Variant report

Variant	rs9906036
Chromosome Location	chr17:15454088-15454089
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11651787	0.80[EUR][1000 genomes]
rs11653403	0.83[EUR][1000 genomes]
rs1465251	0.83[EUR][1000 genomes]
rs1988028	0.81[AMR][1000 genomes]
rs28411195	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4365325	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4572441	0.80[EUR][1000 genomes]
rs56407841	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62072569	0.80[EUR][1000 genomes]
rs62072571	0.80[EUR][1000 genomes]
rs62072578	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs8076852	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9903674	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9908651	0.80[EUR][1000 genomes]
rs9911005	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9911822	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9913509	0.80[EUR][1000 genomes]
rs9914680	0.91[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[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	nsv492304	chr17:15043353-15611753	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv916652	chr17:15093600-15856310	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
3	nsv1055677	chr17:15294011-15561130	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	nsv1059056	chr17:15294011-15856861	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
5	nsv1058286	chr17:15315763-15561130	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
6	nsv543213	chr17:15315763-15561130	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv960418	chr17:15441505-15470653	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	esv3395445	chr17:15444877-15459575	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv457695	chr17:15447364-15611495	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
10	nsv574462	chr17:15447364-15611495	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
11	esv3434152	chr17:15450327-15455625	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	inside rSNPs	diseases
12	esv3508601	chr17:15450327-15459525	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	esv3508602	chr17:15450327-15459525	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15383400-15455000	Weak transcription	Gastric	stomach
2	chr17:15416200-15466000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr17:15417600-15466400	Weak transcription	Ovary	ovary
4	chr17:15420600-15459600	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr17:15421800-15465600	Weak transcription	Hela-S3	cervix
6	chr17:15422800-15465800	Weak transcription	Fetal Intestine Small	intestine
7	chr17:15429800-15466000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr17:15429800-15466400	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr17:15431000-15465400	Weak transcription	K562	blood
10	chr17:15439000-15466000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr17:15439600-15456000	Weak transcription	Colon Smooth Muscle	Colon
12	chr17:15439600-15466000	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr17:15439800-15466400	Weak transcription	Primary B cells from peripheral blood	blood
14	chr17:15440200-15466400	Weak transcription	Left Ventricle	heart
15	chr17:15440800-15466000	Weak transcription	NHEK	skin
16	chr17:15441000-15466000	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr17:15442600-15465400	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr17:15442600-15466000	Weak transcription	A549	lung
19	chr17:15442600-15466400	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr17:15442800-15462600	Weak transcription	Thymus	Thymus
21	chr17:15442800-15465800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr17:15442800-15466400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr17:15442800-15466400	Weak transcription	Lung	lung
24	chr17:15445200-15462000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr17:15447200-15465200	Weak transcription	HUVEC	blood vessel
26	chr17:15449000-15455000	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr17:15449000-15465200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr17:15449000-15466000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr17:15449000-15466000	Weak transcription	Brain Anterior Caudate	brain
30	chr17:15449000-15466000	Weak transcription	HSMMtube	muscle
31	chr17:15449200-15454600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr17:15449200-15454800	Weak transcription	Fetal Muscle Leg	muscle
33	chr17:15449200-15459200	Weak transcription	Duodenum Mucosa	Duodenum
34	chr17:15449200-15465400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr17:15449200-15466000	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr17:15449200-15466000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr17:15449200-15466000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr17:15449200-15466000	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr17:15449200-15466000	Weak transcription	NH-A	brain
40	chr17:15449400-15454200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr17:15449400-15458600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr17:15449400-15462800	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr17:15449600-15462600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr17:15449600-15463600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr17:15449600-15463600	Weak transcription	HepG2	liver
46	chr17:15449600-15465200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr17:15449600-15465200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr17:15449600-15465800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr17:15449600-15466000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr17:15449600-15466000	Weak transcription	Osteobl	bone

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