Variant report

Variant	rs34654815
Chromosome Location	chr9:95777029-95777030
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs12682842	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs12684564	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12685906	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3934851	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4072566	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs41273408	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][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	nsv526296	chr9:95708192-96030392	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv1054767	chr9:95738134-95875977	Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1035230	chr9:95770249-95934982	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95761600-95785800	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr9:95761600-95785800	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr9:95762000-95786400	Strong transcription	Primary monocytes fromperipheralblood	blood
4	chr9:95762600-95790200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr9:95763600-95787200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
6	chr9:95763800-95789400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr9:95766400-95785600	Strong transcription	Primary B cells from peripheral blood	blood
8	chr9:95766600-95778000	Weak transcription	Gastric	stomach
9	chr9:95766600-95780200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr9:95766600-95783400	Weak transcription	Placenta	Placenta
11	chr9:95766600-95790400	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr9:95766600-95790800	Weak transcription	Right Ventricle	heart
13	chr9:95766600-95791000	Weak transcription	Colonic Mucosa	Colon
14	chr9:95766600-95791000	Weak transcription	Rectal Smooth Muscle	rectum
15	chr9:95766600-95794000	Weak transcription	Brain Hippocampus Middle	brain
16	chr9:95766800-95782400	Weak transcription	Liver	Liver
17	chr9:95766800-95786400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr9:95767000-95781800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr9:95767000-95787200	Strong transcription	Fetal Thymus	thymus
20	chr9:95767200-95781600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr9:95767400-95781800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr9:95767400-95782000	Strong transcription	Primary T cells from cord blood	blood
23	chr9:95769000-95781600	Weak transcription	Adipose Nuclei	Adipose
24	chr9:95770200-95780000	Weak transcription	Left Ventricle	heart
25	chr9:95770200-95793600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr9:95771000-95777800	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr9:95772600-95781200	Strong transcription	Primary T helper cells PMA-I stimulated	--
28	chr9:95772600-95783000	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr9:95773200-95779600	Strong transcription	Primary T helper cells fromperipheralblood	blood
30	chr9:95773400-95778000	Weak transcription	Fetal Stomach	stomach
31	chr9:95773400-95780000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr9:95773400-95781600	Strong transcription	Primary T helper naive cells from peripheral blood	blood
33	chr9:95773400-95781800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr9:95773400-95786600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr9:95773600-95783000	Weak transcription	Fetal Muscle Leg	muscle
36	chr9:95774200-95783800	Weak transcription	Fetal Brain Male	brain
37	chr9:95774800-95788400	Strong transcription	Thymus	Thymus
38	chr9:95775000-95786600	Strong transcription	Primary B cells from cord blood	blood
39	chr9:95775600-95778000	Weak transcription	Esophagus	oesophagus
40	chr9:95776400-95778000	Weak transcription	Fetal Intestine Large	intestine
41	chr9:95776400-95778000	Weak transcription	Lung	lung
42	chr9:95776400-95783200	Weak transcription	Fetal Brain Female	brain
43	chr9:95776600-95778000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr9:95776600-95778000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr9:95776600-95778000	Weak transcription	Brain Germinal Matrix	brain
46	chr9:95776600-95778000	Weak transcription	Pancreas	Pancrea
47	chr9:95776600-95778000	Weak transcription	Spleen	Spleen
48	chr9:95776600-95778200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr9:95776600-95780400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr9:95776600-95780400	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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