Variant report

Variant	rs74075204
Chromosome Location	chr1:56414356-56414357
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs56248222	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59073332	1.00[AMR][1000 genomes]
rs59121815	1.00[AMR][1000 genomes]
rs59641326	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60466904	0.86[AFR][1000 genomes]
rs61213965	1.00[AMR][1000 genomes]
rs6588604	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6689869	1.00[AMR][1000 genomes]
rs74072808	1.00[AMR][1000 genomes]
rs74075209	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74075217	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74075221	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74075222	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74075224	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74075225	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74075226	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74075233	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74075234	0.88[AFR][1000 genomes];1.00[AMR][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	nsv870513	chr1:56407227-56493106	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv528440	chr1:56412081-56420193	Enhancers ZNF genes & repeats Weak transcription	TF binding region lncRNA	1 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	chr1:56402000-56416800	Weak transcription	Aorta	Aorta
2	chr1:56404600-56416200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:56410600-56418600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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