Variant report

Variant	rs73756267
Chromosome Location	chr5:52138990-52138991
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10038615	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10046016	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10513000	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10513001	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11949835	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11952083	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11956627	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12110170	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1478445	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16880353	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59192299	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60422098	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6860395	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6880226	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6884370	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6886404	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6894627	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6895807	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6896699	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73102285	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73754051	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73754052	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73754053	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73754054	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73754055	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73754057	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73756268	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73756272	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7704305	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][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	esv2754787	chr5:51688543-52193243	Enhancers Active TSS Genic enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv462187	chr5:51758804-52333420	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv598163	chr5:51758804-52333420	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
4	nsv471013	chr5:51779197-52339114	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
5	nsv830295	chr5:52084532-52257696	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv1032554	chr5:52126688-52174119	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:52130400-52141200	Weak transcription	Ovary	ovary
2	chr5:52133200-52141200	Weak transcription	Left Ventricle	heart
3	chr5:52133200-52143400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:52134200-52140800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr5:52134600-52140800	Weak transcription	Hela-S3	cervix
6	chr5:52134600-52141200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr5:52135000-52141200	Weak transcription	Esophagus	oesophagus
8	chr5:52135800-52145400	Weak transcription	Liver	Liver
9	chr5:52136200-52161400	Weak transcription	Duodenum Mucosa	Duodenum
10	chr5:52136400-52140200	Weak transcription	Stomach Smooth Muscle	stomach
11	chr5:52136400-52140400	Weak transcription	HUVEC	blood vessel
12	chr5:52136400-52140600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr5:52136400-52140600	Weak transcription	HSMMtube	muscle
14	chr5:52136400-52140800	Weak transcription	NH-A	brain
15	chr5:52136400-52140800	Weak transcription	Osteobl	bone
16	chr5:52136400-52141200	Weak transcription	Fetal Thymus	thymus
17	chr5:52136400-52141200	Weak transcription	Right Atrium	heart
18	chr5:52136400-52141800	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr5:52136800-52139800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr5:52136800-52140200	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr5:52137000-52140200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr5:52137000-52140200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr5:52137000-52140200	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr5:52137000-52140200	Weak transcription	NHLF	lung
25	chr5:52137000-52140600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr5:52137000-52140800	Weak transcription	Adipose Nuclei	Adipose
27	chr5:52137000-52140800	Weak transcription	NHDF-Ad	bronchial
28	chr5:52137000-52141000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr5:52137000-52141000	Weak transcription	HSMM	muscle
30	chr5:52137200-52140000	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr5:52137400-52139400	Weak transcription	Dnd41	blood
32	chr5:52137400-52140000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr5:52137400-52140000	Weak transcription	Fetal Lung	lung
34	chr5:52137400-52140600	Weak transcription	Fetal Stomach	stomach
35	chr5:52138000-52139400	Enhancers	Spleen	Spleen
36	chr5:52138000-52141200	Weak transcription	Aorta	Aorta
37	chr5:52138200-52139400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr5:52138200-52139400	Weak transcription	Rectal Smooth Muscle	rectum
39	chr5:52138200-52139400	Weak transcription	Small Intestine	intestine
40	chr5:52138200-52140000	Weak transcription	Fetal Kidney	kidney
41	chr5:52138400-52141200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr5:52138600-52139000	Weak transcription	Colon Smooth Muscle	Colon

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