Variant report

Variant	rs570241649
Chromosome Location	chr12:40864893-40864894
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899033	chr12:40758652-41122288	Bivalent/Poised TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv518952	chr12:40857620-40867333	Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	esv2476758	chr12:40864242-40865712	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2048308	chr12:40864827-40865263	Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv3496898	chr12:40864834-40865217	Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv3496900	chr12:40864858-40865197	Weak transcription	n/a	n/a	inside rSNPs	diseases
7	esv3496899	chr12:40864878-40865170	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40864000-40867600	Weak transcription	Fetal Heart	heart

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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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