Variant report

Variant	rs9847107
Chromosome Location	chr3:143545699-143545700
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10433437	1.00[CHB][hapmap]
rs12497227	1.00[CHB][hapmap];0.80[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1394403	0.90[CHB][hapmap]
rs1504603	1.00[GIH][hapmap]
rs1504604	1.00[GIH][hapmap]
rs1504605	1.00[GIH][hapmap]
rs16834862	1.00[GIH][hapmap]
rs16854417	0.90[CHB][hapmap]
rs16854421	0.90[CHB][hapmap]
rs16854423	0.90[CHB][hapmap]
rs16854424	0.90[CHB][hapmap]
rs16854463	0.90[CHB][hapmap]
rs16854493	0.90[CHB][hapmap]
rs16854503	1.00[CHB][hapmap]
rs16854525	0.90[CHB][hapmap]
rs16854543	1.00[GIH][hapmap]
rs1823220	1.00[CEU][hapmap];0.90[CHB][hapmap];0.92[EUR][1000 genomes]
rs1900643	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs1900644	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs1989180	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1995529	1.00[GIH][hapmap]
rs1995530	1.00[GIH][hapmap]
rs2134913	0.80[AMR][1000 genomes]
rs2361199	0.90[CHB][hapmap]
rs2361204	1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[MEX][hapmap];0.80[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4593022	0.92[EUR][1000 genomes]
rs4839612	1.00[CEU][hapmap]
rs4839614	0.90[CHB][hapmap]
rs4839659	0.90[CHB][hapmap]
rs4839660	0.90[CHB][hapmap]
rs4839661	0.90[CHB][hapmap]
rs4839663	0.90[CHB][hapmap]
rs4839670	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6763660	0.82[CHB][hapmap]
rs6764661	1.00[CHB][hapmap];0.95[CHD][hapmap];0.85[MEX][hapmap];0.80[AMR][1000 genomes]
rs6765414	0.90[CHB][hapmap]
rs6769847	0.90[CHB][hapmap]
rs6773087	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs6776336	1.00[CHB][hapmap];0.80[AMR][1000 genomes]
rs6780027	1.00[GIH][hapmap]
rs6792031	0.90[CHB][hapmap]
rs6801948	1.00[CEU][hapmap]
rs6804065	1.00[CEU][hapmap];0.90[CHB][hapmap];0.92[EUR][1000 genomes]
rs7434217	1.00[GIH][hapmap]
rs7621206	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7624170	1.00[GIH][hapmap]
rs7651412	0.90[CHB][hapmap]
rs7652644	0.90[CHB][hapmap]
rs7653164	1.00[GIH][hapmap]
rs9289669	1.00[GIH][hapmap]
rs9822158	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[TSI][hapmap];0.92[EUR][1000 genomes]
rs9827103	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9832471	1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[MEX][hapmap];0.80[AMR][1000 genomes]
rs9844917	0.92[EUR][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	nsv949288	chr3:142793323-143585882	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	esv3418674	chr3:143457005-143558357	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv1009935	chr3:143497700-143610852	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1001076	chr3:143513526-143547076	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv536747	chr3:143513526-143547076	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143539600-143546600	Weak transcription	Esophagus	oesophagus
2	chr3:143539600-143550000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr3:143539800-143558200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr3:143540000-143549600	Weak transcription	HSMM	muscle
5	chr3:143541000-143554200	Weak transcription	Fetal Muscle Trunk	muscle
6	chr3:143541400-143565200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr3:143541800-143549800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr3:143542000-143553600	Weak transcription	Brain Cingulate Gyrus	brain
9	chr3:143542200-143549800	Weak transcription	Brain Anterior Caudate	brain
10	chr3:143542200-143552400	Weak transcription	Brain Angular Gyrus	brain
11	chr3:143542200-143553600	Weak transcription	Brain Hippocampus Middle	brain
12	chr3:143543200-143545800	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr3:143543200-143545800	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr3:143543200-143545800	Enhancers	NHDF-Ad	bronchial
15	chr3:143543200-143546200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr3:143543200-143547800	Enhancers	Colon Smooth Muscle	Colon
17	chr3:143543400-143545800	Enhancers	Primary B cells from peripheral blood	blood
18	chr3:143543400-143545800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
19	chr3:143543400-143545800	Enhancers	Rectal Smooth Muscle	rectum
20	chr3:143543400-143546000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
21	chr3:143543600-143546200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr3:143543600-143551400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr3:143543800-143545800	Enhancers	Stomach Mucosa	stomach
24	chr3:143544000-143546000	Enhancers	Primary B cells from cord blood	blood
25	chr3:143544000-143546000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr3:143544000-143549800	Weak transcription	Adipose Nuclei	Adipose
27	chr3:143544200-143549200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr3:143544200-143552800	Weak transcription	Fetal Lung	lung
29	chr3:143544400-143549600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr3:143544600-143545800	Enhancers	Primary hematopoietic stem cells	blood
31	chr3:143544800-143545800	Enhancers	GM12878-XiMat	blood
32	chr3:143544800-143549000	Weak transcription	HUVEC	blood vessel
33	chr3:143545000-143546800	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr3:143545000-143548000	Weak transcription	Primary T cells from cord blood	blood
35	chr3:143545000-143549800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr3:143545400-143546000	Weak transcription	Right Atrium	heart
37	chr3:143545400-143549000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr3:143545400-143549800	Weak transcription	Brain Substantia Nigra	brain
39	chr3:143545400-143550000	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr3:143545400-143550000	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr3:143545400-143550200	Weak transcription	Duodenum Mucosa	Duodenum
42	chr3:143545400-143550400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr3:143545400-143550400	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr3:143545400-143558800	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr3:143545600-143546200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr3:143545600-143548800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr3:143545600-143565400	Weak transcription	Primary T cells fromperipheralblood	blood

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