Variant report

Variant	rs79382970
Chromosome Location	chr8:130140026-130140027
allele	A/C/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	nsv891443	chr8:130016499-130220746	Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv2761241	chr8:130139946-130146557	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
3	esv1599688	chr8:130140025-130140026	Strong transcription Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
4	esv2541423	chr8:130140026-130140026	Strong transcription Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
5	esv2028937	chr8:130140026-130140027	Strong transcription Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130126400-130160600	Weak transcription	Fetal Thymus	thymus
2	chr8:130138800-130142600	Strong transcription	Dnd41	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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