Variant report

Variant	rs11165905
Chromosome Location	chr1:98183644-98183645
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs12048413	1.00[AFR][1000 genomes]
rs1333718	1.00[AFR][1000 genomes]
rs1889230	1.00[AFR][1000 genomes]
rs2151562	1.00[AFR][1000 genomes]
rs4970727	1.00[AFR][1000 genomes]
rs6604873	0.83[AFR][1000 genomes]
rs6686280	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491816	chr1:97266403-98223619	Enhancers Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv533039	chr1:97665736-98343102	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv530049	chr1:97883261-98384614	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv830714	chr1:98025090-98229416	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
5	nsv1012958	chr1:98081528-98864746	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	nsv871740	chr1:98165091-98322379	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
7	nsv871472	chr1:98165091-98342417	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
8	nsv870596	chr1:98165091-98365310	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
9	nsv871625	chr1:98165091-98564736	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
10	nsv546868	chr1:98175878-98194845	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS	TF binding region miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:98136200-98188800	Weak transcription	Left Ventricle	heart
2	chr1:98141800-98185400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr1:98148000-98192800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr1:98153400-98187800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr1:98163200-98185400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr1:98166200-98186800	Weak transcription	HSMM	muscle
7	chr1:98167400-98185000	Weak transcription	NHDF-Ad	bronchial
8	chr1:98171600-98185400	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr1:98172600-98185400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr1:98173400-98185200	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr1:98175400-98185200	Weak transcription	Duodenum Mucosa	Duodenum
12	chr1:98176400-98188200	Weak transcription	Right Ventricle	heart
13	chr1:98177000-98188200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr1:98177200-98185800	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr1:98177200-98254600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr1:98177600-98185400	Weak transcription	Adipose Nuclei	Adipose
17	chr1:98178200-98184200	Weak transcription	Esophagus	oesophagus
18	chr1:98179000-98188000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr1:98179000-98220800	Weak transcription	Psoas Muscle	Psoas
20	chr1:98179400-98185400	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr1:98179600-98187400	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr1:98179800-98185200	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr1:98179800-98187400	Strong transcription	Primary monocytes fromperipheralblood	blood
24	chr1:98180200-98187200	Strong transcription	Primary hematopoietic stem cells	blood
25	chr1:98181200-98188600	Weak transcription	Lung	lung
26	chr1:98181400-98204400	Weak transcription	Osteobl	bone
27	chr1:98181600-98188600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr1:98181800-98187400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr1:98182000-98187000	Weak transcription	Brain Substantia Nigra	brain
30	chr1:98182000-98187000	Weak transcription	Small Intestine	intestine
31	chr1:98182000-98187600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr1:98182600-98186600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr1:98182600-98187200	Strong transcription	Dnd41	blood
34	chr1:98182800-98187600	Weak transcription	Fetal Lung	lung
35	chr1:98183200-98183800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr1:98183200-98183800	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr1:98183200-98184000	Strong transcription	Primary T cells from cord blood	blood
38	chr1:98183200-98184000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr1:98183200-98187200	Strong transcription	Liver	Liver
40	chr1:98183400-98183800	ZNF genes & repeats	Fetal Intestine Large	intestine
41	chr1:98183400-98183800	Weak transcription	HSMMtube	muscle
42	chr1:98183400-98184000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr1:98183400-98184200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr1:98183600-98184800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr1:98183600-98185600	Weak transcription	Primary B cells from cord blood	blood
46	chr1:98183600-98189600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr1:98183600-98279600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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