Variant report

Variant	rs10204077
Chromosome Location	chr2:11233884-11233885
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10199233	0.83[AFR][1000 genomes]
rs11678834	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11685699	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11686282	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13019468	0.86[EUR][1000 genomes]
rs13385775	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13385890	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13395933	0.92[EUR][1000 genomes]
rs13425856	0.83[AFR][1000 genomes]
rs35790419	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71439047	0.86[AMR][1000 genomes];0.90[EUR][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	nsv833392	chr2:11054580-11235239	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 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	chr2:11233000-11234200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:11233000-11253000	Weak transcription	Gastric	stomach
3	chr2:11233400-11234400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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