Variant report

Variant	rs72727916
Chromosome Location	chr4:147033634-147033635
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147024600-147035000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr4:147030200-147034800	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr4:147030800-147034400	Enhancers	Primary B cells from cord blood	blood
4	chr4:147031400-147034600	Enhancers	Primary B cells from peripheral blood	blood
5	chr4:147033000-147033800	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr4:147033000-147034000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr4:147033000-147035000	Weak transcription	Fetal Intestine Large	intestine
8	chr4:147033600-147034000	Weak transcription	Fetal Intestine Small	intestine
9	chr4:147033600-147034000	Active TSS	GM12878-XiMat	blood

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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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