Variant report

Variant	rs7295707
Chromosome Location	chr12:41661017-41661018
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11837950	1.00[AMR][1000 genomes]
rs17129118	1.00[CEU][hapmap]
rs17129130	0.94[YRI][hapmap]
rs17129138	1.00[CEU][hapmap]
rs1897230	1.00[CEU][hapmap]
rs73120934	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73120941	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73120943	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73120947	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73120950	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7980336	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv497867	chr12:41286305-41728650	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv899034	chr12:41515090-41698342	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv899035	chr12:41548545-41710912	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv469364	chr12:41631105-41710912	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
5	nsv558699	chr12:41631105-41710912	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
6	nsv517338	chr12:41653979-41662453	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
7	esv3404398	chr12:41658910-41661458	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
8	esv3447263	chr12:41659135-41661133	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:41661000-41661200	Enhancers	Colon Smooth Muscle	Colon

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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

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