Variant report

rs_ID	r²[population]
rs11556354	0.93[GIH][hapmap];0.91[TSI][hapmap]
rs12175928	0.91[JPT][hapmap]
rs2073298	0.91[JPT][hapmap]
rs2180341	0.82[MEX][hapmap]
rs2326567	0.81[MEX][hapmap]
rs3798853	0.82[MEX][hapmap]
rs4141423	0.91[JPT][hapmap]
rs4308584	0.81[EUR][1000 genomes]
rs6569479	0.81[MEX][hapmap]
rs6569485	0.91[JPT][hapmap]
rs6569487	0.85[EUR][1000 genomes]
rs6913350	0.82[ASN][1000 genomes]
rs761842	0.91[JPT][hapmap]
rs7742161	0.82[ASN][1000 genomes]
rs7760652	0.82[ASN][1000 genomes]
rs7764180	0.91[JPT][hapmap]
rs877102	0.91[CHB][hapmap];0.91[JPT][hapmap];0.86[MEX][hapmap];0.80[ASN][1000 genomes]
rs9321072	0.91[JPT][hapmap]
rs9372861	0.86[JPT][hapmap]
rs9372862	0.91[JPT][hapmap]
rs9372863	0.90[JPT][hapmap]
rs9372865	0.91[JPT][hapmap]
rs9372866	0.86[JPT][hapmap]
rs9375493	0.81[ASN][1000 genomes]
rs9375498	0.86[JPT][hapmap]
rs9375500	0.90[JPT][hapmap]
rs9375502	0.91[JPT][hapmap]
rs9385422	0.81[EUR][1000 genomes]
rs9388554	0.82[ASN][1000 genomes]
rs9388557	0.86[JPT][hapmap]
rs9388558	0.91[JPT][hapmap]
rs9388559	0.91[JPT][hapmap]
rs9398840	0.82[MEX][hapmap]
rs9401939	0.86[JPT][hapmap]
rs9401945	0.91[JPT][hapmap]
rs9401947	0.86[JPT][hapmap]
rs9401949	0.91[JPT][hapmap]
rs9401953	0.82[MEX][hapmap]

SNP	Gene	Cis/trans	Tissue	Source
rs4371861	ECHDC1	Cis_1M	lymphoblastoid	RTeQTL
rs4371861	SH3RF2	trans	brain	seeQTL

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:127568200-127568800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr6:127568200-127569000	Enhancers	HMEC	breast
3	chr6:127568200-127569000	Enhancers	NHEK	skin
4	chr6:127568200-127569600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr6:127568200-127569600	Enhancers	Fetal Brain Male	brain
6	chr6:127568400-127569400	Enhancers	NHDF-Ad	bronchial

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