Variant report

Variant	rs370384470
Chromosome Location	chr15:79030651-79030652
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917303	chr15:78491050-79205255	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	122 gene(s)	inside rSNPs	diseases
2	nsv974606	chr15:78996783-79048337	Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv904431	chr15:79006442-79155088	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv977797	chr15:79029383-79031049	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	inside rSNPs	diseases
5	esv3430813	chr15:79030147-79032270	Active TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:79029800-79030800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
2	chr15:79029800-79032800	Weak transcription	Spleen	Spleen
3	chr15:79030400-79030800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr15:79030400-79030800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr15:79030400-79030800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr15:79030400-79030800	Enhancers	Placenta	Placenta
7	chr15:79030400-79031000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr15:79030400-79031000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr15:79030400-79031000	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr15:79030600-79030800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr15:79030600-79031000	Active TSS	HUES6 Cell Line	embryonic stem cell
12	chr15:79030600-79032400	Weak transcription	Stomach Smooth Muscle	stomach
13	chr15:79030600-79032600	Weak transcription	Right Ventricle	heart
14	chr15:79030600-79032600	Weak transcription	K562	blood

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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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