Variant report

Variant	rs1333363
Chromosome Location	chr13:38275877-38275878
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs1298657	1.00[AMR][1000 genomes]
rs1333355	1.00[AMR][1000 genomes]
rs1333356	1.00[AMR][1000 genomes]
rs1333357	1.00[AMR][1000 genomes]
rs1413000	1.00[AMR][1000 genomes]
rs1415600	1.00[AMR][1000 genomes]
rs1475245	1.00[AMR][1000 genomes]
rs1538141	1.00[AMR][1000 genomes]
rs1538147	1.00[AMR][1000 genomes]
rs1538150	1.00[AMR][1000 genomes]
rs1538151	1.00[AMR][1000 genomes]
rs1570610	1.00[CEU][hapmap];1.00[AMR][1000 genomes]
rs1577008	1.00[AMR][1000 genomes]
rs17056136	1.00[CEU][hapmap]
rs17056209	1.00[CEU][hapmap]
rs1924282	1.00[AMR][1000 genomes]
rs1924284	1.00[AMR][1000 genomes]
rs1924287	1.00[AMR][1000 genomes]
rs1924294	1.00[AMR][1000 genomes]
rs1924297	1.00[AMR][1000 genomes]
rs1924305	1.00[CEU][hapmap];1.00[AMR][1000 genomes]
rs1924308	1.00[CEU][hapmap];1.00[AMR][1000 genomes]
rs1981057	1.00[AMR][1000 genomes]
rs2031272	1.00[AMR][1000 genomes]
rs2031273	1.00[AMR][1000 genomes]
rs2181773	1.00[CEU][hapmap]
rs2957213	1.00[AMR][1000 genomes]
rs2985157	1.00[AMR][1000 genomes]
rs2985158	1.00[AMR][1000 genomes]
rs2985166	1.00[AMR][1000 genomes]
rs2985171	1.00[CEU][hapmap];1.00[AMR][1000 genomes]
rs2985172	1.00[CEU][hapmap];1.00[AMR][1000 genomes]
rs4343144	1.00[AMR][1000 genomes]
rs4418936	1.00[AMR][1000 genomes]
rs4480663	1.00[AMR][1000 genomes]
rs4485231	1.00[AMR][1000 genomes]
rs4595666	1.00[AMR][1000 genomes]
rs4943530	1.00[AMR][1000 genomes]
rs545636	1.00[AMR][1000 genomes]
rs604068	1.00[CEU][hapmap]
rs615491	1.00[AMR][1000 genomes]
rs6563568	1.00[CEU][hapmap];1.00[AMR][1000 genomes]
rs662478	1.00[AMR][1000 genomes]
rs669862	1.00[AMR][1000 genomes]
rs7334202	1.00[AMR][1000 genomes]
rs7984439	1.00[AMR][1000 genomes]
rs7989413	1.00[AMR][1000 genomes]
rs7990804	1.00[AMR][1000 genomes]
rs8002347	1.00[AMR][1000 genomes]
rs817616	1.00[AMR][1000 genomes]
rs860144	1.00[AMR][1000 genomes]
rs912386	1.00[AMR][1000 genomes]
rs9285117	1.00[AMR][1000 genomes]
rs9315519	1.00[AMR][1000 genomes]
rs9547981	1.00[AMR][1000 genomes]
rs9547989	1.00[AMR][1000 genomes]
rs9548002	1.00[CEU][hapmap];1.00[AMR][1000 genomes]
rs9548019	1.00[AMR][1000 genomes]
rs959269	1.00[AMR][1000 genomes]
rs9603229	1.00[AMR][1000 genomes]
rs963953	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	nsv948975	chr13:37281203-38280430	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	esv34109	chr13:37843819-38276391	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv1045716	chr13:37952062-38394595	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv915901	chr13:38199035-39032633	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:38257400-38282000	Weak transcription	Ovary	ovary
2	chr13:38273600-38277600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr13:38273800-38276800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr13:38274000-38277000	Enhancers	NHLF	lung
5	chr13:38274000-38277200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr13:38274000-38277200	Enhancers	HSMMtube	muscle
7	chr13:38274000-38277800	Enhancers	NHDF-Ad	bronchial
8	chr13:38274400-38276800	Enhancers	NH-A	brain
9	chr13:38275200-38276200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr13:38275200-38277200	Enhancers	HSMM	muscle
11	chr13:38275600-38276000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr13:38275600-38276000	Enhancers	Adipose Nuclei	Adipose
13	chr13:38275600-38276000	Flanking Active TSS	Osteobl	bone
14	chr13:38275600-38276400	Enhancers	Rectal Smooth Muscle	rectum
15	chr13:38275600-38276400	Enhancers	Stomach Smooth Muscle	stomach
16	chr13:38275600-38276600	Enhancers	HUVEC	blood vessel
17	chr13:38275800-38277400	Enhancers	Muscle Satellite Cultured Cells	--

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