Variant report

Variant	rs67778216
Chromosome Location	chr3:101650205-101650206
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs1611792	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1615244	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1616007	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1620838	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1622608	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1626282	0.83[ASN][1000 genomes]
rs1672375	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1672394	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1672395	0.80[ASN][1000 genomes]
rs1672396	0.80[ASN][1000 genomes]
rs1707601	0.82[AMR][1000 genomes]
rs1707602	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1707603	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1707606	0.87[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1707607	0.81[ASN][1000 genomes]
rs1707614	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1707616	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1707617	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2203234	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2203235	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2221909	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2942708	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2942715	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2942716	0.82[ASN][1000 genomes]
rs2951443	0.83[ASN][1000 genomes]
rs2951446	0.83[ASN][1000 genomes]
rs2951449	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34922383	0.81[ASN][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	nsv497784	chr3:101315009-102092989	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	esv3351469	chr3:101511702-101866448	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	nsv1010762	chr3:101584836-101803821	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:101643600-101654000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr3:101643800-101658400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr3:101644000-101654400	Weak transcription	Primary B cells from cord blood	blood
4	chr3:101644400-101651600	Weak transcription	Esophagus	oesophagus
5	chr3:101644600-101652800	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr3:101644800-101654000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr3:101645800-101650800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr3:101648200-101655600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr3:101648400-101651200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr3:101648400-101654400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr3:101648400-101655000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr3:101648400-101655400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr3:101648400-101655600	Weak transcription	NHLF	lung
14	chr3:101648600-101651600	Weak transcription	NHDF-Ad	bronchial
15	chr3:101648600-101654800	Weak transcription	Osteobl	bone
16	chr3:101648600-101655600	Weak transcription	Hela-S3	cervix
17	chr3:101648800-101651200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr3:101648800-101651200	Weak transcription	Fetal Muscle Leg	muscle
19	chr3:101648800-101651200	Weak transcription	HSMMtube	muscle
20	chr3:101648800-101655600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr3:101648800-101655600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr3:101649000-101650800	Weak transcription	HSMM	muscle
23	chr3:101649000-101651200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr3:101649000-101651200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr3:101649200-101650800	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr3:101649600-101653200	Weak transcription	Primary monocytes fromperipheralblood	blood

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