Variant report

Variant	rs377324492
Chromosome Location	chr9:110249101-110249102
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:110247849..110250590-chr9:111329415..111332131,3	MCF-7	breast:
2	chr9:110248541..110250333-chr9:110285200..110286705,2	MCF-7	breast:
3	chr9:110247080..110249421-chr9:111323616..111326393,2	MCF-7	breast:
4	chr9:110243041..110245201-chr9:110246252..110249576,3	K562	blood:
5	chr9:110246852..110249468-chr9:110266978..110269904,2	MCF-7	breast:
6	chr9:110246511..110249498-chr9:111190126..111191677,2	MCF-7	breast:
7	chr9:110248220..110250527-chr9:111302470..111304423,3	MCF-7	breast:
8	chr9:110246319..110249443-chr9:111522237..111525040,3	MCF-7	breast:
9	chr9:109425556..109427280-chr9:110248781..110250709,2	MCF-7	breast:
10	chr6:27114514..27116900-chr9:110249066..110251372,2	MCF-7	breast:
11	chr9:110247496..110249786-chr9:111257923..111260578,2	MCF-7	breast:
12	chr9:110248605..110250352-chr9:110763897..110765598,2	MCF-7	breast:
13	chr9:110248029..110249543-chr9:110331066..110332921,2	MCF-7	breast:
14	chr9:110246769..110253919-chr9:110298442..110306182,20	MCF-7	breast:
15	chr9:110246987..110249540-chr9:110886248..110888523,2	MCF-7	breast:
16	chr9:110247156..110249811-chr9:110250115..110251860,2	K562	blood:
17	chr9:110242425..110245039-chr9:110248076..110250038,3	K562	blood:
18	chr9:110247513..110249830-chr9:110339098..110341617,2	MCF-7	breast:
19	chr9:110248818..110250564-chr9:110802870..110804460,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000227350	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000234229	Chromatin interaction
ENSG00000136826	Chromatin interaction
ENSG00000265565	Chromatin interaction

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530948	chr9:109760752-110413602	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	nsv825028	chr9:110248596-110252543	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110243000-110249600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:110244000-110249200	Weak transcription	A549	lung
3	chr9:110244000-110250400	Weak transcription	HSMMtube	muscle
4	chr9:110246000-110249800	Transcr. at gene 5' and 3'	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr9:110246200-110253800	Active TSS	Right Atrium	heart
6	chr9:110247000-110249600	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr9:110247000-110249800	Transcr. at gene 5' and 3'	Rectal Mucosa Donor 29	rectum
8	chr9:110247000-110249800	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
9	chr9:110247000-110250600	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr9:110247200-110249600	Transcr. at gene 5' and 3'	NHEK	skin
11	chr9:110247200-110250000	Transcr. at gene 5' and 3'	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr9:110247200-110250400	Transcr. at gene 5' and 3'	Adipose Nuclei	Adipose
13	chr9:110247200-110250600	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr9:110247200-110250800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr9:110247200-110254000	Active TSS	Duodenum Smooth Muscle	Duodenum
16	chr9:110247400-110249200	Active TSS	Pancreatic Islets	Pancreatic Islet
17	chr9:110247400-110249200	Active TSS	Right Ventricle	heart
18	chr9:110247400-110249400	Transcr. at gene 5' and 3'	Fetal Intestine Large	intestine
19	chr9:110247400-110249600	Transcr. at gene 5' and 3'	Placenta Amnion	Placenta Amnion
20	chr9:110247400-110249600	Transcr. at gene 5' and 3'	NHDF-Ad	bronchial
21	chr9:110247400-110249800	Transcr. at gene 5' and 3'	Primary monocytes fromperipheralblood	blood
22	chr9:110247400-110251400	Transcr. at gene 5' and 3'	Rectal Mucosa Donor 31	rectum
23	chr9:110247400-110253800	Active TSS	Psoas Muscle	Psoas
24	chr9:110247600-110250400	Transcr. at gene 5' and 3'	Stomach Smooth Muscle	stomach
25	chr9:110247600-110250600	Active TSS	Brain Hippocampus Middle	brain
26	chr9:110247600-110250600	Active TSS	Small Intestine	intestine
27	chr9:110247600-110250600	Transcr. at gene 5' and 3'	NHLF	lung
28	chr9:110247800-110249400	Active TSS	Left Ventricle	heart
29	chr9:110248000-110250800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr9:110248200-110250400	Weak transcription	Aorta	Aorta
31	chr9:110248400-110249200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
32	chr9:110248400-110249200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr9:110248400-110249400	Transcr. at gene 5' and 3'	HMEC	breast
34	chr9:110248400-110250000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
35	chr9:110248400-110254200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
36	chr9:110248600-110249200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
37	chr9:110248600-110249200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
38	chr9:110248600-110249200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr9:110248600-110249200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr9:110248600-110249200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
41	chr9:110248600-110250800	Transcr. at gene 5' and 3'	Sigmoid Colon	Sigmoid Colon
42	chr9:110248600-110252800	Active TSS	Brain Cingulate Gyrus	brain
43	chr9:110248800-110249200	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
44	chr9:110248800-110249800	Transcr. at gene 5' and 3'	Placenta	Placenta
45	chr9:110248800-110249800	Flanking Active TSS	Hela-S3	cervix
46	chr9:110248800-110250200	Transcr. at gene 5' and 3'	Rectal Smooth Muscle	rectum
47	chr9:110249000-110249200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
48	chr9:110249000-110249200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
49	chr9:110249000-110249200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
50	chr9:110249000-110249200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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