Variant report

Variant	rs12232205
Chromosome Location	chr14:71159710-71159711
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71133200-71173000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:71141000-71160800	Weak transcription	Primary T cells from cord blood	blood
3	chr14:71143000-71177800	Weak transcription	Primary B cells from cord blood	blood
4	chr14:71153400-71165200	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr14:71154400-71165000	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr14:71154600-71165000	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr14:71154600-71165200	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr14:71157600-71162400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr14:71158400-71160000	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr14:71158400-71160200	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr14:71158600-71160200	Enhancers	Placenta	Placenta

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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