Variant report

Variant	rs7925677
Chromosome Location	chr11:119720281-119720282
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119716200-119723400	Weak transcription	Fetal Intestine Large	intestine
2	chr11:119716200-119725200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr11:119716400-119724400	Weak transcription	Right Atrium	heart
4	chr11:119717200-119723600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr11:119717800-119723400	Weak transcription	Fetal Intestine Small	intestine
6	chr11:119718000-119721600	Weak transcription	Right Ventricle	heart
7	chr11:119718600-119722000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:119719000-119724400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr11:119720000-119722000	Weak transcription	Breast Myoepithelial Primary Cells	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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