Variant report

Variant	rs12634529
Chromosome Location	chr3:80282712-80282713
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10511115	0.88[AMR][1000 genomes]
rs12629039	0.81[ASN][1000 genomes]
rs12631344	0.88[AMR][1000 genomes]
rs12639169	0.89[ASN][1000 genomes]
rs17017626	0.88[AMR][1000 genomes]
rs2202859	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6795725	1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73852658	0.88[AMR][1000 genomes]
rs73852661	0.88[AMR][1000 genomes]
rs73852680	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73852695	0.81[ASN][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	nsv590740	chr3:79999534-80575042	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv997786	chr3:80008898-80489031	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv536598	chr3:80008898-80489031	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv877030	chr3:80013063-80444843	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1014658	chr3:80035786-80716259	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv536599	chr3:80035786-80716259	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv997720	chr3:80035786-80745662	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv1012046	chr3:80125918-80482086	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	esv3391878	chr3:80254971-80474866	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:80281400-80283000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr3:80281400-80284000	Enhancers	NH-A	brain
3	chr3:80281600-80282800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr3:80281600-80282800	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr3:80281600-80283000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr3:80281600-80283200	Enhancers	NHEK	skin
7	chr3:80281800-80282800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
8	chr3:80281800-80282800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr3:80281800-80282800	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr3:80281800-80282800	Enhancers	Hela-S3	cervix
11	chr3:80281800-80283000	Enhancers	H9 Cell Line	embryonic stem cell
12	chr3:80281800-80283200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr3:80281800-80283200	Enhancers	Muscle Satellite Cultured Cells	--
14	chr3:80281800-80283200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr3:80281800-80283200	Enhancers	HMEC	breast
16	chr3:80282000-80283000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr3:80282000-80283000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr3:80282200-80282800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr3:80282200-80282800	Enhancers	NHDF-Ad	bronchial
20	chr3:80282200-80283000	Enhancers	Osteobl	bone
21	chr3:80282200-80283600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr3:80282200-80287200	Weak transcription	HUVEC	blood vessel
23	chr3:80282400-80283000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr3:80282600-80283000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr3:80282600-80283000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr3:80282600-80283800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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