Variant report

Variant	rs190362024
Chromosome Location	chr11:59616032-59616033
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv825935	chr11:59615227-59626656	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv442233	chr11:59615391-59626011	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59614200-59619400	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr11:59614600-59622000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr11:59614600-59624800	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr11:59615200-59616200	Weak transcription	Stomach Mucosa	stomach
5	chr11:59615400-59616400	Weak transcription	K562	blood
6	chr11:59616000-59616600	Enhancers	Pancreas	Pancrea
7	chr11:59616000-59617200	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr11:59616000-59617400	Enhancers	Fetal Intestine Large	intestine
9	chr11:59616000-59617400	Enhancers	Fetal Intestine Small	intestine
10	chr11:59616000-59617400	Enhancers	Sigmoid Colon	Sigmoid Colon

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