Variant report

Variant	rs2100807
Chromosome Location	chr3:116023990-116023991
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11924642	0.80[MEX][hapmap]
rs11928524	0.86[MEX][hapmap]
rs12494652	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13070962	0.80[MEX][hapmap]
rs1367770	0.86[MEX][hapmap]
rs1731596	0.80[MEX][hapmap]
rs1993733	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35300468	0.80[ASN][1000 genomes]
rs4831092	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6775293	0.80[ASN][1000 genomes]
rs7611085	1.00[CHB][hapmap]
rs7621652	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7634137	0.86[MEX][hapmap]
rs7637573	0.80[MEX][hapmap]
rs9809878	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9838534	0.80[MEX][hapmap]
rs9872860	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][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	nsv877360	chr3:115916171-116023990	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv3957	chr3:115986950-116032625	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv877361	chr3:116017931-116138039	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2100807	C3orf30	cis	cerebellum	SCAN
rs2100807	NR1I2	cis	cerebellum	SCAN
rs2100807	KLHL11	trans	cerebellum	SCAN

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:116017000-116029600	Enhancers	Colon Smooth Muscle	Colon
2	chr3:116019200-116025600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr3:116019200-116028400	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr3:116019400-116025000	Weak transcription	Brain Angular Gyrus	brain
5	chr3:116019400-116025000	Weak transcription	Brain Cingulate Gyrus	brain
6	chr3:116019400-116025000	Weak transcription	Brain Substantia Nigra	brain
7	chr3:116019600-116037000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr3:116020400-116024000	Enhancers	Rectal Smooth Muscle	rectum
9	chr3:116022200-116033000	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr3:116023200-116024000	Enhancers	Brain Anterior Caudate	brain
11	chr3:116023800-116025000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr3:116023800-116026000	Enhancers	Brain Hippocampus Middle	brain

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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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