Variant report

Variant	rs7321219
Chromosome Location	chr13:65012566-65012567
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:6)

rs_ID	r²[population]
rs11841634	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17086815	1.00[AMR][1000 genomes]
rs17087329	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34647155	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34965553	1.00[AMR][1000 genomes]
rs41367248	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv455914	chr13:64432922-65368490	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv561965	chr13:64432922-65368490	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv430577	chr13:64602899-65034099	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv3367739	chr13:64805577-65549276	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv900344	chr13:64868768-65193124	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1050887	chr13:64989770-65058348	Weak transcription Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1047916	chr13:64993852-65024851	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
8	nsv900346	chr13:64999866-65198145	Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv561968	chr13:65006281-65062206	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv428606	chr13:65008453-65158452	Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:65011600-65014800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr13:65012000-65012800	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr13:65012200-65012600	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr13:65012200-65012600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr13:65012200-65012600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr13:65012200-65012800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr13:65012200-65012800	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr13:65012200-65012800	Enhancers	Fetal Lung	lung
9	chr13:65012200-65013200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr13:65012400-65012800	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr13:65012400-65012800	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr13:65012400-65012800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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Input of quick search could be:

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

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