Variant report

Variant	rs73244824
Chromosome Location	chr8:66799832-66799833
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs16932444	1.00[EUR][1000 genomes]
rs73242979	1.00[AMR][1000 genomes]
rs73242992	1.00[AMR][1000 genomes]
rs73244816	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73244820	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73244823	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73244826	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73244833	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73247075	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73247076	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73247084	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73248904	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73248977	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7842488	1.00[AMR][1000 genomes];1.00[EUR][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	esv3446467	chr8:66749863-67667068	Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	nsv1023239	chr8:66775321-66904124	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:66792400-66801000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr8:66799000-66802200	Enhancers	Primary B cells from peripheral blood	blood
3	chr8:66799600-66800000	Flanking Active TSS	Duodenum Mucosa	Duodenum
4	chr8:66799600-66800400	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr8:66799800-66800000	Enhancers	Primary T cells from cord blood	blood
6	chr8:66799800-66800400	Enhancers	Dnd41	blood
7	chr8:66799800-66801000	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr8:66799800-66801000	Enhancers	Fetal Intestine Small	intestine
9	chr8:66799800-66801000	Enhancers	Small Intestine	intestine

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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

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