Variant report

Variant	rs555076635
Chromosome Location	chr11:45908364-45908365
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:45868641..45870553-chr11:45905537..45909020,4	K562	blood:
2	chr11:45904999..45908778-chr11:45926674..45929138,4	MCF-7	breast:
3	chr11:45907661..45910600-chr11:45912657..45914797,3	MCF-7	breast:
4	chr11:45892807..45894535-chr11:45907209..45909004,2	K562	blood:
5	chr11:45867854..45870393-chr11:45906869..45909551,2	MCF-7	breast:
6	chr11:45868680..45870553-chr11:45907106..45909020,2	K562	blood:
7	chr11:45907546..45909448-chr11:45934193..45936568,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000234776	Chromatin interaction
ENSG00000255498	Chromatin interaction
ENSG00000121671	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	nsv897314	chr11:45816020-45965129	Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
2	nsv1047462	chr11:45898630-45953696	Active TSS Genic enhancers Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv516442	chr11:45899962-45983385	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	esv1794798	chr11:45903280-45953636	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
5	esv3435139	chr11:45906376-45908374	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45906600-45908400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
2	chr11:45906600-45908400	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr11:45907000-45908400	Active TSS	Brain Anterior Caudate	brain
4	chr11:45907000-45908400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
5	chr11:45907000-45908600	Active TSS	Brain Hippocampus Middle	brain
6	chr11:45907000-45908600	Active TSS	Brain Inferior Temporal Lobe	brain
7	chr11:45907400-45908400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr11:45907600-45908400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
9	chr11:45907600-45908600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
10	chr11:45907600-45912400	Weak transcription	Liver	Liver
11	chr11:45907600-45920800	Weak transcription	Right Atrium	heart
12	chr11:45907800-45908400	Bivalent/Poised TSS	Fetal Intestine Small	intestine
13	chr11:45907800-45908800	Flanking Active TSS	Brain Germinal Matrix	brain
14	chr11:45908000-45908400	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:45908000-45908400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
16	chr11:45908000-45908400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
17	chr11:45908000-45908600	Active TSS	Brain Cingulate Gyrus	brain
18	chr11:45908000-45909200	Flanking Active TSS	Fetal Brain Female	brain
19	chr11:45908000-45910000	Weak transcription	Esophagus	oesophagus
20	chr11:45908000-45912400	Weak transcription	Pancreas	Pancrea
21	chr11:45908000-45912800	Enhancers	Fetal Brain Male	brain
22	chr11:45908000-45913000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr11:45908200-45908400	Flanking Active TSS	H1 Cell Line	embryonic stem cell
24	chr11:45908200-45908400	Enhancers	H9 Cell Line	embryonic stem cell
25	chr11:45908200-45908400	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr11:45908200-45908400	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
27	chr11:45908200-45908400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
28	chr11:45908200-45908400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr11:45908200-45908600	Active TSS	iPS-18 Cell Line	embryonic stem cell
30	chr11:45908200-45908600	Flanking Active TSS	Brain Angular Gyrus	brain
31	chr11:45908200-45908800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr11:45908200-45909400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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