Variant report

Variant	rs2448915
Chromosome Location	chr8:95354736-95354737
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:95342938..95344823-chr8:95354569..95356336,2	K562	blood:

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10956912	0.88[ASN][1000 genomes]
rs11778733	0.88[ASN][1000 genomes]
rs11786007	0.88[ASN][1000 genomes]
rs2244209	0.89[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2255130	0.98[ASN][1000 genomes]
rs2263133	0.88[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs2445698	0.97[ASN][1000 genomes]
rs2445701	0.90[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2445702	0.98[ASN][1000 genomes]
rs2445713	0.89[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2448907	0.86[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2448914	0.86[ASN][1000 genomes]
rs2450248	0.84[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2450249	0.82[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2450550	0.82[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2450551	0.92[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2450552	0.97[ASN][1000 genomes]
rs2450555	0.89[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs2450560	0.89[ASN][1000 genomes]
rs2450562	0.94[ASN][1000 genomes]
rs2450563	0.88[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2450564	0.84[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2450565	0.93[ASN][1000 genomes]
rs2450566	0.86[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs2450571	0.89[ASN][1000 genomes]
rs2450574	0.87[ASN][1000 genomes]
rs2450576	0.98[ASN][1000 genomes]
rs2450577	0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2450579	0.88[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs2470727	0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2470729	0.98[ASN][1000 genomes]
rs2470730	0.90[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2470734	0.89[ASN][1000 genomes]
rs2470736	0.89[ASN][1000 genomes]
rs2470737	0.88[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs2470738	0.82[ASN][1000 genomes]
rs2470741	0.86[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2470743	0.94[ASN][1000 genomes]
rs2470744	0.94[ASN][1000 genomes]
rs2470745	0.94[ASN][1000 genomes]
rs2470747	0.89[ASN][1000 genomes]
rs2515097	0.92[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2515101	0.88[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs2515102	0.94[ASN][1000 genomes]
rs2515104	0.89[ASN][1000 genomes]
rs2515105	0.89[ASN][1000 genomes]
rs2515106	0.86[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2515109	0.84[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2515119	0.86[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs2515120	0.89[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2515121	0.89[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2515122	0.97[ASN][1000 genomes]
rs2515132	0.89[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2515142	0.82[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2515151	0.87[ASN][1000 genomes]
rs2515152	0.94[ASN][1000 genomes]
rs2515158	0.97[ASN][1000 genomes]
rs2515159	0.92[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2515160	0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2515162	0.98[ASN][1000 genomes]
rs2515163	0.98[ASN][1000 genomes]
rs2515164	0.94[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2515166	0.89[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs2515168	0.97[ASN][1000 genomes]
rs28503419	0.87[ASN][1000 genomes]
rs3098702	0.87[ASN][1000 genomes]
rs3098704	0.88[ASN][1000 genomes]
rs3136400	0.89[ASN][1000 genomes]
rs3136407	0.89[ASN][1000 genomes]
rs3136414	0.83[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs56303696	0.88[ASN][1000 genomes]
rs7007534	0.88[ASN][1000 genomes]
rs882521	0.89[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	nsv831401	chr8:95218297-95393968	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1017301	chr8:95273503-96248352	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv539680	chr8:95273503-96248352	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
4	nsv532338	chr8:95296118-95971825	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95347400-95355400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr8:95353800-95359000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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