Variant report

Variant	rs2622430
Chromosome Location	chr11:63912060-63912061
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:63903545..63905452-chr11:63911377..63913056,2	MCF-7	breast:
2	chr11:63906755..63909220-chr11:63909551..63912410,2	MCF-7	breast:
3	chr11:63604849..63606605-chr11:63911575..63914169,2	K562	blood:
4	chr11:63910019..63912556-chr11:63923747..63925482,2	MCF-7	breast:
5	chr11:63907528..63910274-chr11:63911901..63915955,5	K562	blood:

Variant related genes	Relation type
ENSG00000072518	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 2 )

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

rs_ID	r²[population]
rs11549691	0.81[EUR][1000 genomes]
rs1544538	0.85[EUR][1000 genomes]
rs17851033	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1938817	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2070232	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2154984	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2186571	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2245837	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2622420	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2622422	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2622424	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2622428	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2701530	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2701536	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2701537	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2701539	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4980506	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs583799	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59250939	0.85[EUR][1000 genomes]
rs599549	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs615924	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs616652	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs639406	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs688241	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897630	chr11:63664882-63924446	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
2	nsv897631	chr11:63664882-64129722	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	254 gene(s)	inside rSNPs	diseases
3	esv1802079	chr11:63746066-64151373	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	247 gene(s)	inside rSNPs	diseases
4	nsv897646	chr11:63754986-64150370	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	245 gene(s)	inside rSNPs	diseases
5	nsv832184	chr11:63787702-63925084	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	nsv1035875	chr11:63800238-64132030	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	234 gene(s)	inside rSNPs	diseases
7	nsv832185	chr11:63819946-63963532	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	89 gene(s)	inside rSNPs	diseases
8	nsv469961	chr11:63822940-64085967	Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases
9	nsv897660	chr11:63860826-64125142	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	231 gene(s)	inside rSNPs	diseases
10	nsv897661	chr11:63863405-64129722	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
11	nsv356	chr11:63868847-63913129	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv897662	chr11:63889749-64150370	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
13	esv1801661	chr11:63894054-63937949	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
14	nsv897663	chr11:63910153-63962152	Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	86 gene(s)	inside rSNPs	n/a

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2622430	PRDX5	Cis_1M	lymphoblastoid	RTeQTL
rs2622430	HSPC152	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63890600-63913600	Weak transcription	Esophagus	oesophagus
2	chr11:63892000-63915800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr11:63895800-63920000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr11:63897200-63918400	Weak transcription	Dnd41	blood
5	chr11:63898800-63916400	Weak transcription	Hela-S3	cervix
6	chr11:63900200-63931800	Weak transcription	Lung	lung
7	chr11:63900400-63916000	Weak transcription	Fetal Intestine Large	intestine
8	chr11:63900800-63916200	Weak transcription	Liver	Liver
9	chr11:63902000-63916600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr11:63902800-63915600	Weak transcription	Fetal Intestine Small	intestine
11	chr11:63903600-63915600	Weak transcription	Left Ventricle	heart
12	chr11:63904200-63913400	Weak transcription	K562	blood
13	chr11:63906200-63913400	Weak transcription	Pancreas	Pancrea
14	chr11:63906800-63912200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:63907000-63915400	Weak transcription	Fetal Heart	heart
16	chr11:63907000-63915600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr11:63907000-63915600	Weak transcription	Fetal Brain Female	brain
18	chr11:63909400-63912800	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr11:63909400-63913000	Weak transcription	Brain Cingulate Gyrus	brain
20	chr11:63909600-63912800	Weak transcription	Brain Hippocampus Middle	brain
21	chr11:63909600-63912800	Weak transcription	Fetal Brain Male	brain
22	chr11:63909600-63912800	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr11:63909600-63913000	Weak transcription	Brain Anterior Caudate	brain
24	chr11:63909600-63913000	Weak transcription	Brain Substantia Nigra	brain
25	chr11:63909600-63913000	Weak transcription	Right Ventricle	heart
26	chr11:63909600-63913800	Weak transcription	Fetal Muscle Leg	muscle
27	chr11:63909600-63915400	Weak transcription	Stomach Smooth Muscle	stomach
28	chr11:63909600-63915600	Weak transcription	Psoas Muscle	Psoas
29	chr11:63909600-63916000	Weak transcription	Brain Angular Gyrus	brain
30	chr11:63909800-63912800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr11:63909800-63915400	Weak transcription	Colon Smooth Muscle	Colon
32	chr11:63910200-63913600	Weak transcription	HepG2	liver
33	chr11:63910800-63915400	Enhancers	Brain Germinal Matrix	brain
34	chr11:63911000-63915600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr11:63911200-63912200	Enhancers	Fetal Muscle Trunk	muscle
36	chr11:63911200-63912200	Strong transcription	Ovary	ovary
37	chr11:63911200-63912400	Strong transcription	Gastric	stomach
38	chr11:63911200-63915400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr11:63911400-63913000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr11:63911400-63920200	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr11:63911600-63912200	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr11:63911600-63915600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr11:63911600-63915800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr11:63911600-63919800	Weak transcription	Primary B cells from cord blood	blood
45	chr11:63911600-63920400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr11:63911600-63932600	Weak transcription	Primary T cells from cord blood	blood
47	chr11:63911800-63912600	Strong transcription	Spleen	Spleen
48	chr11:63911800-63913600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr11:63911800-63916000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr11:63911800-63916000	Weak transcription	Fetal Thymus	thymus

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links