Variant report

Variant	rs7185008
Chromosome Location	chr16:79943738-79943739
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs28552565	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7187277	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs74040136	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8055558	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8057246	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9930729	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9931748	0.96[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	nsv573285	chr16:79158182-80127326	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:79938400-79949200	Weak transcription	Ovary	ovary
2	chr16:79943000-79944400	Enhancers	Fetal Lung	lung
3	chr16:79943400-79944000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr16:79943400-79944200	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr16:79943400-79944200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr16:79943400-79944200	Enhancers	NHEK	skin
7	chr16:79943400-79944400	Enhancers	Fetal Stomach	stomach
8	chr16:79943400-79944600	Enhancers	Fetal Brain Male	brain
9	chr16:79943400-79944800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr16:79943400-79945400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr16:79943600-79943800	Enhancers	Stomach Smooth Muscle	stomach

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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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