Variant report

Variant	rs11564133
Chromosome Location	chr12:40483459-40483460
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:40480723..40487168-chr12:40489659..40495663,7	K562	blood:
2	chr12:40483377..40487149-chr12:40498015..40500549,4	K562	blood:
3	chr12:40481786..40484578-chr12:40492831..40495668,2	MCF-7	breast:
4	chr12:40478482..40480663-chr12:40481421..40484352,2	MCF-7	breast:
5	chr12:40481016..40484666-chr12:40485206..40488003,4	K562	blood:

Variant related genes	Relation type
ENSG00000151229	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10506145	0.93[CEU][hapmap];1.00[JPT][hapmap];0.93[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs1086490	1.00[JPT][hapmap]
rs10877837	1.00[JPT][hapmap]
rs11174370	1.00[JPT][hapmap]
rs11564137	0.93[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs11564139	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes]
rs11564160	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11564194	1.00[JPT][hapmap]
rs11564223	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11564282	1.00[JPT][hapmap]
rs12312535	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12371119	1.00[JPT][hapmap]
rs12810368	1.00[JPT][hapmap]
rs12827948	1.00[JPT][hapmap]
rs1388599	1.00[YRI][hapmap]
rs1482282	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1491926	0.93[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs1491937	1.00[YRI][hapmap]
rs17442108	1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17442304	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17442469	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17442756	1.00[JPT][hapmap]
rs17442805	0.85[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs17443112	1.00[JPT][hapmap];0.93[AFR][1000 genomes]
rs17458299	0.85[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17458396	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17458403	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17461082	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs17461492	0.93[AFR][1000 genomes]
rs17465400	0.93[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs17465519	0.85[AFR][1000 genomes]
rs17465540	0.85[AFR][1000 genomes]
rs17483628	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17559478	1.00[JPT][hapmap]
rs2046929	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2086598	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2404346	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2404574	0.93[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs2708404	1.00[JPT][hapmap]
rs28370644	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28370654	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28370656	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs28370659	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28370681	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28740188	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs55707305	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs55993200	0.93[AFR][1000 genomes]
rs7136434	1.00[YRI][hapmap]
rs7305377	0.93[AFR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7306718	1.00[JPT][hapmap]
rs7484475	1.00[JPT][hapmap]
rs7969495	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7971935	1.00[YRI][hapmap]
rs7974522	1.00[JPT][hapmap];0.93[AFR][1000 genomes]
rs7974972	1.00[JPT][hapmap]
rs992851	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv558596	chr12:40413698-40591117	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv899028	chr12:40478652-40524180	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
3	nsv899029	chr12:40478652-40536061	Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40453800-40487400	Weak transcription	Left Ventricle	heart
2	chr12:40464400-40493200	Weak transcription	Colon Smooth Muscle	Colon
3	chr12:40466400-40498200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:40471400-40496800	Weak transcription	Stomach Smooth Muscle	stomach
5	chr12:40474400-40497000	Weak transcription	Ovary	ovary
6	chr12:40475400-40497200	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr12:40475600-40496400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr12:40476200-40485400	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr12:40476400-40486200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr12:40476400-40492400	Weak transcription	K562	blood
11	chr12:40476400-40497400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr12:40476600-40484600	Weak transcription	Fetal Intestine Large	intestine
13	chr12:40476600-40492600	Weak transcription	Lung	lung
14	chr12:40476600-40498400	Weak transcription	Fetal Stomach	stomach
15	chr12:40476800-40497800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:40477000-40492000	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr12:40477000-40497000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr12:40477200-40495200	Weak transcription	Hela-S3	cervix
19	chr12:40477400-40496800	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr12:40478600-40492600	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr12:40479000-40493400	Weak transcription	Duodenum Mucosa	Duodenum
22	chr12:40479200-40493200	Weak transcription	Fetal Heart	heart
23	chr12:40480200-40493400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr12:40480600-40485800	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr12:40480600-40496800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr12:40481200-40492800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr12:40482000-40497800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr12:40482400-40483800	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr12:40482400-40493400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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