Variant report

Variant	rs558654894
Chromosome Location	chr6:24332264-24332265
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv33852	chr6:24331709-24334480	Weak transcription Enhancers Genic enhancers Strong transcription	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	chr6:24327400-24339200	Weak transcription	Pancreas	Pancrea
2	chr6:24330200-24338400	Weak transcription	Fetal Intestine Large	intestine
3	chr6:24330400-24332400	Enhancers	HepG2	liver
4	chr6:24331000-24334200	Enhancers	A549	lung
5	chr6:24332000-24332600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr6:24332000-24333800	Enhancers	HMEC	breast
7	chr6:24332200-24332800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr6:24332200-24333200	Enhancers	Fetal Kidney	kidney
9	chr6:24332200-24333400	Enhancers	HSMMtube	muscle
10	chr6:24332200-24333400	Enhancers	NH-A	brain
11	chr6:24332200-24333600	Enhancers	NHEK	skin
12	chr6:24332200-24334400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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