Variant report

Variant	rs73367074
Chromosome Location	chr14:104289238-104289239
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11623518	0.83[EUR][1000 genomes]
rs11625216	0.96[EUR][1000 genomes]
rs11625521	0.81[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs11625613	0.81[EUR][1000 genomes]
rs11625676	0.83[EUR][1000 genomes]
rs11626714	0.81[EUR][1000 genomes]
rs11627337	0.91[EUR][1000 genomes]
rs11851462	0.85[EUR][1000 genomes]
rs12432763	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12435668	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12436297	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17101871	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs45604035	0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4641668	0.83[EUR][1000 genomes]
rs56971743	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs57560950	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs57952067	0.83[EUR][1000 genomes]
rs58369398	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs58411502	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59320483	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs60431526	0.83[EUR][1000 genomes]
rs73350555	0.86[EUR][1000 genomes]
rs73350563	0.81[EUR][1000 genomes]
rs8006493	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8016928	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3332028	chr14:103581471-104328811	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
2	nsv1045162	chr14:104140525-104594841	Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv542204	chr14:104140525-104594841	Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
4	esv2758368	chr14:104147525-104412813	Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
5	esv2760013	chr14:104147525-104412813	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
6	nsv902313	chr14:104162263-104378087	Bivalent Enhancer Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
7	nsv902318	chr14:104255083-104464809	Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
8	nsv902319	chr14:104255083-104620077	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	64 gene(s)	inside rSNPs	diseases
9	nsv902320	chr14:104274294-104308095	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	esv1838047	chr14:104283104-104359121	Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
11	nsv902321	chr14:104283104-104378087	Strong transcription Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	23 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	chr14:104280800-104294800	Weak transcription	Small Intestine	intestine
2	chr14:104286200-104294800	Weak transcription	Rectal Smooth Muscle	rectum
3	chr14:104286600-104291400	Weak transcription	Fetal Intestine Large	intestine
4	chr14:104286600-104294800	Weak transcription	Brain Angular Gyrus	brain
5	chr14:104286600-104303400	Weak transcription	Spleen	Spleen
6	chr14:104286800-104289600	Weak transcription	Stomach Mucosa	stomach
7	chr14:104286800-104291200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr14:104286800-104291200	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr14:104286800-104291200	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr14:104287000-104289600	Weak transcription	Right Atrium	heart
11	chr14:104287000-104294800	Weak transcription	Adipose Nuclei	Adipose
12	chr14:104287200-104291000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr14:104287200-104291400	Weak transcription	Fetal Intestine Small	intestine
14	chr14:104287200-104291400	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr14:104287200-104294800	Weak transcription	Ovary	ovary
16	chr14:104287200-104294800	Weak transcription	Right Ventricle	heart
17	chr14:104287400-104290200	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr14:104287400-104291200	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr14:104287400-104291400	Weak transcription	Fetal Kidney	kidney
20	chr14:104287600-104291200	Weak transcription	Liver	Liver
21	chr14:104287600-104294800	Weak transcription	Fetal Lung	lung
22	chr14:104288000-104292400	Weak transcription	Left Ventricle	heart
23	chr14:104288400-104289800	Weak transcription	HepG2	liver
24	chr14:104288400-104291200	Weak transcription	Duodenum Mucosa	Duodenum
25	chr14:104289200-104290200	Enhancers	Pancreas	Pancrea
26	chr14:104289200-104292800	Enhancers	Fetal Heart	heart

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