Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10201348	0.80[CEU][hapmap]
rs1033213	1.00[JPT][hapmap]
rs10497548	0.82[JPT][hapmap]
rs10803927	0.93[JPT][hapmap]
rs13408749	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17821260	0.93[JPT][hapmap]
rs1877941	0.93[JPT][hapmap]
rs2203461	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2276573	0.87[JPT][hapmap]
rs3106718	0.93[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs3106720	0.93[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs3106722	0.94[JPT][hapmap]
rs3112932	0.93[JPT][hapmap]
rs3112935	1.00[JPT][hapmap];0.96[YRI][hapmap];0.80[AFR][1000 genomes]
rs3112972	0.81[JPT][hapmap];0.96[YRI][hapmap]
rs6708189	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6708429	0.84[CEU][hapmap]
rs6708458	0.83[CEU][hapmap]
rs7569621	0.82[CEU][hapmap]
rs7581866	0.82[CEU][hapmap]
rs7607628	0.82[CEU][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180535200-180540200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:180536200-180541600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr2:180536600-180537400	Enhancers	Fetal Intestine Large	intestine
4	chr2:180536800-180539400	Weak transcription	Gastric	stomach
5	chr2:180536800-180541200	Weak transcription	HSMMtube	muscle

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