Variant report

Variant	rs68084394
Chromosome Location	chr10:99295513-99295514
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:99293705..99296189-chr10:99297526..99301633,5	MCF-7	breast:
2	chr10:99295454..99297833-chr10:99302850..99305384,2	MCF-7	breast:
3	chr10:99256672..99259054-chr10:99294869..99296403,2	MCF-7	breast:
4	chr10:99258502..99260593-chr10:99293993..99296377,2	K562	blood:

Variant related genes	Relation type
ENSG00000165886	Chromatin interaction
ENSG00000155229	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10748698	0.81[EUR][1000 genomes]
rs10882957	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10882959	0.83[EUR][1000 genomes]
rs10882963	0.92[ASN][1000 genomes]
rs10882967	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1107517	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1107518	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11189267	0.93[ASN][1000 genomes]
rs11189270	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11189274	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11189280	0.93[ASN][1000 genomes]
rs11189284	0.81[ASN][1000 genomes]
rs11511362	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11814566	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12243136	0.86[EUR][1000 genomes]
rs12355384	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12357750	0.93[ASN][1000 genomes]
rs12415338	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12766074	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12767760	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12774288	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12775868	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12779451	0.82[ASN][1000 genomes]
rs12783481	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1417408	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3814554	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4244325	0.85[ASN][1000 genomes]
rs4244326	0.83[ASN][1000 genomes]
rs4919108	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4919109	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7077976	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7094973	0.85[ASN][1000 genomes]
rs7342022	0.83[ASN][1000 genomes]
rs7475851	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7911122	0.82[AMR][1000 genomes];0.97[ASN][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	esv1817777	chr10:99196035-99558169	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv1036494	chr10:99267639-99345207	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
3	nsv7508	chr10:99285375-99330501	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
4	esv3419391	chr10:99295228-99295589	Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:99277800-99301800	Weak transcription	Gastric	stomach
2	chr10:99278000-99302600	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr10:99278200-99298800	Weak transcription	Aorta	Aorta
4	chr10:99278400-99301800	Weak transcription	Spleen	Spleen
5	chr10:99278600-99300200	Weak transcription	Stomach Smooth Muscle	stomach
6	chr10:99281400-99302200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr10:99282200-99301800	Weak transcription	Pancreas	Pancrea
8	chr10:99282400-99298200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr10:99282800-99299400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr10:99285200-99298600	Weak transcription	Right Atrium	heart
11	chr10:99286200-99299200	Weak transcription	Ovary	ovary
12	chr10:99287200-99298200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr10:99290000-99298200	Weak transcription	Adipose Nuclei	Adipose
14	chr10:99290000-99299400	Weak transcription	Right Ventricle	heart
15	chr10:99291800-99297800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr10:99292000-99298200	Weak transcription	HUVEC	blood vessel
17	chr10:99292000-99298200	Weak transcription	NHDF-Ad	bronchial
18	chr10:99292000-99298600	Weak transcription	Lung	lung
19	chr10:99292800-99298200	Weak transcription	NHEK	skin
20	chr10:99293200-99298200	Weak transcription	A549	lung
21	chr10:99293200-99298600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr10:99293200-99301800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr10:99293400-99297800	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr10:99293400-99297800	Weak transcription	Osteobl	bone
25	chr10:99293400-99298200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr10:99293400-99298600	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr10:99293400-99298800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr10:99293400-99298800	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr10:99293400-99299400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr10:99293400-99299600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr10:99293400-99300400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr10:99293600-99298200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr10:99293600-99298600	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr10:99294000-99296000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr10:99294000-99297800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr10:99294000-99297800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr10:99294000-99298200	Weak transcription	HSMM	muscle
38	chr10:99294000-99298600	Weak transcription	Psoas Muscle	Psoas
39	chr10:99294200-99296200	Weak transcription	Placenta Amnion	Placenta Amnion
40	chr10:99294200-99296600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr10:99294200-99297800	Weak transcription	NH-A	brain
42	chr10:99294200-99298600	Weak transcription	Fetal Muscle Leg	muscle
43	chr10:99294400-99301800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr10:99294600-99297400	Weak transcription	HSMMtube	muscle
45	chr10:99294600-99298200	Weak transcription	NHLF	lung
46	chr10:99294600-99298800	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr10:99294800-99299400	Weak transcription	Esophagus	oesophagus
48	chr10:99295000-99296400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr10:99295000-99297000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr10:99295000-99297200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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