Variant report

Variant	rs11724810
Chromosome Location	chr4:166315689-166315690
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:166314486..166316368-chr4:166318044..166320457,2	K562	blood:
2	chr4:166299654..166301660-chr4:166314118..166315958,2	MCF-7	breast:
3	chr4:166309664..166311443-chr4:166315170..166317373,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000109472	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11100610	0.82[ASN][1000 genomes]
rs13110854	0.86[ASN][1000 genomes]
rs1438109	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17686863	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28503877	0.84[AMR][1000 genomes]
rs28604413	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28729471	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34405858	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35212926	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35355030	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4691190	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4691191	0.85[ASN][1000 genomes]
rs72701678	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9308104	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9631752	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9631753	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9631765	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9997245	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9997470	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9997481	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:166304400-166332400	Weak transcription	Brain Angular Gyrus	brain
2	chr4:166305200-166319400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr4:166305800-166330400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:166306600-166324800	Weak transcription	Fetal Stomach	stomach
5	chr4:166307200-166322200	Weak transcription	HepG2	liver
6	chr4:166311400-166319600	Weak transcription	Brain Hippocampus Middle	brain
7	chr4:166311400-166327400	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr4:166312200-166318800	Weak transcription	Fetal Brain Male	brain
9	chr4:166313200-166316200	Weak transcription	Fetal Brain Female	brain
10	chr4:166314800-166315800	Enhancers	Ovary	ovary
11	chr4:166315000-166316000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:166315000-166316800	Weak transcription	Brain Anterior Caudate	brain
13	chr4:166315000-166325200	Weak transcription	Aorta	Aorta
14	chr4:166315200-166315800	Enhancers	HSMM	muscle
15	chr4:166315400-166316200	Enhancers	NHDF-Ad	bronchial
16	chr4:166315400-166317000	Weak transcription	Fetal Lung	lung
17	chr4:166315400-166318600	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr4:166315400-166319600	Weak transcription	Brain Substantia Nigra	brain
19	chr4:166315600-166315800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain

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