Variant report

Variant	rs191278808
Chromosome Location	chr1:217057516-217057517
allele	C/G
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	nsv873179	chr1:217056893-217112871	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	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	chr1:217055600-217062200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr1:217056800-217058400	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr1:217056800-217058800	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr1:217057000-217058800	Enhancers	Fetal Intestine Small	intestine
5	chr1:217057000-217061200	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr1:217057400-217058400	Enhancers	Small Intestine	intestine
7	chr1:217057400-217058600	Enhancers	HMEC	breast

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