Variant report

Variant	rs571034443
Chromosome Location	chr3:115867401-115867402
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012260	chr3:115680931-115935968	Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	esv2756413	chr3:115721898-115908480	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	esv2751975	chr3:115766285-115902901	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	esv2755046	chr3:115818840-115942952	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv591345	chr3:115819376-115902901	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2752728	chr3:115833212-115902901	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv2751976	chr3:115867310-115903310	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:115865200-115867800	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr3:115866600-115867800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr3:115866600-115869000	Enhancers	Brain Cingulate Gyrus	brain
4	chr3:115866800-115871600	Enhancers	Brain Germinal Matrix	brain
5	chr3:115867000-115867600	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr3:115867200-115867800	Enhancers	Brain Hippocampus Middle	brain
7	chr3:115867200-115868400	Enhancers	Brain Anterior Caudate	brain
8	chr3:115867200-115868600	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr3:115867200-115869000	Enhancers	Brain Substantia Nigra	brain
10	chr3:115867200-115869800	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr3:115867200-115870200	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr3:115867200-115870200	Enhancers	Brain Angular Gyrus	brain
13	chr3:115867400-115868200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:115867400-115868800	Enhancers	Fetal Lung	lung
15	chr3:115867400-115869200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr3:115867400-115869600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

Quick Search:

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

what's new

Quick links