Variant report

Variant	rs6569007
Chromosome Location	chr6:118541098-118541099
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs1034247	0.83[ASN][1000 genomes]
rs1889465	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs1889466	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs1931976	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs2050312	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs2050313	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs205917	0.83[ASN][1000 genomes]
rs205919	0.82[AFR][1000 genomes]
rs205920	0.83[ASN][1000 genomes]
rs205923	0.83[ASN][1000 genomes]
rs2095406	0.83[ASN][1000 genomes]
rs2105021	0.83[ASN][1000 genomes]
rs2184365	0.83[ASN][1000 genomes]
rs2883847	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs2883848	0.83[ASN][1000 genomes]
rs455227	0.83[ASN][1000 genomes]
rs455338	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs456384	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs457162	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs457210	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs458588	0.83[ASN][1000 genomes]
rs460399	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs465226	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs4945614	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs4945615	0.83[ASN][1000 genomes]
rs4945617	0.83[ASN][1000 genomes]
rs4946328	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs6911094	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs6917963	0.83[ASN][1000 genomes]
rs6921633	0.83[ASN][1000 genomes]
rs6921657	0.83[ASN][1000 genomes]
rs6933344	0.83[ASN][1000 genomes]
rs7748215	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs7768436	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs9320645	0.83[ASN][1000 genomes]
rs9481771	0.83[ASN][1000 genomes]
rs9481772	0.83[ASN][1000 genomes]
rs9489324	0.83[ASN][1000 genomes]
rs980916	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530526	chr6:118027339-118718476	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv428153	chr6:118430517-118586974	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1030089	chr6:118436482-118604516	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv538427	chr6:118436482-118604516	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:118533600-118541600	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr6:118536800-118542000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:118537400-118541600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:118539400-118541800	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr6:118540000-118541400	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr6:118540000-118541600	Weak transcription	Fetal Heart	heart
7	chr6:118540000-118542200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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