Variant report

Variant	rs10276216
Chromosome Location	chr7:18697996-18697997
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10229062	0.81[AMR][1000 genomes]
rs10259495	0.82[AMR][1000 genomes]
rs17139571	0.83[AMR][1000 genomes]
rs17139630	0.81[AMR][1000 genomes]
rs17139658	0.85[AMR][1000 genomes]
rs17150245	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2269752	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2285439	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2285440	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58397191	0.81[EUR][1000 genomes]
rs6973548	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs73067100	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73069011	0.94[AMR][1000 genomes];0.93[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	esv2755157	chr7:18337660-18805860	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv830917	chr7:18612436-18817712	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv531368	chr7:18677922-18836920	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv498112	chr7:18677922-18991946	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18645200-18708000	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr7:18645400-18721000	Weak transcription	Psoas Muscle	Psoas
3	chr7:18645800-18706000	Weak transcription	HMEC	breast
4	chr7:18656000-18706000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr7:18661800-18699800	Weak transcription	Right Ventricle	heart
6	chr7:18671400-18705600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr7:18673200-18707000	Weak transcription	Fetal Kidney	kidney
8	chr7:18678400-18702000	Weak transcription	Spleen	Spleen
9	chr7:18678400-18721200	Weak transcription	Brain Substantia Nigra	brain
10	chr7:18679600-18698000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr7:18682400-18706000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr7:18686800-18699400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr7:18688400-18699200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:18688400-18699200	Weak transcription	Fetal Stomach	stomach
15	chr7:18688400-18699200	Weak transcription	NHDF-Ad	bronchial
16	chr7:18688400-18706000	Weak transcription	NHEK	skin
17	chr7:18688400-18715200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr7:18688600-18706000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr7:18688800-18702400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr7:18688800-18703400	Weak transcription	Brain Cingulate Gyrus	brain
21	chr7:18688800-18705800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr7:18688800-18706600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr7:18688800-18746400	Weak transcription	Primary hematopoietic stem cells	blood
24	chr7:18689000-18707400	Weak transcription	Fetal Muscle Trunk	muscle
25	chr7:18689200-18704800	Weak transcription	Fetal Brain Female	brain
26	chr7:18689400-18701200	Weak transcription	Fetal Muscle Leg	muscle
27	chr7:18689400-18705800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr7:18689400-18708200	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr7:18689400-18713200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr7:18689600-18699000	Weak transcription	Brain Hippocampus Middle	brain
31	chr7:18689600-18699000	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr7:18689600-18699200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr7:18689600-18699200	Weak transcription	Brain Angular Gyrus	brain
34	chr7:18689600-18701400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr7:18689600-18705800	Weak transcription	Left Ventricle	heart
36	chr7:18689600-18706800	Weak transcription	NH-A	brain
37	chr7:18690000-18708200	Weak transcription	Fetal Heart	heart
38	chr7:18690600-18702000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr7:18693200-18704200	Strong transcription	Primary B cells from peripheral blood	blood
40	chr7:18694600-18705800	Weak transcription	Esophagus	oesophagus
41	chr7:18695400-18703000	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr7:18695800-18706400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr7:18696200-18701000	Strong transcription	Primary B cells from cord blood	blood
44	chr7:18696200-18715000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr7:18696600-18702400	Weak transcription	Adipose Nuclei	Adipose
46	chr7:18696800-18698000	Strong transcription	HSMMtube	muscle
47	chr7:18696800-18710800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr7:18697400-18699400	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr7:18697400-18700400	Strong transcription	Monocytes-CD14+_RO01746	blood
50	chr7:18697600-18698000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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