Variant report

Variant	rs2173726
Chromosome Location	chr19:21614655-21614656
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:21614539..21617498-chr19:21618431..21621735,3	K562	blood:

Extended variants
information (count: 88 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs10410362	1.00[MEX][hapmap];0.81[YRI][hapmap];1.00[AMR][1000 genomes]
rs10412054	1.00[AMR][1000 genomes]
rs10424079	0.82[YRI][hapmap]
rs11878543	1.00[AMR][1000 genomes]
rs11879610	1.00[CHB][hapmap]
rs11879647	1.00[AMR][1000 genomes]
rs11880701	1.00[AMR][1000 genomes]
rs11880751	1.00[AMR][1000 genomes]
rs11881331	1.00[AMR][1000 genomes]
rs11881379	1.00[AMR][1000 genomes]
rs11881619	1.00[ASN][1000 genomes]
rs11881648	1.00[ASN][1000 genomes]
rs11882304	1.00[AMR][1000 genomes]
rs1401927	1.00[CHB][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs1645806	1.00[MEX][hapmap]
rs1762561	1.00[AMR][1000 genomes]
rs1762562	1.00[AMR][1000 genomes]
rs1762569	1.00[AMR][1000 genomes]
rs1781849	1.00[AMR][1000 genomes]
rs1781854	1.00[AMR][1000 genomes]
rs1781859	1.00[AMR][1000 genomes]
rs1846713	1.00[AMR][1000 genomes]
rs1909772	1.00[AMR][1000 genomes]
rs1963057	1.00[MEX][hapmap];0.86[YRI][hapmap];1.00[AMR][1000 genomes]
rs2011379	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs2088759	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2359147	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2359148	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2434998	1.00[AMR][1000 genomes]
rs2454922	1.00[MEX][hapmap];0.81[YRI][hapmap];1.00[AMR][1000 genomes]
rs2537693	1.00[AMR][1000 genomes]
rs2537695	1.00[AMR][1000 genomes]
rs2562412	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2562434	1.00[AMR][1000 genomes]
rs2562460	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2650772	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2650811	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2650838	1.00[AMR][1000 genomes]
rs2650839	1.00[AMR][1000 genomes]
rs2801860	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs28857324	1.00[AMR][1000 genomes]
rs2914643	1.00[AMR][1000 genomes]
rs2914644	0.84[YRI][hapmap];1.00[AMR][1000 genomes]
rs2928219	1.00[AMR][1000 genomes]
rs2928220	1.00[AMR][1000 genomes]
rs2968029	1.00[AMR][1000 genomes]
rs2968031	1.00[MEX][hapmap];0.81[YRI][hapmap];1.00[AMR][1000 genomes]
rs2968071	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs57144387	1.00[ASN][1000 genomes]
rs57470621	1.00[ASN][1000 genomes]
rs57626552	1.00[AMR][1000 genomes]
rs57785081	1.00[ASN][1000 genomes]
rs57847044	1.00[AMR][1000 genomes]
rs58638125	1.00[AMR][1000 genomes]
rs58878959	1.00[ASN][1000 genomes]
rs59087535	1.00[AMR][1000 genomes]
rs59268487	1.00[AMR][1000 genomes]
rs60355060	1.00[ASN][1000 genomes]
rs61334868	1.00[AMR][1000 genomes]
rs7249229	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7258384	1.00[CHB][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs73534731	1.00[ASN][1000 genomes]
rs73539807	1.00[AMR][1000 genomes]
rs73543179	1.00[ASN][1000 genomes]
rs73543709	1.00[AMR][1000 genomes]
rs73545768	1.00[AMR][1000 genomes]
rs73545790	1.00[AMR][1000 genomes]
rs73546772	1.00[ASN][1000 genomes]
rs73546788	1.00[ASN][1000 genomes]
rs73546793	1.00[ASN][1000 genomes]
rs73547713	1.00[AMR][1000 genomes]
rs73547779	1.00[AMR][1000 genomes]
rs73548623	1.00[ASN][1000 genomes]
rs73548627	1.00[ASN][1000 genomes]
rs73548629	1.00[ASN][1000 genomes]
rs73548644	1.00[ASN][1000 genomes]
rs73549716	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs73551246	1.00[ASN][1000 genomes]
rs73551256	1.00[ASN][1000 genomes]
rs73551258	1.00[ASN][1000 genomes]
rs8112786	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3518033	chr19:21278465-21747567	Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	esv3518034	chr19:21278465-21747567	ZNF genes & repeats Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	esv3414204	chr19:21301761-21839451	ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	esv3325271	chr19:21445407-21792817	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	esv2751783	chr19:21465822-21726337	Strong transcription ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
6	esv3363678	chr19:21483148-21756908	Strong transcription Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
7	nsv578952	chr19:21535707-21868584	Genic enhancers Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21607600-21630200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr19:21613400-21618600	ZNF genes & repeats	Liver	Liver
3	chr19:21614400-21614800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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