Variant report

Variant	rs12827587
Chromosome Location	chr12:76233869-76233870
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:76229938..76232810-chr12:76233252..76234908,2	K562	blood:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10431516	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10431517	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10431594	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10431595	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11180698	0.91[EUR][1000 genomes]
rs11180699	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11180700	0.91[EUR][1000 genomes]
rs11180702	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11180704	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11180706	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11180707	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11180708	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11180715	0.98[ASN][1000 genomes]
rs11180717	0.98[ASN][1000 genomes]
rs11180718	0.97[ASN][1000 genomes]
rs1275563	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12809551	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12810244	0.92[ASN][1000 genomes]
rs12819031	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12822358	0.96[ASN][1000 genomes]
rs12831736	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1532294	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1565771	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17115780	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34148649	0.84[EUR][1000 genomes]
rs34198570	0.80[EUR][1000 genomes]
rs35319713	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35906325	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35916241	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4531531	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71460148	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs71460149	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs937245	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]

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	nsv1040583	chr12:75742802-76360276	Enhancers Genic enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv832463	chr12:76136551-76316703	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv899315	chr12:76163309-76385096	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv1041730	chr12:76198863-76331900	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:76225600-76234200	Weak transcription	Fetal Brain Female	brain
2	chr12:76228600-76239800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:76228600-76250000	Weak transcription	Pancreas	Pancrea
4	chr12:76230600-76234600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr12:76231000-76237800	Weak transcription	HepG2	liver
6	chr12:76231800-76235400	Weak transcription	Fetal Muscle Leg	muscle
7	chr12:76232200-76235000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr12:76232200-76241400	Weak transcription	Fetal Stomach	stomach
9	chr12:76232400-76235400	Weak transcription	Fetal Brain Male	brain
10	chr12:76232800-76234200	Weak transcription	Fetal Lung	lung
11	chr12:76232800-76237400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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