Variant report

Variant	rs35496464
Chromosome Location	chr10:50290505-50290506
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10508910	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12762834	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12762859	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12763447	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12770345	0.80[AMR][1000 genomes]
rs12772732	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12774117	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12776211	0.80[AMR][1000 genomes]
rs12777282	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17175928	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17782595	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17782649	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17782673	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17782691	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17782733	0.87[AMR][1000 genomes]
rs2137914	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2246937	0.89[EUR][1000 genomes]
rs34056748	0.87[AMR][1000 genomes]
rs34347666	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34373855	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34436721	0.87[AMR][1000 genomes]
rs34712064	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34786393	0.83[AMR][1000 genomes]
rs35007047	0.87[AMR][1000 genomes]
rs35285557	0.83[AMR][1000 genomes]
rs35311796	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35586957	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35621290	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3924984	0.89[EUR][1000 genomes]
rs3924985	0.89[EUR][1000 genomes]
rs4012666	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4293050	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4298825	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4310535	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4342944	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4445564	0.90[ASN][1000 genomes]
rs4468264	0.91[EUR][1000 genomes]
rs4483510	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4488117	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4497319	0.91[EUR][1000 genomes]
rs4550151	0.91[EUR][1000 genomes]
rs4617506	0.88[ASN][1000 genomes]
rs7084112	0.89[EUR][1000 genomes]
rs7098134	0.89[EUR][1000 genomes]
rs71500261	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs71500264	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs71500265	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7904272	0.91[EUR][1000 genomes]
rs7907959	0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831866	chr10:50165180-50335276	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
2	esv2761593	chr10:50276812-50336129	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50272600-50294200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr10:50283200-50298200	Weak transcription	Spleen	Spleen
3	chr10:50284800-50292400	Enhancers	Liver	Liver
4	chr10:50285200-50292400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr10:50286000-50292400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr10:50287200-50292200	Enhancers	Adipose Nuclei	Adipose
7	chr10:50287200-50292400	Enhancers	Brain Substantia Nigra	brain
8	chr10:50288000-50291400	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr10:50288000-50291400	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr10:50288200-50291000	Enhancers	Fetal Muscle Leg	muscle
11	chr10:50288200-50291400	Enhancers	Brain Angular Gyrus	brain
12	chr10:50288200-50292000	Enhancers	Fetal Muscle Trunk	muscle
13	chr10:50288200-50292000	Genic enhancers	Fetal Stomach	stomach
14	chr10:50288200-50292200	Enhancers	Colon Smooth Muscle	Colon
15	chr10:50288200-50292200	Enhancers	Left Ventricle	heart
16	chr10:50288200-50292200	Enhancers	Skeletal Muscle Male	skeletal muscle
17	chr10:50288200-50293200	Enhancers	Right Ventricle	heart
18	chr10:50288400-50291000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr10:50288400-50291400	Enhancers	Brain Cingulate Gyrus	brain
20	chr10:50288400-50291600	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr10:50288400-50292400	Enhancers	Brain Hippocampus Middle	brain
22	chr10:50288400-50292600	Enhancers	Brain Anterior Caudate	brain
23	chr10:50288400-50292800	Enhancers	Ovary	ovary
24	chr10:50288400-50293600	Enhancers	HSMMtube	muscle
25	chr10:50288600-50290800	Weak transcription	Brain Germinal Matrix	brain
26	chr10:50288600-50291600	Enhancers	Placenta	Placenta
27	chr10:50288600-50292200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr10:50289000-50291000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr10:50289000-50291200	Enhancers	H1 Cell Line	embryonic stem cell
30	chr10:50289000-50291400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr10:50289000-50291400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr10:50289000-50291800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr10:50289000-50291800	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr10:50289000-50292200	Enhancers	Fetal Brain Male	brain
35	chr10:50289000-50294200	Weak transcription	Rectal Smooth Muscle	rectum
36	chr10:50289200-50291600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr10:50289200-50292200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr10:50289200-50292200	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr10:50289200-50294400	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr10:50289400-50291200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr10:50289400-50291400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr10:50289400-50291600	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr10:50289400-50291800	Enhancers	Fetal Kidney	kidney
44	chr10:50289400-50292200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr10:50289400-50294200	Weak transcription	Primary hematopoietic stem cells	blood
46	chr10:50289600-50290800	Weak transcription	Fetal Brain Female	brain
47	chr10:50289600-50291000	Weak transcription	Aorta	Aorta
48	chr10:50289600-50298800	Weak transcription	Fetal Thymus	thymus
49	chr10:50289800-50290800	Weak transcription	Lung	lung
50	chr10:50289800-50290800	Weak transcription	Right Atrium	heart

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