Variant report

Variant	rs1892335
Chromosome Location	chr10:90846055-90846056
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:90837544..90840360-chr10:90843799..90846492,3	K562	blood:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10788634	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10887893	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10887897	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10887904	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10887907	0.86[AFR][1000 genomes]
rs10887908	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11202975	0.85[AFR][1000 genomes]
rs11202976	0.85[AFR][1000 genomes]
rs11202977	0.85[AFR][1000 genomes]
rs1937332	0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs1937334	0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs2211595	0.99[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2211598	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4933492	0.80[AFR][1000 genomes]
rs4934439	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4934450	0.81[AFR][1000 genomes]
rs7079195	0.86[AFR][1000 genomes]
rs7086087	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7091729	0.93[AFR][1000 genomes]
rs7092725	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7897422	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7897437	0.83[ASN][1000 genomes]
rs7918678	0.83[CHB][hapmap];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1042848	chr10:90466032-91318474	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv540741	chr10:90466032-91318474	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
3	nsv831943	chr10:90664836-90865834	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv467416	chr10:90815975-90889997	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
5	nsv551842	chr10:90815975-90889997	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
6	nsv895880	chr10:90816060-90874029	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
7	nsv831944	chr10:90822654-90967018	Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
8	nsv467418	chr10:90826252-90874468	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv551843	chr10:90826252-90874468	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	esv2829934	chr10:90826779-90874468	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	esv2758235	chr10:90835064-91017486	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	esv2759775	chr10:90835064-91017486	Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv895881	chr10:90842431-90940003	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:90840800-90846400	Weak transcription	K562	blood
2	chr10:90841000-90846200	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr10:90841800-90861000	Weak transcription	Aorta	Aorta
4	chr10:90842000-90851600	Weak transcription	Brain Cingulate Gyrus	brain
5	chr10:90842200-90846600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr10:90842400-90846600	Weak transcription	Left Ventricle	heart
7	chr10:90843800-90847400	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr10:90844200-90850400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr10:90844400-90846200	Enhancers	NHDF-Ad	bronchial
10	chr10:90844400-90846400	Enhancers	NHLF	lung
11	chr10:90844400-90847400	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr10:90844600-90846200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr10:90844600-90846600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr10:90844600-90847200	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr10:90845000-90846200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr10:90845000-90846600	Weak transcription	GM12878-XiMat	blood
17	chr10:90845200-90846200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr10:90845200-90846400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr10:90845200-90846600	Weak transcription	Psoas Muscle	Psoas
20	chr10:90845200-90850600	Weak transcription	Primary hematopoietic stem cells	blood
21	chr10:90845200-90855000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr10:90845400-90846200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr10:90845400-90846400	Weak transcription	Brain Angular Gyrus	brain
24	chr10:90845400-90846600	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr10:90845400-90846600	Weak transcription	Brain Anterior Caudate	brain
26	chr10:90845400-90847000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr10:90845400-90850000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr10:90845400-90850600	Weak transcription	Brain Substantia Nigra	brain
29	chr10:90845600-90846400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr10:90845600-90847000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr10:90845800-90847200	Enhancers	H9 Cell Line	embryonic stem cell
32	chr10:90845800-90847400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr10:90845800-90847400	Flanking Active TSS	Dnd41	blood
34	chr10:90846000-90846200	Enhancers	HSMMtube	muscle
35	chr10:90846000-90846400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr10:90846000-90846400	Enhancers	Adipose Nuclei	Adipose
37	chr10:90846000-90846400	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr10:90846000-90846600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
39	chr10:90846000-90846600	Enhancers	Right Atrium	heart
40	chr10:90846000-90846600	Enhancers	HSMM	muscle
41	chr10:90846000-90846800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr10:90846000-90847000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr10:90846000-90847200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr10:90846000-90847400	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr10:90846000-90847400	Enhancers	HUES64 Cell Line	embryonic stem cell

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