Item | Value |
---|---|
geneid | 116113 |
ensemblid | ENSG00000137166.18 |
hgncid | 20842 |
symbol | FOXP4 |
name | forkhead box P4 |
refseq_nuc | NM_001012426.2 |
refseq_prot | NP_001012426.1 |
ensembl_nuc | ENST00000307972.10 |
ensembl_prot | ENSP00000309823.4 |
mane_status | MANE Select |
chr | chr6 |
start | 41546381 |
end | 41602384 |
strand | + |
ver | v1.2 |
region | chr6:41546381-41602384 |
region5000 | chr6:41541381-41607384 |
regionname0 | FOXP4_chr6_41546381_41602384 |
regionname5000 | FOXP4_chr6_41541381_41607384 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 680 | 345 | 83 | 71 | 129 | 18 | 42 | 96 | FOXP4_chr6_41541381_41607384 | FOXP4 | MMVES others(675): Show |
chr6 | 41541381 | 41607384 |
a0002 | 0/0 | 680 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | MMVES others(675): Show |
chr6 | 41541381 | 41607384 |
a0003 | 0/0 | 680 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FOXP4_chr6_41541381_41607384 | FOXP4 | MMVES others(675): Show |
chr6 | 41541381 | 41607384 |
a0004 | 0/0 | 680 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | MMVES others(675): Show |
chr6 | 41541381 | 41607384 |
a0005 | 0/0 | 680 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | MMVES others(675): Show |
chr6 | 41541381 | 41607384 |
a0006 | 0/0 | 680 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | MMVES others(675): Show |
chr6 | 41541381 | 41607384 |
a0007 | 0/0 | 680 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | MMVES others(675): Show |
chr6 | 41541381 | 41607384 |
a0008 | 0/0 | 680 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | MMVES others(675): Show |
chr6 | 41541381 | 41607384 |
a0009 | 0/0 | 680 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | MMVES others(675): Show |
chr6 | 41541381 | 41607384 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2040 | 178 | 31 | 41 | 75 | 9 | 21 | FOXP4_chr6_41541381_41607384 | FOXP4 | ATGAT others(2035): Show |
chr6 | 41541381 | 41607384 | ||
a0001c0002 | 0/0 | 2040 | 134 | 39 | 23 | 53 | 7 | 12 | FOXP4_chr6_41541381_41607384 | FOXP4 | ATGAT others(2035): Show |
chr6 | 41541381 | 41607384 | ||
a0001c0003 | 0/0 | 2040 | 15 | 0 | 5 | 0 | 2 | 8 | FOXP4_chr6_41541381_41607384 | FOXP4 | ATGAT others(2035): Show |
chr6 | 41541381 | 41607384 | ||
a0001c0004 | 0/0 | 2040 | 5 | 5 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ATGAT others(2035): Show |
chr6 | 41541381 | 41607384 | ||
a0001c0005 | 0/1 | 2040 | 4 | 0 | 2 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | ATGAT others(2035): Show |
chr6 | 41541381 | 41607384 | ||
a0001c0006 | 0/0 | 2040 | 3 | 3 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ATGAT others(2035): Show |
chr6 | 41541381 | 41607384 | ||
a0001c0008 | 0/0 | 2040 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ATGAT others(2035): Show |
chr6 | 41541381 | 41607384 | ||
a0001c0010 | 0/0 | 2040 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ATGAT others(2035): Show |
chr6 | 41541381 | 41607384 | ||
a0001c0012 | 0/0 | 2040 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ATGAT others(2035): Show |
chr6 | 41541381 | 41607384 | ||
a0001c0018 | 0/0 | 2040 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ATGAT others(2035): Show |
chr6 | 41541381 | 41607384 | ||
a0002c0007 | 0/0 | 2040 | 3 | 0 | 3 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ATGAT others(2035): Show |
chr6 | 41541381 | 41607384 | ||
a0003c0009 | 0/0 | 2040 | 2 | 0 | 0 | 2 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ATGAT others(2035): Show |
chr6 | 41541381 | 41607384 | ||
a0004c0013 | 0/0 | 2040 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ATGAT others(2035): Show |
chr6 | 41541381 | 41607384 | ||
a0005c0015 | 0/0 | 2040 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ATGAT others(2035): Show |
chr6 | 41541381 | 41607384 | ||
a0006c0016 | 0/0 | 2040 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ATGAT others(2035): Show |
chr6 | 41541381 | 41607384 | ||
a0007c0014 | 0/0 | 2040 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ATGAT others(2035): Show |
chr6 | 41541381 | 41607384 | ||
a0008c0017 | 0/0 | 2040 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ATGAT others(2035): Show |
chr6 | 41541381 | 41607384 | ||
a0009c0011 | 0/0 | 2040 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ATGAT others(2035): Show |
chr6 | 41541381 | 41607384 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5994 | 137 | 17 | 36 | 58 | 8 | 17 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0001t0002 | 0/0 | 5994 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0001t0004 | 0/0 | 5994 | 11 | 4 | 2 | 3 | 1 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0001t0005 | 0/0 | 5995 | 11 | 1 | 3 | 7 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5990): Show |
chr6 | 41541381 | 41607384 |
a0001c0001t0010 | 0/0 | 5994 | 3 | 0 | 0 | 1 | 0 | 2 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0001t0011 | 0/0 | 5993 | 5 | 5 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5988): Show |
chr6 | 41541381 | 41607384 |
a0001c0001t0021 | 0/0 | 5994 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0001t0027 | 0/0 | 6005 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(6000): Show |
chr6 | 41541381 | 41607384 |
a0001c0001t0028 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0001t0030 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0001t0031 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0001t0032 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0001t0033 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0001t0034 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0002 | 0/0 | 5994 | 26 | 14 | 1 | 10 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0003 | 0/0 | 5994 | 31 | 1 | 6 | 22 | 0 | 2 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0004 | 0/0 | 5994 | 12 | 5 | 2 | 5 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0007 | 0/0 | 5994 | 10 | 0 | 4 | 4 | 1 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0008 | 0/0 | 6000 | 9 | 6 | 1 | 1 | 1 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5995): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0009 | 0/0 | 5994 | 8 | 0 | 4 | 0 | 2 | 2 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0010 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0012 | 0/0 | 5994 | 3 | 1 | 0 | 1 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0013 | 0/0 | 5995 | 3 | 1 | 0 | 2 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5990): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0014 | 0/0 | 5995 | 4 | 0 | 1 | 3 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5990): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0015 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0017 | 0/0 | 5994 | 3 | 3 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0019 | 0/0 | 5994 | 2 | 0 | 0 | 0 | 0 | 2 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0022 | 0/0 | 5994 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0023 | 0/0 | 5994 | 2 | 0 | 0 | 2 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0024 | 0/0 | 5994 | 2 | 0 | 0 | 0 | 2 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0025 | 0/0 | 5994 | 2 | 0 | 0 | 0 | 1 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0026 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0036 | 0/0 | 5995 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5990): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0037 | 0/0 | 6001 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5996): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0038 | 0/0 | 5995 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5990): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0039 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0040 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0041 | 0/0 | 5994 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0042 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0043 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0044 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0045 | 0/0 | 5995 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5990): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0046 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0002t0047 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0003t0006 | 0/0 | 5994 | 11 | 0 | 5 | 0 | 2 | 4 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0003t0018 | 0/0 | 5994 | 3 | 0 | 0 | 0 | 0 | 3 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0003t0035 | 0/0 | 5995 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5990): Show |
chr6 | 41541381 | 41607384 |
a0001c0004t0010 | 0/0 | 5994 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0004t0016 | 0/0 | 5994 | 3 | 3 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0005t0002 | 0/1 | 5994 | 4 | 0 | 2 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0006t0002 | 0/0 | 5994 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0006t0013 | 0/0 | 5995 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5990): Show |
chr6 | 41541381 | 41607384 |
a0001c0008t0020 | 0/0 | 5994 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0010t0001 | 0/0 | 5994 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0012t0012 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0001c0018t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0002c0007t0015 | 0/0 | 5994 | 3 | 0 | 3 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0003c0009t0001 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0003c0009t0005 | 0/0 | 5995 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5990): Show |
chr6 | 41541381 | 41607384 |
a0004c0013t0002 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0005c0015t0001 | 0/0 | 5994 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0006c0016t0005 | 0/0 | 5995 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5990): Show |
chr6 | 41541381 | 41607384 |
a0007c0014t0001 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0008c0017t0029 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
a0009c0011t0012 | 0/0 | 5994 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | ACTCG others(5989): Show |
chr6 | 41541381 | 41607384 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0013 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0004g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0004g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0005g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0005g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0005g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0010g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0010g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0010g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0011g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0011g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0011g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0011g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0021g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0027g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0028g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0030g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0031g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0032g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0033g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0001t0034g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0007g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0007g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0007g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0007g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0007g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0007g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0007g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0007g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0007g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0008g0015 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0008g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0008g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0009g0007 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0009g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0009g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0009g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0009g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0009g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0010g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0012g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0012g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0012g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0013g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0013g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0013g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0014g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0014g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0014g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0015g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0017g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0019g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0019g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0022g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0022g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0023g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0023g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0024g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0025g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0025g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0026g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0036g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0037g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0038g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0039g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0040g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0041g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0042g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0043g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0044g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0045g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0046g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0002t0047g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0003t0006g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0003t0006g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0003t0006g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0003t0006g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0003t0006g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0003t0006g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0003t0006g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0003t0006g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0003t0006g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0003t0018g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0003t0018g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0003t0018g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0003t0035g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0004t0010g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0004t0010g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0004t0016g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0004t0016g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0004t0016g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0005t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0005t0002g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0005t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0006t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0006t0013g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0008t0020g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0008t0020g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0010t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0010t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0012t0012g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0001c0018t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0002c0007t0015g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0003c0009t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0003c0009t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0004c0013t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0005c0015t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0006c0016t0005g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0007c0014t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0008c0017t0029g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
a0009c0011t0012g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | GBR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00099 | hp2 | a0001 | c0002 | t0025 | g0114 | EUR | GBR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00140 | hp1 | a0001 | c0002 | t0009 | g0107 | EUR | GBR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00280 | hp1 | a0001 | c0002 | t0007 | g0147 | EUR | FIN | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00323 | hp1 | a0001 | c0002 | t0008 | g0015 | EUR | FIN | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00323 | hp2 | a0001 | c0002 | t0009 | g0007 | EUR | FIN | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00408 | hp1 | a0001 | c0002 | t0007 | g0121 | EAS | CHS | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00438 | hp2 | a0001 | c0002 | t0013 | g0076 | EAS | CHS | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0116 | EAS | CHS | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0115 | EAS | CHS | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00609 | hp1 | a0001 | c0018 | t0001 | g0185 | EAS | CHS | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00609 | hp2 | a0004 | c0013 | t0002 | g0019 | EAS | CHS | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00639 | hp2 | a0001 | c0003 | t0006 | g0040 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00642 | hp1 | a0001 | c0003 | t0006 | g0283 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00733 | hp1 | a0001 | c0002 | t0044 | g0120 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00738 | hp1 | a0001 | c0003 | t0006 | g0282 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0174 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01069 | hp1 | a0002 | c0007 | t0015 | g0004 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01074 | hp1 | a0001 | c0002 | t0009 | g0113 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01074 | hp2 | a0001 | c0005 | t0002 | g0016 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01081 | hp1 | a0001 | c0005 | t0002 | g0016 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01099 | hp2 | a0002 | c0007 | t0015 | g0004 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01109 | hp1 | a0002 | c0007 | t0015 | g0004 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01167 | hp1 | a0001 | c0002 | t0009 | g0110 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01169 | hp2 | a0001 | c0002 | t0009 | g0112 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0046 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01243 | hp1 | a0001 | c0002 | t0004 | g0106 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01256 | hp2 | a0001 | c0003 | t0006 | g0040 | AMR | CLM | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01257 | hp2 | a0001 | c0002 | t0003 | g0129 | AMR | CLM | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01258 | hp1 | a0001 | c0002 | t0003 | g0022 | AMR | CLM | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01346 | hp1 | a0001 | c0002 | t0009 | g0108 | AMR | CLM | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01358 | hp1 | a0001 | c0002 | t0015 | g0004 | AMR | CLM | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0082 | AMR | CLM | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0175 | AMR | CLM | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01433 | hp2 | a0001 | c0002 | t0004 | g0093 | AMR | CLM | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01496 | hp1 | a0001 | c0002 | t0003 | g0022 | AMR | CLM | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01496 | hp2 | a0005 | c0015 | t0001 | g0197 | AMR | CLM | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01515 | hp1 | a0001 | c0002 | t0024 | g0018 | EUR | IBS | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01516 | hp1 | a0001 | c0003 | t0006 | g0284 | EUR | IBS | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01517 | hp1 | a0001 | c0003 | t0006 | g0285 | EUR | IBS | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01517 | hp2 | a0001 | c0002 | t0024 | g0018 | EUR | IBS | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0059 | AFR | ACB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0066 | AFR | ACB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01891 | hp1 | a0001 | c0008 | t0020 | g0087 | AFR | ACB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01891 | hp2 | a0001 | c0002 | t0008 | g0095 | AFR | ACB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01928 | hp1 | a0001 | c0002 | t0007 | g0021 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01928 | hp2 | a0006 | c0016 | t0005 | g0205 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01943 | hp1 | a0001 | c0002 | t0003 | g0138 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01952 | hp1 | a0001 | c0002 | t0014 | g0023 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01952 | hp2 | a0001 | c0002 | t0038 | g0004 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01975 | hp2 | a0001 | c0002 | t0007 | g0021 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01978 | hp1 | a0001 | c0002 | t0026 | g0133 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01981 | hp2 | a0001 | c0002 | t0008 | g0096 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02040 | hp2 | a0001 | c0002 | t0003 | g0152 | EAS | KHV | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | ACB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02074 | hp1 | a0001 | c0001 | t0032 | g0030 | EAS | KHV | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02074 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | KHV | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02129 | hp2 | a0001 | c0002 | t0007 | g0025 | EAS | KHV | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02145 | hp1 | a0001 | c0002 | t0040 | g0061 | AFR | ACB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | ACB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02148 | hp1 | a0001 | c0002 | t0007 | g0131 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02148 | hp2 | a0001 | c0002 | t0003 | g0135 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02165 | hp1 | a0001 | c0002 | t0008 | g0015 | EAS | CDX | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02257 | hp1 | a0001 | c0006 | t0002 | g0006 | AFR | ACB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02257 | hp2 | a0001 | c0012 | t0012 | g0063 | AFR | ACB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02273 | hp1 | a0001 | c0002 | t0007 | g0132 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | ACB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0103 | AFR | ACB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02293 | hp1 | a0001 | c0002 | t0003 | g0142 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02451 | hp1 | a0001 | c0002 | t0043 | g0057 | AFR | ACB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02451 | hp2 | a0001 | c0001 | t0011 | g0265 | AFR | ACB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02523 | hp1 | a0001 | c0001 | t0028 | g0217 | EAS | KHV | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02572 | hp1 | a0001 | c0002 | t0008 | g0053 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02622 | hp1 | a0007 | c0014 | t0001 | g0013 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02622 | hp2 | a0001 | c0002 | t0012 | g0065 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02630 | hp1 | a0001 | c0002 | t0008 | g0092 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0074 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0085 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02647 | hp2 | a0001 | c0002 | t0002 | g0099 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02683 | hp2 | a0001 | c0005 | t0002 | g0097 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02698 | hp1 | a0001 | c0003 | t0018 | g0279 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02717 | hp1 | a0001 | c0002 | t0002 | g0094 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02723 | hp1 | a0001 | c0002 | t0008 | g0101 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02809 | hp1 | a0001 | c0004 | t0016 | g0260 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02809 | hp2 | a0001 | c0002 | t0047 | g0073 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02818 | hp2 | a0001 | c0002 | t0004 | g0017 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02886 | hp2 | a0001 | c0002 | t0017 | g0012 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0084 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02896 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02896 | hp2 | a0001 | c0002 | t0004 | g0060 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02897 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02922 | hp1 | a0001 | c0008 | t0020 | g0088 | AFR | ESN | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02922 | hp2 | a0001 | c0002 | t0004 | g0017 | AFR | ESN | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02965 | hp1 | a0001 | c0004 | t0016 | g0258 | AFR | ESN | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02965 | hp2 | a0001 | c0002 | t0017 | g0012 | AFR | ESN | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0052 | AFR | ESN | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02970 | hp2 | a0001 | c0002 | t0036 | g0081 | AFR | ESN | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02976 | hp1 | a0001 | c0001 | t0011 | g0229 | AFR | ESN | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02976 | hp2 | a0001 | c0002 | t0008 | g0089 | AFR | ESN | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03017 | hp1 | a0001 | c0002 | t0025 | g0111 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03017 | hp2 | a0001 | c0001 | t0010 | g0238 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03098 | hp1 | a0001 | c0002 | t0037 | g0102 | AFR | MSL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03098 | hp2 | a0001 | c0002 | t0002 | g0056 | AFR | MSL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03130 | hp1 | a0001 | c0001 | t0005 | g0157 | AFR | ESN | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03130 | hp2 | a0001 | c0002 | t0017 | g0012 | AFR | ESN | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03139 | hp1 | a0001 | c0002 | t0022 | g0104 | AFR | ESN | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03139 | hp2 | a0001 | c0004 | t0010 | g0224 | AFR | ESN | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03195 | hp1 | a0001 | c0006 | t0002 | g0006 | AFR | ESN | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03195 | hp2 | a0008 | c0017 | t0029 | g0237 | AFR | ESN | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03209 | hp1 | a0001 | c0002 | t0004 | g0109 | AFR | MSL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03225 | hp1 | a0001 | c0002 | t0002 | g0058 | AFR | MSL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | MSL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03239 | hp1 | a0001 | c0002 | t0010 | g0262 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03486 | hp1 | a0001 | c0001 | t0011 | g0036 | AFR | MSL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03486 | hp2 | a0009 | c0011 | t0012 | g0064 | AFR | MSL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03490 | hp1 | a0001 | c0002 | t0002 | g0075 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03490 | hp2 | a0001 | c0003 | t0006 | g0038 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03491 | hp1 | a0001 | c0003 | t0006 | g0039 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03491 | hp2 | a0001 | c0002 | t0019 | g0068 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03492 | hp1 | a0001 | c0002 | t0019 | g0069 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03492 | hp2 | a0001 | c0003 | t0006 | g0038 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03516 | hp1 | a0001 | c0002 | t0013 | g0048 | AFR | ESN | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03516 | hp2 | a0001 | c0006 | t0013 | g0006 | AFR | ESN | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03540 | hp1 | a0001 | c0010 | t0001 | g0277 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03654 | hp1 | a0001 | c0003 | t0018 | g0278 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03669 | hp2 | a0001 | c0003 | t0006 | g0281 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03704 | hp2 | a0001 | c0001 | t0010 | g0274 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03831 | hp1 | a0001 | c0002 | t0007 | g0148 | SAS | BEB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03834 | hp1 | a0001 | c0003 | t0035 | g0039 | SAS | BEB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0001 | SAS | BEB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03927 | hp2 | a0001 | c0002 | t0041 | g0072 | SAS | BEB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03942 | hp1 | a0001 | c0003 | t0018 | g0280 | SAS | BEB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG04115 | hp2 | a0001 | c0002 | t0009 | g0007 | SAS | STU | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG04184 | hp1 | a0001 | c0002 | t0012 | g0067 | SAS | BEB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG04199 | hp2 | a0001 | c0002 | t0003 | g0144 | SAS | STU | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG04228 | hp2 | a0001 | c0001 | t0033 | g0213 | SAS | STU | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18522 | hp1 | a0001 | c0004 | t0010 | g0225 | AFR | YRI | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18522 | hp2 | a0001 | c0001 | t0011 | g0264 | AFR | YRI | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18747 | hp2 | a0001 | c0002 | t0023 | g0049 | EAS | CHB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18906 | hp1 | a0001 | c0002 | t0039 | g0098 | AFR | YRI | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0077 | AFR | YRI | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18939 | hp2 | a0001 | c0002 | t0003 | g0025 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18941 | hp2 | a0001 | c0002 | t0003 | g0123 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18942 | hp2 | a0001 | c0001 | t0030 | g0219 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18943 | hp2 | a0001 | c0002 | t0007 | g0155 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18944 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18945 | hp1 | a0001 | c0002 | t0003 | g0023 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18948 | hp1 | a0001 | c0002 | t0012 | g0043 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18948 | hp2 | a0001 | c0002 | t0003 | g0154 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18951 | hp1 | a0003 | c0009 | t0001 | g0246 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18951 | hp2 | a0001 | c0002 | t0003 | g0151 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18956 | hp2 | a0001 | c0002 | t0003 | g0130 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18957 | hp1 | a0001 | c0001 | t0034 | g0208 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18957 | hp2 | a0001 | c0002 | t0003 | g0143 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18969 | hp1 | a0001 | c0001 | t0031 | g0227 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18970 | hp1 | a0001 | c0002 | t0007 | g0134 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18971 | hp1 | a0001 | c0002 | t0046 | g0146 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18971 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18978 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18978 | hp2 | a0001 | c0001 | t0005 | g0243 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18979 | hp2 | a0001 | c0002 | t0004 | g0062 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18981 | hp2 | a0001 | c0002 | t0003 | g0024 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18985 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18985 | hp2 | a0001 | c0002 | t0003 | g0125 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18986 | hp1 | a0001 | c0002 | t0003 | g0124 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18986 | hp2 | a0001 | c0002 | t0004 | g0071 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18988 | hp1 | a0001 | c0002 | t0045 | g0003 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18989 | hp1 | a0001 | c0001 | t0010 | g0273 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18989 | hp2 | a0001 | c0002 | t0003 | g0149 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18990 | hp1 | a0001 | c0001 | t0005 | g0177 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18990 | hp2 | a0001 | c0001 | t0005 | g0192 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18994 | hp1 | a0001 | c0002 | t0003 | g0137 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18997 | hp1 | a0001 | c0002 | t0003 | g0127 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA18997 | hp2 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19000 | hp2 | a0001 | c0002 | t0003 | g0136 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19003 | hp1 | a0001 | c0002 | t0004 | g0045 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19003 | hp2 | a0001 | c0002 | t0003 | g0156 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19004 | hp1 | a0001 | c0002 | t0003 | g0139 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19005 | hp1 | a0001 | c0002 | t0003 | g0024 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19005 | hp2 | a0001 | c0002 | t0004 | g0044 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19007 | hp2 | a0001 | c0002 | t0003 | g0140 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19011 | hp2 | a0001 | c0001 | t0005 | g0222 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | LWK | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19030 | hp2 | a0001 | c0002 | t0022 | g0105 | AFR | LWK | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19043 | hp1 | a0001 | c0010 | t0001 | g0257 | AFR | LWK | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19043 | hp2 | a0001 | c0001 | t0021 | g0041 | AFR | LWK | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19055 | hp1 | a0001 | c0002 | t0042 | g0153 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19060 | hp1 | a0001 | c0002 | t0014 | g0026 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19060 | hp2 | a0001 | c0001 | t0027 | g0241 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19063 | hp1 | a0001 | c0002 | t0003 | g0126 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19067 | hp1 | a0001 | c0002 | t0013 | g0083 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19067 | hp2 | a0001 | c0002 | t0014 | g0122 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19074 | hp2 | a0001 | c0002 | t0003 | g0145 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19080 | hp2 | a0001 | c0002 | t0023 | g0003 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19081 | hp1 | a0001 | c0002 | t0014 | g0026 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19084 | hp2 | a0001 | c0002 | t0004 | g0070 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19087 | hp2 | a0001 | c0002 | t0003 | g0141 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA19090 | hp2 | a0003 | c0009 | t0005 | g0231 | EAS | JPT | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA20129 | hp1 | a0001 | c0004 | t0016 | g0259 | AFR | ASW | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA20129 | hp2 | a0001 | c0002 | t0003 | g0128 | AFR | ASW | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | TSI | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | TSI | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0091 | EUR | TSI | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA20905 | hp1 | a0001 | c0002 | t0003 | g0150 | SAS | GIH | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA20905 | hp2 | a0001 | c0002 | t0009 | g0007 | SAS | GIH | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG01123 | hp2 | a0001 | c0003 | t0006 | g0286 | AMR | CLM | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | ACB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG02559 | hp2 | a0001 | c0002 | t0008 | g0100 | AFR | ACB | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03471 | hp1 | a0001 | c0002 | t0004 | g0090 | AFR | MSL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0119 | AFR | USA | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
HG06807 | hp2 | a0001 | c0001 | t0021 | g0041 | AFR | USA | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | USA | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
NA20300 | hp2 | a0001 | c0001 | t0011 | g0036 | AFR | USA | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
homoSapiens | chm13v2 | a0001 | c0005 | t0002 | g0086 | REF | REF | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0013 | REF | REF | FOXP4_chr6_41541381_41607384 | FOXP4 | chr6 | 41541381 | 41607384 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:41584808 | A | G | 1 | a0004 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.340A>G | p.Thr114Ala | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 4/17 | 843/5994 | 340/2043 | 114/680 | chr6 | 41584808 | |||
chr6:41587352 | G | A | 1 | a0002 | 3 | HG01069.hp1 HG01099.hp2 HG01109.hp1 |
missense_variant | MODERATE | c.712G>A | p.Gly238Arg | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 7/17 | 1215/5994 | 712/2043 | 238/680 | chr6 | 41587352 | |||
chr6:41589829 | C | T | 1 | a0003 | 2 | NA18951.hp1 NA19090.hp2 |
missense_variant | MODERATE | c.1124C>T | p.Ser375Leu | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 10/17 | 1627/5994 | 1124/2043 | 375/680 | chr6 | 41589829 | |||
chr6:41589970 | C | T | 1 | a0008 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.1157C>T | p.Pro386Leu | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 11/17 | 1660/5994 | 1157/2043 | 386/680 | chr6 | 41589970 | |||
chr6:41590059 | G | A | 1 | a0007 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.1246G>A | p.Ala416Thr | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 11/17 | 1749/5994 | 1246/2043 | 416/680 | chr6 | 41590059 | |||
chr6:41590107 | C | A | 1 | a0009 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.1294C>A | p.Leu432Met | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 11/17 | 1797/5994 | 1294/2043 | 432/680 | chr6 | 41590107 | |||
chr6:41597812 | T | A | 1 | a0005 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1757T>A | p.Leu586His | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 16/17 | 2260/5994 | 1757/2043 | 586/680 | chr6 | 41597812 | |||
chr6:41597844 | G | A | 1 | a0006 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.1789G>A | p.Ala597Thr | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 16/17 | 2292/5994 | 1789/2043 | 597/680 | chr6 | 41597844 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:41565835 | G | A | 1 | a0001c0003 | 15 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
synonymous_variant | LOW | c.75G>A | p.Gly25Gly | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/17 | 578/5994 | 75/2043 | 25/680 | chr6 | 41565835 | |||
chr6:41565841 | C | A | 9 | a0001c0002 a0001c0003 a0001c0005 others(6): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
synonymous_variant | LOW | c.81C>A | p.Ala27Ala | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/17 | 584/5994 | 81/2043 | 27/680 | chr6 | 41565841 | |||
chr6:41565958 | G | A | 1 | a0001c0006 | 3 | HG02257.hp1 HG03195.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.198G>A | p.Gln66Gln | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/17 | 701/5994 | 198/2043 | 66/680 | chr6 | 41565958 | |||
chr6:41578069 | C | T | 1 | a0001c0005 | 3 | HG01074.hp2 HG01081.hp1 HG02683.hp2 |
synonymous_variant | LOW | c.288C>T | p.Ala96Ala | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/17 | 791/5994 | 288/2043 | 96/680 | chr6 | 41578069 | |||
chr6:41587351 | C | T | 1 | a0001c0018 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.711C>T | p.Pro237Pro | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 7/17 | 1214/5994 | 711/2043 | 237/680 | chr6 | 41587351 | |||
chr6:41587474 | C | T | 1 | a0001c0010 | 2 | HG03540.hp1 NA19043.hp1 |
synonymous_variant | LOW | c.834C>T | p.Pro278Pro | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 7/17 | 1337/5994 | 834/2043 | 278/680 | chr6 | 41587474 | |||
chr6:41588647 | C | T | 1 | a0001c0012 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.981C>T | p.His327His | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 9/17 | 1484/5994 | 981/2043 | 327/680 | chr6 | 41588647 | |||
chr6:41590305 | C | T | 2 | a0001c0004 a0001c0008 |
7 | HG01891.hp1 HG02809.hp1 HG02922.hp1 others(4): Show |
synonymous_variant | LOW | c.1392C>T | p.Ala464Ala | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 12/17 | 1895/5994 | 1392/2043 | 464/680 | chr6 | 41590305 | |||
chr6:41597843 | C | T | 1 | a0001c0010 | 2 | HG03540.hp1 NA19043.hp1 |
synonymous_variant | LOW | c.1788C>T | p.Ser596Ser | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 16/17 | 2291/5994 | 1788/2043 | 596/680 | chr6 | 41597843 | |||
chr6:41597939 | G | A | 1 | a0001c0006 | 3 | HG02257.hp1 HG03195.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.1884G>A | p.Pro628Pro | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 16/17 | 2387/5994 | 1884/2043 | 628/680 | chr6 | 41597939 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:41546580 | G | C | 1 | a0001c0002t0026 | 1 | HG01978.hp1 | 5_prime_UTR_variant | MODIFIER | c.-304G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/17 | 19181 | chr6 | 41546580 | ||||||
chr6:41546634 | A | G | 42 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0021 others(39): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
5_prime_UTR_variant | MODIFIER | c.-250A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/17 | 19127 | chr6 | 41546634 | ||||||
chr6:41546666 | A | G | 1 | a0001c0002t0047 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-218A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/17 | 19095 | chr6 | 41546666 | ||||||
chr6:41546673 | C | G | 42 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0021 others(39): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
5_prime_UTR_variant | MODIFIER | c.-211C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/17 | 19088 | chr6 | 41546673 | ||||||
chr6:41546710 | C | T | 1 | a0001c0001t0034 | 1 | NA18957.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-174C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/17 | chr6 | 41546710 | |||||||
chr6:41599062 | C | T | 1 | a0001c0002t0046 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*126C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 126 | chr6 | 41599062 | ||||||
chr6:41599170 | T | G | 1 | a0001c0001t0027 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*234T>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 234 | chr6 | 41599170 | ||||||
chr6:41599216 | C | T | 1 | a0001c0001t0033 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*280C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 280 | chr6 | 41599216 | ||||||
chr6:41599290 | C | A | 1 | a0001c0001t0027 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*354C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 354 | chr6 | 41599290 | ||||||
chr6:41599295 | G | GCTTGGAC others(4): Show |
1 | a0001c0001t0027 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*360_*361insTTGGAC others(5): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 361 | INFO_REALIGN_3_PRIME | chr6 | 41599295 | |||||
chr6:41599298 | G | C | 1 | a0001c0001t0027 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*362G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 362 | chr6 | 41599298 | ||||||
chr6:41599390 | C | T | 4 | a0001c0002t0009 a0001c0002t0017 a0001c0002t0024 others(1): Show |
15 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*454C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 454 | chr6 | 41599390 | ||||||
chr6:41599544 | G | A | 1 | a0001c0001t0028 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*608G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 608 | chr6 | 41599544 | ||||||
chr6:41599619 | C | A | 1 | a0001c0001t0027 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*683C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 683 | chr6 | 41599619 | ||||||
chr6:41599620 | A | C | 1 | a0001c0001t0027 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*684A>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 684 | chr6 | 41599620 | ||||||
chr6:41599641 | C | T | 2 | a0001c0002t0023 a0001c0002t0045 |
3 | NA18747.hp2 NA18988.hp1 NA19080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*705C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 705 | chr6 | 41599641 | ||||||
chr6:41599672 | A | AC | 11 | a0001c0001t0005 a0001c0002t0013 a0001c0002t0014 others(8): Show |
26 | HG00438.hp2 HG00741.hp1 HG01361.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*738dupC | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 739 | INFO_REALIGN_3_PRIME | chr6 | 41599672 | |||||
chr6:41599675 | G | T | 1 | a0001c0001t0027 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*739G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 739 | chr6 | 41599675 | ||||||
chr6:41599676 | C | G | 1 | a0001c0001t0027 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*740C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 740 | chr6 | 41599676 | ||||||
chr6:41599678 | T | A | 1 | a0001c0001t0027 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*742T>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 742 | chr6 | 41599678 | ||||||
chr6:41599682 | C | A | 1 | a0001c0001t0027 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*746C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 746 | chr6 | 41599682 | ||||||
chr6:41599686 | A | G | 1 | a0001c0001t0027 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*750A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 750 | chr6 | 41599686 | ||||||
chr6:41599687 | G | T | 1 | a0001c0001t0027 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*751G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 751 | chr6 | 41599687 | ||||||
chr6:41599886 | GC | G | 1 | a0001c0001t0011 | 5 | HG02451.hp2 HG02976.hp1 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*953delC | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 953 | INFO_REALIGN_3_PRIME | chr6 | 41599886 | |||||
chr6:41599889 | C | T | 1 | a0001c0002t0022 | 2 | HG03139.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*953C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 953 | chr6 | 41599889 | ||||||
chr6:41600238 | C | T | 3 | a0001c0002t0015 a0001c0002t0038 a0002c0007t0015 |
5 | HG01069.hp1 HG01099.hp2 HG01109.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1302C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 1302 | chr6 | 41600238 | ||||||
chr6:41600326 | G | A | 34 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0011 others(31): Show |
104 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1390G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 1390 | chr6 | 41600326 | ||||||
chr6:41600425 | G | A | 1 | a0008c0017t0029 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1489G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 1489 | chr6 | 41600425 | ||||||
chr6:41600716 | C | T | 2 | a0001c0004t0016 a0001c0008t0020 |
5 | HG01891.hp1 HG02809.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1780C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 1780 | chr6 | 41600716 | ||||||
chr6:41600717 | G | A | 8 | a0001c0001t0030 a0001c0001t0031 a0001c0002t0003 others(5): Show |
50 | HG00280.hp1 HG00408.hp1 HG01257.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1781G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 1781 | chr6 | 41600717 | ||||||
chr6:41600945 | G | A | 1 | a0001c0002t0024 | 2 | HG01515.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2009G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 2009 | chr6 | 41600945 | ||||||
chr6:41601129 | T | C | 2 | a0001c0002t0003 a0001c0002t0014 |
2 | HG01952.hp1 NA19003.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2193T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 2193 | chr6 | 41601129 | ||||||
chr6:41601168 | G | A | 35 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0011 others(32): Show |
105 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*2232G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 2232 | chr6 | 41601168 | ||||||
chr6:41601242 | A | AAAGGGG | 2 | a0001c0002t0008 a0001c0002t0037 |
10 | HG00323.hp1 HG01891.hp2 HG01981.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2307_*2308insAGGG others(2): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 2308 | INFO_REALIGN_3_PRIME | chr6 | 41601242 | |||||
chr6:41601251 | A | T | 1 | a0001c0002t0041 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2315A>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 2315 | chr6 | 41601251 | ||||||
chr6:41601318 | C | G | 9 | a0001c0001t0030 a0001c0001t0031 a0001c0002t0003 others(6): Show |
51 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*2382C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 2382 | chr6 | 41601318 | ||||||
chr6:41601318 | C | T | 5 | a0001c0002t0012 a0001c0002t0019 a0001c0012t0012 others(2): Show |
8 | HG02257.hp2 HG02622.hp2 HG03195.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2382C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 2382 | chr6 | 41601318 | ||||||
chr6:41601380 | T | G | 7 | a0001c0002t0009 a0001c0002t0017 a0001c0002t0024 others(4): Show |
21 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2444T>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 2444 | chr6 | 41601380 | ||||||
chr6:41601395 | C | A | 3 | a0001c0002t0015 a0001c0002t0038 a0002c0007t0015 |
5 | HG01069.hp1 HG01099.hp2 HG01109.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2459C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 2459 | chr6 | 41601395 | ||||||
chr6:41601395 | C | T | 1 | a0001c0002t0042 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2459C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 2459 | chr6 | 41601395 | ||||||
chr6:41601419 | G | A | 47 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0011 others(44): Show |
168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*2483G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 2483 | chr6 | 41601419 | ||||||
chr6:41601423 | C | T | 2 | a0001c0001t0011 a0001c0002t0036 |
6 | HG02451.hp2 HG02970.hp2 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2487C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 2487 | chr6 | 41601423 | ||||||
chr6:41601449 | G | A | 1 | a0001c0004t0016 | 3 | HG02809.hp1 HG02965.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2513G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 2513 | chr6 | 41601449 | ||||||
chr6:41601459 | G | A | 1 | a0001c0002t0040 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2523G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 2523 | chr6 | 41601459 | ||||||
chr6:41601468 | G | A | 1 | a0001c0001t0032 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2532G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 2532 | chr6 | 41601468 | ||||||
chr6:41601516 | A | G | 1 | a0001c0002t0019 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2580A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 2580 | chr6 | 41601516 | ||||||
chr6:41601639 | A | C | 3 | a0001c0003t0006 a0001c0003t0018 a0001c0003t0035 |
15 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2703A>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 2703 | chr6 | 41601639 | ||||||
chr6:41601665 | G | A | 4 | a0001c0002t0012 a0001c0002t0019 a0001c0012t0012 others(1): Show |
7 | HG02257.hp2 HG02622.hp2 HG03486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2729G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 2729 | chr6 | 41601665 | ||||||
chr6:41602100 | A | C | 4 | a0001c0001t0031 a0001c0002t0007 a0001c0002t0026 others(1): Show |
13 | HG00280.hp1 HG00408.hp1 HG01928.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3164A>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 3164 | chr6 | 41602100 | ||||||
chr6:41602110 | C | T | 1 | a0001c0002t0025 | 2 | HG00099.hp2 HG03017.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3174C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 3174 | chr6 | 41602110 | ||||||
chr6:41602199 | G | A | 1 | a0001c0003t0018 | 3 | HG02698.hp1 HG03654.hp1 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3263G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 17/17 | 3263 | chr6 | 41602199 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:41547077 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-17+210C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41547077 | |||||||
chr6:41547261 | C | T | 1 | a0001c0001t0021g0041 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-17+394C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41547261 | |||||||
chr6:41547441 | GC | G | 13 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0040 others(10): Show |
15 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17+575delC | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41547441 | |||||||
chr6:41547486 | G | A | 108 | a0001c0001t0002g0055 a0001c0001t0002g0118 a0001c0001t0004g0020 others(105): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-17+619G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41547486 | |||||||
chr6:41547486 | G | C | 44 | a0001c0002t0003g0022 a0001c0002t0003g0023 a0001c0002t0003g0024 others(41): Show |
48 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.-17+619G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41547486 | |||||||
chr6:41547487 | G | C | 1 | a0001c0002t0003g0156 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-17+620G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41547487 | |||||||
chr6:41547529 | A | T | 1 | a0001c0010t0001g0277 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-17+662A>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41547529 | |||||||
chr6:41547709 | G | T | 3 | a0001c0001t0002g0118 a0001c0001t0004g0020 a0001c0001t0004g0119 |
4 | HG01081.hp2 HG02280.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17+842G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41547709 | |||||||
chr6:41547757 | G | A | 1 | a0001c0001t0005g0157 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-17+890G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41547757 | |||||||
chr6:41547777 | A | AC | 51 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(48): Show |
56 | HG00408.hp1 HG00438.hp2 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.-17+919dupC | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 41547777 | ||||||
chr6:41547777 | A | ACC | 14 | a0001c0001t0004g0042 a0001c0001t0004g0051 a0001c0002t0002g0003 others(11): Show |
16 | HG00733.hp1 HG01175.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17+918_-17+919dup others(2): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 41547777 | ||||||
chr6:41547784 | C | CCA | 13 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0040 others(10): Show |
15 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17+918_-17+919ins others(2): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 41547784 | ||||||
chr6:41548062 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-17+1195C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548062 | |||||||
chr6:41548074 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-17+1207T>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548074 | |||||||
chr6:41548085 | G | A | 1 | a0001c0002t0002g0052 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-17+1218G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548085 | |||||||
chr6:41548190 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG01358.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-17+1323G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548190 | |||||||
chr6:41548224 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-17+1357G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548224 | |||||||
chr6:41548234 | G | T | 50 | a0001c0001t0004g0051 a0001c0001t0004g0078 a0001c0001t0004g0079 others(47): Show |
55 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.-17+1367G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548234 | |||||||
chr6:41548257 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-17+1390C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548257 | |||||||
chr6:41548288 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-17+1421G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548288 | |||||||
chr6:41548491 | A | G | 2 | a0001c0002t0002g0084 a0001c0002t0002g0085 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-17+1624A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548491 | |||||||
chr6:41548512 | G | T | 42 | a0001c0002t0003g0022 a0001c0002t0003g0023 a0001c0002t0003g0024 others(39): Show |
46 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.-17+1645G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548512 | |||||||
chr6:41548547 | GGCCTGTA | G | 13 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0040 others(10): Show |
15 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17+1683_-17+1689d others(9): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 41548547 | ||||||
chr6:41548613 | A | G | 150 | a0001c0001t0002g0118 a0001c0001t0004g0020 a0001c0001t0004g0051 others(147): Show |
169 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.-17+1746A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548613 | |||||||
chr6:41548680 | A | C | 1 | a0001c0002t0003g0156 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-17+1813A>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548680 | |||||||
chr6:41548682 | C | A | 1 | a0001c0002t0003g0156 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-17+1815C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548682 | |||||||
chr6:41548685 | C | A | 1 | a0001c0002t0002g0056 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-17+1818C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548685 | |||||||
chr6:41548686 | T | C | 1 | a0001c0002t0003g0156 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-17+1819T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548686 | |||||||
chr6:41548687 | C | T | 1 | a0001c0002t0003g0156 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-17+1820C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548687 | |||||||
chr6:41548823 | CCTTT | C | 28 | a0001c0001t0004g0051 a0001c0001t0004g0078 a0001c0001t0004g0079 others(25): Show |
33 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.-17+1957_-17+1960d others(6): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548823 | |||||||
chr6:41548823 | CCTTTT | C | 14 | a0001c0002t0002g0066 a0001c0002t0004g0044 a0001c0002t0004g0045 others(11): Show |
14 | HG01884.hp2 HG02257.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.-17+1957_-17+1961d others(7): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548823 | |||||||
chr6:41548823 | CCTTTTT | C | 6 | a0001c0002t0002g0058 a0001c0002t0002g0059 a0001c0002t0002g0084 others(3): Show |
6 | HG01884.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17+1957_-17+1962d others(8): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548823 | |||||||
chr6:41548824 | CT | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(134): Show |
169 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.-17+1978delT | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 41548824 | ||||||
chr6:41548824 | CTTT | C | 18 | a0001c0002t0002g0056 a0001c0002t0014g0122 a0001c0002t0043g0057 others(15): Show |
21 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17+1976_-17+1978d others(5): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 41548824 | ||||||
chr6:41548824 | CTTTT | C | 80 | a0001c0001t0002g0118 a0001c0001t0004g0020 a0001c0001t0004g0091 others(77): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.-17+1975_-17+1978d others(6): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 41548824 | ||||||
chr6:41548827 | T | A | 2 | a0001c0002t0002g0117 a0001c0002t0013g0083 |
2 | NA19066.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-17+1960T>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548827 | |||||||
chr6:41548828 | T | A | 28 | a0001c0001t0004g0051 a0001c0001t0004g0078 a0001c0001t0004g0079 others(25): Show |
33 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.-17+1961T>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548828 | |||||||
chr6:41548829 | T | A | 14 | a0001c0002t0002g0066 a0001c0002t0004g0044 a0001c0002t0004g0045 others(11): Show |
14 | HG01884.hp2 HG02257.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.-17+1962T>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548829 | |||||||
chr6:41548830 | T | A | 6 | a0001c0002t0002g0058 a0001c0002t0002g0059 a0001c0002t0002g0084 others(3): Show |
6 | HG01884.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17+1963T>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41548830 | |||||||
chr6:41549116 | G | C | 2 | a0001c0008t0020g0087 a0001c0008t0020g0088 |
2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-17+2249G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41549116 | |||||||
chr6:41549147 | C | G | 1 | a0001c0001t0001g0272 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-17+2280C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41549147 | |||||||
chr6:41549337 | G | A | 50 | a0001c0001t0004g0051 a0001c0001t0004g0078 a0001c0001t0004g0079 others(47): Show |
55 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.-17+2470G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41549337 | |||||||
chr6:41549360 | C | G | 1 | a0001c0002t0024g0018 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-17+2493C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41549360 | |||||||
chr6:41549380 | C | G | 2 | a0001c0008t0020g0087 a0001c0008t0020g0088 |
2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-17+2513C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41549380 | |||||||
chr6:41549446 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0167 |
3 | HG01106.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-17+2579G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41549446 | |||||||
chr6:41549664 | C | A | 1 | a0001c0002t0008g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-17+2797C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41549664 | |||||||
chr6:41549710 | G | A | 45 | a0001c0002t0003g0022 a0001c0002t0003g0023 a0001c0002t0003g0024 others(42): Show |
49 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.-17+2843G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41549710 | |||||||
chr6:41549719 | G | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(78): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-17+2852G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41549719 | |||||||
chr6:41549746 | A | G | 148 | a0001c0001t0002g0118 a0001c0001t0004g0020 a0001c0001t0004g0051 others(145): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.-17+2879A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41549746 | |||||||
chr6:41549812 | G | A | 1 | a0001c0002t0008g0053 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-17+2945G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41549812 | |||||||
chr6:41549826 | G | A | 148 | a0001c0001t0002g0118 a0001c0001t0004g0020 a0001c0001t0004g0051 others(145): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.-17+2959G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41549826 | |||||||
chr6:41549924 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-17+3057G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41549924 | |||||||
chr6:41550003 | C | A | 1 | a0001c0001t0005g0169 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-17+3136C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41550003 | |||||||
chr6:41550006 | T | C | 1 | a0001c0001t0005g0169 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-17+3139T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41550006 | |||||||
chr6:41550060 | T | C | 1 | a0001c0001t0005g0169 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-17+3193T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41550060 | |||||||
chr6:41550061 | A | T | 1 | a0001c0001t0005g0169 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-17+3194A>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41550061 | |||||||
chr6:41550119 | A | T | 1 | a0001c0001t0005g0169 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-17+3252A>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41550119 | |||||||
chr6:41550148 | A | G | 4 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(1): Show |
4 | HG01169.hp1 HG01175.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17+3281A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41550148 | |||||||
chr6:41550167 | C | A | 1 | a0001c0001t0005g0169 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-17+3300C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41550167 | |||||||
chr6:41550198 | TGGCATTA others(6): Show |
T | 1 | a0001c0001t0005g0169 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-17+3334_-17+3346d others(15): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 41550198 | ||||||
chr6:41550203 | T | C | 3 | a0001c0001t0001g0166 a0001c0001t0005g0243 a0001c0001t0027g0241 |
3 | NA18978.hp2 NA18988.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-17+3336T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41550203 | |||||||
chr6:41550275 | T | C | 50 | a0001c0001t0004g0051 a0001c0001t0004g0078 a0001c0001t0004g0079 others(47): Show |
55 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.-17+3408T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41550275 | |||||||
chr6:41550341 | G | T | 1 | a0001c0001t0005g0169 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-17+3474G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41550341 | |||||||
chr6:41550345 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0267 |
3 | HG02723.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-17+3478C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41550345 | |||||||
chr6:41550581 | G | A | 1 | a0001c0002t0004g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-17+3714G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41550581 | |||||||
chr6:41550769 | C | A | 1 | a0001c0001t0005g0169 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-17+3902C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41550769 | |||||||
chr6:41550770 | A | G | 1 | a0001c0001t0005g0169 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-17+3903A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41550770 | |||||||
chr6:41550772 | G | C | 1 | a0001c0001t0005g0169 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-17+3905G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41550772 | |||||||
chr6:41550889 | A | G | 1 | a0001c0001t0005g0169 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-17+4022A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41550889 | |||||||
chr6:41550926 | A | T | 17 | a0001c0002t0004g0017 a0001c0002t0004g0090 a0001c0002t0004g0106 others(14): Show |
21 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.-17+4059A>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41550926 | |||||||
chr6:41550938 | A | G | 17 | a0001c0002t0004g0017 a0001c0002t0004g0090 a0001c0002t0004g0106 others(14): Show |
21 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.-17+4071A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41550938 | |||||||
chr6:41551018 | C | T | 1 | a0001c0002t0025g0114 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-17+4151C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41551018 | |||||||
chr6:41551069 | A | G | 148 | a0001c0001t0002g0118 a0001c0001t0004g0020 a0001c0001t0004g0051 others(145): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.-17+4202A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41551069 | |||||||
chr6:41551233 | G | T | 1 | a0001c0001t0005g0169 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-17+4366G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41551233 | |||||||
chr6:41551254 | G | A | 2 | a0001c0004t0010g0224 a0001c0004t0010g0225 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-17+4387G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41551254 | |||||||
chr6:41551300 | G | A | 13 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0040 others(10): Show |
15 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17+4433G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41551300 | |||||||
chr6:41551376 | C | T | 1 | a0001c0002t0002g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-17+4509C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41551376 | |||||||
chr6:41551441 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-17+4574T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41551441 | |||||||
chr6:41551657 | C | T | 1 | a0001c0001t0005g0169 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-17+4790C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41551657 | |||||||
chr6:41551692 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0027 others(21): Show |
31 | HG00408.hp2 HG01070.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.-17+4825G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41551692 | |||||||
chr6:41551769 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-17+4902C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41551769 | |||||||
chr6:41551772 | C | A | 1 | a0001c0001t0005g0169 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-17+4905C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41551772 | |||||||
chr6:41551784 | G | A | 148 | a0001c0001t0002g0118 a0001c0001t0004g0020 a0001c0001t0004g0051 others(145): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.-17+4917G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41551784 | |||||||
chr6:41551789 | T | C | 1 | a0001c0002t0043g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-17+4922T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41551789 | |||||||
chr6:41551807 | G | A | 1 | a0001c0001t0031g0227 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-17+4940G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41551807 | |||||||
chr6:41551813 | G | C | 1 | a0001c0002t0024g0018 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-17+4946G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41551813 | |||||||
chr6:41551852 | A | G | 60 | a0001c0001t0004g0051 a0001c0001t0004g0078 a0001c0001t0004g0079 others(57): Show |
68 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.-17+4985A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41551852 | |||||||
chr6:41551897 | C | T | 3 | a0001c0002t0008g0100 a0001c0002t0008g0101 a0001c0002t0037g0102 |
3 | HG02559.hp2 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-17+5030C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41551897 | |||||||
chr6:41551906 | G | T | 1 | a0001c0002t0041g0072 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-17+5039G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41551906 | |||||||
chr6:41551916 | A | G | 148 | a0001c0001t0002g0118 a0001c0001t0004g0020 a0001c0001t0004g0051 others(145): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.-17+5049A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41551916 | |||||||
chr6:41551988 | C | T | 3 | a0001c0002t0002g0099 a0001c0002t0002g0103 a0001c0002t0039g0098 |
3 | HG02280.hp2 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-17+5121C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41551988 | |||||||
chr6:41552260 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-17+5393A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41552260 | |||||||
chr6:41552547 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-17+5680G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41552547 | |||||||
chr6:41552614 | G | C | 1 | a0001c0002t0002g0046 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-17+5747G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41552614 | |||||||
chr6:41552679 | G | A | 60 | a0001c0001t0004g0051 a0001c0001t0004g0078 a0001c0001t0004g0079 others(57): Show |
68 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.-17+5812G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41552679 | |||||||
chr6:41552709 | C | T | 3 | a0001c0001t0011g0036 a0001c0001t0011g0264 a0001c0001t0011g0265 |
4 | HG02451.hp2 HG03486.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17+5842C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41552709 | |||||||
chr6:41552715 | G | A | 60 | a0001c0001t0004g0051 a0001c0001t0004g0078 a0001c0001t0004g0079 others(57): Show |
68 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.-17+5848G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41552715 | |||||||
chr6:41552852 | C | T | 14 | a0001c0001t0011g0036 a0001c0001t0011g0265 a0001c0002t0002g0094 others(11): Show |
17 | HG00323.hp1 HG01074.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.-17+5985C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41552852 | |||||||
chr6:41553088 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-17+6221C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41553088 | |||||||
chr6:41553098 | C | A | 1 | a0001c0001t0001g0171 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-17+6231C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41553098 | |||||||
chr6:41553153 | T | C | 144 | a0001c0001t0004g0051 a0001c0001t0004g0078 a0001c0001t0004g0079 others(141): Show |
162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-17+6286T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41553153 | |||||||
chr6:41553324 | G | GGA | 57 | a0001c0002t0002g0094 a0001c0002t0003g0022 a0001c0002t0003g0023 others(54): Show |
63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.-17+6465_-17+6466d others(4): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 41553324 | ||||||
chr6:41553337 | C | T | 12 | a0001c0002t0002g0094 a0001c0002t0004g0093 a0001c0002t0008g0015 others(9): Show |
14 | HG00323.hp1 HG01074.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.-17+6470C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41553337 | |||||||
chr6:41553372 | T | C | 144 | a0001c0001t0004g0051 a0001c0001t0004g0078 a0001c0001t0004g0079 others(141): Show |
162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-17+6505T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41553372 | |||||||
chr6:41553639 | C | T | 3 | a0001c0002t0002g0099 a0001c0002t0002g0103 a0001c0002t0039g0098 |
3 | HG02280.hp2 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-17+6772C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41553639 | |||||||
chr6:41553661 | G | A | 5 | a0001c0002t0002g0019 a0001c0002t0002g0047 a0001c0002t0002g0115 others(2): Show |
5 | HG00597.hp2 HG00609.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17+6794G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41553661 | |||||||
chr6:41553759 | T | C | 1 | a0001c0002t0002g0115 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-17+6892T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41553759 | |||||||
chr6:41553835 | G | A | 3 | a0001c0003t0018g0278 a0001c0003t0018g0279 a0001c0003t0018g0280 |
3 | HG02698.hp1 HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-17+6968G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41553835 | |||||||
chr6:41554068 | C | T | 1 | a0001c0002t0043g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-17+7201C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41554068 | |||||||
chr6:41554205 | A | G | 45 | a0001c0002t0003g0022 a0001c0002t0003g0023 a0001c0002t0003g0024 others(42): Show |
49 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.-17+7338A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41554205 | |||||||
chr6:41554278 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0172 others(3): Show |
10 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17+7411G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41554278 | |||||||
chr6:41554357 | C | T | 12 | a0001c0002t0002g0094 a0001c0002t0004g0093 a0001c0002t0008g0015 others(9): Show |
14 | HG00323.hp1 HG01074.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.-17+7490C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41554357 | |||||||
chr6:41554443 | C | T | 2 | a0001c0006t0002g0006 a0001c0006t0013g0006 |
3 | HG02257.hp1 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-17+7576C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41554443 | |||||||
chr6:41554544 | T | C | 1 | a0001c0001t0004g0042 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-17+7677T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41554544 | |||||||
chr6:41554549 | G | A | 2 | a0001c0002t0002g0103 a0001c0002t0039g0098 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-17+7682G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41554549 | |||||||
chr6:41554696 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-17+7829C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41554696 | |||||||
chr6:41554721 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-17+7854G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41554721 | |||||||
chr6:41555199 | AGATCGC | A | 12 | a0001c0002t0002g0094 a0001c0002t0004g0093 a0001c0002t0008g0015 others(9): Show |
14 | HG00323.hp1 HG01074.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.-17+8334_-17+8339d others(8): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 41555199 | ||||||
chr6:41555228 | G | A | 53 | a0001c0001t0004g0051 a0001c0001t0004g0078 a0001c0001t0004g0079 others(50): Show |
59 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-17+8361G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41555228 | |||||||
chr6:41555244 | C | T | 2 | a0001c0004t0010g0224 a0001c0004t0010g0225 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-17+8377C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41555244 | |||||||
chr6:41555262 | G | A | 2 | a0001c0002t0002g0103 a0001c0002t0039g0098 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-17+8395G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41555262 | |||||||
chr6:41555328 | A | G | 45 | a0001c0002t0003g0022 a0001c0002t0003g0023 a0001c0002t0003g0024 others(42): Show |
49 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.-17+8461A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41555328 | |||||||
chr6:41555581 | C | T | 1 | a0001c0001t0005g0222 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-17+8714C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41555581 | |||||||
chr6:41555612 | G | A | 5 | a0001c0002t0004g0106 a0001c0002t0022g0104 a0001c0002t0022g0105 others(2): Show |
5 | HG01243.hp1 HG01891.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17+8745G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41555612 | |||||||
chr6:41555646 | A | G | 2 | a0001c0001t0004g0082 a0001c0002t0036g0081 |
2 | HG01361.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-17+8779A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41555646 | |||||||
chr6:41555808 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0178 a0001c0001t0005g0010 others(1): Show |
5 | NA18939.hp1 NA18963.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17+8941T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41555808 | |||||||
chr6:41555966 | C | CT | 5 | a0001c0002t0004g0044 a0001c0002t0004g0045 a0001c0002t0004g0070 others(2): Show |
5 | HG03239.hp1 NA18986.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17+9107dupT | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 41555966 | ||||||
chr6:41555992 | G | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0179 a0001c0001t0001g0180 others(3): Show |
7 | HG01192.hp2 HG01516.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17+9125G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41555992 | |||||||
chr6:41556058 | G | C | 1 | a0001c0002t0022g0104 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-17+9191G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41556058 | |||||||
chr6:41556127 | C | A | 1 | a0001c0001t0001g0228 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-17+9260C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41556127 | |||||||
chr6:41556275 | G | T | 13 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0040 others(10): Show |
15 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17+9408G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41556275 | |||||||
chr6:41556282 | G | A | 2 | a0001c0006t0002g0006 a0001c0006t0013g0006 |
3 | HG02257.hp1 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-17+9415G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41556282 | |||||||
chr6:41556325 | G | GT | 50 | a0001c0001t0001g0166 a0001c0001t0001g0221 a0001c0001t0001g0261 others(47): Show |
54 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.-16-9404dupT | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 41556325 | ||||||
chr6:41556325 | GT | G | 31 | a0001c0001t0001g0230 a0001c0001t0004g0051 a0001c0001t0004g0078 others(28): Show |
36 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.-16-9404delT | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 41556325 | ||||||
chr6:41556531 | A | G | 2 | a0001c0002t0019g0068 a0001c0002t0019g0069 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-16-9214A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41556531 | |||||||
chr6:41556546 | G | A | 42 | a0001c0001t0004g0082 a0001c0001t0011g0036 a0001c0001t0011g0229 others(39): Show |
49 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.-16-9199G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41556546 | |||||||
chr6:41556614 | G | A | 10 | a0001c0002t0004g0109 a0001c0002t0009g0007 a0001c0002t0009g0107 others(7): Show |
13 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.-16-9131G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41556614 | |||||||
chr6:41556700 | A | C | 4 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0005g0169 others(1): Show |
4 | NA18942.hp2 NA18997.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16-9045A>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41556700 | |||||||
chr6:41556872 | C | T | 3 | a0001c0004t0016g0258 a0001c0004t0016g0259 a0001c0004t0016g0260 |
3 | HG02809.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-16-8873C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41556872 | |||||||
chr6:41556939 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-16-8806T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41556939 | |||||||
chr6:41556942 | G | T | 1 | a0001c0002t0008g0100 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-16-8803G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41556942 | |||||||
chr6:41557126 | C | T | 4 | a0001c0002t0002g0066 a0001c0002t0012g0065 a0001c0012t0012g0063 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16-8619C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41557126 | |||||||
chr6:41557131 | A | G | 1 | a0001c0004t0016g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-16-8614A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41557131 | |||||||
chr6:41557246 | A | G | 1 | a0001c0002t0002g0014 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-16-8499A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41557246 | |||||||
chr6:41557554 | G | A | 2 | a0001c0008t0020g0087 a0001c0008t0020g0088 |
2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-16-8191G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41557554 | |||||||
chr6:41557669 | A | G | 30 | a0001c0002t0004g0017 a0001c0002t0004g0090 a0001c0002t0004g0106 others(27): Show |
36 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.-16-8076A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41557669 | |||||||
chr6:41557728 | G | A | 2 | a0001c0001t0004g0082 a0001c0002t0036g0081 |
2 | HG01361.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-16-8017G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41557728 | |||||||
chr6:41557810 | C | T | 6 | a0001c0002t0002g0058 a0001c0002t0002g0059 a0001c0002t0002g0084 others(3): Show |
6 | HG01884.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16-7935C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41557810 | |||||||
chr6:41557985 | A | G | 1 | a0001c0001t0028g0217 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-16-7760A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41557985 | |||||||
chr6:41558001 | A | G | 90 | a0001c0002t0002g0094 a0001c0002t0002g0103 a0001c0002t0003g0022 others(87): Show |
102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-16-7744A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41558001 | |||||||
chr6:41558082 | CA | C | 14 | a0001c0002t0002g0058 a0001c0002t0002g0059 a0001c0002t0002g0066 others(11): Show |
14 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.-16-7662delA | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41558082 | |||||||
chr6:41558221 | A | G | 2 | a0001c0005t0002g0016 a0001c0005t0002g0097 |
3 | HG01074.hp2 HG01081.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-16-7524A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41558221 | |||||||
chr6:41558256 | C | T | 2 | a0001c0002t0002g0103 a0001c0002t0039g0098 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-16-7489C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41558256 | |||||||
chr6:41558264 | A | T | 17 | a0001c0002t0004g0017 a0001c0002t0004g0090 a0001c0002t0004g0106 others(14): Show |
21 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.-16-7481A>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41558264 | |||||||
chr6:41558448 | C | T | 1 | a0001c0002t0007g0155 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-16-7297C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41558448 | |||||||
chr6:41558729 | G | A | 5 | a0001c0002t0007g0021 a0001c0002t0007g0121 a0001c0002t0007g0131 others(2): Show |
6 | HG00408.hp1 HG01928.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-7016G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41558729 | |||||||
chr6:41558731 | C | T | 30 | a0001c0002t0004g0017 a0001c0002t0004g0090 a0001c0002t0004g0106 others(27): Show |
36 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.-16-7014C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41558731 | |||||||
chr6:41558947 | C | A | 2 | a0001c0002t0002g0103 a0001c0002t0039g0098 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-16-6798C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41558947 | |||||||
chr6:41559017 | C | T | 1 | a0001c0010t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-16-6728C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41559017 | |||||||
chr6:41559108 | T | A | 1 | a0001c0002t0047g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-16-6637T>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41559108 | |||||||
chr6:41559305 | T | C | 1 | a0001c0001t0004g0078 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-16-6440T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41559305 | |||||||
chr6:41559396 | G | A | 2 | a0001c0001t0031g0227 a0003c0009t0005g0231 |
2 | NA18969.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-16-6349G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41559396 | |||||||
chr6:41559431 | A | G | 4 | a0001c0002t0003g0154 a0001c0002t0014g0026 a0001c0002t0014g0122 others(1): Show |
5 | NA18948.hp2 NA19055.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16-6314A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41559431 | |||||||
chr6:41559593 | A | G | 1 | a0001c0002t0010g0262 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-16-6152A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41559593 | |||||||
chr6:41559629 | G | A | 2 | a0001c0001t0001g0232 a0001c0010t0001g0257 |
2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-16-6116G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41559629 | |||||||
chr6:41559658 | C | G | 1 | a0001c0002t0002g0014 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-16-6087C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41559658 | |||||||
chr6:41559873 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-16-5872A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41559873 | |||||||
chr6:41559921 | A | G | 45 | a0001c0002t0003g0022 a0001c0002t0003g0023 a0001c0002t0003g0024 others(42): Show |
49 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.-16-5824A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41559921 | |||||||
chr6:41559953 | A | C | 3 | a0001c0002t0002g0056 a0001c0006t0002g0006 a0001c0006t0013g0006 |
4 | HG02257.hp1 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16-5792A>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41559953 | |||||||
chr6:41559960 | G | C | 145 | a0001c0001t0004g0082 a0001c0001t0010g0273 a0001c0001t0010g0274 others(142): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-16-5785G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41559960 | |||||||
chr6:41560157 | G | A | 58 | a0001c0002t0002g0094 a0001c0002t0003g0022 a0001c0002t0003g0023 others(55): Show |
64 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-16-5588G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41560157 | |||||||
chr6:41560163 | T | C | 12 | a0001c0002t0002g0094 a0001c0002t0004g0093 a0001c0002t0008g0015 others(9): Show |
14 | HG00323.hp1 HG01074.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.-16-5582T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41560163 | |||||||
chr6:41560269 | A | G | 1 | a0001c0002t0009g0113 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-16-5476A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41560269 | |||||||
chr6:41560321 | G | A | 13 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0040 others(10): Show |
15 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.-16-5424G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41560321 | |||||||
chr6:41560423 | C | G | 1 | a0001c0001t0004g0079 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-16-5322C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41560423 | |||||||
chr6:41560438 | A | G | 3 | a0001c0002t0004g0017 a0001c0002t0004g0090 a0001c0002t0004g0106 |
4 | HG01243.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16-5307A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41560438 | |||||||
chr6:41560461 | G | A | 143 | a0001c0001t0004g0082 a0001c0002t0002g0003 a0001c0002t0002g0014 others(140): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-16-5284G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41560461 | |||||||
chr6:41560476 | G | A | 143 | a0001c0001t0004g0082 a0001c0002t0002g0003 a0001c0002t0002g0014 others(140): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-16-5269G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41560476 | |||||||
chr6:41560806 | G | C | 3 | a0001c0002t0012g0065 a0001c0012t0012g0063 a0009c0011t0012g0064 |
3 | HG02257.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-16-4939G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41560806 | |||||||
chr6:41560917 | C | G | 1 | a0001c0001t0001g0256 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-16-4828C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41560917 | |||||||
chr6:41560920 | C | CAAAAGCA others(347): Show |
1 | a0001c0002t0008g0096 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-16-4812_-16-4811i others(356): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 41560920 | ||||||
chr6:41561215 | C | G | 13 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0040 others(10): Show |
15 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.-16-4530C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41561215 | |||||||
chr6:41561322 | TC | T | 142 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0019 others(139): Show |
162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-16-4420delC | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 41561322 | ||||||
chr6:41561886 | G | T | 1 | a0001c0001t0001g0223 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-16-3859G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41561886 | |||||||
chr6:41561912 | C | T | 2 | a0001c0002t0002g0084 a0001c0002t0002g0085 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-16-3833C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41561912 | |||||||
chr6:41561926 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0178 a0001c0001t0005g0010 others(1): Show |
5 | NA18939.hp1 NA18963.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16-3819C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41561926 | |||||||
chr6:41562011 | C | A | 2 | a0001c0002t0002g0103 a0001c0002t0039g0098 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-16-3734C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41562011 | |||||||
chr6:41562085 | G | A | 3 | a0001c0002t0015g0004 a0001c0002t0038g0004 a0002c0007t0015g0004 |
5 | HG01069.hp1 HG01099.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16-3660G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41562085 | |||||||
chr6:41562096 | G | A | 2 | a0001c0008t0020g0087 a0001c0008t0020g0088 |
2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-16-3649G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41562096 | |||||||
chr6:41562128 | C | A | 1 | a0001c0010t0001g0277 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-16-3617C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41562128 | |||||||
chr6:41562157 | G | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0214 a0001c0001t0001g0215 |
4 | HG01070.hp1 HG01934.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16-3588G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41562157 | |||||||
chr6:41562206 | C | T | 1 | a0001c0008t0020g0088 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-16-3539C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41562206 | |||||||
chr6:41562229 | G | A | 1 | a0001c0002t0009g0107 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-16-3516G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41562229 | |||||||
chr6:41562304 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-16-3441A>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41562304 | |||||||
chr6:41562477 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-16-3268G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41562477 | |||||||
chr6:41562546 | T | C | 2 | a0001c0002t0002g0103 a0001c0002t0039g0098 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-16-3199T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41562546 | |||||||
chr6:41562551 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-16-3194C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41562551 | |||||||
chr6:41562581 | A | T | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0005g0157 others(1): Show |
5 | HG02572.hp2 HG02717.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16-3164A>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41562581 | |||||||
chr6:41562848 | C | A | 6 | a0001c0002t0002g0058 a0001c0002t0002g0059 a0001c0002t0002g0084 others(3): Show |
6 | HG01884.hp1 HG02145.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16-2897C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41562848 | |||||||
chr6:41562940 | C | G | 13 | a0001c0002t0002g0094 a0001c0002t0004g0093 a0001c0002t0008g0015 others(10): Show |
15 | HG00323.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.-16-2805C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41562940 | |||||||
chr6:41562980 | A | G | 3 | a0001c0003t0018g0278 a0001c0003t0018g0279 a0001c0003t0018g0280 |
3 | HG02698.hp1 HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-16-2765A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41562980 | |||||||
chr6:41563263 | C | T | 1 | a0001c0001t0033g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-16-2482C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41563263 | |||||||
chr6:41563276 | A | G | 1 | a0001c0002t0043g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-16-2469A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41563276 | |||||||
chr6:41563324 | G | A | 1 | a0001c0002t0007g0134 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-16-2421G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41563324 | |||||||
chr6:41563429 | G | A | 13 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0040 others(10): Show |
15 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.-16-2316G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41563429 | |||||||
chr6:41563483 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-16-2262C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41563483 | |||||||
chr6:41563485 | G | A | 81 | a0001c0002t0002g0094 a0001c0002t0002g0103 a0001c0002t0003g0022 others(78): Show |
90 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.-16-2260G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41563485 | |||||||
chr6:41563504 | C | G | 1 | a0001c0005t0002g0097 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-16-2241C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41563504 | |||||||
chr6:41563506 | A | G | 3 | a0001c0002t0002g0056 a0001c0006t0002g0006 a0001c0006t0013g0006 |
4 | HG02257.hp1 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16-2239A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41563506 | |||||||
chr6:41563630 | T | C | 2 | a0001c0002t0002g0058 a0001c0002t0002g0059 |
2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-16-2115T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41563630 | |||||||
chr6:41563713 | A | G | 1 | a0001c0002t0012g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-16-2032A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41563713 | |||||||
chr6:41563860 | A | T | 1 | a0001c0002t0008g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-16-1885A>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41563860 | |||||||
chr6:41564108 | C | T | 7 | a0001c0002t0004g0017 a0001c0002t0004g0090 a0001c0002t0004g0106 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-16-1637C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41564108 | |||||||
chr6:41564317 | G | C | 1 | a0001c0002t0009g0107 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-16-1428G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41564317 | |||||||
chr6:41564378 | C | T | 1 | a0001c0005t0002g0097 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-16-1367C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41564378 | |||||||
chr6:41564530 | C | T | 45 | a0001c0002t0003g0022 a0001c0002t0003g0023 a0001c0002t0003g0024 others(42): Show |
49 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.-16-1215C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41564530 | |||||||
chr6:41564559 | G | A | 1 | a0001c0002t0012g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-16-1186G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41564559 | |||||||
chr6:41564651 | C | G | 17 | a0001c0002t0004g0017 a0001c0002t0004g0090 a0001c0002t0004g0106 others(14): Show |
21 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.-16-1094C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41564651 | |||||||
chr6:41564656 | G | T | 3 | a0001c0003t0018g0278 a0001c0003t0018g0279 a0001c0003t0018g0280 |
3 | HG02698.hp1 HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-16-1089G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41564656 | |||||||
chr6:41564674 | T | C | 2 | a0001c0002t0002g0103 a0001c0002t0039g0098 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-16-1071T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41564674 | |||||||
chr6:41564774 | A | AGTCAAAA others(11): Show |
1 | a0001c0002t0008g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-16-970_-16-969ins others(18): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr6 | 41564774 | ||||||
chr6:41564776 | G | A | 1 | a0001c0002t0008g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-16-969G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41564776 | |||||||
chr6:41564935 | G | A | 1 | a0001c0002t0039g0098 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-16-810G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41564935 | |||||||
chr6:41565103 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-16-642A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41565103 | |||||||
chr6:41565133 | A | G | 5 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
5 | HG00408.hp2 HG02132.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16-612A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41565133 | |||||||
chr6:41565166 | G | A | 62 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0019 others(59): Show |
73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.-16-579G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41565166 | |||||||
chr6:41565294 | A | G | 1 | a0001c0002t0003g0130 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-16-451A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41565294 | |||||||
chr6:41565308 | C | T | 143 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0019 others(140): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-16-437C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41565308 | |||||||
chr6:41565612 | G | T | 2 | a0001c0002t0002g0103 a0001c0002t0039g0098 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-16-133G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 1/16 | chr6 | 41565612 | |||||||
chr6:41566196 | G | A | 1 | a0001c0001t0004g0079 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.204+232G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41566196 | |||||||
chr6:41566202 | G | A | 17 | a0001c0001t0001g0034 a0001c0001t0001g0160 a0001c0001t0001g0161 others(14): Show |
19 | HG00733.hp2 HG01099.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.204+238G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41566202 | |||||||
chr6:41566226 | G | A | 7 | a0001c0002t0004g0017 a0001c0002t0004g0090 a0001c0002t0004g0106 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+262G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41566226 | |||||||
chr6:41566283 | A | G | 2 | a0001c0002t0009g0007 a0001c0002t0009g0107 |
4 | HG00140.hp1 HG00323.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+319A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41566283 | |||||||
chr6:41566357 | G | T | 1 | a0001c0001t0034g0208 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.204+393G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41566357 | |||||||
chr6:41566366 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.204+402G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41566366 | |||||||
chr6:41566905 | G | T | 1 | a0001c0001t0001g0207 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.204+941G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41566905 | |||||||
chr6:41567641 | A | G | 144 | a0001c0001t0010g0273 a0001c0001t0010g0274 a0001c0002t0002g0003 others(141): Show |
164 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.204+1677A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41567641 | |||||||
chr6:41567660 | T | G | 1 | a0001c0001t0001g0029 | 2 | HG00639.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.204+1696T>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41567660 | |||||||
chr6:41567865 | C | T | 1 | a0001c0002t0003g0152 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.204+1901C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41567865 | |||||||
chr6:41568048 | A | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0167 |
3 | HG01106.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.204+2084A>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41568048 | |||||||
chr6:41568100 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.204+2136G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41568100 | |||||||
chr6:41568219 | A | G | 1 | a0001c0002t0012g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.204+2255A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41568219 | |||||||
chr6:41568324 | A | G | 45 | a0001c0002t0003g0022 a0001c0002t0003g0023 a0001c0002t0003g0024 others(42): Show |
49 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.204+2360A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41568324 | |||||||
chr6:41568370 | T | C | 2 | a0001c0005t0002g0016 a0001c0005t0002g0097 |
3 | HG01074.hp2 HG01081.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.204+2406T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41568370 | |||||||
chr6:41568508 | A | G | 4 | a0001c0001t0001g0027 a0001c0001t0001g0167 a0001c0001t0001g0206 others(1): Show |
5 | HG01106.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+2544A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41568508 | |||||||
chr6:41568620 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.204+2656C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41568620 | |||||||
chr6:41568630 | G | C | 13 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0040 others(10): Show |
15 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.204+2666G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41568630 | |||||||
chr6:41568653 | GTCTGTGG others(7): Show |
G | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.204+2690_204+2703d others(16): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41568653 | |||||||
chr6:41568689 | C | T | 144 | a0001c0001t0010g0273 a0001c0001t0010g0274 a0001c0002t0002g0003 others(141): Show |
164 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.204+2725C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41568689 | |||||||
chr6:41568849 | T | G | 144 | a0001c0001t0010g0273 a0001c0001t0010g0274 a0001c0002t0002g0003 others(141): Show |
164 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.204+2885T>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41568849 | |||||||
chr6:41568935 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.204+2971G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41568935 | |||||||
chr6:41569085 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0167 |
3 | HG01106.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.204+3121A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41569085 | |||||||
chr6:41569606 | G | A | 61 | a0001c0001t0010g0273 a0001c0001t0010g0274 a0001c0002t0002g0003 others(58): Show |
72 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.204+3642G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41569606 | |||||||
chr6:41569830 | C | A | 45 | a0001c0002t0003g0022 a0001c0002t0003g0023 a0001c0002t0003g0024 others(42): Show |
49 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.204+3866C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41569830 | |||||||
chr6:41569848 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.204+3884G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41569848 | |||||||
chr6:41569935 | T | C | 6 | a0001c0002t0004g0017 a0001c0002t0004g0060 a0001c0002t0004g0090 others(3): Show |
7 | HG01243.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.204+3971T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41569935 | |||||||
chr6:41570069 | A | C | 5 | a0001c0002t0002g0058 a0001c0002t0002g0059 a0001c0002t0002g0084 others(2): Show |
5 | HG01884.hp1 HG02145.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.204+4105A>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41570069 | |||||||
chr6:41570079 | G | GAC | 82 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(79): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.204+4152_204+4153d others(4): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 41570079 | ||||||
chr6:41570079 | G | GACAC | 21 | a0001c0001t0001g0029 a0001c0001t0001g0173 a0001c0001t0001g0179 others(18): Show |
24 | HG00544.hp2 HG00609.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.204+4150_204+4153d others(6): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 41570079 | ||||||
chr6:41570079 | G | GACACAC | 4 | a0001c0002t0003g0151 a0001c0002t0007g0155 a0001c0002t0026g0133 others(1): Show |
4 | HG01978.hp1 HG02451.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+4148_204+4153d others(8): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 41570079 | ||||||
chr6:41570079 | G | GACACACA others(1): Show |
11 | a0001c0002t0003g0025 a0001c0002t0003g0124 a0001c0002t0003g0125 others(8): Show |
12 | HG00280.hp1 HG01123.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.204+4146_204+4153d others(10): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 41570079 | ||||||
chr6:41570079 | G | GACACACA others(3): Show |
19 | a0001c0002t0003g0023 a0001c0002t0003g0024 a0001c0002t0003g0123 others(16): Show |
22 | HG00323.hp1 HG00408.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.204+4144_204+4153d others(12): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 41570079 | ||||||
chr6:41570079 | G | GACACACA others(5): Show |
27 | a0001c0001t0004g0042 a0001c0002t0002g0059 a0001c0002t0002g0084 others(24): Show |
29 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.204+4142_204+4153d others(14): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 41570079 | ||||||
chr6:41570079 | G | GACACACA others(7): Show |
7 | a0001c0002t0003g0136 a0001c0002t0003g0137 a0001c0002t0003g0138 others(4): Show |
7 | HG01943.hp1 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.204+4140_204+4153d others(16): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 41570079 | ||||||
chr6:41570079 | G | GACACACA others(9): Show |
4 | a0001c0002t0003g0135 a0001c0003t0006g0039 a0001c0003t0006g0281 others(1): Show |
4 | HG02148.hp2 HG03491.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+4138_204+4153d others(18): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 41570079 | ||||||
chr6:41570079 | G | GACACACA others(11): Show |
1 | a0001c0003t0006g0038 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.204+4136_204+4153d others(20): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 41570079 | ||||||
chr6:41570079 | G | GACACACA others(13): Show |
1 | a0001c0004t0010g0225 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.204+4134_204+4153d others(22): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 41570079 | ||||||
chr6:41570079 | G | GACACACA others(15): Show |
4 | a0001c0001t0002g0055 a0001c0001t0004g0054 a0001c0004t0010g0224 others(1): Show |
4 | HG02145.hp2 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+4132_204+4153d others(24): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 41570079 | ||||||
chr6:41570079 | G | GACACACA others(17): Show |
1 | a0001c0002t0008g0096 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.204+4130_204+4153d others(26): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 41570079 | ||||||
chr6:41570079 | G | GACACACA others(19): Show |
3 | a0001c0002t0002g0058 a0001c0004t0016g0258 a0001c0004t0016g0260 |
3 | HG02809.hp1 HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.204+4128_204+4153d others(28): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 41570079 | ||||||
chr6:41570079 | G | GACACACA others(23): Show |
3 | a0001c0001t0011g0036 a0001c0001t0011g0229 a0001c0001t0011g0264 |
4 | HG02976.hp1 HG03486.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+4124_204+4153d others(32): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 41570079 | ||||||
chr6:41570079 | G | GACACACA others(27): Show |
1 | a0001c0001t0011g0265 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.204+4120_204+4153d others(36): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 41570079 | ||||||
chr6:41570079 | GAC | G | 28 | a0001c0001t0001g0211 a0001c0001t0001g0215 a0001c0001t0001g0255 others(25): Show |
33 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.204+4152_204+4153d others(4): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 41570079 | ||||||
chr6:41570335 | A | C | 1 | a0001c0002t0043g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.204+4371A>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41570335 | |||||||
chr6:41570491 | C | G | 1 | a0001c0002t0002g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.204+4527C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41570491 | |||||||
chr6:41570562 | C | A | 9 | a0001c0002t0002g0103 a0001c0002t0004g0017 a0001c0002t0004g0090 others(6): Show |
10 | HG01243.hp1 HG01891.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.204+4598C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41570562 | |||||||
chr6:41570807 | T | C | 157 | a0001c0001t0002g0055 a0001c0001t0004g0042 a0001c0001t0004g0054 others(154): Show |
178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.204+4843T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41570807 | |||||||
chr6:41570921 | A | G | 7 | a0001c0002t0004g0017 a0001c0002t0004g0090 a0001c0002t0004g0106 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+4957A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41570921 | |||||||
chr6:41571183 | T | TTGC | 45 | a0001c0002t0003g0022 a0001c0002t0003g0023 a0001c0002t0003g0024 others(42): Show |
49 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.204+5222_204+5224d others(5): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 41571183 | ||||||
chr6:41571390 | A | G | 1 | a0001c0002t0043g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.204+5426A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41571390 | |||||||
chr6:41571499 | G | A | 1 | a0001c0002t0008g0053 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.204+5535G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41571499 | |||||||
chr6:41571553 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.204+5589C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41571553 | |||||||
chr6:41571622 | G | T | 1 | a0001c0002t0002g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.204+5658G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41571622 | |||||||
chr6:41571908 | T | G | 1 | a0001c0001t0005g0157 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.204+5944T>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41571908 | |||||||
chr6:41571940 | G | A | 1 | a0001c0002t0007g0147 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.204+5976G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41571940 | |||||||
chr6:41572154 | A | G | 22 | a0001c0002t0002g0103 a0001c0002t0004g0017 a0001c0002t0004g0090 others(19): Show |
25 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.205-5832A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41572154 | |||||||
chr6:41572317 | C | T | 1 | a0001c0001t0005g0175 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.205-5669C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41572317 | |||||||
chr6:41572337 | C | T | 2 | a0001c0008t0020g0087 a0001c0008t0020g0088 |
2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.205-5649C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41572337 | |||||||
chr6:41572857 | T | G | 2 | a0001c0004t0010g0224 a0001c0004t0010g0225 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.205-5129T>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41572857 | |||||||
chr6:41573071 | C | T | 35 | a0001c0001t0010g0273 a0001c0001t0010g0274 a0001c0002t0002g0003 others(32): Show |
42 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.205-4915C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41573071 | |||||||
chr6:41573112 | G | A | 1 | a0009c0011t0012g0064 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.205-4874G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41573112 | |||||||
chr6:41573135 | G | C | 1 | a0001c0002t0003g0139 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.205-4851G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41573135 | |||||||
chr6:41573137 | G | A | 13 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0040 others(10): Show |
15 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.205-4849G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41573137 | |||||||
chr6:41573231 | A | T | 62 | a0001c0001t0010g0273 a0001c0001t0010g0274 a0001c0002t0002g0003 others(59): Show |
73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.205-4755A>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41573231 | |||||||
chr6:41573511 | G | A | 1 | a0001c0002t0022g0105 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.205-4475G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41573511 | |||||||
chr6:41573687 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.205-4299T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41573687 | |||||||
chr6:41573747 | G | C | 3 | a0001c0001t0004g0051 a0001c0001t0004g0078 a0001c0001t0004g0079 |
3 | NA18944.hp1 NA18971.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.205-4239G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41573747 | |||||||
chr6:41573772 | T | G | 13 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0040 others(10): Show |
15 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.205-4214T>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41573772 | |||||||
chr6:41573847 | G | T | 1 | a0001c0001t0033g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.205-4139G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41573847 | |||||||
chr6:41573854 | C | T | 1 | a0001c0002t0002g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.205-4132C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41573854 | |||||||
chr6:41573937 | A | G | 1 | a0001c0002t0036g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.205-4049A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41573937 | |||||||
chr6:41574476 | T | C | 143 | a0001c0001t0010g0273 a0001c0001t0010g0274 a0001c0002t0002g0003 others(140): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.205-3510T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41574476 | |||||||
chr6:41574503 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0245 |
2 | HG01070.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.205-3483G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41574503 | |||||||
chr6:41574651 | G | C | 1 | a0001c0008t0020g0087 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.205-3335G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41574651 | |||||||
chr6:41574667 | C | T | 1 | a0001c0002t0002g0099 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.205-3319C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41574667 | |||||||
chr6:41574668 | G | A | 1 | a0001c0001t0010g0238 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.205-3318G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41574668 | |||||||
chr6:41574679 | C | T | 143 | a0001c0001t0010g0273 a0001c0001t0010g0274 a0001c0002t0002g0003 others(140): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.205-3307C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41574679 | |||||||
chr6:41574705 | T | C | 1 | a0001c0001t0034g0208 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.205-3281T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41574705 | |||||||
chr6:41574788 | C | T | 1 | a0001c0001t0005g0169 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.205-3198C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41574788 | |||||||
chr6:41574945 | CGTGTTTT others(10): Show |
C | 1 | a0001c0002t0043g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.205-3021_205-3005d others(19): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 41574945 | ||||||
chr6:41575661 | A | G | 1 | a0001c0001t0001g0251 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.205-2325A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41575661 | |||||||
chr6:41575674 | A | T | 1 | a0001c0001t0001g0186 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.205-2312A>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41575674 | |||||||
chr6:41575811 | A | T | 1 | a0006c0016t0005g0205 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.205-2175A>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41575811 | |||||||
chr6:41575846 | G | A | 2 | a0001c0002t0002g0103 a0001c0002t0039g0098 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.205-2140G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41575846 | |||||||
chr6:41575880 | C | G | 13 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0040 others(10): Show |
15 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.205-2106C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41575880 | |||||||
chr6:41576035 | C | T | 5 | a0001c0002t0002g0058 a0001c0002t0002g0059 a0001c0002t0002g0084 others(2): Show |
5 | HG01884.hp1 HG02145.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.205-1951C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41576035 | |||||||
chr6:41576046 | G | A | 13 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0040 others(10): Show |
15 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.205-1940G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41576046 | |||||||
chr6:41576049 | A | AC | 35 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0159 others(32): Show |
38 | HG00609.hp1 HG00642.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.205-1926dupC | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr6 | 41576049 | ||||||
chr6:41576055 | C | A | 144 | a0001c0001t0010g0273 a0001c0001t0010g0274 a0001c0002t0002g0003 others(141): Show |
164 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.205-1931C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41576055 | |||||||
chr6:41576061 | A | C | 1 | a0001c0001t0001g0204 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.205-1925A>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41576061 | |||||||
chr6:41576101 | G | C | 1 | a0001c0001t0001g0027 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.205-1885G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41576101 | |||||||
chr6:41576146 | T | A | 1 | a0001c0002t0004g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.205-1840T>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41576146 | |||||||
chr6:41576362 | G | A | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0005g0157 others(1): Show |
5 | HG02572.hp2 HG02717.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.205-1624G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41576362 | |||||||
chr6:41576657 | C | A | 11 | a0001c0002t0002g0094 a0001c0002t0004g0093 a0001c0002t0008g0015 others(8): Show |
12 | HG00323.hp1 HG01433.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.205-1329C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41576657 | |||||||
chr6:41576657 | C | T | 1 | a0001c0002t0046g0146 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.205-1329C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41576657 | |||||||
chr6:41576756 | A | G | 147 | a0001c0001t0010g0273 a0001c0001t0010g0274 a0001c0001t0031g0227 others(144): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.205-1230A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41576756 | |||||||
chr6:41576989 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.205-997G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41576989 | |||||||
chr6:41577143 | A | C | 1 | a0001c0001t0001g0234 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.205-843A>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41577143 | |||||||
chr6:41577716 | G | C | 13 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0040 others(10): Show |
15 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.205-270G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41577716 | |||||||
chr6:41577736 | C | T | 22 | a0001c0002t0002g0103 a0001c0002t0004g0017 a0001c0002t0004g0090 others(19): Show |
25 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.205-250C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41577736 | |||||||
chr6:41577822 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.205-164C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41577822 | |||||||
chr6:41577850 | T | C | 9 | a0001c0002t0002g0103 a0001c0002t0004g0017 a0001c0002t0004g0090 others(6): Show |
10 | HG01243.hp1 HG01891.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.205-136T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 2/16 | chr6 | 41577850 | |||||||
chr6:41578366 | T | C | 1 | a0001c0002t0009g0113 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.300+285T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41578366 | |||||||
chr6:41578456 | G | C | 1 | a0001c0002t0007g0148 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.300+375G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41578456 | |||||||
chr6:41578553 | A | G | 1 | a0001c0010t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.300+472A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41578553 | |||||||
chr6:41578717 | C | T | 2 | a0001c0004t0010g0224 a0001c0004t0010g0225 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.300+636C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41578717 | |||||||
chr6:41578720 | G | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0244 |
2 | NA18983.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.300+639G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41578720 | |||||||
chr6:41578795 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.300+714T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41578795 | |||||||
chr6:41579120 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.300+1039A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41579120 | |||||||
chr6:41579123 | T | C | 1 | a0001c0002t0017g0012 | 3 | HG02886.hp2 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.300+1042T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41579123 | |||||||
chr6:41579269 | C | T | 1 | a0001c0001t0028g0217 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.300+1188C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41579269 | |||||||
chr6:41579296 | G | T | 1 | a0001c0002t0014g0122 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.300+1215G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41579296 | |||||||
chr6:41579526 | A | T | 1 | a0008c0017t0029g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.300+1445A>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41579526 | |||||||
chr6:41579574 | T | C | 145 | a0001c0001t0010g0273 a0001c0001t0010g0274 a0001c0001t0031g0227 others(142): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.300+1493T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41579574 | |||||||
chr6:41579676 | A | G | 2 | a0001c0008t0020g0087 a0001c0008t0020g0088 |
2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.300+1595A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41579676 | |||||||
chr6:41579801 | ATACT | A | 8 | a0001c0002t0002g0066 a0001c0002t0012g0043 a0001c0002t0012g0065 others(5): Show |
8 | HG01884.hp2 HG02257.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.300+1725_300+1728d others(6): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr6 | 41579801 | ||||||
chr6:41579859 | G | A | 3 | a0001c0002t0002g0056 a0001c0006t0002g0006 a0001c0006t0013g0006 |
4 | HG02257.hp1 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+1778G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41579859 | |||||||
chr6:41580044 | C | CT | 76 | a0001c0001t0001g0037 a0001c0001t0010g0273 a0001c0001t0010g0274 others(73): Show |
87 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.300+1981dupT | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr6 | 41580044 | ||||||
chr6:41580044 | C | CTT | 61 | a0001c0001t0031g0227 a0001c0002t0002g0046 a0001c0002t0002g0074 others(58): Show |
71 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.300+1980_300+1981d others(4): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr6 | 41580044 | ||||||
chr6:41580102 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.300+2021C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41580102 | |||||||
chr6:41580115 | C | T | 1 | a0001c0002t0043g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.300+2034C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41580115 | |||||||
chr6:41580152 | C | G | 3 | a0001c0003t0018g0278 a0001c0003t0018g0279 a0001c0003t0018g0280 |
3 | HG02698.hp1 HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.300+2071C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41580152 | |||||||
chr6:41580178 | A | T | 1 | a0001c0002t0043g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.300+2097A>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41580178 | |||||||
chr6:41580254 | G | A | 1 | a0001c0002t0002g0099 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.300+2173G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41580254 | |||||||
chr6:41580322 | C | T | 2 | a0001c0005t0002g0016 a0001c0005t0002g0097 |
3 | HG01074.hp2 HG01081.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.300+2241C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41580322 | |||||||
chr6:41580449 | A | G | 6 | a0001c0002t0003g0022 a0001c0002t0003g0128 a0001c0002t0003g0129 others(3): Show |
7 | HG01257.hp2 HG01258.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.300+2368A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41580449 | |||||||
chr6:41580462 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.300+2381G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41580462 | |||||||
chr6:41580490 | G | A | 3 | a0001c0002t0002g0056 a0001c0006t0002g0006 a0001c0006t0013g0006 |
4 | HG02257.hp1 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+2409G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41580490 | |||||||
chr6:41580525 | G | C | 1 | a0001c0002t0002g0075 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.300+2444G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41580525 | |||||||
chr6:41580563 | T | C | 2 | a0001c0005t0002g0016 a0001c0005t0002g0097 |
3 | HG01074.hp2 HG01081.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.300+2482T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41580563 | |||||||
chr6:41580674 | G | A | 13 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0040 others(10): Show |
15 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.300+2593G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41580674 | |||||||
chr6:41580685 | T | C | 1 | a0001c0002t0003g0156 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.300+2604T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41580685 | |||||||
chr6:41580692 | A | G | 146 | a0001c0001t0002g0118 a0001c0001t0010g0273 a0001c0001t0010g0274 others(143): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.300+2611A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41580692 | |||||||
chr6:41580708 | T | C | 1 | a0001c0002t0002g0056 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.300+2627T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41580708 | |||||||
chr6:41580802 | C | G | 146 | a0001c0001t0002g0118 a0001c0001t0010g0273 a0001c0001t0010g0274 others(143): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.300+2721C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41580802 | |||||||
chr6:41580893 | C | G | 4 | a0001c0002t0003g0154 a0001c0002t0014g0026 a0001c0002t0014g0122 others(1): Show |
5 | NA18948.hp2 NA19055.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.300+2812C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41580893 | |||||||
chr6:41580933 | A | T | 59 | a0001c0001t0031g0227 a0001c0002t0002g0094 a0001c0002t0003g0022 others(56): Show |
65 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.300+2852A>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41580933 | |||||||
chr6:41580949 | C | T | 1 | a0001c0002t0043g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.300+2868C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41580949 | |||||||
chr6:41581017 | A | G | 148 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0002g0118 others(145): Show |
168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.300+2936A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41581017 | |||||||
chr6:41581055 | A | G | 46 | a0001c0001t0031g0227 a0001c0002t0003g0022 a0001c0002t0003g0023 others(43): Show |
50 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.300+2974A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41581055 | |||||||
chr6:41581165 | G | C | 1 | a0001c0003t0006g0282 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.300+3084G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41581165 | |||||||
chr6:41581370 | C | T | 13 | a0001c0002t0002g0094 a0001c0002t0004g0093 a0001c0002t0008g0015 others(10): Show |
15 | HG00323.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.300+3289C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41581370 | |||||||
chr6:41581380 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.300+3299G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41581380 | |||||||
chr6:41581729 | G | A | 4 | a0001c0002t0004g0060 a0001c0003t0018g0278 a0001c0003t0018g0279 others(1): Show |
4 | HG02698.hp1 HG02896.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.301-3040G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41581729 | |||||||
chr6:41581747 | C | G | 1 | a0001c0002t0004g0109 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.301-3022C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41581747 | |||||||
chr6:41581980 | C | G | 1 | a0001c0002t0002g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.301-2789C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41581980 | |||||||
chr6:41582155 | GAATTTAA others(30): Show |
G | 1 | a0001c0002t0003g0127 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.301-2613_301-2577d others(39): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582155 | |||||||
chr6:41582205 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.301-2564C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582205 | |||||||
chr6:41582211 | A | G | 57 | a0001c0001t0001g0186 a0001c0001t0001g0194 a0001c0001t0001g0275 others(54): Show |
66 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.301-2558A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582211 | |||||||
chr6:41582306 | C | T | 5 | a0001c0002t0002g0058 a0001c0002t0002g0059 a0001c0002t0002g0084 others(2): Show |
5 | HG01884.hp1 HG02145.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.301-2463C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582306 | |||||||
chr6:41582328 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.301-2441C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582328 | |||||||
chr6:41582391 | A | G | 2 | a0001c0004t0010g0224 a0001c0004t0010g0225 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.301-2378A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582391 | |||||||
chr6:41582434 | C | A | 90 | a0001c0001t0001g0008 a0001c0001t0001g0173 a0001c0001t0030g0219 others(87): Show |
104 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.301-2335C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582434 | |||||||
chr6:41582554 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.301-2215G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582554 | |||||||
chr6:41582575 | A | G | 1 | a0001c0002t0003g0127 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.301-2194A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582575 | |||||||
chr6:41582576 | G | A | 1 | a0001c0002t0003g0127 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.301-2193G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582576 | |||||||
chr6:41582579 | A | G | 1 | a0001c0002t0003g0127 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.301-2190A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582579 | |||||||
chr6:41582587 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.301-2182G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582587 | |||||||
chr6:41582606 | T | A | 1 | a0001c0002t0003g0127 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.301-2163T>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582606 | |||||||
chr6:41582656 | A | G | 10 | a0001c0002t0002g0094 a0001c0002t0008g0015 a0001c0002t0008g0053 others(7): Show |
11 | HG00323.hp1 HG01891.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.301-2113A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582656 | |||||||
chr6:41582669 | G | C | 1 | a0001c0002t0013g0076 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.301-2100G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582669 | |||||||
chr6:41582689 | A | C | 1 | a0001c0002t0003g0127 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.301-2080A>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582689 | |||||||
chr6:41582696 | T | TATGTTGT others(24): Show |
1 | a0001c0002t0003g0127 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.301-2073_301-2072i others(33): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582696 | |||||||
chr6:41582698 | T | C | 1 | a0001c0002t0003g0127 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.301-2071T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582698 | |||||||
chr6:41582702 | C | A | 1 | a0001c0002t0003g0127 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.301-2067C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582702 | |||||||
chr6:41582705 | T | C | 1 | a0001c0002t0003g0127 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.301-2064T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582705 | |||||||
chr6:41582706 | T | C | 1 | a0001c0002t0003g0127 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.301-2063T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582706 | |||||||
chr6:41582721 | C | A | 1 | a0001c0002t0003g0127 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.301-2048C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582721 | |||||||
chr6:41582726 | C | G | 1 | a0001c0002t0003g0127 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.301-2043C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582726 | |||||||
chr6:41582728 | CA | C | 144 | a0001c0001t0005g0175 a0001c0001t0010g0273 a0001c0001t0010g0274 others(141): Show |
164 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.301-2040delA | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582728 | |||||||
chr6:41582889 | G | A | 2 | a0001c0002t0002g0052 a0001c0002t0002g0077 |
2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.301-1880G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41582889 | |||||||
chr6:41583021 | A | AAAC | 7 | a0001c0002t0003g0024 a0001c0002t0003g0126 a0001c0002t0003g0136 others(4): Show |
8 | HG03540.hp1 NA18981.hp2 NA18994.hp1 others(5): Show |
intron_variant | MODIFIER | c.301-1733_301-1731d others(5): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr6 | 41583021 | ||||||
chr6:41583136 | T | G | 1 | a0001c0002t0003g0144 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.301-1633T>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41583136 | |||||||
chr6:41583193 | G | A | 18 | a0001c0001t0001g0035 a0001c0001t0001g0164 a0001c0001t0001g0165 others(15): Show |
19 | HG01069.hp2 HG01070.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.301-1576G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41583193 | |||||||
chr6:41583208 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.301-1561G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41583208 | |||||||
chr6:41583271 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.301-1498C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41583271 | |||||||
chr6:41583327 | GT | G | 2 | a0001c0005t0002g0016 a0001c0005t0002g0097 |
3 | HG01074.hp2 HG01081.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.301-1441delT | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41583327 | |||||||
chr6:41583487 | G | T | 2 | a0001c0001t0010g0273 a0001c0001t0010g0274 |
2 | HG03704.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.301-1282G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41583487 | |||||||
chr6:41583497 | G | A | 8 | a0001c0004t0010g0224 a0001c0004t0010g0225 a0001c0004t0016g0258 others(5): Show |
8 | HG01891.hp1 HG02809.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.301-1272G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41583497 | |||||||
chr6:41583595 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.301-1174T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41583595 | |||||||
chr6:41583687 | A | C | 1 | a0001c0002t0003g0127 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.301-1082A>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41583687 | |||||||
chr6:41583691 | C | G | 1 | a0001c0002t0003g0127 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.301-1078C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41583691 | |||||||
chr6:41583944 | T | G | 10 | a0001c0002t0002g0094 a0001c0002t0008g0015 a0001c0002t0008g0053 others(7): Show |
11 | HG00323.hp1 HG01891.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.301-825T>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41583944 | |||||||
chr6:41584209 | G | A | 1 | a0001c0002t0010g0262 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.301-560G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41584209 | |||||||
chr6:41584267 | C | T | 44 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0027 others(41): Show |
54 | HG00408.hp2 HG00423.hp2 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.301-502C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41584267 | |||||||
chr6:41584302 | T | C | 146 | a0001c0001t0010g0238 a0001c0001t0010g0273 a0001c0001t0010g0274 others(143): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.301-467T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41584302 | |||||||
chr6:41584363 | T | C | 146 | a0001c0001t0010g0238 a0001c0001t0010g0273 a0001c0001t0010g0274 others(143): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.301-406T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41584363 | |||||||
chr6:41584472 | A | C | 1 | a0001c0001t0001g0191 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.301-297A>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41584472 | |||||||
chr6:41584537 | G | A | 33 | a0001c0002t0002g0094 a0001c0002t0008g0015 a0001c0002t0008g0053 others(30): Show |
37 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.301-232G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41584537 | |||||||
chr6:41584679 | C | T | 1 | a0001c0001t0010g0238 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.301-90C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41584679 | |||||||
chr6:41584691 | G | A | 99 | a0001c0001t0010g0238 a0001c0001t0010g0273 a0001c0001t0010g0274 others(96): Show |
115 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.301-78G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 3/16 | chr6 | 41584691 | |||||||
chr6:41584991 | C | T | 30 | a0001c0001t0010g0238 a0001c0001t0010g0273 a0001c0001t0010g0274 others(27): Show |
35 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.423+100C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 4/16 | chr6 | 41584991 | |||||||
chr6:41585301 | T | A | 1 | a0001c0001t0001g0180 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.424-130T>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 4/16 | chr6 | 41585301 | |||||||
chr6:41585319 | C | T | 10 | a0001c0002t0002g0094 a0001c0002t0008g0015 a0001c0002t0008g0053 others(7): Show |
11 | HG00323.hp1 HG01891.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.424-112C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 4/16 | chr6 | 41585319 | |||||||
chr6:41585425 | C | A | 1 | a0005c0015t0001g0197 | 1 | HG01496.hp2 | splice_region_variant&intron_variant | LOW | c.424-6C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 4/16 | chr6 | 41585425 | |||||||
chr6:41585546 | G | A | 1 | a0001c0002t0002g0074 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.510+29G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 5/16 | chr6 | 41585546 | |||||||
chr6:41585696 | C | A | 1 | a0001c0002t0026g0133 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.510+179C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 5/16 | chr6 | 41585696 | |||||||
chr6:41585775 | C | T | 2 | a0001c0004t0010g0224 a0001c0004t0010g0225 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.510+258C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 5/16 | chr6 | 41585775 | |||||||
chr6:41585786 | C | T | 1 | a0001c0002t0002g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.510+269C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 5/16 | chr6 | 41585786 | |||||||
chr6:41585973 | G | T | 2 | a0001c0001t0004g0020 a0001c0001t0004g0119 |
3 | HG01081.hp2 HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.510+456G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 5/16 | chr6 | 41585973 | |||||||
chr6:41586127 | C | T | 1 | a0001c0002t0013g0048 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.510+610C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 5/16 | chr6 | 41586127 | |||||||
chr6:41586444 | A | G | 148 | a0001c0001t0002g0055 a0001c0001t0002g0118 a0001c0001t0010g0238 others(145): Show |
168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.511-565A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 5/16 | chr6 | 41586444 | |||||||
chr6:41586491 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0245 |
2 | HG01070.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.511-518C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 5/16 | chr6 | 41586491 | |||||||
chr6:41586789 | C | T | 2 | a0001c0001t0010g0238 a0001c0002t0041g0072 |
2 | HG03017.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.511-220C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 5/16 | chr6 | 41586789 | |||||||
chr6:41586850 | A | G | 1 | a0001c0002t0003g0145 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.511-159A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 5/16 | chr6 | 41586850 | |||||||
chr6:41587181 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.658+25C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 6/16 | chr6 | 41587181 | |||||||
chr6:41587208 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.658+52G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 6/16 | chr6 | 41587208 | |||||||
chr6:41587235 | T | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0178 a0001c0001t0001g0199 others(3): Show |
7 | NA18939.hp1 NA18956.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.659-64T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 6/16 | chr6 | 41587235 | |||||||
chr6:41587255 | G | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(87): Show |
117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.659-44G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 6/16 | chr6 | 41587255 | |||||||
chr6:41587573 | C | G | 1 | a0001c0002t0002g0050 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.872+61C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 7/16 | chr6 | 41587573 | |||||||
chr6:41587625 | T | TCACTCCC others(4): Show |
1 | a0001c0001t0001g0189 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.872+126_872+136dup others(11): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr6 | 41587625 | ||||||
chr6:41587625 | TCACTCCC others(4): Show |
T | 56 | a0001c0001t0030g0219 a0001c0001t0031g0227 a0001c0002t0003g0022 others(53): Show |
60 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.872+126_872+136del others(11): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr6 | 41587625 | ||||||
chr6:41587655 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0180 a0001c0001t0001g0200 others(1): Show |
4 | HG02015.hp1 HG02074.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.873-138G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 7/16 | chr6 | 41587655 | |||||||
chr6:41588052 | G | A | 2 | a0001c0004t0010g0224 a0001c0004t0010g0225 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.977+155G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 8/16 | chr6 | 41588052 | |||||||
chr6:41588089 | T | G | 3 | a0001c0001t0001g0242 a0001c0001t0001g0248 a0001c0001t0001g0252 |
3 | HG00741.hp2 HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.977+192T>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 8/16 | chr6 | 41588089 | |||||||
chr6:41588124 | G | A | 147 | a0001c0001t0002g0055 a0001c0001t0010g0238 a0001c0001t0010g0273 others(144): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.977+227G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 8/16 | chr6 | 41588124 | |||||||
chr6:41588133 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.977+236G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 8/16 | chr6 | 41588133 | |||||||
chr6:41588210 | G | A | 17 | a0001c0002t0002g0058 a0001c0002t0002g0059 a0001c0002t0002g0084 others(14): Show |
22 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.977+313G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 8/16 | chr6 | 41588210 | |||||||
chr6:41588256 | C | T | 63 | a0001c0001t0002g0055 a0001c0001t0010g0238 a0001c0001t0010g0273 others(60): Show |
71 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.977+359C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 8/16 | chr6 | 41588256 | |||||||
chr6:41588308 | A | G | 2 | a0001c0005t0002g0016 a0001c0005t0002g0097 |
3 | HG01074.hp2 HG01081.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.978-336A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 8/16 | chr6 | 41588308 | |||||||
chr6:41588357 | C | A | 2 | a0001c0005t0002g0016 a0001c0005t0002g0097 |
3 | HG01074.hp2 HG01081.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.978-287C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 8/16 | chr6 | 41588357 | |||||||
chr6:41588478 | G | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(38): Show |
54 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.978-166G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 8/16 | chr6 | 41588478 | |||||||
chr6:41588607 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.978-37G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 8/16 | chr6 | 41588607 | |||||||
chr6:41588740 | C | T | 2 | a0001c0002t0002g0084 a0001c0002t0002g0085 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1065+9C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 9/16 | chr6 | 41588740 | |||||||
chr6:41589097 | C | T | 1 | a0001c0002t0043g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1065+366C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 9/16 | chr6 | 41589097 | |||||||
chr6:41589282 | C | A | 1 | a0001c0001t0001g0198 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1066-489C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 9/16 | chr6 | 41589282 | |||||||
chr6:41589327 | T | C | 1 | a0001c0002t0003g0140 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1066-444T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 9/16 | chr6 | 41589327 | |||||||
chr6:41589379 | A | C | 154 | a0001c0001t0002g0055 a0001c0001t0002g0118 a0001c0001t0010g0238 others(151): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1066-392A>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 9/16 | chr6 | 41589379 | |||||||
chr6:41589453 | C | G | 5 | a0001c0002t0004g0044 a0001c0002t0004g0045 a0001c0002t0004g0062 others(2): Show |
5 | NA18979.hp2 NA18986.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.1066-318C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 9/16 | chr6 | 41589453 | |||||||
chr6:41589609 | C | G | 3 | a0001c0002t0002g0056 a0001c0006t0002g0006 a0001c0006t0013g0006 |
4 | HG02257.hp1 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1066-162C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 9/16 | chr6 | 41589609 | |||||||
chr6:41589638 | G | A | 1 | a0001c0002t0010g0262 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1066-133G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 9/16 | chr6 | 41589638 | |||||||
chr6:41589677 | C | T | 6 | a0001c0001t0011g0036 a0001c0001t0011g0229 a0001c0001t0011g0264 others(3): Show |
7 | HG02451.hp2 HG02523.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1066-94C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 9/16 | chr6 | 41589677 | |||||||
chr6:41589909 | C | A | 5 | a0001c0002t0002g0058 a0001c0002t0002g0059 a0001c0002t0002g0084 others(2): Show |
5 | HG01884.hp1 HG02145.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1150-54C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 10/16 | chr6 | 41589909 | |||||||
chr6:41590207 | G | A | 10 | a0001c0002t0039g0098 a0001c0004t0010g0224 a0001c0004t0010g0225 others(7): Show |
10 | HG01891.hp1 HG02809.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.1357+37G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 11/16 | chr6 | 41590207 | |||||||
chr6:41590460 | G | A | 10 | a0001c0002t0002g0094 a0001c0002t0008g0015 a0001c0002t0008g0053 others(7): Show |
11 | HG00323.hp1 HG01891.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.1434+113G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 12/16 | chr6 | 41590460 | |||||||
chr6:41590498 | G | A | 2 | a0001c0010t0001g0257 a0001c0010t0001g0277 |
2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1434+151G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 12/16 | chr6 | 41590498 | |||||||
chr6:41590536 | A | G | 10 | a0001c0002t0002g0094 a0001c0002t0008g0015 a0001c0002t0008g0053 others(7): Show |
11 | HG00323.hp1 HG01891.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.1434+189A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 12/16 | chr6 | 41590536 | |||||||
chr6:41590552 | C | T | 1 | a0001c0002t0041g0072 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1434+205C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 12/16 | chr6 | 41590552 | |||||||
chr6:41590558 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1434+211G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 12/16 | chr6 | 41590558 | |||||||
chr6:41590561 | C | T | 31 | a0001c0001t0002g0055 a0001c0001t0002g0118 a0001c0001t0010g0238 others(28): Show |
36 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.1434+214C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 12/16 | chr6 | 41590561 | |||||||
chr6:41590620 | A | G | 148 | a0001c0001t0002g0055 a0001c0001t0002g0118 a0001c0001t0010g0238 others(145): Show |
168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1434+273A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 12/16 | chr6 | 41590620 | |||||||
chr6:41590627 | G | C | 148 | a0001c0001t0002g0055 a0001c0001t0002g0118 a0001c0001t0010g0238 others(145): Show |
168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1434+280G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 12/16 | chr6 | 41590627 | |||||||
chr6:41590664 | T | C | 3 | a0001c0002t0008g0100 a0001c0002t0008g0101 a0001c0002t0037g0102 |
3 | HG02559.hp2 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1434+317T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 12/16 | chr6 | 41590664 | |||||||
chr6:41590705 | A | G | 148 | a0001c0001t0002g0055 a0001c0001t0002g0118 a0001c0001t0010g0238 others(145): Show |
168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1434+358A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 12/16 | chr6 | 41590705 | |||||||
chr6:41590773 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1434+426C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 12/16 | chr6 | 41590773 | |||||||
chr6:41590920 | G | A | 5 | a0001c0002t0004g0044 a0001c0002t0004g0045 a0001c0002t0004g0062 others(2): Show |
5 | NA18979.hp2 NA18986.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.1435-301G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 12/16 | chr6 | 41590920 | |||||||
chr6:41591148 | G | A | 2 | a0001c0008t0020g0087 a0001c0008t0020g0088 |
2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1435-73G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 12/16 | chr6 | 41591148 | |||||||
chr6:41591214 | C | T | 18 | a0001c0002t0003g0152 a0001c0002t0004g0109 a0001c0002t0009g0007 others(15): Show |
23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
splice_region_variant&intron_variant | LOW | c.1435-7C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 12/16 | chr6 | 41591214 | |||||||
chr6:41591599 | G | A | 1 | a0001c0001t0033g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1536+277G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41591599 | |||||||
chr6:41591670 | TCA | T | 80 | a0001c0001t0002g0055 a0001c0001t0010g0238 a0001c0001t0010g0273 others(77): Show |
91 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1536+351_1536+352d others(4): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr6 | 41591670 | ||||||
chr6:41591745 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1536+423G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41591745 | |||||||
chr6:41591992 | G | T | 41 | a0001c0001t0031g0227 a0001c0002t0003g0022 a0001c0002t0003g0023 others(38): Show |
45 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.1536+670G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41591992 | |||||||
chr6:41592123 | C | A | 13 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0040 others(10): Show |
15 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1536+801C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41592123 | |||||||
chr6:41592189 | G | T | 1 | a0001c0002t0025g0114 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1536+867G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41592189 | |||||||
chr6:41592365 | C | G | 4 | a0001c0002t0003g0154 a0001c0002t0014g0026 a0001c0002t0014g0122 others(1): Show |
5 | NA18948.hp2 NA19055.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.1536+1043C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41592365 | |||||||
chr6:41592549 | G | A | 13 | a0001c0003t0006g0038 a0001c0003t0006g0039 a0001c0003t0006g0040 others(10): Show |
15 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1536+1227G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41592549 | |||||||
chr6:41592604 | A | C | 1 | a0001c0002t0025g0114 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1536+1282A>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41592604 | |||||||
chr6:41592750 | A | G | 3 | a0001c0002t0004g0017 a0001c0002t0004g0090 a0001c0002t0004g0106 |
4 | HG01243.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1536+1428A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41592750 | |||||||
chr6:41592975 | G | A | 10 | a0001c0002t0002g0094 a0001c0002t0008g0015 a0001c0002t0008g0053 others(7): Show |
11 | HG00323.hp1 HG01891.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.1536+1653G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41592975 | |||||||
chr6:41592991 | TTGCCAGT others(6): Show |
T | 55 | a0001c0001t0002g0055 a0001c0001t0002g0118 a0001c0001t0010g0238 others(52): Show |
62 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1536+1672_1536+168 others(17): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr6 | 41592991 | ||||||
chr6:41593006 | G | A | 2 | a0001c0001t0001g0235 a0001c0001t0001g0261 |
2 | HG01099.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1536+1684G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41593006 | |||||||
chr6:41593320 | G | A | 1 | a0001c0002t0002g0050 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1537-1550G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41593320 | |||||||
chr6:41593344 | T | C | 5 | a0001c0001t0011g0036 a0001c0001t0011g0229 a0001c0001t0011g0264 others(2): Show |
6 | HG02451.hp2 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1537-1526T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41593344 | |||||||
chr6:41593381 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0167 |
3 | HG01106.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1537-1489C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41593381 | |||||||
chr6:41593417 | C | T | 5 | a0001c0001t0011g0036 a0001c0001t0011g0229 a0001c0001t0011g0264 others(2): Show |
6 | HG02451.hp2 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1537-1453C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41593417 | |||||||
chr6:41593442 | G | A | 55 | a0001c0001t0002g0055 a0001c0001t0002g0118 a0001c0001t0010g0238 others(52): Show |
62 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1537-1428G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41593442 | |||||||
chr6:41593503 | C | A | 32 | a0001c0001t0002g0055 a0001c0001t0002g0118 a0001c0001t0010g0238 others(29): Show |
37 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.1537-1367C>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41593503 | |||||||
chr6:41593503 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0214 others(2): Show |
7 | HG01070.hp1 HG01255.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1537-1367C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41593503 | |||||||
chr6:41593555 | G | A | 1 | a0001c0001t0005g0157 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1537-1315G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41593555 | |||||||
chr6:41593616 | G | A | 18 | a0001c0002t0002g0094 a0001c0002t0003g0022 a0001c0002t0003g0128 others(15): Show |
21 | HG00323.hp1 HG01074.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.1537-1254G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41593616 | |||||||
chr6:41593853 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1537-1017C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41593853 | |||||||
chr6:41593910 | A | G | 1 | a0001c0001t0001g0218 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1537-960A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41593910 | |||||||
chr6:41593917 | G | C | 1 | a0001c0001t0001g0234 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1537-953G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41593917 | |||||||
chr6:41593940 | T | TAACAGGG others(5): Show |
19 | a0001c0002t0002g0094 a0001c0002t0003g0022 a0001c0002t0003g0128 others(16): Show |
22 | HG00323.hp1 HG01074.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.1537-929_1537-918d others(14): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr6 | 41593940 | ||||||
chr6:41593989 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1537-881C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41593989 | |||||||
chr6:41594172 | C | G | 1 | a0001c0001t0001g0218 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1537-698C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41594172 | |||||||
chr6:41594216 | C | G | 1 | a0001c0001t0001g0255 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1537-654C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41594216 | |||||||
chr6:41594258 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1537-612C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41594258 | |||||||
chr6:41594447 | T | A | 1 | a0001c0002t0003g0154 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1537-423T>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41594447 | |||||||
chr6:41594468 | C | G | 1 | a0001c0001t0001g0193 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1537-402C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41594468 | |||||||
chr6:41594571 | T | C | 43 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(40): Show |
58 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1537-299T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41594571 | |||||||
chr6:41594703 | G | A | 1 | a0001c0002t0039g0098 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1537-167G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41594703 | |||||||
chr6:41594708 | C | T | 18 | a0001c0002t0004g0109 a0001c0002t0009g0007 a0001c0002t0009g0107 others(15): Show |
23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.1537-162C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41594708 | |||||||
chr6:41594726 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1537-144T>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41594726 | |||||||
chr6:41594740 | C | G | 2 | a0001c0008t0020g0087 a0001c0008t0020g0088 |
2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1537-130C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41594740 | |||||||
chr6:41594776 | C | T | 11 | a0001c0002t0008g0015 a0001c0002t0008g0053 a0001c0002t0008g0089 others(8): Show |
13 | HG00323.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1537-94C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41594776 | |||||||
chr6:41594782 | T | G | 1 | a0001c0001t0002g0055 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1537-88T>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41594782 | |||||||
chr6:41594792 | A | G | 157 | a0001c0001t0002g0055 a0001c0001t0002g0118 a0001c0001t0004g0042 others(154): Show |
178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1537-78A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 13/16 | chr6 | 41594792 | |||||||
chr6:41595019 | G | C | 1 | a0001c0001t0001g0181 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1658+28G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41595019 | |||||||
chr6:41595069 | A | G | 2 | a0001c0001t0030g0219 a0001c0002t0003g0139 |
2 | NA18942.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1658+78A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41595069 | |||||||
chr6:41595172 | G | A | 2 | a0001c0004t0010g0224 a0001c0004t0010g0225 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1658+181G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41595172 | |||||||
chr6:41595281 | T | A | 1 | a0001c0001t0005g0222 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1658+290T>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41595281 | |||||||
chr6:41595295 | G | A | 1 | a0001c0003t0006g0281 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1658+304G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41595295 | |||||||
chr6:41595312 | TGCCAGCC others(1308): Show |
T | 1 | a0001c0002t0043g0057 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1658+326_1659-545d others(2): Show |
FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr6 | 41595312 | ||||||
chr6:41595389 | C | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0159 a0001c0001t0001g0183 others(5): Show |
8 | HG00438.hp1 HG02071.hp2 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.1658+398C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41595389 | |||||||
chr6:41595419 | C | T | 17 | a0001c0002t0009g0007 a0001c0002t0009g0107 a0001c0002t0009g0108 others(14): Show |
22 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.1658+428C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41595419 | |||||||
chr6:41595448 | A | G | 47 | a0001c0001t0030g0219 a0001c0001t0031g0227 a0001c0002t0003g0022 others(44): Show |
51 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.1658+457A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41595448 | |||||||
chr6:41595614 | T | G | 10 | a0001c0002t0009g0007 a0001c0002t0009g0107 a0001c0002t0009g0108 others(7): Show |
15 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.1658+623T>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41595614 | |||||||
chr6:41595761 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1658+770C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41595761 | |||||||
chr6:41595960 | C | T | 6 | a0001c0002t0003g0022 a0001c0002t0003g0128 a0001c0002t0003g0129 others(3): Show |
7 | HG01257.hp2 HG01258.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.1658+969C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41595960 | |||||||
chr6:41596042 | C | T | 1 | a0001c0002t0002g0099 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1658+1051C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41596042 | |||||||
chr6:41596043 | G | A | 56 | a0001c0001t0002g0055 a0001c0001t0002g0118 a0001c0001t0010g0238 others(53): Show |
64 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1658+1052G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41596043 | |||||||
chr6:41596086 | C | T | 17 | a0001c0002t0009g0007 a0001c0002t0009g0107 a0001c0002t0009g0108 others(14): Show |
22 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.1659-1090C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41596086 | |||||||
chr6:41596178 | G | A | 1 | a0001c0002t0037g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1659-998G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41596178 | |||||||
chr6:41596235 | G | A | 4 | a0001c0002t0012g0043 a0001c0002t0012g0067 a0001c0002t0019g0068 others(1): Show |
4 | HG03491.hp2 HG03492.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1659-941G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41596235 | |||||||
chr6:41596246 | G | T | 47 | a0001c0001t0030g0219 a0001c0001t0031g0227 a0001c0002t0003g0022 others(44): Show |
51 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.1659-930G>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41596246 | |||||||
chr6:41596288 | G | C | 145 | a0001c0001t0002g0055 a0001c0001t0002g0118 a0001c0001t0010g0238 others(142): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1659-888G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41596288 | |||||||
chr6:41596295 | A | G | 11 | a0001c0002t0002g0094 a0001c0002t0008g0015 a0001c0002t0008g0053 others(8): Show |
12 | HG00323.hp1 HG01891.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.1659-881A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41596295 | |||||||
chr6:41596323 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1659-853T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41596323 | |||||||
chr6:41596578 | T | A | 1 | a0001c0001t0028g0217 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1659-598T>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41596578 | |||||||
chr6:41596841 | G | A | 1 | a0001c0010t0001g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1659-335G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41596841 | |||||||
chr6:41596856 | G | A | 1 | a0001c0002t0002g0115 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1659-320G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41596856 | |||||||
chr6:41596948 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1659-228A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 14/16 | chr6 | 41596948 | |||||||
chr6:41597340 | G | A | 1 | a0001c0002t0002g0099 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1725+98G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 15/16 | chr6 | 41597340 | |||||||
chr6:41597413 | T | C | 1 | a0001c0002t0002g0099 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1725+171T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 15/16 | chr6 | 41597413 | |||||||
chr6:41597595 | C | T | 2 | a0001c0004t0010g0224 a0001c0004t0010g0225 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1726-186C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 15/16 | chr6 | 41597595 | |||||||
chr6:41597596 | A | G | 2 | a0001c0004t0010g0224 a0001c0004t0010g0225 |
2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1726-185A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 15/16 | chr6 | 41597596 | |||||||
chr6:41597670 | A | G | 2 | a0001c0005t0002g0016 a0001c0005t0002g0097 |
3 | HG01074.hp2 HG01081.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1726-111A>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 15/16 | chr6 | 41597670 | |||||||
chr6:41597734 | C | T | 58 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0244 others(55): Show |
65 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1726-47C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 15/16 | chr6 | 41597734 | |||||||
chr6:41598216 | C | CT | 6 | a0001c0001t0004g0042 a0001c0001t0004g0054 a0001c0001t0027g0241 others(3): Show |
6 | HG02055.hp2 HG02148.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1895+284dupT | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr6 | 41598216 | ||||||
chr6:41598216 | CT | C | 35 | a0001c0001t0001g0170 a0001c0001t0001g0178 a0001c0001t0001g0182 others(32): Show |
36 | HG01167.hp1 HG01255.hp2 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.1895+284delT | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr6 | 41598216 | ||||||
chr6:41598352 | A | T | 2 | a0001c0002t0003g0022 a0001c0002t0003g0129 |
3 | HG01257.hp2 HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1895+402A>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 16/16 | chr6 | 41598352 | |||||||
chr6:41598363 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1895+413C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 16/16 | chr6 | 41598363 | |||||||
chr6:41598545 | C | T | 1 | a0001c0002t0039g0098 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1896-244C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 16/16 | chr6 | 41598545 | |||||||
chr6:41598546 | G | A | 9 | a0001c0002t0008g0015 a0001c0002t0008g0053 a0001c0002t0008g0089 others(6): Show |
10 | HG00323.hp1 HG01891.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.1896-243G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 16/16 | chr6 | 41598546 | |||||||
chr6:41598560 | C | T | 2 | a0001c0008t0020g0087 a0001c0008t0020g0088 |
2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1896-229C>T | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 16/16 | chr6 | 41598560 | |||||||
chr6:41598614 | C | G | 1 | a0001c0002t0002g0014 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1896-175C>G | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 16/16 | chr6 | 41598614 | |||||||
chr6:41598675 | G | C | 6 | a0001c0002t0002g0058 a0001c0002t0002g0059 a0001c0002t0002g0084 others(3): Show |
6 | HG01884.hp1 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1896-114G>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 16/16 | chr6 | 41598675 | |||||||
chr6:41598710 | T | C | 1 | a0001c0002t0002g0099 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1896-79T>C | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 16/16 | chr6 | 41598710 | |||||||
chr6:41598720 | T | A | 1 | a0001c0002t0003g0152 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1896-69T>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 16/16 | chr6 | 41598720 | |||||||
chr6:41598771 | G | A | 6 | a0001c0002t0002g0058 a0001c0002t0002g0059 a0001c0002t0002g0084 others(3): Show |
6 | HG01884.hp1 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1896-18G>A | FOXP4 | ENSG00000137166.18 | transcript | ENST00000307972.10 | protein_coding | 16/16 | chr6 | 41598771 |