Variant report

Variant	rs35405235
Chromosome Location	chr6:78016178-78016179
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs13193803	0.83[EUR][1000 genomes]
rs13196365	0.83[EUR][1000 genomes]
rs13200984	0.82[EUR][1000 genomes]
rs13204564	0.83[EUR][1000 genomes]
rs13208313	0.83[EUR][1000 genomes]
rs13214068	0.83[EUR][1000 genomes]
rs1342632	0.82[ASN][1000 genomes]
rs16888809	0.80[ASN][1000 genomes]
rs1935723	0.82[EUR][1000 genomes]
rs2211407	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2211409	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2211412	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2226149	0.97[ASN][1000 genomes]
rs2320295	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4499895	0.86[ASN][1000 genomes]
rs4708328	0.83[ASN][1000 genomes]
rs4708329	0.86[ASN][1000 genomes]
rs4708330	0.86[ASN][1000 genomes]
rs58535979	0.86[ASN][1000 genomes]
rs58816934	0.86[ASN][1000 genomes]
rs60136329	0.93[ASN][1000 genomes]
rs61003419	0.95[ASN][1000 genomes]
rs6453970	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6932428	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs71537194	0.83[EUR][1000 genomes]
rs71537195	0.80[EUR][1000 genomes]
rs7772083	0.83[EUR][1000 genomes]
rs9294070	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9343598	0.84[EUR][1000 genomes]
rs9352465	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9359260	0.83[EUR][1000 genomes]
rs9359261	0.85[EUR][1000 genomes]
rs9443397	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9443399	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9448053	0.80[EUR][1000 genomes]
rs9448071	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017082	chr6:77585310-78258237	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv534282	chr6:77764575-78351994	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1034979	chr6:77781244-78426249	Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv538324	chr6:77781244-78426249	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv2753543	chr6:77791848-78059351	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1015307	chr6:77902559-78352291	Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:78003400-78016200	Weak transcription	Aorta	Aorta
2	chr6:78004400-78017000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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