Variant report

Variant	rs187775294
Chromosome Location	chr6:55962161-55962162
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	nsv1034037	chr6:55222409-56069600	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv885911	chr6:55789704-56143231	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
3	nsv526703	chr6:55810482-56023811	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
4	nsv1029182	chr6:55910866-55991956	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
5	esv3444681	chr6:55962018-55964341	Weak transcription Enhancers Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3404892	chr6:55962143-55964191	Weak transcription Enhancers Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:55920600-56018400	Weak transcription	Ovary	ovary
2	chr6:55956600-55965800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr6:55956600-55978400	Weak transcription	Aorta	Aorta
4	chr6:55956800-55965600	Weak transcription	NHLF	lung
5	chr6:55957800-55962200	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr6:55958200-55965600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr6:55958600-55962200	Strong transcription	Fetal Muscle Trunk	muscle
8	chr6:55959600-55969600	Weak transcription	Fetal Lung	lung
9	chr6:55960600-55977800	Weak transcription	Fetal Muscle Leg	muscle
10	chr6:55960600-55978000	Weak transcription	Stomach Smooth Muscle	stomach
11	chr6:55961200-55962200	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr6:55961200-55962400	Enhancers	NHDF-Ad	bronchial
13	chr6:55961200-55962600	Enhancers	HUVEC	blood vessel
14	chr6:55961200-55964400	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr6:55961400-55969600	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr6:55961600-55962200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr6:55961600-55962400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr6:55961600-55964400	Weak transcription	Pancreas	Pancrea
19	chr6:55962000-55962200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr6:55962000-55962400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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