Variant report

Variant	rs56153341
Chromosome Location	chr2:55310960-55310961
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:55299200-55318000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:55308800-55312000	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr2:55309200-55312000	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr2:55309200-55315200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr2:55310000-55311200	Enhancers	Hela-S3	cervix
6	chr2:55310200-55311000	Enhancers	Primary B cells from cord blood	blood
7	chr2:55310200-55313400	Enhancers	Fetal Lung	lung
8	chr2:55310400-55311000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
9	chr2:55310600-55311000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr2:55310600-55311000	Flanking Active TSS	HUVEC	blood vessel
11	chr2:55310800-55312200	Enhancers	Adipose Nuclei	Adipose

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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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