Variant report

Variant	rs67697939
Chromosome Location	chr2:168369551-168369552
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:168342324..168343828-chr2:168369519..168372114,2	K562	blood:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1112983	0.80[EUR][1000 genomes]
rs11897803	0.81[ASN][1000 genomes]
rs11899757	0.90[ASN][1000 genomes]
rs12105560	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1227120	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1238298	0.81[EUR][1000 genomes]
rs12470779	0.86[AMR][1000 genomes]
rs12478609	0.86[ASN][1000 genomes]
rs12613660	0.91[AMR][1000 genomes]
rs12623916	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12989813	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12990145	0.90[ASN][1000 genomes]
rs12996381	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13032189	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13383575	0.81[ASN][1000 genomes]
rs13406065	0.81[ASN][1000 genomes]
rs1541889	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1583216	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1583217	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1653420	0.86[EUR][1000 genomes]
rs1653425	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1653430	0.83[EUR][1000 genomes]
rs16853634	0.81[ASN][1000 genomes]
rs16853644	0.81[ASN][1000 genomes]
rs16853648	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs16853653	0.81[ASN][1000 genomes]
rs16853655	0.81[ASN][1000 genomes]
rs1730713	0.84[EUR][1000 genomes]
rs1730725	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1813255	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1919851	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1919854	0.84[EUR][1000 genomes]
rs1919855	0.80[EUR][1000 genomes]
rs2052982	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2052984	0.88[AMR][1000 genomes]
rs34653091	0.88[AMR][1000 genomes]
rs35523753	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35580310	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4667955	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs59149606	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6710395	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6725601	0.84[ASN][1000 genomes]
rs6731834	0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs67321550	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6753105	0.81[ASN][1000 genomes]
rs7567362	0.82[AMR][1000 genomes];0.85[EUR][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	nsv491872	chr2:168220323-168737986	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	esv3388045	chr2:168289403-168424317	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv834449	chr2:168340043-168511856	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv583592	chr2:168356232-168721539	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	esv3415767	chr2:168368306-168370204	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:168366600-168384800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr2:168366800-168374200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr2:168367000-168385200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr2:168367200-168371200	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr2:168367200-168371200	Weak transcription	Muscle Satellite Cultured Cells	--

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