Variant report

Variant	rs2711868
Chromosome Location	chr7:103195622-103195623
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs2535756	1.00[EUR][1000 genomes]
rs2535758	1.00[EUR][1000 genomes]
rs2535761	1.00[EUR][1000 genomes]
rs2535767	1.00[EUR][1000 genomes]
rs2535775	1.00[EUR][1000 genomes]
rs2535776	1.00[EUR][1000 genomes]
rs2535779	1.00[EUR][1000 genomes]
rs2535780	1.00[EUR][1000 genomes]
rs2535782	1.00[EUR][1000 genomes]
rs2711841	1.00[EUR][1000 genomes]
rs2711855	1.00[EUR][1000 genomes]
rs2711856	1.00[EUR][1000 genomes]
rs2711857	1.00[EUR][1000 genomes]
rs2711858	1.00[EUR][1000 genomes]
rs2711859	1.00[EUR][1000 genomes]
rs2711866	1.00[EUR][1000 genomes]
rs2711872	1.00[EUR][1000 genomes]
rs2711880	1.00[EUR][1000 genomes]
rs28396636	1.00[EUR][1000 genomes]
rs28417002	1.00[EUR][1000 genomes]
rs2907932	1.00[EUR][1000 genomes]
rs362657	1.00[EUR][1000 genomes]
rs362751	1.00[EUR][1000 genomes]
rs362775	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030446	chr7:102932689-103221638	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv491911	chr7:102967150-103403622	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv831085	chr7:103140672-103342388	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv888923	chr7:103143117-103199719	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103158000-103198600	Weak transcription	Liver	Liver
2	chr7:103180400-103199000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr7:103181800-103209400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr7:103182200-103198600	Weak transcription	Brain Anterior Caudate	brain
5	chr7:103190600-103197200	Weak transcription	K562	blood
6	chr7:103191800-103204400	Weak transcription	HepG2	liver
7	chr7:103195600-103197200	Weak transcription	Fetal Heart	heart

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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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