Variant report

No.	Distal block	Cell Line	Cell type
1	chr4:127341836..127344814-chr4:127351235..127352909,2	K562	blood:
2	chr17:57920736..57923200-chr4:127350568..127352705,2	MCF-7	breast:
3	chr4:127350740..127352427-chr4:127352755..127354537,2	K562	blood:

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

rs_ID	r²[population]
rs10857113	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11939675	0.92[ASN][1000 genomes]
rs13106216	0.92[ASN][1000 genomes]
rs13126578	0.81[ASN][1000 genomes]
rs1355109	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17011076	0.92[ASN][1000 genomes]
rs17011079	0.94[ASN][1000 genomes]
rs1858092	0.95[ASN][1000 genomes]
rs2391051	0.92[ASN][1000 genomes]
rs2391052	0.92[ASN][1000 genomes]
rs2391053	0.92[ASN][1000 genomes]
rs2391054	0.92[ASN][1000 genomes]
rs2391055	0.94[ASN][1000 genomes]
rs2391056	0.95[ASN][1000 genomes]
rs28419042	0.92[ASN][1000 genomes]
rs28765400	0.92[ASN][1000 genomes]
rs2893184	0.92[ASN][1000 genomes]
rs34210608	0.89[ASN][1000 genomes]
rs4834119	0.84[AMR][1000 genomes]
rs7697549	0.92[ASN][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	nsv526498	chr4:127347399-127362391	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:127346200-127388400	Weak transcription	K562	blood

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