Variant report

Variant	rs12776687
Chromosome Location	chr10:21701447-21701448
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10047291	0.83[EUR][1000 genomes]
rs10047346	0.80[EUR][1000 genomes]
rs10082390	0.82[EUR][1000 genomes]
rs10828243	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11012716	0.81[EUR][1000 genomes]
rs11012717	0.81[EUR][1000 genomes]
rs11594201	0.83[CEU][hapmap];1.00[CHB][hapmap];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11594724	0.81[EUR][1000 genomes]
rs12098603	0.82[EUR][1000 genomes]
rs12248483	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12249704	0.82[EUR][1000 genomes]
rs12412917	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16921815	0.81[EUR][1000 genomes]
rs2360051	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34017213	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58747541	0.81[EUR][1000 genomes]
rs6482181	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs67206878	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7067553	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7070904	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7074328	0.87[EUR][1000 genomes]
rs7080252	0.82[EUR][1000 genomes]
rs7087431	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7098776	0.81[EUR][1000 genomes]
rs7895825	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7899812	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7900593	0.85[ASN][1000 genomes]
rs7907233	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7922464	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs959652	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.82[MKK][hapmap];0.95[TSI][hapmap];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9664320	0.88[EUR][1000 genomes];0.81[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	nsv530148	chr10:21065080-21724565	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12776687	STAM	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:21697600-21706200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr10:21699800-21707600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr10:21701400-21707600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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