Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs244776	0.89[ASN][1000 genomes]
rs244779	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28580	0.84[ASN][1000 genomes]
rs32767	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs32768	0.89[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs32770	0.85[ASN][1000 genomes]
rs32771	0.85[ASN][1000 genomes]
rs32774	0.85[ASN][1000 genomes]
rs32775	0.85[ASN][1000 genomes]
rs32776	0.85[ASN][1000 genomes]
rs32777	0.85[ASN][1000 genomes]
rs32780	0.84[ASN][1000 genomes]
rs32783	0.84[ASN][1000 genomes]
rs32784	0.83[ASN][1000 genomes]
rs32786	0.84[ASN][1000 genomes]
rs32787	0.84[ASN][1000 genomes]
rs391090	0.85[ASN][1000 genomes]
rs393791	0.84[ASN][1000 genomes]
rs401590	0.84[ASN][1000 genomes]
rs413206	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:35364800-35371800	Weak transcription	Placenta	Placenta
2	chr5:35366400-35370200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr5:35367800-35370600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr5:35368400-35370000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:35369800-35370600	Enhancers	Monocytes-CD14+_RO01746	blood

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