Variant report

Variant	rs6710930
Chromosome Location	chr2:67923789-67923790
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10190216	0.93[ASN][1000 genomes]
rs10210921	0.94[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs1367460	0.82[JPT][hapmap]
rs1367462	0.86[CEU][hapmap]
rs1430760	0.89[AFR][1000 genomes]
rs1430761	0.93[AFR][1000 genomes]
rs1430767	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1835462	0.93[AFR][1000 genomes]
rs2060042	0.95[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs4233941	0.93[ASN][1000 genomes]
rs4671195	0.97[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs4671196	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4671830	0.87[CEU][hapmap];0.82[JPT][hapmap];0.84[EUR][1000 genomes]
rs4671842	0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6724226	0.94[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs6733362	0.85[JPT][hapmap]
rs934311	0.93[AFR][1000 genomes]
rs966442	0.93[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534389	chr2:67388428-68225338	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
2	nsv1007345	chr2:67870225-67980094	Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Weak transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv834250	chr2:67897722-68051532	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67922200-67927800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:67923200-67924000	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr2:67923400-67924000	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr2:67923400-67924200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr2:67923400-67924200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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