Variant report

Variant	rs572708713
Chromosome Location	chr20:16080477-16080478
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869328	chr20:15325423-16213898	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv3447866	chr20:15799286-16115291	Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1059778	chr20:15999519-16165895	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv544207	chr20:15999519-16165895	Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv1061301	chr20:16007489-16097070	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv979489	chr20:16077754-16084263	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
7	nsv520909	chr20:16078767-16087405	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
8	nsv828692	chr20:16078779-16084992	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
9	esv3454146	chr20:16078865-16085497	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
10	nsv828693	chr20:16078906-16084992	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
11	esv3454145	chr20:16078916-16085462	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
12	esv3454142	chr20:16078930-16085379	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
13	esv3454144	chr20:16078931-16085437	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
14	esv3454143	chr20:16079034-16085377	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
15	esv3454147	chr20:16079050-16085373	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:16078200-16084000	Enhancers	Primary B cells from cord blood	blood
2	chr20:16079400-16082400	Enhancers	HepG2	liver
3	chr20:16079600-16081600	Enhancers	Ovary	ovary
4	chr20:16079800-16082400	Enhancers	Liver	Liver
5	chr20:16080400-16080600	Enhancers	Psoas Muscle	Psoas
6	chr20:16080400-16081400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr20:16080400-16081800	Weak transcription	Primary B cells from peripheral blood	blood

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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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