Variant report

Variant	rs2901100
Chromosome Location	chr10:118009806-118009807
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10218849	0.80[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10787638	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs10787639	0.81[CEU][hapmap];0.82[MEX][hapmap]
rs10885889	0.93[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs11197596	1.00[LWK][hapmap];0.89[MKK][hapmap]
rs11197611	0.81[CEU][hapmap];0.91[MEX][hapmap]
rs11197612	0.81[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap];0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs11599593	0.90[ASN][1000 genomes]
rs12774375	0.81[CEU][hapmap];0.91[MEX][hapmap]
rs2420253	0.89[CEU][hapmap]
rs2901101	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs3740572	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs4554795	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs7078853	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs7087136	0.90[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	esv3449389	chr10:117806874-118102404	Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv832000	chr10:117944492-118116253	Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:117999800-118011200	Weak transcription	Liver	Liver
2	chr10:118003600-118011200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr10:118007800-118013200	Weak transcription	HSMMtube	muscle
4	chr10:118008000-118014000	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr10:118008600-118010200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr10:118008600-118012600	Weak transcription	Fetal Muscle Trunk	muscle
7	chr10:118008600-118013400	Weak transcription	HSMM	muscle
8	chr10:118008600-118014000	Weak transcription	Fetal Stomach	stomach
9	chr10:118009000-118013200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr10:118009200-118010200	Weak transcription	Fetal Muscle Leg	muscle

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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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