Variant report

Variant	rs72734662
Chromosome Location	chr9:78771392-78771393
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs72734660	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72738796	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831627	chr9:78651134-78817669	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
2	nsv869152	chr9:78742197-79583399	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv893474	chr9:78753324-78784325	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv893475	chr9:78753324-78817288	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
5	nsv893476	chr9:78768830-78887992	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:78688000-78774000	Weak transcription	Left Ventricle	heart
2	chr9:78751600-78773200	Weak transcription	Fetal Stomach	stomach
3	chr9:78752200-78772000	Weak transcription	Fetal Intestine Large	intestine
4	chr9:78752400-78773400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr9:78753600-78773400	Weak transcription	Ovary	ovary
6	chr9:78757200-78776400	Weak transcription	Psoas Muscle	Psoas
7	chr9:78760600-78771800	Weak transcription	Primary T cells from cord blood	blood
8	chr9:78760600-78773800	Weak transcription	Pancreas	Pancrea
9	chr9:78762400-78771800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr9:78762600-78773600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr9:78762800-78780200	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr9:78763400-78776400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr9:78763800-78776200	Weak transcription	Right Atrium	heart
14	chr9:78765800-78776000	Weak transcription	Fetal Lung	lung
15	chr9:78766000-78773400	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr9:78766200-78772000	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr9:78766200-78773200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr9:78766400-78776000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr9:78766400-78790000	Weak transcription	Spleen	Spleen
20	chr9:78766600-78771800	Weak transcription	Thymus	Thymus
21	chr9:78766600-78772000	Weak transcription	Fetal Thymus	thymus
22	chr9:78766600-78773800	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr9:78766600-78774200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr9:78766600-78785200	Weak transcription	Fetal Kidney	kidney
25	chr9:78767200-78771800	Weak transcription	Fetal Intestine Small	intestine
26	chr9:78767400-78776800	Weak transcription	Small Intestine	intestine
27	chr9:78767600-78773800	Weak transcription	Esophagus	oesophagus
28	chr9:78768400-78772000	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr9:78769000-78777000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr9:78769200-78772000	Weak transcription	Adipose Nuclei	Adipose
31	chr9:78769200-78773800	Weak transcription	Colonic Mucosa	Colon
32	chr9:78769400-78772000	Weak transcription	Fetal Muscle Leg	muscle
33	chr9:78769400-78773400	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr9:78769400-78773600	Weak transcription	Fetal Muscle Trunk	muscle
35	chr9:78769600-78771600	Weak transcription	Duodenum Mucosa	Duodenum
36	chr9:78769600-78771800	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr9:78769600-78773400	Weak transcription	Liver	Liver
38	chr9:78769600-78773400	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr9:78769800-78772600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr9:78770400-78773200	Weak transcription	Stomach Smooth Muscle	stomach
41	chr9:78770400-78773400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr9:78770400-78781600	Weak transcription	Brain Substantia Nigra	brain
43	chr9:78770600-78772200	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr9:78770600-78773200	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr9:78770600-78773800	Weak transcription	Gastric	stomach
46	chr9:78770600-78774000	Weak transcription	Lung	lung
47	chr9:78770600-78790000	Weak transcription	Brain Hippocampus Middle	brain
48	chr9:78770800-78773400	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr9:78771000-78771600	Weak transcription	Aorta	Aorta
50	chr9:78771000-78773800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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