Variant report

Variant	rs17024738
Chromosome Location	chr4:96759296-96759297
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11733580	1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.90[YRI][hapmap];0.88[AFR][1000 genomes]
rs11733585	1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap]
rs11934350	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11936396	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1436546	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17024664	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61674077	0.83[AFR][1000 genomes]
rs7681496	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

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	nsv997304	chr4:96575198-96861349	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv1010830	chr4:96607025-96862878	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv537191	chr4:96607025-96862878	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv594915	chr4:96628653-97086618	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv428767	chr4:96676384-96831793	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv879628	chr4:96739251-96778499	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv879629	chr4:96747135-96818263	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv10537	chr4:96757571-96956294	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:96757200-96759400	Weak transcription	Brain Substantia Nigra	brain
2	chr4:96758600-96760200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:96758600-96760600	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr4:96758600-96760800	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr4:96758800-96760200	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr4:96758800-96760200	Enhancers	Fetal Heart	heart
7	chr4:96758800-96761000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr4:96759000-96759600	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr4:96759200-96760000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:96759200-96760200	Enhancers	H1 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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