Variant report

Variant	rs10085055
Chromosome Location	chr5:106752322-106752323
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:106751855..106753579-chr5:106758119..106760914,2	MCF-7	breast:
2	chr5:106750740..106753168-chr5:106754133..106755799,2	K562	blood:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11242636	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11956440	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13178242	0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13182976	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1975009	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28683545	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34366978	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34583348	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35021422	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3756544	0.85[EUR][1000 genomes]
rs3776792	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3797514	0.85[EUR][1000 genomes]
rs3797516	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs3797517	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3797521	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3797527	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3822565	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3873122	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3873123	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58696640	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59863014	0.85[EUR][1000 genomes]
rs66505151	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6868410	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72785818	0.85[EUR][1000 genomes]
rs72785829	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7703776	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030118	chr5:106006097-106847949	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv1034276	chr5:106461538-106944163	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv537851	chr5:106461538-106944163	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	esv34018	chr5:106720912-107110506	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 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	chr5:106732200-106753200	Weak transcription	Fetal Kidney	kidney
2	chr5:106738800-106761600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:106739000-106754600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:106739000-106758200	Weak transcription	Left Ventricle	heart
5	chr5:106739600-106762600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr5:106741000-106758200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr5:106742000-106753800	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr5:106745000-106754000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr5:106745600-106758400	Weak transcription	Right Ventricle	heart
10	chr5:106745600-106758400	Weak transcription	HMEC	breast
11	chr5:106745800-106753800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr5:106746600-106753400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr5:106748400-106753000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:106750000-106758200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr5:106750000-106758400	Weak transcription	Aorta	Aorta
16	chr5:106751200-106753800	Enhancers	Muscle Satellite Cultured Cells	--
17	chr5:106751400-106752400	Enhancers	HSMM	muscle
18	chr5:106751400-106758000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr5:106751400-106759400	Enhancers	A549	lung
20	chr5:106751600-106752400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr5:106751600-106752600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr5:106751600-106753400	Enhancers	Fetal Heart	heart
23	chr5:106751600-106753400	Weak transcription	Fetal Lung	lung
24	chr5:106751600-106764400	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr5:106751800-106752600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr5:106751800-106758200	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr5:106751800-106765800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr5:106751800-106767800	Weak transcription	Stomach Mucosa	stomach
29	chr5:106752000-106752600	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr5:106752000-106761600	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr5:106752200-106752600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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