Variant report

Variant	rs61035513
Chromosome Location	chr3:112964558-112964559
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1499898	1.00[ASN][1000 genomes]
rs16845106	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs16860709	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16860720	1.00[ASN][1000 genomes]
rs16860770	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17320040	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17320242	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2399476	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34600669	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs41271353	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs57104308	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59590258	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs60070011	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9820139	0.95[ASN][1000 genomes]
rs9832953	0.93[ASN][1000 genomes]
rs9849714	1.00[ASN][1000 genomes]
rs9855011	1.00[ASN][1000 genomes]
rs9872998	0.95[ASN][1000 genomes]
rs9878424	0.95[ASN][1000 genomes]
rs998647	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs999365	1.00[EUR][1000 genomes];0.95[ASN][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	esv3431441	chr3:112453467-113213252	Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv829677	chr3:112857075-113038987	Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	nsv1003511	chr3:112858775-112989045	Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1013506	chr3:112890608-113680951	Weak transcription Bivalent/Poised TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
5	nsv877348	chr3:112914756-113012509	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112932000-112972800	Weak transcription	Aorta	Aorta
2	chr3:112951200-112967000	Weak transcription	Colonic Mucosa	Colon
3	chr3:112953800-112965600	Weak transcription	Right Atrium	heart
4	chr3:112954200-112965600	Weak transcription	Brain Substantia Nigra	brain
5	chr3:112958600-112969000	Weak transcription	Spleen	Spleen
6	chr3:112960400-112965800	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr3:112960800-112964600	Weak transcription	Fetal Muscle Trunk	muscle
8	chr3:112960800-112965600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr3:112960800-112965600	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr3:112960800-112967000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr3:112961000-112965600	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr3:112961400-112964600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr3:112961400-112964600	Weak transcription	HSMMtube	muscle
14	chr3:112961400-112964600	Weak transcription	NHLF	lung
15	chr3:112961400-112965600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr3:112961400-112969400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr3:112961600-112965600	Weak transcription	Brain Angular Gyrus	brain
18	chr3:112961600-112966400	Weak transcription	Fetal Thymus	thymus
19	chr3:112961600-112967400	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr3:112961600-112983000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr3:112961800-112965400	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr3:112961800-112965600	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr3:112962000-112965600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr3:112962000-112968200	Genic enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr3:112962000-112968800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr3:112962200-112964600	Weak transcription	NH-A	brain
27	chr3:112962200-112965600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr3:112962400-112969000	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr3:112962600-112964600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr3:112962800-112964600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr3:112962800-112964600	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr3:112962800-112964800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr3:112962800-112968000	Weak transcription	Gastric	stomach
34	chr3:112962800-112972400	Weak transcription	Brain Germinal Matrix	brain
35	chr3:112963000-112964600	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr3:112963000-112964600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr3:112963000-112964600	Weak transcription	Ovary	ovary
38	chr3:112963000-112964800	Weak transcription	Fetal Brain Male	brain
39	chr3:112963000-112965600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr3:112963000-112965600	Weak transcription	Esophagus	oesophagus
41	chr3:112963000-112968000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr3:112963000-112969200	Weak transcription	Pancreas	Pancrea
43	chr3:112963000-112972800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr3:112963600-112964800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:112963600-112965800	Enhancers	Stomach Smooth Muscle	stomach
46	chr3:112963600-112967200	Enhancers	Fetal Lung	lung
47	chr3:112964000-112968000	Enhancers	Fetal Kidney	kidney
48	chr3:112964000-112969000	Enhancers	HSMM	muscle
49	chr3:112964200-112964800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr3:112964200-112964800	Active TSS	Fetal Brain Female	brain

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