Variant report

Variant	rs41266913
Chromosome Location	chr1:160522787-160522788
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	chr1:160515112..160518077-chr1:160519420..160523438,5	K562	blood:

Variant related genes	Relation type
ENSG00000264286	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1553459	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1570707	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3737791	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3766386	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6427538	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6665409	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73014378	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs73016361	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73016371	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73016376	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1829614	chr1:160465291-160595000	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv872491	chr1:160470258-160580549	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv831703	chr1:160496124-160643024	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:160511800-160527800	Weak transcription	Colonic Mucosa	Colon
2	chr1:160512200-160524600	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr1:160516000-160526200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr1:160516200-160523800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr1:160516600-160523800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr1:160517400-160523800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr1:160517400-160524000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr1:160517400-160528000	Weak transcription	Placenta	Placenta
9	chr1:160517600-160523800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr1:160517600-160528400	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr1:160517800-160524000	Weak transcription	Adipose Nuclei	Adipose
12	chr1:160519200-160524000	Strong transcription	Primary hematopoietic stem cells	blood
13	chr1:160519400-160524200	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr1:160519600-160526000	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr1:160519800-160523800	Strong transcription	Primary T helper cells fromperipheralblood	blood
16	chr1:160519800-160531000	Weak transcription	Duodenum Mucosa	Duodenum
17	chr1:160520000-160523800	Genic enhancers	GM12878-XiMat	blood
18	chr1:160520000-160524000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
19	chr1:160520200-160523600	Strong transcription	Dnd41	blood
20	chr1:160520400-160523800	Genic enhancers	Primary B cells from peripheral blood	blood
21	chr1:160520400-160524000	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr1:160520600-160522800	Weak transcription	Spleen	Spleen
23	chr1:160520600-160523800	Strong transcription	Primary T killer memory cells from peripheral blood	blood
24	chr1:160520600-160524000	Strong transcription	Fetal Thymus	thymus
25	chr1:160520600-160525600	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr1:160520800-160523800	Strong transcription	Primary T cells from cord blood	blood
27	chr1:160520800-160524000	Strong transcription	Primary T helper naive cells from peripheral blood	blood
28	chr1:160521000-160524600	Strong transcription	Primary B cells from cord blood	blood
29	chr1:160521200-160524000	Strong transcription	Thymus	Thymus
30	chr1:160521600-160524000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr1:160521600-160524600	Strong transcription	Primary T cells fromperipheralblood	blood
32	chr1:160521800-160523200	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr1:160522000-160523800	Strong transcription	Pancreas	Pancrea
34	chr1:160522000-160524000	Strong transcription	Primary T helper cells PMA-I stimulated	--
35	chr1:160522200-160527600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr1:160522200-160529600	Weak transcription	Stomach Mucosa	stomach
37	chr1:160522600-160522800	Weak transcription	Gastric	stomach
38	chr1:160522600-160523800	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr1:160522600-160527600	Weak transcription	K562	blood

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