Variant report

Variant	rs13313977
Chromosome Location	chr3:160639895-160639896
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs12634108	1.00[EUR][1000 genomes]
rs12636473	1.00[EUR][1000 genomes]
rs16831667	1.00[EUR][1000 genomes]
rs16831679	1.00[EUR][1000 genomes]
rs34853143	1.00[AMR][1000 genomes]
rs34865754	1.00[AMR][1000 genomes]
rs34868645	1.00[EUR][1000 genomes]
rs57649180	1.00[EUR][1000 genomes]
rs58404146	1.00[EUR][1000 genomes]
rs61560039	1.00[EUR][1000 genomes]
rs61631170	1.00[EUR][1000 genomes]
rs61693724	1.00[EUR][1000 genomes]
rs6766476	1.00[EUR][1000 genomes]
rs6773475	1.00[EUR][1000 genomes]
rs6774622	1.00[EUR][1000 genomes]
rs6784487	1.00[EUR][1000 genomes]
rs6790257	1.00[EUR][1000 genomes]
rs6794409	1.00[EUR][1000 genomes]
rs6802169	1.00[EUR][1000 genomes]
rs6802417	1.00[EUR][1000 genomes]
rs6807237	1.00[EUR][1000 genomes]
rs73875444	1.00[EUR][1000 genomes]
rs9852671	1.00[EUR][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	nsv532666	chr3:159777847-160703202	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 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	chr3:160630200-160641400	Weak transcription	Psoas Muscle	Psoas
2	chr3:160635400-160644000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr3:160635400-160649200	Weak transcription	Fetal Brain Female	brain
4	chr3:160636000-160644000	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr3:160638200-160641800	Weak transcription	Left Ventricle	heart
6	chr3:160638200-160647200	Weak transcription	Right Ventricle	heart
7	chr3:160638400-160643800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr3:160638400-160643800	Weak transcription	Right Atrium	heart
9	chr3:160639000-160644400	Weak transcription	Fetal Brain Male	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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