Variant report

Variant	rs818427
Chromosome Location	chr5:112221869-112221870
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:112221269..112223827-chr5:112227698..112230274,2	K562	blood:

Variant related genes	Relation type
ENSG00000270067	Chromatin interaction

Extended variants
information (count: 103 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:95)

rs_ID	r²[population]
rs1069061	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1093611	0.84[CEU][hapmap];0.87[EUR][1000 genomes]
rs1093677	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1441375	0.85[CEU][hapmap]
rs151976	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs151977	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs151978	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs153545	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs153546	0.96[CEU][hapmap];0.87[EUR][1000 genomes]
rs153548	0.84[CEU][hapmap];0.82[EUR][1000 genomes]
rs153550	0.84[EUR][1000 genomes]
rs153562	0.83[AMR][1000 genomes]
rs1661035	0.89[CEU][hapmap]
rs173466	0.80[AMR][1000 genomes]
rs193527	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2431238	0.85[CHB][hapmap]
rs2439591	0.84[CEU][hapmap]
rs2464805	0.84[CEU][hapmap]
rs2545162	0.88[CEU][hapmap]
rs2545163	0.88[CEU][hapmap];0.86[CHB][hapmap];0.81[ASN][1000 genomes]
rs2545166	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2545167	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2545169	0.88[CEU][hapmap];0.85[CHB][hapmap];0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs2545751	0.89[ASN][1000 genomes]
rs2909904	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs351767	0.91[EUR][1000 genomes]
rs351769	0.96[CEU][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs351770	0.85[CEU][hapmap];0.85[EUR][1000 genomes]
rs35726351	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs372492	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs380144	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs382260	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs386830	0.80[AMR][1000 genomes]
rs392907	0.89[CEU][hapmap];0.86[CHB][hapmap]
rs411356	0.88[CEU][hapmap]
rs419632	0.96[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs429427	0.88[CEU][hapmap];0.83[EUR][1000 genomes]
rs430665	0.84[CEU][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs431287	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs433429	0.80[AMR][1000 genomes]
rs434090	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs434157	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs438252	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs439456	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs442507	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs446567	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs448162	0.84[CEU][hapmap]
rs455412	0.87[CEU][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs455469	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs456313	0.96[CEU][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs458451	0.85[CEU][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs459102	0.90[EUR][1000 genomes]
rs459552	0.85[CHB][hapmap];0.83[ASN][1000 genomes]
rs460301	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs460832	0.84[CEU][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs461424	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs461866	0.85[CEU][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs463229	1.00[CEU][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs464002	0.88[CEU][hapmap]
rs464708	0.88[CEU][hapmap]
rs465454	0.96[CEU][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs468101	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs468610	0.83[EUR][1000 genomes]
rs468783	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs468854	0.84[EUR][1000 genomes]
rs469663	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs469727	0.84[CEU][hapmap];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs469760	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs469827	0.85[CEU][hapmap];0.84[EUR][1000 genomes]
rs481789	0.84[AMR][1000 genomes]
rs495794	0.96[CEU][hapmap];0.94[EUR][1000 genomes]
rs497844	0.84[CEU][hapmap];0.87[AMR][1000 genomes]
rs501250	0.85[CHB][hapmap];0.86[JPT][hapmap]
rs514763	0.92[CEU][hapmap];0.94[EUR][1000 genomes]
rs519397	0.96[CEU][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs544243	0.85[CHB][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs563556	0.85[CEU][hapmap];0.86[CHB][hapmap]
rs565453	0.87[AMR][1000 genomes]
rs565603	0.85[AMR][1000 genomes]
rs580237	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs698405	0.84[CEU][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs712662	0.84[CEU][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs712663	0.87[EUR][1000 genomes]
rs712664	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs712665	0.84[CEU][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs712666	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs712668	1.00[CEU][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs712671	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7213	0.96[CEU][hapmap];0.96[EUR][1000 genomes]
rs818423	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs818424	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs818425	0.96[CEU][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs818429	0.90[EUR][1000 genomes]
rs864682	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9011	0.96[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][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	esv33290	chr5:112110808-112238295	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv1029271	chr5:112113308-112325943	Strong transcription Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv529536	chr5:112174106-112269758	Genic enhancers Strong transcription Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv599394	chr5:112185491-112446323	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
5	nsv870231	chr5:112192379-112247084	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
6	nsv1029595	chr5:112197662-112242375	Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv1030103	chr5:112197662-112255712	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
8	nsv537863	chr5:112197662-112255712	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs818427	SRP19	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:112199000-112226000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:112200600-112242000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr5:112206400-112242800	Weak transcription	Fetal Brain Male	brain
4	chr5:112208200-112225800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr5:112209600-112225000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr5:112209600-112226400	Strong transcription	Fetal Muscle Trunk	muscle
7	chr5:112209600-112226800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr5:112209800-112224600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr5:112209800-112238600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:112210600-112225000	Strong transcription	Liver	Liver
11	chr5:112210800-112225000	Strong transcription	Duodenum Mucosa	Duodenum
12	chr5:112210800-112232400	Strong transcription	Primary B cells from peripheral blood	blood
13	chr5:112211200-112222600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr5:112211200-112240000	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr5:112211600-112256400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr5:112211800-112223400	Strong transcription	Rectal Mucosa Donor 29	rectum
17	chr5:112211800-112239200	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr5:112212200-112256400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr5:112212400-112225200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr5:112212400-112225400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr5:112212600-112251400	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr5:112213000-112223000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
23	chr5:112213000-112223200	Strong transcription	Fetal Lung	lung
24	chr5:112213000-112223200	Strong transcription	Stomach Smooth Muscle	stomach
25	chr5:112213000-112224600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr5:112213200-112222800	Strong transcription	Rectal Mucosa Donor 31	rectum
27	chr5:112213200-112223200	Strong transcription	Brain Germinal Matrix	brain
28	chr5:112213200-112223400	Strong transcription	Adipose Nuclei	Adipose
29	chr5:112213200-112223400	Strong transcription	Fetal Brain Female	brain
30	chr5:112213200-112229400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr5:112213600-112223000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr5:112213800-112225000	Strong transcription	Fetal Intestine Large	intestine
33	chr5:112214000-112223400	Strong transcription	HUES64 Cell Line	embryonic stem cell
34	chr5:112214000-112224400	Strong transcription	Cortex derived primary cultured neurospheres	brain
35	chr5:112214200-112232200	Strong transcription	Primary neutrophils fromperipheralblood	blood
36	chr5:112214800-112223400	Strong transcription	HUES48 Cell Line	embryonic stem cell
37	chr5:112214800-112223400	Strong transcription	Fetal Thymus	thymus
38	chr5:112214800-112226600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr5:112214800-112234800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr5:112215000-112223000	Strong transcription	Fetal Stomach	stomach
41	chr5:112215200-112223000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr5:112215200-112224800	Strong transcription	HUES6 Cell Line	embryonic stem cell
43	chr5:112215200-112255800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr5:112215400-112222600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
45	chr5:112215400-112223000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr5:112215400-112223200	Strong transcription	HMEC	breast
47	chr5:112215400-112223400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr5:112215400-112223400	Strong transcription	Placenta	Placenta
49	chr5:112215800-112222200	Strong transcription	H1 Cell Line	embryonic stem cell
50	chr5:112215800-112222800	Strong transcription	Esophagus	oesophagus

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links