Variant report

Variant	rs144506682
Chromosome Location	chr2:211528981-211528982
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	esv3398091	chr2:211315261-211634200	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1013658	chr2:211447246-211809945	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv536135	chr2:211447246-211809945	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv536136	chr2:211497528-211830019	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv821631	chr2:211528918-211658981	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:211498200-211529000	Strong transcription	Hela-S3	cervix
2	chr2:211501000-211540600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:211525800-211530000	Genic enhancers	Liver	Liver
4	chr2:211526200-211537600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:211526400-211540400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr2:211527600-211538800	Weak transcription	Fetal Intestine Small	intestine
7	chr2:211527800-211530000	Strong transcription	Duodenum Mucosa	Duodenum
8	chr2:211527800-211530000	Strong transcription	Fetal Intestine Large	intestine
9	chr2:211528400-211529000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:211528600-211529000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr2:211528600-211529000	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr2:211528600-211529000	Enhancers	Adipose Nuclei	Adipose
13	chr2:211528600-211529000	Enhancers	Brain Angular Gyrus	brain
14	chr2:211528600-211529000	Flanking Active TSS	Brain Cingulate Gyrus	brain
15	chr2:211528600-211529000	Flanking Active TSS	Brain Hippocampus Middle	brain
16	chr2:211528600-211529000	Enhancers	Brain Substantia Nigra	brain
17	chr2:211528600-211529200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr2:211528800-211542400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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