Variant report

Variant	rs373826792
Chromosome Location	chr20:23146690-23146691
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	esv2758516	chr20:23029404-23173240	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	esv2758789	chr20:23029404-23179604	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv912817	chr20:23127661-23240969	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	esv2756735	chr20:23146607-23179604	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23142800-23146800	Enhancers	Fetal Intestine Large	intestine
2	chr20:23142800-23148000	Weak transcription	NH-A	brain
3	chr20:23143000-23148000	Weak transcription	NHDF-Ad	bronchial
4	chr20:23143200-23147400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr20:23143400-23148000	Weak transcription	NHEK	skin
6	chr20:23143800-23147400	Weak transcription	Esophagus	oesophagus
7	chr20:23144000-23148400	Weak transcription	Right Atrium	heart
8	chr20:23144000-23150800	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr20:23144000-23151000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr20:23144400-23147000	Enhancers	Fetal Intestine Small	intestine
11	chr20:23145200-23150800	Weak transcription	Lung	lung
12	chr20:23145400-23146800	Enhancers	Duodenum Mucosa	Duodenum
13	chr20:23145400-23147800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr20:23146000-23147600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr20:23146200-23150800	Weak transcription	Spleen	Spleen
16	chr20:23146400-23149400	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr20:23146400-23149400	Weak transcription	Gastric	stomach
18	chr20:23146600-23146800	Enhancers	Small Intestine	intestine
19	chr20:23146600-23146800	Enhancers	Stomach Smooth Muscle	stomach

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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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