Variant report

Variant	rs60953408
Chromosome Location	chr6:24308803-24308804
allele	C/T
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	chr6:24294600-24312000	Weak transcription	Fetal Intestine Small	intestine
2	chr6:24303000-24310000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:24308000-24309200	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr6:24308400-24313600	Weak transcription	Fetal Kidney	kidney
5	chr6:24308400-24313800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:24308600-24309400	Enhancers	HepG2	liver
7	chr6:24308600-24309800	Weak transcription	A549	lung
8	chr6:24308600-24311000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr6:24308600-24311200	Weak transcription	HSMMtube	muscle
10	chr6:24308600-24311800	Weak transcription	HUES6 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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