Variant report

Variant	rs73387152
Chromosome Location	chr8:130377832-130377833
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130369400-130383800	Strong transcription	K562	blood
2	chr8:130375400-130379400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:130375600-130378200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr8:130375600-130379600	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr8:130377200-130378200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr8:130377400-130383800	Enhancers	Dnd41	blood
7	chr8:130377600-130378200	Strong transcription	Fetal Thymus	thymus

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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