Variant report

Variant	rs9868919
Chromosome Location	chr3:70176819-70176820
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	GATA2	chr3:70176304-70176915	SH-SY5Y	brain:	n/a	n/a
2	EP300	chr3:70175893-70177012	SK-N-SH	brain:	n/a	n/a
3	RFX5	chr3:70176104-70176917	SK-N-SH	brain:	n/a	n/a

Variant related genes	Relation type
ENSG00000271034	TF binding region

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10084760	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12494970	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13324738	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13327166	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13327169	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17006722	0.82[AMR][1000 genomes]
rs4132502	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4974261	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs59260955	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59312808	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6549275	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6549281	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6806567	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6807288	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs73108022	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73108030	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73108033	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7340562	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9310182	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9817459	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9817902	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9824741	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9849979	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9880622	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533396	chr3:69964029-70538306	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:70166000-70182400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:70169600-70182400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr3:70172800-70186800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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