Variant report

No.	Distal block	Cell Line	Cell type
1	chr6:15785339..15788012-chr6:15788868..15790666,2	MCF-7	breast:
2	chr6:15785790..15789204-chr6:16129110..16133019,3	K562	blood:
3	chr6:15786898..15789429-chr6:15792470..15795145,2	K562	blood:
4	chr6:15786648..15788654-chr6:16128086..16130862,2	K562	blood:

Variant related genes	Relation type
ENSG00000007944	Chromatin interaction

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10949314	0.97[ASN][1000 genomes]
rs10949315	0.99[ASN][1000 genomes]
rs12192181	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12332848	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12333139	0.85[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1883449	0.88[EUR][1000 genomes]
rs1927575	0.97[ASN][1000 genomes]
rs2149146	0.98[ASN][1000 genomes]
rs4712256	0.99[ASN][1000 genomes]
rs4712257	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4715997	0.99[ASN][1000 genomes]
rs6911160	0.97[ASN][1000 genomes]
rs6925866	0.97[ASN][1000 genomes]
rs6935121	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs742387	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7739472	0.99[ASN][1000 genomes]
rs7739977	0.99[ASN][1000 genomes]
rs7756956	0.99[ASN][1000 genomes]
rs9476906	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9476911	0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs9476912	0.97[ASN][1000 genomes]
rs9476920	0.96[ASN][1000 genomes]
rs9476921	0.99[ASN][1000 genomes]
rs9476922	0.99[ASN][1000 genomes]
rs9476923	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9476934	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15782400-15789200	Weak transcription	Fetal Intestine Large	intestine
2	chr6:15785600-15791200	Weak transcription	Gastric	stomach

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