Variant report

rs_ID	r²[population]
rs1079654	1.00[JPT][hapmap]
rs11760080	1.00[JPT][hapmap]
rs15017	1.00[JPT][hapmap]
rs1569526	1.00[JPT][hapmap]
rs1569527	1.00[JPT][hapmap]
rs1883339	0.89[EUR][1000 genomes]
rs2092236	1.00[JPT][hapmap]
rs6569789	1.00[JPT][hapmap]
rs6903616	1.00[JPT][hapmap]
rs72992830	0.87[AMR][1000 genomes]
rs760811	1.00[JPT][hapmap]
rs7739007	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9483425	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9483433	1.00[JPT][hapmap]
rs9493273	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9493275	1.00[JPT][hapmap]

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:132594200-132599200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:132596600-132597400	Enhancers	Fetal Intestine Small	intestine
3	chr6:132596600-132600800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr6:132596600-132600800	Weak transcription	Fetal Muscle Trunk	muscle
5	chr6:132596800-132600800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr6:132596800-132600800	Weak transcription	Fetal Muscle Leg	muscle
7	chr6:132597000-132600800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr6:132597000-132600800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr6:132597000-132600800	Weak transcription	Duodenum Mucosa	Duodenum
10	chr6:132597000-132600800	Weak transcription	Fetal Intestine Large	intestine
11	chr6:132597000-132600800	Weak transcription	Stomach Mucosa	stomach

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