Variant report

Variant	rs114683352
Chromosome Location	chr6:100676043-100676044
allele	C/G
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	nsv604262	chr6:100661336-100701917	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv1001991	chr6:100674651-100685935	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv1795039	chr6:100674799-100691977	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:100674600-100676400	Enhancers	HUVEC	blood vessel
2	chr6:100674800-100676200	Enhancers	K562	blood
3	chr6:100675600-100676200	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr6:100675800-100676200	Enhancers	GM12878-XiMat	blood
5	chr6:100675800-100676400	Enhancers	Fetal Intestine Large	intestine
6	chr6:100676000-100676200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr6:100676000-100676200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr6:100676000-100676200	Enhancers	Rectal Mucosa Donor 29	rectum
9	chr6:100676000-100676200	Enhancers	NHEK	skin
10	chr6:100676000-100676400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr6:100676000-100676400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr6:100676000-100676600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr6:100676000-100676600	Enhancers	NHLF	lung
14	chr6:100676000-100676800	Active TSS	Fetal Brain Male	brain
15	chr6:100676000-100677600	Enhancers	Fetal Heart	heart

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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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