Variant report

Variant	rs186722422
Chromosome Location	chr2:213228644-213228645
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:213223218..213224821-chr2:213227410..213229033,2	MCF-7	breast:

Extended variants
information (count: 11 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006051	chr2:213052804-213273642	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv584346	chr2:213067749-213258622	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv834526	chr2:213114901-213237146	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
4	nsv834527	chr2:213115966-213334308	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1014680	chr2:213142147-213301614	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1004573	chr2:213186537-213365252	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
7	nsv875811	chr2:213200920-213347104	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
8	nsv3149	chr2:213204282-213248966	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv584422	chr2:213214303-213270427	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv1003694	chr2:213216431-213290523	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv962099	chr2:213227283-213230590	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:213219200-213233600	Weak transcription	Psoas Muscle	Psoas
2	chr2:213224600-213228800	Weak transcription	Brain Germinal Matrix	brain
3	chr2:213225200-213228800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr2:213225200-213229000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr2:213225200-213229200	Weak transcription	Fetal Kidney	kidney
6	chr2:213225200-213231600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:213225400-213228800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr2:213225400-213228800	Weak transcription	Brain Angular Gyrus	brain
9	chr2:213226400-213228800	Weak transcription	Brain Cingulate Gyrus	brain
10	chr2:213226400-213229200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr2:213226600-213229000	Weak transcription	HepG2	liver
12	chr2:213226600-213229200	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr2:213228000-213229200	Enhancers	Brain Substantia Nigra	brain
14	chr2:213228200-213229000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr2:213228400-213228800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr2:213228400-213228800	Enhancers	Brain Anterior Caudate	brain
17	chr2:213228400-213229000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr2:213228400-213229000	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr2:213228400-213229600	Enhancers	NHDF-Ad	bronchial
20	chr2:213228400-213231000	Enhancers	Fetal Heart	heart
21	chr2:213228600-213229000	Enhancers	Brain Hippocampus Middle	brain
22	chr2:213228600-213229400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr2:213228600-213229400	Enhancers	HUVEC	blood vessel
24	chr2:213228600-213229600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr2:213228600-213229600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:213228600-213229600	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr2:213228600-213229600	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr2:213228600-213229600	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr2:213228600-213229600	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr2:213228600-213229600	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr2:213228600-213229600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr2:213228600-213229800	Enhancers	HUES64 Cell Line	embryonic stem cell

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