Variant report

Variant	rs2221404
Chromosome Location	chr13:90207427-90207428
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	TCF12	chr13:90206932-90207546	A549	lung:	n/a	n/a
2	KAP1	chr13:90206948-90207513	HEK293	kidney:	n/a	n/a
3	TCF7L2	chr13:90206668-90207598	HEK293	kidney:	n/a	chr13:90207170-90207177
4	KAP1	chr13:90206905-90207438	U2OS	brain:	n/a	n/a
5	FOXA2	chr13:90207054-90207485	A549	lung:	n/a	n/a
6	FOXA2	chr13:90207050-90207434	HepG2	liver:	n/a	n/a
7	FOXA1	chr13:90206977-90207454	HepG2	liver:	n/a	n/a

Variant related genes	Relation type
LINC00353	TF binding region

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11069934	1.00[ASN][1000 genomes]
rs11617569	1.00[ASN][1000 genomes]
rs12584606	0.99[ASN][1000 genomes]
rs1504434	1.00[ASN][1000 genomes]
rs1504436	1.00[ASN][1000 genomes]
rs17630679	0.84[ASN][1000 genomes]
rs17729533	1.00[ASN][1000 genomes]
rs35855604	0.99[ASN][1000 genomes]
rs4576939	0.99[ASN][1000 genomes]
rs61194221	1.00[ASN][1000 genomes]
rs7993695	0.94[ASN][1000 genomes]
rs7996895	0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9301583	0.87[ASN][1000 genomes]
rs9555914	0.81[ASN][1000 genomes]
rs9588641	1.00[ASN][1000 genomes]
rs9588642	1.00[ASN][1000 genomes]
rs9588643	1.00[ASN][1000 genomes]
rs9588647	1.00[ASN][1000 genomes]
rs9588653	0.99[ASN][1000 genomes]
rs9588655	0.99[ASN][1000 genomes]
rs9588656	0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048574	chr13:89650680-90232894	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1044807	chr13:89991827-90263328	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1039775	chr13:89995537-90260944	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv900860	chr13:90008941-90259291	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv533455	chr13:90041897-90255725	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1053657	chr13:90100510-90578568	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv1038982	chr13:90199563-90345091	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS	TF binding region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:90205200-90208000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr13:90207400-90211400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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