Variant report

Variant	rs9848498
Chromosome Location	chr3:118703009-118703010
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs28392691	1.00[AMR][1000 genomes]
rs28484956	0.81[AFR][1000 genomes]
rs28565574	0.81[AFR][1000 genomes]
rs58420381	1.00[AMR][1000 genomes]
rs6768020	1.00[AMR][1000 genomes]
rs6795721	0.80[AFR][1000 genomes]
rs6796798	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72966895	0.80[AFR][1000 genomes]
rs72966899	1.00[AMR][1000 genomes]
rs72968606	1.00[AMR][1000 genomes]
rs72968612	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72968632	1.00[AMR][1000 genomes]
rs72968638	0.80[AFR][1000 genomes]
rs72968654	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72970438	1.00[AMR][1000 genomes]
rs72970470	1.00[AMR][1000 genomes]
rs72970472	1.00[AMR][1000 genomes]
rs7623832	1.00[AMR][1000 genomes]
rs7624134	1.00[AMR][1000 genomes]
rs7625109	1.00[AMR][1000 genomes]
rs9289118	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9811829	0.80[AFR][1000 genomes]
rs9814712	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9817851	0.85[AFR][1000 genomes]
rs9826100	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9827711	1.00[AMR][1000 genomes]
rs9835052	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9840552	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9841148	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9847137	1.00[AMR][1000 genomes]
rs9854365	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9857367	1.00[AMR][1000 genomes]
rs9859319	1.00[AMR][1000 genomes]
rs9862313	1.00[AMR][1000 genomes]
rs9862556	1.00[AMR][1000 genomes]
rs9876041	1.00[AMR][1000 genomes]
rs9882006	1.00[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	esv3487859	chr3:118570588-119419623	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	esv3487860	chr3:118570588-119419623	Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	nsv1010475	chr3:118657382-118789714	Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv877369	chr3:118681771-118824418	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	esv2756586	chr3:118688611-118863998	Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr3:118688800-118706000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:118689000-118703600	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr3:118692600-118704400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr3:118693400-118704400	Weak transcription	Stomach Smooth Muscle	stomach
5	chr3:118697200-118703600	Weak transcription	Ovary	ovary
6	chr3:118697400-118704200	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr3:118697400-118704800	Weak transcription	Pancreas	Pancrea
8	chr3:118697600-118704200	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr3:118699200-118706000	Enhancers	Brain Substantia Nigra	brain
10	chr3:118700000-118704600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr3:118700200-118706200	Enhancers	Brain Hippocampus Middle	brain
12	chr3:118700400-118705800	Enhancers	Brain Cingulate Gyrus	brain
13	chr3:118700400-118706000	Enhancers	Brain Angular Gyrus	brain
14	chr3:118700400-118707800	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr3:118700800-118703600	Weak transcription	Right Atrium	heart
16	chr3:118701000-118706200	Weak transcription	Psoas Muscle	Psoas
17	chr3:118701200-118704400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr3:118701600-118709800	Enhancers	Brain Anterior Caudate	brain
19	chr3:118702000-118704000	Weak transcription	Brain Germinal Matrix	brain
20	chr3:118702200-118710600	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr3:118702400-118703200	Weak transcription	K562	blood
22	chr3:118702800-118704600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:118703000-118703600	Weak transcription	Primary T cells from cord blood	blood
24	chr3:118703000-118703600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr3:118703000-118703800	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr3:118703000-118707800	Enhancers	Fetal Heart	heart

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