Variant report

Variant	rs190262802
Chromosome Location	chr6:144388715-144388716
allele	A/C
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	nsv886738	chr6:144387698-144428387	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:144386400-144408800	Weak transcription	Right Ventricle	heart
2	chr6:144387400-144388800	Enhancers	Primary B cells from peripheral blood	blood
3	chr6:144388000-144389400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr6:144388200-144389200	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr6:144388400-144389800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr6:144388400-144396600	Weak transcription	K562	blood
7	chr6:144388600-144389200	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr6:144388600-144390200	Enhancers	GM12878-XiMat	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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