Variant report

Variant	rs17246769
Chromosome Location	chr9:108179836-108179837
allele	C/T
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:18)

rs_ID	r²[population]
rs10991638	0.82[EUR][1000 genomes]
rs10991641	0.86[EUR][1000 genomes]
rs10991643	0.82[EUR][1000 genomes]
rs10991644	0.86[EUR][1000 genomes]
rs10991645	0.83[EUR][1000 genomes]
rs11096	1.00[YRI][hapmap];0.89[EUR][1000 genomes]
rs12379533	0.86[EUR][1000 genomes]
rs1360087	0.89[EUR][1000 genomes]
rs1410838	0.86[EUR][1000 genomes]
rs1969981	0.89[EUR][1000 genomes]
rs2149591	0.82[EUR][1000 genomes]
rs2417641	0.89[EUR][1000 genomes]
rs2771032	0.89[EUR][1000 genomes]
rs2771034	0.86[EUR][1000 genomes]
rs2771043	0.86[EUR][1000 genomes]
rs2812313	0.89[EUR][1000 genomes]
rs2812317	0.89[EUR][1000 genomes]
rs73514068	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045108	chr9:107509553-108188550	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv1037750	chr9:108027692-108251733	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:108175600-108181200	Enhancers	HepG2	liver
2	chr9:108175800-108181800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr9:108176200-108181000	Weak transcription	Adipose Nuclei	Adipose
4	chr9:108176200-108188200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr9:108176400-108180800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr9:108177600-108186400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr9:108177800-108180800	Weak transcription	Fetal Lung	lung
8	chr9:108177800-108180800	Weak transcription	Stomach Mucosa	stomach
9	chr9:108177800-108181000	Weak transcription	Brain Cingulate Gyrus	brain
10	chr9:108177800-108181000	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr9:108177800-108181000	Weak transcription	A549	lung
12	chr9:108177800-108182200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr9:108177800-108194200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr9:108177800-108194200	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr9:108178000-108180800	Weak transcription	Brain Angular Gyrus	brain
16	chr9:108178000-108181000	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr9:108178000-108181800	Weak transcription	Fetal Intestine Small	intestine
18	chr9:108178200-108180600	Weak transcription	Fetal Intestine Large	intestine
19	chr9:108178200-108181000	Weak transcription	Brain Anterior Caudate	brain
20	chr9:108179200-108183200	Enhancers	Fetal Brain Male	brain
21	chr9:108179400-108180000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr9:108179400-108180000	Enhancers	Brain Hippocampus Middle	brain
23	chr9:108179400-108180400	Flanking Active TSS	Liver	Liver
24	chr9:108179600-108180000	Enhancers	GM12878-XiMat	blood
25	chr9:108179600-108184200	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr9:108179800-108180800	Weak transcription	Brain Substantia Nigra	brain

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