Variant report

Variant	rs1330471
Chromosome Location	chr13:92648841-92648842
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1536375	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1854738	0.85[CEU][hapmap]
rs1972350	1.00[CHB][hapmap]
rs2352190	1.00[CHB][hapmap]
rs4630398	1.00[CHB][hapmap]
rs59551510	0.86[ASN][1000 genomes]
rs6492565	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7988651	0.93[CEU][hapmap]
rs7990703	1.00[CHB][hapmap]
rs7992791	0.93[CEU][hapmap];1.00[CHB][hapmap]
rs9523438	1.00[CHB][hapmap]
rs9523439	1.00[CHB][hapmap]
rs9523441	1.00[CHB][hapmap]
rs9556130	0.93[CEU][hapmap];0.87[AMR][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	esv3378326	chr13:92445514-92816367	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv2756005	chr13:92584199-93080799	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv562722	chr13:92607374-92733984	Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:92647000-92649400	Weak transcription	Brain Substantia Nigra	brain

Quick Search:

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

what's new

Quick links