Variant report

Variant	rs10052817
Chromosome Location	chr5:150941839-150941840
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:150939504..150942408-chr5:150945212..150947600,2	MCF-7	breast:
2	chr5:150933953..150936226-chr5:150941566..150943074,2	K562	blood:
3	chr5:150933361..150936096-chr5:150939863..150943066,3	K562	blood:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10054406	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10060613	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10060662	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10069540	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10069901	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10085060	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12055366	0.96[ASN][1000 genomes]
rs13158643	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1432862	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1541910	0.89[ASN][1000 genomes]
rs2163769	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2304053	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2304054	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28449749	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34335300	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34346367	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35908499	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35957412	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3734055	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3734057	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3734058	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3734059	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3734060	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4320248	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6859217	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6878528	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6878532	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6878556	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6878627	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6879740	0.86[ASN][1000 genomes]
rs6883153	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6883216	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6890712	0.87[AFR][1000 genomes]
rs7724472	0.90[ASN][1000 genomes]
rs7726769	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7727173	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9324698	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9324699	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9324700	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv20633	chr5:150941705-150955343	Strong transcription Enhancers Genic enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:150908200-150948000	Strong transcription	HMEC	breast
2	chr5:150908400-150944000	Strong transcription	NHEK	skin
3	chr5:150909200-150942400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr5:150911600-150942800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr5:150918200-150945400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr5:150931000-150942800	Weak transcription	Brain Angular Gyrus	brain
7	chr5:150934200-150949600	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr5:150937000-150948600	Weak transcription	Right Atrium	heart
9	chr5:150937600-150948600	Weak transcription	Adipose Nuclei	Adipose
10	chr5:150940800-150942600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr5:150940800-150943200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr5:150941400-150942200	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr5:150941400-150942600	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr5:150941600-150942000	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr5:150941600-150942200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr5:150941800-150942200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr5:150941800-150942200	Genic enhancers	Esophagus	oesophagus

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