Variant report

Variant	rs145862132
Chromosome Location	chr2:183765097-183765098
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:183764300..183766706-chr2:183778634..183780515,2	MCF-7	breast:
2	chr2:183757338..183762208-chr2:183763229..183766079,6	K562	blood:
3	chr2:183759211..183762247-chr2:183762468..183766311,3	K562	blood:

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009882	chr2:183213152-184171519	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	esv2757842	chr2:183437700-183835084	Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	esv2759104	chr2:183437700-183835084	Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	esv34847	chr2:183537399-183786763	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv1006265	chr2:183666013-183777604	Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
6	nsv536071	chr2:183666013-183777604	Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
7	nsv818096	chr2:183701588-183827018	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
8	nsv978955	chr2:183764044-183768268	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	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	chr2:183752400-183772000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr2:183755000-183772200	Weak transcription	HSMM	muscle
3	chr2:183757000-183773800	Weak transcription	Fetal Intestine Large	intestine
4	chr2:183757400-183797800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr2:183758800-183771600	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr2:183759000-183772000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr2:183759000-183774000	Weak transcription	Left Ventricle	heart
8	chr2:183759200-183766600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr2:183759200-183772200	Weak transcription	Fetal Intestine Small	intestine
10	chr2:183759200-183775000	Weak transcription	Stomach Smooth Muscle	stomach
11	chr2:183759200-183775200	Weak transcription	Pancreas	Pancrea
12	chr2:183759600-183774400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr2:183759600-183777000	Weak transcription	HSMMtube	muscle
14	chr2:183759800-183771800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr2:183759800-183774000	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr2:183760000-183774000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr2:183760200-183769600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr2:183761000-183768600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr2:183762000-183778000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr2:183762200-183774600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr2:183762400-183772200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr2:183762400-183775000	Weak transcription	Osteobl	bone
23	chr2:183762400-183775200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr2:183762600-183775800	Weak transcription	NHDF-Ad	bronchial
25	chr2:183762600-183778000	Weak transcription	NHLF	lung
26	chr2:183762800-183772000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr2:183763600-183765400	Enhancers	Placenta	Placenta
28	chr2:183764000-183766600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr2:183764200-183772200	Weak transcription	Fetal Stomach	stomach
30	chr2:183764600-183765200	Enhancers	HepG2	liver
31	chr2:183765000-183774400	Weak transcription	Fetal Muscle Trunk	muscle
32	chr2:183765000-183774800	Weak transcription	Esophagus	oesophagus

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