Variant report

Variant	rs28612399
Chromosome Location	chr2:231492302-231492303
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10168790	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10177471	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10183030	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10190300	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10206720	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11886067	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11902476	0.84[ASN][1000 genomes]
rs12694877	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12988735	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13004009	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1474101	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28802613	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28871949	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4343455	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4972964	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4973338	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6436952	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6436953	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6436955	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6436956	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6436957	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6436958	0.81[ASN][1000 genomes]
rs6436959	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6726627	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6748337	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6754758	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7572912	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7575688	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7587015	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7595572	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv875955	chr2:231440555-231500805	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:231472800-231497200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:231481800-231493000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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