Variant report

Variant	rs7715693
Chromosome Location	chr5:154496059-154496060
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ESR1	chr5:154496028-154496883	T-47D	breast:	n/a	n/a
2	HNF4A	chr5:154495977-154496320	HepG2	liver:	n/a	chr5:154496177-154496192 chr5:154496179-154496192 chr5:154496179-154496192 chr5:154496179-154496192 chr5:154496177-154496192 chr5:154496178-154496191 chr5:154496179-154496191 chr5:154496177-154496192 chr5:154496176-154496194 chr5:154496179-154496191 chr5:154496178-154496186 chr5:154496179-154496191 chr5:154496177-154496192 chr5:154496179-154496191
3	GATA3	chr5:154495927-154497013	T-47D	breast:	n/a	n/a
4	ESR1	chr5:154495969-154496967	T-47D	breast:	n/a	n/a
5	ESR1	chr5:154495963-154496905	T-47D	breast:	n/a	n/a
6	EP300	chr5:154495955-154496979	T-47D	breast:	n/a	n/a
7	FOXA2	chr5:154496039-154496300	HepG2	liver:	n/a	n/a
8	FOXA1	chr5:154495986-154497114	T-47D	breast:	n/a	n/a
9	GATA3	chr5:154496040-154497008	T-47D	breast:	n/a	n/a
10	HNF4G	chr5:154495925-154496378	HepG2	liver:	n/a	chr5:154496177-154496192 chr5:154496179-154496192 chr5:154496179-154496192 chr5:154496179-154496192 chr5:154496177-154496192 chr5:154496178-154496191 chr5:154496179-154496191 chr5:154496176-154496194 chr5:154496179-154496191 chr5:154496178-154496186 chr5:154496178-154496193 chr5:154496179-154496191 chr5:154496177-154496192 chr5:154496179-154496191
11	EP300	chr5:154496052-154496919	T-47D	breast:	n/a	n/a
12	HNF4A	chr5:154496013-154496261	HepG2	liver:	n/a	chr5:154496177-154496192 chr5:154496179-154496192 chr5:154496179-154496192 chr5:154496179-154496192 chr5:154496177-154496192 chr5:154496178-154496191 chr5:154496179-154496191 chr5:154496177-154496192 chr5:154496176-154496194 chr5:154496179-154496191 chr5:154496178-154496186 chr5:154496179-154496191 chr5:154496177-154496192 chr5:154496179-154496191
13	HNF4G	chr5:154496022-154496351	HepG2	liver:	n/a	chr5:154496177-154496192 chr5:154496179-154496192 chr5:154496179-154496192 chr5:154496179-154496192 chr5:154496177-154496192 chr5:154496178-154496191 chr5:154496179-154496191 chr5:154496176-154496194 chr5:154496179-154496191 chr5:154496178-154496186 chr5:154496178-154496193 chr5:154496179-154496191 chr5:154496177-154496192 chr5:154496179-154496191
14	FOXA1	chr5:154496046-154496937	T-47D	breast:	n/a	n/a
15	ESR1	chr5:154495965-154496924	T-47D	breast:	n/a	n/a

Variant related genes	Relation type
ENSG00000253646	TF binding region

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10077934	0.88[ASN][1000 genomes]
rs10454998	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11167710	1.00[CEU][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12153388	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12187203	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13154769	0.81[EUR][1000 genomes]
rs13158970	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13159706	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13165083	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13167540	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13172264	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13172496	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13186839	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13187205	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17116912	0.82[ASN][1000 genomes]
rs17116922	0.82[ASN][1000 genomes]
rs17650275	0.83[EUR][1000 genomes]
rs286595	1.00[JPT][hapmap]
rs34317195	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs34549773	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs36059089	0.85[EUR][1000 genomes]
rs4958397	0.92[CEU][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4958778	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4958781	1.00[CEU][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4958782	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4958783	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs66859046	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67047831	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67562605	0.82[EUR][1000 genomes]
rs6859744	0.88[ASN][1000 genomes]
rs6883288	0.88[ASN][1000 genomes]
rs71597682	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72799591	0.98[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7719709	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7722477	0.88[ASN][1000 genomes]
rs7724975	0.85[EUR][1000 genomes]
rs7733613	0.88[ASN][1000 genomes]
rs7733811	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv883059	chr5:154457905-154556230	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv462492	chr5:154489393-154523910	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv600091	chr5:154489393-154523910	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:154495400-154496800	Enhancers	HepG2	liver
2	chr5:154495800-154496800	Enhancers	Placenta Amnion	Placenta Amnion

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