Variant report

Variant	rs568741146
Chromosome Location	chr6:35105480-35105481
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3441631	chr6:35103524-35106522	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv511879	chr6:35103668-35106088	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3364376	chr6:35103875-35105623	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2633690	chr6:35103902-35106024	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3388382	chr6:35104024-35105922	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35104000-35108600	Weak transcription	Ovary	ovary
2	chr6:35104200-35108000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr6:35104200-35108000	Weak transcription	Fetal Lung	lung
4	chr6:35104400-35114000	Weak transcription	Brain Cingulate Gyrus	brain
5	chr6:35105000-35108800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr6:35105400-35106000	Enhancers	Adipose Nuclei	Adipose
7	chr6:35105400-35106200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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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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