Variant report

Variant	rs7823285
Chromosome Location	chr8:49547651-49547652
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10087993	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs16938333	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs16938348	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2004390	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4582590	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57572174	1.00[EUR][1000 genomes]
rs66764967	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs67193056	1.00[EUR][1000 genomes]
rs6999204	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs878995	0.82[EUR][1000 genomes]

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49534400-49556000	Weak transcription	Pancreas	Pancrea
2	chr8:49543200-49548000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:49543200-49548400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr8:49543400-49548000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr8:49543600-49548200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:49544200-49548200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr8:49544400-49555400	Weak transcription	Osteobl	bone
8	chr8:49546600-49554400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr8:49547000-49548800	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr8:49547200-49551200	Weak transcription	Ovary	ovary
11	chr8:49547400-49553400	Weak transcription	Fetal Lung	lung

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

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