Variant report

Variant	rs80241482
Chromosome Location	chr6:72289367-72289368
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830685	chr6:72244007-72410757	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv3442082	chr6:72287826-72291575	Enhancers Weak transcription	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
3	esv3359534	chr6:72287829-72291581	Enhancers Weak transcription	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:72288800-72289600	Enhancers	Pancreas	Pancrea
2	chr6:72289200-72289400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:72289200-72289600	Enhancers	Fetal Intestine Large	intestine
4	chr6:72289200-72289600	Enhancers	Fetal Intestine Small	intestine
5	chr6:72289200-72290200	Enhancers	HUVEC	blood vessel

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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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