Variant report

Variant	rs73274423
Chromosome Location	chr12:41760575-41760576
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs59015177	1.00[AFR][1000 genomes]
rs7136410	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7136514	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73274413	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73274416	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73274425	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73274449	0.94[AFR][1000 genomes]
rs73274455	0.94[AFR][1000 genomes]
rs73274457	0.94[AFR][1000 genomes]
rs73274468	0.87[AFR][1000 genomes]
rs73274472	0.91[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832383	chr12:41693298-41846934	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:41760000-41762200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:41760200-41760800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr12:41760200-41761000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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