Variant report

Variant	rs377282876
Chromosome Location	chr1:213645954-213645955
allele	-/TCTA
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	nsv832525	chr1:213580476-213782815	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv526119	chr1:213637483-213652148	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv549179	chr1:213641943-213674732	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv520354	chr1:213645844-213652148	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:213640000-213649200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:213645200-213646400	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr1:213645400-213646400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
4	chr1:213645400-213646400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr1:213645800-213646000	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr1:213645800-213646000	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr1:213645800-213646600	Enhancers	HepG2	liver
8	chr1:213645800-213647200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr1:213645800-213649800	Weak transcription	HUES64 Cell Line	embryonic stem cell

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