Variant report

Variant	rs559236407
Chromosome Location	chr12:120809254-120809255
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899555	chr12:120519124-120840522	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	499 gene(s)	inside rSNPs	diseases
2	esv14211	chr12:120801254-120809932	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv560437	chr12:120803783-120809590	Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv975533	chr12:120808952-120809553	Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:120807800-120814000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr12:120808200-120809400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr12:120808200-120809800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr12:120808200-120809800	Weak transcription	Right Atrium	heart
5	chr12:120808600-120809600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr12:120808600-120813800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr12:120808800-120809400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
8	chr12:120808800-120809400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr12:120808800-120809400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
10	chr12:120808800-120809800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
11	chr12:120809000-120809400	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
12	chr12:120809000-120809400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
13	chr12:120809200-120809400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
14	chr12:120809200-120809600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
15	chr12:120809200-120809800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
16	chr12:120809200-120809800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
17	chr12:120809200-120813600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr12:120809200-120813600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured 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

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