Variant report

Variant	rs145442787
Chromosome Location	chr9:92733453-92733454
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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	nsv893561	chr9:92732368-92802101	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:92725600-92738200	Weak transcription	Lung	lung
2	chr9:92729600-92733800	Enhancers	Fetal Intestine Small	intestine
3	chr9:92730800-92733800	Enhancers	Fetal Intestine Large	intestine
4	chr9:92732600-92733600	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr9:92733000-92733600	Enhancers	Colonic Mucosa	Colon
6	chr9:92733000-92736600	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr9:92733400-92733600	ZNF genes & repeats	HSMMtube	muscle
8	chr9:92733400-92740200	Weak transcription	Monocytes-CD14+_RO01746	blood

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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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