Variant report

Variant	rs2361698
Chromosome Location	chr7:139505708-139505709
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10237429	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10253277	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10256282	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10277705	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12534299	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs194152	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1990354	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2107900	0.83[EUR][1000 genomes]
rs2267679	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4590360	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4726815	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4726838	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4727013	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs56147462	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6464800	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6951759	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6952322	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6980375	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs764745	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs764746	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1020234	chr7:139377822-139661964	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1032711	chr7:139411404-139684043	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv464732	chr7:139424022-139654256	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv608472	chr7:139424022-139654256	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv1018712	chr7:139429703-139658014	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv464733	chr7:139491967-139539218	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv608473	chr7:139491967-139539218	Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr7:139503200-139508400	Weak transcription	Esophagus	oesophagus
2	chr7:139503800-139506200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:139504000-139506600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr7:139504000-139511400	Weak transcription	Fetal Stomach	stomach
5	chr7:139504200-139508200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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