Variant report

Variant	rs7070972
Chromosome Location	chr10:56234234-56234235
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10825335	1.00[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs10825336	0.95[CHB][hapmap];0.94[JPT][hapmap]
rs10825338	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs11004321	0.82[CHB][hapmap]
rs11004326	1.00[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs11004328	1.00[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs11004329	0.95[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs11004332	0.95[CHB][hapmap];0.88[JPT][hapmap]
rs11004333	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs1157587	0.95[CHB][hapmap];0.89[JPT][hapmap]
rs12219968	0.89[CHB][hapmap]
rs12220423	1.00[CHB][hapmap];0.88[JPT][hapmap]
rs12268378	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs12415777	0.92[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap]
rs12570763	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs1342309	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16906167	0.95[CHB][hapmap];0.89[JPT][hapmap]
rs2104891	1.00[CHB][hapmap];0.93[JPT][hapmap];0.81[ASN][1000 genomes]
rs7912610	0.83[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052386	chr10:56075990-56273476	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv895440	chr10:56212367-56286068	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv895441	chr10:56212367-56286068	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv895442	chr10:56212367-56295820	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1050405	chr10:56224676-56800009	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
6	nsv540635	chr10:56224676-56800009	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:56233800-56234400	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr10:56233800-56234600	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr10:56234000-56234400	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr10:56234000-56234400	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr10:56234000-56234600	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr10:56234000-56234800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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