Variant report

Variant	rs148499432
Chromosome Location	chr3:118945658-118945659
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	chr3:118944759..118947412-chr3:118958236..118960502,3	MCF-7	breast:
2	chr3:118943120..118945710-chr3:118958108..118960423,2	K562	blood:

Variant related genes	Relation type
ENSG00000121578	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3487859	chr3:118570588-119419623	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	esv3487860	chr3:118570588-119419623	Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	esv18354	chr3:118855337-119000251	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv591362	chr3:118906442-118948155	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv3386832	chr3:118944762-118948560	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118924400-118959000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr3:118927000-118952600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr3:118927000-118953800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr3:118927000-118953800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr3:118927200-118953800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr3:118927200-118955200	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr3:118927400-118950200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr3:118927400-118953000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr3:118927600-118952400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr3:118927800-118956400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
11	chr3:118928000-118955600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
12	chr3:118928200-118951000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr3:118928800-118950000	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr3:118929200-118956200	Strong transcription	HUES48 Cell Line	embryonic stem cell
15	chr3:118929200-118956200	Strong transcription	HUES64 Cell Line	embryonic stem cell
16	chr3:118929200-118956400	Strong transcription	H1 Cell Line	embryonic stem cell
17	chr3:118929200-118956600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
18	chr3:118930000-118949800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr3:118930000-118955400	Strong transcription	Primary B cells from peripheral blood	blood
20	chr3:118930200-118955800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr3:118930200-118958400	Weak transcription	Hela-S3	cervix
22	chr3:118931600-118957400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr3:118931800-118946400	Genic enhancers	A549	lung
24	chr3:118932600-118955800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr3:118935800-118947600	Weak transcription	HUVEC	blood vessel
26	chr3:118937200-118952600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr3:118938400-118947200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr3:118938400-118951200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr3:118938600-118947200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr3:118938600-118947800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr3:118939200-118947800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr3:118940200-118950000	Strong transcription	Dnd41	blood
33	chr3:118940200-118950000	Strong transcription	GM12878-XiMat	blood
34	chr3:118941000-118953000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr3:118941800-118952400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr3:118942000-118949800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr3:118942400-118946200	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr3:118942400-118947200	Weak transcription	Fetal Brain Male	brain
39	chr3:118942800-118946200	Weak transcription	Pancreas	Pancrea
40	chr3:118943000-118946400	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr3:118943000-118946600	Weak transcription	Gastric	stomach
42	chr3:118943000-118946800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr3:118943000-118947600	Weak transcription	Right Ventricle	heart
44	chr3:118943000-118947800	Weak transcription	HSMMtube	muscle
45	chr3:118943000-118948600	Weak transcription	K562	blood
46	chr3:118943200-118947600	Weak transcription	Fetal Kidney	kidney
47	chr3:118943800-118946000	Genic enhancers	Primary T helper cells fromperipheralblood	blood
48	chr3:118943800-118948200	Genic enhancers	Primary T helper cells PMA-I stimulated	--
49	chr3:118944000-118946200	Genic enhancers	Primary T cells from cord blood	blood
50	chr3:118944000-118949400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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