Variant report

Variant	rs73072156
Chromosome Location	chr1:203351782-203351783
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs34961776	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4291556	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6428005	0.94[ASN][1000 genomes]
rs6428006	0.94[ASN][1000 genomes]
rs6428008	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6661852	0.81[ASN][1000 genomes]
rs6662062	0.87[ASN][1000 genomes]
rs73072176	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:203347600-203351800	Enhancers	Fetal Stomach	stomach
2	chr1:203347600-203351800	Enhancers	Ovary	ovary
3	chr1:203347800-203352200	Enhancers	Right Atrium	heart
4	chr1:203348000-203351800	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr1:203348600-203352200	Enhancers	Primary B cells from peripheral blood	blood
6	chr1:203349400-203351800	Enhancers	Rectal Smooth Muscle	rectum
7	chr1:203349600-203352000	Enhancers	Stomach Smooth Muscle	stomach
8	chr1:203350200-203351800	Enhancers	Primary B cells from cord blood	blood
9	chr1:203350600-203351800	Enhancers	Spleen	Spleen
10	chr1:203350800-203351800	Genic enhancers	Adipose Nuclei	Adipose
11	chr1:203350800-203351800	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr1:203351600-203351800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:203351600-203353400	Weak transcription	Fetal Heart	heart

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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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