Variant report

Variant	rs782637
Chromosome Location	chr2:55894247-55894248
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	chr2:55893661..55895607-chr2:55919705..55921512,2	K562	blood:
2	chr2:55891954..55894358-chr2:55898574..55900895,2	K562	blood:

Variant related genes	Relation type
ENSG00000138035	Chromatin interaction

Extended variants
information (count: 66 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10460508	0.94[ASW][hapmap];0.81[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.96[MEX][hapmap];0.94[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10496050	0.88[ASW][hapmap];0.97[GIH][hapmap];0.87[MEX][hapmap];0.82[MKK][hapmap];0.89[TSI][hapmap];1.00[YRI][hapmap]
rs1084522	0.82[ASW][hapmap];0.97[GIH][hapmap];0.83[JPT][hapmap];0.87[MEX][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap]
rs1084525	0.83[ASW][hapmap];0.89[CEU][hapmap];0.94[GIH][hapmap];0.83[JPT][hapmap];0.95[LWK][hapmap];0.92[MEX][hapmap];0.96[MKK][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs12329050	0.90[YRI][hapmap]
rs17278044	0.83[JPT][hapmap];1.00[YRI][hapmap]
rs17369191	0.90[YRI][hapmap]
rs1823893	1.00[YRI][hapmap]
rs1975487	0.81[CEU][hapmap];0.85[YRI][hapmap]
rs2586950	0.83[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs2586952	0.90[AFR][1000 genomes]
rs2586954	0.94[ASW][hapmap];0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.97[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2586969	1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap]
rs2586970	1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap]
rs2627765	0.94[ASW][hapmap];1.00[CHD][hapmap];0.92[JPT][hapmap];0.83[LWK][hapmap];0.92[MEX][hapmap];0.88[MKK][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2627766	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2627767	1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2627769	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2627772	0.97[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2627773	0.96[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2627775	0.88[ASW][hapmap];0.97[GIH][hapmap];0.83[JPT][hapmap];0.83[MEX][hapmap];0.83[MKK][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs2627776	0.82[CEU][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs2627777	0.86[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs2627779	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35504023	0.88[ASW][hapmap];0.97[GIH][hapmap];0.87[MEX][hapmap];0.82[MKK][hapmap];0.87[TSI][hapmap];1.00[YRI][hapmap]
rs4290693	0.88[ASW][hapmap];0.97[GIH][hapmap];0.82[MKK][hapmap];0.87[TSI][hapmap];1.00[YRI][hapmap]
rs4312532	0.95[YRI][hapmap]
rs62165255	0.82[AMR][1000 genomes]
rs6545506	0.88[ASW][hapmap];0.97[GIH][hapmap];0.87[MEX][hapmap];0.82[MKK][hapmap];0.87[TSI][hapmap];1.00[YRI][hapmap]
rs706548	0.82[GIH][hapmap];0.83[JPT][hapmap]
rs7582278	0.83[JPT][hapmap];1.00[YRI][hapmap]
rs7596377	0.91[YRI][hapmap]
rs782566	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs782567	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs782568	0.94[ASW][hapmap];0.82[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.96[MEX][hapmap];0.96[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs782572	0.92[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs782573	0.92[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs782579	0.86[ASN][1000 genomes]
rs782584	0.92[CEU][hapmap];0.97[GIH][hapmap];0.83[JPT][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];0.98[TSI][hapmap];0.86[YRI][hapmap];0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs782585	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs782586	0.88[ASW][hapmap];0.97[GIH][hapmap];0.83[JPT][hapmap];0.87[MEX][hapmap];0.87[TSI][hapmap];1.00[YRI][hapmap]
rs782588	0.94[GIH][hapmap];0.83[JPT][hapmap];0.87[MEX][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap]
rs782590	0.82[ASW][hapmap];0.94[GIH][hapmap];0.82[JPT][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap]
rs782595	0.83[JPT][hapmap];1.00[YRI][hapmap]
rs782599	1.00[YRI][hapmap]
rs782602	0.88[ASW][hapmap];0.94[GIH][hapmap];0.83[JPT][hapmap];0.87[MEX][hapmap];0.86[MKK][hapmap];0.87[TSI][hapmap];1.00[YRI][hapmap]
rs782606	0.94[ASW][hapmap];0.82[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.97[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs782619	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs782622	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs782629	1.00[ASW][hapmap];0.96[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs782630	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs782632	0.96[CEU][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs782633	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs782634	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs782641	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs782642	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs782652	0.88[ASW][hapmap];0.82[CEU][hapmap];0.97[GIH][hapmap];0.83[JPT][hapmap];0.83[LWK][hapmap];0.96[MEX][hapmap];0.89[MKK][hapmap];0.93[TSI][hapmap];0.95[YRI][hapmap];0.83[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs809732	0.92[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs935177	0.90[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv520581	chr2:55622825-55903016	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv531374	chr2:55653723-56299784	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
3	nsv834080	chr2:55741036-55927928	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
4	esv2757798	chr2:55747239-55981074	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	esv2759050	chr2:55747239-55981074	Strong transcription Active TSS Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
6	nsv1008452	chr2:55809191-55987274	Strong transcription Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
7	esv2762645	chr2:55892248-55963418	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs782637	ENSG00000138035	cis	multi-tissue	Pritchard
rs782637	PNPT1	Cis_1M	lymphoblastoid	RTeQTL
rs782637	CCDC104	cis	parietal	SCAN
rs782637	PNPT1	cis	cerebellum	SCAN
rs782637	PNPT1	cis	lymphoblastoid	seeQTL
rs782637	SMEK2	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:55846800-55919800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:55847400-55911000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr2:55858200-55920400	Weak transcription	Fetal Heart	heart
4	chr2:55860400-55905400	Weak transcription	Fetal Brain Male	brain
5	chr2:55864400-55919600	Weak transcription	NHLF	lung
6	chr2:55866600-55920000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr2:55870400-55920000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr2:55870600-55920000	Weak transcription	Rectal Smooth Muscle	rectum
9	chr2:55870800-55903600	Weak transcription	Gastric	stomach
10	chr2:55870800-55909000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr2:55870800-55920400	Weak transcription	Aorta	Aorta
12	chr2:55871000-55920000	Weak transcription	Spleen	Spleen
13	chr2:55871200-55905200	Weak transcription	Brain Angular Gyrus	brain
14	chr2:55871400-55905200	Weak transcription	Fetal Kidney	kidney
15	chr2:55873200-55919800	Weak transcription	Small Intestine	intestine
16	chr2:55873800-55899400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr2:55874800-55920200	Weak transcription	Pancreas	Pancrea
18	chr2:55879000-55896200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr2:55879000-55917600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr2:55879200-55902800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr2:55879400-55914200	Strong transcription	HUES64 Cell Line	embryonic stem cell
22	chr2:55881200-55913000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr2:55881800-55898000	Weak transcription	NHDF-Ad	bronchial
24	chr2:55882200-55909600	Weak transcription	Brain Germinal Matrix	brain
25	chr2:55883000-55906800	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr2:55883000-55919800	Weak transcription	HSMMtube	muscle
27	chr2:55883200-55906600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr2:55883400-55906800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr2:55883800-55897600	Weak transcription	Brain Substantia Nigra	brain
30	chr2:55884000-55897800	Weak transcription	HMEC	breast
31	chr2:55885600-55902600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr2:55886000-55896000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr2:55887400-55896000	Strong transcription	Monocytes-CD14+_RO01746	blood
34	chr2:55887600-55898400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr2:55887800-55900200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr2:55887800-55900400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr2:55888000-55907200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr2:55888400-55895600	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr2:55888600-55899600	Weak transcription	Fetal Brain Female	brain
40	chr2:55888600-55904200	Weak transcription	Esophagus	oesophagus
41	chr2:55888800-55905200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr2:55888800-55909600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr2:55889800-55918400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
44	chr2:55890200-55902400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
45	chr2:55890200-55915600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr2:55890400-55898400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr2:55890400-55898400	Strong transcription	Hela-S3	cervix
48	chr2:55890400-55914200	Strong transcription	Primary T helper cells PMA-I stimulated	--
49	chr2:55891000-55896600	Strong transcription	Primary T helper cells fromperipheralblood	blood
50	chr2:55891200-55895000	Strong transcription	HUVEC	blood vessel

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links