Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:181816772..181818990-chr2:181821114..181822961,2	K562	blood:
2	chr2:181808930..181811570-chr2:181816470..181818302,2	K562	blood:

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10167039	0.85[ASN][1000 genomes]
rs10180373	0.94[ASN][1000 genomes]
rs10180999	0.94[ASN][1000 genomes]
rs10190282	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10203057	0.94[ASN][1000 genomes]
rs10203106	0.94[ASN][1000 genomes]
rs10206321	0.85[ASN][1000 genomes]
rs13389513	0.94[ASN][1000 genomes]
rs13396254	1.00[CHB][hapmap];0.94[ASN][1000 genomes]
rs13399193	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs13406482	0.94[ASN][1000 genomes]
rs13409312	0.85[ASN][1000 genomes]
rs13420661	0.85[ASN][1000 genomes]
rs13425162	0.85[ASN][1000 genomes]
rs13425730	0.85[ASN][1000 genomes]
rs28887797	0.94[ASN][1000 genomes]
rs4077214	0.94[ASN][1000 genomes]
rs4618006	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6706552	0.85[ASN][1000 genomes]
rs6721173	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs6722001	0.85[ASN][1000 genomes]
rs6761219	0.85[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	nsv875476	chr2:181767757-181854997	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	n/a
2	esv275458	chr2:181816046-181819377	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:181817000-181818000	Enhancers	GM12878-XiMat	blood

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