Variant report

Variant	rs17003255
Chromosome Location	chr4:79378000-79378001
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs17003128	1.00[AMR][1000 genomes]
rs17003130	1.00[AMR][1000 genomes]
rs17003157	1.00[AMR][1000 genomes]
rs17003170	1.00[AMR][1000 genomes]
rs17003190	1.00[AMR][1000 genomes]
rs17003217	1.00[AMR][1000 genomes]
rs17003229	1.00[AMR][1000 genomes]
rs17003249	1.00[AMR][1000 genomes]
rs17003269	1.00[AMR][1000 genomes]
rs17003281	1.00[AMR][1000 genomes]
rs17003344	1.00[AMR][1000 genomes]
rs1995061	1.00[AMR][1000 genomes]
rs34358235	1.00[AMR][1000 genomes]
rs36067699	1.00[AMR][1000 genomes]
rs6533643	1.00[AMR][1000 genomes]
rs6830611	1.00[AMR][1000 genomes]
rs6843017	1.00[AMR][1000 genomes]
rs6849354	1.00[AMR][1000 genomes]
rs7670643	1.00[AMR][1000 genomes]
rs7678493	1.00[AMR][1000 genomes]
rs7690611	1.00[AMR][1000 genomes]
rs7691528	1.00[AMR][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	nsv534024	chr4:78785189-79437403	ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv1009633	chr4:78887573-79652236	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	nsv1010782	chr4:79057839-79387207	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:79320000-79400200	Weak transcription	Psoas Muscle	Psoas
2	chr4:79333200-79391000	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr4:79343200-79431800	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr4:79348400-79378000	Weak transcription	Right Ventricle	heart
5	chr4:79354000-79391000	Weak transcription	Left Ventricle	heart
6	chr4:79354000-79401600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr4:79354200-79391000	Weak transcription	Fetal Kidney	kidney
8	chr4:79354400-79385200	Weak transcription	Pancreas	Pancrea
9	chr4:79359800-79382800	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr4:79362400-79378000	Weak transcription	HSMMtube	muscle
11	chr4:79363200-79409800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr4:79363400-79455200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr4:79363800-79464200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr4:79365600-79406400	Strong transcription	HUES48 Cell Line	embryonic stem cell
15	chr4:79365800-79388200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:79366200-79408200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
17	chr4:79366600-79382800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
18	chr4:79366800-79382200	Strong transcription	H1 Cell Line	embryonic stem cell
19	chr4:79367200-79385400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr4:79368000-79385600	Weak transcription	Aorta	Aorta
21	chr4:79369200-79379000	Strong transcription	HepG2	liver
22	chr4:79369200-79382000	Strong transcription	H9 Cell Line	embryonic stem cell
23	chr4:79369400-79397800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr4:79372000-79379200	Weak transcription	Fetal Heart	heart
25	chr4:79372600-79379400	Strong transcription	Fetal Intestine Large	intestine
26	chr4:79372600-79395000	Weak transcription	Stomach Smooth Muscle	stomach
27	chr4:79373600-79385400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr4:79374000-79397600	Weak transcription	Fetal Lung	lung
29	chr4:79374200-79398800	Weak transcription	Esophagus	oesophagus
30	chr4:79374600-79391000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr4:79375800-79391000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr4:79376000-79381600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr4:79376000-79385200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr4:79376200-79382000	Strong transcription	HUES6 Cell Line	embryonic stem cell
35	chr4:79376200-79387400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr4:79376200-79390000	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr4:79376200-79398600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr4:79376200-79411600	Weak transcription	Fetal Stomach	stomach
39	chr4:79377000-79396200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr4:79377400-79378000	Weak transcription	Fetal Intestine Small	intestine
41	chr4:79377800-79378200	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr4:79377800-79378800	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr4:79378000-79378600	Strong transcription	Fetal Intestine Small	intestine
44	chr4:79378000-79378600	Strong transcription	Right Ventricle	heart
45	chr4:79378000-79379200	Strong transcription	HSMMtube	muscle

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