Variant report

No.	Distal block	Cell Line	Cell type
1	chr11:74805066..74808860-chr11:74814569..74816963,4	K562	blood:
2	chr11:74790844..74792497-chr11:74804407..74806198,2	MCF-7	breast:
3	chr11:74669969..74672134-chr11:74806047..74808621,2	K562	blood:
4	chr11:74802408..74809371-chr11:74811514..74814356,7	K562	blood:

Variant related genes	Relation type
ENSG00000137491	Chromatin interaction
ENSG00000213333	Chromatin interaction

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

rs_ID	r²[population]
rs11236326	0.87[ASN][1000 genomes]
rs11827488	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12270538	0.82[EUR][1000 genomes]
rs12281823	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12288006	0.82[EUR][1000 genomes]
rs12292336	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12361277	0.80[ASN][1000 genomes]
rs12421194	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17133732	0.88[ASN][1000 genomes]
rs4944072	0.88[ASN][1000 genomes]
rs4944974	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4944975	0.87[ASN][1000 genomes]
rs58626404	0.91[ASN][1000 genomes]
rs61117837	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6592598	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6592602	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs66687047	0.88[ASN][1000 genomes]
rs67947132	0.80[ASN][1000 genomes]
rs7119732	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7122309	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72996586	0.80[ASN][1000 genomes]
rs7946082	0.80[AMR][1000 genomes];0.82[EUR][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	esv3478707	chr11:74782633-74842791	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
2	esv3478718	chr11:74782633-74842791	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74804800-74806200	Weak transcription	A549	lung
2	chr11:74805800-74806600	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr11:74805800-74806600	Flanking Active TSS	K562	blood
4	chr11:74805800-74807400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr11:74805800-74807600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr11:74806000-74806200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr11:74806000-74806200	Bivalent Enhancer	Fetal Intestine Large	intestine

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