Variant report

Variant	rs202117076
Chromosome Location	chr5:167081460-167081461
allele	-/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932627	chr5:166744408-167290959	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1032559	chr5:167070888-167210684	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv2763892	chr5:167080980-167101161	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:167067200-167084200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:167079000-167081600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr5:167079000-167081600	Enhancers	Osteobl	bone
4	chr5:167079200-167081600	Enhancers	Hela-S3	cervix
5	chr5:167079600-167081600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr5:167079600-167081600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr5:167079800-167081600	Enhancers	NH-A	brain
8	chr5:167080000-167081600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr5:167080600-167081600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr5:167080800-167084000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr5:167081000-167081800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr5:167081200-167081600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr5:167081400-167081800	Enhancers	Muscle Satellite Cultured Cells	--
14	chr5:167081400-167082800	Enhancers	A549	lung
15	chr5:167081400-167085000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr5:167081400-167090400	Weak transcription	HSMM	muscle

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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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