Variant report

Variant	rs1463790
Chromosome Location	chr13:97978704-97978705
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1316549	0.91[JPT][hapmap]
rs1553012	0.83[CHB][hapmap]
rs1553013	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1973419	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2011452	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2291785	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3782983	0.96[CEU][hapmap];0.90[CHB][hapmap];0.83[JPT][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4771270	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61974439	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6491350	0.96[CEU][hapmap];0.90[CHB][hapmap];0.83[JPT][hapmap];0.82[EUR][1000 genomes]
rs7318250	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7320865	1.00[CHB][hapmap];0.86[JPT][hapmap];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7338689	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7995199	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs949741	0.91[JPT][hapmap];0.86[AMR][1000 genomes]
rs9513235	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9513237	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9516902	0.91[JPT][hapmap];0.84[AMR][1000 genomes]
rs9516904	0.91[JPT][hapmap]
rs9516907	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9516914	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9556701	0.82[CHB][hapmap]
rs9556702	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9556706	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832694	chr13:97930561-98137882	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:97925800-97987200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr13:97942800-97995200	Weak transcription	Thymus	Thymus
3	chr13:97954400-97986200	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr13:97955000-97987000	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr13:97955200-97986800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr13:97959400-97988800	Weak transcription	Fetal Intestine Large	intestine
7	chr13:97961400-97987200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr13:97962000-97979200	Weak transcription	HUVEC	blood vessel
9	chr13:97962000-97991200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr13:97963000-97984400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr13:97965200-97985800	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr13:97965600-97988800	Weak transcription	Primary hematopoietic stem cells	blood
13	chr13:97965800-97987200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr13:97967000-97980400	Weak transcription	Fetal Thymus	thymus
15	chr13:97967400-97991400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr13:97969200-97979200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr13:97969400-97981600	Weak transcription	Spleen	Spleen
18	chr13:97969400-97981800	Weak transcription	Esophagus	oesophagus
19	chr13:97969600-97982000	Weak transcription	Primary B cells from cord blood	blood
20	chr13:97969600-97987200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr13:97969800-97986600	Weak transcription	Primary B cells from peripheral blood	blood
22	chr13:97971400-97979800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr13:97971400-97981800	Weak transcription	Gastric	stomach
24	chr13:97971600-97979800	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr13:97971600-97981600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr13:97971600-97991400	Weak transcription	Stomach Mucosa	stomach
27	chr13:97971800-97979800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr13:97971800-97980200	Weak transcription	Placenta	Placenta
29	chr13:97971800-97980600	Weak transcription	Pancreas	Pancrea
30	chr13:97971800-97981600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr13:97971800-97986400	Weak transcription	Primary T cells from cord blood	blood
32	chr13:97971800-97986400	Weak transcription	Aorta	Aorta
33	chr13:97971800-97986400	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr13:97971800-97987200	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr13:97971800-97987600	Weak transcription	Fetal Intestine Small	intestine
36	chr13:97971800-97987800	Weak transcription	Colonic Mucosa	Colon
37	chr13:97971800-97991800	Weak transcription	Small Intestine	intestine
38	chr13:97972000-97980000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr13:97972000-97987200	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr13:97972200-97980200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr13:97972400-97981800	Weak transcription	Liver	Liver
42	chr13:97972400-97986400	Weak transcription	Duodenum Mucosa	Duodenum
43	chr13:97973000-97979600	Enhancers	Brain Hippocampus Middle	brain
44	chr13:97973000-97983200	Enhancers	Brain Cingulate Gyrus	brain
45	chr13:97973200-97983400	Enhancers	Rectal Smooth Muscle	rectum
46	chr13:97974400-97979200	Weak transcription	A549	lung
47	chr13:97974600-97980200	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr13:97974800-97979800	Weak transcription	Fetal Heart	heart
49	chr13:97974800-97980400	Enhancers	Stomach Smooth Muscle	stomach
50	chr13:97975000-97980200	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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