Variant report

Variant	rs1859700
Chromosome Location	chr7:41065849-41065850
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:41060800-41066600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr7:41062800-41082200	Weak transcription	Aorta	Aorta
3	chr7:41064000-41066600	Weak transcription	Osteobl	bone
4	chr7:41065600-41069200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:41065600-41069200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:41065800-41066800	Weak transcription	NHDF-Ad	bronchial
7	chr7:41065800-41067600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:41065800-41068800	Enhancers	HSMMtube	muscle
9	chr7:41065800-41069000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr7:41065800-41071000	Enhancers	HMEC	breast

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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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