Variant report

Variant	rs491240
Chromosome Location	chr1:175796465-175796466
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs16849314	1.00[AMR][1000 genomes]
rs16849325	1.00[AMR][1000 genomes]
rs16849347	1.00[AMR][1000 genomes]
rs2994686	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs476146	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs508911	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs511759	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs531377	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs535108	1.00[AMR][1000 genomes]
rs539235	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs545285	1.00[EUR][1000 genomes]
rs545497	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs548159	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs556934	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs560031	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7524237	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv33328	chr1:175446583-175910001	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv872560	chr1:175648631-175869554	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv3447472	chr1:175796181-175796678	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:175793400-175799400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:175795800-175797000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:175795800-175797000	Weak transcription	Placenta	Placenta

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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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