Variant report

Variant	rs12705213
Chromosome Location	chr7:104091465-104091466
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:104090683..104093466-chr7:104097985..104100510,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10232719	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10239251	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10248554	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10248577	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10248586	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10248725	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10248853	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10253179	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10258646	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10267229	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10267467	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10278196	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10279103	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11763095	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12705211	0.83[EUR][1000 genomes]
rs12705212	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12705217	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13223335	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs28504445	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6977154	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7806966	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7807089	0.83[AMR][1000 genomes];0.96[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	nsv888925	chr7:104047599-104170560	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104084600-104092800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr7:104091400-104092000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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