Variant report

Variant	rs2282620
Chromosome Location	chr11:71183477-71183478
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:71182002..71184181-chr11:71185465..71188579,3	K562	blood:
2	chr11:71163024..71164713-chr11:71182379..71183959,2	MCF-7	breast:
3	chr11:71177769..71179272-chr11:71180854..71183536,2	K562	blood:

Variant related genes	Relation type
ENSG00000172893	Chromatin interaction
ENSG00000172890	Chromatin interaction

Extended variants
information (count: 67 )
Associated
traits (count: 12 )

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs1044482	0.94[CEU][hapmap];0.85[EUR][1000 genomes]
rs11233746	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11233747	0.82[CHB][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11233789	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11546509	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11600569	1.00[CEU][hapmap];0.83[CHB][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11600860	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11603330	0.95[CEU][hapmap];0.85[EUR][1000 genomes]
rs11604642	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11606033	0.95[CEU][hapmap];0.85[EUR][1000 genomes]
rs11606612	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11606631	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12278461	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12419279	1.00[CEU][hapmap];0.82[CHB][hapmap];0.81[EUR][1000 genomes]
rs12419334	0.94[CEU][hapmap];0.81[EUR][1000 genomes]
rs12422045	0.95[CEU][hapmap];0.85[EUR][1000 genomes]
rs12785878	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12789751	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12790010	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12790558	1.00[CEU][hapmap];0.83[CHB][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12791871	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12792306	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12793224	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12793530	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12794668	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12797951	0.95[CEU][hapmap];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12800438	1.00[CEU][hapmap];0.83[CHB][hapmap];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12806844	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12807718	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12807827	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12808368	1.00[CEU][hapmap];0.83[CHB][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1981412	0.81[EUR][1000 genomes]
rs2002063	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2040323	1.00[CEU][hapmap];0.83[CHB][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2276360	1.00[CEU][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2276361	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2276362	1.00[CEU][hapmap];0.83[CHB][hapmap];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2282621	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][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]
rs28364617	0.91[EUR][1000 genomes]
rs2852853	0.94[CEU][hapmap];0.85[EUR][1000 genomes]
rs3750997	0.95[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3794060	1.00[CEU][hapmap];0.83[CHB][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4423214	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4488226	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4944062	1.00[CEU][hapmap];0.82[CHB][hapmap];0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4944946	0.88[EUR][1000 genomes]
rs4944955	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4944956	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4944957	1.00[CEU][hapmap]
rs4944958	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4944959	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4945008	0.95[CEU][hapmap];0.83[CHB][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs732934	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7928249	1.00[CEU][hapmap];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7935125	1.00[CEU][hapmap];0.81[CHB][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7938885	1.00[CEU][hapmap];0.84[CHB][hapmap];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7944926	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs909217	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048123	chr11:70795222-71231382	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
2	nsv526973	chr11:71088949-71215880	Weak transcription Strong transcription Active TSS Enhancers 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	14 gene(s)	inside rSNPs	diseases
3	nsv897897	chr11:71088949-71217571	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
4	nsv530623	chr11:71088949-72020418	Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	134 gene(s)	inside rSNPs	diseases
5	nsv897898	chr11:71103143-71211654	Weak transcription ZNF genes & repeats Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
6	nsv519224	chr11:71108341-71215880	Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
7	nsv1037357	chr11:71162241-71209628	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
8	nsv541085	chr11:71162241-71209628	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
9	nsv1052432	chr11:71167449-71213007	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:12)

SNP	Gene	Cis/trans	Tissue	Source
rs2282620	RP11-660L16.2	cis	Skin Sun Exposed Lower leg	GTEx
rs2282620	RP11-660L16.2	cis	Adipose Subcutaneous	GTEx
rs2282620	RP11-660L16.2	cis	Artery Aorta	GTEx
rs2282620	NADSYN1	cis	Nerve Tibial	GTEx
rs2282620	NADSYN1	cis	Thyroid	GTEx
rs2282620	NADSYN1	cis	lung	GTEx
rs2282620	RP11-660L16.2	cis	Esophagus Muscularis	GTEx
rs2282620	RP11-660L16.2	cis	Heart Left Ventricle	GTEx
rs2282620	RP11-660L16.2	cis	Thyroid	GTEx
rs2282620	RP11-660L16.2	cis	lung	GTEx
rs2282620	RP11-660L16.2	cis	Muscle Skeletal	GTEx
rs2282620	RP11-660L16.2	cis	Whole Blood	GTEx

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71165000-71210000	Weak transcription	Psoas Muscle	Psoas
2	chr11:71165200-71199200	Weak transcription	Right Atrium	heart
3	chr11:71165400-71194200	Weak transcription	Fetal Heart	heart
4	chr11:71165800-71218400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
5	chr11:71166000-71194200	Weak transcription	Fetal Brain Male	brain
6	chr11:71167400-71194000	Weak transcription	Fetal Kidney	kidney
7	chr11:71170600-71184600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr11:71170600-71187600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr11:71171000-71183600	Weak transcription	Fetal Lung	lung
10	chr11:71171000-71184000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr11:71171000-71184200	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr11:71171400-71184200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr11:71171400-71184200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr11:71171400-71184200	Weak transcription	NH-A	brain
15	chr11:71171600-71183600	Weak transcription	Small Intestine	intestine
16	chr11:71171600-71194000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr11:71171800-71189000	Weak transcription	Stomach Mucosa	stomach
18	chr11:71172200-71195000	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr11:71173200-71184000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr11:71174800-71183800	Weak transcription	HMEC	breast
21	chr11:71177800-71188400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr11:71178000-71184400	Weak transcription	Colon Smooth Muscle	Colon
23	chr11:71178400-71183800	Weak transcription	Right Ventricle	heart
24	chr11:71178400-71192600	Weak transcription	K562	blood
25	chr11:71179600-71190400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr11:71180400-71184800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr11:71180600-71183600	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr11:71180600-71199000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr11:71180800-71184400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr11:71180800-71197600	Strong transcription	Fetal Intestine Small	intestine
31	chr11:71180800-71198400	Strong transcription	Cortex derived primary cultured neurospheres	brain
32	chr11:71180800-71199400	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr11:71181000-71183600	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr11:71181400-71217800	Strong transcription	Primary monocytes fromperipheralblood	blood
35	chr11:71181800-71183600	Strong transcription	Primary neutrophils fromperipheralblood	blood
36	chr11:71181800-71218000	Strong transcription	Monocytes-CD14+_RO01746	blood
37	chr11:71182000-71191200	Strong transcription	Placenta	Placenta
38	chr11:71182000-71197600	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr11:71182000-71197800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr11:71182000-71198400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr11:71182000-71198800	Strong transcription	Fetal Muscle Trunk	muscle
42	chr11:71182000-71217600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr11:71182200-71189200	Strong transcription	Esophagus	oesophagus
44	chr11:71182200-71191600	Strong transcription	Gastric	stomach
45	chr11:71182200-71195800	Strong transcription	Lung	lung
46	chr11:71182200-71197800	Strong transcription	Brain Cingulate Gyrus	brain
47	chr11:71182200-71197800	Strong transcription	Brain Inferior Temporal Lobe	brain
48	chr11:71182200-71198000	Strong transcription	Brain Hippocampus Middle	brain
49	chr11:71182200-71198400	Strong transcription	Primary T helper cells PMA-I stimulated	--
50	chr11:71182200-71198400	Strong transcription	Brain Anterior Caudate	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links