Variant report

Variant	rs10466960
Chromosome Location	chr12:83249247-83249248
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10506884	1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11115457	1.00[ASW][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.88[MEX][hapmap];0.87[MKK][hapmap];0.90[YRI][hapmap];0.99[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11115458	1.00[CHB][hapmap];0.95[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.98[ASN][1000 genomes]
rs11115459	1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12300038	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12304267	0.91[ASN][1000 genomes]
rs12317660	0.95[ASN][1000 genomes]
rs17010056	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs17010066	0.88[JPT][hapmap]
rs17010069	0.88[CEU][hapmap];0.88[JPT][hapmap];0.80[EUR][1000 genomes]
rs1703105	0.88[JPT][hapmap];0.88[MEX][hapmap]
rs1703107	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs6539694	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs6539695	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.88[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.90[YRI][hapmap];0.97[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7137977	1.00[ASN][1000 genomes]
rs7301204	0.96[ASN][1000 genomes]
rs7304237	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7313758	1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs73358271	0.84[ASN][1000 genomes]
rs73358284	0.84[ASN][1000 genomes]
rs73358290	0.83[ASN][1000 genomes]
rs7979960	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.97[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9651971	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1053093	chr12:82645292-83287809	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv541551	chr12:82645292-83287809	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv427917	chr12:82917031-83279712	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv521849	chr12:83013783-83991479	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv469490	chr12:83089431-83507269	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
6	nsv559542	chr12:83089431-83507269	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
7	esv2758315	chr12:83101045-83357621	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	esv2759911	chr12:83101045-83357621	Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv430520	chr12:83166956-83271602	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
10	nsv437765	chr12:83230454-83271933	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
11	nsv832472	chr12:83248283-83419753	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:83196400-83250800	Weak transcription	Fetal Muscle Leg	muscle
2	chr12:83206600-83250000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr12:83206600-83255200	Weak transcription	Fetal Muscle Trunk	muscle
4	chr12:83212400-83257000	Weak transcription	Gastric	stomach
5	chr12:83214200-83250800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr12:83229600-83252000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr12:83236000-83250800	Weak transcription	Fetal Lung	lung
8	chr12:83236000-83264000	Weak transcription	Stomach Smooth Muscle	stomach
9	chr12:83236200-83253200	Weak transcription	Fetal Brain Male	brain
10	chr12:83240000-83250800	Weak transcription	Fetal Stomach	stomach
11	chr12:83242200-83289800	Weak transcription	Stomach Mucosa	stomach
12	chr12:83243200-83249600	Weak transcription	Brain Angular Gyrus	brain
13	chr12:83243400-83249600	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr12:83244400-83250800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr12:83244400-83251200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr12:83244400-83252000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr12:83246400-83253600	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr12:83246800-83256000	Weak transcription	Brain Germinal Matrix	brain
19	chr12:83247600-83249400	Weak transcription	Brain Cingulate Gyrus	brain
20	chr12:83248600-83255800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr12:83249000-83249400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr12:83249000-83249400	Enhancers	Fetal Heart	heart
23	chr12:83249000-83249600	Enhancers	Colon Smooth Muscle	Colon
24	chr12:83249000-83250400	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr12:83249000-83250800	Weak transcription	Fetal Intestine Small	intestine
26	chr12:83249000-83251200	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr12:83249000-83251400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr12:83249000-83252200	Enhancers	Brain Substantia Nigra	brain
29	chr12:83249200-83249400	Enhancers	Brain Hippocampus Middle	brain
30	chr12:83249200-83249600	Enhancers	Fetal Brain Female	brain
31	chr12:83249200-83249600	Enhancers	Rectal Smooth Muscle	rectum
32	chr12:83249200-83250000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr12:83249200-83250600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr12:83249200-83250600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr12:83249200-83250800	Enhancers	Brain Anterior Caudate	brain
36	chr12:83249200-83256000	Weak transcription	Placenta Amnion	Placenta Amnion

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