Variant report

Variant	rs2309433
Chromosome Location	chr2:99271011-99271012
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10189698	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1028144	0.92[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11123746	0.86[CEU][hapmap];0.83[EUR][1000 genomes]
rs12468113	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12613547	0.83[EUR][1000 genomes]
rs12613577	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12616821	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1514914	0.86[CEU][hapmap];0.83[EUR][1000 genomes]
rs1599827	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1599828	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17448190	1.00[YRI][hapmap]
rs2063780	0.86[CEU][hapmap];0.83[EUR][1000 genomes]
rs2271670	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];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2309432	0.83[EUR][1000 genomes]
rs2871234	0.85[CEU][hapmap];0.83[EUR][1000 genomes]
rs34457904	0.83[EUR][1000 genomes]
rs34622150	0.83[EUR][1000 genomes]
rs3754870	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3769689	1.00[YRI][hapmap]
rs3769691	0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4508652	0.82[CEU][hapmap];0.81[EUR][1000 genomes]
rs4513341	0.81[EUR][1000 genomes]
rs6542835	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6719489	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6750281	0.86[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7557647	0.86[CEU][hapmap];0.83[EUR][1000 genomes]
rs9308813	0.96[CEU][hapmap];0.86[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9308814	0.96[CEU][hapmap];0.86[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap]

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	nsv1013941	chr2:99116255-99317933	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv535834	chr2:99116255-99317933	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv582516	chr2:99254031-99304794	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:99231200-99286200	Weak transcription	Stomach Mucosa	stomach
2	chr2:99234600-99310600	Weak transcription	Small Intestine	intestine
3	chr2:99234800-99296400	Weak transcription	Esophagus	oesophagus
4	chr2:99235400-99273600	Weak transcription	Fetal Kidney	kidney
5	chr2:99249800-99318000	Weak transcription	Psoas Muscle	Psoas
6	chr2:99251400-99277800	Weak transcription	Spleen	Spleen
7	chr2:99251400-99295600	Weak transcription	Fetal Stomach	stomach
8	chr2:99251600-99275400	Weak transcription	Gastric	stomach
9	chr2:99251600-99302000	Weak transcription	Brain Angular Gyrus	brain
10	chr2:99251600-99306600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr2:99251800-99275600	Weak transcription	Aorta	Aorta
12	chr2:99252200-99271200	Weak transcription	Primary hematopoietic stem cells	blood
13	chr2:99253200-99277400	Weak transcription	Brain Hippocampus Middle	brain
14	chr2:99253200-99293000	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr2:99255600-99306800	Weak transcription	Colonic Mucosa	Colon
16	chr2:99256400-99296000	Weak transcription	Rectal Smooth Muscle	rectum
17	chr2:99259000-99281800	Weak transcription	Left Ventricle	heart
18	chr2:99260000-99288000	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr2:99260600-99290400	Weak transcription	Liver	Liver
20	chr2:99260600-99290800	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr2:99264600-99299000	Weak transcription	Colon Smooth Muscle	Colon
22	chr2:99265200-99275400	Weak transcription	Pancreas	Pancrea
23	chr2:99265200-99291800	Weak transcription	Placenta	Placenta
24	chr2:99265400-99271600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr2:99265400-99271800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
26	chr2:99265400-99290800	Weak transcription	Stomach Smooth Muscle	stomach
27	chr2:99265600-99271200	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr2:99265600-99306600	Weak transcription	Lung	lung
29	chr2:99265800-99271200	Weak transcription	Thymus	Thymus
30	chr2:99265800-99271400	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr2:99265800-99275400	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr2:99265800-99303800	Weak transcription	Brain Substantia Nigra	brain
33	chr2:99266200-99290400	Weak transcription	Adipose Nuclei	Adipose
34	chr2:99266200-99296200	Weak transcription	Brain Cingulate Gyrus	brain
35	chr2:99266400-99271200	Weak transcription	Fetal Thymus	thymus
36	chr2:99266400-99271400	Weak transcription	Primary B cells from peripheral blood	blood
37	chr2:99266400-99275400	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr2:99266400-99278000	Weak transcription	HUVEC	blood vessel
39	chr2:99266400-99304200	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr2:99267200-99271800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr2:99267400-99271400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr2:99267400-99272800	Weak transcription	Fetal Intestine Large	intestine
43	chr2:99267600-99271200	Enhancers	Primary T helper naive cells from peripheral blood	blood
44	chr2:99267600-99284200	Weak transcription	Fetal Intestine Small	intestine
45	chr2:99267800-99271200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr2:99268000-99273000	Enhancers	Primary T killer memory cells from peripheral blood	blood
47	chr2:99268600-99273400	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr2:99269000-99273400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr2:99269400-99271200	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr2:99269400-99272800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links