Variant report

Variant	rs7704382
Chromosome Location	chr5:112448114-112448115
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10040400	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10067901	0.89[ASN][1000 genomes]
rs10478110	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11241191	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11241192	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11241193	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11743369	0.90[ASN][1000 genomes]
rs11953203	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12187718	0.86[EUR][1000 genomes]
rs12187866	0.86[EUR][1000 genomes]
rs12188482	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12517185	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12517187	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12523053	0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs13156718	0.96[ASN][1000 genomes]
rs13174483	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13179421	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13183472	0.86[EUR][1000 genomes]
rs13183638	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13184187	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs36041392	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3884576	0.95[ASN][1000 genomes]
rs3922563	0.93[ASN][1000 genomes]
rs3922583	0.93[ASN][1000 genomes]
rs4078253	0.91[ASN][1000 genomes]
rs4078254	0.91[ASN][1000 genomes]
rs4235793	0.90[ASN][1000 genomes]
rs4262097	0.91[ASN][1000 genomes]
rs4705542	0.97[ASN][1000 genomes]
rs4705543	0.97[ASN][1000 genomes]
rs4705544	0.89[ASN][1000 genomes]
rs4705545	0.90[ASN][1000 genomes]
rs4705778	0.87[EUR][1000 genomes]
rs4705779	0.87[EUR][1000 genomes]
rs4705780	0.90[ASN][1000 genomes]
rs4705783	0.82[ASN][1000 genomes]
rs4705786	0.80[ASN][1000 genomes]
rs4705787	0.90[ASN][1000 genomes]
rs4705788	0.90[ASN][1000 genomes]
rs62374710	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6594682	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6594683	0.92[ASN][1000 genomes]
rs6859963	0.89[ASN][1000 genomes]
rs6860460	0.81[EUR][1000 genomes]
rs6869399	0.90[ASN][1000 genomes]
rs7700271	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7707142	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7731180	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9326877	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9326878	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9326879	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9885385	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][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	nsv1018344	chr5:112390951-112458853	Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv599396	chr5:112408944-112853189	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:112384000-112453000	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr5:112426600-112453000	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr5:112426800-112450200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:112426800-112450600	Weak transcription	Primary T cells from cord blood	blood
5	chr5:112426800-112450600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr5:112426800-112453800	Weak transcription	HSMMtube	muscle
7	chr5:112427000-112453800	Weak transcription	Fetal Kidney	kidney
8	chr5:112427200-112448200	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr5:112431200-112461600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr5:112432200-112450200	Weak transcription	Spleen	Spleen
11	chr5:112432200-112454600	Weak transcription	Pancreas	Pancrea
12	chr5:112434000-112459200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr5:112437800-112454400	Weak transcription	Fetal Muscle Trunk	muscle
14	chr5:112438000-112450600	Weak transcription	Aorta	Aorta
15	chr5:112438000-112454200	Weak transcription	Psoas Muscle	Psoas
16	chr5:112438200-112450000	Weak transcription	Adipose Nuclei	Adipose
17	chr5:112438200-112450200	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr5:112438200-112452800	Weak transcription	Brain Anterior Caudate	brain
19	chr5:112439600-112454600	Weak transcription	Esophagus	oesophagus
20	chr5:112439800-112452600	Weak transcription	Fetal Lung	lung
21	chr5:112440000-112450000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr5:112440200-112450000	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr5:112440200-112450000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr5:112440200-112450000	Weak transcription	Fetal Stomach	stomach
25	chr5:112440200-112454200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr5:112442800-112452600	Weak transcription	Stomach Smooth Muscle	stomach
27	chr5:112443400-112448600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr5:112444400-112448600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr5:112444800-112448600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr5:112444800-112450000	Weak transcription	Lung	lung
31	chr5:112445000-112448600	Weak transcription	HMEC	breast
32	chr5:112446400-112448200	Enhancers	Left Ventricle	heart
33	chr5:112446400-112450200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr5:112446600-112449000	Enhancers	Right Ventricle	heart
35	chr5:112446600-112450000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr5:112446600-112450000	Weak transcription	Liver	Liver
37	chr5:112447000-112448400	Weak transcription	Fetal Heart	heart
38	chr5:112447200-112450000	Weak transcription	Ovary	ovary
39	chr5:112447600-112448200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr5:112447800-112448800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr5:112447800-112449000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr5:112447800-112449000	Enhancers	Right Atrium	heart
43	chr5:112447800-112449200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr5:112448000-112449000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr5:112448000-112449000	Enhancers	Fetal Muscle Leg	muscle
46	chr5:112448000-112449000	Genic enhancers	NHEK	skin

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