Variant report

Variant	rs543007964
Chromosome Location	chr20:11175677-11175678
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1065969	chr20:10850562-11464172	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv544181	chr20:10850562-11464172	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv585415	chr20:11134907-11383327	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv585416	chr20:11156775-11190087	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1056067	chr20:11174581-11213919	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:11167600-11176400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr20:11168000-11176800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr20:11168400-11176200	Weak transcription	HMEC	breast
4	chr20:11171000-11176200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr20:11173600-11175800	Weak transcription	Fetal Stomach	stomach
6	chr20:11174200-11176400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr20:11174600-11175800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr20:11174800-11175800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr20:11175000-11176400	Enhancers	NHEK	skin
10	chr20:11175400-11176400	Enhancers	Left Ventricle	heart
11	chr20:11175400-11177200	Enhancers	Fetal Intestine Large	intestine
12	chr20:11175400-11177400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr20:11175400-11177400	Enhancers	Fetal Intestine Small	intestine
14	chr20:11175400-11177600	Enhancers	Fetal Heart	heart
15	chr20:11175600-11176400	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr20:11175600-11176600	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr20:11175600-11177200	Enhancers	Fetal Lung	lung
18	chr20:11175600-11177200	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr20:11175600-11177600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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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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