Variant report

Variant	rs9785091
Chromosome Location	chr8:61330886-61330887
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	POLR2A	chr8:61330649-61331007	K562	blood:	n/a	n/a
2	TCF7L2	chr8:61330705-61331139	PANC-1	pancreas:	n/a	chr8:61330941-61330957 chr8:61330945-61330954
3	TCF7L2	chr8:61330750-61331126	HEK293	kidney:	n/a	chr8:61330941-61330957 chr8:61330945-61330954

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:61325999..61328203-chr8:61328768..61330939,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000251396	TF binding region
ENSG00000251396	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 2 )

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

rs_ID	r²[population]
rs10087760	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10092773	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10102945	0.88[ASN][1000 genomes]
rs10504312	0.88[ASN][1000 genomes]
rs11988766	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11988798	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12548711	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1318227	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1552070	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1842388	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1893277	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1893279	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1941467	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2012856	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2068587	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2155831	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6471877	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6471880	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6471881	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6982032	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6986664	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6994192	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6998307	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6999822	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7004236	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7814226	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7819947	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7824474	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7824671	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7828383	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7831106	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7841648	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917756	chr8:60942299-61862796	Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
2	esv3371465	chr8:61115030-61356658	Bivalent Enhancer Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs9785091	RP11-163N6.2	cis	Thyroid	GTEx
rs9785091	RAB2A	Cis_1M	lymphoblastoid	RTeQTL

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

No data

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