Variant report

Variant	rs2921343
Chromosome Location	chr11:70687149-70687150
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs2921332	0.81[EUR][1000 genomes]
rs2921333	0.81[EUR][1000 genomes]
rs2921337	0.86[AFR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2921338	0.86[AFR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2921339	0.89[AFR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2921340	0.94[AFR][1000 genomes];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2921341	0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2921342	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3017499	0.81[EUR][1000 genomes]
rs3019838	0.89[AFR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3019839	0.89[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs3019841	0.86[AFR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3019849	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs930585	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:70670000-70731800	Weak transcription	Gastric	stomach
2	chr11:70673000-70688800	Weak transcription	Pancreas	Pancrea
3	chr11:70681800-70701400	Weak transcription	Liver	Liver
4	chr11:70682400-70689800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr11:70682400-70690400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr11:70684000-70687400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr11:70684800-70697000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr11:70685200-70691600	Weak transcription	Fetal Brain Female	brain
9	chr11:70686000-70690200	Strong transcription	Fetal Intestine Small	intestine
10	chr11:70686200-70687600	Weak transcription	HepG2	liver
11	chr11:70686400-70690800	Weak transcription	Right Atrium	heart
12	chr11:70686600-70687400	Weak transcription	Lung	lung

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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