Variant report

Variant	rs185001785
Chromosome Location	chr6:30207689-30207690
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3412822	chr6:30207123-30209221	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv2428476	chr6:30207271-30208835	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3473887	chr6:30207648-30208353	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3430366	chr6:30207668-30208330	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30205600-30213000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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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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