Variant report

Variant	rs4673601
Chromosome Location	chr2:212069927-212069928
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10195210	0.85[ASN][1000 genomes]
rs10497936	1.00[ASN][1000 genomes]
rs12611962	0.97[ASN][1000 genomes]
rs12619699	0.85[ASN][1000 genomes]
rs12620783	1.00[ASN][1000 genomes]
rs12620896	0.91[ASN][1000 genomes]
rs12694230	0.86[ASN][1000 genomes]
rs13025294	0.85[ASN][1000 genomes]
rs13389611	0.86[ASN][1000 genomes]
rs13419011	0.85[ASN][1000 genomes]
rs13432611	0.85[ASN][1000 genomes]
rs13432618	0.85[ASN][1000 genomes]
rs1437916	0.94[ASN][1000 genomes]
rs1465827	1.00[ASN][1000 genomes]
rs1465828	0.91[ASN][1000 genomes]
rs16845716	0.98[ASN][1000 genomes]
rs1836732	0.86[ASN][1000 genomes]
rs2043790	0.97[ASN][1000 genomes]
rs4672608	0.95[ASN][1000 genomes]
rs57474880	0.91[ASN][1000 genomes]
rs71422736	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012193	chr2:211684524-212072213	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv460064	chr2:212045919-212101698	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv470511	chr2:212045919-212101698	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv584312	chr2:212045919-212101698	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv834522	chr2:212066442-212225328	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212069600-212072000	Enhancers	Hela-S3	cervix

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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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