Variant report

Variant	rs7849196
Chromosome Location	chr9:101095620-101095621
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10125457	1.00[ASN][1000 genomes]
rs28564647	0.84[ASN][1000 genomes]
rs28653687	1.00[ASN][1000 genomes]
rs7021314	1.00[AMR][1000 genomes]
rs7031028	1.00[AMR][1000 genomes]
rs7034571	1.00[AMR][1000 genomes]
rs7037748	1.00[AMR][1000 genomes]
rs7041874	1.00[AMR][1000 genomes]
rs7043006	1.00[CHD][hapmap];0.84[ASN][1000 genomes]
rs72759627	1.00[ASN][1000 genomes]
rs72759646	1.00[ASN][1000 genomes]
rs7849698	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7863839	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7871796	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7871923	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs7872003	1.00[AMR][1000 genomes]
rs7875502	0.92[ASN][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	nsv430085	chr9:100928245-101339645	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv831663	chr9:100941048-101109492	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv831664	chr9:101024862-101205637	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:101087400-101096000	Weak transcription	Osteobl	bone
2	chr9:101087400-101096400	Weak transcription	NH-A	brain
3	chr9:101089000-101096000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr9:101090400-101098400	Enhancers	HUVEC	blood vessel
5	chr9:101092000-101096000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr9:101092200-101095800	Weak transcription	HMEC	breast
7	chr9:101092600-101097000	Weak transcription	Fetal Intestine Large	intestine
8	chr9:101094200-101096200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr9:101094400-101096000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr9:101094400-101096000	Weak transcription	NHDF-Ad	bronchial
11	chr9:101094400-101104400	Weak transcription	Brain Angular Gyrus	brain
12	chr9:101095000-101096000	Weak transcription	Spleen	Spleen
13	chr9:101095000-101098400	Enhancers	K562	blood
14	chr9:101095200-101096400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr9:101095400-101095800	Weak transcription	NHLF	lung
16	chr9:101095400-101096600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr9:101095400-101096600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr9:101095400-101097400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr9:101095400-101102800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr9:101095600-101096800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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