Variant report

Variant	rs10161209
Chromosome Location	chr12:47191685-47191686
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:47189132..47192118-chr12:47192545..47194252,2	K562	blood:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10437941	0.85[ASN][1000 genomes]
rs11183610	0.85[CHB][hapmap];0.86[CHD][hapmap];0.84[LWK][hapmap]
rs11183618	0.92[CEU][hapmap];0.89[YRI][hapmap];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12301214	0.85[CHB][hapmap]
rs12305532	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12306007	0.82[YRI][hapmap]
rs12307687	0.82[CHB][hapmap]
rs12318924	0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12321267	0.92[CEU][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.89[YRI][hapmap];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12424453	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12581848	0.92[CEU][hapmap];0.85[CHB][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17097246	0.85[CHB][hapmap];0.86[CHD][hapmap];0.84[LWK][hapmap]
rs17097332	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1860371	0.84[AFR][1000 genomes]
rs1860372	1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2079787	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs2465585	0.89[YRI][hapmap]
rs2715788	0.89[YRI][hapmap]
rs3862137	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4447249	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs4482114	1.00[JPT][hapmap];0.85[LWK][hapmap];0.84[YRI][hapmap];0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4768758	0.85[CHB][hapmap]
rs4768759	0.85[CHB][hapmap]
rs6582676	0.85[CHB][hapmap]
rs73283958	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs73283960	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049525	chr12:46721742-47264172	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
2	nsv541486	chr12:46721742-47264172	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
3	esv1845143	chr12:47051076-47431496	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv826361	chr12:47159545-47200894	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:47181000-47194200	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr12:47182400-47194200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr12:47185000-47192200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:47186200-47193800	Weak transcription	Pancreas	Pancrea
5	chr12:47187800-47209400	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr12:47189000-47197000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr12:47189400-47195400	Weak transcription	HSMM	muscle
8	chr12:47189800-47193600	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr12:47190400-47192000	Genic enhancers	Liver	Liver
10	chr12:47191600-47192400	Flanking Active TSS	HepG2	liver

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