Variant report

Variant	rs7597877
Chromosome Location	chr2:184905255-184905256
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10931115	0.86[ASN][1000 genomes]
rs11677862	0.94[ASN][1000 genomes]
rs11883925	0.95[ASN][1000 genomes]
rs11901460	0.95[ASN][1000 genomes]
rs12104934	0.96[ASN][1000 genomes]
rs12104943	0.94[ASN][1000 genomes]
rs12613881	0.93[ASN][1000 genomes]
rs12615504	0.93[ASN][1000 genomes]
rs12615512	0.93[ASN][1000 genomes]
rs12616364	0.85[ASN][1000 genomes]
rs12617300	0.92[ASN][1000 genomes]
rs12619090	0.93[ASN][1000 genomes]
rs12622086	0.94[ASN][1000 genomes]
rs12693367	0.96[ASN][1000 genomes]
rs12988863	0.96[ASN][1000 genomes]
rs4233781	0.91[ASN][1000 genomes]
rs4335910	0.93[ASN][1000 genomes]
rs4396672	0.93[ASN][1000 genomes]
rs4556942	0.93[ASN][1000 genomes]
rs4564742	0.93[ASN][1000 genomes]
rs4583423	0.92[ASN][1000 genomes]
rs4595929	0.92[ASN][1000 genomes]
rs4666648	0.93[ASN][1000 genomes]
rs4666955	0.96[ASN][1000 genomes]
rs55921900	0.93[ASN][1000 genomes]
rs58741881	0.84[ASN][1000 genomes]
rs59285257	0.93[ASN][1000 genomes]
rs59641790	0.92[ASN][1000 genomes]
rs60126067	0.84[ASN][1000 genomes]
rs62196426	0.81[ASN][1000 genomes]
rs66769153	0.85[ASN][1000 genomes]
rs6726069	0.82[ASN][1000 genomes]
rs6742505	0.93[ASN][1000 genomes]
rs6760489	0.94[ASN][1000 genomes]
rs7591437	0.93[ASN][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	nsv1002074	chr2:184697897-184955330	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv875487	chr2:184737282-185186670	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv997475	chr2:184828307-184993186	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv583991	chr2:184855828-184954425	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:184883800-184911600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:184905000-184905400	Enhancers	Rectal Mucosa Donor 29	rectum

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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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