Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11807180	1.00[EUR][1000 genomes]
rs11807502	1.00[EUR][1000 genomes]
rs1340156	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1538765	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs17098321	1.00[EUR][1000 genomes]
rs17098354	1.00[EUR][1000 genomes]
rs17101286	1.00[EUR][1000 genomes]
rs17101443	1.00[EUR][1000 genomes]
rs17101553	1.00[EUR][1000 genomes]
rs17101560	1.00[EUR][1000 genomes]
rs17101563	1.00[EUR][1000 genomes]
rs17101578	1.00[EUR][1000 genomes]
rs17101728	1.00[EUR][1000 genomes]
rs17101736	1.00[EUR][1000 genomes]
rs17101744	1.00[EUR][1000 genomes]
rs532357	1.00[EUR][1000 genomes]
rs55717739	1.00[EUR][1000 genomes]
rs57065621	1.00[EUR][1000 genomes]
rs9628620	1.00[EUR][1000 genomes]
rs9628623	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013008	chr1:78463173-78958701	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv535012	chr1:78463173-78958701	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv871835	chr1:78528803-79501129	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 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	chr1:78747000-78754600	Weak transcription	NHDF-Ad	bronchial
2	chr1:78747400-78754000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr1:78751000-78754600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:78751400-78758200	Weak transcription	Liver	Liver
5	chr1:78751600-78753200	Enhancers	HUVEC	blood vessel
6	chr1:78752200-78752800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr1:78752200-78752800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr1:78752200-78752800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr1:78752200-78752800	Enhancers	Osteobl	bone
10	chr1:78752200-78753000	Enhancers	Muscle Satellite Cultured Cells	--
11	chr1:78752200-78753000	Enhancers	NH-A	brain
12	chr1:78752200-78753000	Enhancers	NHLF	lung
13	chr1:78752200-78753200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr1:78752200-78753400	Enhancers	Hela-S3	cervix
15	chr1:78752400-78752800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr1:78752400-78752800	Enhancers	HMEC	breast
17	chr1:78752600-78752800	Enhancers	Sigmoid Colon	Sigmoid Colon

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