Variant report

Variant	rs60901740
Chromosome Location	chr5:126769546-126769547
allele	A/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:49)

rs_ID	r²[population]
rs10519936	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11743934	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11949330	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11950427	0.82[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs11952366	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11952552	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11959505	0.82[EUR][1000 genomes]
rs12233927	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12234066	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1363388	0.88[EUR][1000 genomes]
rs1363631	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1422318	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1593949	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1593950	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17164902	0.89[EUR][1000 genomes]
rs17164903	0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17164915	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17164995	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17165090	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17839693	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2173978	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2408871	0.82[EUR][1000 genomes]
rs2408873	0.96[EUR][1000 genomes]
rs2434620	0.93[EUR][1000 genomes]
rs2898044	0.87[EUR][1000 genomes]
rs3756721	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3844184	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3851469	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3909351	0.85[EUR][1000 genomes]
rs4395678	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4604231	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4637594	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs55663031	0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs55763657	0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56006993	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57411417	0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs59745967	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs60153933	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61175766	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs67425941	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6874521	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6874752	0.82[EUR][1000 genomes]
rs6881894	0.88[EUR][1000 genomes]
rs6886487	0.85[EUR][1000 genomes]
rs72790422	0.82[EUR][1000 genomes]
rs72790424	0.82[EUR][1000 genomes]
rs72790426	0.82[EUR][1000 genomes]
rs72790443	0.86[EUR][1000 genomes]
rs7700469	0.81[AMR][1000 genomes];0.96[EUR][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	nsv1033607	chr5:126385181-127304459	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv1019821	chr5:126658200-126934917	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv537894	chr5:126658200-126934917	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1032587	chr5:126691103-126826978	Genic enhancers Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv830478	chr5:126721368-126937408	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:126742800-126782000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:126742800-126792400	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr5:126743000-126784800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr5:126755400-126774400	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr5:126756000-126770400	Weak transcription	Fetal Muscle Trunk	muscle
6	chr5:126759200-126774000	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr5:126760400-126778600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr5:126761000-126774800	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr5:126761000-126783400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr5:126761600-126774000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr5:126761800-126776600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr5:126761800-126779600	Weak transcription	Right Atrium	heart
13	chr5:126762800-126778400	Weak transcription	Pancreas	Pancrea
14	chr5:126763000-126770000	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr5:126763200-126770600	Enhancers	Brain Substantia Nigra	brain
16	chr5:126763400-126794000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr5:126764600-126770400	Weak transcription	HSMMtube	muscle
18	chr5:126765800-126782000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr5:126766000-126770200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr5:126766000-126770400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr5:126766200-126770400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr5:126768000-126773600	Weak transcription	Fetal Muscle Leg	muscle
23	chr5:126768200-126770400	Weak transcription	Brain Cingulate Gyrus	brain
24	chr5:126768200-126770400	Weak transcription	Brain Hippocampus Middle	brain
25	chr5:126768200-126776200	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr5:126768200-126782000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr5:126768600-126770400	Weak transcription	Brain Angular Gyrus	brain
28	chr5:126768800-126770000	Weak transcription	Fetal Stomach	stomach
29	chr5:126769200-126772200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr5:126769200-126775400	Weak transcription	Fetal Brain Male	brain
31	chr5:126769400-126774200	Weak transcription	Brain Anterior Caudate	brain

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