Variant report

Variant	rs575122397
Chromosome Location	chr9:103965272-103965273
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

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	nsv831671	chr9:103858107-104020816	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv3388399	chr9:103965184-103965405	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:103963400-103965600	Enhancers	Fetal Heart	heart
2	chr9:103963800-103965800	Enhancers	Brain Hippocampus Middle	brain
3	chr9:103964200-103965400	Enhancers	Brain Cingulate Gyrus	brain
4	chr9:103964400-103965600	Enhancers	Brain Angular Gyrus	brain
5	chr9:103964600-103978400	Weak transcription	HepG2	liver
6	chr9:103964800-103969800	Weak transcription	Brain Anterior Caudate	brain
7	chr9:103965200-103969600	Weak transcription	Brain Substantia Nigra	brain

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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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