Variant report

No.	Distal block	Cell Line	Cell type
1	chr1:211686791..211692090-chr1:211692436..211697358,7	K562	blood:
2	chr1:211694815..211696668-chr1:211701298..211704318,3	K562	blood:
3	chr1:211687723..211692261-chr1:211692405..211697712,7	MCF-7	breast:
4	chr1:211692018..211701005-chr1:211746984..211755135,17	MCF-7	breast:
5	chr1:211692714..211696685-chr1:211696869..211699786,3	K562	blood:

Variant related genes	Relation type
ENSG00000170385	Chromatin interaction

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10863898	0.84[YRI][hapmap]
rs11119751	0.83[YRI][hapmap]
rs11800588	0.91[ASN][1000 genomes]
rs11805325	0.91[ASN][1000 genomes]
rs11805328	0.86[ASN][1000 genomes]
rs12040334	0.85[YRI][hapmap]
rs12062602	0.91[ASN][1000 genomes]
rs17017569	1.00[CHB][hapmap]
rs17017668	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17189035	1.00[CHB][hapmap]
rs2120669	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2120670	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2120671	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2166104	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs57302235	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6669700	0.89[CEU][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6699104	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7527404	0.83[YRI][hapmap]
rs7542785	0.97[ASN][1000 genomes]
rs7553035	0.97[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832514	chr1:211630247-211794963	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211688200-211701200	Weak transcription	Gastric	stomach
2	chr1:211689400-211701200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:211689400-211715000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr1:211690200-211698400	Enhancers	Liver	Liver
5	chr1:211691000-211700400	Weak transcription	Fetal Thymus	thymus
6	chr1:211693400-211697800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr1:211694800-211698000	Weak transcription	Fetal Muscle Leg	muscle
8	chr1:211695000-211697400	Weak transcription	K562	blood
9	chr1:211695000-211697800	Weak transcription	Fetal Muscle Trunk	muscle
10	chr1:211695000-211698400	Enhancers	HepG2	liver
11	chr1:211695200-211701200	Weak transcription	Right Atrium	heart
12	chr1:211696200-211699200	Weak transcription	GM12878-XiMat	blood
13	chr1:211696400-211696800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr1:211696400-211696800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr1:211696400-211697800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:211696400-211700400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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