Variant report

Variant	rs11115463
Chromosome Location	chr12:83257472-83257473
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs10466961	1.00[CEU][hapmap]
rs17010561	1.00[CEU][hapmap]
rs73358271	0.95[EUR][1000 genomes]
rs7962040	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1053093	chr12:82645292-83287809	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv541551	chr12:82645292-83287809	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv427917	chr12:82917031-83279712	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv521849	chr12:83013783-83991479	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv469490	chr12:83089431-83507269	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
6	nsv559542	chr12:83089431-83507269	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
7	esv2758315	chr12:83101045-83357621	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	esv2759911	chr12:83101045-83357621	Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv430520	chr12:83166956-83271602	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
10	nsv437765	chr12:83230454-83271933	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
11	nsv832472	chr12:83248283-83419753	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:83236000-83264000	Weak transcription	Stomach Smooth Muscle	stomach
2	chr12:83242200-83289800	Weak transcription	Stomach Mucosa	stomach
3	chr12:83249400-83261000	Weak transcription	Fetal Heart	heart
4	chr12:83249600-83261200	Weak transcription	Rectal Smooth Muscle	rectum
5	chr12:83250000-83264600	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr12:83251400-83258000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr12:83251400-83259000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr12:83251400-83265000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr12:83251600-83260800	Weak transcription	Fetal Muscle Leg	muscle
10	chr12:83252200-83258600	Weak transcription	Fetal Intestine Small	intestine
11	chr12:83252200-83260400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr12:83252200-83261600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr12:83252200-83264000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr12:83252200-83273000	Weak transcription	Pancreas	Pancrea
15	chr12:83252400-83257600	Weak transcription	Duodenum Mucosa	Duodenum
16	chr12:83252800-83261800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr12:83252800-83262000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr12:83252800-83262000	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr12:83252800-83264000	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr12:83255600-83258000	Enhancers	Brain Cingulate Gyrus	brain
21	chr12:83255800-83257600	Enhancers	Brain Substantia Nigra	brain
22	chr12:83255800-83257800	Enhancers	Brain Anterior Caudate	brain
23	chr12:83256000-83257600	Enhancers	Brain Angular Gyrus	brain
24	chr12:83256000-83259200	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr12:83256000-83259200	Enhancers	Brain Germinal Matrix	brain
26	chr12:83256200-83257800	Enhancers	Brain Hippocampus Middle	brain
27	chr12:83256200-83258600	Weak transcription	Fetal Stomach	stomach
28	chr12:83256200-83261600	Weak transcription	Fetal Lung	lung
29	chr12:83256600-83257800	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr12:83256600-83258000	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr12:83256600-83258000	Enhancers	Small Intestine	intestine
32	chr12:83256800-83257800	Enhancers	Fetal Brain Female	brain
33	chr12:83256800-83258200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr12:83256800-83258200	Enhancers	Fetal Brain Male	brain
35	chr12:83256800-83258200	Strong transcription	Monocytes-CD14+_RO01746	blood
36	chr12:83257000-83258200	Strong transcription	Primary monocytes fromperipheralblood	blood
37	chr12:83257200-83261600	Weak transcription	Colon Smooth Muscle	Colon
38	chr12:83257200-83261800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr12:83257200-83261800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr12:83257200-83263800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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