Variant report

Variant	rs35906325
Chromosome Location	chr12:76231025-76231026
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:76229938..76232810-chr12:76233252..76234908,2	K562	blood:
2	chr12:76226887..76228730-chr12:76230537..76233430,2	K562	blood:
3	chr12:76230979..76233331-chr12:76235384..76238133,2	MCF-7	breast:

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

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

rs_ID	r²[population]
rs10431516	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10431517	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10431594	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10431595	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11180698	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11180699	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11180700	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11180702	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11180704	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11180706	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11180707	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11180708	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11180715	0.96[ASN][1000 genomes]
rs11180717	0.96[ASN][1000 genomes]
rs11180718	0.95[ASN][1000 genomes]
rs1275563	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12809551	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12810244	0.90[ASN][1000 genomes]
rs12819031	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12822358	0.94[ASN][1000 genomes]
rs12827587	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12831736	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1532294	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1565771	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17115780	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34148649	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34198570	0.84[EUR][1000 genomes]
rs35319713	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35916241	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4531531	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs71460148	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs71460149	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs937245	0.89[AMR][1000 genomes];0.96[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:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:76225600-76231400	Weak transcription	NHDF-Ad	bronchial
2	chr12:76225600-76234200	Weak transcription	Fetal Brain Female	brain
3	chr12:76227400-76232000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr12:76228200-76232800	Enhancers	Fetal Lung	lung
5	chr12:76228600-76239800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:76228600-76250000	Weak transcription	Pancreas	Pancrea
7	chr12:76229400-76231400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr12:76229600-76232200	Enhancers	Fetal Stomach	stomach
9	chr12:76229800-76231800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr12:76229800-76231800	Enhancers	Fetal Muscle Leg	muscle
11	chr12:76230200-76232800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr12:76230600-76232000	Enhancers	Fetal Brain Male	brain
13	chr12:76230600-76234600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr12:76230800-76231800	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr12:76231000-76231200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr12:76231000-76232200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr12:76231000-76232200	Enhancers	HSMMtube	muscle
18	chr12:76231000-76232200	Enhancers	K562	blood
19	chr12:76231000-76237800	Weak transcription	HepG2	liver

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