Variant report

Variant	rs73678638
Chromosome Location	chr7:12211550-12211551
allele	C/G
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:11)

rs_ID	r²[population]
rs12699318	0.86[AFR][1000 genomes]
rs2080607	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56967414	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57765130	1.00[AMR][1000 genomes]
rs73678623	1.00[AMR][1000 genomes]
rs73678626	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73678630	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73678633	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73678653	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73678679	1.00[AMR][1000 genomes]
rs73678681	1.00[AMR][1000 genomes]

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	nsv606199	chr7:11506143-12486659	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv1023608	chr7:12064114-12247520	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv534432	chr7:12148960-12693032	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv1021710	chr7:12164993-12251790	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
5	nsv887627	chr7:12178793-12227892	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv887628	chr7:12186502-12227892	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	2 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	chr7:12209200-12212000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
2	chr7:12209400-12211800	Enhancers	Primary T helper cells fromperipheralblood	blood
3	chr7:12209400-12211800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
4	chr7:12210200-12211800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr7:12210200-12212000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
6	chr7:12210400-12211600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr7:12211200-12211600	Enhancers	A549	lung
8	chr7:12211400-12212200	Enhancers	HepG2	liver
9	chr7:12211400-12212800	Weak transcription	Primary T helper cells PMA-I stimulated	--

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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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