Variant report

Variant	rs1361779
Chromosome Location	chr1:215816929-215816930
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs2677111	0.87[ASN][1000 genomes]
rs2677112	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2797224	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2797229	0.82[ASN][1000 genomes]
rs2797254	0.84[ASN][1000 genomes]
rs2797386	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[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	nsv430324	chr1:215649163-216082605	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215810600-215820000	Weak transcription	Left Ventricle	heart
2	chr1:215810800-215821800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:215810800-215823000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr1:215811400-215820600	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr1:215816800-215817200	Flanking Active TSS	Liver	Liver
6	chr1:215816800-215817800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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