Variant report

Variant	rs10842820
Chromosome Location	chr12:9228823-9228824
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:9227774..9229320-chr12:9231610..9234265,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000175899	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10771307	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10771309	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10771310	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10842789	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10842795	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10842845	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10842898	0.95[EUR][1000 genomes]
rs11048789	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805651	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805652	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805653	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805654	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805655	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805656	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805657	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805658	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805659	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805660	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805661	0.91[AFR][1000 genomes]
rs1805664	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1805666	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1805667	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1805678	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805681	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2193005	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs226379	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs226383	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs226384	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs226393	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs226395	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2300147	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2300148	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2377682	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6487574	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6487581	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6487585	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6487587	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs669	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7135781	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7299282	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7299600	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7309361	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7310089	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7310167	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7310884	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7310921	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7955940	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7965184	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7968640	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7976461	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs881376	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832327	chr12:9081779-9246220	Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv1045317	chr12:9113216-9544655	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
3	nsv898738	chr12:9205030-9274394	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv1048491	chr12:9208806-9544655	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9217800-9234200	Weak transcription	Primary T cells from cord blood	blood
2	chr12:9218000-9234000	Weak transcription	Primary hematopoietic stem cells	blood
3	chr12:9218200-9232200	Weak transcription	Fetal Muscle Leg	muscle
4	chr12:9218200-9236200	Weak transcription	Psoas Muscle	Psoas
5	chr12:9218200-9266200	Weak transcription	Fetal Kidney	kidney
6	chr12:9218400-9230800	Weak transcription	Brain Hippocampus Middle	brain
7	chr12:9218400-9231000	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr12:9218400-9234400	Weak transcription	Right Atrium	heart
9	chr12:9218400-9236600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr12:9218400-9236600	Weak transcription	Brain Substantia Nigra	brain
11	chr12:9218400-9237200	Weak transcription	Brain Cingulate Gyrus	brain
12	chr12:9218600-9229400	Weak transcription	Colonic Mucosa	Colon
13	chr12:9218600-9235600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr12:9218600-9235800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr12:9218600-9236400	Weak transcription	Brain Angular Gyrus	brain
16	chr12:9218800-9230400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr12:9218800-9236200	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr12:9218800-9236200	Weak transcription	Fetal Heart	heart
19	chr12:9219000-9233200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr12:9219200-9229200	Weak transcription	Gastric	stomach
21	chr12:9219200-9234600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
22	chr12:9219200-9266000	Weak transcription	Esophagus	oesophagus
23	chr12:9219400-9233200	Strong transcription	Stomach Smooth Muscle	stomach
24	chr12:9219800-9233200	Strong transcription	Skeletal Muscle Female	skeletal muscle
25	chr12:9219800-9235800	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr12:9220600-9232600	Strong transcription	Skeletal Muscle Male	skeletal muscle
27	chr12:9220800-9232400	Strong transcription	Duodenum Smooth Muscle	Duodenum
28	chr12:9222200-9230600	Genic enhancers	Liver	Liver
29	chr12:9222600-9232600	Strong transcription	Fetal Lung	lung
30	chr12:9222600-9233400	Strong transcription	Left Ventricle	heart
31	chr12:9224200-9232800	Strong transcription	Right Ventricle	heart
32	chr12:9225400-9230600	Weak transcription	Small Intestine	intestine
33	chr12:9225400-9231400	Weak transcription	Rectal Smooth Muscle	rectum
34	chr12:9225600-9229200	Weak transcription	Ovary	ovary
35	chr12:9225600-9233200	Strong transcription	Adipose Nuclei	Adipose
36	chr12:9225600-9236200	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr12:9226200-9233200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr12:9226400-9229400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr12:9226600-9230200	Weak transcription	Fetal Intestine Large	intestine
40	chr12:9227000-9229200	Weak transcription	Placenta	Placenta
41	chr12:9227000-9231200	Weak transcription	Colon Smooth Muscle	Colon
42	chr12:9227200-9234400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr12:9227400-9229200	Weak transcription	Fetal Stomach	stomach
44	chr12:9227400-9234200	Strong transcription	HepG2	liver
45	chr12:9227600-9229200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr12:9227600-9229200	Weak transcription	Aorta	Aorta
47	chr12:9227600-9229200	Weak transcription	Duodenum Mucosa	Duodenum
48	chr12:9227600-9229200	Weak transcription	Lung	lung
49	chr12:9227600-9229200	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr12:9228000-9229000	Weak transcription	Spleen	Spleen

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