Variant report

Variant	rs553473964
Chromosome Location	chr7:150952487-150952488
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:150948703..150950863-chr7:150952432..150955323,2	K562	blood:
2	chr7:150938571..150942838-chr7:150950941..150954111,4	MCF-7	breast:
3	chr7:150952243..150954405-chr7:150956858..150959573,2	K562	blood:
4	chr7:150928662..150932139-chr7:150946772..150952684,6	MCF-7	breast:

Variant related genes	Relation type
ENSG00000082014	Chromatin interaction
ENSG00000033100	Chromatin interaction

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	esv1821419	chr7:150593315-150974269	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	128 gene(s)	inside rSNPs	diseases
2	nsv609035	chr7:150896223-150955765	Bivalent Enhancer Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
3	nsv889487	chr7:150922952-150988172	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
4	nsv889488	chr7:150926775-150955765	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
5	nsv465216	chr7:150951819-150991795	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
6	nsv609036	chr7:150951819-150991795	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150950000-150952800	Enhancers	Right Ventricle	heart
2	chr7:150950200-150952800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
3	chr7:150950200-150953600	Weak transcription	Brain Anterior Caudate	brain
4	chr7:150950200-150953600	Weak transcription	Brain Hippocampus Middle	brain
5	chr7:150950400-150973400	Weak transcription	Brain Substantia Nigra	brain
6	chr7:150950600-150952600	Weak transcription	Colon Smooth Muscle	Colon
7	chr7:150950600-150953600	Weak transcription	Gastric	stomach
8	chr7:150950600-150953800	Weak transcription	Brain Cingulate Gyrus	brain
9	chr7:150950600-150955400	Weak transcription	Lung	lung
10	chr7:150950600-150955600	Weak transcription	Esophagus	oesophagus
11	chr7:150950600-150957200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr7:150950600-150957800	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr7:150950600-150958400	Weak transcription	Right Atrium	heart
14	chr7:150950600-150961400	Weak transcription	Spleen	Spleen
15	chr7:150950600-150965200	Weak transcription	Brain Angular Gyrus	brain
16	chr7:150950600-150967600	Weak transcription	Pancreas	Pancrea
17	chr7:150950800-150953600	Weak transcription	Fetal Heart	heart
18	chr7:150951000-150965400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr7:150951000-150969800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr7:150951000-150970800	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr7:150951200-150952600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr7:150951200-150952800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr7:150951200-150953600	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr7:150951600-150952600	Enhancers	Stomach Smooth Muscle	stomach
25	chr7:150951600-150968000	Weak transcription	Brain Germinal Matrix	brain
26	chr7:150951800-150952600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:150951800-150953600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr7:150951800-150967600	Weak transcription	Fetal Brain Female	brain
29	chr7:150952000-150953000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
30	chr7:150952000-150953800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr7:150952000-150954400	Enhancers	Ovary	ovary
32	chr7:150952400-150952600	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
33	chr7:150952400-150952600	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr7:150952400-150952800	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr7:150952400-150953000	Bivalent Enhancer	Fetal Muscle Leg	muscle

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