Variant report

Variant	rs57279023
Chromosome Location	chr11:74919347-74919348
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:74918789..74920470-chr11:74922172..74924054,2	K562	blood:
2	chr11:74918103..74919811-chr11:74924513..74927138,2	K562	blood:
3	chr11:74718841..74721499-chr11:74918282..74920055,2	K562	blood:
4	chr11:74918789..74921667-chr11:74922172..74926062,5	K562	blood:

Variant related genes	Relation type
ENSG00000255136	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11823030	0.84[ASN][1000 genomes]
rs17133818	0.88[ASN][1000 genomes]
rs17133831	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17133844	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17133848	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17133858	0.82[EUR][1000 genomes]
rs1801906	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2035208	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3781725	0.84[ASN][1000 genomes]
rs3781727	0.88[ASN][1000 genomes]
rs3824904	0.81[ASN][1000 genomes]
rs41298117	0.82[EUR][1000 genomes]
rs41298121	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4362167	0.82[EUR][1000 genomes]
rs56253315	0.92[ASN][1000 genomes]
rs56738638	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56958854	0.82[EUR][1000 genomes]
rs57277559	0.82[EUR][1000 genomes]
rs57654883	0.82[EUR][1000 genomes]
rs58769063	0.88[ASN][1000 genomes]
rs59390914	0.82[EUR][1000 genomes]
rs60893479	0.82[EUR][1000 genomes]
rs61265142	0.82[EUR][1000 genomes]
rs61443691	0.88[ASN][1000 genomes]
rs67495709	0.82[EUR][1000 genomes]
rs67947456	0.82[EUR][1000 genomes]
rs72998587	0.82[EUR][1000 genomes]
rs72998590	0.82[EUR][1000 genomes]
rs72998594	0.82[EUR][1000 genomes]
rs72998602	0.82[EUR][1000 genomes]
rs73488755	0.83[ASN][1000 genomes]
rs73488760	0.88[ASN][1000 genomes]
rs73488764	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7924924	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7927925	0.82[EUR][1000 genomes]
rs7951787	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74911400-74919800	Weak transcription	Spleen	Spleen
2	chr11:74915800-74919600	Weak transcription	Lung	lung
3	chr11:74916000-74919600	Weak transcription	Pancreas	Pancrea
4	chr11:74916000-74920800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr11:74916800-74919600	Weak transcription	Liver	Liver
6	chr11:74917200-74919800	Weak transcription	Fetal Intestine Small	intestine
7	chr11:74917200-74920400	Weak transcription	Fetal Intestine Large	intestine
8	chr11:74919200-74920400	Enhancers	K562	blood

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