Variant report

Variant	rs7985262
Chromosome Location	chr13:52997161-52997162
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	chr13:52995666..52997611-chr13:53023270..53025763,2	K562	blood:

Variant related genes	Relation type
ENSG00000136100	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1056335	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11148252	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11618716	0.91[ASN][1000 genomes]
rs11620062	0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13431	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1815669	0.87[ASN][1000 genomes]
rs3803262	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3803264	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3886077	0.88[ASN][1000 genomes]
rs4286007	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4884320	0.99[ASN][1000 genomes]
rs4884354	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4884452	0.87[ASN][1000 genomes]
rs4885953	0.89[ASN][1000 genomes]
rs4886018	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4886077	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61958050	1.00[ASN][1000 genomes]
rs6561665	0.83[ASN][1000 genomes]
rs7323666	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7333451	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7336679	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7399631	0.86[ASN][1000 genomes]
rs7987115	0.88[ASN][1000 genomes]
rs8001624	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9379	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9526913	0.89[ASN][1000 genomes]
rs9526914	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9536046	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9536048	0.93[ASN][1000 genomes]
rs9536052	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9536069	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9568728	0.87[ASN][1000 genomes]
rs9596643	0.80[ASN][1000 genomes]
rs9596648	0.85[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	nsv934070	chr13:52362588-53174923	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
2	nsv1040931	chr13:52564792-53350914	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
3	nsv541773	chr13:52564792-53350914	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv428288	chr13:52728370-53068132	Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	nsv900084	chr13:52835231-53119704	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
6	esv1838257	chr13:52971893-53231454	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs7985262	CKAP2	cis	Thyroid	GTEx
rs7985262	CKAP2	cis	Adipose Subcutaneous	GTEx
rs7985262	CKAP2	cis	Artery Tibial	GTEx
rs7985262	VPS36	cis	Esophagus Mucosa	GTEx
rs7985262	CKAP2	cis	Skin Sun Exposed Lower leg	GTEx
rs7985262	CKAP2	cis	Heart Left Ventricle	GTEx
rs7985262	CKAP2	cis	Muscle Skeletal	GTEx
rs7985262	CKAP2	cis	Nerve Tibial	GTEx

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52980200-53002000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr13:52980200-53021600	Weak transcription	Small Intestine	intestine
3	chr13:52981000-53022800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr13:52982800-53012600	Weak transcription	Fetal Brain Male	brain
5	chr13:52983600-53000800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr13:52983800-53016600	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr13:52984000-53002400	Weak transcription	Hela-S3	cervix
8	chr13:52984400-53023400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr13:52984800-53013400	Strong transcription	Dnd41	blood
10	chr13:52985000-53000600	Strong transcription	Duodenum Smooth Muscle	Duodenum
11	chr13:52985000-53001400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr13:52985000-53002400	Weak transcription	K562	blood
13	chr13:52985000-53013400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr13:52985000-53017400	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr13:52985000-53019400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr13:52985600-53000800	Strong transcription	Fetal Muscle Trunk	muscle
17	chr13:52985600-53004000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr13:52985600-53010600	Strong transcription	Rectal Mucosa Donor 29	rectum
19	chr13:52985800-53001400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
20	chr13:52986000-53017000	Strong transcription	Primary B cells from peripheral blood	blood
21	chr13:52986200-53001600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr13:52986600-53013400	Strong transcription	Liver	Liver
23	chr13:52986800-53002400	Weak transcription	Stomach Mucosa	stomach
24	chr13:52987000-53004200	Strong transcription	Primary T helper cells PMA-I stimulated	--
25	chr13:52987200-53023600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
26	chr13:52988000-53001200	Strong transcription	Skeletal Muscle Female	skeletal muscle
27	chr13:52988200-52999400	Strong transcription	Fetal Muscle Leg	muscle
28	chr13:52988200-53001200	Strong transcription	Stomach Smooth Muscle	stomach
29	chr13:52988400-53001400	Strong transcription	Fetal Thymus	thymus
30	chr13:52988800-53002600	Weak transcription	Psoas Muscle	Psoas
31	chr13:52988800-53010000	Weak transcription	Esophagus	oesophagus
32	chr13:52989000-53003400	Weak transcription	Gastric	stomach
33	chr13:52989000-53006000	Weak transcription	NHLF	lung
34	chr13:52989000-53015000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr13:52989000-53016200	Strong transcription	Adipose Nuclei	Adipose
36	chr13:52989000-53021600	Weak transcription	Fetal Heart	heart
37	chr13:52989000-53022800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr13:52989400-53003400	Weak transcription	Spleen	Spleen
39	chr13:52989400-53015000	Weak transcription	Lung	lung
40	chr13:52990400-52998600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr13:52990400-53002400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr13:52990400-53003000	Weak transcription	Brain Angular Gyrus	brain
43	chr13:52990600-53001400	Strong transcription	Osteobl	bone
44	chr13:52990800-53001600	Strong transcription	Fetal Intestine Small	intestine
45	chr13:52990800-53015000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr13:52991000-53000200	Strong transcription	Fetal Stomach	stomach
47	chr13:52991000-53007200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr13:52991200-53001400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr13:52991200-53017000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
50	chr13:52991400-52999600	Weak transcription	NHDF-Ad	bronchial

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