152969369 | C | A | 13 | a0001c0010t0003g0251 a0001c0010t0003g0253 a0001c0010t0022g0143 others(10): Show |
13 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1218+1272C>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969369 | |||||||
chr4:152969494 | C | T | 271 | a0001c0002t0001g0103 a0001c0002t0001g0145 a0001c0002t0001g0189 others(268): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.1218+1397C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969494 | |||||||
chr4:152969641 | C | T | 210 | a0001c0002t0002g0065 a0001c0002t0002g0183 a0001c0005t0001g0029 others(207): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1218+1544C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969641 | |||||||
chr4:152969665 | G | GT | 61 | a0001c0002t0002g0024 a0001c0002t0002g0076 a0001c0002t0002g0084 others(58): Show |
62 | HG00438.hp2 HG00621.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1218+1587dupT | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 152969665 | ||||||
chr4:152969665 | G | T | 3 | a0002c0001t0001g0085 a0002c0001t0001g0223 a0004c0003t0001g0401 |
3 | HG02165.hp1 NA18943.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1218+1568G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969665 | |||||||
chr4:152969672 | T | C | 8 | a0001c0002t0001g0195 a0001c0002t0001g0301 a0003c0004t0001g0021 others(5): Show |
9 | HG01168.hp1 HG02738.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.1218+1575T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969672 | |||||||
chr4:152969684 | T | C | 1 | a0001c0002t0005g0325 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1218+1587T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969684 | |||||||
chr4:152969732 | C | T | 40 | a0001c0002t0003g0082 a0001c0002t0003g0106 a0001c0002t0003g0132 others(37): Show |
40 | HG00597.hp1 HG01081.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.1218+1635C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969732 | |||||||
chr4:152969870 | C | T | 186 | a0001c0007t0027g0365 a0002c0001t0001g0001 a0002c0001t0001g0004 others(183): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.1218+1773C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969870 | |||||||
chr4:152969871 | G | A | 8 | a0001c0010t0003g0251 a0001c0010t0003g0253 a0001c0010t0022g0143 others(5): Show |
8 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1218+1774G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969871 | |||||||
chr4:152969916 | A | G | 401 | a0001c0002t0001g0103 a0001c0002t0001g0145 a0001c0002t0001g0164 others(398): Show |
429 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(426): Show |
intron_variant | MODIFIER | c.1218+1819A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969916 | |||||||
chr4:152969989 | C | T | 1 | a0035c0031t0001g0163 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1218+1892C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152969989 | |||||||
chr4:152970120 | A | T | 2 | a0002c0001t0001g0007 a0002c0001t0016g0032 |
3 | HG01516.hp2 HG01517.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1218+2023A>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152970120 | |||||||
chr4:152970171 | T | C | 6 | a0001c0002t0001g0189 a0001c0007t0007g0058 a0001c0007t0007g0154 others(3): Show |
6 | HG01891.hp2 HG02257.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1218+2074T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152970171 | |||||||
chr4:152970502 | C | T | 1 | a0001c0007t0027g0365 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1219-1875C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152970502 | |||||||
chr4:152970541 | G | C | 1 | a0001c0002t0003g0229 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1219-1836G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152970541 | |||||||
chr4:152970632 | A | G | 2 | a0001c0013t0003g0136 a0001c0013t0003g0138 |
2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1219-1745A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152970632 | |||||||
chr4:152970789 | G | A | 1 | a0001c0002t0003g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1219-1588G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152970789 | |||||||
chr4:152971150 | G | T | 38 | a0001c0002t0003g0082 a0001c0002t0003g0106 a0001c0002t0003g0140 others(35): Show |
38 | HG00597.hp1 HG01891.hp1 HG02083.hp1 others(35): Show |
intron_variant | MODIFIER | c.1219-1227G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971150 | |||||||
chr4:152971152 | G | A | 1 | a0035c0031t0001g0163 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1219-1225G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971152 | |||||||
chr4:152971209 | A | C | 1 | a0004c0003t0001g0341 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1219-1168A>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971209 | |||||||
chr4:152971273 | T | C | 7 | a0001c0002t0001g0103 a0001c0002t0001g0145 a0006c0039t0044g0144 others(4): Show |
7 | HG00621.hp2 HG02559.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1219-1104T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971273 | |||||||
chr4:152971519 | C | T | 2 | a0002c0001t0001g0093 a0004c0003t0001g0337 |
2 | NA18984.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1219-858C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971519 | |||||||
chr4:152971532 | C | T | 1 | a0001c0002t0001g0103 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1219-845C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971532 | |||||||
chr4:152971543 | T | C | 2 | a0012c0046t0023g0123 a0012c0047t0023g0153 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1219-834T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971543 | |||||||
chr4:152971704 | A | G | 190 | a0001c0002t0003g0132 a0002c0001t0001g0001 a0002c0001t0001g0004 others(187): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1219-673A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971704 | |||||||
chr4:152971786 | C | T | 2 | a0002c0001t0001g0007 a0002c0001t0016g0032 |
3 | HG01516.hp2 HG01517.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1219-591C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971786 | |||||||
chr4:152971850 | G | C | 1 | a0002c0001t0001g0111 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1219-527G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971850 | |||||||
chr4:152971920 | A | G | 125 | a0001c0002t0001g0164 a0001c0002t0001g0187 a0001c0002t0001g0255 others(122): Show |
138 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.1219-457A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971920 | |||||||
chr4:152971945 | A | G | 20 | a0001c0005t0001g0029 a0001c0005t0001g0030 a0001c0005t0001g0131 others(17): Show |
20 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1219-432A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152971945 | |||||||
chr4:152972113 | G | A | 249 | a0001c0002t0001g0103 a0001c0002t0003g0082 a0001c0002t0003g0106 others(246): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1219-264G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152972113 | |||||||
chr4:152972190 | G | T | 1 | a0001c0002t0005g0260 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1219-187G>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152972190 | |||||||
chr4:152972202 | G | A | 181 | a0002c0001t0001g0001 a0002c0001t0001g0004 a0002c0001t0001g0007 others(178): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1219-175G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152972202 | |||||||
chr4:152972317 | C | G | 1 | a0006c0039t0044g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1219-60C>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152972317 | |||||||
chr4:152972325 | C | T | 1 | a0006c0039t0044g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1219-52C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 10/11 | chr4 | 152972325 | |||||||
chr4:152972706 | T | C | 8 | a0001c0010t0003g0251 a0001c0010t0003g0253 a0001c0010t0022g0143 others(5): Show |
8 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1383+165T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152972706 | |||||||
chr4:152972957 | C | T | 3 | a0001c0002t0004g0033 a0001c0002t0004g0034 a0001c0002t0051g0049 |
3 | HG03239.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1383+416C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152972957 | |||||||
chr4:152972990 | G | C | 1 | a0001c0002t0003g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1383+449G>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152972990 | |||||||
chr4:152973047 | C | T | 21 | a0001c0005t0001g0029 a0001c0005t0001g0030 a0001c0005t0001g0131 others(18): Show |
22 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1383+506C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152973047 | |||||||
chr4:152973091 | G | A | 256 | a0001c0002t0001g0103 a0001c0002t0003g0082 a0001c0002t0003g0106 others(253): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1383+550G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152973091 | |||||||
chr4:152973229 | T | C | 50 | a0001c0002t0003g0082 a0001c0002t0003g0106 a0001c0002t0003g0132 others(47): Show |
50 | HG00597.hp1 HG01081.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.1383+688T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152973229 | |||||||
chr4:152973282 | C | T | 1 | a0001c0002t0001g0255 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1383+741C>T | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152973282 | |||||||
chr4:152973727 | A | G | 2 | a0001c0002t0031g0175 a0003c0027t0041g0191 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1384-948A>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152973727 | |||||||
chr4:152973852 | T | G | 3 | a0006c0039t0044g0144 a0012c0046t0023g0123 a0012c0047t0023g0153 |
3 | HG02922.hp1 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1384-823T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152973852 | |||||||
chr4:152974126 | T | C | 2 | a0001c0002t0001g0187 a0022c0035t0001g0329 |
2 | HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1384-549T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152974126 | |||||||
chr4:152974206 | T | C | 1 | a0002c0001t0001g0274 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1384-469T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152974206 | |||||||
chr4:152974393 | T | C | 20 | a0001c0005t0001g0029 a0001c0005t0001g0030 a0001c0005t0001g0131 others(17): Show |
20 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1384-282T>C | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152974393 | |||||||
chr4:152974393 | TAAA | T | 181 | a0002c0001t0001g0001 a0002c0001t0001g0004 a0002c0001t0001g0007 others(178): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1384-279_1384-277d others(5): Show |
FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 152974393 | ||||||
chr4:152974460 | G | A | 3 | a0001c0002t0019g0135 a0001c0002t0019g0200 a0001c0002t0047g0040 |
3 | HG02970.hp1 HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1384-215G>A | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152974460 | |||||||
chr4:152974517 | T | G | 1 | a0001c0002t0002g0296 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1384-158T>G | FHDC1 | ENSG00000137460.10 | transcript | ENST00000511601.6 | protein_coding | 11/11 | chr4 | 152974517 |