Variant report

Variant	rs565900876
Chromosome Location	chr2:63665800-63665801
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	chr15:86367748..86369747-chr2:63664289..63665809,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000264406	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3417336	chr2:62957866-63749654	Strong transcription Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	esv1800788	chr2:63473443-63900292	ZNF genes & repeats Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv834241	chr2:63490262-63668205	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv874234	chr2:63606001-63666590	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv874235	chr2:63622470-63709708	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv819228	chr2:63664455-63666590	Weak transcription Enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:63628200-63668200	Weak transcription	Fetal Kidney	kidney
2	chr2:63631800-63675800	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr2:63631800-63677200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr2:63631800-63681200	Weak transcription	Aorta	Aorta
5	chr2:63631800-63688000	Weak transcription	Right Ventricle	heart
6	chr2:63634200-63665800	Weak transcription	Fetal Heart	heart
7	chr2:63643000-63673200	Weak transcription	Left Ventricle	heart
8	chr2:63652600-63666600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr2:63652600-63673800	Weak transcription	Primary hematopoietic stem cells	blood
10	chr2:63653200-63673800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr2:63654000-63668000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr2:63654600-63670600	Weak transcription	Fetal Muscle Leg	muscle
13	chr2:63654600-63678200	Weak transcription	Psoas Muscle	Psoas
14	chr2:63655000-63679000	Weak transcription	Primary T cells from cord blood	blood
15	chr2:63656200-63675600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr2:63657400-63675400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr2:63658600-63666800	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr2:63658600-63669400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr2:63658800-63668000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr2:63658800-63674000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr2:63659200-63679200	Weak transcription	Brain Hippocampus Middle	brain
22	chr2:63659600-63679000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr2:63659800-63667400	Weak transcription	A549	lung
24	chr2:63660400-63667400	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr2:63661800-63673400	Weak transcription	Fetal Brain Female	brain
26	chr2:63662000-63698000	Weak transcription	Ovary	ovary
27	chr2:63662200-63667800	Weak transcription	Fetal Brain Male	brain
28	chr2:63662200-63681400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr2:63662600-63665800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr2:63662800-63688000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr2:63663400-63667000	Strong transcription	Adipose Nuclei	Adipose
32	chr2:63663400-63670600	Weak transcription	Primary B cells from peripheral blood	blood
33	chr2:63664400-63667600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr2:63665600-63666400	Strong transcription	Primary B cells from cord blood	blood
35	chr2:63665800-63666000	Enhancers	Fetal Heart	heart
36	chr2:63665800-63666600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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