Variant report

Variant	rs2250146
Chromosome Location	chr10:50250732-50250733
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs12269023	0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs12765128	0.82[CEU][hapmap]
rs12770345	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs12776211	1.00[CEU][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes]
rs17175928	0.88[MEX][hapmap]
rs2246463	0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs2246937	0.80[AMR][1000 genomes]
rs2250257	0.95[ASN][1000 genomes]
rs2250349	0.95[ASN][1000 genomes]
rs2250602	0.87[ASN][1000 genomes]
rs2943253	1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs2943254	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3924984	0.80[AMR][1000 genomes]
rs3924985	0.80[AMR][1000 genomes]
rs4128908	0.86[ASN][1000 genomes]
rs4129035	0.83[ASN][1000 genomes]
rs4240498	0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs4293050	0.94[MEX][hapmap]
rs4298825	0.83[MEX][hapmap]
rs4317903	0.83[ASN][1000 genomes]
rs4317904	0.83[ASN][1000 genomes]
rs4403731	0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs4421674	0.83[ASN][1000 genomes]
rs4488117	0.88[MEX][hapmap]
rs4497319	0.84[GIH][hapmap];0.89[MEX][hapmap]
rs4550151	0.84[GIH][hapmap];0.84[MEX][hapmap]
rs6537493	0.87[JPT][hapmap];0.87[ASN][1000 genomes]
rs6537494	0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs7074818	0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs7082096	1.00[CEU][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.80[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7084112	0.84[GIH][hapmap];0.89[MEX][hapmap]
rs7093398	0.83[ASN][1000 genomes]
rs7097933	0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs7897289	0.81[JPT][hapmap];0.86[ASN][1000 genomes]
rs7906722	0.86[ASN][1000 genomes]
rs7916825	0.81[JPT][hapmap];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 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

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50222800-50279000	Weak transcription	Brain Cingulate Gyrus	brain
2	chr10:50223000-50254200	Weak transcription	NHDF-Ad	bronchial
3	chr10:50224400-50258200	Weak transcription	Brain Anterior Caudate	brain
4	chr10:50232400-50279200	Weak transcription	Brain Hippocampus Middle	brain
5	chr10:50232800-50255400	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr10:50233000-50266000	Weak transcription	Colon Smooth Muscle	Colon
7	chr10:50233800-50261400	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr10:50233800-50261400	Weak transcription	Spleen	Spleen
9	chr10:50234000-50254200	Weak transcription	Left Ventricle	heart
10	chr10:50241600-50263200	Weak transcription	NHLF	lung
11	chr10:50242400-50258000	Weak transcription	Fetal Kidney	kidney
12	chr10:50242400-50259200	Weak transcription	Brain Substantia Nigra	brain
13	chr10:50243400-50261200	Weak transcription	Lung	lung
14	chr10:50243800-50278800	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr10:50245400-50258200	Weak transcription	Osteobl	bone
16	chr10:50245600-50264200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr10:50245800-50257800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr10:50247000-50259000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr10:50247000-50282600	Weak transcription	Brain Angular Gyrus	brain
20	chr10:50247200-50253800	Weak transcription	Adipose Nuclei	Adipose
21	chr10:50247800-50253600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr10:50247800-50255000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr10:50247800-50271600	Weak transcription	Fetal Intestine Small	intestine
24	chr10:50248000-50255000	Weak transcription	Right Ventricle	heart
25	chr10:50248200-50251200	Strong transcription	Fetal Muscle Trunk	muscle
26	chr10:50248200-50253400	Weak transcription	Stomach Smooth Muscle	stomach
27	chr10:50249200-50258000	Weak transcription	Liver	Liver
28	chr10:50250000-50251200	Strong transcription	Fetal Lung	lung
29	chr10:50250200-50251000	Strong transcription	HSMMtube	muscle
30	chr10:50250200-50251200	Strong transcription	Fetal Muscle Leg	muscle
31	chr10:50250400-50251200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr10:50250400-50251200	Strong transcription	Ovary	ovary
33	chr10:50250400-50252400	Strong transcription	Aorta	Aorta
34	chr10:50250400-50255000	Weak transcription	Fetal Stomach	stomach
35	chr10:50250600-50251000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr10:50250600-50255000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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