Variant report

Variant	rs1452312
Chromosome Location	chr2:183665161-183665162
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:183660311..183663383-chr2:183663723..183666825,3	K562	blood:
2	chr2:183648162..183650730-chr2:183663988..183666770,2	K562	blood:
3	chr2:183664890..183667245-chr2:183673485..183675403,2	K562	blood:
4	chr2:183659213..183661128-chr2:183664377..183666463,2	MCF-7	breast:

Extended variants
information (count: 47 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10931040	0.80[EUR][1000 genomes]
rs13509	0.83[CEU][hapmap];0.92[YRI][hapmap];0.83[AFR][1000 genomes]
rs17356762	0.84[CEU][hapmap]
rs190830	0.80[CEU][hapmap]
rs192618	0.92[YRI][hapmap];0.81[AFR][1000 genomes]
rs208393	0.84[CEU][hapmap]
rs288239	0.85[AFR][1000 genomes]
rs288240	0.83[CEU][hapmap]
rs288241	0.88[CEU][hapmap];0.93[YRI][hapmap];0.83[AFR][1000 genomes]
rs288253	0.84[CEU][hapmap];0.93[YRI][hapmap]
rs288256	0.81[AFR][1000 genomes]
rs288258	0.84[CEU][hapmap]
rs288259	0.83[CEU][hapmap]
rs288264	0.88[YRI][hapmap]
rs288265	0.80[CEU][hapmap];0.92[YRI][hapmap]
rs288280	0.83[CEU][hapmap]
rs288283	0.83[CEU][hapmap]
rs288285	0.83[AFR][1000 genomes]
rs288287	0.85[AFR][1000 genomes]
rs288291	0.81[AFR][1000 genomes]
rs288292	0.81[AFR][1000 genomes]
rs288293	0.80[AFR][1000 genomes]
rs288306	0.83[CEU][hapmap];0.88[YRI][hapmap]
rs288307	0.84[CEU][hapmap];0.89[YRI][hapmap]
rs288310	0.83[CEU][hapmap]
rs288311	0.84[CEU][hapmap]
rs288312	0.86[AFR][1000 genomes]
rs288313	0.88[AFR][1000 genomes]
rs288331	0.82[AFR][1000 genomes]
rs288342	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs288343	0.87[AFR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs288344	0.88[AFR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs288346	0.88[AFR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs288349	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs288354	0.94[ASN][1000 genomes]
rs3115425	0.80[AFR][1000 genomes]
rs438248	0.83[CEU][hapmap];0.96[YRI][hapmap]
rs825660	0.83[CEU][hapmap]
rs825668	0.83[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009882	chr2:183213152-184171519	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh 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	35 gene(s)	inside rSNPs	diseases
2	esv2757842	chr2:183437700-183835084	Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	esv2759104	chr2:183437700-183835084	Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	esv2756954	chr2:183528670-183764930	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	esv34847	chr2:183537399-183786763	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
6	esv3693445	chr2:183542825-183725221	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
7	nsv1004531	chr2:183648083-183698793	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv536070	chr2:183648083-183698793	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1452312	DNAJC10	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183664400-183665800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr2:183664800-183665400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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