Variant report

Variant	rs2795312
Chromosome Location	chr1:220129357-220129358
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs1061160	0.81[EUR][1000 genomes]
rs1498393	0.83[EUR][1000 genomes]
rs1624678	0.80[EUR][1000 genomes]
rs2647463	0.81[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	nsv427930	chr1:220120379-220333434	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	744 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	chr1:220128800-220130000	Enhancers	Liver	Liver
2	chr1:220128800-220130200	Weak transcription	Fetal Intestine Large	intestine
3	chr1:220128800-220131400	Weak transcription	Duodenum Mucosa	Duodenum
4	chr1:220128800-220131400	Weak transcription	Fetal Intestine Small	intestine
5	chr1:220128800-220132200	Weak transcription	K562	blood
6	chr1:220129200-220145800	Weak transcription	HepG2	liver

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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