Variant report

Variant	rs7815436
Chromosome Location	chr8:127894008-127894009
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1819408	chr8:127835876-127898165	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv831456	chr8:127861583-128025508	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv429940	chr8:127881818-127929818	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:127889400-127894600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:127889400-127899400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:127889600-127894600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:127890200-127898200	Weak transcription	Primary T cells from cord blood	blood
5	chr8:127891600-127897200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr8:127891600-127897400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr8:127891800-127897000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr8:127892000-127897000	Weak transcription	NHEK	skin
9	chr8:127892000-127897200	Weak transcription	HMEC	breast
10	chr8:127892600-127894200	Enhancers	Stomach Smooth Muscle	stomach
11	chr8:127893000-127894400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr8:127893200-127894200	Enhancers	Fetal Stomach	stomach
13	chr8:127893200-127894200	Enhancers	HSMMtube	muscle
14	chr8:127893200-127894200	Enhancers	HUVEC	blood vessel
15	chr8:127893400-127894800	Enhancers	Fetal Muscle Trunk	muscle

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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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