Variant report

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10934239	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10934240	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11914863	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11918910	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11921407	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12486414	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12489192	0.87[AMR][1000 genomes]
rs12490048	0.81[AMR][1000 genomes]
rs12490651	0.87[AMR][1000 genomes]
rs12491540	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12492290	0.87[AMR][1000 genomes]
rs12492542	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12492783	0.81[AMR][1000 genomes]
rs12493602	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12493935	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12494777	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12495298	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12495713	0.87[AMR][1000 genomes]
rs12496604	0.87[AMR][1000 genomes]
rs12496617	0.81[AMR][1000 genomes]
rs12497754	0.87[AMR][1000 genomes]
rs16861230	0.81[AMR][1000 genomes]
rs16861233	0.81[AMR][1000 genomes]
rs16861235	0.81[AMR][1000 genomes]
rs16861331	0.87[AMR][1000 genomes]
rs2292512	0.81[AMR][1000 genomes]
rs3773686	0.81[AMR][1000 genomes]
rs57010522	0.87[AMR][1000 genomes]
rs58929900	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013506	chr3:112890608-113680951	Weak transcription Bivalent/Poised TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv1004000	chr3:113116778-113513899	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:113342600-113375800	Weak transcription	Pancreas	Pancrea
2	chr3:113365800-113367000	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr3:113365800-113368000	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr3:113365800-113368400	Weak transcription	Psoas Muscle	Psoas
5	chr3:113365800-113375200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr3:113366000-113373800	Weak transcription	Primary B cells from cord blood	blood
7	chr3:113366000-113373800	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr3:113366000-113376200	Weak transcription	Primary hematopoietic stem cells	blood
9	chr3:113366000-113377000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr3:113366000-113377000	Weak transcription	Liver	Liver
11	chr3:113366200-113368400	Weak transcription	Primary T cells from cord blood	blood
12	chr3:113366200-113373400	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr3:113366200-113373800	Weak transcription	Primary B cells from peripheral blood	blood
14	chr3:113366200-113374400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr3:113366200-113375400	Weak transcription	Duodenum Mucosa	Duodenum

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