Variant report

Variant	rs35960583
Chromosome Location	chr12:30937602-30937603
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10771771	0.83[EUR][1000 genomes]
rs11051080	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11051081	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11051084	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12810332	0.93[EUR][1000 genomes]
rs12816066	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1485351	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2195236	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7312385	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]

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	esv3343291	chr12:30455597-30992837	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv832361	chr12:30794030-30997241	Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	nsv949148	chr12:30800040-31131712	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
4	esv34091	chr12:30927650-31061815	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:30936000-30939400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
2	chr12:30936000-30945000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:30936800-30939400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
4	chr12:30937000-30938400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
5	chr12:30937000-30938600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
6	chr12:30937200-30938200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
7	chr12:30937200-30938800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr12:30937200-30939600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
9	chr12:30937600-30939400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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