Variant report

No.	Distal block	Cell Line	Cell type
1	chr7:103528310..103530000-chr7:103532562..103534288,2	K562	blood:
2	chr7:103527274..103529978-chr7:103557277..103559784,3	K562	blood:
3	chr7:103527274..103529840-chr7:103557277..103559784,2	K562	blood:

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

rs_ID	r²[population]
rs10233074	0.83[MEX][hapmap]
rs10244283	0.89[ASN][1000 genomes]
rs10262803	0.83[MEX][hapmap]
rs10953394	1.00[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs12536007	1.00[ASW][hapmap];0.90[CEU][hapmap];1.00[GIH][hapmap];0.94[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12669883	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1510857	0.88[MEX][hapmap]
rs17156394	0.88[MEX][hapmap]
rs17157063	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1848959	0.88[MEX][hapmap]
rs1877109	0.95[CHB][hapmap];0.95[CHD][hapmap];0.90[JPT][hapmap];0.83[MEX][hapmap];0.89[ASN][1000 genomes]
rs2237643	1.00[CHB][hapmap];0.93[CHD][hapmap];0.90[JPT][hapmap];0.89[ASN][1000 genomes]
rs2237646	0.95[ASN][1000 genomes]
rs2299393	0.93[ASN][1000 genomes]
rs3213725	1.00[YRI][hapmap]
rs3914129	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs4440548	0.99[ASN][1000 genomes]
rs73181912	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9641319	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs9656085	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.96[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	esv1843940	chr7:103421702-103590285	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103520800-103529200	Weak transcription	HepG2	liver
2	chr7:103526800-103531000	Enhancers	K562	blood
3	chr7:103527800-103529600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr7:103528200-103530400	Enhancers	Fetal Heart	heart
5	chr7:103528800-103529200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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