Variant report

Variant	rs73522572
Chromosome Location	chr9:95648703-95648704
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs16908618	1.00[AMR][1000 genomes]
rs57248419	0.95[AFR][1000 genomes]
rs7036069	0.82[AFR][1000 genomes]
rs73522512	1.00[AMR][1000 genomes]
rs73524291	0.97[AFR][1000 genomes]
rs73526840	0.95[AFR][1000 genomes]
rs73526854	0.80[AFR][1000 genomes]
rs73526860	0.89[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831654	chr9:95542920-95720961	ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv893574	chr9:95580376-95688099	Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv972781	chr9:95639258-95671744	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95640600-95648800	Weak transcription	Thymus	Thymus
2	chr9:95646600-95648800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr9:95646800-95649000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr9:95647800-95651600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr9:95648400-95649600	Enhancers	Primary T helper cells PMA-I stimulated	--
6	chr9:95648400-95651400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr9:95648400-95651600	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr9:95648600-95649600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr9:95648600-95649800	Enhancers	Primary T cells from cord blood	blood
10	chr9:95648600-95650800	Enhancers	Dnd41	blood
11	chr9:95648600-95651000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
12	chr9:95648600-95651400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr9:95648600-95651600	Enhancers	Primary T cells fromperipheralblood	blood

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

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