Variant report

Variant	rs4952876
Chromosome Location	chr2:47435722-47435723
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:47423169..47425083-chr2:47433358..47436246,2	K562	blood:
2	chr2:47433849..47436405-chr2:47465797..47467993,2	MCF-7	breast:
3	chr2:47434249..47437300-chr2:47437596..47440193,3	K562	blood:
4	chr2:47426377..47428396-chr2:47434799..47437160,2	K562	blood:
5	chr2:47429443..47431361-chr2:47434372..47436330,2	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1021609	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1021610	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1039162	0.94[CHB][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11899830	0.91[CEU][hapmap];0.88[CHB][hapmap];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11899833	0.91[CEU][hapmap];0.88[CHB][hapmap];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12612040	0.91[CEU][hapmap]
rs13391158	0.91[CEU][hapmap];0.94[CHB][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17557422	0.87[ASN][1000 genomes]
rs1874668	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1874669	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2132923	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2132924	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4952877	0.91[CEU][hapmap];0.94[CHB][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4953477	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4953478	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4953479	0.94[CHB][hapmap];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61371951	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6544972	0.86[CEU][hapmap]
rs6721098	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs67882902	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7575670	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs904166	0.91[CEU][hapmap];0.88[CHB][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs904167	0.88[CHB][hapmap];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817517	chr2:46819371-47715140	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
2	nsv1004828	chr2:47056849-47814482	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
3	nsv457374	chr2:47313624-47448865	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	87 gene(s)	inside rSNPs	diseases
4	nsv581754	chr2:47313624-47448865	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	87 gene(s)	inside rSNPs	diseases
5	esv10649	chr2:47429316-47472670	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv531348	chr2:47433147-47827310	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:47427000-47435800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr2:47428400-47437800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr2:47428800-47441000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:47428800-47442000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr2:47429000-47438400	Weak transcription	Brain Anterior Caudate	brain
6	chr2:47429200-47435800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr2:47430800-47435800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr2:47431400-47447200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr2:47433000-47438400	Weak transcription	Liver	Liver
10	chr2:47433200-47435800	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr2:47433200-47435800	Weak transcription	Fetal Lung	lung
12	chr2:47433200-47435800	Weak transcription	NHLF	lung
13	chr2:47433200-47436000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr2:47433200-47442200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr2:47433400-47435800	Weak transcription	Fetal Intestine Small	intestine
16	chr2:47433400-47435800	Weak transcription	Osteobl	bone
17	chr2:47433400-47436000	Weak transcription	HSMM	muscle
18	chr2:47433400-47442200	Weak transcription	Duodenum Mucosa	Duodenum
19	chr2:47433400-47445200	Weak transcription	Fetal Kidney	kidney
20	chr2:47433600-47435800	Weak transcription	Stomach Mucosa	stomach
21	chr2:47433600-47435800	Weak transcription	HUVEC	blood vessel
22	chr2:47433600-47438400	Weak transcription	Fetal Heart	heart
23	chr2:47433800-47435800	Weak transcription	Fetal Intestine Large	intestine
24	chr2:47433800-47436000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr2:47434200-47435800	Weak transcription	K562	blood
26	chr2:47435000-47435800	Weak transcription	Placenta	Placenta
27	chr2:47435200-47435800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr2:47435200-47436000	Enhancers	Hela-S3	cervix
29	chr2:47435600-47436000	Enhancers	A549	lung
30	chr2:47435600-47436200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr2:47435600-47436400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr2:47435600-47437000	Enhancers	NH-A	brain

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