Variant report

Variant	rs3752449
Chromosome Location	chr3:50623193-50623194
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:50621137..50623770-chr3:50625680..50628111,2	K562	blood:
2	chr3:50613663..50623986-chr3:50635558..50652363,41	MCF-7	breast:
3	chr3:50619029..50623920-chr3:50628439..50631863,6	MCF-7	breast:
4	chr3:50607065..50611118-chr3:50617412..50623416,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000114738	Chromatin interaction
ENSG00000088543	Chromatin interaction
ENSG00000114737	Chromatin interaction

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs1077215	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1107312	0.80[ASN][1000 genomes]
rs12486143	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12486717	0.85[ASN][1000 genomes]
rs12487817	0.80[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12489607	0.87[ASN][1000 genomes]
rs12491440	0.87[ASN][1000 genomes]
rs12491812	0.89[ASN][1000 genomes]
rs12492093	0.87[ASN][1000 genomes]
rs12492540	0.87[ASN][1000 genomes]
rs12492982	0.88[ASN][1000 genomes]
rs12494094	0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12494326	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12494707	0.91[AMR][1000 genomes]
rs17050991	0.89[ASN][1000 genomes]
rs17050995	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs17051000	0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs17051043	0.87[ASN][1000 genomes]
rs17051045	0.87[ASN][1000 genomes]
rs17051403	0.80[ASN][1000 genomes]
rs1872184	0.98[ASN][1000 genomes]
rs1894459	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2035484	0.80[ASN][1000 genomes]
rs2076927	0.83[ASN][1000 genomes]
rs2170840	0.87[ASN][1000 genomes]
rs2227292	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2227293	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2239750	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2239751	0.98[ASN][1000 genomes]
rs2239752	0.98[ASN][1000 genomes]
rs2239753	0.98[ASN][1000 genomes]
rs2285090	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3749265	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs3792323	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3806706	0.81[ASN][1000 genomes]
rs4476497	0.90[ASN][1000 genomes]
rs4640555	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4688705	0.87[ASN][1000 genomes]
rs4688707	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4688709	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4688710	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4688713	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4688715	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4688716	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56170012	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs56856095	0.82[ASN][1000 genomes]
rs57910827	0.87[ASN][1000 genomes]
rs58427389	0.87[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs58529408	0.80[ASN][1000 genomes]
rs59036236	0.85[ASN][1000 genomes]
rs60552073	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs60877431	0.86[ASN][1000 genomes]
rs61193866	0.88[ASN][1000 genomes]
rs61316441	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61574029	0.89[ASN][1000 genomes]
rs61613532	0.90[ASN][1000 genomes]
rs616689	0.93[ASN][1000 genomes]
rs6446208	0.86[ASN][1000 genomes]
rs650655	0.88[ASN][1000 genomes]
rs6766638	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6771348	0.90[ASN][1000 genomes]
rs6783922	0.90[ASN][1000 genomes]
rs6794155	0.85[ASN][1000 genomes]
rs728902	0.87[ASN][1000 genomes]
rs72938758	0.90[ASN][1000 genomes]
rs72942785	0.87[ASN][1000 genomes]
rs72942794	0.85[ASN][1000 genomes]
rs72944726	0.80[ASN][1000 genomes]
rs72944730	0.80[ASN][1000 genomes]
rs73835531	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs743753	0.98[ASN][1000 genomes]
rs745356	0.90[ASN][1000 genomes]
rs762889	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs808148	0.90[ASN][1000 genomes]
rs876103	0.88[ASN][1000 genomes]
rs876104	0.88[ASN][1000 genomes]
rs876105	0.88[ASN][1000 genomes]
rs9868889	0.90[ASN][1000 genomes]
rs9879397	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1821728	chr3:50156142-50657253	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
2	nsv1001993	chr3:50187646-50640808	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
3	esv3584502	chr3:50368278-50659741	Strong transcription Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
4	nsv432419	chr3:50388396-50637496	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	nsv1013225	chr3:50440826-50700448	Flanking Active TSS Enhancers Genic enhancers Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
6	nsv536566	chr3:50440826-50700448	Genic enhancers Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
7	nsv984540	chr3:50473691-50669310	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
8	nsv1012501	chr3:50483037-50679591	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
9	nsv536567	chr3:50483037-50679591	Bivalent Enhancer Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
10	nsv460533	chr3:50574213-50678151	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
11	nsv590273	chr3:50574213-50678151	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50607400-50628200	Weak transcription	Small Intestine	intestine
2	chr3:50607600-50628400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:50607800-50628200	Weak transcription	HSMMtube	muscle
4	chr3:50607800-50628600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr3:50608200-50624000	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr3:50608200-50628400	Weak transcription	A549	lung
7	chr3:50608200-50637400	Weak transcription	Fetal Kidney	kidney
8	chr3:50608400-50625600	Weak transcription	NHDF-Ad	bronchial
9	chr3:50610200-50623600	Strong transcription	Fetal Muscle Leg	muscle
10	chr3:50610200-50624400	Strong transcription	Fetal Stomach	stomach
11	chr3:50610200-50628000	Weak transcription	Stomach Mucosa	stomach
12	chr3:50610400-50623200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
13	chr3:50610400-50623200	Strong transcription	Stomach Smooth Muscle	stomach
14	chr3:50610400-50628400	Weak transcription	HSMM	muscle
15	chr3:50610600-50627600	Weak transcription	Primary hematopoietic stem cells	blood
16	chr3:50613400-50628000	Weak transcription	HMEC	breast
17	chr3:50616000-50625800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr3:50616000-50628600	Weak transcription	Colon Smooth Muscle	Colon
19	chr3:50617600-50626200	Enhancers	Liver	Liver
20	chr3:50617800-50628200	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr3:50618000-50623200	Strong transcription	Fetal Muscle Trunk	muscle
22	chr3:50618000-50628000	Weak transcription	Rectal Smooth Muscle	rectum
23	chr3:50618200-50626200	Enhancers	Right Ventricle	heart
24	chr3:50618200-50626800	Enhancers	Left Ventricle	heart
25	chr3:50618600-50623200	Enhancers	Right Atrium	heart
26	chr3:50619000-50627000	Enhancers	Psoas Muscle	Psoas
27	chr3:50619200-50623600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr3:50619200-50624200	Weak transcription	Brain Cingulate Gyrus	brain
29	chr3:50619400-50623600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr3:50619400-50625400	Enhancers	HepG2	liver
31	chr3:50619400-50628200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr3:50619400-50628200	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr3:50619600-50624400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr3:50619600-50624600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr3:50619600-50624600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr3:50619600-50624600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr3:50619600-50628400	Weak transcription	Brain Angular Gyrus	brain
38	chr3:50619800-50623400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr3:50619800-50628200	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr3:50620000-50623600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr3:50620000-50628600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr3:50620200-50623600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr3:50620200-50624000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr3:50620200-50624000	Weak transcription	Brain Hippocampus Middle	brain
45	chr3:50620200-50625800	Weak transcription	Primary B cells from peripheral blood	blood
46	chr3:50620200-50626000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr3:50620200-50626000	Weak transcription	NHEK	skin
48	chr3:50620200-50628200	Weak transcription	Fetal Heart	heart
49	chr3:50620400-50628000	Weak transcription	Primary B cells from cord blood	blood
50	chr3:50620400-50628200	Weak transcription	Sigmoid Colon	Sigmoid Colon

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