Variant report

Variant	rs74146615
Chromosome Location	chr1:225230425-225230426
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	chr1:225229374..225230956-chr1:225231061..225233757,2	K562	blood:
2	chr1:225226692..225229117-chr1:225229791..225231600,2	K562	blood:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs4484895	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs55692366	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs56030006	1.00[AMR][1000 genomes]
rs56386111	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs56981420	0.85[AFR][1000 genomes]
rs57762550	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs58253035	1.00[EUR][1000 genomes]
rs58465537	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs59384753	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs60258106	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs60266138	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74146292	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74146297	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74146299	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74146300	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74146620	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74146622	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74147103	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74147105	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74147108	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74147112	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74147113	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74147114	1.00[AMR][1000 genomes]
rs74147127	1.00[AMR][1000 genomes]
rs74147130	1.00[AMR][1000 genomes]
rs74147132	1.00[AMR][1000 genomes]
rs74147133	1.00[AMR][1000 genomes]
rs74149407	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74149408	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74149409	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74149411	0.92[AFR][1000 genomes]
rs74149412	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74149413	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74149415	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74149424	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757773	chr1:225087924-225253274	Active TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	esv2759001	chr1:225087924-225253274	Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	esv3438976	chr1:225133567-225248753	Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv873225	chr1:225162060-225373936	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv549262	chr1:225191852-225319898	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv549263	chr1:225202426-225319898	ZNF genes & repeats Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv998899	chr1:225210813-225496353	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv1004856	chr1:225228287-225271137	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv526708	chr1:225229866-225273248	ZNF genes & repeats Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:225205600-225235600	Weak transcription	Pancreas	Pancrea
2	chr1:225215600-225242200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr1:225223400-225236000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr1:225225200-225232000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:225227000-225238400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr1:225227000-225240200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:225228000-225231000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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