Variant report

Variant	rs73391358
Chromosome Location	chr9:5876488-5876489
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:5868662..5871145-chr9:5874957..5877904,2	MCF-7	breast:
2	chr9:5875561..5878927-chr9:6007054..6010083,3	K562	blood:
3	chr9:5869625..5872282-chr9:5874318..5876632,2	K562	blood:
4	chr9:5871955..5874825-chr9:5876474..5878566,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000263575	Chromatin interaction
ENSG00000183354	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs10975331	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017103	chr9:5509431-5987907	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv539965	chr9:5509431-5987907	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv948847	chr9:5712626-6417677	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	esv3331803	chr9:5766129-5905103	Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv1031086	chr9:5806949-6630686	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
6	nsv539967	chr9:5806949-6630686	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
7	nsv892155	chr9:5825768-6044937	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
8	nsv613203	chr9:5841438-5877948	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1033546	chr9:5875201-5900427	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:5834400-5886000	Weak transcription	Brain Cingulate Gyrus	brain
2	chr9:5840400-5921600	Weak transcription	Right Ventricle	heart
3	chr9:5840600-5879800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr9:5852200-5897000	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr9:5852400-5878800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr9:5853800-5895600	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr9:5854400-5886200	Weak transcription	Brain Anterior Caudate	brain
8	chr9:5855600-5876600	Weak transcription	Fetal Stomach	stomach
9	chr9:5856600-5880000	Weak transcription	Esophagus	oesophagus
10	chr9:5856800-5895600	Weak transcription	Brain Substantia Nigra	brain
11	chr9:5858600-5876600	Weak transcription	Aorta	Aorta
12	chr9:5858600-5885800	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr9:5859000-5876800	Weak transcription	Left Ventricle	heart
14	chr9:5859000-5895600	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr9:5859000-5906600	Weak transcription	Ovary	ovary
16	chr9:5859200-5919800	Weak transcription	Fetal Brain Female	brain
17	chr9:5859800-5876600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr9:5863400-5876800	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr9:5863400-5895600	Weak transcription	Fetal Intestine Small	intestine
20	chr9:5863600-5896600	Weak transcription	Pancreas	Pancrea
21	chr9:5864800-5880800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr9:5864800-5881400	Weak transcription	Spleen	Spleen
23	chr9:5864800-5895600	Weak transcription	Gastric	stomach
24	chr9:5865200-5881000	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr9:5865200-5886000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr9:5870000-5886400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr9:5870200-5876600	Weak transcription	Placenta	Placenta
28	chr9:5870400-5876800	Weak transcription	HepG2	liver
29	chr9:5870800-5895600	Weak transcription	Stomach Smooth Muscle	stomach
30	chr9:5871000-5895600	Weak transcription	Brain Hippocampus Middle	brain
31	chr9:5871000-5920000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr9:5871200-5898400	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr9:5872600-5879400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr9:5873200-5876800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr9:5874200-5876600	Weak transcription	Hela-S3	cervix
36	chr9:5874200-5877200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
37	chr9:5875400-5876600	Enhancers	GM12878-XiMat	blood
38	chr9:5875600-5876600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr9:5875600-5881600	Weak transcription	Primary T cells from cord blood	blood
40	chr9:5875600-5884800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr9:5875800-5876600	Enhancers	Primary B cells from peripheral blood	blood
42	chr9:5876000-5876800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr9:5876000-5885000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr9:5876200-5877200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr9:5876200-5877200	Strong transcription	Brain Angular Gyrus	brain
46	chr9:5876400-5876800	Genic enhancers	K562	blood

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