Variant report

Variant	rs10002144
Chromosome Location	chr4:7621448-7621449
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10001358	1.00[EUR][1000 genomes]
rs10002768	1.00[EUR][1000 genomes]
rs10804999	1.00[EUR][1000 genomes]
rs10805000	1.00[EUR][1000 genomes]
rs13435331	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16840543	1.00[EUR][1000 genomes]
rs16840589	1.00[EUR][1000 genomes]
rs16840614	1.00[EUR][1000 genomes]
rs16840635	1.00[EUR][1000 genomes]
rs16840725	1.00[EUR][1000 genomes]
rs16840743	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16840756	1.00[EUR][1000 genomes]
rs4234819	1.00[EUR][1000 genomes]
rs4234820	1.00[EUR][1000 genomes]
rs4330351	1.00[EUR][1000 genomes]
rs4346650	1.00[EUR][1000 genomes]
rs4572883	1.00[EUR][1000 genomes]
rs4689757	1.00[EUR][1000 genomes]
rs59256904	1.00[EUR][1000 genomes]
rs6446604	1.00[EUR][1000 genomes]
rs6446618	1.00[EUR][1000 genomes]
rs757245	1.00[EUR][1000 genomes]
rs7683873	1.00[EUR][1000 genomes]
rs7690364	1.00[EUR][1000 genomes]
rs7691525	1.00[EUR][1000 genomes]
rs7692130	1.00[EUR][1000 genomes]
rs7693764	1.00[EUR][1000 genomes]
rs871943	1.00[EUR][1000 genomes]
rs9884448	1.00[EUR][1000 genomes]
rs9884644	1.00[EUR][1000 genomes]
rs9884725	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916610	chr4:7238883-7731946	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv593569	chr4:7291363-7626136	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1011547	chr4:7318232-7637410	Active TSS ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv537017	chr4:7318232-7637410	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
5	esv34156	chr4:7526515-7750588	Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
6	nsv878570	chr4:7534603-7836835	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
7	nsv491712	chr4:7582506-8155069	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
8	nsv461213	chr4:7584560-7637297	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv593618	chr4:7584560-7637297	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv508272	chr4:7591967-7722112	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7614800-7622600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:7615400-7622200	Weak transcription	Brain Germinal Matrix	brain
3	chr4:7618000-7632200	Weak transcription	Right Atrium	heart
4	chr4:7621000-7622600	Enhancers	Brain Substantia Nigra	brain
5	chr4:7621200-7621800	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr4:7621200-7622600	Enhancers	Brain Cingulate Gyrus	brain
7	chr4:7621400-7621600	Enhancers	Brain Hippocampus Middle	brain
8	chr4:7621400-7622000	Enhancers	Brain Angular Gyrus	brain
9	chr4:7621400-7623000	Enhancers	Fetal Brain Male	brain

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