Variant report

Variant	rs4285965
Chromosome Location	chr12:10026194-10026195
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:10024279..10026522-chr12:10046207..10048850,2	K562	blood:
2	chr12:10024036..10026643-chr12:10029276..10031174,3	K562	blood:

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10219684	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10844994	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10844998	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1814494	0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1814495	0.87[ASN][1000 genomes]
rs4287401	0.95[ASN][1000 genomes]
rs4764045	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4764046	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4764047	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs5017882	0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs5017883	0.99[ASN][1000 genomes]
rs5017884	0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs5017885	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs5017886	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs5017887	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7134094	0.87[ASN][1000 genomes]
rs7138292	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7297667	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7300903	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7305724	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7312942	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7313246	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs935537	0.86[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10024200-10026200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:10024400-10026200	Enhancers	HMEC	breast
3	chr12:10025600-10033400	Weak transcription	Primary hematopoietic stem cells	blood

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