Variant report

Variant	rs12322826
Chromosome Location	chr12:67271264-67271265
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs7309285	0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040682	chr12:66750103-67328053	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1053250	chr12:67067995-67381411	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1050547	chr12:67122154-67314886	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv541521	chr12:67122154-67314886	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1037144	chr12:67203280-67325187	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1044939	chr12:67207260-67377982	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA	4 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	chr12:67258000-67292600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:67268000-67271800	Weak transcription	Fetal Brain Female	brain
3	chr12:67269400-67271600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr12:67269600-67272200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr12:67270000-67272400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr12:67270000-67274000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr12:67270200-67271600	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr12:67270200-67271800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr12:67270200-67271800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr12:67270200-67271800	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr12:67270200-67273000	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr12:67270200-67274000	Enhancers	Fetal Brain Male	brain
13	chr12:67270400-67274000	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr12:67271000-67271800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr12:67271000-67272200	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr12:67271200-67271600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr12:67271200-67271800	Weak transcription	H1 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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