Variant report

Variant	rs71336046
Chromosome Location	chr3:135682756-135682757
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:135678002..135681918-chr3:135682555..135686339,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000241905	Chromatin interaction

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10935175	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13072596	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13097946	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13098245	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13325914	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1403766	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1403770	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1523595	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1523596	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1523597	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17196987	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17197552	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17250445	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs28449384	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34311570	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34409306	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs34522617	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs34767379	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35257855	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs36039354	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4073308	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs67039922	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6771224	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6771997	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6774289	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6786769	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6807058	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6807242	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6807565	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6809006	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6810223	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73222222	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7427833	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7433567	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7621331	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7621396	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7621425	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7641070	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7643661	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9289502	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9289503	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9808979	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9812561	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9814557	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9825239	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9826806	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9834104	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9836374	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9836758	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9837355	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9842840	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9842864	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9843725	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9846137	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9848322	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9851361	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9853577	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9862264	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9862743	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9862763	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9862777	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9864247	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9864514	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9868246	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9872542	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9875328	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9877082	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9880721	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460860	chr3:135107678-135769006	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv591829	chr3:135107678-135769006	Flanking Active TSS Strong transcription Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv829732	chr3:135561706-135756840	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv869409	chr3:135649101-136164174	Strong transcription Genic enhancers Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
5	esv3374702	chr3:135649303-135686527	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:135682400-135683400	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr3:135682400-135684000	Enhancers	H1 Cell Line	embryonic stem cell
3	chr3:135682600-135682800	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr3:135682600-135684000	Enhancers	Fetal Intestine Small	intestine

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