Variant report

Variant	rs2100369
Chromosome Location	chr2:11195795-11195796
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs16857111	0.86[ASN][1000 genomes]
rs2056101	0.80[ASN][1000 genomes]
rs2056102	0.80[ASN][1000 genomes]
rs2357891	0.97[ASN][1000 genomes]
rs4669684	0.81[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs56218122	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6720704	0.95[EUR][1000 genomes]
rs72783448	0.86[ASN][1000 genomes]
rs7586836	0.86[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	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	nsv580971	chr2:11175395-11226507	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11191000-11196800	Weak transcription	Fetal Brain Female	brain
2	chr2:11194400-11196600	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr2:11195400-11196600	Weak transcription	Fetal Brain Male	brain
4	chr2:11195400-11198400	Weak transcription	Spleen	Spleen
5	chr2:11195600-11195800	Enhancers	Brain Germinal Matrix	brain

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

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