Variant report

Variant	rs13191059
Chromosome Location	chr6:15099687-15099688
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:15099407..15102397-chr6:15106486..15108344,2	K562	blood:
2	chr6:15097373..15100226-chr6:15101243..15103987,3	K562	blood:

Extended variants
information (count: 31 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs13210483	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16876061	0.94[CHB][hapmap];0.81[ASN][1000 genomes]
rs35957683	0.84[ASN][1000 genomes]
rs4715965	0.91[ASN][1000 genomes]
rs6906466	0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[ASN][1000 genomes]
rs6928159	0.94[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs6928936	0.94[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs6936729	0.86[ASN][1000 genomes]
rs72832873	0.84[ASN][1000 genomes]
rs72832876	0.84[ASN][1000 genomes]
rs72832881	0.97[ASN][1000 genomes]
rs72832884	0.99[ASN][1000 genomes]
rs72832887	0.89[ASN][1000 genomes]
rs72832890	0.90[ASN][1000 genomes]
rs72832892	0.88[ASN][1000 genomes]
rs7756288	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7767571	0.90[ASN][1000 genomes]
rs9349965	0.94[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs9358050	0.88[CHB][hapmap];0.91[CHD][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs9367859	0.93[ASN][1000 genomes]
rs9367860	0.99[ASN][1000 genomes]
rs9383020	0.92[ASN][1000 genomes]
rs9383022	0.90[ASN][1000 genomes]
rs9383023	0.89[ASW][hapmap];1.00[CEU][hapmap];0.83[CHB][hapmap];0.85[CHD][hapmap];0.96[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.97[TSI][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9383024	0.89[ASN][1000 genomes]
rs9383025	0.87[ASN][1000 genomes]
rs9396557	0.89[ASN][1000 genomes]
rs9396558	0.89[ASN][1000 genomes]
rs9800553	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[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	nsv830593	chr6:15049636-15244190	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1016007	chr6:15099585-15159098	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs13191059	NOL7	cis	parietal	SCAN

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15087400-15117600	Weak transcription	Right Atrium	heart
2	chr6:15090400-15109000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:15098400-15103600	Weak transcription	K562	blood

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