Variant report

Variant	rs2623370
Chromosome Location	chr3:99146033-99146034
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs1031966	0.85[ASN][1000 genomes]
rs1031967	0.85[ASN][1000 genomes]
rs12487192	0.81[ASN][1000 genomes]
rs12490465	0.81[ASN][1000 genomes]
rs12632463	1.00[AMR][1000 genomes]
rs1383857	0.93[ASN][1000 genomes]
rs1481531	0.93[ASN][1000 genomes]
rs1481547	0.93[ASN][1000 genomes]
rs1481548	0.93[ASN][1000 genomes]
rs1994036	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2062042	0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2086520	0.85[ASN][1000 genomes]
rs2101107	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2101108	0.85[ASN][1000 genomes]
rs2128021	0.85[ASN][1000 genomes]
rs2128022	1.00[ASN][1000 genomes]
rs2170385	0.85[ASN][1000 genomes]
rs2170386	0.85[ASN][1000 genomes]
rs2219971	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2245932	0.81[ASN][1000 genomes]
rs2245940	0.85[ASN][1000 genomes]
rs2464150	0.93[ASN][1000 genomes]
rs2470690	0.93[ASN][1000 genomes]
rs2623345	0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2623354	0.85[ASN][1000 genomes]
rs2623356	0.85[ASN][1000 genomes]
rs2623358	0.85[ASN][1000 genomes]
rs2623359	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2623360	0.95[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2623361	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2623369	0.93[ASN][1000 genomes]
rs2623377	0.93[ASN][1000 genomes]
rs2700589	0.93[ASN][1000 genomes]
rs2700591	0.93[ASN][1000 genomes]
rs2700607	0.81[ASN][1000 genomes]
rs2700609	0.82[ASN][1000 genomes]
rs2700612	0.93[ASN][1000 genomes]
rs2700613	1.00[ASN][1000 genomes]
rs2700614	0.95[ASN][1000 genomes]
rs2700615	0.85[ASN][1000 genomes]
rs2700616	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2700621	0.85[ASN][1000 genomes]
rs2700625	0.93[ASN][1000 genomes]
rs2700638	0.93[ASN][1000 genomes]
rs2700644	0.81[ASN][1000 genomes]
rs2929436	0.81[ASN][1000 genomes]
rs2929438	0.93[ASN][1000 genomes]
rs2960090	0.93[ASN][1000 genomes]
rs34794291	0.93[ASN][1000 genomes]
rs7625600	0.85[ASN][1000 genomes]
rs900058	0.93[ASN][1000 genomes]
rs969004	0.93[ASN][1000 genomes]
rs9835548	0.85[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	nsv1007140	chr3:98421229-99202458	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv536663	chr3:98421229-99202458	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1007486	chr3:98597738-99249081	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv530026	chr3:98837320-99340537	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv877216	chr3:99065296-99161022	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr3:99145200-99147600	Weak transcription	NHDF-Ad	bronchial
2	chr3:99145200-99148600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr3:99145200-99148600	Weak transcription	HSMMtube	muscle

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