Variant report

Variant	rs561839895
Chromosome Location	chr11:106785575-106785576
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898362	chr11:106715879-106809457	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv556231	chr11:106737224-106815963	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv474	chr11:106757020-106795146	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv531938	chr11:106760733-107156814	Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv3466197	chr11:106784242-106789940	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv1819607	chr11:106784955-106789492	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
7	esv3486333	chr11:106785042-106790740	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
8	nsv556232	chr11:106785139-106787540	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
9	nsv556233	chr11:106785139-106787809	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
10	nsv556234	chr11:106785139-106788876	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
11	nsv556235	chr11:106785139-106789414	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
12	nsv556236	chr11:106785139-106789492	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
13	nsv556237	chr11:106785139-106795127	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
14	esv3486336	chr11:106785492-106790590	Enhancers Weak transcription ZNF genes & repeats	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	chr11:106783800-106785800	Weak transcription	Fetal Lung	lung

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