Variant report

Variant	rs555009911
Chromosome Location	chr8:58835993-58835994
allele	C/G
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	nsv831323	chr8:58692548-58849862	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv611411	chr8:58835639-58878786	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58833200-58836400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:58833200-58837800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr8:58833200-58838400	Weak transcription	Fetal Muscle Leg	muscle
4	chr8:58833400-58838800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr8:58833400-58839000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr8:58833600-58838000	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr8:58833600-58838800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr8:58833600-58839000	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr8:58833600-58839000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr8:58835800-58836200	Enhancers	HUES64 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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