Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11687033	0.86[CHB][hapmap]
rs11688746	0.80[CHB][hapmap]
rs1356065	0.84[JPT][hapmap]
rs1356066	0.84[JPT][hapmap]
rs1399686	0.80[CHB][hapmap];0.84[JPT][hapmap]
rs1399687	0.85[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs1515277	0.82[JPT][hapmap]
rs1515278	0.82[JPT][hapmap]
rs1515282	0.81[CHB][hapmap]
rs1554103	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16866876	0.82[JPT][hapmap]
rs17819812	0.81[CEU][hapmap]
rs1996240	0.81[CEU][hapmap];0.84[AFR][1000 genomes]
rs3106694	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3112944	0.84[ASN][1000 genomes]
rs4894114	0.81[CEU][hapmap]
rs62176332	0.85[ASN][1000 genomes]
rs62176333	0.85[ASN][1000 genomes]
rs62176334	0.85[ASN][1000 genomes]
rs6741320	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6743733	0.81[CEU][hapmap]
rs6756679	0.86[CHB][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs954649	0.81[CEU][hapmap];0.84[AFR][1000 genomes]
rs9750247	0.80[CHB][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180502400-180511600	Weak transcription	Fetal Heart	heart
2	chr2:180506800-180511200	Weak transcription	Fetal Brain Female	brain
3	chr2:180508400-180517000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr2:180510200-180511200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr2:180510200-180512200	Enhancers	Fetal Lung	lung
6	chr2:180510200-180512400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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