Variant report

Variant	rs576765147
Chromosome Location	chr4:30819224-30819225
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv4285	chr4:30815642-30838784	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv499039	chr4:30819213-30830142	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:30795800-30824000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:30804800-30819400	Weak transcription	Aorta	Aorta
3	chr4:30813800-30835800	Weak transcription	Colon Smooth Muscle	Colon
4	chr4:30817600-30820400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr4:30817600-30824000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:30817800-30819800	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr4:30817800-30820200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr4:30818000-30823000	Weak transcription	Stomach Smooth Muscle	stomach
9	chr4:30818400-30819600	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr4:30818600-30823600	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr4:30819000-30819600	Weak transcription	Fetal Lung	lung
12	chr4:30819000-30821600	Enhancers	Fetal Heart	heart

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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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