Variant report

Variant	rs7122109
Chromosome Location	chr11:15597135-15597136
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:15595876..15598536-chr11:15605124..15607978,2	K562	blood:
2	chr11:15595531..15597893-chr11:15599482..15601771,2	K562	blood:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10741679	0.90[EUR][1000 genomes]
rs10766262	0.84[EUR][1000 genomes]
rs10766265	0.96[EUR][1000 genomes]
rs10766266	0.96[EUR][1000 genomes]
rs10766270	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10832451	0.82[EUR][1000 genomes]
rs10832458	0.84[EUR][1000 genomes]
rs10832459	0.84[EUR][1000 genomes]
rs10832473	0.96[EUR][1000 genomes]
rs10832477	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10832478	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10832482	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11023639	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1552304	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2068036	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2351041	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2351049	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2351051	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2351052	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2351054	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2351055	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2351056	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2351058	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2882567	0.96[EUR][1000 genomes]
rs2882568	0.95[EUR][1000 genomes]
rs2882569	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4129901	0.84[EUR][1000 genomes]
rs4757337	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6486248	0.84[EUR][1000 genomes]
rs6486255	0.95[EUR][1000 genomes]
rs6486256	0.97[EUR][1000 genomes]
rs6486257	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6486258	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7110995	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7114130	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7117412	0.84[EUR][1000 genomes]
rs7119351	0.96[EUR][1000 genomes]
rs7120823	0.85[EUR][1000 genomes]
rs7124172	0.85[EUR][1000 genomes]
rs7124173	0.85[EUR][1000 genomes]
rs7126988	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7128205	0.96[EUR][1000 genomes]
rs7129098	0.84[EUR][1000 genomes]
rs7481721	0.84[EUR][1000 genomes]
rs7483088	0.90[EUR][1000 genomes]
rs7924910	0.90[EUR][1000 genomes]
rs7930552	0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7935111	0.84[EUR][1000 genomes]
rs7936873	0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7939544	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7943582	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[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	nsv1050475	chr11:15584061-15620602	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:15585200-15610600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:15588200-15606000	Weak transcription	Left Ventricle	heart
3	chr11:15592400-15601200	Weak transcription	Right Atrium	heart
4	chr11:15596000-15597800	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr11:15596400-15601600	Weak transcription	Psoas Muscle	Psoas
6	chr11:15596800-15601400	Weak transcription	Stomach Mucosa	stomach
7	chr11:15597000-15603000	Enhancers	Primary monocytes fromperipheralblood	blood

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