Variant report

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10490844	1.00[CEU][hapmap]
rs1104799	0.82[ASN][1000 genomes]
rs1109959	1.00[CEU][hapmap]
rs17053459	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17053480	1.00[CEU][hapmap];0.86[CHB][hapmap]
rs2362424	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3774598	0.82[JPT][hapmap];0.85[EUR][1000 genomes]
rs3796346	1.00[CEU][hapmap]
rs3821864	1.00[CEU][hapmap];0.86[CHB][hapmap]
rs920253	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 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	nsv1002452	chr3:53742148-53802811	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:53768600-53801000	Strong transcription	Fetal Lung	lung
2	chr3:53773000-53807600	Strong transcription	Fetal Intestine Large	intestine
3	chr3:53774800-53807200	Strong transcription	Fetal Intestine Small	intestine
4	chr3:53778600-53806400	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr3:53778800-53797000	Weak transcription	Pancreas	Pancrea
6	chr3:53779000-53806400	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr3:53780400-53807000	Weak transcription	Fetal Brain Female	brain
8	chr3:53781800-53807400	Weak transcription	Brain Anterior Caudate	brain
9	chr3:53785000-53811200	Weak transcription	Spleen	Spleen
10	chr3:53785400-53795400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr3:53785800-53806600	Weak transcription	Brain Cingulate Gyrus	brain
12	chr3:53786000-53795600	Weak transcription	Brain Angular Gyrus	brain
13	chr3:53786000-53808200	Weak transcription	Liver	Liver
14	chr3:53788200-53797400	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr3:53788600-53795600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr3:53788800-53795200	Weak transcription	Duodenum Mucosa	Duodenum
17	chr3:53788800-53798400	Weak transcription	Lung	lung
18	chr3:53788800-53807000	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr3:53789400-53797600	Weak transcription	Fetal Brain Male	brain
20	chr3:53789800-53795600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr3:53789800-53814600	Weak transcription	Brain Substantia Nigra	brain

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