Variant report

Variant	rs2450000
Chromosome Location	chr12:30736401-30736402
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1087340	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1087342	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1087345	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12426381	1.00[ASN][1000 genomes]
rs1371050	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1438909	0.85[AFR][1000 genomes]
rs1630788	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1659284	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1659286	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs794160	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs794161	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs794162	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3343291	chr12:30455597-30992837	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:30724600-30738600	Weak transcription	Pancreas	Pancrea
2	chr12:30726600-30740400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr12:30727800-30752800	Weak transcription	Left Ventricle	heart
4	chr12:30732400-30752000	Weak transcription	HSMMtube	muscle
5	chr12:30733400-30752600	Weak transcription	Right Ventricle	heart
6	chr12:30734000-30741400	Weak transcription	Stomach Smooth Muscle	stomach
7	chr12:30734200-30741000	Weak transcription	Lung	lung
8	chr12:30734200-30749800	Weak transcription	Aorta	Aorta
9	chr12:30735800-30736600	Enhancers	Adipose Derived Mesenchymal Stem Cell 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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