Variant report

Variant	rs73523917
Chromosome Location	chr9:96429979-96429980
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	chr9:96425679..96427989-chr9:96428974..96431016,3	K562	blood:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs16909167	1.00[AMR][1000 genomes]
rs16909308	1.00[AMR][1000 genomes]
rs16912641	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2001587	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2001588	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2398854	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35505758	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41274432	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41276200	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs57824368	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59044538	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60016166	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61687771	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6479486	1.00[AMR][1000 genomes]
rs7030805	1.00[AMR][1000 genomes]
rs7035026	1.00[AMR][1000 genomes]
rs73522240	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73522243	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73522252	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73522271	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73522273	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73522292	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73522296	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73523904	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73523906	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73523907	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73523908	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73523910	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73523922	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73523932	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73523933	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73523934	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73523942	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73523944	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73523946	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73527828	1.00[EUR][1000 genomes]
rs7870558	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893586	chr9:96363859-96493773	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
2	nsv1036609	chr9:96375217-96477641	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
3	nsv893587	chr9:96383605-96451784	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96400400-96430600	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr9:96401000-96430000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:96401000-96438600	Weak transcription	Psoas Muscle	Psoas
4	chr9:96402600-96430200	Strong transcription	Cortex derived primary cultured neurospheres	brain
5	chr9:96402600-96433600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
6	chr9:96403400-96430800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr9:96403400-96430800	Strong transcription	Liver	Liver
8	chr9:96405200-96431400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr9:96405400-96430000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr9:96405400-96430600	Strong transcription	Primary T cells from cord blood	blood
11	chr9:96405400-96431400	Strong transcription	Fetal Brain Female	brain
12	chr9:96405400-96433200	Strong transcription	Fetal Intestine Small	intestine
13	chr9:96405600-96430000	Strong transcription	Brain Germinal Matrix	brain
14	chr9:96405600-96430400	Strong transcription	Stomach Smooth Muscle	stomach
15	chr9:96406200-96438600	Weak transcription	Small Intestine	intestine
16	chr9:96406800-96430600	Strong transcription	Brain Hippocampus Middle	brain
17	chr9:96407200-96430400	Strong transcription	Skeletal Muscle Female	skeletal muscle
18	chr9:96410000-96430200	Strong transcription	Fetal Muscle Trunk	muscle
19	chr9:96410400-96432600	Strong transcription	Rectal Mucosa Donor 31	rectum
20	chr9:96410400-96433200	Strong transcription	Gastric	stomach
21	chr9:96412400-96430000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr9:96412600-96430000	Weak transcription	K562	blood
23	chr9:96412600-96439400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr9:96412600-96442800	Weak transcription	NHDF-Ad	bronchial
25	chr9:96412600-96445000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr9:96412800-96430600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr9:96412800-96442800	Weak transcription	HMEC	breast
28	chr9:96412800-96443600	Weak transcription	Stomach Mucosa	stomach
29	chr9:96413000-96432000	Strong transcription	Placenta	Placenta
30	chr9:96413000-96442000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr9:96413000-96444800	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr9:96413200-96430800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr9:96413200-96440800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr9:96413400-96441600	Weak transcription	GM12878-XiMat	blood
35	chr9:96414200-96434800	Weak transcription	Right Atrium	heart
36	chr9:96414400-96435800	Weak transcription	HSMM	muscle
37	chr9:96416400-96443400	Weak transcription	HepG2	liver
38	chr9:96417800-96439000	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr9:96419000-96431800	Weak transcription	Hela-S3	cervix
40	chr9:96419200-96440000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr9:96420800-96435600	Weak transcription	A549	lung
42	chr9:96422000-96439800	Weak transcription	Osteobl	bone
43	chr9:96424000-96430200	Strong transcription	Brain Inferior Temporal Lobe	brain
44	chr9:96424200-96430200	Strong transcription	Primary T cells fromperipheralblood	blood
45	chr9:96424200-96430800	Strong transcription	Adipose Nuclei	Adipose
46	chr9:96424200-96430800	Strong transcription	Fetal Intestine Large	intestine
47	chr9:96424400-96430000	Strong transcription	Primary monocytes fromperipheralblood	blood
48	chr9:96424400-96431400	Strong transcription	Primary neutrophils fromperipheralblood	blood
49	chr9:96424600-96430000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr9:96424600-96430600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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