Variant report

Variant	rs10090044
Chromosome Location	chr8:49604591-49604592
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49595800-49607600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:49595800-49616800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:49600800-49607600	Weak transcription	Lung	lung
4	chr8:49603200-49608800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:49604200-49604600	Enhancers	Muscle Satellite Cultured Cells	--
6	chr8:49604200-49604600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr8:49604200-49611400	Weak transcription	Fetal Brain Female	brain
8	chr8:49604400-49604800	Enhancers	HSMM	muscle

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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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