Variant report

Variant	rs8020687
Chromosome Location	chr14:37785560-37785561
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:37776717..37778378-chr14:37785144..37786956,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000151338	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10132727	1.00[ASW][hapmap];0.87[YRI][hapmap]
rs10134469	1.00[ASW][hapmap];1.00[AMR][1000 genomes]
rs10136240	1.00[ASW][hapmap]
rs10140854	1.00[LWK][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs10141073	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10143648	1.00[ASW][hapmap];0.85[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10148340	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10148472	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10150559	1.00[ASW][hapmap]
rs10150564	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10151539	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10782385	1.00[ASW][hapmap]
rs10872901	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1474885	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1884406	1.00[ASW][hapmap]
rs1950516	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1950519	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1950885	0.85[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1950887	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1950888	1.00[YRI][hapmap];0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1955931	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1955941	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.85[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1955948	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1955952	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1955955	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1956520	0.85[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2103891	1.00[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2103892	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2103893	1.00[ASW][hapmap]
rs2103894	0.84[AFR][1000 genomes]
rs2144584	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2224344	1.00[ASW][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2415396	0.82[AFR][1000 genomes]
rs2415399	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2899857	0.92[AFR][1000 genomes]
rs4900834	1.00[ASW][hapmap]
rs4900835	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4900867	1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs6571800	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6571813	1.00[AMR][1000 genomes]
rs7142072	1.00[ASW][hapmap]
rs7145905	1.00[ASW][hapmap]
rs7146351	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7150214	1.00[ASW][hapmap]
rs7153565	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7157931	1.00[ASW][hapmap];0.87[YRI][hapmap]
rs7161369	1.00[AMR][1000 genomes]
rs719135	1.00[ASW][hapmap]
rs761818	1.00[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8004838	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8013599	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs8016268	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.85[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8017263	1.00[ASW][hapmap];1.00[LWK][hapmap];0.85[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8018605	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8019384	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8019983	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.85[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8021838	1.00[AMR][1000 genomes]
rs987859	1.00[ASW][hapmap]
rs9989228	1.00[ASW][hapmap]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530038	chr14:37590543-38336191	Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv915783	chr14:37607836-38002966	Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1036854	chr14:37609535-38013533	Active TSS ZNF genes & repeats Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv542045	chr14:37609535-38013533	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv901638	chr14:37702799-37814824	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv1797813	chr14:37738197-37846877	Weak transcription Active TSS ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	esv1820642	chr14:37738197-37846877	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	esv1822817	chr14:37738197-37846877	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	esv1851834	chr14:37738197-37846877	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv901639	chr14:37743583-38038468	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
11	esv1813852	chr14:37768769-37810699	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
12	nsv901640	chr14:37782273-37963104	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv949227	chr14:37785560-37963104	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37752400-37796200	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr14:37759000-37810600	Weak transcription	Psoas Muscle	Psoas
3	chr14:37762600-37812400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr14:37763200-37797400	Weak transcription	Left Ventricle	heart
5	chr14:37769400-37800000	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr14:37774200-37785600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr14:37775200-37817000	Weak transcription	Aorta	Aorta
8	chr14:37776200-37792400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr14:37780400-37786200	Weak transcription	HUVEC	blood vessel
10	chr14:37780400-37795000	Weak transcription	Ovary	ovary
11	chr14:37780600-37796800	Weak transcription	HepG2	liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links