Variant report

Variant	rs570455272
Chromosome Location	chr14:25364535-25364536
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

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	nsv1041336	chr14:24726564-25527319	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv542000	chr14:24726564-25527319	Genic enhancers Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv901504	chr14:25184210-25646203	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv901506	chr14:25295551-25377188	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1041445	chr14:25326692-25388290	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv12764	chr14:25364369-25365119	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:25350600-25364600	Weak transcription	NHDF-Ad	bronchial
2	chr14:25358400-25369800	Weak transcription	HSMM	muscle
3	chr14:25359200-25369000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr14:25360400-25364600	Weak transcription	Psoas Muscle	Psoas
5	chr14:25360600-25369200	Weak transcription	Fetal Lung	lung
6	chr14:25362200-25364600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr14:25362200-25369400	Weak transcription	Fetal Muscle Leg	muscle
8	chr14:25362400-25378400	Weak transcription	Lung	lung
9	chr14:25362600-25364600	Weak transcription	Brain Cingulate Gyrus	brain
10	chr14:25362800-25364600	Weak transcription	Pancreas	Pancrea
11	chr14:25363400-25365400	Enhancers	Right Ventricle	heart
12	chr14:25363400-25366000	Enhancers	Brain Substantia Nigra	brain
13	chr14:25363600-25364600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr14:25363600-25364800	Enhancers	Fetal Intestine Small	intestine
15	chr14:25363600-25365400	Enhancers	Brain Anterior Caudate	brain
16	chr14:25363600-25365600	Enhancers	Left Ventricle	heart
17	chr14:25363800-25364600	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr14:25363800-25365200	Enhancers	Brain Hippocampus Middle	brain
19	chr14:25364000-25365000	Enhancers	Colon Smooth Muscle	Colon
20	chr14:25364000-25367400	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr14:25364400-25364600	Enhancers	Brain Angular Gyrus	brain
22	chr14:25364400-25364800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr14:25364400-25364800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr14:25364400-25364800	Enhancers	Right Atrium	heart
25	chr14:25364400-25365000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr14:25364400-25366200	Enhancers	Fetal Heart	heart

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