Variant report

Variant	rs35541760
Chromosome Location	chr3:70106810-70106811
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs13062402	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13064441	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13069643	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13071266	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13077347	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13080062	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13081786	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13086024	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13094951	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13099113	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2131123	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34313089	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34514277	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34584406	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34771518	1.00[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs35066679	0.87[EUR][1000 genomes]
rs35286473	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35527992	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs36001908	0.88[ASN][1000 genomes]
rs36042309	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs66533134	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6809108	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs71298324	0.89[ASN][1000 genomes]
rs73102056	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73102066	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73104062	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73104068	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533396	chr3:69964029-70538306	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:70104800-70107800	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr3:70104800-70107800	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr3:70105000-70107400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr3:70105000-70107600	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr3:70105000-70107600	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr3:70106000-70107000	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr3:70106200-70107400	Enhancers	Fetal Brain Male	brain
8	chr3:70106400-70107600	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr3:70106800-70107000	Enhancers	Fetal Lung	lung
10	chr3:70106800-70107400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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