Variant report

Variant	rs202036982
Chromosome Location	chr3:134419873-134419874
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3417440	chr3:134419312-134421360	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv231242	chr3:134419873-134419873	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv2115157	chr3:134419873-134419874	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:134411600-134420600	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr3:134418400-134428000	Weak transcription	Right Atrium	heart
3	chr3:134418600-134428800	Weak transcription	Brain Hippocampus Middle	brain
4	chr3:134419000-134423000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr3:134419000-134423400	Weak transcription	Fetal Muscle Leg	muscle
6	chr3:134419800-134427600	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr3:134419800-134432200	Weak transcription	Esophagus	oesophagus

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