Variant report

Variant	rs141691490
Chromosome Location	chr13:29647665-29647666
allele	-/GGCG
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533835	chr13:29141132-29962069	Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	esv3406145	chr13:29616606-29917459	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	esv2079300	chr13:29647665-29647669	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:29640800-29650600	Weak transcription	Aorta	Aorta
2	chr13:29644200-29647800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr13:29646000-29648800	Enhancers	Fetal Heart	heart
4	chr13:29646400-29647800	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr13:29647000-29647800	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr13:29647000-29648000	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr13:29647000-29648800	Enhancers	H1 Cell Line	embryonic stem cell
8	chr13:29647200-29648600	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr13:29647600-29649000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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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

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