Variant report

Variant	rs17034210
Chromosome Location	chr2:67944842-67944843
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10496148	0.82[ASN][1000 genomes]
rs11126148	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs17034147	0.87[ASN][1000 genomes]
rs17034224	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2195683	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2195684	0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs58113451	0.89[ASN][1000 genomes]
rs60157569	0.91[ASN][1000 genomes]
rs60205859	0.89[ASN][1000 genomes]
rs6747212	0.85[ASN][1000 genomes]
rs72621591	0.90[ASN][1000 genomes]
rs72621593	0.90[ASN][1000 genomes]
rs72621594	0.89[ASN][1000 genomes]
rs72621595	0.89[ASN][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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67940000-67945400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:67944200-67945600	Enhancers	NHDF-Ad	bronchial

Quick Search:

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

what's new

Quick links