Variant report

Variant	rs59256904
Chromosome Location	chr4:7546044-7546045
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10001358	1.00[EUR][1000 genomes]
rs10002144	1.00[EUR][1000 genomes]
rs10002768	1.00[EUR][1000 genomes]
rs10804999	1.00[EUR][1000 genomes]
rs10805000	1.00[EUR][1000 genomes]
rs11932649	1.00[AMR][1000 genomes]
rs13435331	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[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]
rs4572883	1.00[EUR][1000 genomes]
rs4689757	1.00[EUR][1000 genomes]
rs60046977	1.00[AMR][1000 genomes]
rs6446604	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	nsv469758	chr4:7370083-7546250	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
6	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
7	nsv461211	chr4:7530451-7548862	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv528667	chr4:7533674-7547547	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
9	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
10	esv3426446	chr4:7544102-7546900	ZNF genes & repeats Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7541000-7549000	Weak transcription	Brain Angular Gyrus	brain
2	chr4:7541200-7547400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr4:7541200-7549000	Weak transcription	Brain Cingulate Gyrus	brain
4	chr4:7541400-7548200	Weak transcription	Ovary	ovary
5	chr4:7542400-7548800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr4:7543000-7548000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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