Variant report

Variant	rs71568531
Chromosome Location	chr7:108170370-108170371
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11971386	0.87[ASN][1000 genomes]
rs11983802	0.82[ASN][1000 genomes]
rs11983842	0.82[ASN][1000 genomes]
rs12530879	0.82[ASN][1000 genomes]
rs12538539	0.82[ASN][1000 genomes]
rs12540029	0.82[ASN][1000 genomes]
rs12705474	0.92[ASN][1000 genomes]
rs13238345	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs13239792	0.92[ASN][1000 genomes]
rs16872576	0.87[ASN][1000 genomes]
rs16872577	0.87[ASN][1000 genomes]
rs34164886	0.92[ASN][1000 genomes]
rs34459886	0.92[ASN][1000 genomes]
rs34771129	0.92[ASN][1000 genomes]
rs34827770	0.92[ASN][1000 genomes]
rs34915298	0.82[ASN][1000 genomes]
rs34959248	0.90[ASN][1000 genomes]
rs35220845	0.87[ASN][1000 genomes]
rs35418774	0.96[EUR][1000 genomes]
rs35444439	0.82[ASN][1000 genomes]
rs3752639	0.82[ASN][1000 genomes]
rs3763460	0.92[ASN][1000 genomes]
rs60117684	0.85[ASN][1000 genomes]
rs6964631	0.82[ASN][1000 genomes]
rs6980319	0.82[ASN][1000 genomes]
rs71568529	0.92[ASN][1000 genomes]
rs71568533	0.92[ASN][1000 genomes]
rs7786180	0.82[ASN][1000 genomes]
rs9641410	0.82[ASN][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	esv3348839	chr7:107377311-108286538	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	91 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:108167400-108173400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:108167600-108176200	Weak transcription	Primary B cells from cord blood	blood
3	chr7:108167800-108170400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr7:108168800-108175800	Weak transcription	K562	blood
5	chr7:108170000-108170600	Enhancers	Placenta	Placenta

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