Variant report

Variant	rs73649933
Chromosome Location	chr9:21685811-21685812
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:21588453..21590122-chr9:21684881..21686548,2	MCF-7	breast:

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs55689357	1.00[AFR][1000 genomes]
rs56322499	1.00[AFR][1000 genomes]
rs61145696	1.00[AFR][1000 genomes]
rs73649930	0.87[AFR][1000 genomes]
rs73649938	1.00[AFR][1000 genomes]
rs73649946	1.00[AFR][1000 genomes]
rs73649948	0.87[AFR][1000 genomes]
rs73649955	1.00[AFR][1000 genomes]
rs73649956	1.00[AFR][1000 genomes]
rs73649957	1.00[AFR][1000 genomes]
rs73649958	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029634	chr9:21542970-21765286	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv1015623	chr9:21579110-21694039	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
3	nsv892742	chr9:21589041-21707372	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv892743	chr9:21675545-21772064	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21678000-21688200	Enhancers	HMEC	breast
2	chr9:21678400-21687400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:21680400-21686000	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr9:21680400-21688200	Flanking Active TSS	A549	lung
5	chr9:21680400-21688200	Enhancers	Osteobl	bone
6	chr9:21680400-21691000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr9:21682200-21687800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr9:21682200-21688000	Enhancers	NHDF-Ad	bronchial
9	chr9:21683200-21688000	Weak transcription	Small Intestine	intestine
10	chr9:21684000-21686000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr9:21684400-21686000	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr9:21684400-21686000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr9:21684600-21687200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr9:21684600-21688400	Enhancers	NHLF	lung
15	chr9:21684800-21686000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr9:21684800-21686200	Enhancers	HSMM	muscle
17	chr9:21684800-21686600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr9:21684800-21688200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr9:21685000-21686000	Enhancers	Esophagus	oesophagus
20	chr9:21685000-21688000	Enhancers	Stomach Mucosa	stomach
21	chr9:21685000-21688200	Enhancers	NH-A	brain
22	chr9:21685200-21691000	Enhancers	Hela-S3	cervix
23	chr9:21685200-21695600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr9:21685400-21688200	Weak transcription	Duodenum Mucosa	Duodenum
25	chr9:21685400-21688400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr9:21685600-21686000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr9:21685600-21688000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr9:21685800-21686000	Flanking Active TSS	NHEK	skin
29	chr9:21685800-21686400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr9:21685800-21690200	Enhancers	HUVEC	blood vessel

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