Variant report

Variant	rs326525
Chromosome Location	chr13:29635157-29635158
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs167832	0.82[ASN][1000 genomes]
rs167834	0.82[ASN][1000 genomes]
rs191266	0.82[ASN][1000 genomes]
rs226906	0.82[ASN][1000 genomes]
rs226909	0.82[ASN][1000 genomes]
rs2475513	0.82[ASN][1000 genomes]
rs2475516	0.82[ASN][1000 genomes]
rs2475517	0.82[ASN][1000 genomes]
rs2475522	0.82[ASN][1000 genomes]
rs2475527	0.82[ASN][1000 genomes]
rs2479772	0.82[ASN][1000 genomes]
rs2479777	0.82[ASN][1000 genomes]
rs2479780	0.82[ASN][1000 genomes]
rs2479782	0.82[ASN][1000 genomes]
rs2479783	0.82[ASN][1000 genomes]
rs2479788	0.82[ASN][1000 genomes]
rs326504	0.82[ASN][1000 genomes]
rs326512	0.82[ASN][1000 genomes]
rs326516	0.82[ASN][1000 genomes]
rs326521	0.82[ASN][1000 genomes]
rs326522	0.82[ASN][1000 genomes]
rs326523	0.82[ASN][1000 genomes]
rs4768998	0.82[ASN][1000 genomes]
rs4769671	0.82[ASN][1000 genomes]
rs4769673	0.82[ASN][1000 genomes]
rs7325000	0.82[ASN][1000 genomes]
rs9506090	0.82[ASN][1000 genomes]
rs9508258	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533835	chr13:29141132-29962069	Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	esv3406145	chr13:29616606-29917459	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:29634200-29636800	Weak transcription	Fetal Heart	heart
2	chr13:29634400-29640000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr13:29634600-29640000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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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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