Variant report

Variant	rs11064857
Chromosome Location	chr12:120067084-120067085
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10732608	0.86[ASN][1000 genomes]
rs10744742	0.83[AFR][1000 genomes]
rs10774507	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs10774509	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs10849685	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs11064856	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs11064858	0.84[AFR][1000 genomes]
rs11064861	0.84[ASN][1000 genomes]
rs11064864	0.86[ASN][1000 genomes]
rs1154836	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs12708371	0.81[AFR][1000 genomes]
rs1319529	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs1858982	0.86[ASN][1000 genomes]
rs2078938	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2301653	0.86[ASN][1000 genomes]
rs2301654	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2893805	0.88[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs4766944	0.86[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs4766945	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs4767834	0.86[ASN][1000 genomes]
rs4767835	0.86[ASN][1000 genomes]
rs6490260	0.87[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs6490261	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs7138785	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs7310741	0.83[AFR][1000 genomes]
rs7955441	0.86[ASN][1000 genomes]
rs7957284	0.83[AFR][1000 genomes]
rs7958547	0.86[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs7959425	0.82[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs7965791	0.85[AFR][1000 genomes]
rs7978341	0.83[AFR][1000 genomes]

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	nsv832529	chr12:119863378-120071646	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1052595	chr12:119992580-120132038	Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv541616	chr12:119992580-120132038	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:120059200-120083400	Weak transcription	Fetal Muscle Trunk	muscle
2	chr12:120063000-120068400	Weak transcription	Psoas Muscle	Psoas
3	chr12:120063800-120067400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr12:120065000-120067400	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr12:120065400-120078400	Weak transcription	Right Atrium	heart
6	chr12:120065600-120067200	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr12:120065600-120067400	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr12:120065800-120067200	Weak transcription	HSMM	muscle
9	chr12:120065800-120068000	Weak transcription	HSMMtube	muscle
10	chr12:120065800-120069800	Weak transcription	HepG2	liver
11	chr12:120065800-120071200	Weak transcription	Fetal Muscle Leg	muscle

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links