Variant report

Variant	rs2851282
Chromosome Location	chr4:100018169-100018170
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs1133485	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1154405	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1154406	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1154407	0.82[AMR][1000 genomes]
rs1154410	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12506256	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1311615	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1311616	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1311617	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1311618	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1311619	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1377689	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1453873	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1453874	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1840228	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1840230	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1840231	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2034696	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2602837	0.92[AMR][1000 genomes]
rs2602842	0.81[AMR][1000 genomes]
rs2602845	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2602846	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2602847	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2602855	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2602858	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2602859	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2602865	0.81[AMR][1000 genomes]
rs2602866	0.81[AMR][1000 genomes]
rs2602873	0.81[AMR][1000 genomes]
rs2602876	0.83[AMR][1000 genomes]
rs2602877	0.83[AMR][1000 genomes]
rs2602878	0.83[AMR][1000 genomes]
rs2851256	0.81[AMR][1000 genomes]
rs2851257	0.81[AMR][1000 genomes]
rs2851260	0.81[AMR][1000 genomes]
rs2851263	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2851265	0.84[AMR][1000 genomes]
rs2851266	0.82[EUR][1000 genomes]
rs2851267	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2851268	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2851269	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2851272	0.83[EUR][1000 genomes]
rs2851277	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2851278	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2851283	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2851285	0.83[AMR][1000 genomes]
rs2851286	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2924580	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3018047	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3018048	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3100629	0.86[AMR][1000 genomes]
rs3133153	0.81[AMR][1000 genomes]
rs4235436	0.81[AMR][1000 genomes]
rs6532779	0.82[EUR][1000 genomes]
rs6822830	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6831225	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9761048	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009017	chr4:99669441-100406394	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	nsv1002927	chr4:99952472-100148690	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv879656	chr4:99976646-100533722	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers 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	36 gene(s)	inside rSNPs	diseases
4	nsv1005446	chr4:99988287-100121669	Strong transcription Enhancers ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
5	nsv537196	chr4:99988287-100121669	Strong transcription ZNF genes & repeats Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
6	esv1849572	chr4:100007243-100024396	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2851282	ADH5	cis	Whole Blood	GTEx

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100011400-100025800	Weak transcription	Esophagus	oesophagus
2	chr4:100011600-100025600	Weak transcription	Primary T cells from cord blood	blood
3	chr4:100011800-100020600	Weak transcription	Fetal Intestine Small	intestine
4	chr4:100012800-100063800	Weak transcription	Aorta	Aorta
5	chr4:100013000-100020200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr4:100014000-100022000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:100014400-100021200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr4:100014400-100024000	Weak transcription	HMEC	breast

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