Variant report

Variant	rs6706854
Chromosome Location	chr2:212508134-212508135
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10203821	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10205275	0.87[AMR][1000 genomes]
rs10932385	1.00[CHB][hapmap]
rs16846637	1.00[CHB][hapmap]
rs17335001	1.00[CHB][hapmap]
rs17335057	1.00[CHB][hapmap]
rs17413177	1.00[CHB][hapmap]
rs17413281	1.00[CHB][hapmap]
rs1851177	0.83[LWK][hapmap]
rs6435647	0.94[EUR][1000 genomes]
rs6435649	1.00[MEX][hapmap];0.82[YRI][hapmap];0.80[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs6435650	0.86[YRI][hapmap];0.88[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs6707492	1.00[MEX][hapmap]
rs6733265	1.00[CHB][hapmap]
rs73078781	0.83[EUR][1000 genomes]
rs73078782	0.83[EUR][1000 genomes]
rs7422464	1.00[MEX][hapmap];0.91[AMR][1000 genomes]
rs7576417	0.89[AFR][1000 genomes]
rs7576673	1.00[CHB][hapmap]

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	nsv584321	chr2:212446818-212511895	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv2754366	chr2:212470494-212541494	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
3	nsv460070	chr2:212492764-212541377	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
4	nsv584322	chr2:212492764-212541377	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region	1 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	chr2:212467400-212546800	Weak transcription	Aorta	Aorta
2	chr2:212508000-212508600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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