Variant report

Variant	rs17649066
Chromosome Location	chr9:8456219-8456220
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs11790547	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs16928175	1.00[LWK][hapmap]
rs17564174	1.00[AFR][1000 genomes]
rs1886020	1.00[CEU][hapmap];0.90[AMR][1000 genomes];1.00[EUR][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	nsv892227	chr9:8445066-8461714	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	inside rSNPs	diseases
6	nsv613289	chr9:8456020-8473169	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8418200-8476000	Weak transcription	Fetal Brain Male	brain
2	chr9:8419200-8491000	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr9:8420600-8466000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr9:8420600-8557600	Weak transcription	Aorta	Aorta
5	chr9:8421400-8456400	Weak transcription	Ovary	ovary
6	chr9:8422000-8464800	Weak transcription	Brain Germinal Matrix	brain
7	chr9:8424200-8485000	Weak transcription	Fetal Kidney	kidney
8	chr9:8430200-8465000	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr9:8434200-8485200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr9:8438200-8457600	Weak transcription	Fetal Heart	heart
11	chr9:8438600-8459800	Weak transcription	Brain Angular Gyrus	brain
12	chr9:8442000-8458000	Weak transcription	Brain Hippocampus Middle	brain
13	chr9:8442200-8522200	Weak transcription	Liver	Liver
14	chr9:8447800-8468200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr9:8448000-8468200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr9:8448000-8494800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr9:8448400-8472800	Weak transcription	Fetal Stomach	stomach
18	chr9:8449000-8465000	Weak transcription	Fetal Brain Female	brain
19	chr9:8449800-8460000	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr9:8449800-8460600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr9:8450200-8457600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr9:8450400-8457800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr9:8451400-8457600	Weak transcription	Brain Substantia Nigra	brain
24	chr9:8451400-8460000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr9:8451400-8492000	Weak transcription	Psoas Muscle	Psoas
26	chr9:8451800-8456600	Weak transcription	Primary hematopoietic stem cells	blood
27	chr9:8451800-8457600	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr9:8451800-8464800	Weak transcription	Fetal Muscle Trunk	muscle
29	chr9:8452400-8475800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr9:8453400-8456400	Strong transcription	Fetal Lung	lung
31	chr9:8453800-8476200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr9:8454800-8457600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr9:8455600-8459800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr9:8456000-8456800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr9:8456000-8456800	Strong transcription	Fetal Muscle Leg	muscle
36	chr9:8456200-8456600	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr9:8456200-8456600	Enhancers	Esophagus	oesophagus
38	chr9:8456200-8456800	Enhancers	Brain Cingulate Gyrus	brain
39	chr9:8456200-8458800	Enhancers	Brain Anterior Caudate	brain

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