Variant report

Variant	rs266089
Chromosome Location	chr10:44869427-44869428
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11239017	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11239018	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1144471	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1147872	0.88[EUR][1000 genomes]
rs1746039	0.82[AMR][1000 genomes]
rs266091	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs266094	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs266096	0.82[JPT][hapmap]
rs266097	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs266098	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[YRI][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2781551	0.81[JPT][hapmap]
rs2839685	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.85[AFR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2839688	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2839693	0.82[CHB][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2861440	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs524280	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1038511	chr10:44596885-44870030	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv1054649	chr10:44848921-44889713	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
3	nsv550699	chr10:44868257-44882203	Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 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	chr10:44850600-44877600	Weak transcription	Duodenum Mucosa	Duodenum
2	chr10:44859000-44871800	Weak transcription	Psoas Muscle	Psoas
3	chr10:44860000-44879000	Weak transcription	Gastric	stomach
4	chr10:44864600-44871600	Strong transcription	Skeletal Muscle Female	skeletal muscle
5	chr10:44864600-44876200	Weak transcription	Brain Anterior Caudate	brain
6	chr10:44864600-44876800	Strong transcription	Fetal Stomach	stomach
7	chr10:44864800-44877800	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr10:44865000-44873000	Weak transcription	Esophagus	oesophagus
9	chr10:44865400-44876200	Weak transcription	Right Atrium	heart
10	chr10:44865600-44878000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr10:44865800-44872200	Strong transcription	Fetal Intestine Small	intestine
12	chr10:44866000-44876200	Strong transcription	Left Ventricle	heart
13	chr10:44866000-44877600	Weak transcription	Fetal Brain Female	brain
14	chr10:44866200-44876000	Strong transcription	Osteobl	bone
15	chr10:44866400-44870000	Strong transcription	Fetal Muscle Leg	muscle
16	chr10:44866400-44875600	Weak transcription	Fetal Brain Male	brain
17	chr10:44866400-44878600	Weak transcription	Liver	Liver
18	chr10:44866600-44870600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr10:44866600-44876200	Weak transcription	Brain Germinal Matrix	brain
20	chr10:44866600-44877600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr10:44866800-44871800	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr10:44866800-44875600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
23	chr10:44867000-44872200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr10:44867000-44878200	Weak transcription	Brain Hippocampus Middle	brain
25	chr10:44867200-44872000	Strong transcription	Colon Smooth Muscle	Colon
26	chr10:44867200-44872000	Strong transcription	Fetal Lung	lung
27	chr10:44867400-44869600	Strong transcription	Aorta	Aorta
28	chr10:44867400-44871000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr10:44867400-44871800	Strong transcription	Stomach Smooth Muscle	stomach
30	chr10:44867400-44875200	Strong transcription	Ovary	ovary
31	chr10:44867400-44876000	Strong transcription	Adipose Nuclei	Adipose
32	chr10:44867400-44876400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr10:44867400-44878000	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr10:44867600-44871600	Strong transcription	Duodenum Smooth Muscle	Duodenum
35	chr10:44867600-44878600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr10:44867800-44871400	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr10:44867800-44872400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr10:44867800-44875400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
39	chr10:44868000-44869600	Strong transcription	Fetal Kidney	kidney
40	chr10:44868000-44869600	Strong transcription	NHLF	lung
41	chr10:44868000-44869800	Strong transcription	Spleen	Spleen
42	chr10:44868000-44875600	Strong transcription	HUES64 Cell Line	embryonic stem cell
43	chr10:44868200-44870200	Strong transcription	H9 Cell Line	embryonic stem cell
44	chr10:44868200-44870800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr10:44868200-44870800	Strong transcription	HUES6 Cell Line	embryonic stem cell
46	chr10:44868200-44873600	Weak transcription	NHDF-Ad	bronchial
47	chr10:44868400-44870400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr10:44868400-44872000	Strong transcription	Fetal Intestine Large	intestine
49	chr10:44868400-44873800	Strong transcription	HUES48 Cell Line	embryonic stem cell
50	chr10:44868800-44869800	Strong transcription	iPS-18 Cell Line	embryonic stem cell

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