Variant report

Variant	rs7522617
Chromosome Location	chr1:185164378-185164379
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10218496	0.83[EUR][1000 genomes]
rs10453829	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10489579	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10489580	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10798000	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10911693	0.81[EUR][1000 genomes]
rs12024023	0.95[EUR][1000 genomes]
rs12028408	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12045671	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12096987	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12118722	0.84[EUR][1000 genomes]
rs12119471	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12120377	0.81[EUR][1000 genomes]
rs12127840	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12135172	0.81[EUR][1000 genomes]
rs12141722	0.97[EUR][1000 genomes]
rs12404187	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1336752	0.80[EUR][1000 genomes]
rs1415072	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1591585	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1969750	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2025227	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2050566	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2146328	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2383269	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3766717	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57188163	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs57731138	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6424972	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6424974	0.84[EUR][1000 genomes]
rs6660169	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6666742	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6670117	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6673303	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6698109	0.99[EUR][1000 genomes]
rs6698122	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7512290	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7533198	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7535064	0.81[EUR][1000 genomes]
rs7539658	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7543962	0.99[EUR][1000 genomes]
rs7550586	0.84[EUR][1000 genomes]
rs7552662	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7556183	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs951428	0.84[EUR][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	nsv1001323	chr1:184525419-185315876	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats 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 miRNA target site	69 gene(s)	inside rSNPs	diseases
2	nsv535222	chr1:184525419-185315876	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
3	nsv521613	chr1:185071831-185171869	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv548398	chr1:185136458-186003094	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:185127200-185169800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:185127400-185192000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr1:185127600-185170000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr1:185127600-185184600	Weak transcription	Psoas Muscle	Psoas
5	chr1:185127600-185218200	Weak transcription	Right Ventricle	heart
6	chr1:185128000-185166400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr1:185128400-185193800	Weak transcription	Brain Angular Gyrus	brain
8	chr1:185128400-185201800	Weak transcription	Gastric	stomach
9	chr1:185128600-185168200	Weak transcription	Fetal Heart	heart
10	chr1:185128600-185171400	Weak transcription	Fetal Brain Male	brain
11	chr1:185131600-185173000	Weak transcription	Brain Substantia Nigra	brain
12	chr1:185134000-185170600	Weak transcription	Lung	lung
13	chr1:185134600-185193200	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr1:185136600-185167200	Weak transcription	Duodenum Mucosa	Duodenum
15	chr1:185136800-185171200	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr1:185137200-185166800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:185137200-185177200	Weak transcription	Primary B cells from cord blood	blood
18	chr1:185137200-185191400	Weak transcription	Brain Anterior Caudate	brain
19	chr1:185137400-185168000	Weak transcription	Fetal Intestine Large	intestine
20	chr1:185137400-185177400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr1:185137400-185191200	Weak transcription	Brain Hippocampus Middle	brain
22	chr1:185137400-185191400	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr1:185138000-185182200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr1:185138000-185186200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr1:185138000-185204000	Weak transcription	Colon Smooth Muscle	Colon
26	chr1:185138200-185171400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr1:185139600-185177400	Weak transcription	Fetal Kidney	kidney
28	chr1:185139800-185165400	Weak transcription	Thymus	Thymus
29	chr1:185139800-185167000	Weak transcription	Fetal Lung	lung
30	chr1:185139800-185168000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr1:185139800-185191400	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr1:185140000-185190800	Weak transcription	Primary B cells from peripheral blood	blood
33	chr1:185140000-185191600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr1:185144800-185181200	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr1:185145000-185170400	Weak transcription	Pancreas	Pancrea
36	chr1:185145000-185182400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr1:185145200-185166200	Weak transcription	Primary hematopoietic stem cells	blood
38	chr1:185145200-185191400	Weak transcription	Stomach Smooth Muscle	stomach
39	chr1:185148400-185193400	Weak transcription	Fetal Thymus	thymus
40	chr1:185151000-185193200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr1:185152200-185200800	Weak transcription	Primary T cells fromperipheralblood	blood
42	chr1:185153200-185191600	Weak transcription	Aorta	Aorta
43	chr1:185154400-185167200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr1:185154400-185167200	Weak transcription	Primary T cells from cord blood	blood
45	chr1:185154400-185191600	Weak transcription	Ovary	ovary
46	chr1:185158600-185169600	Weak transcription	Fetal Stomach	stomach
47	chr1:185158600-185176400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr1:185159600-185177600	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr1:185160000-185192600	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr1:185160400-185167200	Weak transcription	Liver	Liver

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