Variant report

Variant	rs62093960
Chromosome Location	chr18:29832839-29832840
allele	A/C
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	nsv1056007	chr18:29711974-29899564	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv833616	chr18:29792336-29964212	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv528846	chr18:29832147-29890042	Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29823800-29848000	Weak transcription	Aorta	Aorta
2	chr18:29831400-29833000	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr18:29831400-29847600	Weak transcription	Pancreas	Pancrea
4	chr18:29831600-29833400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr18:29831800-29833000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr18:29832400-29837000	Weak transcription	Fetal Intestine Large	intestine
7	chr18:29832600-29836000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr18:29832600-29837400	Weak transcription	Fetal Intestine Small	intestine
9	chr18:29832800-29834800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr18:29832800-29835600	Weak transcription	Primary hematopoietic stem cells	blood

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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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