Variant report

Variant	rs10784327
Chromosome Location	chr12:63460835-63460836
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs12425328	0.96[CEU][hapmap];0.94[CHB][hapmap];0.88[JPT][hapmap]
rs3847909	0.82[CEU][hapmap]
rs3913039	0.92[ASW][hapmap];0.96[CEU][hapmap];0.94[CHB][hapmap];0.87[CHD][hapmap];0.84[GIH][hapmap];0.89[JPT][hapmap];0.91[MEX][hapmap];0.84[TSI][hapmap];0.85[YRI][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3913040	0.83[CEU][hapmap]
rs3913041	0.85[CEU][hapmap]
rs7969362	0.92[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];0.94[EUR][1000 genomes];0.91[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	esv3415227	chr12:63228121-63591615	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1046836	chr12:63392391-64377169	Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
3	esv2751108	chr12:63445933-63503952	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63456000-63462400	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr12:63456600-63462600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr12:63458400-63462800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr12:63458400-63469200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr12:63458600-63462400	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr12:63458800-63462400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr12:63460000-63461200	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr12:63460600-63461000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr12:63460600-63461000	Enhancers	Fetal Intestine Small	intestine
10	chr12:63460600-63461200	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr12:63460600-63461200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr12:63460800-63461000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr12:63460800-63461000	Enhancers	HepG2	liver

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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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