Variant report

Variant	rs3782991
Chromosome Location	chr13:96665390-96665391
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10454558	0.85[EUR][1000 genomes]
rs13378684	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28895285	0.90[AFR][1000 genomes]
rs35405829	0.95[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs3825423	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4406928	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs58509921	0.83[AFR][1000 genomes]
rs61152555	0.98[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs61422359	0.87[EUR][1000 genomes]
rs7318577	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7327257	0.82[CHB][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs7332461	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7988464	0.89[AFR][1000 genomes]
rs7990333	0.87[EUR][1000 genomes]
rs7990743	0.87[EUR][1000 genomes]
rs9584330	0.90[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs9584331	1.00[YRI][hapmap];0.95[AFR][1000 genomes]
rs9584332	0.82[CHB][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs9584335	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9590335	0.87[AFR][1000 genomes]
rs9590338	0.92[AFR][1000 genomes]
rs9590340	0.85[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs9590341	0.88[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs9590351	0.95[AFR][1000 genomes]
rs9590352	0.82[CHB][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs9590353	0.82[CHB][hapmap];0.94[YRI][hapmap];0.89[AFR][1000 genomes]
rs9590354	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9590356	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9590357	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9590359	0.96[ASN][1000 genomes]
rs9590361	0.85[EUR][1000 genomes]
rs9590362	0.85[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	nsv1050430	chr13:96508530-97020734	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv541883	chr13:96508530-97020734	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1041165	chr13:96522021-96966520	Enhancers Bivalent/Poised TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv1051574	chr13:96550653-96779248	Strong transcription Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv1040320	chr13:96573646-96790859	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv869471	chr13:96622327-97223956	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 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	chr13:96612200-96668600	Weak transcription	Pancreas	Pancrea
2	chr13:96613200-96694200	Weak transcription	A549	lung
3	chr13:96616200-96668600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr13:96616800-96668400	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr13:96621600-96668600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr13:96622000-96668600	Weak transcription	Aorta	Aorta
7	chr13:96622200-96668600	Weak transcription	Fetal Kidney	kidney
8	chr13:96622200-96671400	Weak transcription	Hela-S3	cervix
9	chr13:96622200-96677200	Weak transcription	NH-A	brain
10	chr13:96622400-96668200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr13:96623600-96668200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr13:96634800-96668200	Weak transcription	Fetal Stomach	stomach
13	chr13:96647600-96668200	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr13:96648000-96668200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr13:96648200-96668000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr13:96651000-96671800	Weak transcription	HSMM	muscle
17	chr13:96652600-96668400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr13:96652800-96668000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr13:96655400-96668400	Weak transcription	Fetal Brain Male	brain
20	chr13:96655600-96668000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr13:96656000-96668000	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr13:96656000-96668000	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr13:96656000-96668200	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr13:96656000-96668200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr13:96657600-96668600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr13:96657800-96668200	Weak transcription	Stomach Smooth Muscle	stomach
27	chr13:96657800-96677200	Weak transcription	HSMMtube	muscle
28	chr13:96658400-96668600	Weak transcription	Left Ventricle	heart
29	chr13:96658400-96668600	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr13:96659200-96668200	Weak transcription	Brain Germinal Matrix	brain
31	chr13:96659400-96668200	Weak transcription	Fetal Intestine Large	intestine
32	chr13:96659400-96672600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr13:96660200-96682200	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr13:96660400-96668000	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr13:96660400-96668600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr13:96660400-96678600	Weak transcription	Duodenum Mucosa	Duodenum
37	chr13:96660600-96676600	Weak transcription	Osteobl	bone
38	chr13:96660800-96668600	Weak transcription	Ovary	ovary
39	chr13:96660800-96672600	Weak transcription	Liver	Liver
40	chr13:96660800-96684800	Weak transcription	Psoas Muscle	Psoas
41	chr13:96661000-96668000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr13:96661000-96668000	Weak transcription	Fetal Lung	lung
43	chr13:96661000-96668200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr13:96661200-96668200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr13:96661200-96669200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr13:96661400-96668000	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr13:96661400-96668000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr13:96661400-96668400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr13:96661600-96668200	Weak transcription	Fetal Muscle Leg	muscle
50	chr13:96662800-96668000	Weak transcription	Adipose Nuclei	Adipose

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