Variant report

Variant	rs4233345
Chromosome Location	chr1:169004176-169004177
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs11589212	0.82[ASN][1000 genomes]
rs11589804	0.99[ASN][1000 genomes]
rs4233344	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4486430	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869415	chr1:168467284-169153863	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
2	esv3522071	chr1:168978325-169339044	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
3	esv3522072	chr1:168978325-169339044	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
4	nsv548146	chr1:169000109-169006682	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv548147	chr1:169002599-169005084	Inactive region	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv1836513	chr1:169002599-169005138	Inactive region	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv548148	chr1:169002599-169005138	Inactive region	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	esv1837209	chr1:169002599-169005304	Inactive region	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv3320797	chr1:169003896-169005512	Inactive region	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv820513	chr1:169004137-169005382	Inactive region	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv825320	chr1:169004137-169005382	Inactive region	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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