Variant report

Variant	rs11068687
Chromosome Location	chr12:118256497-118256498
allele	A/C/G/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	chr12:118253800-118266400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr12:118254200-118264000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:118254800-118257400	Enhancers	Dnd41	blood
4	chr12:118256200-118257000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr12:118256200-118257200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr12:118256200-118257200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:118256200-118260600	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr12:118256400-118256600	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr12:118256400-118256800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr12:118256400-118257000	Enhancers	Rectal Mucosa Donor 29	rectum
11	chr12:118256400-118257200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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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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