Variant report

Variant	rs6883244
Chromosome Location	chr5:94086822-94086823
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94074200-94127600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:94083000-94088000	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr5:94083000-94108000	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr5:94083000-94125800	Weak transcription	HUVEC	blood vessel
5	chr5:94084800-94088600	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr5:94085000-94090400	Weak transcription	Hela-S3	cervix
7	chr5:94085200-94105800	Weak transcription	Fetal Thymus	thymus
8	chr5:94085400-94087600	Enhancers	Fetal Heart	heart
9	chr5:94086200-94087600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr5:94086200-94101800	Weak transcription	Primary hematopoietic stem cells	blood
11	chr5:94086400-94087200	Weak transcription	Spleen	Spleen
12	chr5:94086400-94088200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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

what's new

Quick links