Variant report

Variant	rs2724602
Chromosome Location	chr12:11907856-11907857
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10491988	1.00[EUR][1000 genomes]
rs11054431	1.00[EUR][1000 genomes]
rs12303444	1.00[EUR][1000 genomes]
rs12306221	1.00[MEX][hapmap]
rs12310333	1.00[EUR][1000 genomes]
rs13377661	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs16907274	1.00[MEX][hapmap]
rs2710267	0.86[ASW][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2710284	1.00[MEX][hapmap]
rs2724598	1.00[EUR][1000 genomes]
rs2724637	1.00[EUR][1000 genomes]
rs2855706	1.00[MEX][hapmap]
rs2856340	0.86[ASW][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57222202	1.00[EUR][1000 genomes]
rs59302227	1.00[EUR][1000 genomes]
rs7133092	1.00[EUR][1000 genomes]
rs7302827	1.00[EUR][1000 genomes]
rs7307437	1.00[EUR][1000 genomes]
rs73288792	1.00[EUR][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	nsv870039	chr12:11800363-11996598	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
2	nsv1053609	chr12:11898099-11933906	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11873200-11909400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr12:11885800-11911600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr12:11893200-11915000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr12:11894600-11908400	Weak transcription	Psoas Muscle	Psoas
5	chr12:11895000-11912600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr12:11895400-11914400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr12:11895600-11908800	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr12:11897000-11908800	Weak transcription	Brain Anterior Caudate	brain
9	chr12:11899400-11908000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr12:11899400-11908200	Weak transcription	HSMMtube	muscle
11	chr12:11899400-11908400	Weak transcription	HSMM	muscle
12	chr12:11900400-11910600	Weak transcription	Colonic Mucosa	Colon
13	chr12:11900600-11915000	Weak transcription	NHEK	skin
14	chr12:11901400-11911000	Weak transcription	Fetal Lung	lung
15	chr12:11902800-11910600	Weak transcription	Brain Angular Gyrus	brain
16	chr12:11902800-11910600	Weak transcription	Brain Hippocampus Middle	brain
17	chr12:11902800-11910600	Weak transcription	Brain Substantia Nigra	brain
18	chr12:11903200-11910200	Weak transcription	Brain Cingulate Gyrus	brain
19	chr12:11903400-11910400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr12:11904000-11908600	Genic enhancers	Fetal Thymus	thymus
21	chr12:11904000-11918000	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr12:11904200-11913000	Strong transcription	Dnd41	blood
23	chr12:11904400-11910600	Genic enhancers	GM12878-XiMat	blood
24	chr12:11905200-11908000	Weak transcription	Small Intestine	intestine
25	chr12:11905200-11908000	Genic enhancers	Thymus	Thymus
26	chr12:11905200-11908400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr12:11905200-11908600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr12:11905200-11908600	Strong transcription	Fetal Intestine Large	intestine
29	chr12:11905200-11909600	Strong transcription	Primary T helper cells fromperipheralblood	blood
30	chr12:11905200-11910400	Strong transcription	Fetal Stomach	stomach
31	chr12:11905200-11911400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr12:11905400-11910800	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr12:11905400-11911600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr12:11905600-11909600	Strong transcription	Primary T cells from cord blood	blood
35	chr12:11905600-11909600	Strong transcription	Lung	lung
36	chr12:11905800-11918400	Weak transcription	Fetal Brain Male	brain
37	chr12:11906000-11908600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr12:11906000-11909200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr12:11906000-11909200	Strong transcription	Liver	Liver
40	chr12:11906000-11909800	Enhancers	Colon Smooth Muscle	Colon
41	chr12:11906000-11912000	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr12:11906200-11908000	Weak transcription	Fetal Heart	heart
43	chr12:11906200-11908600	Strong transcription	Cortex derived primary cultured neurospheres	brain
44	chr12:11906200-11909000	Strong transcription	Fetal Muscle Leg	muscle
45	chr12:11906200-11909400	Strong transcription	Primary T helper cells PMA-I stimulated	--
46	chr12:11906200-11910600	Weak transcription	Esophagus	oesophagus
47	chr12:11906200-11911000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr12:11906400-11908000	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr12:11906400-11908400	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr12:11906400-11909200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood

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