Variant report

Variant	rs9524408
Chromosome Location	chr13:94943545-94943546
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs34546989	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9516383	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9516384	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9516385	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9524407	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9524409	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9524411	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9524412	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9524413	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9524415	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9524416	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9524417	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9524418	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9524419	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9524420	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9524422	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9524423	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9524425	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948455	chr13:94451368-94988900	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv916640	chr13:94521959-95101443	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv533063	chr13:94560362-95101443	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv34004	chr13:94906537-95392644	Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 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	chr13:94924200-94948600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr13:94936600-94956000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr13:94937400-94944600	Weak transcription	Fetal Intestine Large	intestine
4	chr13:94940200-94943800	Weak transcription	HSMM	muscle
5	chr13:94942800-94946400	Enhancers	Liver	Liver
6	chr13:94943200-94945000	Enhancers	HepG2	liver
7	chr13:94943200-94945600	Enhancers	Fetal Intestine Small	intestine
8	chr13:94943400-94948800	Weak transcription	Pancreas	Pancrea

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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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