Variant report

Variant	rs735737
Chromosome Location	chr2:86177101-86177102
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:86160879..86165285-chr2:86176010..86181999,6	MCF-7	breast:
2	chr2:86174630..86176169-chr2:86176338..86177867,2	MCF-7	breast:
3	chr2:86112745..86122516-chr2:86175080..86185190,27	MCF-7	breast:
4	chr2:86171021..86172691-chr2:86174826..86177732,2	MCF-7	breast:
5	chr2:86124693..86128492-chr2:86175649..86178541,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000232504	Chromatin interaction
ENSG00000115525	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1158729	0.83[AMR][1000 genomes]
rs11891333	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17026666	0.81[AMR][1000 genomes]
rs17026701	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs17026729	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2012798	0.90[ASN][1000 genomes]
rs2366959	0.83[AMR][1000 genomes]
rs4292089	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs55716007	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs57150081	0.81[AMR][1000 genomes]
rs57178127	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs58515922	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs58672934	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs58686314	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs59968392	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs60981340	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61477982	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6547646	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6705122	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6717839	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6718632	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6747424	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6759489	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73943909	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73943920	0.89[ASN][1000 genomes]
rs73945524	0.81[AMR][1000 genomes]
rs73945530	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs73945535	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7570836	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:86175000-86183600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr2:86175800-86177600	Enhancers	Pancreas	Pancrea
3	chr2:86175800-86180600	Enhancers	Liver	Liver
4	chr2:86176200-86177200	Enhancers	Fetal Lung	lung
5	chr2:86176200-86177200	Enhancers	Left Ventricle	heart
6	chr2:86176200-86177200	Enhancers	Right Atrium	heart
7	chr2:86176200-86177200	Enhancers	Spleen	Spleen
8	chr2:86176200-86180400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr2:86176400-86177200	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr2:86176400-86177800	Enhancers	Fetal Thymus	thymus
11	chr2:86176600-86178800	Weak transcription	Fetal Muscle Leg	muscle
12	chr2:86177000-86177200	Bivalent Enhancer	HepG2	liver
13	chr2:86177000-86177800	Enhancers	Ovary	ovary
14	chr2:86177000-86178000	Weak transcription	K562	blood
15	chr2:86177000-86178600	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr2:86177000-86180800	Weak transcription	Adipose Nuclei	Adipose

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