Variant report

Variant	rs7304812
Chromosome Location	chr12:121040703-121040704
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	chr12:121036400-121041000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr12:121038000-121056800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr12:121038400-121041200	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr12:121038600-121041200	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr12:121038600-121041200	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr12:121038600-121050600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr12:121039000-121041000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr12:121039000-121041000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr12:121040000-121040800	Enhancers	Primary B cells from cord blood	blood
10	chr12:121040000-121041200	Enhancers	Primary hematopoietic stem cells	blood
11	chr12:121040400-121040800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr12:121040400-121041000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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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