Variant report

Variant	rs2384982
Chromosome Location	chr7:103706400-103706401
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:103705230..103707654-chr7:103709368..103711788,2	K562	blood:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10215768	0.86[ASN][1000 genomes]
rs10240155	0.85[ASN][1000 genomes]
rs10240408	0.90[ASN][1000 genomes]
rs10240682	0.90[ASN][1000 genomes]
rs1024817	0.88[MEX][hapmap]
rs10252269	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10255340	0.90[ASN][1000 genomes]
rs10256829	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10281061	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10282214	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11971200	0.80[AMR][1000 genomes]
rs1858811	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs194845	0.87[MEX][hapmap]
rs2157800	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34714175	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4727586	0.81[ASN][1000 genomes]
rs4729945	0.90[ASN][1000 genomes]
rs4729946	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4729947	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55914768	0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs58765880	0.90[ASN][1000 genomes]
rs60297107	0.81[AMR][1000 genomes]
rs66918163	0.90[ASN][1000 genomes]
rs6955592	0.93[ASN][1000 genomes]
rs756742	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7797592	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7797632	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7797741	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7797777	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv888924	chr7:103637906-103706936	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1018253	chr7:103669491-103731850	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103705800-103706400	Flanking Active TSS	HepG2	liver
2	chr7:103706400-103708600	Enhancers	HepG2	liver

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