Variant report

Variant	rs12435295
Chromosome Location	chr14:105875434-105875435
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	chr14:105863559..105868687-chr14:105874310..105880497,10	K562	blood:

Variant related genes	Relation type
ENSG00000226174	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10147154	0.86[YRI][hapmap];1.00[ASN][1000 genomes]
rs11621365	0.93[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28529463	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28541433	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4983613	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4983614	0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6576085	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6576086	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6576087	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6576088	0.93[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7149988	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73361094	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7492842	0.83[AMR][1000 genomes]
rs8014777	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530813	chr14:105607701-106453697	Strong transcription Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	149 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105866400-105877400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr14:105866600-105877200	Weak transcription	Brain Cingulate Gyrus	brain
3	chr14:105866600-105877400	Weak transcription	Brain Angular Gyrus	brain
4	chr14:105866800-105877400	Weak transcription	Psoas Muscle	Psoas
5	chr14:105867000-105877200	Weak transcription	Pancreas	Pancrea
6	chr14:105867000-105877200	Weak transcription	Right Ventricle	heart
7	chr14:105867000-105877400	Weak transcription	Left Ventricle	heart
8	chr14:105867200-105877400	Weak transcription	HSMM	muscle
9	chr14:105867600-105875600	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr14:105867600-105876800	Weak transcription	Gastric	stomach
11	chr14:105867600-105877000	Weak transcription	Primary hematopoietic stem cells	blood
12	chr14:105867600-105877000	Weak transcription	Ovary	ovary
13	chr14:105867600-105877000	Weak transcription	Hela-S3	cervix
14	chr14:105867600-105877200	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr14:105867600-105877400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr14:105867600-105877400	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr14:105867600-105877400	Weak transcription	HSMMtube	muscle
18	chr14:105867800-105876800	Weak transcription	Fetal Heart	heart
19	chr14:105868000-105876800	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr14:105868400-105876800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr14:105871600-105875600	Weak transcription	Primary B cells from cord blood	blood
22	chr14:105871600-105875600	Weak transcription	Primary B cells from peripheral blood	blood
23	chr14:105871600-105877200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr14:105873400-105875600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr14:105874200-105877000	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr14:105874800-105876400	Weak transcription	Brain Substantia Nigra	brain
27	chr14:105875000-105875600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr14:105875000-105875600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr14:105875000-105875600	Enhancers	Brain Anterior Caudate	brain
30	chr14:105875000-105876000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr14:105875000-105876800	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr14:105875200-105875600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr14:105875200-105875600	Enhancers	Brain Germinal Matrix	brain
34	chr14:105875400-105875600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
35	chr14:105875400-105875600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
36	chr14:105875400-105875600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
37	chr14:105875400-105875600	Enhancers	Fetal Brain Female	brain
38	chr14:105875400-105875800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
39	chr14:105875400-105875800	Enhancers	Brain Hippocampus Middle	brain
40	chr14:105875400-105876000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
41	chr14:105875400-105876200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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