Variant report

Variant	rs578124135
Chromosome Location	chr11:76360807-76360808
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043912	chr11:76301316-76439095	Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1039451	chr11:76301316-76440221	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	esv1810781	chr11:76311021-76464814	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv555448	chr11:76354115-76383806	Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
5	nsv527708	chr11:76359722-76363817	Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76350800-76365000	Weak transcription	Lung	lung
2	chr11:76359200-76364800	Weak transcription	Right Atrium	heart
3	chr11:76359400-76361600	Enhancers	Fetal Muscle Leg	muscle
4	chr11:76360000-76362400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr11:76360200-76361400	Enhancers	Fetal Lung	lung
6	chr11:76360200-76361800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr11:76360200-76361800	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr11:76360400-76361600	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr11:76360400-76362400	Enhancers	Adipose Nuclei	Adipose
10	chr11:76360600-76361200	Weak transcription	Fetal Stomach	stomach
11	chr11:76360800-76361000	Enhancers	Colonic Mucosa	Colon
12	chr11:76360800-76361400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr11:76360800-76361400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr11:76360800-76361400	Enhancers	Aorta	Aorta
15	chr11:76360800-76361400	Enhancers	Fetal Kidney	kidney
16	chr11:76360800-76361400	Enhancers	Fetal Muscle Trunk	muscle
17	chr11:76360800-76361400	Enhancers	Left Ventricle	heart
18	chr11:76360800-76361400	Enhancers	Right Ventricle	heart
19	chr11:76360800-76361400	Enhancers	Stomach Smooth Muscle	stomach
20	chr11:76360800-76361600	Enhancers	Ovary	ovary

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