Variant report

Variant	rs569805737
Chromosome Location	chr21:17775329-17775330
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1064857	chr21:17628760-18533131	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	345 gene(s)	inside rSNPs	diseases
2	nsv544382	chr21:17628760-18533131	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	345 gene(s)	inside rSNPs	diseases
3	nsv913416	chr21:17728224-17863882	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv913417	chr21:17762340-17777827	ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription	lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv913418	chr21:17767773-17786219	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
6	esv3455310	chr21:17770886-17775518	Enhancers Weak transcription Strong transcription	n/a	n/a	inside rSNPs	diseases
7	esv3455312	chr21:17770886-17775518	Weak transcription Enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases
8	esv3455311	chr21:17770913-17775515	Enhancers Weak transcription Strong transcription	n/a	n/a	inside rSNPs	diseases
9	nsv979496	chr21:17772425-17789214	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv913419	chr21:17775056-17826260	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17761600-17780200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr21:17771000-17775400	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr21:17771400-17791200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr21:17774800-17775400	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr21:17775000-17775400	Enhancers	Brain Angular Gyrus	brain
6	chr21:17775000-17775400	Enhancers	Ovary	ovary
7	chr21:17775000-17775600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr21:17775000-17775600	Enhancers	Brain Anterior Caudate	brain
9	chr21:17775000-17775600	Enhancers	Brain Cingulate Gyrus	brain
10	chr21:17775000-17775600	Enhancers	Brain Substantia Nigra	brain
11	chr21:17775000-17775600	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr21:17775000-17775800	Enhancers	Left Ventricle	heart
13	chr21:17775200-17775400	Enhancers	Adipose Nuclei	Adipose
14	chr21:17775200-17775600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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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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