Variant report

Variant	rs528897362
Chromosome Location	chr20:23011581-23011582
allele	C/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	nsv912816	chr20:22757960-23062927	Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv524981	chr20:23011468-23021597	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23001000-23015800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr20:23008600-23011800	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr20:23009000-23011600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr20:23010200-23011600	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr20:23010200-23012600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr20:23010200-23012800	Weak transcription	Primary hematopoietic stem cells	blood
7	chr20:23010600-23011800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr20:23010600-23012800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr20:23011000-23011800	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr20:23011200-23011600	Enhancers	H9 Cell Line	embryonic stem cell
11	chr20:23011200-23012600	Enhancers	Fetal Heart	heart
12	chr20:23011200-23013800	Enhancers	Left Ventricle	heart
13	chr20:23011400-23011800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr20:23011400-23014600	Enhancers	Dnd41	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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