Variant report

Variant	rs573765951
Chromosome Location	chr6:12769935-12769936
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	esv3521000	chr6:12561306-13128519	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv3521001	chr6:12561306-13128519	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv830587	chr6:12769661-12939875	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:12762200-12780600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr6:12763000-12770000	Weak transcription	HSMMtube	muscle
3	chr6:12766400-12770600	Weak transcription	Aorta	Aorta
4	chr6:12769400-12770200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr6:12769400-12770200	Enhancers	NHDF-Ad	bronchial
6	chr6:12769400-12770400	Enhancers	Brain Germinal Matrix	brain
7	chr6:12769400-12773800	Enhancers	Fetal Brain Female	brain
8	chr6:12769600-12770200	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr6:12769600-12770600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr6:12769600-12770600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr6:12769600-12770800	Enhancers	HSMM	muscle
12	chr6:12769600-12774000	Enhancers	Fetal Brain Male	brain
13	chr6:12769800-12770400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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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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