Variant report

Variant	rs193229884
Chromosome Location	chr7:104053682-104053683
allele	C/T
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	nsv888925	chr7:104047599-104170560	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104052800-104054200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr7:104053000-104055600	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr7:104053400-104054600	Weak transcription	Brain Germinal Matrix	brain
4	chr7:104053600-104053800	Bivalent Enhancer	Fetal Brain Male	brain
5	chr7:104053600-104054800	Weak transcription	Brain Cingulate Gyrus	brain
6	chr7:104053600-104055000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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