Variant report

Variant	rs73441297
Chromosome Location	chr9:22122794-22122795
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

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

rs_ID	r²[population]
rs59995170	1.00[AFR][1000 genomes]
rs60123355	1.00[AFR][1000 genomes]
rs60601001	1.00[AFR][1000 genomes]
rs61650117	1.00[AFR][1000 genomes]
rs73438868	1.00[AFR][1000 genomes]
rs73441209	1.00[AFR][1000 genomes]
rs73441213	1.00[AFR][1000 genomes]
rs73441281	1.00[AFR][1000 genomes]
rs73441296	1.00[AFR][1000 genomes]
rs73441298	1.00[AFR][1000 genomes]
rs73443203	0.94[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	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	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
4	nsv1029889	chr9:22118046-22161828	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:22119000-22128200	Weak transcription	HSMMtube	muscle
2	chr9:22119600-22124400	Weak transcription	HUVEC	blood vessel
3	chr9:22119600-22124600	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr9:22119600-22124600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr9:22119800-22124400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr9:22119800-22124600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr9:22119800-22129000	Weak transcription	HMEC	breast
8	chr9:22120000-22124600	Weak transcription	NH-A	brain
9	chr9:22120000-22129200	Weak transcription	Stomach Mucosa	stomach
10	chr9:22120200-22123400	Weak transcription	Hela-S3	cervix
11	chr9:22120400-22123400	Weak transcription	Fetal Intestine Small	intestine
12	chr9:22120400-22123800	Weak transcription	Duodenum Mucosa	Duodenum
13	chr9:22120400-22123800	Weak transcription	Fetal Intestine Large	intestine
14	chr9:22121800-22125200	Enhancers	Rectal Mucosa Donor 31	rectum

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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