Variant report

Variant	rs9805696
Chromosome Location	chr13:39313361-39313362
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs7325603	0.92[AFR][1000 genomes]
rs7329184	0.95[AFR][1000 genomes]
rs74048110	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7991794	0.92[AFR][1000 genomes]
rs9315610	0.92[YRI][hapmap]
rs9576609	0.95[AFR][1000 genomes]
rs9603410	0.90[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832585	chr13:39233307-39424375	Weak transcription Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:39294800-39325000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr13:39298200-39339600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr13:39308000-39317600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr13:39310800-39325400	Weak transcription	Fetal Kidney	kidney
5	chr13:39312200-39319800	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr13:39313200-39313800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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