Variant report

Variant	rs73652841
Chromosome Location	chr9:22033362-22033363
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs16935753	0.83[AMR][1000 genomes]
rs2069420	0.83[AMR][1000 genomes]
rs2151279	0.83[AMR][1000 genomes]
rs3217980	0.83[AMR][1000 genomes]
rs3217994	0.83[AMR][1000 genomes]
rs3217997	0.83[AMR][1000 genomes]
rs3217999	0.83[AMR][1000 genomes]
rs3218003	0.83[AMR][1000 genomes]
rs3218021	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs3218022	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs3218023	0.83[AMR][1000 genomes]
rs56272822	0.81[AFR][1000 genomes]
rs60693449	0.83[AMR][1000 genomes]
rs61564778	0.83[AMR][1000 genomes]
rs73650003	0.83[AMR][1000 genomes]
rs73652816	0.83[AMR][1000 genomes]
rs73652817	0.83[AMR][1000 genomes]
rs73652818	0.83[AMR][1000 genomes]
rs73652821	0.83[AMR][1000 genomes]
rs73652824	0.83[AMR][1000 genomes]
rs73652825	0.83[AMR][1000 genomes]
rs73652839	0.83[AMR][1000 genomes]
rs73652842	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73652845	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73652846	0.83[AMR][1000 genomes]
rs73652847	0.83[AMR][1000 genomes]
rs73652848	0.83[AMR][1000 genomes]
rs73652849	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529609	chr9:21708371-22537069	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv8426	chr9:21763810-22176200	Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv1018514	chr9:21944275-22075326	Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv892747	chr9:21984661-22068646	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	nsv531617	chr9:21985057-22809676	Genic enhancers Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:22009800-22037000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr9:22025000-22033800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:22025400-22039800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr9:22029400-22034200	Enhancers	HMEC	breast
5	chr9:22030000-22034200	Enhancers	NHEK	skin
6	chr9:22030200-22037400	Weak transcription	Primary B cells from cord blood	blood
7	chr9:22030400-22035400	Weak transcription	HSMM	muscle
8	chr9:22030400-22038000	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr9:22030400-22040000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr9:22030600-22036800	Weak transcription	Fetal Intestine Large	intestine
11	chr9:22030800-22035400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr9:22030800-22035400	Weak transcription	Osteobl	bone
13	chr9:22030800-22035600	Weak transcription	HSMMtube	muscle
14	chr9:22030800-22036800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr9:22030800-22037200	Weak transcription	Fetal Intestine Small	intestine
16	chr9:22030800-22041800	Weak transcription	Stomach Mucosa	stomach
17	chr9:22031000-22036600	Weak transcription	Hela-S3	cervix
18	chr9:22031000-22037200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr9:22031000-22037200	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr9:22031600-22034200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr9:22031800-22034200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr9:22032000-22033800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr9:22032000-22035400	Weak transcription	Esophagus	oesophagus
24	chr9:22032200-22034600	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr9:22032200-22037600	Weak transcription	GM12878-XiMat	blood
26	chr9:22032400-22035200	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr9:22032600-22033800	Strong transcription	Dnd41	blood
28	chr9:22032600-22036800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr9:22032600-22037800	Weak transcription	NHDF-Ad	bronchial
30	chr9:22033000-22033400	Enhancers	H1 Cell Line	embryonic stem cell
31	chr9:22033000-22035400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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