Variant report

Variant	rs148902942
Chromosome Location	chr2:113879397-113879398
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	chr2:113875025..113876736-chr2:113878416..113881099,2	MCF-7	breast:
2	chr2:113874395..113876014-chr2:113879125..113882509,3	K562	blood:

Variant related genes	Relation type
ENSG00000136689	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv997348	chr2:113688093-113986508	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv1007254	chr2:113726982-113887782	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv535894	chr2:113726982-113887782	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv1003928	chr2:113846503-113887782	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv979338	chr2:113869830-113880320	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1013513	chr2:113876914-113893482	Weak transcription Active TSS Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv961490	chr2:113879376-113880320	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113875400-113887400	Weak transcription	Spleen	Spleen
2	chr2:113875600-113881000	Weak transcription	Primary hematopoietic stem cells	blood
3	chr2:113875800-113880800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr2:113875800-113881000	Weak transcription	Lung	lung
5	chr2:113876000-113887400	Weak transcription	Gastric	stomach
6	chr2:113876000-113896200	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr2:113876200-113881400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr2:113876600-113885000	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr2:113877200-113880800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr2:113877200-113881600	Weak transcription	HMEC	breast
11	chr2:113877600-113881600	Weak transcription	Stomach Mucosa	stomach
12	chr2:113878400-113879400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr2:113878600-113880200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr2:113878800-113879400	Enhancers	Primary B cells from cord blood	blood
15	chr2:113878800-113879600	Enhancers	NHEK	skin
16	chr2:113878800-113880000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr2:113878800-113880400	Bivalent Enhancer	HepG2	liver
18	chr2:113879000-113880800	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr2:113879000-113880800	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr2:113879000-113881400	Weak transcription	GM12878-XiMat	blood
21	chr2:113879200-113879400	Enhancers	Duodenum Mucosa	Duodenum
22	chr2:113879200-113879400	Flanking Active TSS	Esophagus	oesophagus
23	chr2:113879200-113879400	Enhancers	Right Atrium	heart

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