Variant report

Variant	rs10099433
Chromosome Location	chr8:91666520-91666521
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000251136	Chromatin interaction
ENSG00000196562	Chromatin interaction
ENSG00000104320	Chromatin interaction
ENSG00000104312	Chromatin interaction

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91660600-91667400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:91666000-91666600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
3	chr8:91666000-91666600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
4	chr8:91666200-91666800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr8:91666400-91666600	Enhancers	H9 Cell Line	embryonic stem cell
6	chr8:91666400-91666800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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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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