Variant report

Variant	rs11902608
Chromosome Location	chr2:9870314-9870315
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:9870027..9872978-chr2:9873410..9875751,2	K562	blood:
2	chr2:9845748..9848155-chr2:9867890..9870403,2	K562	blood:
3	chr2:9845674..9847302-chr2:9868513..9870809,2	MCF-7	breast:

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10164660	0.84[ASN][1000 genomes]
rs10202938	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10929596	0.90[ASN][1000 genomes]
rs10929597	0.90[ASN][1000 genomes]
rs10929598	0.90[ASN][1000 genomes]
rs10929600	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10929602	0.93[ASN][1000 genomes]
rs10929605	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11695437	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11892176	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11901380	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11902412	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12472594	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12991432	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12993968	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13024852	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1877949	0.85[ASN][1000 genomes]
rs1877950	0.86[ASN][1000 genomes]
rs1877951	0.86[ASN][1000 genomes]
rs1877953	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2357264	0.92[ASN][1000 genomes]
rs2357265	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4459704	0.92[ASN][1000 genomes]
rs4507070	0.88[ASN][1000 genomes]
rs4668636	0.84[ASN][1000 genomes]
rs4668637	0.89[ASN][1000 genomes]
rs4668638	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4668639	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4668640	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4668641	0.83[ASN][1000 genomes]
rs4668642	0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4668643	0.85[ASN][1000 genomes]
rs4669427	0.88[ASN][1000 genomes]
rs4669428	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4669429	0.90[ASN][1000 genomes]
rs4669430	0.90[ASN][1000 genomes]
rs4669432	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4669433	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4669435	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4669437	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4669441	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4669445	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4669446	0.85[ASN][1000 genomes]
rs5020306	0.90[ASN][1000 genomes]
rs58577971	0.83[ASN][1000 genomes]
rs58961346	0.93[ASN][1000 genomes]
rs6432033	0.90[ASN][1000 genomes]
rs6724483	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6727688	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6736421	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6752842	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs74171467	0.82[ASN][1000 genomes]
rs7592044	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7602784	0.82[ASN][1000 genomes]
rs7605675	0.82[ASN][1000 genomes]
rs885572	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]

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	nsv469405	chr2:9814374-9964947	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
2	nsv580930	chr2:9814374-9964947	Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
3	nsv1003026	chr2:9854939-10012516	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	nsv470443	chr2:9857018-9975557	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
5	nsv1014911	chr2:9863969-9905959	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:9868800-9870400	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr2:9869600-9875800	Weak transcription	Fetal Thymus	thymus
3	chr2:9869800-9870400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr2:9869800-9871200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr2:9870000-9870400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr2:9870000-9870400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin

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