Variant report

Variant	rs7653869
Chromosome Location	chr3:98692137-98692138
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs13321323	1.00[EUR][1000 genomes]
rs2949162	1.00[EUR][1000 genomes]
rs6800403	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7634027	1.00[AMR][1000 genomes]
rs7638893	1.00[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	nsv591065	chr3:98204198-98766326	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv1007140	chr3:98421229-99202458	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription 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	17 gene(s)	inside rSNPs	diseases
3	nsv536663	chr3:98421229-99202458	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv877214	chr3:98445324-98738006	Enhancers Genic enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
5	nsv1007486	chr3:98597738-99249081	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers 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	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:98690800-98692200	Enhancers	HUVEC	blood vessel
2	chr3:98690800-98692800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr3:98691000-98693600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr3:98691000-98696200	Weak transcription	Hela-S3	cervix
5	chr3:98691400-98696400	Weak transcription	HSMM	muscle
6	chr3:98691600-98693600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr3:98691600-98696400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr3:98691800-98696000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr3:98691800-98696400	Weak transcription	NHLF	lung
10	chr3:98692000-98692600	Weak transcription	A549	lung
11	chr3:98692000-98692800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr3:98692000-98692800	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr3:98692000-98692800	Weak transcription	NHDF-Ad	bronchial
14	chr3:98692000-98693000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr3:98692000-98695000	Weak transcription	HMEC	breast
16	chr3:98692000-98695200	Weak transcription	NH-A	brain
17	chr3:98692000-98695400	Weak transcription	Osteobl	bone
18	chr3:98692000-98696000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr3:98692000-98696000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr3:98692000-98696200	Weak transcription	NHEK	skin
21	chr3:98692000-98696400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr3:98692000-98699600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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