Variant report

Variant	rs71762324
Chromosome Location	chr6:72290191-72290192
allele	-/TTTTT
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	nsv830685	chr6:72244007-72410757	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv3442082	chr6:72287826-72291575	Enhancers Weak transcription	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
3	esv3359534	chr6:72287829-72291581	Enhancers Weak transcription	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
4	esv1614236	chr6:72290190-72290192	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
5	nsv344504	chr6:72290191-72290194	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv2164648	chr6:72290191-72290195	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:72289200-72290200	Enhancers	HUVEC	blood vessel
2	chr6:72289400-72295400	Weak transcription	H1 Derived Mesenchymal Stem 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