Variant report

Variant	rs147213728
Chromosome Location	chr2:11205737-11205738
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833392	chr2:11054580-11235239	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv580971	chr2:11175395-11226507	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv527179	chr2:11204654-11208294	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
4	nsv519160	chr2:11205359-11208294	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11205400-11205800	Enhancers	Rectal Mucosa Donor 29	rectum
2	chr2:11205600-11205800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
3	chr2:11205600-11206000	Bivalent Enhancer	Fetal Intestine Large	intestine
4	chr2:11205600-11206400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr2:11205600-11206400	Enhancers	Fetal Lung	lung
6	chr2:11205600-11206600	Enhancers	Colonic Mucosa	Colon
7	chr2:11205600-11206600	Enhancers	Fetal Intestine Small	intestine
8	chr2:11205600-11206600	Enhancers	Fetal Stomach	stomach
9	chr2:11205600-11206600	Enhancers	Sigmoid Colon	Sigmoid Colon

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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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