Variant report

Variant	rs17010056
Chromosome Location	chr12:83247188-83247189
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10466960	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs10506884	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11115457	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs11115458	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs11115459	0.84[ASN][1000 genomes]
rs12300038	1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs17010066	0.88[JPT][hapmap]
rs17010069	0.88[JPT][hapmap]
rs1703105	0.88[JPT][hapmap]
rs6539694	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6539695	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs7137977	0.83[ASN][1000 genomes]
rs7301204	0.86[ASN][1000 genomes]
rs7304237	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs7313758	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs73358271	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73358284	0.94[ASN][1000 genomes]
rs73358290	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7979960	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs9651971	1.00[JPT][hapmap];0.83[ASN][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	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	esv2755991	chr12:83105631-83248605	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	esv2755875	chr12:83166956-83248605	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
11	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
12	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

No data

Chromatin state (count:29 , 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	chr12:83234000-83249200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr12:83236000-83249000	Weak transcription	Colon Smooth Muscle	Colon
9	chr12:83236000-83249200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr12:83236000-83250800	Weak transcription	Fetal Lung	lung
11	chr12:83236000-83264000	Weak transcription	Stomach Smooth Muscle	stomach
12	chr12:83236200-83253200	Weak transcription	Fetal Brain Male	brain
13	chr12:83240000-83250800	Weak transcription	Fetal Stomach	stomach
14	chr12:83242200-83289800	Weak transcription	Stomach Mucosa	stomach
15	chr12:83243200-83249600	Weak transcription	Brain Angular Gyrus	brain
16	chr12:83243400-83249600	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr12:83243600-83249200	Weak transcription	Brain Anterior Caudate	brain
18	chr12:83244400-83249000	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr12:83244400-83250800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr12:83244400-83251200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr12:83244400-83252000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr12:83245600-83249000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr12:83245800-83247600	Enhancers	Brain Cingulate Gyrus	brain
24	chr12:83246400-83253600	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr12:83246600-83249000	Weak transcription	Brain Substantia Nigra	brain
26	chr12:83246600-83249200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr12:83246800-83249000	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr12:83246800-83256000	Weak transcription	Brain Germinal Matrix	brain
29	chr12:83247000-83249200	Weak transcription	Brain Hippocampus Middle	brain

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