Variant report

Variant	rs537787111
Chromosome Location	chr3:133132665-133132666
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:133127092..133128594-chr3:133130623..133133431,2	K562	blood:

Extended variants
information (count: 9 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877504	chr3:133122216-133172374	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv3356798	chr3:133131662-133135760	Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	esv16435	chr3:133132004-133137072	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3430009	chr3:133132212-133137110	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv591802	chr3:133132464-133135002	Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv591803	chr3:133132464-133136961	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv591804	chr3:133132464-133137016	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv591805	chr3:133132496-133136961	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv591806	chr3:133132496-133137016	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133124600-133138400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr3:133131000-133133000	Enhancers	Fetal Brain Male	brain
3	chr3:133131400-133132800	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr3:133131400-133132800	Active TSS	NHLF	lung
5	chr3:133131400-133133000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr3:133131400-133133200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr3:133131600-133132800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr3:133131600-133132800	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr3:133131600-133132800	Active TSS	Stomach Smooth Muscle	stomach
10	chr3:133131600-133133000	Bivalent Enhancer	Fetal Muscle Leg	muscle
11	chr3:133131600-133133000	Enhancers	Placenta	Placenta
12	chr3:133131800-133132800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
13	chr3:133131800-133132800	Bivalent Enhancer	Fetal Intestine Small	intestine
14	chr3:133131800-133132800	Flanking Active TSS	Osteobl	bone
15	chr3:133131800-133133000	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr3:133131800-133133000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr3:133132000-133132800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr3:133132000-133132800	Flanking Active TSS	Brain Cingulate Gyrus	brain
19	chr3:133132000-133133000	Enhancers	Fetal Muscle Trunk	muscle
20	chr3:133132000-133133200	Enhancers	Fetal Stomach	stomach
21	chr3:133132200-133132800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr3:133132200-133132800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr3:133132200-133132800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr3:133132200-133132800	Flanking Active TSS	Brain Substantia Nigra	brain
25	chr3:133132200-133132800	Flanking Active TSS	Fetal Lung	lung
26	chr3:133132200-133132800	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
27	chr3:133132400-133132800	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr3:133132400-133132800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr3:133132400-133132800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
30	chr3:133132400-133132800	Active TSS	HSMM	muscle
31	chr3:133132400-133133000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr3:133132600-133132800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr3:133132600-133132800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr3:133132600-133132800	Enhancers	Muscle Satellite Cultured Cells	--
35	chr3:133132600-133132800	Enhancers	Adipose Nuclei	Adipose
36	chr3:133132600-133132800	Flanking Active TSS	Brain Hippocampus Middle	brain
37	chr3:133132600-133132800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
38	chr3:133132600-133132800	Enhancers	Rectal Smooth Muscle	rectum
39	chr3:133132600-133132800	Flanking Bivalent TSS/Enh	A549	lung
40	chr3:133132600-133132800	Active TSS	HSMMtube	muscle
41	chr3:133132600-133133000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr3:133132600-133133000	Active TSS	Brain Anterior Caudate	brain

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