Variant report

Variant	rs557847146
Chromosome Location	chr5:128072049-128072050
allele	A/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	nsv427734	chr5:127805281-128088632	Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv830484	chr5:127936347-128087308	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1023405	chr5:127955360-128190069	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv882836	chr5:127999225-128136519	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv4995	chr5:128047181-128092021	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:128071400-128072600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr5:128071600-128072200	Enhancers	Brain Anterior Caudate	brain
3	chr5:128071600-128072200	Enhancers	Brain Inferior Temporal Lobe	brain
4	chr5:128071600-128072400	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr5:128071600-128072400	Enhancers	Brain Substantia Nigra	brain
6	chr5:128071600-128072800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:128071600-128073000	Enhancers	HMEC	breast
8	chr5:128071600-128073200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr5:128071600-128073800	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr5:128071800-128072600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr5:128071800-128072800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr5:128071800-128073000	Flanking Active TSS	Brain Hippocampus Middle	brain
13	chr5:128071800-128073400	Enhancers	Brain Angular Gyrus	brain
14	chr5:128071800-128073400	Enhancers	Brain Cingulate Gyrus	brain
15	chr5:128071800-128073800	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr5:128072000-128072600	Enhancers	Fetal Lung	lung
17	chr5:128072000-128073400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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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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