Variant report

Variant	rs545504502
Chromosome Location	chr3:115868409-115868410
allele	C/T
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:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:115866600-115869000	Enhancers	Brain Cingulate Gyrus	brain
2	chr3:115866800-115871600	Enhancers	Brain Germinal Matrix	brain
3	chr3:115867200-115868600	Enhancers	Brain Inferior Temporal Lobe	brain
4	chr3:115867200-115869000	Enhancers	Brain Substantia Nigra	brain
5	chr3:115867200-115869800	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr3:115867200-115870200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr3:115867200-115870200	Enhancers	Brain Angular Gyrus	brain
8	chr3:115867400-115868800	Enhancers	Fetal Lung	lung
9	chr3:115867400-115869200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr3:115867400-115869600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr3:115867600-115868800	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr3:115867600-115869200	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr3:115867600-115869800	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr3:115867600-115870200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr3:115867800-115868600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr3:115867800-115868600	Active TSS	Pancreatic Islets	Pancreatic Islet
17	chr3:115867800-115868800	Enhancers	Muscle Satellite Cultured Cells	--
18	chr3:115867800-115869400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr3:115867800-115870400	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr3:115868000-115868600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr3:115868200-115869400	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr3:115868400-115868600	Flanking Active TSS	Brain Anterior Caudate	brain
23	chr3:115868400-115868800	Enhancers	NH-A	brain
24	chr3:115868400-115869200	Enhancers	Brain Hippocampus Middle	brain
25	chr3:115868400-115872000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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