Variant report

Variant	rs7791225
Chromosome Location	chr7:6261683-6261684
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 93 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10046499	1.00[JPT][hapmap]
rs10224504	1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap]
rs10225119	1.00[JPT][hapmap]
rs10227013	0.83[ASN][1000 genomes]
rs10240510	1.00[JPT][hapmap]
rs10241174	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10241580	1.00[ASN][1000 genomes]
rs10244640	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs10245186	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10247585	1.00[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap]
rs10252947	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10253501	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs10255662	1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10255914	1.00[JPT][hapmap]
rs10261217	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs10263878	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10267982	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10268916	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[GIH][hapmap];0.91[TSI][hapmap]
rs10270609	0.90[EUR][1000 genomes]
rs10274992	0.83[ASN][1000 genomes]
rs10275021	1.00[JPT][hapmap]
rs10279137	1.00[JPT][hapmap]
rs10280585	1.00[JPT][hapmap]
rs11768047	1.00[JPT][hapmap]
rs11768749	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs11976961	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs12667392	1.00[JPT][hapmap]
rs13237896	0.82[EUR][1000 genomes]
rs13437890	1.00[JPT][hapmap]
rs17136048	1.00[JPT][hapmap]
rs34073302	0.85[EUR][1000 genomes]
rs34312608	0.93[EUR][1000 genomes]
rs34904930	0.85[EUR][1000 genomes]
rs34939060	0.97[EUR][1000 genomes]
rs35257722	0.95[EUR][1000 genomes]
rs35372475	0.85[EUR][1000 genomes]
rs35402521	0.95[EUR][1000 genomes]
rs35868999	0.95[EUR][1000 genomes]
rs35882223	0.95[EUR][1000 genomes]
rs35934233	0.85[EUR][1000 genomes]
rs59180903	0.95[ASN][1000 genomes]
rs59568570	0.83[ASN][1000 genomes]
rs6463535	0.93[EUR][1000 genomes]
rs6463540	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.91[TSI][hapmap];0.81[YRI][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6463541	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs6463542	0.83[ASN][1000 genomes]
rs6463543	0.83[ASN][1000 genomes]
rs6463544	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs6942707	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6944071	1.00[JPT][hapmap]
rs6944216	0.95[ASN][1000 genomes]
rs6946205	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6949823	1.00[JPT][hapmap]
rs6955065	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6960965	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs6961095	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6962767	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6969814	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6969863	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6976305	0.83[ASN][1000 genomes]
rs71531366	0.95[EUR][1000 genomes]
rs71531367	0.95[EUR][1000 genomes]
rs71531368	0.95[EUR][1000 genomes]
rs71531370	0.95[EUR][1000 genomes]
rs71531372	0.85[EUR][1000 genomes]
rs71531373	0.82[EUR][1000 genomes]
rs71549618	0.85[EUR][1000 genomes]
rs7777433	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.91[TSI][hapmap];0.81[YRI][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7780269	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs7780702	0.87[EUR][1000 genomes]
rs7783018	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7783827	0.87[EUR][1000 genomes]
rs7784025	1.00[ASN][1000 genomes]
rs7800777	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs7807841	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];0.82[MKK][hapmap];0.84[YRI][hapmap];0.86[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs7811702	0.83[ASN][1000 genomes]
rs886675	0.90[YRI][hapmap]
rs958329	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533108	chr7:5488018-6316581	Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	390 gene(s)	inside rSNPs	diseases
2	nsv948912	chr7:5803903-6623553	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
3	nsv1034060	chr7:5814823-6745710	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	138 gene(s)	inside rSNPs	diseases
4	nsv538711	chr7:5814823-6745710	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	138 gene(s)	inside rSNPs	diseases
5	nsv1028242	chr7:5819084-6645024	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	127 gene(s)	inside rSNPs	diseases
6	nsv538712	chr7:5819084-6645024	Weak transcription Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	127 gene(s)	inside rSNPs	diseases
7	nsv949531	chr7:5949371-6753694	Strong transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	129 gene(s)	inside rSNPs	diseases
8	nsv1021037	chr7:6070792-6426966	Strong transcription Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
9	nsv538713	chr7:6070792-6426966	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
10	nsv530989	chr7:6176729-6438197	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
11	nsv5629	chr7:6217866-6263131	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
12	nsv482829	chr7:6231809-6407606	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
13	nsv1032987	chr7:6246313-6373054	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
14	nsv538714	chr7:6246313-6373054	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
15	nsv1020236	chr7:6248930-6690377	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7791225	PSCD3	Cis_1M	lymphoblastoid	RTeQTL
rs7791225	CYTH3	cis	lymphoblastoid	seeQTL

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6229400-6270600	Weak transcription	Gastric	stomach
2	chr7:6240800-6265400	Weak transcription	HSMM	muscle
3	chr7:6241000-6265200	Weak transcription	Fetal Stomach	stomach
4	chr7:6241200-6265600	Weak transcription	Fetal Intestine Small	intestine
5	chr7:6249600-6265800	Weak transcription	Stomach Smooth Muscle	stomach
6	chr7:6249800-6265400	Weak transcription	HSMMtube	muscle
7	chr7:6249800-6265600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr7:6254600-6267800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:6257200-6262200	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr7:6258000-6265400	Weak transcription	Rectal Smooth Muscle	rectum
11	chr7:6258000-6266000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr7:6258400-6265600	Weak transcription	Colon Smooth Muscle	Colon
13	chr7:6259200-6265600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr7:6259400-6263600	Weak transcription	Small Intestine	intestine
15	chr7:6259400-6265600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr7:6259400-6276800	Weak transcription	Aorta	Aorta
17	chr7:6260000-6265800	Weak transcription	NHEK	skin
18	chr7:6260400-6262200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr7:6260600-6262000	Enhancers	Primary hematopoietic stem cells	blood
20	chr7:6260600-6262000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr7:6260600-6262000	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr7:6260600-6262000	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr7:6260600-6262000	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr7:6260600-6262400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr7:6260600-6263000	Enhancers	A549	lung
26	chr7:6260800-6261800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr7:6260800-6261800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr7:6260800-6261800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr7:6260800-6262000	Enhancers	Primary B cells from cord blood	blood
30	chr7:6260800-6262000	Enhancers	K562	blood
31	chr7:6260800-6262200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr7:6260800-6262200	Enhancers	NHLF	lung
33	chr7:6260800-6262800	Enhancers	Fetal Heart	heart
34	chr7:6261000-6261800	Enhancers	Primary B cells from peripheral blood	blood
35	chr7:6261000-6261800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr7:6261000-6261800	Enhancers	Duodenum Mucosa	Duodenum
37	chr7:6261000-6261800	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr7:6261000-6261800	Enhancers	Spleen	Spleen
39	chr7:6261000-6262000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr7:6261000-6262000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr7:6261000-6262000	Enhancers	Adipose Nuclei	Adipose
42	chr7:6261000-6262000	Enhancers	Placenta	Placenta
43	chr7:6261000-6262000	Enhancers	Psoas Muscle	Psoas
44	chr7:6261000-6262000	Enhancers	Right Atrium	heart
45	chr7:6261000-6262000	Enhancers	Right Ventricle	heart
46	chr7:6261000-6262000	Enhancers	GM12878-XiMat	blood
47	chr7:6261000-6262000	Enhancers	Osteobl	bone
48	chr7:6261000-6262200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr7:6261000-6262200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr7:6261000-6262200	Enhancers	Skeletal Muscle Female	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links