Variant report

Variant	rs9768020
Chromosome Location	chr7:98900165-98900166
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	chr7:98899578..98901452-chr7:98910011..98912501,2	MCF-7	breast:
2	chr7:98899191..98901926-chr7:98970485..98972382,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000130429	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs1002172	0.85[ASN][1000 genomes]
rs10155966	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10232076	0.88[ASN][1000 genomes]
rs10236149	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10243678	0.87[AMR][1000 genomes]
rs10249167	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10255399	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10258757	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10267346	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10270459	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10270917	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10272998	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10274407	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10953287	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11762273	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11771702	0.86[EUR][1000 genomes]
rs12112936	0.86[EUR][1000 genomes]
rs12113440	0.86[EUR][1000 genomes]
rs17161652	0.82[ASN][1000 genomes]
rs17161677	0.85[ASN][1000 genomes]
rs17161692	0.88[ASN][1000 genomes]
rs2072181	0.87[AMR][1000 genomes]
rs2107705	0.83[ASN][1000 genomes]
rs2286162	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2301889	0.89[ASN][1000 genomes]
rs2404323	0.86[AMR][1000 genomes]
rs28468623	0.89[ASN][1000 genomes]
rs28495024	0.83[AMR][1000 genomes]
rs28820905	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3801288	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs58421977	0.82[ASN][1000 genomes]
rs58660994	0.89[ASN][1000 genomes]
rs58999322	0.85[ASN][1000 genomes]
rs59725656	0.87[ASN][1000 genomes]
rs6943920	0.86[AMR][1000 genomes]
rs6948775	0.88[ASN][1000 genomes]
rs6953476	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6957987	0.85[EUR][1000 genomes]
rs6958704	0.86[EUR][1000 genomes]
rs6972337	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6973408	0.86[EUR][1000 genomes]
rs6975099	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73395547	0.89[ASN][1000 genomes]
rs73395557	0.89[ASN][1000 genomes]
rs73395580	0.88[ASN][1000 genomes]
rs733991	0.85[EUR][1000 genomes]
rs73709637	0.86[ASN][1000 genomes]
rs73709641	0.85[ASN][1000 genomes]
rs9641253	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9918551	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3433144	chr7:98777878-99060209	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers 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	62 gene(s)	inside rSNPs	diseases
2	nsv831068	chr7:98819572-99006481	Weak transcription Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9768020	ARPC1B	cis	Thyroid	GTEx

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:98873200-98905800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:98874800-98906800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr7:98890800-98905800	Weak transcription	Pancreas	Pancrea
4	chr7:98893200-98906600	Weak transcription	Fetal Intestine Small	intestine
5	chr7:98893800-98906000	Weak transcription	HMEC	breast
6	chr7:98897200-98903200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr7:98899200-98907800	Weak transcription	Aorta	Aorta
8	chr7:98899400-98901800	Weak transcription	Gastric	stomach
9	chr7:98899400-98907000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr7:98899400-98907200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr7:98899600-98900600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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