Variant report

Variant	rs35420031
Chromosome Location	chr5:29238803-29238804
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs13163147	0.82[EUR][1000 genomes]
rs13163290	0.83[EUR][1000 genomes]
rs13163695	0.98[EUR][1000 genomes]
rs13169841	0.80[EUR][1000 genomes]
rs13170090	0.80[EUR][1000 genomes]
rs13173392	0.86[EUR][1000 genomes]
rs34286636	0.83[EUR][1000 genomes]
rs34424405	1.00[EUR][1000 genomes]
rs34745063	0.80[EUR][1000 genomes]
rs34946282	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35166177	0.80[EUR][1000 genomes]
rs35229135	1.00[EUR][1000 genomes]
rs35346985	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs35767223	1.00[EUR][1000 genomes]
rs35998955	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71621769	0.90[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs71621777	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3528360	chr5:29069255-29548659	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
2	esv3528361	chr5:29069255-29548659	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
3	nsv1016603	chr5:29102713-29843965	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
4	nsv537712	chr5:29102713-29843965	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
5	nsv1031329	chr5:29177677-29760923	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
6	nsv537713	chr5:29177677-29760923	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
7	nsv880414	chr5:29194872-29495564	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv881552	chr5:29219030-29466930	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv1024756	chr5:29220387-29501672	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:29237000-29239200	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr5:29237600-29239000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr5:29238000-29239600	Enhancers	Hela-S3	cervix
4	chr5:29238600-29239200	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr5:29238800-29239000	Enhancers	iPS-20b Cell Line	embryonic stem cell

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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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