Variant report

Variant	rs4132457
Chromosome Location	chr13:89631811-89631812
allele	A/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	TEAD4	chr13:89631719-89631992	H1-hESC	embryonic stem cell:	n/a	n/a

Variant related genes	Relation type
GRPEL2P1	TF binding region

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs1832259	0.80[AFR][1000 genomes]
rs4369519	0.80[AFR][1000 genomes]
rs4573801	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55661501	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55911606	1.00[EUR][1000 genomes]
rs55931359	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56105607	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs56112031	1.00[EUR][1000 genomes]
rs56144304	1.00[EUR][1000 genomes]
rs60920942	0.82[AFR][1000 genomes]
rs7320386	1.00[AMR][1000 genomes]
rs7320663	1.00[AMR][1000 genomes]
rs7321416	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7325384	0.85[AFR][1000 genomes]
rs7325941	0.91[AMR][1000 genomes]
rs7329082	0.80[AFR][1000 genomes]
rs7329725	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7329893	1.00[EUR][1000 genomes]
rs7331144	0.80[AFR][1000 genomes]
rs7331975	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs7332112	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7335030	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs73577934	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73577943	0.85[AFR][1000 genomes]
rs73579841	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73579843	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73585445	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73585492	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73587201	1.00[AMR][1000 genomes]
rs73588288	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73590225	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73590241	0.87[AFR][1000 genomes]
rs73590246	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73590290	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73590294	0.80[AFR][1000 genomes]
rs73590296	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73592132	0.80[AFR][1000 genomes]
rs73592133	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73594035	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73594053	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73594054	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7984249	0.91[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs7985020	0.86[EUR][1000 genomes]
rs7985913	1.00[EUR][1000 genomes]
rs7986157	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7987472	1.00[EUR][1000 genomes]
rs7990594	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7995825	1.00[EUR][1000 genomes]
rs7997170	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7998558	0.90[AFR][1000 genomes]
rs7999389	0.80[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv900820	chr13:89302824-89686507	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv900821	chr13:89302824-89941209	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv915862	chr13:89408920-90118030	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv2758339	chr13:89411081-89875974	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	esv2759957	chr13:89411081-89875974	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv900826	chr13:89466123-89686507	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv900828	chr13:89474702-89642526	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv915623	chr13:89476229-89668705	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv826739	chr13:89477707-89830601	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv900839	chr13:89510330-89637081	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	esv34578	chr13:89515664-89822799	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv900840	chr13:89516104-89686507	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv1043687	chr13:89523570-89673179	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	esv2757546	chr13:89539415-89864593	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv900843	chr13:89583854-89686507	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv1040210	chr13:89584630-90156186	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:89631600-89632000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr13:89631600-89632200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr13:89631600-89632200	Flanking Active TSS	Fetal Heart	heart
4	chr13:89631800-89632200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr13:89631800-89632200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr13:89631800-89632200	Enhancers	Brain Substantia Nigra	brain
7	chr13:89631800-89632200	Enhancers	Fetal Lung	lung
8	chr13:89631800-89632400	Enhancers	Breast Myoepithelial Primary Cells	Breast

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