Variant report

Variant	rs561182055
Chromosome Location	chr8:94967555-94967556
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754970	chr8:94675324-94991724	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv982128	chr8:94966644-94973304	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 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	chr8:94965400-94967600	Weak transcription	HepG2	liver
2	chr8:94965400-94969800	Weak transcription	Fetal Lung	lung
3	chr8:94965600-94969000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr8:94965600-94971800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr8:94965800-94967800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr8:94965800-94968600	Weak transcription	Fetal Intestine Large	intestine
7	chr8:94965800-94968600	Weak transcription	Fetal Intestine Small	intestine
8	chr8:94965800-94970200	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr8:94966000-94969200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr8:94966200-94968400	Enhancers	Placenta	Placenta
11	chr8:94967400-94967600	Enhancers	Left Ventricle	heart
12	chr8:94967400-94968000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr8:94967400-94968000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr8:94967400-94968000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr8:94967400-94968000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
16	chr8:94967400-94968000	Enhancers	Ovary	ovary
17	chr8:94967400-94968400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr8:94967400-94969200	Enhancers	HUVEC	blood vessel
19	chr8:94967400-94969400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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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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