Variant report

Variant	rs4374807
Chromosome Location	chr6:166617246-166617247
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166611200-166618600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:166611800-166618400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:166614200-166618600	Enhancers	Primary B cells from peripheral blood	blood
4	chr6:166614800-166618600	Enhancers	Primary B cells from cord blood	blood
5	chr6:166615200-166617400	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr6:166616000-166617400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr6:166616200-166617600	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr6:166616800-166618600	Enhancers	GM12878-XiMat	blood
9	chr6:166617200-166617400	Enhancers	Spleen	Spleen
10	chr6:166617200-166619200	Weak transcription	Adipose Derived Mesenchymal Stem Cell 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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