Variant report

Variant	rs368452869
Chromosome Location	chr6:35105167-35105168
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3441631	chr6:35103524-35106522	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv511879	chr6:35103668-35106088	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3364376	chr6:35103875-35105623	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2633690	chr6:35103902-35106024	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3388382	chr6:35104024-35105922	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv1001098	chr6:35104162-35105220	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35104000-35108600	Weak transcription	Ovary	ovary
2	chr6:35104200-35105400	Weak transcription	Adipose Nuclei	Adipose
3	chr6:35104200-35108000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr6:35104200-35108000	Weak transcription	Fetal Lung	lung
5	chr6:35104400-35114000	Weak transcription	Brain Cingulate Gyrus	brain
6	chr6:35105000-35108800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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