Variant report

Variant	rs567549111
Chromosome Location	chr16:47887828-47887829
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv520355	chr16:47424828-48164777	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv525976	chr16:47583872-48035026	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv428657	chr16:47748036-47913816	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv833218	chr16:47869819-48051745	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	esv3351124	chr16:47886851-47890349	Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	inside rSNPs	n/a
6	esv3433157	chr16:47886851-47891049	Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:47882800-47889200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr16:47883000-47890600	Weak transcription	Fetal Brain Female	brain
3	chr16:47883200-47889800	Weak transcription	Gastric	stomach
4	chr16:47883400-47899600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr16:47883800-47893000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr16:47885400-47891000	Weak transcription	Fetal Brain Male	brain
7	chr16:47885600-47892400	Weak transcription	Brain Anterior Caudate	brain
8	chr16:47886000-47888000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr16:47886000-47888600	Weak transcription	Brain Germinal Matrix	brain
10	chr16:47886600-47888200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr16:47887200-47888400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr16:47887600-47888000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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