Variant report

Variant	rs10815951
Chromosome Location	chr9:8800353-8800354
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10115018	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10119916	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10120008	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10739169	0.89[EUR][1000 genomes]
rs1434269	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4255195	0.86[ASN][1000 genomes]
rs4562389	0.86[ASN][1000 genomes]
rs7032107	0.97[EUR][1000 genomes]
rs765802	0.94[EUR][1000 genomes]
rs7867313	0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	nsv892235	chr9:8700396-8865925	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1025800	chr9:8712487-9030627	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv539980	chr9:8712487-9030627	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv892236	chr9:8745520-8870553	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv1015898	chr9:8753534-9011443	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv892239	chr9:8773599-8805462	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region	1 gene(s)	inside rSNPs	diseases
8	nsv892240	chr9:8796449-8834108	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8794200-8821800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr9:8794800-8825600	Weak transcription	Ovary	ovary
3	chr9:8797600-8800600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr9:8798400-8800800	Enhancers	Brain Angular Gyrus	brain
5	chr9:8798400-8815400	Weak transcription	Fetal Brain Male	brain
6	chr9:8798600-8800600	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr9:8798600-8800600	Enhancers	Brain Hippocampus Middle	brain
8	chr9:8798600-8800800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr9:8798800-8800800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr9:8799000-8800600	Enhancers	Brain Anterior Caudate	brain
11	chr9:8799000-8800800	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr9:8799200-8800400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr9:8799200-8800600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr9:8799200-8800800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr9:8799200-8809000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr9:8799400-8800600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr9:8799400-8806400	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr9:8799600-8801800	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr9:8799600-8806400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr9:8799800-8800600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr9:8799800-8802000	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr9:8799800-8806200	Weak transcription	Brain Substantia Nigra	brain
23	chr9:8800000-8800400	Enhancers	Fetal Heart	heart
24	chr9:8800000-8800600	Enhancers	H9 Cell Line	embryonic stem cell
25	chr9:8800000-8807800	Weak transcription	Brain Cingulate Gyrus	brain
26	chr9:8800000-8809000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr9:8800200-8800600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr9:8800200-8802000	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr9:8800200-8802200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr9:8800200-8802200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr9:8800200-8802400	Weak transcription	Fetal Lung	lung

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