Variant report

Variant	rs60163503
Chromosome Location	chr8:39929031-39929032
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11997199	0.92[ASN][1000 genomes]
rs59258191	1.00[ASN][1000 genomes]
rs60223559	0.87[AMR][1000 genomes]
rs6990154	1.00[AMR][1000 genomes]
rs6990187	0.92[ASN][1000 genomes]
rs6990874	0.81[AMR][1000 genomes]
rs72632084	1.00[AMR][1000 genomes]
rs72632085	1.00[AMR][1000 genomes]
rs72632088	1.00[AMR][1000 genomes]
rs72632098	0.87[AMR][1000 genomes]
rs73619620	0.92[ASN][1000 genomes]
rs73674759	0.92[ASN][1000 genomes]
rs7813461	0.87[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv539555	chr8:39683857-40673606	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv534582	chr8:39884590-40653224	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 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	chr8:39913000-39939000	Weak transcription	Right Atrium	heart
2	chr8:39927400-39929400	Enhancers	Fetal Intestine Large	intestine
3	chr8:39927400-39929400	Enhancers	Fetal Intestine Small	intestine
4	chr8:39927400-39930000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr8:39928600-39929400	Enhancers	Small Intestine	intestine
6	chr8:39928600-39932000	Weak transcription	A549	lung

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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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