Variant report

Variant	rs192284702
Chromosome Location	chr20:52637712-52637713
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:52636698..52639265-chr20:52824391..52826497,2	MCF-7	breast:
2	chr20:52637066..52638758-chr20:52814521..52816313,2	MCF-7	breast:
3	chr20:52637571..52639350-chr20:52639396..52641959,2	K562	blood:
4	chr10:6752413..6755027-chr20:52637066..52638701,2	MCF-7	breast:
5	chr20:52637587..52640113-chr20:52663021..52665849,2	MCF-7	breast:
6	chr17:69373468..69375354-chr20:52636085..52637962,2	MCF-7	breast:
7	chr20:52628739..52630363-chr20:52636022..52638678,2	K562	blood:
8	chr20:52637408..52640155-chr20:52655059..52656752,2	MCF-7	breast:

No data

No data

No data

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34060	chr20:52251863-52702186	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	296 gene(s)	inside rSNPs	diseases
2	nsv586224	chr20:52474850-53279490	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	338 gene(s)	inside rSNPs	diseases
3	esv2763673	chr20:52637074-52668126	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	13 gene(s)	inside rSNPs	diseases
4	nsv3419	chr20:52637581-52672115	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	15 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:52566400-52644800	Weak transcription	Gastric	stomach
2	chr20:52618800-52644400	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr20:52631400-52641400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr20:52633800-52638600	Weak transcription	Brain Cingulate Gyrus	brain
5	chr20:52633800-52641200	Weak transcription	Brain Angular Gyrus	brain
6	chr20:52634000-52638600	Weak transcription	Brain Anterior Caudate	brain
7	chr20:52634800-52645400	Weak transcription	Fetal Lung	lung
8	chr20:52635800-52641800	Enhancers	Brain Substantia Nigra	brain
9	chr20:52636000-52641200	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr20:52636600-52640600	Weak transcription	Stomach Mucosa	stomach
11	chr20:52637200-52638800	Enhancers	Brain Hippocampus Middle	brain
12	chr20:52637600-52640400	Weak transcription	Rectal Mucosa Donor 31	rectum

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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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