Variant report

Variant	rs536522555
Chromosome Location	chr3:51989463-51989464
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:51980605..51983550-chr3:51988202..51990542,2	MCF-7	breast:
2	chr3:51987928..51991924-chr3:52001407..52003695,4	MCF-7	breast:
3	chr3:51988009..51992311-chr3:51992660..51997455,6	K562	blood:
4	chr3:51976311..51979172-chr3:51989239..51992217,2	K562	blood:
5	chr3:51987614..51990073-chr3:52025987..52029912,3	K562	blood:
6	chr3:51988573..51991523-chr3:52028412..52030001,2	K562	blood:

Variant related genes	Relation type
ENSG00000162244	Chromatin interaction
ENSG00000041880	Chromatin interaction
ENSG00000090097	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv520211	chr3:51772347-52166147	Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv1012847	chr3:51811062-52056727	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	68 gene(s)	inside rSNPs	diseases
3	nsv536571	chr3:51811062-52056727	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	68 gene(s)	inside rSNPs	diseases
4	nsv1003453	chr3:51962081-52099441	Active TSS Genic enhancers Strong transcription Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
5	esv1804090	chr3:51962081-52140591	Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
6	esv1835339	chr3:51962081-52140591	Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
7	nsv1003581	chr3:51973395-52108645	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
8	nsv1001062	chr3:51973395-52134638	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
9	nsv876780	chr3:51981021-52101799	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
10	nsv876781	chr3:51985664-52009612	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
11	nsv876782	chr3:51985664-52022779	Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
12	nsv876783	chr3:51987224-52009612	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
13	nsv876784	chr3:51987224-52013242	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
14	esv3438711	chr3:51987612-51992410	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
15	esv3405551	chr3:51989162-51991160	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:51977200-51992000	Weak transcription	Aorta	Aorta
2	chr3:51983800-51990200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr3:51986200-51993400	Weak transcription	HepG2	liver
4	chr3:51987600-51990200	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
5	chr3:51987600-51992000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr3:51988000-51989600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr3:51988000-51990600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr3:51988000-51990800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr3:51988000-51990800	Weak transcription	HSMM	muscle
10	chr3:51988000-51992400	Weak transcription	HSMMtube	muscle
11	chr3:51988200-51989600	Weak transcription	Osteobl	bone
12	chr3:51988400-52000600	Weak transcription	Hela-S3	cervix
13	chr3:51988800-51989600	Bivalent Enhancer	Fetal Muscle Leg	muscle
14	chr3:51989000-51989600	Flanking Active TSS	Brain Anterior Caudate	brain
15	chr3:51989000-51989600	Flanking Active TSS	Brain Hippocampus Middle	brain
16	chr3:51989000-51989800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
17	chr3:51989000-51989800	Flanking Active TSS	Brain Cingulate Gyrus	brain
18	chr3:51989000-51989800	Enhancers	Pancreas	Pancrea
19	chr3:51989000-51990000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
20	chr3:51989200-51989600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr3:51989200-51989600	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr3:51989200-51989600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
23	chr3:51989200-51989600	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr3:51989200-51989600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
25	chr3:51989200-51989600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr3:51989200-51989600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr3:51989200-51989600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr3:51989200-51989600	Enhancers	Adipose Nuclei	Adipose
29	chr3:51989200-51989600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
30	chr3:51989200-51989600	Enhancers	Gastric	stomach
31	chr3:51989200-51989600	Enhancers	Ovary	ovary
32	chr3:51989200-51989600	Enhancers	Psoas Muscle	Psoas
33	chr3:51989200-51989600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
34	chr3:51989200-51989800	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr3:51989200-51989800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
36	chr3:51989200-51989800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
37	chr3:51989200-51990000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr3:51989200-51990400	Active TSS	Brain Angular Gyrus	brain
39	chr3:51989200-51990800	Active TSS	Brain Inferior Temporal Lobe	brain
40	chr3:51989200-51991000	Enhancers	Fetal Brain Male	brain
41	chr3:51989200-51991000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
42	chr3:51989200-51991200	Enhancers	Spleen	Spleen
43	chr3:51989200-51991400	Enhancers	Liver	Liver
44	chr3:51989200-51991400	Enhancers	Fetal Heart	heart
45	chr3:51989400-51989600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
46	chr3:51989400-51989600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
47	chr3:51989400-51989600	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
48	chr3:51989400-51989600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr3:51989400-51989600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr3:51989400-51989600	Enhancers	Colon Smooth Muscle	Colon

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