Variant report

Variant	rs73167845
Chromosome Location	chr2:10757532-10757533
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:10754918..10757554-chr2:10759036..10761540,2	K562	blood:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs2171771	1.00[AMR][1000 genomes]
rs56702784	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56914795	1.00[AMR][1000 genomes]
rs57125237	1.00[AMR][1000 genomes]
rs57309175	1.00[AMR][1000 genomes]
rs57382387	1.00[AMR][1000 genomes]
rs57464659	1.00[AMR][1000 genomes]
rs57597544	1.00[AMR][1000 genomes]
rs58214362	1.00[AMR][1000 genomes]
rs58838965	1.00[AMR][1000 genomes]
rs58886768	1.00[AMR][1000 genomes]
rs59114654	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59640725	1.00[AMR][1000 genomes]
rs60016454	1.00[AMR][1000 genomes]
rs60286502	1.00[AMR][1000 genomes]
rs60384217	1.00[AMR][1000 genomes]
rs60489255	1.00[AMR][1000 genomes]
rs61167760	1.00[AMR][1000 genomes]
rs6749287	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73165980	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73167824	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73167849	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73167864	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73167887	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73167897	1.00[AMR][1000 genomes]
rs73167901	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73169906	1.00[AMR][1000 genomes]
rs73169907	1.00[AMR][1000 genomes]
rs73169908	1.00[AMR][1000 genomes]
rs73169912	0.86[AFR][1000 genomes]
rs73169917	1.00[AMR][1000 genomes]
rs73169921	1.00[AMR][1000 genomes]
rs73169922	1.00[AMR][1000 genomes]
rs73169924	1.00[AMR][1000 genomes]
rs73169925	1.00[AMR][1000 genomes]
rs73169929	1.00[AMR][1000 genomes]
rs73169933	1.00[AMR][1000 genomes]
rs7587281	1.00[AMR][1000 genomes]
rs7607468	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007185	chr2:10540386-10791743	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv833370	chr2:10625149-10785402	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv1000953	chr2:10717304-10921805	Strong transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv535584	chr2:10717304-10921805	Bivalent Enhancer Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
5	nsv833381	chr2:10723465-10911284	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10725600-10758800	Weak transcription	Stomach Mucosa	stomach
2	chr2:10725600-10793400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr2:10725800-10787000	Weak transcription	Fetal Heart	heart
4	chr2:10729200-10760000	Weak transcription	Brain Angular Gyrus	brain
5	chr2:10729400-10781800	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr2:10729400-10798400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr2:10730800-10774400	Weak transcription	Psoas Muscle	Psoas
8	chr2:10732000-10777600	Weak transcription	Rectal Smooth Muscle	rectum
9	chr2:10738400-10766600	Weak transcription	Fetal Kidney	kidney
10	chr2:10740200-10759800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr2:10740200-10782000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr2:10742200-10757600	Weak transcription	Brain Hippocampus Middle	brain
13	chr2:10742400-10757600	Weak transcription	Brain Cingulate Gyrus	brain
14	chr2:10742400-10773800	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr2:10742400-10774400	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr2:10742600-10760800	Weak transcription	Ovary	ovary
17	chr2:10742600-10772200	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr2:10742600-10791000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr2:10742800-10760000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr2:10742800-10760000	Weak transcription	Fetal Brain Female	brain
21	chr2:10742800-10760600	Weak transcription	Brain Anterior Caudate	brain
22	chr2:10742800-10782400	Weak transcription	Esophagus	oesophagus
23	chr2:10743800-10760800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr2:10744400-10777000	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr2:10745200-10772400	Weak transcription	Colon Smooth Muscle	Colon
26	chr2:10745600-10759200	Weak transcription	Primary B cells from cord blood	blood
27	chr2:10746000-10760600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr2:10746400-10757600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr2:10746400-10759800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr2:10746400-10764000	Weak transcription	Primary hematopoietic stem cells	blood
31	chr2:10746600-10760000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr2:10746600-10760400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr2:10746600-10760400	Weak transcription	Placenta	Placenta
34	chr2:10746600-10760600	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr2:10746600-10760800	Weak transcription	Fetal Thymus	thymus
36	chr2:10746600-10761000	Weak transcription	Aorta	Aorta
37	chr2:10746600-10761000	Weak transcription	Left Ventricle	heart
38	chr2:10746600-10777000	Weak transcription	Colonic Mucosa	Colon
39	chr2:10746600-10781800	Weak transcription	Right Ventricle	heart
40	chr2:10746800-10760600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr2:10746800-10761000	Weak transcription	Gastric	stomach
42	chr2:10746800-10774000	Weak transcription	Spleen	Spleen
43	chr2:10746800-10774400	Weak transcription	HSMMtube	muscle
44	chr2:10746800-10781800	Weak transcription	Pancreas	Pancrea
45	chr2:10747000-10759600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr2:10747000-10759800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr2:10747000-10759800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr2:10747000-10760000	Weak transcription	Primary B cells from peripheral blood	blood
49	chr2:10747000-10781800	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr2:10747200-10760000	Weak transcription	K562	blood

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