Variant report

Variant	rs10931461
Chromosome Location	chr2:191405280-191405281
allele	A/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	chr2:191402000-191405600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:191402000-191405800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr2:191402400-191406600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
4	chr2:191402800-191409600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:191403000-191416800	Weak transcription	Gastric	stomach
6	chr2:191403800-191406600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr2:191404600-191405400	ZNF genes & repeats	Brain Hippocampus Middle	brain
8	chr2:191404600-191405600	ZNF genes & repeats	Colon Smooth Muscle	Colon
9	chr2:191404800-191405400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
10	chr2:191405000-191405400	ZNF genes & repeats	Aorta	Aorta
11	chr2:191405000-191405400	ZNF genes & repeats	Esophagus	oesophagus
12	chr2:191405000-191405400	ZNF genes & repeats	Right Atrium	heart

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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