Variant report

Variant	rs4737504
Chromosome Location	chr8:59540579-59540580
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs12334684	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2255834	0.92[CEU][hapmap];0.90[JPT][hapmap];0.83[YRI][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2279460	0.80[JPT][hapmap]
rs2279462	0.81[JPT][hapmap]
rs2634530	0.93[CEU][hapmap];0.91[JPT][hapmap];0.85[YRI][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2634531	0.82[CEU][hapmap];0.86[JPT][hapmap]
rs2634534	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2680897	0.93[CEU][hapmap];0.91[JPT][hapmap];0.95[YRI][hapmap];0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2680899	0.96[CEU][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2680901	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28819228	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2946578	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6985007	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6985643	0.88[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6987187	0.89[CEU][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7820921	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7836960	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7844231	0.81[JPT][hapmap]
rs901954	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv890938	chr8:59355053-59809785	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv890939	chr8:59471187-59544413	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases
3	nsv831325	chr8:59492580-59694443	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:59467400-59559400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr8:59498600-59548400	Weak transcription	Stomach Mucosa	stomach
3	chr8:59503000-59545400	Weak transcription	Esophagus	oesophagus
4	chr8:59507400-59561200	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr8:59507600-59545400	Weak transcription	Gastric	stomach
6	chr8:59508000-59545400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr8:59508200-59542200	Weak transcription	Aorta	Aorta
8	chr8:59508200-59542400	Weak transcription	Psoas Muscle	Psoas
9	chr8:59509000-59542200	Weak transcription	Brain Cingulate Gyrus	brain
10	chr8:59509000-59543000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr8:59509000-59560400	Weak transcription	Brain Substantia Nigra	brain
12	chr8:59509800-59542400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr8:59510200-59542400	Weak transcription	Lung	lung
14	chr8:59510200-59554800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr8:59510400-59551000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr8:59510400-59570200	Weak transcription	Colonic Mucosa	Colon
17	chr8:59512000-59542200	Weak transcription	Right Ventricle	heart
18	chr8:59512200-59542200	Weak transcription	NH-A	brain
19	chr8:59513000-59541600	Weak transcription	Brain Germinal Matrix	brain
20	chr8:59513000-59542000	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr8:59513000-59561200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr8:59520200-59542200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr8:59520600-59541600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr8:59520600-59554600	Weak transcription	HMEC	breast
25	chr8:59521000-59542800	Weak transcription	Hela-S3	cervix
26	chr8:59521800-59542200	Weak transcription	Colon Smooth Muscle	Colon
27	chr8:59521800-59542400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr8:59521800-59542400	Weak transcription	Rectal Smooth Muscle	rectum
29	chr8:59522000-59570200	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr8:59522200-59541400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr8:59522200-59542400	Weak transcription	HUVEC	blood vessel
32	chr8:59522200-59542800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr8:59522200-59545200	Weak transcription	Spleen	Spleen
34	chr8:59522400-59541800	Weak transcription	NHLF	lung
35	chr8:59524000-59542400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr8:59524200-59554400	Weak transcription	NHEK	skin
37	chr8:59525200-59542200	Weak transcription	Stomach Smooth Muscle	stomach
38	chr8:59525400-59541000	Weak transcription	HepG2	liver
39	chr8:59526600-59542400	Weak transcription	Fetal Heart	heart
40	chr8:59527200-59542200	Weak transcription	Brain Angular Gyrus	brain
41	chr8:59527400-59542200	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr8:59529200-59542600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr8:59529400-59554600	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr8:59529600-59543000	Weak transcription	HSMM	muscle
45	chr8:59531800-59542200	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr8:59532000-59543800	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr8:59532000-59545600	Weak transcription	NHDF-Ad	bronchial
48	chr8:59533000-59542200	Weak transcription	Brain Anterior Caudate	brain
49	chr8:59533600-59542400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr8:59533800-59553000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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