Variant report

Variant	rs66555646
Chromosome Location	chr19:45062496-45062497
allele	lengthTooLong
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	nsv1062812	chr19:45042262-45214796	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
2	esv3357953	chr19:45061712-45063710	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	esv3428859	chr19:45062305-45062699	Inactive region	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv3443702	chr19:45062342-45062552	Inactive region	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv3420965	chr19:45062356-45062637	Inactive region	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv3381739	chr19:45062418-45062628	Inactive region	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv1393126	chr19:45062495-45062597	Inactive region	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No data

Quick Search:

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

what's new

Quick links