Variant report

Variant	rs576883304
Chromosome Location	chr11:46161366-46161367
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3460785	chr11:46160626-46162733	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
2	nsv512221	chr11:46160845-46162559	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
3	esv3460763	chr11:46160872-46162508	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
4	esv3460774	chr11:46160933-46162476	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
5	esv3460796	chr11:46160951-46162428	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
6	esv3460807	chr11:46161011-46162469	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
7	esv3460818	chr11:46161018-46162401	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
8	esv16657	chr11:46161028-46162404	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
9	nsv511476	chr11:46161054-46169659	Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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