Variant report

rs_ID	r²[population]
rs10497544	0.81[MEX][hapmap]
rs11901346	0.81[JPT][hapmap]
rs12373725	0.83[JPT][hapmap]
rs12622727	0.86[EUR][1000 genomes]
rs12623583	0.83[JPT][hapmap]
rs13419649	0.82[JPT][hapmap]
rs1399687	0.83[CHB][hapmap]
rs1515282	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1515289	0.83[JPT][hapmap]
rs16866903	0.81[JPT][hapmap]
rs16866915	0.83[JPT][hapmap]
rs2292652	0.82[JPT][hapmap]
rs3106689	0.83[JPT][hapmap]
rs3112968	0.82[JPT][hapmap]
rs3112970	0.83[JPT][hapmap]
rs58011887	0.86[EUR][1000 genomes]
rs61241001	0.86[EUR][1000 genomes]
rs62175160	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62175161	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62175162	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62175169	0.86[EUR][1000 genomes]
rs62175183	0.86[EUR][1000 genomes]
rs62175184	0.86[EUR][1000 genomes]
rs62175187	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7421557	0.83[JPT][hapmap]
rs7558784	0.83[JPT][hapmap]
rs7590028	0.83[JPT][hapmap]
rs932115	0.83[JPT][hapmap]

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180517400-180521400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:180520800-180521600	Weak transcription	Fetal Brain Male	brain
3	chr2:180521200-180522000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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