Variant report

Variant	rs73718120
Chromosome Location	chr7:112504741-112504742
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:112503704..112506152-chr7:112507913..112510486,2	MCF-7	breast:
2	chr7:112497079..112499499-chr7:112502379..112504783,2	K562	blood:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10233800	1.00[EUR][1000 genomes]
rs10236439	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10236707	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10237085	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10240478	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10241725	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10247997	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10252311	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10259048	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10263057	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10269437	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10277476	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10279386	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10280036	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10280117	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10441329	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28378392	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28542840	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28589798	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28634829	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28832579	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs500280	1.00[EUR][1000 genomes]
rs59569539	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61680362	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73718121	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73718123	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73718124	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73718131	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73718132	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73718133	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73718138	0.87[AMR][1000 genomes]
rs73718141	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9648966	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][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	nsv531436	chr7:111856171-112585407	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	105 gene(s)	inside rSNPs	diseases
2	esv1794529	chr7:112400060-112588376	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv5905	chr7:112445425-112521797	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
4	esv2754368	chr7:112483049-112588049	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv2758131	chr7:112492127-112768628	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	esv2759556	chr7:112492127-112768628	Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:112468600-112550000	Weak transcription	Aorta	Aorta
2	chr7:112469800-112529000	Weak transcription	Brain Anterior Caudate	brain
3	chr7:112470800-112506800	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr7:112470800-112533200	Weak transcription	HSMM	muscle
5	chr7:112471800-112511200	Weak transcription	HSMMtube	muscle
6	chr7:112471800-112545200	Weak transcription	Ovary	ovary
7	chr7:112472000-112506400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr7:112472000-112524600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:112472200-112513200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr7:112472200-112517800	Weak transcription	Osteobl	bone
11	chr7:112472600-112533200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr7:112472800-112505400	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr7:112478400-112506400	Weak transcription	Primary B cells from peripheral blood	blood
14	chr7:112486200-112506400	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr7:112490800-112533000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr7:112491200-112508600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr7:112492200-112506400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr7:112492600-112505000	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr7:112492600-112508800	Weak transcription	Dnd41	blood
20	chr7:112493800-112507800	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr7:112493800-112509200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr7:112494200-112508600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr7:112494200-112532400	Weak transcription	Primary T cells fromperipheralblood	blood
24	chr7:112494400-112506600	Weak transcription	Adipose Nuclei	Adipose
25	chr7:112494400-112506600	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr7:112494400-112508800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr7:112495600-112508400	Weak transcription	Right Ventricle	heart
28	chr7:112495600-112515000	Weak transcription	Pancreas	Pancrea
29	chr7:112495800-112508400	Weak transcription	Fetal Intestine Large	intestine
30	chr7:112496200-112509000	Weak transcription	Spleen	Spleen
31	chr7:112496200-112533400	Weak transcription	Stomach Smooth Muscle	stomach
32	chr7:112496600-112506400	Weak transcription	Left Ventricle	heart
33	chr7:112496600-112506400	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr7:112498000-112508600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr7:112498000-112508600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr7:112498000-112515000	Weak transcription	Gastric	stomach
37	chr7:112498200-112505600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr7:112498200-112506400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr7:112498200-112508800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr7:112499200-112509200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr7:112499400-112517600	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr7:112499600-112518000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr7:112500600-112506400	Weak transcription	Psoas Muscle	Psoas
44	chr7:112500600-112521200	Weak transcription	Thymus	Thymus
45	chr7:112501400-112518000	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr7:112502200-112509200	Weak transcription	Esophagus	oesophagus
47	chr7:112502400-112504800	Weak transcription	Fetal Stomach	stomach
48	chr7:112502600-112513200	Weak transcription	Primary B cells from cord blood	blood
49	chr7:112502800-112504800	Weak transcription	Fetal Intestine Small	intestine
50	chr7:112503400-112506600	Weak transcription	Fetal Lung	lung

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