Variant report

Variant	rs3763231
Chromosome Location	chr6:87645858-87645859
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RAD21	chr6:87645691-87647792	SK-N-SH	brain:	n/a	chr6:87646950-87646962 chr6:87646947-87646966 chr6:87646953-87646962 chr6:87646950-87646963
2	CTCF	chr6:87645820-87645970	HEK293	kidney:	n/a	chr6:87645907-87645916

Variant related genes	Relation type
HTR1E	TF binding region

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1013019	1.00[ASN][1000 genomes]
rs10498959	1.00[ASN][1000 genomes]
rs12663746	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1408447	1.00[ASN][1000 genomes]
rs1535228	1.00[ASN][1000 genomes]
rs16877863	1.00[ASN][1000 genomes]
rs16877883	1.00[ASN][1000 genomes]
rs16877984	1.00[ASN][1000 genomes]
rs16877987	1.00[ASN][1000 genomes]
rs16877991	1.00[ASN][1000 genomes]
rs17545444	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1884740	1.00[ASN][1000 genomes]
rs2145050	0.83[ASN][1000 genomes]
rs4371828	1.00[ASN][1000 genomes]
rs55859404	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55982849	1.00[ASN][1000 genomes]
rs56152175	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56364606	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62439115	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62439116	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62439143	1.00[ASN][1000 genomes]
rs62439144	0.95[ASN][1000 genomes]
rs62439145	1.00[ASN][1000 genomes]
rs62439146	1.00[ASN][1000 genomes]
rs62439147	0.95[ASN][1000 genomes]
rs62440765	1.00[ASN][1000 genomes]
rs62440766	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62440767	1.00[ASN][1000 genomes]
rs62440790	1.00[ASN][1000 genomes]
rs62440822	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6940008	1.00[ASN][1000 genomes]
rs73751775	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73751802	1.00[ASN][1000 genomes]
rs9444442	1.00[ASN][1000 genomes]
rs9444447	1.00[ASN][1000 genomes]
rs9450536	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9450544	1.00[ASN][1000 genomes]
rs9450568	0.81[ASN][1000 genomes]
rs9450569	1.00[ASN][1000 genomes]
rs9450573	0.81[ASN][1000 genomes]
rs9450587	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018878	chr6:86778852-87691755	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv1031639	chr6:86815397-87721507	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv1024751	chr6:87433199-87908721	Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases

No data

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

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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