Variant report

Variant	rs57519519
Chromosome Location	chr1:155409866-155409867
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10158037	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10158433	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10465954	0.84[AFR][1000 genomes]
rs13375379	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16836851	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16836867	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16836868	0.81[AFR][1000 genomes]
rs28438500	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28491466	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28507559	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56035547	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56770523	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57134822	0.81[AFR][1000 genomes]
rs57334798	0.88[AFR][1000 genomes]
rs57807227	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58621120	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58647953	0.84[AFR][1000 genomes]
rs58850753	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59633238	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59815288	1.00[AMR][1000 genomes]
rs59913551	0.90[AFR][1000 genomes]
rs59992966	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60568057	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60818259	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61403978	1.00[AFR][1000 genomes]
rs61631408	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6427277	0.94[AFR][1000 genomes]
rs6658401	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6659913	0.90[AFR][1000 genomes]
rs6665660	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6665939	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6669216	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6670530	0.80[AFR][1000 genomes]
rs6692952	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72993428	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72993486	0.93[AFR][1000 genomes]
rs72995115	0.96[AFR][1000 genomes]
rs72995140	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72995165	0.90[AFR][1000 genomes]
rs72995166	0.89[AFR][1000 genomes]
rs72995171	0.89[AFR][1000 genomes]
rs72995173	0.89[AFR][1000 genomes]
rs72995177	0.91[AFR][1000 genomes]
rs73008931	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73008968	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73008999	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73010906	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73010909	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73010921	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7517139	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7517777	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7532714	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7541017	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9988453	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9988540	0.89[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529709	chr1:155154933-155757219	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	450 gene(s)	inside rSNPs	diseases
2	nsv831636	chr1:155219223-155444864	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
3	esv33869	chr1:155223283-155917961	Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	187 gene(s)	inside rSNPs	diseases
4	esv1799856	chr1:155305059-155534616	Enhancers Weak transcription Genic enhancers Strong transcription Active TSS 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 miRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
5	esv1795662	chr1:155305059-155540660	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Genic enhancers 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 miRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
6	esv1795478	chr1:155334933-155510824	Genic enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	esv1803551	chr1:155334933-155522572	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	esv1800974	chr1:155367680-155510824	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155362200-155433400	Weak transcription	Psoas Muscle	Psoas
2	chr1:155362800-155442400	Weak transcription	Right Ventricle	heart
3	chr1:155364400-155450800	Weak transcription	HUVEC	blood vessel
4	chr1:155367400-155426000	Weak transcription	Stomach Mucosa	stomach
5	chr1:155384800-155425600	Weak transcription	Colon Smooth Muscle	Colon
6	chr1:155392800-155422800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr1:155397400-155410400	Strong transcription	Fetal Intestine Small	intestine
8	chr1:155399400-155418200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:155399800-155411000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr1:155400000-155410000	Strong transcription	Primary T helper cells fromperipheralblood	blood
11	chr1:155400600-155410000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr1:155402400-155426800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr1:155403400-155411800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr1:155403800-155410200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr1:155404600-155441400	Weak transcription	Esophagus	oesophagus
16	chr1:155404800-155410200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr1:155405200-155410000	Strong transcription	Placenta	Placenta
18	chr1:155405400-155417400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr1:155405600-155410000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr1:155405600-155410800	Strong transcription	Fetal Thymus	thymus
21	chr1:155406600-155410200	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr1:155407000-155411000	Strong transcription	Primary hematopoietic stem cells	blood
23	chr1:155407600-155411800	Weak transcription	HMEC	breast
24	chr1:155407600-155417600	Weak transcription	Fetal Heart	heart
25	chr1:155407600-155425800	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr1:155408400-155428000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr1:155408600-155410600	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr1:155408600-155411800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr1:155408600-155444200	Weak transcription	Fetal Brain Male	brain
30	chr1:155408600-155448400	Weak transcription	Fetal Brain Female	brain
31	chr1:155408800-155410400	Weak transcription	Osteobl	bone
32	chr1:155408800-155411600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:155408800-155411600	Weak transcription	Small Intestine	intestine
34	chr1:155408800-155412600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr1:155408800-155416200	Weak transcription	HSMM	muscle
36	chr1:155408800-155417400	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr1:155408800-155417400	Weak transcription	Fetal Kidney	kidney
38	chr1:155408800-155417800	Weak transcription	Fetal Lung	lung
39	chr1:155408800-155418000	Weak transcription	Fetal Stomach	stomach
40	chr1:155408800-155418200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr1:155408800-155419200	Weak transcription	A549	lung
42	chr1:155408800-155419600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr1:155408800-155419600	Weak transcription	Adipose Nuclei	Adipose
44	chr1:155408800-155419800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr1:155408800-155419800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr1:155408800-155419800	Weak transcription	NH-A	brain
47	chr1:155408800-155420000	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr1:155408800-155420000	Weak transcription	Fetal Intestine Large	intestine
49	chr1:155408800-155420200	Weak transcription	Colonic Mucosa	Colon
50	chr1:155408800-155420400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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