Variant report

Variant	rs112162485
Chromosome Location	chr12:117797175-117797176
allele	A/T
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	nsv455724	chr12:117786105-117845806	Bivalent Enhancer Bivalent/Poised TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv560385	chr12:117786105-117845806	Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv3433275	chr12:117796919-117800317	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117790000-117798000	Weak transcription	Psoas Muscle	Psoas
2	chr12:117796400-117800400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
3	chr12:117796600-117797200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr12:117796600-117797200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr12:117796800-117797200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
6	chr12:117796800-117797400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
7	chr12:117796800-117797400	Weak transcription	NHEK	skin
8	chr12:117796800-117797800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
9	chr12:117797000-117797200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr12:117797000-117799600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
11	chr12:117797000-117799600	Bivalent/Poised TSS	iPS-20b 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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