Variant report

Variant	rs569292239
Chromosome Location	chr11:105765518-105765519
allele	-/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832257	chr11:105662753-105817576	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	esv1825856	chr11:105672706-105775768	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	esv3337437	chr11:105764792-105766790	Enhancers Weak transcription Active TSS	n/a	n/a	inside rSNPs	diseases
4	esv6086	chr11:105765279-105766052	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv3472130	chr11:105765396-105765935	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv3524924	chr11:105765416-105765915	Weak transcription	n/a	n/a	inside rSNPs	diseases
7	esv3524926	chr11:105765420-105765932	Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv3524927	chr11:105765438-105765861	Weak transcription	n/a	n/a	inside rSNPs	diseases
9	esv3472119	chr11:105765442-105765904	Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv3472141	chr11:105765452-105765901	Weak transcription	n/a	n/a	inside rSNPs	diseases
11	esv3524925	chr11:105765456-105765883	Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv3524923	chr11:105765467-105765896	Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv4809	chr11:105765472-105766006	Weak transcription	n/a	n/a	inside rSNPs	diseases
14	esv3472108	chr11:105765492-105765829	Weak transcription	n/a	n/a	inside rSNPs	diseases
15	esv3524928	chr11:105765502-105765843	Weak transcription	n/a	n/a	inside rSNPs	diseases
16	nsv39020	chr11:105765506-105765824	Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv3472152	chr11:105765506-105765841	Weak transcription	n/a	n/a	inside rSNPs	diseases
18	esv3524930	chr11:105765506-105765841	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:105747600-105766400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr11:105762600-105767400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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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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