Variant report

Variant	rs4737518
Chromosome Location	chr8:54631879-54631880
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:54631323..54633867-chr8:54635784..54637550,2	K562	blood:

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs1031980	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10435587	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11996300	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12056486	0.85[EUR][1000 genomes]
rs12056719	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12115070	0.82[AMR][1000 genomes]
rs12234972	0.87[EUR][1000 genomes]
rs1552148	0.87[EUR][1000 genomes]
rs16919507	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16919508	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16919522	0.83[EUR][1000 genomes]
rs16919534	0.81[EUR][1000 genomes]
rs16919537	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs16919541	0.90[EUR][1000 genomes]
rs16919563	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1872063	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1905061	0.85[EUR][1000 genomes]
rs2128150	0.83[EUR][1000 genomes]
rs2376011	0.81[EUR][1000 genomes]
rs3735831	0.87[EUR][1000 genomes]
rs3757954	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs41321146	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4236945	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4737554	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4737558	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4737753	0.86[ASN][1000 genomes]
rs4737761	0.86[ASN][1000 genomes]
rs4737764	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4737821	0.82[AMR][1000 genomes]
rs4737974	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4738027	0.84[EUR][1000 genomes]
rs4738470	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4738646	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4738701	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4738884	0.90[EUR][1000 genomes]
rs4738916	0.83[EUR][1000 genomes]
rs55682919	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56956173	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs56973376	0.83[EUR][1000 genomes]
rs57071607	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs57550901	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs58473841	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs58558817	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58970885	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61070518	0.84[EUR][1000 genomes]
rs6473893	0.81[ASN][1000 genomes]
rs6984257	0.84[EUR][1000 genomes]
rs6986372	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6987427	0.83[EUR][1000 genomes]
rs6988009	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6988082	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6988808	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6988812	0.84[EUR][1000 genomes]
rs6994851	0.81[ASN][1000 genomes]
rs6997003	0.84[EUR][1000 genomes]
rs6999454	0.83[EUR][1000 genomes]
rs7005696	0.88[ASN][1000 genomes]
rs7006934	0.88[ASN][1000 genomes]
rs7009705	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73587624	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs73587627	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs73680316	0.82[AMR][1000 genomes]
rs73680321	0.84[EUR][1000 genomes]
rs73682549	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73682551	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73682552	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73682555	0.83[EUR][1000 genomes]
rs73682570	0.87[EUR][1000 genomes]
rs7387704	0.86[AMR][1000 genomes]
rs7843701	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs900163	0.83[EUR][1000 genomes]
rs958268	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9643480	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9643819	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9643820	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758159	chr8:54474589-54737473	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv2759616	chr8:54474589-54737473	Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1021775	chr8:54631303-54827173	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv539621	chr8:54631303-54827173	Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:54613600-54634800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr8:54620800-54636200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:54620800-54636200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:54621400-54643600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr8:54622200-54632800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr8:54624200-54635800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr8:54624200-54640600	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr8:54624200-54643600	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr8:54624600-54639200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr8:54625000-54640000	Weak transcription	Fetal Thymus	thymus
11	chr8:54625000-54642000	Weak transcription	Brain Substantia Nigra	brain
12	chr8:54625200-54634600	Weak transcription	Pancreas	Pancrea
13	chr8:54625200-54635800	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr8:54625200-54639800	Weak transcription	Thymus	Thymus
15	chr8:54625200-54641200	Weak transcription	Brain Angular Gyrus	brain
16	chr8:54625200-54649000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr8:54625200-54649600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr8:54625400-54634000	Weak transcription	NHDF-Ad	bronchial
19	chr8:54625400-54634200	Weak transcription	Primary hematopoietic stem cells	blood
20	chr8:54625400-54634600	Weak transcription	Esophagus	oesophagus
21	chr8:54625400-54634800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr8:54625400-54634800	Weak transcription	Brain Cingulate Gyrus	brain
23	chr8:54625400-54634800	Weak transcription	Left Ventricle	heart
24	chr8:54625400-54636200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr8:54625400-54636200	Weak transcription	Aorta	Aorta
26	chr8:54625400-54639200	Weak transcription	Brain Anterior Caudate	brain
27	chr8:54625400-54639400	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr8:54625400-54639600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr8:54625400-54639600	Weak transcription	Fetal Lung	lung
30	chr8:54625400-54639800	Weak transcription	Fetal Intestine Large	intestine
31	chr8:54625400-54639800	Weak transcription	Fetal Muscle Trunk	muscle
32	chr8:54625400-54639800	Weak transcription	HMEC	breast
33	chr8:54625400-54639800	Weak transcription	NH-A	brain
34	chr8:54625400-54640000	Weak transcription	Duodenum Mucosa	Duodenum
35	chr8:54625400-54640600	Weak transcription	Fetal Brain Female	brain
36	chr8:54625400-54640600	Weak transcription	Psoas Muscle	Psoas
37	chr8:54625400-54640600	Weak transcription	Right Ventricle	heart
38	chr8:54625400-54640600	Weak transcription	NHLF	lung
39	chr8:54625400-54641800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr8:54625400-54641800	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr8:54625400-54641800	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr8:54625400-54642000	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr8:54625400-54642000	Weak transcription	Fetal Muscle Leg	muscle
44	chr8:54625400-54645200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr8:54625400-54645800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr8:54625400-54646800	Weak transcription	Fetal Kidney	kidney
47	chr8:54625400-54649400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr8:54625600-54634600	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr8:54625600-54635600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr8:54625600-54635800	Weak transcription	NHEK	skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links