Variant report

Variant	rs11585741
Chromosome Location	chr1:247045119-247045120
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	chr1:247041147..247045524-chr1:247051435..247055344,4	K562	blood:
2	chr1:246996938..246999359-chr1:247044207..247046740,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1039009	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1039010	0.82[EUR][1000 genomes]
rs1472275	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1612610	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1613209	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1619941	0.83[EUR][1000 genomes]
rs1691240	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1691241	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1691242	0.81[ASN][1000 genomes]
rs1691252	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1691254	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1691255	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1779964	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1779968	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1779969	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2172796	0.90[EUR][1000 genomes]
rs2642975	0.84[EUR][1000 genomes]
rs2642977	0.82[EUR][1000 genomes]
rs2642991	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2800214	0.89[EUR][1000 genomes]
rs2800215	0.85[EUR][1000 genomes]
rs2800219	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2800220	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2800221	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2818888	0.88[EUR][1000 genomes]
rs7542895	0.88[EUR][1000 genomes]
rs768197	0.90[EUR][1000 genomes]
rs9729306	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9729316	0.80[EUR][1000 genomes];0.84[ASN][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	nsv949571	chr1:246688635-247240863	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	esv2762192	chr1:246823857-247069232	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Active TSS 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	21 gene(s)	inside rSNPs	diseases
3	nsv1006271	chr1:246832606-247276182	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
4	nsv535416	chr1:246832606-247276182	Strong transcription ZNF genes & repeats Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
5	nsv1011346	chr1:246868799-247133898	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	esv1810844	chr1:246988018-247054824	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
7	nsv873424	chr1:246991094-247366380	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
8	nsv5276	chr1:247028364-247073098	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
9	nsv1005208	chr1:247037441-247597975	Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
10	nsv1000602	chr1:247044627-247226568	Enhancers Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:247002200-247082400	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr1:247002400-247081000	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr1:247004000-247053600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr1:247004200-247083400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr1:247005200-247079800	Weak transcription	Stomach Mucosa	stomach
6	chr1:247006600-247071600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr1:247018400-247056400	Weak transcription	Fetal Heart	heart
8	chr1:247020400-247072800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr1:247024200-247052000	Weak transcription	Pancreas	Pancrea
10	chr1:247025200-247048000	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr1:247025200-247052000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr1:247031600-247071400	Strong transcription	Primary T helper cells fromperipheralblood	blood
13	chr1:247032800-247051600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr1:247033200-247060800	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr1:247033600-247058000	Weak transcription	Colonic Mucosa	Colon
16	chr1:247033800-247046000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:247033800-247051600	Weak transcription	HSMMtube	muscle
18	chr1:247033800-247070800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr1:247035000-247051600	Weak transcription	Psoas Muscle	Psoas
20	chr1:247035800-247051600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr1:247036200-247052000	Weak transcription	Small Intestine	intestine
22	chr1:247037200-247051800	Weak transcription	Brain Germinal Matrix	brain
23	chr1:247037400-247052000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr1:247038000-247050200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr1:247039000-247049000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr1:247039000-247051600	Weak transcription	Spleen	Spleen
27	chr1:247039000-247057200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr1:247039000-247070400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr1:247039200-247047600	Weak transcription	Fetal Brain Female	brain
30	chr1:247039200-247050000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr1:247039200-247051600	Weak transcription	Brain Cingulate Gyrus	brain
32	chr1:247039200-247051600	Weak transcription	Lung	lung
33	chr1:247039200-247052000	Weak transcription	Fetal Brain Male	brain
34	chr1:247039200-247052000	Weak transcription	Rectal Smooth Muscle	rectum
35	chr1:247039400-247051400	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr1:247039400-247052000	Weak transcription	Esophagus	oesophagus
37	chr1:247039800-247051400	Weak transcription	Right Ventricle	heart
38	chr1:247040200-247045800	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr1:247040200-247050600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr1:247040200-247050800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr1:247040400-247045800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr1:247040400-247046000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr1:247040400-247046000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr1:247040400-247047400	Weak transcription	Fetal Kidney	kidney
45	chr1:247040400-247048000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr1:247040400-247048000	Weak transcription	Brain Anterior Caudate	brain
47	chr1:247040400-247048000	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr1:247040400-247048000	Weak transcription	Fetal Lung	lung
49	chr1:247040400-247048000	Weak transcription	NHDF-Ad	bronchial
50	chr1:247040400-247048200	Weak transcription	Colon Smooth Muscle	Colon

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