Variant report

Variant	rs531974986
Chromosome Location	chr3:53822582-53822583
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	nsv1003621	chr3:53448934-54425322	Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv1001128	chr3:53659570-53927842	Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1013783	chr3:53694418-53934781	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv1003204	chr3:53820070-53877149	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv1002375	chr3:53822319-53872753	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr3:53807600-53829800	Weak transcription	Brain Angular Gyrus	brain
2	chr3:53808200-53827800	Strong transcription	Fetal Intestine Small	intestine
3	chr3:53808800-53830200	Weak transcription	Pancreas	Pancrea
4	chr3:53809400-53824400	Strong transcription	Fetal Intestine Large	intestine
5	chr3:53811400-53838600	Weak transcription	Spleen	Spleen
6	chr3:53811600-53843600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr3:53815200-53829000	Weak transcription	Brain Anterior Caudate	brain
8	chr3:53815200-53829400	Weak transcription	Brain Hippocampus Middle	brain
9	chr3:53815400-53829800	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr3:53816600-53822800	Strong transcription	Fetal Lung	lung
11	chr3:53818200-53826800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr3:53819600-53830000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr3:53821600-53822800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr3:53822200-53822800	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr3:53822400-53822800	Enhancers	H1 Cell Line	embryonic stem cell
16	chr3:53822400-53823000	Enhancers	ES-UCSF4 Cell Line	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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