Variant report

Variant	rs202162
Chromosome Location	chr7:101635248-101635249
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:101635097..101635843-chr7:101647196..101647966,2	MCF-7	breast:
2	chr7:101634892..101635843-chr7:101647115..101648070,5	MCF-7	breast:
3	chr7:101624015..101626714-chr7:101633341..101635563,2	MCF-7	breast:
4	chr7:101627337..101631221-chr7:101631346..101635612,7	MCF-7	breast:
5	chr7:101634157..101637054-chr7:101638722..101641195,2	MCF-7	breast:
6	chr7:101630321..101633242-chr7:101633881..101635594,2	K562	blood:

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs202154	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs202155	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs202156	1.00[ASN][1000 genomes]
rs202157	0.83[ASN][1000 genomes]
rs202158	1.00[ASN][1000 genomes]
rs202159	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024319	chr7:101368299-101668159	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	nsv539047	chr7:101368299-101668159	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv1020372	chr7:101420819-101718950	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	nsv482846	chr7:101539981-101707666	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv888827	chr7:101562674-101650302	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv482521	chr7:101604002-101718950	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv831080	chr7:101629121-101718950	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv981839	chr7:101632578-101663728	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101578200-101671200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr7:101597000-101642000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr7:101614400-101646400	Weak transcription	Fetal Brain Female	brain
4	chr7:101620200-101642000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr7:101622200-101635600	Weak transcription	Pancreas	Pancrea
6	chr7:101625600-101635400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr7:101625600-101635400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr7:101627000-101647400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr7:101627000-101671200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr7:101628000-101651600	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr7:101629000-101651600	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr7:101629600-101641400	Weak transcription	Brain Hippocampus Middle	brain
13	chr7:101630000-101638000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr7:101630000-101641000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr7:101630000-101641200	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr7:101630000-101641400	Weak transcription	Aorta	Aorta
17	chr7:101630000-101668000	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr7:101630400-101635400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr7:101630400-101640000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr7:101630400-101641200	Weak transcription	Stomach Smooth Muscle	stomach
21	chr7:101630400-101643800	Weak transcription	Right Atrium	heart
22	chr7:101630400-101646600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr7:101630600-101635600	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr7:101630600-101635600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr7:101630600-101639400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr7:101630600-101641200	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr7:101630600-101641200	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr7:101630600-101641400	Weak transcription	Psoas Muscle	Psoas
29	chr7:101630600-101641400	Weak transcription	Spleen	Spleen
30	chr7:101630600-101641600	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr7:101630600-101642000	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr7:101630600-101642000	Weak transcription	Rectal Smooth Muscle	rectum
33	chr7:101630800-101635600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr7:101630800-101637800	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr7:101630800-101652400	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr7:101631000-101635600	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr7:101631000-101644000	Weak transcription	Esophagus	oesophagus
38	chr7:101632000-101639000	Weak transcription	Right Ventricle	heart
39	chr7:101632000-101641400	Weak transcription	Fetal Heart	heart
40	chr7:101632400-101641400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr7:101632600-101640000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr7:101632800-101635400	Weak transcription	Placenta	Placenta
43	chr7:101632800-101639400	Weak transcription	Left Ventricle	heart
44	chr7:101633000-101640200	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr7:101633000-101646600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr7:101633200-101649000	Weak transcription	Lung	lung
47	chr7:101633400-101651400	Weak transcription	Gastric	stomach
48	chr7:101633600-101641000	Weak transcription	Fetal Muscle Leg	muscle
49	chr7:101633600-101641400	Weak transcription	Fetal Intestine Large	intestine
50	chr7:101634200-101639400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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