Variant report

Variant	rs9344147
Chromosome Location	chr6:82015674-82015675
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1034243	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12055775	0.91[ASN][1000 genomes]
rs12174607	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12216396	0.88[ASN][1000 genomes]
rs12665795	0.91[ASN][1000 genomes]
rs16892963	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72899340	0.87[ASN][1000 genomes]
rs9341869	0.94[ASN][1000 genomes]
rs9344135	0.88[ASN][1000 genomes]
rs9344138	0.91[ASN][1000 genomes]
rs9352972	0.88[ASN][1000 genomes]
rs9359475	0.91[ASN][1000 genomes]
rs9361784	1.00[ASN][1000 genomes]
rs9361785	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9361786	0.98[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	nsv604087	chr6:81792413-82326091	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1032655	chr6:81942397-82225830	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv1034440	chr6:82002417-82044834	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82014000-82016200	Enhancers	Muscle Satellite Cultured Cells	--
2	chr6:82014000-82016400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr6:82014200-82016400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr6:82014800-82018400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:82015000-82016000	Weak transcription	HSMM	muscle
6	chr6:82015400-82016200	Enhancers	Adipose Nuclei	Adipose
7	chr6:82015600-82015800	Enhancers	NHDF-Ad	bronchial
8	chr6:82015600-82016000	Enhancers	Osteobl	bone
9	chr6:82015600-82016200	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr6:82015600-82016200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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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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