Variant report

Variant	rs6822381
Chromosome Location	chr4:47522811-47522812
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11938614	0.88[AFR][1000 genomes]
rs4305497	0.88[AFR][1000 genomes]
rs4695241	0.88[AFR][1000 genomes]
rs6447563	0.88[AFR][1000 genomes]
rs6835123	0.84[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879005	chr4:47408838-47548254	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv829923	chr4:47436139-47678443	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv1008515	chr4:47488431-47906835	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv948568	chr4:47488431-47907524	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv1004939	chr4:47488573-47901460	Bivalent Enhancer Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS 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 miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv537080	chr4:47488573-47901460	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv997471	chr4:47489412-47895223	Weak transcription Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
8	nsv998892	chr4:47493552-47863354	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
9	nsv537081	chr4:47493552-47863354	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
10	nsv1000337	chr4:47493907-47902019	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:47488000-47533800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:47488600-47524600	Weak transcription	Fetal Intestine Small	intestine
3	chr4:47488800-47559800	Weak transcription	Right Ventricle	heart
4	chr4:47489200-47533600	Weak transcription	Esophagus	oesophagus
5	chr4:47501000-47527600	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr4:47502200-47533000	Weak transcription	Rectal Smooth Muscle	rectum
7	chr4:47507800-47526400	Weak transcription	NHDF-Ad	bronchial
8	chr4:47507800-47527800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr4:47510000-47526000	Weak transcription	Pancreas	Pancrea
10	chr4:47512200-47536800	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr4:47512400-47530200	Weak transcription	Fetal Brain Male	brain
12	chr4:47512400-47577200	Weak transcription	Small Intestine	intestine
13	chr4:47512800-47532600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr4:47513000-47527600	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr4:47513600-47533200	Weak transcription	Brain Substantia Nigra	brain
16	chr4:47513800-47530600	Weak transcription	Fetal Heart	heart
17	chr4:47513800-47534000	Weak transcription	Brain Hippocampus Middle	brain
18	chr4:47514000-47524200	Weak transcription	Liver	Liver
19	chr4:47514000-47531400	Weak transcription	Brain Anterior Caudate	brain
20	chr4:47514000-47551000	Weak transcription	Gastric	stomach
21	chr4:47514200-47533800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr4:47515400-47524400	Weak transcription	Fetal Stomach	stomach
23	chr4:47515800-47527800	Weak transcription	Aorta	Aorta
24	chr4:47515800-47530000	Weak transcription	Primary T cells from cord blood	blood
25	chr4:47515800-47531200	Weak transcription	Colon Smooth Muscle	Colon
26	chr4:47515800-47533800	Weak transcription	Brain Cingulate Gyrus	brain
27	chr4:47515800-47533800	Weak transcription	Lung	lung
28	chr4:47516000-47524200	Weak transcription	Fetal Muscle Trunk	muscle
29	chr4:47516000-47525000	Weak transcription	Fetal Kidney	kidney
30	chr4:47516000-47525600	Weak transcription	NHLF	lung
31	chr4:47516000-47527400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr4:47516000-47529600	Weak transcription	Fetal Muscle Leg	muscle
33	chr4:47516000-47534000	Weak transcription	Stomach Mucosa	stomach
34	chr4:47516200-47524200	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr4:47516200-47524200	Weak transcription	Left Ventricle	heart
36	chr4:47516200-47525800	Weak transcription	Stomach Smooth Muscle	stomach
37	chr4:47516200-47526200	Weak transcription	Fetal Lung	lung
38	chr4:47516200-47527800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr4:47516400-47523200	Weak transcription	Duodenum Mucosa	Duodenum
40	chr4:47516400-47547800	Weak transcription	Ovary	ovary
41	chr4:47516400-47548200	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr4:47516600-47527800	Weak transcription	Fetal Intestine Large	intestine
43	chr4:47517600-47524800	Weak transcription	Adipose Nuclei	Adipose
44	chr4:47517800-47525000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr4:47517800-47528800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr4:47518000-47523000	Weak transcription	NH-A	brain
47	chr4:47518000-47525600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr4:47518000-47526400	Weak transcription	NHEK	skin
49	chr4:47518000-47527200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr4:47518000-47527800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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