Variant report

Variant	rs73560914
Chromosome Location	chr6:145797996-145797997
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1396645	1.00[EUR][1000 genomes]
rs4566900	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59400283	1.00[EUR][1000 genomes]
rs59536308	1.00[EUR][1000 genomes]
rs59839423	1.00[EUR][1000 genomes]
rs6899864	1.00[EUR][1000 genomes]
rs6929731	1.00[EUR][1000 genomes]
rs73559143	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73559156	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73562162	1.00[EUR][1000 genomes]
rs73568386	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73568401	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73575448	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7742823	1.00[EUR][1000 genomes]
rs7748474	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7757256	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];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	nsv1017166	chr6:145677071-145808448	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv604838	chr6:145709371-145841146	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145768200-145803800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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