Variant report

Variant	rs563966301
Chromosome Location	chr2:210637644-210637645
allele	A/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	nsv1009129	chr2:210550858-210681136	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv3417338	chr2:210635907-210637905	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island	1 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	chr2:210636000-210638000	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr2:210636000-210638200	Active TSS	Brain Hippocampus Middle	brain
3	chr2:210636000-210638400	Active TSS	Brain Angular Gyrus	brain
4	chr2:210636400-210638400	Active TSS	Brain Anterior Caudate	brain
5	chr2:210636400-210638400	Active TSS	Brain Inferior Temporal Lobe	brain
6	chr2:210636400-210638400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
7	chr2:210637000-210637800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr2:210637000-210638200	Weak transcription	Aorta	Aorta
9	chr2:210637200-210638200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:210637200-210638600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr2:210637400-210637800	Flanking Active TSS	Brain Germinal Matrix	brain
12	chr2:210637400-210641200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr2:210637600-210637800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
14	chr2:210637600-210638200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr2:210637600-210638200	Enhancers	Fetal Brain Female	brain
16	chr2:210637600-210638400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr2:210637600-210638400	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr2:210637600-210638400	Enhancers	Fetal Brain Male	brain
19	chr2:210637600-210653800	Weak transcription	Brain Cingulate Gyrus	brain

Quick Search:

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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