Variant report

Variant	rs3784554
Chromosome Location	chr15:56956079-56956080
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:56954012..56957476-chr15:56973562..56976021,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000137871	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10152127	0.97[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11071280	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11630168	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11633363	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11635333	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11636994	0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11638707	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11852277	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11856558	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11857388	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11857706	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12148500	0.98[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12438709	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12442018	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12442189	0.84[EUR][1000 genomes]
rs12591502	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12592389	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12593286	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12898760	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12903283	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12903336	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12903862	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12906830	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12908906	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12910442	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12911191	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12911381	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12916079	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17238845	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1979467	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1994081	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2170459	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2170463	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2279298	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2279299	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2414480	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28480089	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28620278	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3803457	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3929265	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4774244	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4774884	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4774886	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs559736	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7165831	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7168178	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7169454	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7174432	0.81[EUR][1000 genomes]
rs7178796	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7182187	0.83[ASN][1000 genomes]
rs8025391	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs8036217	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8041540	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8043223	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3422474	chr15:56867190-57244330	Strong transcription ZNF genes & repeats Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv1041239	chr15:56888945-56959028	Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56912800-56957000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr15:56916600-56990800	Weak transcription	Pancreas	Pancrea
3	chr15:56917600-56957000	Weak transcription	Brain Anterior Caudate	brain
4	chr15:56917800-56956800	Weak transcription	Colon Smooth Muscle	Colon
5	chr15:56917800-56959800	Weak transcription	Brain Angular Gyrus	brain
6	chr15:56917800-56990600	Weak transcription	Rectal Smooth Muscle	rectum
7	chr15:56917800-56990600	Weak transcription	NHLF	lung
8	chr15:56918400-56957200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr15:56919800-57016600	Weak transcription	Small Intestine	intestine
10	chr15:56922000-56958000	Weak transcription	Lung	lung
11	chr15:56924000-56990600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr15:56924000-56990800	Weak transcription	NHEK	skin
13	chr15:56924600-56957200	Weak transcription	HUVEC	blood vessel
14	chr15:56928400-56996800	Weak transcription	Gastric	stomach
15	chr15:56937400-57000200	Weak transcription	Colonic Mucosa	Colon
16	chr15:56938600-56968200	Weak transcription	HMEC	breast
17	chr15:56939200-56990800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr15:56939400-56986000	Weak transcription	Brain Substantia Nigra	brain
19	chr15:56941400-56960200	Weak transcription	Spleen	Spleen
20	chr15:56943600-56958000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr15:56944200-56959600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr15:56944400-56957600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr15:56944600-56964600	Weak transcription	K562	blood
24	chr15:56944800-56960800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr15:56944800-56962800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr15:56945200-56963200	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr15:56945800-56963000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr15:56945800-56990800	Weak transcription	Fetal Brain Male	brain
29	chr15:56946000-56957800	Weak transcription	Fetal Intestine Small	intestine
30	chr15:56946000-56990800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr15:56946200-56957400	Weak transcription	GM12878-XiMat	blood
32	chr15:56946200-56971000	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr15:56946200-56990800	Weak transcription	Right Ventricle	heart
34	chr15:56947000-56960200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr15:56947200-56957000	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr15:56948200-56961400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr15:56950200-56969200	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr15:56950400-56957000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr15:56950400-56965000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr15:56950600-56956400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr15:56950600-56957000	Weak transcription	HSMM	muscle
42	chr15:56950600-56967200	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr15:56951000-56956600	Weak transcription	Brain Germinal Matrix	brain
44	chr15:56951800-56960800	Strong transcription	Adipose Nuclei	Adipose
45	chr15:56952400-56960800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr15:56952800-56960800	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr15:56953000-56958600	Strong transcription	Fetal Muscle Trunk	muscle
48	chr15:56953000-56960800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr15:56953200-56959000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr15:56953200-56959800	Strong transcription	Liver	Liver

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