Variant report

Variant	rs532918518
Chromosome Location	chr11:127545247-127545248
allele	A/G
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	nsv898445	chr11:127377733-127713173	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv1043894	chr11:127423435-127637119	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv541202	chr11:127423435-127637119	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1035919	chr11:127500933-127561596	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv541203	chr11:127500933-127561596	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1050596	chr11:127528390-127608257	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv826124	chr11:127545193-127580415	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:127540400-127545600	Weak transcription	Gastric	stomach
2	chr11:127541000-127545400	Weak transcription	Fetal Lung	lung
3	chr11:127545000-127545800	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr11:127545000-127546000	Enhancers	Brain Inferior Temporal Lobe	brain
5	chr11:127545000-127549400	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr11:127545200-127545400	Enhancers	H9 Cell Line	embryonic stem cell
7	chr11:127545200-127545800	Bivalent Enhancer	Aorta	Aorta
8	chr11:127545200-127545800	Enhancers	Left Ventricle	heart
9	chr11:127545200-127545800	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr11:127545200-127546000	Enhancers	Liver	Liver
11	chr11:127545200-127546000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
12	chr11:127545200-127546000	Enhancers	Pancreas	Pancrea
13	chr11:127545200-127546000	Enhancers	Spleen	Spleen
14	chr11:127545200-127546200	Enhancers	Adipose Nuclei	Adipose
15	chr11:127545200-127546200	Enhancers	Brain Hippocampus Middle	brain
16	chr11:127545200-127546200	Enhancers	Fetal Intestine Small	intestine
17	chr11:127545200-127546400	Enhancers	Psoas Muscle	Psoas
18	chr11:127545200-127547400	Enhancers	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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