Variant report

Variant	rs12204363
Chromosome Location	chr6:134098184-134098185
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11154744	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11154745	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1208256	0.91[ASN][1000 genomes]
rs1208259	0.90[ASN][1000 genomes]
rs1209415	0.90[ASN][1000 genomes]
rs12193307	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12196907	0.87[AFR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12203224	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12206782	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12213745	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1414668	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1414670	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17062853	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17062904	0.85[EUR][1000 genomes]
rs1763943	0.88[ASN][1000 genomes]
rs1855895	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4895387	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4895989	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4895990	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4895991	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4895992	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4895994	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6569906	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6909803	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][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	nsv830812	chr6:133993897-134165407	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv34122	chr6:134089019-134378252	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:134086200-134112400	Weak transcription	Aorta	Aorta
2	chr6:134091000-134100000	Weak transcription	Rectal Smooth Muscle	rectum
3	chr6:134095800-134099600	Weak transcription	A549	lung
4	chr6:134096000-134098200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr6:134096000-134099400	Weak transcription	Osteobl	bone
6	chr6:134096000-134100000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr6:134096000-134100000	Weak transcription	NHDF-Ad	bronchial
8	chr6:134096000-134112400	Weak transcription	HSMM	muscle
9	chr6:134096200-134099400	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr6:134097600-134099000	Enhancers	Fetal Lung	lung
11	chr6:134097800-134098600	Weak transcription	Fetal Kidney	kidney
12	chr6:134097800-134102400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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