Variant report

Variant	rs79239018
Chromosome Location	chr1:165317170-165317171
allele	lengthTooLong
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3335311	chr1:165317131-165317274	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3453418	chr1:165317156-165317259	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv1005410	chr1:165317169-165317253	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv1310421	chr1:165317170-165317255	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3453419	chr1:165317170-165317256	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:165311400-165318800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr1:165315000-165318000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:165315000-165318800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr1:165316400-165317600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr1:165316800-165317200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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