Variant report

Variant	rs192747709
Chromosome Location	chr2:210811760-210811761
allele	C/T
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	nsv431969	chr2:210682494-211074494	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv1004426	chr2:210709999-211001680	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv998029	chr2:210751692-210838759	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	esv1795338	chr2:210758078-211098113	Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	esv3337227	chr2:210811745-210812012	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:210796200-210812800	Weak transcription	Fetal Brain Male	brain
2	chr2:210797200-210822800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr2:210799600-210813600	Weak transcription	Brain Cingulate Gyrus	brain
4	chr2:210806600-210825400	Weak transcription	Fetal Brain Female	brain
5	chr2:210806800-210825400	Weak transcription	Brain Anterior Caudate	brain
6	chr2:210807000-210818400	Weak transcription	Brain Germinal Matrix	brain
7	chr2:210807000-210825000	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr2:210807000-210866000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr2:210808400-210812200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr2:210808800-210825400	Weak transcription	Pancreas	Pancrea
11	chr2:210809200-210813600	Weak transcription	Brain Angular Gyrus	brain
12	chr2:210809800-210812000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr2:210810200-210812200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr2:210811000-210812000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr2:210811200-210811800	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr2:210811600-210812000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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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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