Variant report

Variant	rs2479782
Chromosome Location	chr13:29653156-29653157
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs167832	1.00[ASN][1000 genomes]
rs167834	1.00[ASN][1000 genomes]
rs191266	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs226906	1.00[ASN][1000 genomes]
rs226909	1.00[ASN][1000 genomes]
rs2475513	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2475516	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2475517	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2475522	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2475527	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2475547	0.92[ASN][1000 genomes]
rs2479769	0.85[ASN][1000 genomes]
rs2479772	1.00[ASN][1000 genomes]
rs2479777	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2479780	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2479783	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2479788	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs326504	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs326512	1.00[ASN][1000 genomes]
rs326516	1.00[ASN][1000 genomes]
rs326518	0.96[ASN][1000 genomes]
rs326521	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs326522	0.92[ASN][1000 genomes]
rs326523	1.00[ASN][1000 genomes]
rs326525	0.82[ASN][1000 genomes]
rs4768998	1.00[ASN][1000 genomes]
rs4769671	1.00[ASN][1000 genomes]
rs4769673	1.00[ASN][1000 genomes]
rs7325000	1.00[ASN][1000 genomes]
rs9506090	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9508258	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[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:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:29651800-29653200	Enhancers	Dnd41	blood
2	chr13:29651800-29654600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr13:29652200-29655000	Weak transcription	Fetal Heart	heart
4	chr13:29652600-29654600	Weak transcription	Primary T cells from cord blood	blood
5	chr13:29652800-29653400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links