Variant report

Variant	rs6779005
Chromosome Location	chr3:120437864-120437865
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CUX1	chr3:120437763-120437871	GM12878	blood:	n/a	n/a

Variant related genes	Relation type
ENSG00000243257	TF binding region
ENSG00000240452	TF binding region

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11708525	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11708642	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11712360	0.83[ASN][1000 genomes]
rs11713594	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11714216	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11716584	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11718363	0.84[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs11719207	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs11719896	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11720353	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11720614	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs167722	0.83[CEU][hapmap]
rs17183618	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17184204	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17243218	0.81[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs17243933	0.83[ASN][1000 genomes]
rs2059331	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2229308	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2292170	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2877413	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34319994	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34565470	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs41365345	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs55663109	0.80[ASN][1000 genomes]
rs55697401	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55869122	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs56140323	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56267829	0.93[ASN][1000 genomes]
rs6438590	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6769985	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73183728	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73183730	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7637037	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7647895	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007557	chr3:119892894-120764353	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv536706	chr3:119892894-120764353	Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv829699	chr3:120308332-120484695	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
4	nsv869548	chr3:120320731-121076337	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
5	nsv916869	chr3:120360281-120973169	Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
6	nsv877378	chr3:120381530-120606438	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:120398200-120438000	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr3:120398800-120442200	Weak transcription	Fetal Muscle Leg	muscle
3	chr3:120402800-120456600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr3:120412800-120438000	Weak transcription	Fetal Intestine Small	intestine
5	chr3:120415000-120438000	Weak transcription	HepG2	liver
6	chr3:120416400-120460600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr3:120416600-120438000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr3:120416800-120460600	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr3:120417600-120456600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr3:120419000-120450800	Weak transcription	Brain Hippocampus Middle	brain
11	chr3:120422000-120438000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr3:120422000-120438000	Weak transcription	Fetal Stomach	stomach
13	chr3:120422000-120438000	Weak transcription	Fetal Thymus	thymus
14	chr3:120422000-120438000	Weak transcription	Left Ventricle	heart
15	chr3:120422200-120438000	Weak transcription	Adipose Nuclei	Adipose
16	chr3:120422200-120438000	Weak transcription	Fetal Kidney	kidney
17	chr3:120422200-120441000	Weak transcription	Fetal Muscle Trunk	muscle
18	chr3:120422200-120446800	Weak transcription	Ovary	ovary
19	chr3:120422400-120438000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr3:120422400-120444200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr3:120423000-120460200	Weak transcription	HUVEC	blood vessel
22	chr3:120423400-120438000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr3:120423400-120441000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr3:120423600-120438000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr3:120423600-120447200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr3:120424400-120438000	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr3:120424400-120446800	Weak transcription	Fetal Intestine Large	intestine
28	chr3:120424600-120450200	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr3:120424800-120438000	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr3:120425000-120438000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr3:120425000-120451200	Weak transcription	Primary hematopoietic stem cells	blood
32	chr3:120425000-120456600	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr3:120425600-120446600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr3:120428200-120438000	Weak transcription	Duodenum Mucosa	Duodenum
35	chr3:120428400-120446800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr3:120428400-120448000	Weak transcription	Osteobl	bone
37	chr3:120428600-120438000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr3:120428600-120449200	Weak transcription	Placenta	Placenta
39	chr3:120428800-120438000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr3:120428800-120438000	Weak transcription	Fetal Lung	lung
41	chr3:120428800-120440800	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr3:120429200-120456200	Weak transcription	Liver	Liver
43	chr3:120430000-120446600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr3:120434000-120438000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr3:120436600-120438000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr3:120436600-120438000	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr3:120436600-120438000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr3:120436600-120438000	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr3:120437000-120438000	Enhancers	Primary T cells from cord blood	blood
50	chr3:120437000-120438000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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