Variant report

Variant	rs7736032
Chromosome Location	chr5:54002871-54002872
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	chr5:54001087..54003577-chr5:54005143..54007201,4	K562	blood:
2	chr5:54001087..54003577-chr5:54005143..54007201,3	K562	blood:

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10940418	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10940419	0.84[ASN][1000 genomes]
rs12520114	0.84[ASN][1000 genomes]
rs12654571	0.82[ASN][1000 genomes]
rs12655150	0.82[ASN][1000 genomes]
rs12659390	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12659671	0.84[ASN][1000 genomes]
rs1823053	0.96[AFR][1000 genomes];0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2034237	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4288089	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4342279	0.93[AFR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4376219	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4865585	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4865865	0.95[AFR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55774545	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs56341116	0.87[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs56399530	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs57433496	0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs57534013	0.81[ASN][1000 genomes]
rs57569595	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs59617154	0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs60146924	0.84[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs7735895	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7736999	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:53999600-54003600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:53999800-54009400	Weak transcription	Aorta	Aorta
3	chr5:53999800-54009600	Weak transcription	Right Atrium	heart
4	chr5:54000000-54005000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:54000000-54005000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr5:54000200-54005600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr5:54001200-54004000	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr5:54001800-54003200	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr5:54002400-54003200	Enhancers	Fetal Heart	heart
10	chr5:54002600-54003200	Enhancers	Placenta	Placenta
11	chr5:54002600-54003200	Enhancers	Ovary	ovary
12	chr5:54002600-54003600	Weak transcription	Adipose Nuclei	Adipose
13	chr5:54002600-54005000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr5:54002600-54009600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr5:54002800-54003000	Enhancers	Fetal Intestine Large	intestine

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