Variant report

Variant	rs72783159
Chromosome Location	chr10:50233474-50233475
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10218854	0.90[EUR][1000 genomes]
rs17011603	0.92[EUR][1000 genomes]
rs17011698	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17011795	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17011910	0.85[EUR][1000 genomes]
rs17700453	0.95[EUR][1000 genomes]
rs1913524	0.95[EUR][1000 genomes]
rs2137918	0.95[EUR][1000 genomes]
rs2137919	1.00[EUR][1000 genomes]
rs2244085	1.00[EUR][1000 genomes]
rs2244704	0.88[EUR][1000 genomes]
rs2254632	1.00[EUR][1000 genomes]
rs2466749	1.00[EUR][1000 genomes]
rs2466750	1.00[EUR][1000 genomes]
rs4012668	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41301107	0.87[EUR][1000 genomes]
rs4838361	0.92[EUR][1000 genomes]
rs4838362	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4838364	0.90[EUR][1000 genomes]
rs4838368	0.85[EUR][1000 genomes]
rs4838440	0.95[EUR][1000 genomes]
rs4838445	0.90[EUR][1000 genomes]
rs4838459	0.87[EUR][1000 genomes]
rs56192862	0.83[EUR][1000 genomes]
rs57328384	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs58487442	0.92[EUR][1000 genomes]
rs59461690	0.83[EUR][1000 genomes]
rs61167870	0.89[EUR][1000 genomes]
rs61848150	0.89[EUR][1000 genomes]
rs61848154	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61848421	0.89[EUR][1000 genomes]
rs61848427	0.85[EUR][1000 genomes]
rs61848428	0.85[EUR][1000 genomes]
rs61848429	0.85[EUR][1000 genomes]
rs61848430	0.85[EUR][1000 genomes]
rs61848432	0.83[EUR][1000 genomes]
rs61850676	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61850680	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6537495	0.90[EUR][1000 genomes]
rs6537500	0.83[EUR][1000 genomes]
rs7069441	0.90[EUR][1000 genomes]
rs7070829	0.85[EUR][1000 genomes]
rs7078930	0.85[EUR][1000 genomes]
rs7080670	0.90[EUR][1000 genomes]
rs7094220	0.90[EUR][1000 genomes]
rs7096516	0.90[EUR][1000 genomes]
rs7101339	0.90[EUR][1000 genomes]
rs72785049	0.92[EUR][1000 genomes]
rs7393292	0.89[EUR][1000 genomes]
rs7897563	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7899437	0.92[EUR][1000 genomes]
rs7905794	0.81[EUR][1000 genomes]
rs7915922	0.90[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831866	chr10:50165180-50335276	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50218600-50238200	Weak transcription	Esophagus	oesophagus
2	chr10:50220400-50233600	Weak transcription	Gastric	stomach
3	chr10:50222000-50233800	Weak transcription	Lung	lung
4	chr10:50222800-50279000	Weak transcription	Brain Cingulate Gyrus	brain
5	chr10:50223000-50254200	Weak transcription	NHDF-Ad	bronchial
6	chr10:50224400-50258200	Weak transcription	Brain Anterior Caudate	brain
7	chr10:50224600-50244800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr10:50227800-50237400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr10:50227800-50238800	Weak transcription	HSMMtube	muscle
10	chr10:50227800-50243200	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr10:50231400-50233600	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr10:50231400-50233800	Enhancers	Skeletal Muscle Female	skeletal muscle
13	chr10:50231400-50234000	Genic enhancers	Fetal Muscle Leg	muscle
14	chr10:50231400-50234400	Enhancers	Ovary	ovary
15	chr10:50231600-50234000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr10:50231600-50234200	Enhancers	Fetal Intestine Small	intestine
17	chr10:50232200-50234000	Enhancers	Placenta	Placenta
18	chr10:50232200-50234000	Enhancers	Left Ventricle	heart
19	chr10:50232200-50241800	Weak transcription	Fetal Kidney	kidney
20	chr10:50232400-50279200	Weak transcription	Brain Hippocampus Middle	brain
21	chr10:50232600-50233800	Enhancers	Fetal Intestine Large	intestine
22	chr10:50232600-50235000	Weak transcription	Brain Angular Gyrus	brain
23	chr10:50232600-50245000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr10:50232800-50233800	Weak transcription	Aorta	Aorta
25	chr10:50232800-50237000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr10:50232800-50242000	Weak transcription	Brain Substantia Nigra	brain
27	chr10:50232800-50247800	Weak transcription	Right Atrium	heart
28	chr10:50232800-50255400	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr10:50233000-50236600	Weak transcription	Adipose Nuclei	Adipose
30	chr10:50233000-50237400	Weak transcription	Stomach Smooth Muscle	stomach
31	chr10:50233000-50239800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr10:50233000-50266000	Weak transcription	Colon Smooth Muscle	Colon
33	chr10:50233200-50233800	Enhancers	Right Ventricle	heart
34	chr10:50233200-50238200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr10:50233400-50233600	Flanking Active TSS	HepG2	liver
36	chr10:50233400-50233800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr10:50233400-50233800	Enhancers	Spleen	Spleen
38	chr10:50233400-50234000	Enhancers	Liver	Liver
39	chr10:50233400-50234800	Genic enhancers	Fetal Muscle Trunk	muscle
40	chr10:50233400-50235800	Strong transcription	Fetal Stomach	stomach
41	chr10:50233400-50241600	Weak transcription	Fetal Lung	lung

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