Variant report

Variant	rs61950706
Chromosome Location	chr12:86725368-86725369
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs12304593	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12305255	0.81[AMR][1000 genomes]
rs12306280	0.87[EUR][1000 genomes]
rs12306726	0.81[AMR][1000 genomes]
rs12316480	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12582690	0.89[EUR][1000 genomes]
rs17288772	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17289052	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17359446	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17367374	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17367869	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs55649116	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs55733909	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs55820226	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs55956857	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56293486	0.91[EUR][1000 genomes]
rs60436792	0.91[EUR][1000 genomes]
rs61133374	0.95[EUR][1000 genomes]
rs61949011	0.86[AMR][1000 genomes]
rs61949013	0.81[AMR][1000 genomes]
rs61949037	0.81[AMR][1000 genomes]
rs61949038	0.83[AMR][1000 genomes]
rs61949039	0.81[AMR][1000 genomes]
rs61949045	0.83[AMR][1000 genomes]
rs61949047	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs61949048	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61949049	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61949475	1.00[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs61949482	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61949483	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61950663	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61950665	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61950667	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61950671	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61950674	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61950711	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61950712	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61950713	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61950714	0.93[EUR][1000 genomes]
rs61950746	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61950747	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61950748	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61950749	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61950781	0.84[AMR][1000 genomes]
rs767898	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9705580	0.82[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049179	chr12:86056376-86799188	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2761759	chr12:86415936-86747726	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv518059	chr12:86416212-86747726	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1041397	chr12:86438607-86737558	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1053087	chr12:86569126-86733418	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv541564	chr12:86569126-86733418	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1037003	chr12:86610040-86798121	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv1045386	chr12:86616015-86733418	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv541565	chr12:86616015-86733418	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	esv1845250	chr12:86696771-86730126	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	nsv1053234	chr12:86701070-86774957	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
12	esv2754127	chr12:86723232-87576932	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86723800-86725400	Enhancers	Fetal Kidney	kidney
2	chr12:86723800-86726000	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr12:86724600-86726000	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr12:86724600-86726400	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr12:86724800-86725400	Enhancers	Small Intestine	intestine
6	chr12:86724800-86725600	Enhancers	H1 Cell Line	embryonic stem cell
7	chr12:86724800-86725600	Enhancers	Fetal Muscle Leg	muscle
8	chr12:86724800-86725800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr12:86724800-86725800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr12:86724800-86726400	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr12:86724800-86727600	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr12:86725000-86725400	Enhancers	H9 Cell Line	embryonic stem cell
13	chr12:86725000-86725400	Enhancers	Adipose Nuclei	Adipose
14	chr12:86725000-86725400	Enhancers	Brain Germinal Matrix	brain
15	chr12:86725000-86725400	Enhancers	Fetal Lung	lung
16	chr12:86725000-86725600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr12:86725000-86725600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr12:86725000-86726000	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr12:86725000-86726000	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr12:86725200-86726000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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