Variant report

Variant	rs1904103
Chromosome Location	chr4:76364458-76364459
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10029348	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10031553	0.80[EUR][1000 genomes]
rs1046662	0.94[EUR][1000 genomes]
rs11730978	0.81[EUR][1000 genomes]
rs11735018	0.81[EUR][1000 genomes]
rs11935932	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13112378	0.80[EUR][1000 genomes]
rs13145288	0.80[EUR][1000 genomes]
rs1351092	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1389443	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1395359	0.94[CHB][hapmap];0.93[JPT][hapmap];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1395360	0.93[CHB][hapmap];0.93[JPT][hapmap];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1478174	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1564174	0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1580297	0.94[EUR][1000 genomes]
rs1600100	0.94[EUR][1000 genomes]
rs1676917	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1841932	0.94[EUR][1000 genomes]
rs2045863	0.80[EUR][1000 genomes]
rs2126855	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2867920	0.94[EUR][1000 genomes]
rs2867921	0.81[EUR][1000 genomes]
rs4593160	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4859963	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs57749060	0.85[EUR][1000 genomes]
rs59581284	0.92[EUR][1000 genomes]
rs6823674	0.85[EUR][1000 genomes]
rs6833496	0.81[EUR][1000 genomes]
rs6841171	0.94[CHB][hapmap];0.93[JPT][hapmap];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6841882	0.81[EUR][1000 genomes]
rs7698352	0.86[EUR][1000 genomes]
rs786682	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs786684	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs786688	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs949611	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs955545	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv594687	chr4:76154064-76502748	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv998511	chr4:76184807-76398377	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	esv2763368	chr4:76190070-76387413	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv534570	chr4:76214619-76498362	ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1904103	THAP6	cis	multi-tissue	Pritchard

Chromatin state (count:0 , 50 per page) page:

No data

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