Variant report

Variant	rs34787450
Chromosome Location	chr7:117382500-117382501
allele	G/T
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:16)

rs_ID	r²[population]
rs10233110	0.94[EUR][1000 genomes]
rs10257581	0.97[EUR][1000 genomes]
rs10269788	0.91[EUR][1000 genomes]
rs12530721	0.88[EUR][1000 genomes]
rs28414508	0.94[EUR][1000 genomes]
rs28441380	0.94[EUR][1000 genomes]
rs28622152	0.94[EUR][1000 genomes]
rs34151592	0.85[EUR][1000 genomes]
rs34511745	0.85[EUR][1000 genomes]
rs34605897	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34643488	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34830562	0.85[EUR][1000 genomes]
rs35018341	0.94[EUR][1000 genomes]
rs35683365	1.00[EUR][1000 genomes]
rs36073009	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36117041	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv464695	chr7:117342771-117393516	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv608258	chr7:117342771-117393516	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr7:117349600-117385000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:117353200-117384600	Weak transcription	Ovary	ovary
3	chr7:117354800-117417200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr7:117355000-117382800	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr7:117356200-117431400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr7:117358400-117398800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:117359200-117402600	Weak transcription	Spleen	Spleen
8	chr7:117362600-117394000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr7:117363200-117401000	Weak transcription	Rectal Smooth Muscle	rectum
10	chr7:117365600-117407000	Weak transcription	Colon Smooth Muscle	Colon
11	chr7:117369600-117384000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr7:117371800-117396000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr7:117372000-117395800	Weak transcription	Fetal Intestine Small	intestine
14	chr7:117374400-117393800	Weak transcription	Fetal Heart	heart
15	chr7:117374800-117384800	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr7:117375000-117410800	Weak transcription	Left Ventricle	heart
17	chr7:117375200-117395800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr7:117375200-117395800	Weak transcription	Pancreas	Pancrea
19	chr7:117375200-117431600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr7:117375400-117384400	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr7:117375400-117396000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr7:117375400-117402600	Weak transcription	Esophagus	oesophagus
23	chr7:117375600-117384400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr7:117375800-117406800	Weak transcription	Fetal Kidney	kidney
25	chr7:117376400-117385800	Strong transcription	Fetal Brain Female	brain
26	chr7:117378000-117386000	Strong transcription	HUES48 Cell Line	embryonic stem cell
27	chr7:117378000-117389600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
28	chr7:117378600-117383400	Strong transcription	H1 Cell Line	embryonic stem cell
29	chr7:117378600-117384600	Weak transcription	Brain Angular Gyrus	brain
30	chr7:117379000-117384800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr7:117379200-117395800	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr7:117379600-117404000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr7:117380200-117383400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
34	chr7:117380200-117383400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr7:117380600-117383200	Strong transcription	Adipose Nuclei	Adipose
36	chr7:117380800-117382600	Strong transcription	Stomach Smooth Muscle	stomach
37	chr7:117381000-117390400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr7:117381200-117383000	Strong transcription	Brain Hippocampus Middle	brain
39	chr7:117381200-117384600	Weak transcription	Brain Germinal Matrix	brain
40	chr7:117381400-117384600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr7:117381400-117389800	Weak transcription	Brain Substantia Nigra	brain
42	chr7:117381400-117395800	Weak transcription	Aorta	Aorta
43	chr7:117381600-117385600	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr7:117381800-117382800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr7:117381800-117387600	Strong transcription	Brain Inferior Temporal Lobe	brain
46	chr7:117381800-117388000	Strong transcription	Fetal Lung	lung
47	chr7:117382000-117383200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr7:117382200-117382600	Enhancers	Brain Cingulate Gyrus	brain
49	chr7:117382200-117384600	Weak transcription	Fetal Brain Male	brain
50	chr7:117382200-117387400	Strong transcription	Brain Anterior Caudate	brain

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