Variant report

Variant	rs1336522
Chromosome Location	chr6:133642610-133642611
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs1015726	0.94[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs11754045	1.00[CHB][hapmap];0.82[JPT][hapmap];0.98[ASN][1000 genomes]
rs11757185	0.98[ASN][1000 genomes]
rs12524250	0.93[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs12524730	0.98[ASN][1000 genomes]
rs12525252	0.98[ASN][1000 genomes]
rs12525309	0.94[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs12527527	0.94[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs12527741	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1336524	0.94[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1336525	0.94[ASN][1000 genomes]
rs1336526	0.98[ASN][1000 genomes]
rs17242333	0.93[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs17242410	0.98[ASN][1000 genomes]
rs17242466	0.93[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs17301622	0.80[CHB][hapmap];0.86[ASN][1000 genomes]
rs17301712	0.93[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs17301754	0.94[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs17301858	0.93[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs17301872	0.98[ASN][1000 genomes]
rs17301914	0.94[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs17301942	0.98[ASN][1000 genomes]
rs17302199	0.98[ASN][1000 genomes]
rs17302366	0.98[ASN][1000 genomes]
rs1814195	0.94[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs1962598	0.98[ASN][1000 genomes]
rs2027210	0.80[CHB][hapmap];0.84[ASN][1000 genomes]
rs2184784	0.90[YRI][hapmap]
rs2210891	0.86[ASN][1000 genomes]
rs2785238	0.94[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs296414	0.97[ASN][1000 genomes]
rs296417	0.94[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs373884	0.93[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs433294	0.82[CHB][hapmap]
rs445979	0.98[ASN][1000 genomes]
rs55977000	0.98[ASN][1000 genomes]
rs56256859	0.98[ASN][1000 genomes]
rs62428661	0.96[ASN][1000 genomes]
rs62428662	0.98[ASN][1000 genomes]
rs62430320	0.86[ASN][1000 genomes]
rs62430323	0.86[ASN][1000 genomes]
rs62431678	0.98[ASN][1000 genomes]
rs6569877	0.82[YRI][hapmap];0.87[AFR][1000 genomes]
rs68021023	0.94[ASN][1000 genomes]
rs6903792	0.84[AFR][1000 genomes]
rs6924629	1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs6930942	0.87[AFR][1000 genomes]
rs6937974	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71545061	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72993929	0.98[ASN][1000 genomes]
rs7454561	0.93[CHB][hapmap];0.90[JPT][hapmap];0.97[ASN][1000 genomes]
rs9483575	0.84[AFR][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	nsv886680	chr6:133613759-133663021	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133613000-133655000	Weak transcription	Hela-S3	cervix
2	chr6:133637200-133642800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr6:133638000-133643000	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr6:133638200-133646400	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr6:133639200-133646200	Weak transcription	Psoas Muscle	Psoas
6	chr6:133640200-133647200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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