Variant report

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	nsv1045035	chr14:32986003-33543227	Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv542021	chr14:32986003-33543227	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv428624	chr14:33065571-33214223	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv832765	chr14:33188170-33367348	Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	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	chr14:33172600-33191600	Weak transcription	Psoas Muscle	Psoas
2	chr14:33173200-33194800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr14:33178800-33191600	Weak transcription	Right Ventricle	heart
4	chr14:33179000-33193400	Weak transcription	HSMMtube	muscle
5	chr14:33180400-33193400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr14:33180600-33191800	Weak transcription	Left Ventricle	heart
7	chr14:33180600-33193800	Weak transcription	Fetal Stomach	stomach
8	chr14:33180800-33194600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr14:33181000-33193000	Weak transcription	Brain Substantia Nigra	brain
10	chr14:33183400-33193000	Weak transcription	Brain Anterior Caudate	brain
11	chr14:33183600-33194000	Weak transcription	Aorta	Aorta
12	chr14:33186200-33196200	Enhancers	Fetal Heart	heart
13	chr14:33188600-33193000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr14:33189000-33190200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr14:33189000-33193600	Weak transcription	Brain Angular Gyrus	brain
16	chr14:33189200-33198000	Weak transcription	Fetal Brain Female	brain
17	chr14:33189800-33190200	Enhancers	Fetal Muscle Leg	muscle
18	chr14:33189800-33190600	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr14:33190000-33190400	Enhancers	Brain Hippocampus Middle	brain
20	chr14:33190000-33190600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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