Variant report

Variant	rs17025797
Chromosome Location	chr1:216141054-216141055
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:216135175..216136682-chr1:216139501..216141114,2	K562	blood:
2	chr1:216137965..216139586-chr1:216139815..216142602,2	MCF-7	breast:
3	chr1:216139397..216141428-chr1:216167682..216169961,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10495011	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap]
rs11579696	1.00[ASN][1000 genomes]
rs11589643	0.86[CHB][hapmap]
rs12408791	0.95[ASN][1000 genomes]
rs1325520	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1325521	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1347627	1.00[JPT][hapmap]
rs1436772	1.00[JPT][hapmap]
rs17025555	0.82[CHB][hapmap]
rs17025589	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap]
rs17025676	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17025679	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17025680	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17025681	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17025683	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17025684	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17025685	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17025690	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17025699	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17025701	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17025702	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17025758	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17025764	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17025799	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17025802	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17042187	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1821761	1.00[JPT][hapmap]
rs2813727	1.00[JPT][hapmap]
rs4481823	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4481824	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4537521	1.00[JPT][hapmap]
rs566191	1.00[JPT][hapmap]
rs57547189	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs626192	1.00[JPT][hapmap]
rs646378	1.00[JPT][hapmap]
rs6540921	1.00[ASN][1000 genomes]
rs6540922	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6540923	0.86[CHB][hapmap]
rs6658138	1.00[CEU][hapmap]
rs6676313	1.00[JPT][hapmap]
rs6680930	1.00[ASN][1000 genomes]
rs6686550	0.86[CHB][hapmap]
rs6687538	1.00[JPT][hapmap]
rs6690420	0.86[CHB][hapmap]
rs6690523	0.86[CHB][hapmap]
rs6692241	1.00[JPT][hapmap]
rs73092442	1.00[ASN][1000 genomes]
rs73092444	1.00[ASN][1000 genomes]
rs7528148	0.85[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006504	chr1:215890460-216642124	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv535288	chr1:215890460-216642124	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv832548	chr1:215987089-216175724	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv428599	chr1:216086224-216267211	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv1844934	chr1:216132878-216179889	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 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	chr1:216132000-216144000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:216139000-216142600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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