Variant report

Variant	rs149880314
Chromosome Location	chr12:56267996-56267997
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000123353	Chromatin interaction
ENSG00000205323	Chromatin interaction
ENSG00000182796	Chromatin interaction
ENSG00000135392	Chromatin interaction

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	nsv719	chr12:56246405-56290812	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1051961	chr12:56262220-56629427	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	284 gene(s)	inside rSNPs	diseases
3	esv3347258	chr12:56267734-56298106	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:56267400-56268000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:56267400-56269000	Weak transcription	Fetal Thymus	thymus
3	chr12:56267800-56268000	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr12:56267800-56268200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr12:56267800-56268400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr12:56267800-56268400	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr12:56267800-56268600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr12:56267800-56268600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr12:56267800-56268600	Enhancers	Brain Cingulate Gyrus	brain
10	chr12:56267800-56268800	Enhancers	ES-I3 Cell Line	embryonic stem cell

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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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