Variant report

Variant	rs6796981
Chromosome Location	chr3:119130456-119130457
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs1001674	0.83[EUR][1000 genomes]
rs10511391	0.95[CEU][hapmap];0.85[CHD][hapmap];0.89[MEX][hapmap];0.83[TSI][hapmap];0.83[EUR][1000 genomes]
rs12485665	0.83[EUR][1000 genomes]
rs12487191	0.83[EUR][1000 genomes]
rs12487982	0.83[EUR][1000 genomes]
rs12488164	0.83[EUR][1000 genomes]
rs12488535	0.82[EUR][1000 genomes]
rs12489912	0.83[EUR][1000 genomes]
rs12490630	0.83[EUR][1000 genomes]
rs12492315	0.95[CEU][hapmap];0.85[CHD][hapmap];0.89[MEX][hapmap];0.83[TSI][hapmap];0.83[EUR][1000 genomes]
rs12492609	0.95[CEU][hapmap];0.83[EUR][1000 genomes]
rs12492859	0.95[CEU][hapmap];0.83[EUR][1000 genomes]
rs12493175	0.94[CEU][hapmap];0.83[EUR][1000 genomes]
rs12493326	0.95[CEU][hapmap];0.83[EUR][1000 genomes]
rs12493328	0.89[CEU][hapmap]
rs12493965	0.95[CEU][hapmap];0.85[CHD][hapmap];0.89[MEX][hapmap];0.83[TSI][hapmap];0.83[EUR][1000 genomes]
rs12494114	0.83[EUR][1000 genomes]
rs12494943	0.95[CEU][hapmap];0.83[EUR][1000 genomes]
rs12495539	0.95[CEU][hapmap];0.83[EUR][1000 genomes]
rs12495580	0.80[EUR][1000 genomes]
rs12495749	0.95[CEU][hapmap];0.89[CHD][hapmap];0.89[MEX][hapmap];0.83[TSI][hapmap];0.83[EUR][1000 genomes]
rs12496277	0.95[CEU][hapmap];0.83[EUR][1000 genomes]
rs12497394	0.94[CEU][hapmap];0.83[EUR][1000 genomes]
rs13062955	0.95[CEU][hapmap];0.83[EUR][1000 genomes]
rs13078312	0.95[CEU][hapmap];0.85[CHD][hapmap];0.89[MEX][hapmap];0.83[TSI][hapmap];0.83[EUR][1000 genomes]
rs13078816	0.83[EUR][1000 genomes]
rs13081067	0.95[CEU][hapmap];0.83[EUR][1000 genomes]
rs13081197	0.95[CEU][hapmap];0.81[EUR][1000 genomes]
rs13090653	0.90[CEU][hapmap]
rs13093049	0.83[EUR][1000 genomes]
rs13094625	0.95[CEU][hapmap];0.83[EUR][1000 genomes]
rs13096213	0.81[CHD][hapmap];0.83[EUR][1000 genomes]
rs16829838	0.95[CEU][hapmap];0.85[CHD][hapmap];0.89[MEX][hapmap];0.83[TSI][hapmap];0.83[EUR][1000 genomes]
rs16829850	0.83[EUR][1000 genomes]
rs16829853	0.95[CEU][hapmap];0.85[CHD][hapmap];0.89[MEX][hapmap];0.83[TSI][hapmap];0.83[EUR][1000 genomes]
rs16829865	0.83[EUR][1000 genomes]
rs1997341	0.95[CEU][hapmap];0.85[CHD][hapmap];0.89[MEX][hapmap];0.83[TSI][hapmap];0.81[EUR][1000 genomes]
rs2282170	0.95[CEU][hapmap];0.85[CHD][hapmap];0.83[TSI][hapmap];0.83[EUR][1000 genomes]
rs2282174	0.83[EUR][1000 genomes]
rs33958792	0.83[EUR][1000 genomes]
rs34023538	0.83[EUR][1000 genomes]
rs34208844	0.83[EUR][1000 genomes]
rs34250818	0.82[EUR][1000 genomes]
rs34468255	0.83[EUR][1000 genomes]
rs34746401	0.83[EUR][1000 genomes]
rs34834687	0.83[EUR][1000 genomes]
rs34849715	0.83[EUR][1000 genomes]
rs35084408	0.83[EUR][1000 genomes]
rs35169866	0.81[EUR][1000 genomes]
rs35282209	0.83[EUR][1000 genomes]
rs35563598	0.83[EUR][1000 genomes]
rs35761622	0.83[EUR][1000 genomes]
rs3732414	0.80[LWK][hapmap]
rs3732420	0.95[CEU][hapmap];0.85[CHD][hapmap];0.89[MEX][hapmap];0.83[TSI][hapmap];0.83[EUR][1000 genomes]
rs6779137	0.80[LWK][hapmap]
rs71325376	0.83[EUR][1000 genomes]
rs71325378	0.83[EUR][1000 genomes]
rs71325380	0.83[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	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	nsv829694	chr3:119011488-119153579	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv3962	chr3:119094646-119135321	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	esv997290	chr3:119127141-119135667	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:119072000-119133800	Weak transcription	Brain Cingulate Gyrus	brain
2	chr3:119080000-119145600	Weak transcription	Fetal Kidney	kidney
3	chr3:119081200-119135600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr3:119082800-119138000	Weak transcription	Small Intestine	intestine
5	chr3:119085200-119139000	Strong transcription	Cortex derived primary cultured neurospheres	brain
6	chr3:119088000-119134200	Weak transcription	NHDF-Ad	bronchial
7	chr3:119097000-119132600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr3:119098000-119136800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr3:119098400-119138200	Strong transcription	Adipose Nuclei	Adipose
10	chr3:119098600-119137400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr3:119100000-119132600	Weak transcription	Primary B cells from cord blood	blood
12	chr3:119102600-119133200	Weak transcription	NHLF	lung
13	chr3:119102600-119134800	Weak transcription	Primary hematopoietic stem cells	blood
14	chr3:119106400-119131200	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr3:119106800-119137400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr3:119109200-119136400	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr3:119109400-119130800	Strong transcription	Osteobl	bone
18	chr3:119110200-119140800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr3:119110400-119132200	Weak transcription	Brain Substantia Nigra	brain
20	chr3:119111800-119132600	Weak transcription	Thymus	Thymus
21	chr3:119112000-119132600	Weak transcription	Fetal Intestine Small	intestine
22	chr3:119112000-119132600	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr3:119112000-119147400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr3:119112200-119138800	Weak transcription	Colonic Mucosa	Colon
25	chr3:119112400-119132800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr3:119113200-119140400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr3:119113400-119138000	Strong transcription	Fetal Stomach	stomach
28	chr3:119114600-119132200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr3:119116400-119132400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr3:119116600-119133400	Strong transcription	Left Ventricle	heart
31	chr3:119118600-119133200	Weak transcription	Fetal Intestine Large	intestine
32	chr3:119119000-119138800	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr3:119121200-119132800	Weak transcription	Pancreas	Pancrea
34	chr3:119121200-119150000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr3:119121400-119132400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr3:119121400-119132600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr3:119121400-119135800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr3:119121400-119136000	Weak transcription	Esophagus	oesophagus
39	chr3:119123000-119136200	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr3:119123400-119132600	Weak transcription	Brain Hippocampus Middle	brain
41	chr3:119124400-119132600	Weak transcription	Gastric	stomach
42	chr3:119124400-119134400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr3:119124600-119135000	Weak transcription	Brain Angular Gyrus	brain
44	chr3:119125600-119132600	Weak transcription	HSMMtube	muscle
45	chr3:119126000-119130600	Strong transcription	NH-A	brain
46	chr3:119126200-119130800	Strong transcription	HUVEC	blood vessel
47	chr3:119127000-119130600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr3:119127000-119135200	Strong transcription	Fetal Muscle Leg	muscle
49	chr3:119127200-119138200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
50	chr3:119127400-119131400	Strong transcription	Lung	lung

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