Variant report

Variant	rs62554850
Chromosome Location	chr9:93568122-93568123
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:93562623..93567761-chr9:93568030..93571323,5	K562	blood:
2	chr9:93561656..93565893-chr9:93566155..93575937,12	MCF-7	breast:
3	chr9:93566479..93568925-chr9:93571004..93572513,2	MCF-7	breast:
4	chr9:93566130..93568297-chr9:93575356..93577751,2	K562	blood:

Variant related genes	Relation type
ENSG00000165025	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10821508	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10993696	0.99[ASN][1000 genomes]
rs10993697	0.88[ASN][1000 genomes]
rs10993698	0.88[ASN][1000 genomes]
rs11788207	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12551275	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12553524	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1460834	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1460835	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16906825	0.99[ASN][1000 genomes]
rs17488335	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2042983	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2042984	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2115484	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2115485	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2126051	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2162977	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs290233	0.89[ASN][1000 genomes]
rs290239	0.90[ASN][1000 genomes]
rs290240	0.99[ASN][1000 genomes]
rs290241	0.99[ASN][1000 genomes]
rs3789890	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3789891	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3789892	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3789893	0.89[ASN][1000 genomes]
rs4002564	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4002565	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4002566	0.99[ASN][1000 genomes]
rs4501705	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56955255	0.89[ASN][1000 genomes]
rs58668584	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61495376	0.99[ASN][1000 genomes]
rs7020331	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7032733	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7046173	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7046193	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7046316	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72729008	0.89[ASN][1000 genomes]
rs72729009	0.89[ASN][1000 genomes]
rs72729010	0.87[ASN][1000 genomes]
rs72729013	0.88[ASN][1000 genomes]
rs72742789	0.81[ASN][1000 genomes]
rs72746350	0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046989	chr9:93353987-93800416	Transcr. at gene 5' and 3' Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv893567	chr9:93519280-93609668	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv831652	chr9:93527411-93696923	Bivalent Enhancer Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv893568	chr9:93539879-93774385	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv893569	chr9:93552550-93587089	Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1038685	chr9:93556174-93685729	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	esv1813758	chr9:93557698-93573095	Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	esv275555	chr9:93565999-93570451	Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs62554850	SYK	Cis_1M	lymphoblastoid	RTeQTL
rs62554850	SYK	cis	Thyroid	GTEx

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:93564600-93568600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr9:93564600-93572000	Weak transcription	Lung	lung
3	chr9:93565000-93569400	Weak transcription	Primary T cells from cord blood	blood
4	chr9:93565000-93609000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr9:93565200-93568400	Flanking Active TSS	Primary B cells from cord blood	blood
6	chr9:93565400-93570600	Weak transcription	HMEC	breast
7	chr9:93565400-93570800	Weak transcription	Placenta	Placenta
8	chr9:93565400-93577000	Weak transcription	Colonic Mucosa	Colon
9	chr9:93566800-93568400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr9:93566800-93569200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr9:93567000-93572800	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr9:93567200-93568600	Flanking Active TSS	GM12878-XiMat	blood
13	chr9:93567400-93570000	Enhancers	Fetal Stomach	stomach
14	chr9:93567600-93571000	Weak transcription	Fetal Intestine Small	intestine
15	chr9:93567600-93573000	Weak transcription	NHEK	skin
16	chr9:93567800-93568200	Active TSS	Thymus	Thymus
17	chr9:93567800-93568400	Enhancers	Rectal Mucosa Donor 29	rectum
18	chr9:93567800-93569000	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr9:93567800-93569000	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr9:93567800-93569200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr9:93567800-93569200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr9:93567800-93569200	Weak transcription	Duodenum Mucosa	Duodenum
23	chr9:93567800-93569200	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr9:93567800-93569200	Weak transcription	Spleen	Spleen
25	chr9:93567800-93569400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr9:93567800-93569400	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr9:93567800-93569600	Weak transcription	Small Intestine	intestine
28	chr9:93567800-93570800	Weak transcription	Pancreas	Pancrea
29	chr9:93567800-93570800	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr9:93567800-93572000	Weak transcription	Esophagus	oesophagus
31	chr9:93567800-93572000	Weak transcription	K562	blood
32	chr9:93567800-93572400	Weak transcription	Stomach Mucosa	stomach
33	chr9:93567800-93584800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr9:93567800-93584800	Weak transcription	Fetal Intestine Large	intestine
35	chr9:93567800-93597400	Weak transcription	Gastric	stomach
36	chr9:93568000-93568400	Weak transcription	Fetal Thymus	thymus
37	chr9:93568000-93568600	Enhancers	Primary B cells from peripheral blood	blood
38	chr9:93568000-93569200	Enhancers	Primary hematopoietic stem cells	blood
39	chr9:93568000-93569800	Weak transcription	Fetal Kidney	kidney

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links