Variant report

Variant	rs7040035
Chromosome Location	chr9:86367397-86367398
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1421144	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2287372	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55644512	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55850239	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56960569	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs58576276	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs59948934	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62561873	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62561874	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62561875	0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs62561880	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62561921	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7020313	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[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	nsv1044639	chr9:86252505-86412041	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv893513	chr9:86298632-86433459	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	nsv973432	chr9:86330626-86371524	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 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	chr9:86348400-86415400	Weak transcription	Fetal Heart	heart
2	chr9:86350000-86431600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr9:86350200-86374600	Weak transcription	Fetal Muscle Leg	muscle
4	chr9:86350800-86407000	Weak transcription	Primary B cells from cord blood	blood
5	chr9:86351000-86393200	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr9:86351400-86371000	Weak transcription	Colon Smooth Muscle	Colon
7	chr9:86352000-86411800	Weak transcription	Ovary	ovary
8	chr9:86352600-86377800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr9:86352600-86398200	Weak transcription	Fetal Brain Female	brain
10	chr9:86352800-86367400	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr9:86352800-86369200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr9:86352800-86383200	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr9:86353000-86368000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr9:86353000-86432000	Weak transcription	Lung	lung
15	chr9:86353800-86368400	Weak transcription	Esophagus	oesophagus
16	chr9:86354800-86380800	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr9:86356000-86369400	Weak transcription	Primary B cells from peripheral blood	blood
18	chr9:86357800-86398800	Weak transcription	Pancreas	Pancrea
19	chr9:86360400-86367400	Weak transcription	Adipose Nuclei	Adipose
20	chr9:86362600-86376200	Weak transcription	Primary hematopoietic stem cells	blood
21	chr9:86362800-86374800	Weak transcription	Gastric	stomach
22	chr9:86362800-86376400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:86363800-86412400	Weak transcription	HepG2	liver
24	chr9:86363800-86431200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr9:86364800-86367600	Strong transcription	Liver	Liver
26	chr9:86364800-86412000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr9:86364800-86413400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr9:86365200-86367800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr9:86365200-86368000	Strong transcription	Left Ventricle	heart
30	chr9:86365200-86368600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr9:86365600-86372000	Weak transcription	Stomach Smooth Muscle	stomach
32	chr9:86365600-86375200	Weak transcription	Brain Germinal Matrix	brain
33	chr9:86366000-86367600	Strong transcription	Primary T cells from cord blood	blood
34	chr9:86366000-86367600	Strong transcription	Brain Hippocampus Middle	brain
35	chr9:86366200-86367400	Strong transcription	Brain Cingulate Gyrus	brain
36	chr9:86366200-86367600	Strong transcription	Skeletal Muscle Male	skeletal muscle
37	chr9:86366400-86375600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr9:86366600-86369000	Weak transcription	GM12878-XiMat	blood
39	chr9:86366800-86367400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr9:86366800-86367400	Strong transcription	Brain Substantia Nigra	brain
41	chr9:86366800-86367600	Strong transcription	Brain Anterior Caudate	brain
42	chr9:86366800-86367800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr9:86366800-86368000	Strong transcription	Aorta	Aorta
44	chr9:86367000-86367400	Strong transcription	Fetal Intestine Small	intestine
45	chr9:86367000-86367600	Strong transcription	Fetal Intestine Large	intestine
46	chr9:86367000-86367800	Strong transcription	Fetal Stomach	stomach
47	chr9:86367000-86368000	Strong transcription	Thymus	Thymus
48	chr9:86367000-86413600	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr9:86367200-86368000	Strong transcription	Fetal Thymus	thymus
50	chr9:86367200-86368800	Weak transcription	Duodenum Mucosa	Duodenum

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