Variant report

Variant	rs59302389
Chromosome Location	chr1:92784144-92784145
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs35258161	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56871729	1.00[AFR][1000 genomes]
rs56950188	1.00[AFR][1000 genomes]
rs59912348	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60450096	0.93[AFR][1000 genomes]
rs61638989	1.00[AMR][1000 genomes]
rs72956870	1.00[AMR][1000 genomes]
rs72956883	1.00[AMR][1000 genomes]
rs72958741	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72958744	0.93[AFR][1000 genomes]
rs72958751	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72958758	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72958762	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72958788	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72960803	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72960828	0.93[AFR][1000 genomes]
rs72960867	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7531207	1.00[AMR][1000 genomes]
rs7538609	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012864	chr1:92067100-92827761	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv535029	chr1:92067100-92827761	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv530438	chr1:92091957-92827760	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS 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 target site	33 gene(s)	inside rSNPs	diseases
4	nsv530046	chr1:92277460-92799794	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	nsv830592	chr1:92669282-92805629	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
6	nsv870667	chr1:92697188-92813741	Active TSS Strong transcription ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
7	nsv871352	chr1:92761127-92807238	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
8	nsv870854	chr1:92765102-92807238	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases
9	nsv871387	chr1:92765102-92813741	Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92765200-92791600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:92765200-92792000	Weak transcription	Aorta	Aorta
3	chr1:92765200-92792000	Weak transcription	Esophagus	oesophagus
4	chr1:92765600-92789600	Weak transcription	Psoas Muscle	Psoas
5	chr1:92765600-92791000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr1:92765600-92791600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr1:92765600-92791800	Weak transcription	Lung	lung
8	chr1:92765600-92791800	Weak transcription	Pancreas	Pancrea
9	chr1:92765600-92791800	Weak transcription	Right Ventricle	heart
10	chr1:92765600-92792000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:92765600-92792000	Weak transcription	Spleen	Spleen
12	chr1:92765800-92786200	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr1:92765800-92789000	Weak transcription	Ovary	ovary
14	chr1:92765800-92789200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr1:92765800-92791600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr1:92765800-92791800	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr1:92765800-92791800	Weak transcription	Gastric	stomach
18	chr1:92765800-92850000	Weak transcription	Small Intestine	intestine
19	chr1:92766000-92792000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr1:92766200-92789000	Weak transcription	Brain Cingulate Gyrus	brain
21	chr1:92766400-92791600	Weak transcription	Brain Hippocampus Middle	brain
22	chr1:92770600-92789000	Weak transcription	Rectal Smooth Muscle	rectum
23	chr1:92770800-92788800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr1:92771000-92791400	Weak transcription	NHEK	skin
25	chr1:92771800-92789000	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr1:92771800-92789000	Weak transcription	A549	lung
27	chr1:92771800-92794800	Weak transcription	Brain Angular Gyrus	brain
28	chr1:92771800-92823800	Weak transcription	Colonic Mucosa	Colon
29	chr1:92772000-92789000	Weak transcription	HepG2	liver
30	chr1:92772000-92789400	Weak transcription	Fetal Brain Male	brain
31	chr1:92773000-92800800	Weak transcription	NHDF-Ad	bronchial
32	chr1:92773600-92786200	Weak transcription	Brain Germinal Matrix	brain
33	chr1:92773800-92785800	Weak transcription	Liver	Liver
34	chr1:92773800-92791800	Weak transcription	NHLF	lung
35	chr1:92774000-92786200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr1:92774000-92791800	Weak transcription	Brain Anterior Caudate	brain
37	chr1:92774200-92786000	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr1:92774200-92786200	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr1:92774200-92788800	Weak transcription	Left Ventricle	heart
40	chr1:92774200-92789000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr1:92774200-92789000	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr1:92774200-92789000	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr1:92774200-92789200	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr1:92774200-92791800	Weak transcription	Brain Substantia Nigra	brain
45	chr1:92774200-92791800	Weak transcription	Thymus	Thymus
46	chr1:92774400-92786000	Weak transcription	Colon Smooth Muscle	Colon
47	chr1:92774400-92789000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr1:92774800-92785600	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr1:92774800-92785600	Weak transcription	Primary B cells from peripheral blood	blood
50	chr1:92774800-92789000	Weak transcription	Duodenum Mucosa	Duodenum

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