Variant report

Variant	rs6930238
Chromosome Location	chr6:145228890-145228891
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs12175408	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12175421	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13198108	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13201654	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13210889	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13216871	0.86[ASN][1000 genomes]
rs13217690	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1338696	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1338697	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1538401	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1538402	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2153108	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2153109	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2153110	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2185143	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35285375	0.83[ASN][1000 genomes]
rs35946718	0.84[ASN][1000 genomes]
rs4331996	0.87[ASN][1000 genomes]
rs4331997	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4526219	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4637659	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4895660	0.81[EUR][1000 genomes]
rs4896761	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs57590687	0.84[ASN][1000 genomes]
rs6570657	0.80[ASN][1000 genomes]
rs6570659	0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6570660	0.84[ASN][1000 genomes]
rs6570661	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6570662	0.86[ASN][1000 genomes]
rs6909971	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6910398	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6914560	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6934724	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6935054	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6935093	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6935178	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6935436	0.81[EUR][1000 genomes]
rs9283117	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9321998	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9321999	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9322000	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9322001	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9322002	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9376873	0.89[ASN][1000 genomes]
rs9376877	0.90[ASN][1000 genomes]
rs9386088	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9390249	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9390250	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9399516	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9403624	0.87[ASN][1000 genomes]
rs9403625	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9403626	0.86[ASN][1000 genomes]
rs9403630	0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9403636	0.86[ASN][1000 genomes]
rs9497118	0.87[ASN][1000 genomes]
rs9497128	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9497135	0.83[ASN][1000 genomes]
rs9688347	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9688355	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9688729	0.80[EUR][1000 genomes];0.87[ASN][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	nsv1016747	chr6:144917411-145599874	Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	esv1850377	chr6:145199259-145319640	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv3437466	chr6:145226059-145230557	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145228000-145235600	Weak transcription	Right Atrium	heart
2	chr6:145228800-145229400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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