Variant report

Variant	rs7127154
Chromosome Location	chr11:33993398-33993399
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:33877921..33880595-chr11:33992729..33995031,2	K562	blood:
2	chr11:33992595..33994153-chr11:34125657..34127905,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000135372	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10430951	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10444269	0.90[ASN][1000 genomes]
rs10444270	0.90[ASN][1000 genomes]
rs10742309	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10768037	0.89[ASN][1000 genomes]
rs10768038	0.95[ASN][1000 genomes]
rs10768039	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10836133	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10836134	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12273291	0.89[ASN][1000 genomes]
rs2176611	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2421454	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2421467	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2901432	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4755352	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4755353	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4755354	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4756086	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4756088	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4996144	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61199722	0.91[ASN][1000 genomes]
rs6484681	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6484682	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6484683	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6484684	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6484685	0.95[ASN][1000 genomes]
rs6484686	0.86[ASN][1000 genomes]
rs6484687	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7104709	0.85[ASN][1000 genomes]
rs713310	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7481489	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7926558	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7940280	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs939038	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33992800-33993400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr11:33992800-33993400	Enhancers	Fetal Intestine Large	intestine
3	chr11:33992800-33993400	Enhancers	Fetal Intestine Small	intestine
4	chr11:33992800-33993400	Enhancers	Fetal Stomach	stomach
5	chr11:33993000-33993400	Bivalent Enhancer	HepG2	liver
6	chr11:33993000-33998200	Weak transcription	Hela-S3	cervix
7	chr11:33993200-33993400	Flanking Active TSS	Placenta	Placenta
8	chr11:33993200-33997800	Weak transcription	Adipose Nuclei	Adipose
9	chr11:33993200-33998000	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr11:33993200-33998000	Weak transcription	Fetal Lung	lung

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