Variant report

Variant	rs2202900
Chromosome Location	chr6:142962360-142962361
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11155255	0.95[EUR][1000 genomes]
rs12214216	0.82[CEU][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12660529	0.88[ASN][1000 genomes]
rs17527704	0.82[CEU][hapmap];0.95[EUR][1000 genomes]
rs263136	0.81[EUR][1000 genomes]
rs263153	0.81[EUR][1000 genomes]
rs9376699	0.88[ASN][1000 genomes]
rs9376701	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9390013	0.81[ASN][1000 genomes]
rs9403403	0.92[ASN][1000 genomes]
rs9403404	0.92[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	nsv949088	chr6:142561402-143128849	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv830827	chr6:142840734-143015005	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive 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	chr6:142959400-142967200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr6:142960000-142967200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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