Variant report

Variant	rs11617914
Chromosome Location	chr13:76436950-76436951
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs12859511	0.81[ASN][1000 genomes]
rs1323563	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1407963	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1407965	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1407966	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs8001647	0.82[ASN][1000 genomes]
rs9573672	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9670668	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]

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	nsv832646	chr13:76300428-76483102	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	esv2758333	chr13:76321610-76542003	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	esv2759950	chr13:76321610-76542003	Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv832649	chr13:76424872-76657891	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76413800-76437600	Strong transcription	HSMM	muscle
2	chr13:76417400-76443800	Weak transcription	Fetal Brain Female	brain
3	chr13:76417600-76437800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr13:76417600-76444600	Weak transcription	HMEC	breast
5	chr13:76417800-76438800	Weak transcription	A549	lung
6	chr13:76424400-76444200	Weak transcription	Fetal Lung	lung
7	chr13:76427400-76440800	Weak transcription	Ovary	ovary
8	chr13:76428000-76444600	Weak transcription	Fetal Kidney	kidney
9	chr13:76428000-76444800	Weak transcription	Esophagus	oesophagus
10	chr13:76428200-76437400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr13:76428200-76444400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr13:76428400-76444600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr13:76428400-76444600	Weak transcription	Fetal Heart	heart
14	chr13:76429600-76444600	Weak transcription	Fetal Muscle Trunk	muscle
15	chr13:76431000-76438400	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr13:76431000-76444600	Weak transcription	Aorta	Aorta
17	chr13:76431600-76437600	Weak transcription	Duodenum Mucosa	Duodenum
18	chr13:76431600-76444600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr13:76432000-76444600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr13:76432200-76438000	Weak transcription	Left Ventricle	heart
21	chr13:76432200-76438800	Weak transcription	HepG2	liver
22	chr13:76432200-76443600	Weak transcription	Primary T cells from cord blood	blood
23	chr13:76432200-76444200	Weak transcription	GM12878-XiMat	blood
24	chr13:76432200-76444600	Weak transcription	Fetal Intestine Small	intestine
25	chr13:76432200-76444600	Weak transcription	Fetal Muscle Leg	muscle
26	chr13:76432200-76444600	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr13:76432400-76437200	Weak transcription	Fetal Intestine Large	intestine
28	chr13:76433000-76444400	Weak transcription	Liver	Liver
29	chr13:76433400-76444200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr13:76434200-76437600	Weak transcription	Hela-S3	cervix
31	chr13:76434800-76437800	Genic enhancers	Osteobl	bone
32	chr13:76435000-76437400	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr13:76435000-76439000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr13:76435000-76443800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr13:76435200-76438000	Weak transcription	NH-A	brain
36	chr13:76435200-76444200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr13:76435400-76443200	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr13:76435600-76437600	Weak transcription	Placenta	Placenta
39	chr13:76435600-76444400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr13:76436000-76444000	Weak transcription	Fetal Thymus	thymus
41	chr13:76436400-76437200	Strong transcription	HSMMtube	muscle
42	chr13:76436600-76438200	Weak transcription	NHLF	lung
43	chr13:76436800-76437000	Enhancers	Psoas Muscle	Psoas
44	chr13:76436800-76437600	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr13:76436800-76437600	Weak transcription	NHDF-Ad	bronchial
46	chr13:76436800-76438000	Enhancers	Fetal Brain Male	brain
47	chr13:76436800-76439200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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