Variant report

Variant	rs539304338
Chromosome Location	chr6:36154325-36154326
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

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	esv3363467	chr6:35820920-36222197	Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	esv3381036	chr6:36153974-36156172	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 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	chr6:36146000-36163400	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr6:36147400-36155400	Weak transcription	Primary T cells from cord blood	blood
3	chr6:36149000-36163600	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr6:36152600-36163600	Weak transcription	Brain Angular Gyrus	brain
5	chr6:36153200-36155200	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr6:36153400-36155400	Weak transcription	Primary hematopoietic stem cells	blood

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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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