Variant report

Variant	rs571054108
Chromosome Location	chr6:134402930-134402931
allele	G/T
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	esv275229	chr6:134402896-134406409	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:134395600-134405000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:134398800-134404200	Enhancers	Placenta	Placenta
3	chr6:134400200-134404600	Enhancers	Primary B cells from cord blood	blood
4	chr6:134400200-134404600	Enhancers	Primary B cells from peripheral blood	blood
5	chr6:134401800-134403200	Weak transcription	GM12878-XiMat	blood
6	chr6:134402800-134403000	Enhancers	hESC Derived CD184+ Endoderm 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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