Variant report

Variant	rs72723860
Chromosome Location	chr1:95769337-95769338
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:12)

rs_ID	r²[population]
rs1336437	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72720295	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72722107	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72722127	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72722131	1.00[EUR][1000 genomes]
rs72722140	1.00[EUR][1000 genomes]
rs72722148	1.00[EUR][1000 genomes]
rs72722161	1.00[EUR][1000 genomes]
rs72722168	1.00[EUR][1000 genomes]
rs72722178	1.00[EUR][1000 genomes]
rs72723805	1.00[EUR][1000 genomes]
rs72723823	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830648	chr1:95760162-95926264	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1006113	chr1:95768502-96139003	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:95768400-95775000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:95768600-95773800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:95769200-95782000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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