Variant report

Variant	rs538931661
Chromosome Location	chr2:180352675-180352676
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv875468	chr2:180352334-180396869	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180349600-180353000	Enhancers	Fetal Heart	heart
2	chr2:180350200-180357800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr2:180350400-180355200	Weak transcription	Right Atrium	heart
4	chr2:180350600-180367200	Weak transcription	Liver	Liver
5	chr2:180352200-180352800	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr2:180352400-180360200	Weak transcription	Gastric	stomach
7	chr2:180352600-180353600	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr2:180352600-180360600	Weak transcription	Fetal Intestine Large	intestine

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

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