Variant report

Variant	rs73523275
Chromosome Location	chr9:97413416-97413417
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:97413279..97414957-chr9:97431103..97432914,2	MCF-7	breast:
2	chr9:97399795..97401859-chr9:97411374..97414324,3	MCF-7	breast:
3	chr9:97389422..97393205-chr9:97411609..97416128,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000165140	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs58676982	1.00[AMR][1000 genomes]
rs58889952	1.00[AMR][1000 genomes]
rs59596055	1.00[AMR][1000 genomes]
rs60553517	1.00[AMR][1000 genomes]
rs7037239	1.00[AMR][1000 genomes]
rs73521196	1.00[AMR][1000 genomes]
rs73521201	1.00[AMR][1000 genomes]
rs73523253	1.00[AMR][1000 genomes]
rs73523261	1.00[AMR][1000 genomes]
rs73523277	1.00[AMR][1000 genomes]
rs73523285	1.00[AMR][1000 genomes]
rs73523301	1.00[AMR][1000 genomes]
rs73524810	1.00[AMR][1000 genomes]
rs73530354	1.00[AMR][1000 genomes]
rs73532323	1.00[AMR][1000 genomes]
rs73532332	1.00[AMR][1000 genomes]
rs73532340	1.00[AMR][1000 genomes]
rs73532355	1.00[AMR][1000 genomes]
rs73534109	1.00[AMR][1000 genomes]
rs73534113	1.00[AMR][1000 genomes]
rs73534154	1.00[AMR][1000 genomes]
rs73534159	1.00[AMR][1000 genomes]
rs73536042	1.00[AMR][1000 genomes]
rs73536067	1.00[AMR][1000 genomes]
rs73536074	1.00[AMR][1000 genomes]
rs73537487	1.00[AMR][1000 genomes]
rs73539427	1.00[AMR][1000 genomes]
rs73539428	1.00[AMR][1000 genomes]
rs7858775	1.00[AMR][1000 genomes]
rs9695249	0.92[AFR][1000 genomes]
rs9696490	1.00[AMR][1000 genomes]

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	nsv893596	chr9:97321172-97598966	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
2	nsv893597	chr9:97380597-97463435	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:97402400-97420000	Weak transcription	Right Atrium	heart
2	chr9:97402600-97415400	Weak transcription	Spleen	Spleen
3	chr9:97405800-97418400	Weak transcription	Fetal Stomach	stomach
4	chr9:97410000-97418000	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr9:97410200-97413600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr9:97410200-97413600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr9:97410200-97413600	Enhancers	Stomach Mucosa	stomach
8	chr9:97410200-97413800	Enhancers	HMEC	breast
9	chr9:97410400-97413600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr9:97410400-97413600	Enhancers	Duodenum Mucosa	Duodenum
11	chr9:97410800-97413600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr9:97411000-97416200	Weak transcription	Lung	lung
13	chr9:97411000-97417800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr9:97411800-97418000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr9:97412000-97413600	Enhancers	NHEK	skin
16	chr9:97412000-97415600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr9:97412000-97417800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr9:97412000-97417800	Weak transcription	Fetal Muscle Leg	muscle
19	chr9:97412200-97414800	Enhancers	Hela-S3	cervix
20	chr9:97412200-97416600	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr9:97412200-97417800	Weak transcription	Primary B cells from cord blood	blood
22	chr9:97412200-97417800	Weak transcription	HSMMtube	muscle
23	chr9:97412200-97418400	Weak transcription	HSMM	muscle
24	chr9:97412400-97417800	Weak transcription	Primary hematopoietic stem cells	blood
25	chr9:97412800-97415600	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr9:97413200-97413800	Enhancers	Fetal Intestine Small	intestine
27	chr9:97413400-97413600	Enhancers	Muscle Satellite Cultured Cells	--
28	chr9:97413400-97413600	Enhancers	Esophagus	oesophagus
29	chr9:97413400-97413800	Enhancers	Gastric	stomach

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