Variant report

Variant	rs1814231
Chromosome Location	chr12:48392397-48392398
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12579815	1.00[EUR][1000 genomes]
rs12580309	1.00[EUR][1000 genomes]
rs12581263	1.00[EUR][1000 genomes]
rs17122615	1.00[EUR][1000 genomes]
rs17122617	1.00[EUR][1000 genomes]
rs41272785	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs41369448	1.00[EUR][1000 genomes]
rs60275794	1.00[EUR][1000 genomes]
rs915920	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832401	chr12:48347453-48477999	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:48382800-48394600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr12:48383800-48393800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr12:48383800-48394400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:48386800-48392800	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:48390000-48395000	Weak transcription	Right Atrium	heart
6	chr12:48390400-48394600	Weak transcription	Left Ventricle	heart
7	chr12:48390400-48394600	Weak transcription	Right Ventricle	heart
8	chr12:48391200-48394600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:48391600-48392800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr12:48391600-48393000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
11	chr12:48391600-48393200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr12:48391600-48394600	Weak transcription	Placenta	Placenta
13	chr12:48391800-48392600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr12:48392000-48392800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
15	chr12:48392200-48392600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
16	chr12:48392200-48392800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr12:48392200-48392800	Bivalent Enhancer	iPS-15b 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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