Variant report

Variant	rs8095400
Chromosome Location	chr18:7838735-7838736
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10502362	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11081345	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1117814	0.92[EUR][1000 genomes]
rs12457653	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12965898	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1348104	0.92[EUR][1000 genomes]
rs1440995	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1440999	0.84[EUR][1000 genomes]
rs1441000	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1441001	0.85[EUR][1000 genomes]
rs1443614	0.80[EUR][1000 genomes]
rs1822456	0.92[EUR][1000 genomes]
rs2009770	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2197010	0.92[EUR][1000 genomes]
rs2377575	0.92[EUR][1000 genomes]
rs2377576	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2377577	0.90[EUR][1000 genomes]
rs331414	0.85[EUR][1000 genomes]
rs331415	0.84[EUR][1000 genomes]
rs34294315	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs36188935	0.92[EUR][1000 genomes]
rs4797302	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4798598	0.82[EUR][1000 genomes]
rs4798599	0.92[EUR][1000 genomes]
rs4798600	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4798601	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4798602	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4798603	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6506535	0.85[EUR][1000 genomes]
rs6506536	0.82[EUR][1000 genomes]
rs671369	0.85[EUR][1000 genomes]
rs7227367	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7228457	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7232793	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7233704	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7235300	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7239136	0.90[EUR][1000 genomes]
rs7243673	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs727949	0.92[EUR][1000 genomes]
rs727951	0.92[EUR][1000 genomes]
rs8083298	0.92[EUR][1000 genomes]
rs8089088	0.92[EUR][1000 genomes]
rs8095467	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs8098502	0.95[EUR][1000 genomes]
rs9944547	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534374	chr18:7438812-8412546	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv458016	chr18:7488133-7934001	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv576399	chr18:7488133-7934001	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv2762810	chr18:7492090-7924728	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1062911	chr18:7561991-8088274	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv543637	chr18:7561991-8088274	Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv1064345	chr18:7562051-8088274	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv543638	chr18:7562051-8088274	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv576425	chr18:7747873-7859757	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:7815400-7843800	Weak transcription	A549	lung
2	chr18:7818200-7839400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr18:7825200-7839800	Weak transcription	Thymus	Thymus
4	chr18:7825400-7839600	Weak transcription	Fetal Thymus	thymus
5	chr18:7826200-7839000	Weak transcription	Fetal Muscle Leg	muscle
6	chr18:7830800-7843800	Weak transcription	Aorta	Aorta
7	chr18:7836800-7839800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr18:7837200-7841200	Enhancers	Skeletal Muscle Male	skeletal muscle
9	chr18:7837400-7840000	Enhancers	Left Ventricle	heart
10	chr18:7837400-7841200	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr18:7837600-7841800	Weak transcription	Fetal Muscle Trunk	muscle
12	chr18:7837800-7840600	Enhancers	Psoas Muscle	Psoas
13	chr18:7837800-7840800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr18:7837800-7844000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr18:7838600-7839800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr18:7838600-7840000	Enhancers	Right Ventricle	heart

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