Variant report

Variant	rs17243536
Chromosome Location	chr8:122782960-122782961
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:122768400-122788200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:122779600-122785400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:122779800-122787000	Weak transcription	Fetal Lung	lung
4	chr8:122780600-122783400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr8:122780800-122783000	Enhancers	Liver	Liver
6	chr8:122781400-122783600	Weak transcription	HSMM	muscle
7	chr8:122781600-122783600	Weak transcription	NHLF	lung
8	chr8:122781600-122784000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr8:122781600-122784000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr8:122782400-122784000	Enhancers	NHDF-Ad	bronchial
11	chr8:122782600-122783000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr8:122782600-122783200	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr8:122782600-122784200	Enhancers	Adipose Nuclei	Adipose
14	chr8:122782800-122787000	Weak transcription	A549	lung

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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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