Variant report

Variant	rs1702870
Chromosome Location	chr12:56457176-56457177
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:56457158..56459397-chr12:56472051..56473667,2	MCF-7	breast:
2	chr12:56435442..56437276-chr12:56456359..56458729,2	MCF-7	breast:
3	chr12:56450765..56453604-chr12:56456930..56458558,2	K562	blood:

Variant related genes	Relation type
ENSG00000197728	Chromatin interaction
ENSG00000065361	Chromatin interaction
ENSG00000257449	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11171736	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1581007	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1619653	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1689507	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1689516	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs1701705	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1702871	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1702875	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs2452822	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2452826	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs2456445	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2456446	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2456969	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs705706	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7309340	0.88[AFR][1000 genomes]
rs772917	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs772924	0.87[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs772925	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs772926	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs773118	0.94[AFR][1000 genomes]
rs7977521	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs808896	0.87[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs808905	0.88[AFR][1000 genomes]
rs9645818	0.86[AFR][1000 genomes]
rs9738150	0.93[AFR][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	nsv1051961	chr12:56262220-56629427	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	284 gene(s)	inside rSNPs	diseases
2	nsv832424	chr12:56275226-56466917	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
3	nsv1043988	chr12:56348185-56534900	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	189 gene(s)	inside rSNPs	diseases
4	nsv832427	chr12:56392545-56512774	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:56437000-56472800	Weak transcription	Right Atrium	heart
2	chr12:56454400-56467800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr12:56456000-56465800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr12:56456200-56457400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr12:56456400-56457200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr12:56456400-56457200	Enhancers	Muscle Satellite Cultured Cells	--
7	chr12:56456600-56457200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr12:56456600-56457200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:56456600-56457200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr12:56456600-56457200	Enhancers	HMEC	breast
11	chr12:56456800-56457400	Enhancers	HUVEC	blood vessel
12	chr12:56457000-56457200	Enhancers	NHEK	skin
13	chr12:56457000-56457400	Enhancers	Osteobl	bone

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