Variant report

Variant	rs57985308
Chromosome Location	chr11:86098888-86098889
allele	A/C
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	chr11:86086000-86102200	Weak transcription	Left Ventricle	heart
2	chr11:86086000-86106200	Weak transcription	Aorta	Aorta
3	chr11:86089400-86099400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr11:86095200-86106200	Weak transcription	Fetal Brain Female	brain
5	chr11:86097600-86105000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr11:86098200-86099000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr11:86098200-86105000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:86098600-86099600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr11:86098600-86099600	Enhancers	Fetal Brain Male	brain
10	chr11:86098800-86099400	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr11:86098800-86099400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr11:86098800-86099600	Strong transcription	H9 Derived Neuron 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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