Variant report

Variant	rs11171940
Chromosome Location	chr12:39779447-39779448
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:39772032..39774907-chr12:39777578..39779495,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs11171568	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11171662	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11171666	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11171669	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11171682	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11171691	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11171732	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11171786	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11171794	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11171797	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11171834	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11171844	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11171857	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11171949	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11171955	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11171957	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11172024	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11172035	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11172109	0.92[AFR][1000 genomes]
rs11172168	0.82[ASN][1000 genomes]
rs11172175	0.82[ASN][1000 genomes]
rs11172204	0.82[ASN][1000 genomes]
rs11172263	0.83[EUR][1000 genomes]
rs12227642	0.88[ASN][1000 genomes]
rs12228664	0.83[EUR][1000 genomes]
rs12231250	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12231735	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17127036	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17127059	0.92[AFR][1000 genomes]
rs17127072	0.92[AFR][1000 genomes]
rs17127115	0.92[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs17127119	0.82[ASN][1000 genomes]
rs56154721	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56326136	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56885420	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs57785083	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58125663	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58648215	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61101304	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61453715	0.92[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs7964039	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9788260	0.92[AFR][1000 genomes];0.81[EUR][1000 genomes]

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	nsv832375	chr12:39599362-39784722	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
2	nsv832376	chr12:39633080-39808277	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
3	nsv531527	chr12:39680812-40182822	Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:39757000-39784600	Weak transcription	Brain Germinal Matrix	brain
2	chr12:39761800-39806000	Weak transcription	Hela-S3	cervix
3	chr12:39763000-39781400	Weak transcription	A549	lung
4	chr12:39764000-39781000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:39767400-39784800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr12:39767600-39791400	Weak transcription	GM12878-XiMat	blood
7	chr12:39767800-39784800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr12:39772400-39780200	Weak transcription	Brain Substantia Nigra	brain
9	chr12:39776400-39783200	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr12:39776600-39783800	Weak transcription	HMEC	breast
11	chr12:39777000-39783200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr12:39778600-39780600	Weak transcription	Brain Cingulate Gyrus	brain
13	chr12:39778800-39779600	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr12:39778800-39779800	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr12:39778800-39781200	Weak transcription	Pancreas	Pancrea
16	chr12:39778800-39786000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr12:39778800-39787200	Weak transcription	Right Ventricle	heart
18	chr12:39779000-39779800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr12:39779000-39780200	Weak transcription	Brain Hippocampus Middle	brain
20	chr12:39779000-39780400	Weak transcription	Brain Anterior Caudate	brain
21	chr12:39779000-39780600	Weak transcription	Brain Angular Gyrus	brain
22	chr12:39779000-39781000	Weak transcription	Right Atrium	heart
23	chr12:39779000-39782400	Enhancers	Fetal Heart	heart
24	chr12:39779000-39786000	Weak transcription	Left Ventricle	heart
25	chr12:39779200-39779600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr12:39779200-39782400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr12:39779200-39786200	Weak transcription	Psoas Muscle	Psoas

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