Variant report

Variant	rs72689121
Chromosome Location	chr14:85774936-85774937
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12436591	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12436824	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17201916	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60463145	0.90[EUR][1000 genomes]
rs6574813	0.89[EUR][1000 genomes]
rs7140796	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72689116	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72689118	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72689126	0.90[EUR][1000 genomes]
rs72689127	0.90[EUR][1000 genomes]
rs895911	0.87[EUR][1000 genomes]

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:85773000-85775600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr14:85774200-85776400	Enhancers	Primary hematopoietic stem cells	blood
3	chr14:85774600-85775200	Enhancers	HSMMtube	muscle
4	chr14:85774800-85775000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr14:85774800-85775600	Enhancers	Fetal Muscle Leg	muscle
6	chr14:85774800-85775600	Enhancers	Fetal Stomach	stomach
7	chr14:85774800-85776000	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr14:85774800-85776000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr14:85774800-85776200	Enhancers	Fetal Brain Male	brain
10	chr14:85774800-85777800	Enhancers	HUVEC	blood vessel

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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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