Variant report

Variant	rs35790419
Chromosome Location	chr2:11233071-11233072
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:9)

rs_ID	r²[population]
rs10204077	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11678834	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11685699	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11686282	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13019468	0.86[EUR][1000 genomes]
rs13385775	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13385890	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13395933	0.81[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs71439047	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 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
2	esv3421097	chr2:11230076-11233349	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3378591	chr2:11230526-11233474	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11232600-11233400	Enhancers	Brain Substantia Nigra	brain
2	chr2:11232800-11233200	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr2:11232800-11233200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr2:11232800-11233200	Enhancers	Brain Hippocampus Middle	brain
5	chr2:11232800-11233200	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr2:11232800-11233400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr2:11233000-11233200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr2:11233000-11233800	Enhancers	H1 Cell Line	embryonic stem cell
9	chr2:11233000-11233800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr2:11233000-11234200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr2:11233000-11253000	Weak transcription	Gastric	stomach

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Input of quick search could be:

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

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