Variant report

Variant	rs545676860
Chromosome Location	chr20:23861632-23861633
allele	G/T
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	nsv491876	chr20:23436633-24031374	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv833944	chr20:23806288-24021865	Bivalent Enhancer Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv585730	chr20:23809681-23862844	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv964382	chr20:23856148-23862860	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
5	esv3432957	chr20:23858584-23901200	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1062441	chr20:23861343-23955100	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23852400-23864800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr20:23858200-23862800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr20:23859200-23861800	Enhancers	Lung	lung
4	chr20:23859400-23862400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr20:23859800-23862400	Enhancers	Pancreas	Pancrea
6	chr20:23860000-23862200	Enhancers	HepG2	liver
7	chr20:23860600-23861800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr20:23860600-23862200	Enhancers	HMEC	breast
9	chr20:23860600-23862400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr20:23860800-23861800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr20:23860800-23862200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr20:23861000-23864600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr20:23861200-23861800	Enhancers	NHEK	skin
14	chr20:23861400-23862200	Enhancers	Esophagus	oesophagus
15	chr20:23861400-23862400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr20:23861400-23864400	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr20:23861600-23861800	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr20:23861600-23862200	Enhancers	Placenta	Placenta

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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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