Variant report

Variant	rs1395359
Chromosome Location	chr4:76287912-76287913
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:76278035..76280636-chr4:76286764..76289463,2	K562	blood:

Variant related genes	Relation type
ENSG00000251383	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10029348	0.82[EUR][1000 genomes]
rs1046662	0.96[CEU][hapmap];0.81[EUR][1000 genomes]
rs11735018	0.96[CEU][hapmap]
rs11935932	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1351092	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1389443	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1395360	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1478174	0.83[EUR][1000 genomes]
rs1564174	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1580297	0.81[EUR][1000 genomes]
rs1600100	0.81[EUR][1000 genomes]
rs1676917	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1817387	0.96[CEU][hapmap]
rs1841932	0.96[CEU][hapmap];0.81[EUR][1000 genomes]
rs1841934	0.96[CEU][hapmap]
rs1904103	0.94[CHB][hapmap];0.93[JPT][hapmap]
rs2045863	0.93[CEU][hapmap]
rs2126855	0.83[EUR][1000 genomes]
rs2867920	0.81[EUR][1000 genomes]
rs4593160	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4859963	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6833496	0.92[CEU][hapmap]
rs6835579	0.96[CEU][hapmap]
rs6841171	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6841882	0.96[CEU][hapmap]
rs7664140	0.96[CEU][hapmap]
rs7698352	0.85[CEU][hapmap]
rs786682	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs786684	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs786688	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap]
rs949611	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs955545	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010552	chr4:76064415-76325430	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	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
3	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
4	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
5	nsv461557	chr4:76212995-76363477	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv594688	chr4:76212995-76363477	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	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
8	nsv879493	chr4:76264496-76332975	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv879494	chr4:76264496-76337998	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1395359	THAP6	cis	multi-tissue	Pritchard

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

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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