Variant report

Variant	rs182686405
Chromosome Location	chr3:53853269-53853270
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003621	chr3:53448934-54425322	Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv1001128	chr3:53659570-53927842	Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1013783	chr3:53694418-53934781	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv1003204	chr3:53820070-53877149	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv1002375	chr3:53822319-53872753	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv876803	chr3:53822893-53889849	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv518466	chr3:53832903-53882663	Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv521181	chr3:53833509-53881471	Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	nsv876804	chr3:53833509-53934171	Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
10	nsv1010575	chr3:53846741-53934781	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
11	nsv1006990	chr3:53849510-54285212	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
12	nsv997771	chr3:53852695-53926635	Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:53839200-53855200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr3:53839600-53876600	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr3:53840800-53853600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr3:53841600-53855600	Weak transcription	Right Ventricle	heart
5	chr3:53841600-53855800	Weak transcription	Right Atrium	heart
6	chr3:53841800-53853400	Weak transcription	Fetal Brain Female	brain
7	chr3:53841800-53853400	Weak transcription	GM12878-XiMat	blood
8	chr3:53842200-53857200	Strong transcription	Fetal Intestine Large	intestine
9	chr3:53842400-53855600	Weak transcription	Fetal Heart	heart
10	chr3:53846600-53879800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr3:53847000-53856400	Weak transcription	Brain Germinal Matrix	brain
12	chr3:53847000-53862000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr3:53849000-53857200	Strong transcription	Duodenum Mucosa	Duodenum
14	chr3:53849000-53857800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr3:53849000-53858200	Strong transcription	Fetal Stomach	stomach
16	chr3:53849000-53858800	Strong transcription	Liver	Liver
17	chr3:53849000-53859200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr3:53849000-53866800	Weak transcription	Stomach Mucosa	stomach
19	chr3:53849200-53853800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr3:53849600-53875400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr3:53850000-53855200	Strong transcription	Brain Inferior Temporal Lobe	brain
22	chr3:53850600-53857400	Strong transcription	Rectal Mucosa Donor 29	rectum
23	chr3:53850800-53854600	Strong transcription	Pancreatic Islets	Pancreatic Islet
24	chr3:53850800-53858600	Strong transcription	Gastric	stomach
25	chr3:53851000-53854400	Strong transcription	HUES6 Cell Line	embryonic stem cell
26	chr3:53851000-53858000	Strong transcription	Pancreas	Pancrea
27	chr3:53851200-53853400	Strong transcription	Colonic Mucosa	Colon
28	chr3:53851200-53854600	Strong transcription	HUES48 Cell Line	embryonic stem cell
29	chr3:53851200-53857400	Strong transcription	Rectal Mucosa Donor 31	rectum
30	chr3:53851200-53858000	Strong transcription	H1 Cell Line	embryonic stem cell
31	chr3:53851400-53854000	Strong transcription	H9 Cell Line	embryonic stem cell
32	chr3:53851400-53854400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
33	chr3:53851400-53855000	Strong transcription	Brain Hippocampus Middle	brain
34	chr3:53851600-53853400	Enhancers	Fetal Thymus	thymus
35	chr3:53851600-53853600	Strong transcription	Primary neutrophils fromperipheralblood	blood
36	chr3:53851600-53855000	Strong transcription	Brain Cingulate Gyrus	brain
37	chr3:53851600-53856000	Genic enhancers	HepG2	liver
38	chr3:53851600-53858000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr3:53851800-53853800	Strong transcription	Skeletal Muscle Male	skeletal muscle
40	chr3:53851800-53854600	Strong transcription	Brain Angular Gyrus	brain
41	chr3:53851800-53854600	Strong transcription	Brain Anterior Caudate	brain
42	chr3:53852000-53854600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr3:53852000-53856400	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr3:53852000-53857000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr3:53852200-53853400	Weak transcription	Esophagus	oesophagus
46	chr3:53852200-53853600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr3:53852200-53853800	Strong transcription	Skeletal Muscle Female	skeletal muscle
48	chr3:53852200-53855000	Strong transcription	Brain Substantia Nigra	brain
49	chr3:53852400-53853400	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr3:53852400-53865000	Weak transcription	Aorta	Aorta

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