Variant report

Variant	rs7666192
Chromosome Location	chr4:100920216-100920217
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:100870363..100872210-chr4:100920058..100922365,2	K562	blood:
2	chr4:100920168..100921025-chr4:101017073..101017833,2	MCF-7	breast:
3	chr4:100914108..100916821-chr4:100918808..100921223,2	K562	blood:

Variant related genes	Relation type
ENSG00000164032	Chromatin interaction
ENSG00000245322	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs1044044	0.80[ASN][1000 genomes]
rs10516458	0.80[ASN][1000 genomes]
rs11097680	0.83[ASN][1000 genomes]
rs11097681	0.80[ASN][1000 genomes]
rs11097682	0.80[ASN][1000 genomes]
rs11097683	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11097685	0.84[ASN][1000 genomes]
rs11097686	0.80[ASN][1000 genomes]
rs11736218	0.82[ASN][1000 genomes]
rs11736750	0.81[ASN][1000 genomes]
rs11931053	0.80[ASN][1000 genomes]
rs11931551	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11932783	0.84[ASN][1000 genomes]
rs11936309	0.82[ASN][1000 genomes]
rs11938952	0.82[ASN][1000 genomes]
rs11939538	0.80[ASN][1000 genomes]
rs11941520	0.85[ASN][1000 genomes]
rs17029662	0.80[ASN][1000 genomes]
rs17029673	0.82[ASN][1000 genomes]
rs17029724	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2070738	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2081626	0.80[ASN][1000 genomes]
rs2081627	0.80[ASN][1000 genomes]
rs2276939	0.82[ASN][1000 genomes]
rs2866179	0.84[ASN][1000 genomes]
rs4320141	0.84[ASN][1000 genomes]
rs5015717	0.93[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs55726736	0.80[ASN][1000 genomes]
rs56007968	0.84[ASN][1000 genomes]
rs56140620	0.84[ASN][1000 genomes]
rs57322716	0.85[ASN][1000 genomes]
rs61203457	0.82[ASN][1000 genomes]
rs62306101	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6532837	0.85[ASN][1000 genomes]
rs6532839	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6814140	0.95[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs6816635	0.85[ASN][1000 genomes]
rs6824513	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6831193	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6832726	0.80[ASN][1000 genomes]
rs6838495	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6842840	0.95[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs6843247	0.85[ASN][1000 genomes]
rs6845556	0.82[ASN][1000 genomes]
rs72686215	0.81[ASN][1000 genomes]
rs732386	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73832925	0.82[ASN][1000 genomes]
rs7660185	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7666156	0.85[ASN][1000 genomes]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7666192	DAPP1	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100918800-100920600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:100919800-100920600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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