Variant report

Variant	rs562773370
Chromosome Location	chr8:67121427-67121428
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:9 , 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	esv3414665	chr8:66936816-67381935	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	esv3479400	chr8:67120275-67121991	Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	esv3479404	chr8:67120611-67121847	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3479403	chr8:67120654-67121827	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3479401	chr8:67120661-67121810	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3479402	chr8:67120682-67121779	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3479405	chr8:67120682-67121779	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv13418	chr8:67120890-67121680	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:67116800-67135200	Weak transcription	Placenta	Placenta
2	chr8:67118400-67131400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:67118400-67133400	Weak transcription	Liver	Liver
4	chr8:67119600-67135400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:67121400-67122000	Enhancers	Brain Anterior Caudate	brain
6	chr8:67121400-67123400	Enhancers	Cortex derived primary cultured neurospheres	brain

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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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