Variant report

Variant	rs371581766
Chromosome Location	chr7:47707756-47707757
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:47704100..47706174-chr7:47707596..47709114,2	MCF-7	breast:
2	chr7:47672802..47676039-chr7:47707333..47710089,3	MCF-7	breast:
3	chr7:47620142..47622766-chr7:47707651..47710546,2	MCF-7	breast:
4	chr7:47685575..47687990-chr7:47705109..47707807,2	MCF-7	breast:
5	chr7:47662894..47665342-chr7:47707411..47709847,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000136205	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

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	nsv1026223	chr7:47560728-48243287	Genic enhancers Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv888003	chr7:47694270-47907214	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	esv3477663	chr7:47706827-47711425	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv3477665	chr7:47706827-47711425	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1024392	chr7:47707023-47758976	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv3413769	chr7:47707627-47710525	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:47695000-47711000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:47700000-47708800	Weak transcription	Spleen	Spleen
3	chr7:47701000-47708800	Weak transcription	Right Ventricle	heart
4	chr7:47701600-47708400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr7:47701600-47708800	Weak transcription	Fetal Kidney	kidney
6	chr7:47701600-47709000	Weak transcription	Lung	lung
7	chr7:47701800-47707800	Weak transcription	Primary B cells from cord blood	blood
8	chr7:47702600-47708200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr7:47703600-47708800	Weak transcription	Psoas Muscle	Psoas
10	chr7:47703800-47708600	Weak transcription	Duodenum Mucosa	Duodenum
11	chr7:47703800-47708600	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr7:47703800-47708800	Weak transcription	Liver	Liver
13	chr7:47703800-47709000	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr7:47704600-47710400	Weak transcription	Fetal Lung	lung
15	chr7:47705000-47708800	Weak transcription	Fetal Muscle Leg	muscle
16	chr7:47705200-47709000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr7:47705800-47708000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr7:47706000-47721600	Enhancers	Placenta	Placenta
19	chr7:47706200-47708800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:47706200-47709000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr7:47706400-47708600	Weak transcription	A549	lung
22	chr7:47706600-47708600	Weak transcription	Fetal Thymus	thymus
23	chr7:47706600-47708800	Weak transcription	Pancreas	Pancrea
24	chr7:47706600-47708800	Weak transcription	NHDF-Ad	bronchial
25	chr7:47706600-47709000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr7:47706600-47709000	Weak transcription	Fetal Intestine Small	intestine
27	chr7:47706800-47708600	Weak transcription	Aorta	Aorta
28	chr7:47706800-47708800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr7:47706800-47708800	Weak transcription	HepG2	liver
30	chr7:47706800-47708800	Weak transcription	HSMMtube	muscle
31	chr7:47706800-47708800	Weak transcription	NH-A	brain
32	chr7:47706800-47709000	Weak transcription	NHLF	lung
33	chr7:47706800-47709200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr7:47707000-47708400	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr7:47707200-47708400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr7:47707200-47708600	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr7:47707200-47708600	Weak transcription	HSMM	muscle
38	chr7:47707200-47708800	Weak transcription	Osteobl	bone
39	chr7:47707400-47708400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr7:47707400-47708800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr7:47707400-47713000	Weak transcription	Fetal Intestine Large	intestine
42	chr7:47707600-47708600	Weak transcription	Primary hematopoietic stem cells	blood
43	chr7:47707600-47714400	Enhancers	Primary B cells from peripheral blood	blood

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