Variant report

Variant	rs7646915
Chromosome Location	chr3:142795712-142795713
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	chr3:142794271..142797141-chr3:142844007..142845720,2	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs1107771	1.00[EUR][1000 genomes]
rs13322379	0.86[EUR][1000 genomes]
rs13322528	0.86[EUR][1000 genomes]
rs13325630	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16852899	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3821646	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs58531834	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs59540153	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6764683	0.86[EUR][1000 genomes]
rs6771415	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6781061	1.00[ASN][1000 genomes]
rs6782124	1.00[EUR][1000 genomes]
rs6797880	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6805721	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6806835	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72990813	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72992555	0.86[EUR][1000 genomes]
rs9289653	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9839114	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9842812	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9868064	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9871843	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9876889	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9877143	0.86[EUR][1000 genomes]
rs9881229	1.00[EUR][1000 genomes]
rs9881390	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9882184	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9990198	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877562	chr3:142573789-142846370	Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	esv2757893	chr3:142720230-142962932	Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	esv2759183	chr3:142720230-142964373	Strong transcription Weak transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv591921	chr3:142762487-142841740	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv1004467	chr3:142768867-142800605	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
6	nsv1004682	chr3:142768867-142804154	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
7	nsv949288	chr3:142793323-143585882	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142790800-142796400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr3:142793800-142797800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr3:142793800-142798000	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr3:142794000-142798800	Weak transcription	K562	blood

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