Variant report

Variant	rs13286908
Chromosome Location	chr9:8485201-8485202
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10115201	1.00[CEU][hapmap];0.88[TSI][hapmap];0.91[EUR][1000 genomes]
rs10115554	0.87[CEU][hapmap];0.91[EUR][1000 genomes]
rs10116020	0.87[CEU][hapmap];1.00[CHB][hapmap];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10124277	1.00[CEU][hapmap];0.88[MEX][hapmap];0.88[TSI][hapmap];0.91[EUR][1000 genomes]
rs10977144	0.88[CEU][hapmap];0.86[GIH][hapmap]
rs10977154	0.87[CEU][hapmap];0.91[GIH][hapmap]
rs1323592	0.91[EUR][1000 genomes]
rs13283150	0.87[CEU][hapmap]
rs13286274	0.88[MEX][hapmap]
rs13288392	0.97[CHD][hapmap]
rs13290896	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13291309	0.82[CEU][hapmap]
rs13292865	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13294270	0.87[CEU][hapmap]
rs13296910	0.93[CHD][hapmap];0.88[JPT][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.88[AMR][1000 genomes]
rs13298803	0.83[CHB][hapmap];0.86[JPT][hapmap];0.83[YRI][hapmap];0.88[AMR][1000 genomes]
rs13301979	0.95[GIH][hapmap];0.82[ASN][1000 genomes]
rs1359120	0.88[CEU][hapmap]
rs1535678	0.88[CHD][hapmap]
rs16928002	0.87[CEU][hapmap];0.91[GIH][hapmap]
rs16928048	0.87[CEU][hapmap];0.88[JPT][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs16928053	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs16928058	0.85[CHB][hapmap];0.97[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap]
rs16928072	0.97[CHD][hapmap]
rs17650289	1.00[MEX][hapmap];0.83[EUR][1000 genomes]
rs34190427	0.95[EUR][1000 genomes]
rs34599557	0.89[EUR][1000 genomes]
rs35441574	0.95[EUR][1000 genomes]
rs35777094	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35929428	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4409447	0.93[CHD][hapmap];0.88[JPT][hapmap];1.00[MEX][hapmap];0.88[AMR][1000 genomes]
rs4495488	0.93[CHD][hapmap];0.88[JPT][hapmap];0.85[AMR][1000 genomes]
rs4549838	0.88[AMR][1000 genomes]
rs62534039	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62534040	0.88[EUR][1000 genomes]
rs7863060	0.84[ASW][hapmap];1.00[CEU][hapmap];0.92[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv8414	chr9:7827373-8511613	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1031472	chr9:8250901-8712547	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv1022796	chr9:8360729-9110046	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv892226	chr9:8435525-8522326	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv892228	chr9:8482778-8703733	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv892229	chr9:8485201-8520366	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8419200-8491000	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr9:8420600-8557600	Weak transcription	Aorta	Aorta
3	chr9:8442200-8522200	Weak transcription	Liver	Liver
4	chr9:8448000-8494800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr9:8451400-8492000	Weak transcription	Psoas Muscle	Psoas
6	chr9:8464600-8494200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr9:8473600-8491600	Weak transcription	Primary hematopoietic stem cells	blood
8	chr9:8476800-8491400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr9:8477000-8491600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr9:8478000-8487000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr9:8478200-8504000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr9:8478400-8488800	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr9:8478800-8485800	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr9:8479000-8491800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr9:8479200-8504000	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr9:8481200-8500800	Weak transcription	Fetal Intestine Small	intestine
17	chr9:8481600-8488200	Strong transcription	Fetal Lung	lung
18	chr9:8482200-8486400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr9:8482200-8487000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr9:8482400-8491800	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr9:8482600-8486000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr9:8482600-8486200	Strong transcription	Rectal Mucosa Donor 29	rectum
23	chr9:8482800-8486200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr9:8483400-8486200	Strong transcription	Fetal Muscle Leg	muscle
25	chr9:8483400-8486400	Strong transcription	Fetal Brain Male	brain
26	chr9:8483800-8486000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
27	chr9:8483800-8486000	Strong transcription	Brain Cingulate Gyrus	brain
28	chr9:8483800-8486200	Strong transcription	HUES64 Cell Line	embryonic stem cell
29	chr9:8483800-8486600	Strong transcription	Brain Inferior Temporal Lobe	brain
30	chr9:8483800-8487000	Strong transcription	Dnd41	blood
31	chr9:8483800-8524800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr9:8484000-8486000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr9:8484000-8486200	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr9:8484000-8486200	Strong transcription	Brain Anterior Caudate	brain
35	chr9:8484000-8486200	Strong transcription	Fetal Muscle Trunk	muscle
36	chr9:8484000-8486400	Strong transcription	Brain Angular Gyrus	brain
37	chr9:8484200-8485800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr9:8484400-8485400	Enhancers	Primary B cells from cord blood	blood
39	chr9:8484400-8492000	Weak transcription	Fetal Stomach	stomach
40	chr9:8484400-8492800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr9:8484400-8492800	Weak transcription	Brain Substantia Nigra	brain
42	chr9:8484800-8485600	Genic enhancers	Fetal Heart	heart
43	chr9:8484800-8487000	Strong transcription	Brain Germinal Matrix	brain
44	chr9:8485000-8486000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
45	chr9:8485000-8486000	Strong transcription	Cortex derived primary cultured neurospheres	brain
46	chr9:8485000-8486200	Strong transcription	Fetal Kidney	kidney
47	chr9:8485000-8488800	Strong transcription	Fetal Brain Female	brain
48	chr9:8485200-8485400	Genic enhancers	HUES48 Cell Line	embryonic stem cell
49	chr9:8485200-8486000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr9:8485200-8486400	Strong transcription	Brain Hippocampus Middle	brain

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