Variant report

Variant	rs569550820
Chromosome Location	chr6:64254331-64254332
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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	nsv981154	chr6:64253950-64260109	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:64249400-64258200	Weak transcription	Liver	Liver
2	chr6:64252400-64255000	Enhancers	Hela-S3	cervix
3	chr6:64252800-64258800	Weak transcription	HepG2	liver
4	chr6:64253400-64254400	Weak transcription	A549	lung
5	chr6:64254200-64254400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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