Variant report

Variant	rs28417613
Chromosome Location	chr18:30261680-30261681
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:30251800-30262000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr18:30252200-30277200	Weak transcription	Spleen	Spleen
3	chr18:30252800-30262000	Strong transcription	Primary B cells from peripheral blood	blood
4	chr18:30253200-30267200	Strong transcription	HepG2	liver
5	chr18:30253200-30275400	Strong transcription	Primary B cells from cord blood	blood
6	chr18:30260400-30282200	Weak transcription	Fetal Kidney	kidney

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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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