Variant report

Variant	rs551582068
Chromosome Location	chr6:139933673-139933674
allele	A/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	nsv869066	chr6:139777114-140639695	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
2	nsv969451	chr6:139933131-139942320	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:139929200-139941000	Weak transcription	Aorta	Aorta
2	chr6:139929200-139944000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr6:139932000-139933800	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr6:139932200-139935000	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr6:139932600-139933800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:139932800-139934000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr6:139933400-139938600	Weak transcription	K562	blood
8	chr6:139933600-139933800	Enhancers	Primary B cells from cord blood	blood
9	chr6:139933600-139934000	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr6:139933600-139935200	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr6:139933600-139935800	Weak transcription	HUES64 Cell Line	embryonic stem cell

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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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