Variant report

Variant	rs8134766
Chromosome Location	chr21:16501741-16501742
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16494200-16502600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr21:16494400-16502800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr21:16499800-16502600	Weak transcription	Fetal Muscle Leg	muscle
4	chr21:16499800-16506400	Weak transcription	Left Ventricle	heart
5	chr21:16500200-16501800	Enhancers	Primary B cells from peripheral blood	blood
6	chr21:16500400-16505800	Weak transcription	Small Intestine	intestine
7	chr21:16500600-16502000	Weak transcription	Primary hematopoietic stem cells	blood
8	chr21:16500600-16510800	Weak transcription	Psoas Muscle	Psoas
9	chr21:16500800-16502200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr21:16500800-16505800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr21:16501200-16506000	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr21:16501400-16505600	Weak transcription	Primary monocytes fromperipheralblood	blood

Quick Search:

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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